[go: up one dir, main page]

EP2111104A2 - Oil suspension concentrate with micro-encapsulated agrochemical active ingredients - Google Patents

Oil suspension concentrate with micro-encapsulated agrochemical active ingredients

Info

Publication number
EP2111104A2
EP2111104A2 EP08701053A EP08701053A EP2111104A2 EP 2111104 A2 EP2111104 A2 EP 2111104A2 EP 08701053 A EP08701053 A EP 08701053A EP 08701053 A EP08701053 A EP 08701053A EP 2111104 A2 EP2111104 A2 EP 2111104A2
Authority
EP
European Patent Office
Prior art keywords
alkyl
methyl
active ingredients
suspension concentrate
oil suspension
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP08701053A
Other languages
German (de)
French (fr)
Inventor
Ralph Grohs
Roland Deckwer
Frank Rosenfeldt
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Bayer CropScience AG
Original Assignee
Bayer CropScience AG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Bayer CropScience AG filed Critical Bayer CropScience AG
Priority to EP08701053A priority Critical patent/EP2111104A2/en
Publication of EP2111104A2 publication Critical patent/EP2111104A2/en
Withdrawn legal-status Critical Current

Links

Classifications

    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
    • A01N25/04—Dispersions, emulsions, suspoemulsions, suspension concentrates or gels
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/26—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests in coated particulate form
    • A01N25/28—Microcapsules or nanocapsules
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
    • A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
    • A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
    • A01N47/38—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< where at least one nitrogen atom is part of a heterocyclic ring; Thio analogues thereof

Definitions

  • Oil suspension concentrate with microencapsulated agrochemical active ingredients Oil suspension concentrate with microencapsulated agrochemical active ingredients
  • the invention relates to oil suspension concentrates for crop protection and agrochemical active substances contained therein, which are present in encapsulated form.
  • Microcapsule is therefore to be distinguished from other forms of formulations such as emulsion, microsphere, liposome, since these do not have the physical separation characteristic of liquids through a wall made of polymers.
  • oil-in-water microencapsulation there is an oil-in-water emulsion, i. the water-immiscible or water-insoluble material is surrounded by the polymer material of the microcapsule.
  • the aqueous phase is inside the microcapsule. It is therefore also referred to as "inverse microencapsulation”.
  • the present invention predominantly uses water-in-oil microencapsulation unless the multi-microencapsulation process is employed.
  • MuJti microencapsulation a distinction must be made between “water-in-oil-in-water microencapsulation” and “water-in-oil-in-oil microencapsulation”.
  • the implementation of both techniques is possible, wherein the water-in-oil-in-oil microencapsulation is in the foreground.
  • the mentioned forms of microencapsulation are appropriate
  • the formation of the microcapsules takes place from the monomers and prepolymers contained in the oil droplets under the influence of heat and / or by pH change and / or by mechanical stirring.
  • the respective treatment causes the polymerization of the monomer or the prepolymers.
  • EP 1 282 353 B1 discloses the combination of pesticides with organic or inorganic carrier materials for the controlled release of the active ingredients, whereby the use of the oil-in-water microencapsulation is also provided.
  • the disclosed combinations allow for the suppression of antagonization of other drugs in admixture therewith and, at the same time, eliminate the need for time and labor intensive splinter applications.
  • the problem of chemical incompatibility between drugs is not the subject of EP 1 282 353 B1.
  • Water-in-oil microcapsules are prepared from a water-in-oil emulsion by the "water-in-oil process.” Such a process is disclosed in US Patent US 4,157,983 A corresponding process using two monomers and prepolymers is in US Pat. No. 4,534,783.
  • a process for multiple microencapsulation is disclosed in WO 2005/058476 A1. It is a continuous process for microencapsulation of water-in-oil-in-water by in situ interfacial polymerization of the corresponding emulsion.
  • the active compounds included in the microcapsules are beneficial to health and suitable for other biological purposes.
  • the use of the method for the formulation of agrochemical active substances or for the solution of the problem of chemical incompatibility between agrochemical active ingredients is not provided for.
  • Another particular method for "water-in-oil microencapsulation" is disclosed in WO 98/28957 A.
  • the wall of the microcapsules in the presence of an active surface proton transfer proton catalyst by in situ self-condensation of prepolymers which
  • Oil-soluble herbicides include EPTC, butylates, cycloates, molinates, vernolates, acetochlor, metolachlor, alachlor, butachlor, propachlor and trifluralin.
  • the hydrolysis sensitivity always has to be considered when formulating active substances from the class of sulfonylureas.
  • Their chemical stability is very well ensured by the previously established forumulation techniques, provided that the sulfonylureas are used as a single active ingredient or in combination with other sulfonylureas or with safener.
  • a challenge remains the formulation of sulfonylureas in combination with active ingredients or excipients whose structure has an acid function and / or free OH groups.
  • Agents known for their hydrolysis-inducing potential over sulfonylureas are e.g. Glufosinate and glyphosate.
  • the low pH of glyphosate ( ⁇ 7) is detrimental to those sulfonylureas that are stable in the basic range.
  • the chemical incompatibility of drugs is a complex problem.
  • the stability of the active ingredient after dilution of the concentrate in the spray tank can be a problem.
  • the crystallization must be prevented and the distributability and the biological activity of the active ingredient must be ensured.
  • the object of the present invention was to provide an improved, liquid crop protection agent formulation having at least two agrochemical active ingredients, wherein each active ingredient, in particular the chemically unstable active ingredients contained in the formulation, and the formulation as a whole, a high chemical and physical stability and a have high biological effectiveness and crop plant compatibility.
  • This also generally includes the avoidance of antagonistic inactivity or overdose, which otherwise necessitates the application of splinter applications.
  • the present invention thus relates to an oil suspension concentrate containing
  • the core idea of the alternatives is to protect the more hydrolysis-sensitive active ingredient in the case of a combination of active ingredients, in any case in a microencapsulated form, another active ingredient which possibly has a hydrolysis-inducing potential.
  • oil suspension concentrates which contain at least two different agrochemical active substances, at least one of which is water-soluble and is present inside a microcapsule. At least one other, i. the active ingredient present in (b), dispersed or dissolved in the oil phase, is also encapsulated.
  • At least two active substances which differ, for example, in their solubility and / or in their hydrolysis sensitivity are microencapsulated.
  • the hydrolysis-sensitive active ingredient is additionally protected, in front of the active ingredient, which is also present in microencapsulated form due to its hydrolysis-inducing potential.
  • the additional microencapsulation of the active ingredients dispersed or dissolved better in the oil phase can additionally have the advantage that, due to the delayed release of the differently encapsulated active ingredients, splinter applications can be avoided.
  • an oil suspension concentrate which contains at least two different agrochemical active ingredients, at least one of which is present in the interior of a microcapsule and at least one in non-encapsulated form in the oil phase, wherein the present in non-encapsulated form in the oil phase active ingredient Acetolactate synthase (ALS) inhibitor.
  • ALS Acetolactate synthase
  • the third alternative uses an oil suspension concentrate containing at least two different agrochemically active compounds, at least one of which is present inside a microcapsule and at least one in an unencapsulated form in the oil phase, where the microencapsulated agent is an acetolactate synthase (ALS) inhibitor and the active ingredient having high hydrolysis-inducing potential is present in non-encapsulated form in the oil phase. That According to the approach of the third alternative, the additional microencapsulation of the hydrolysis-inducing active ingredients is dispensed with.
  • ALS acetolactate synthase
  • an oil suspension concentrate which contains at least two different agrochemical active ingredients, at least one of which is present in the interior of a microcapsule and at least one in non-encapsulated form in the oil phase, wherein in non-encapsulated form in the oil phase present active substance is a phosphorus-containing herbicide.
  • the active substances were treated according to the multi-microencapsulation method in WO 2005/058476 A1 and are present in appropriate form.
  • the most sensitive to hydrolysis active ingredient, however, is in the oil phase of the oil suspension concentrate, because there is the best protected.
  • the oil suspension concentrate contains at least two different agrochemical active ingredients, wherein at least one active ingredient is water-soluble and at least one active ingredient is dispersed or dissolved in the oil phase and the active ingredients have been treated according to a multi-microencapsulation method and present in appropriate form.
  • the class of compounds of the sulfonylureas belongs to their mode of action according to the group of ALS inhibitors. These inhibit the enzyme acetolactate synthase (ALS) and thus the protein synthesis in the plants.
  • ALS acetolactate synthase
  • oil suspension concentrate oil dispersion
  • OD oil dispersion
  • One or more active substances or safeners are suspended in the organic solvent. In this case, further active ingredients or safeners may be dissolved in the organic solvent.
  • agrochemical active ingredient in the context of this invention includes herbicides, plant growth regulators, safeners. That
  • the oil suspension concentrates according to the invention may also contain one or more safeners, it being possible for the safener to be present in microencapsulated form in addition to the active substance. Possible safeners are mentioned below by way of example in connection with the agrochemical active ingredients.
  • the oil suspension concentrates according to the invention may contain one or more inorganic salts as well as customary auxiliaries and additives.
  • herbicides examples include: herbicides
  • herbicides are e.g. ALS inhibitors (acetolactate synthetase inhibitors) or herbicides from the group of carbamates, thiocarbamates, haloacetanilides, substituted phenoxy, naphthoxy and phenoxyphenoxycarboxylic acid derivatives and heteroaryloxy-phenoxyalkanecarboxylic acid derivatives, such as quinolyloxy, quinoxalyl-oxy, pyridyloxy , Benzoxazolyloxy- and Benzthiazolyloxyphenoxyalkan-carboxylic acid esters, cyclo-hexanedione derivatives, imidazolinones, phosphorus-containing herbicides, eg glufosinate-type or glyphosate-type, pyrimidinyloxypyridinecarboxylic acid derivatives, pyrimidyloxybenzoic acid derivatives, triazolopyrimidine-sulfonamide derivatives and S- (N
  • the herbicides from the group of carbamates, thiocarbamates, haloacetanilides are not provided as active substances present in the oily phase.
  • carbamates, thiocarbamates, haloacetanilides may be present in the aqueous phase inside the microcapsules contained in the oil suspension concentrate.
  • the herbicidal active compounds from the group of ALS inhibitors are always to be understood as meaning, in addition to the neutral compounds, their salts with inorganic and / or organic counterions.
  • sulfonylureas can form, for example, salts in which the hydrogen of the -S ⁇ 2-NH group is replaced by a cation suitable for agriculture.
  • These salts are, for example, metal salts, in particular alkali metal salts or alkaline earth metal salts, in particular sodium and potassium salts, or else ammonium salts or salts with organic amines.
  • salt formation can take place by addition of an acid to basic groups, such as, for example, amino and alkylamino.
  • Suitable acids for this purpose are strong inorganic and organic acids, for example HCl, HBr, H 2 SO 4 or HNO 3 .
  • Preferred ALS inhibitors come from the series of sulfonylureas and / or their salts, for example pyrimidine or triazinylaminocarbonyl [benzene, pyridine, pyrazole, thiophene and (alkylsulfonyl) alkylamino] sulfamides.
  • sulfonylureas are, for example
  • Methyl-S-chloro- ⁇ , ⁇ , ⁇ -dimethoxypyrimidine, ⁇ -ylylcarbamoyl-sulfamoyl-O-methyl-pyrazole-4-carboxylate (EP-A 0 282 613); Methyl 5- (4,6-dimethylpyrimidin-2-ylcarbamoylsulfamoyl) -1- (2-pyridyl) pyrazole-4-carboxylic acid (NC-330, see Brighton Crop Prot. Conference "Weeds 1 1991, Vol.
  • E is CH or N, preferably CH, R 20 is iodine or NR 25 R 26 ,
  • R 21 is hydrogen, halogen, cyano, (Ci-C 3) alkyl, (Ci-C 3) alkoxy, (CrC 3) - haloalkyl, (dC 3) -haloalkoxy, (C r C 3) alkylthio, ( C r C 3 ) -alkoxy- (d-
  • R x, R y are independently hydrogen, (C r C 3) alkyl, (Ci-C 3) -alkenyl, (CrC 3) - alkynyl or together are - (CH 2) 4 -, - (CH 2) 5 - or - (CH 2 ) 2 -O- (CH 2 ) 2, n is 0.1, 2 or 3, preferably 0 or 1,
  • R 22 is hydrogen or CH 3
  • R 23 is halogen, (C 1 -C 2 ) -alkyl, (-C 2) alkoxy, (CrC 2) -haloalkyl, in particular
  • R 25 is (C r C 4 ) alkyl
  • R 26 is (CrC 4 ) alkylsulfonyl or
  • R 25 and R 26 together represent a chain of the formula - (CH 2 ) 3 SO 2 - or - (CH 2 J 4 SO 2 -, for example 3- (4,6-dimethoxypyrimiden-2-yl) -1- (3 -N-methylsulfonyl-N-methyl-aminopyridin-2-yl) -sulfonylurea, or salts thereof;
  • oil suspension concentrate according to the invention is present as the herbicidal active ingredient pyridyl sulfonylurea in suspended form in the organic phase. This means that the herbicidal active ingredient pyridyl sulfonylurea in suspended form in the organic phase.
  • the pyridyl-sulfonylurea in the organic solvent to more than 50 wt .-%, more preferably more than 80 wt .-% suspended, each based on the total amount of pyridyl-sulfonylurea a) in the oil suspension concentrate according to the invention.
  • Preferred pyridyl-sulfonylureas are dioxazine-pyridylsulfonylureas, in particular of the general formula (I) wherein
  • R 11 is hydrogen, alkyl, halogen and haloalkyl
  • R 1 is hydrogen or an optionally substituted radical from the group consisting of alkyl, alkoxy, alkoxyalkyl, alkenyl, alkynyl, cycloalkyl, cycloalkylalkyl, aralkyl and aryl
  • R 2 is hydrogen, halogen or in each case optionally halogen-substituted alkyl, alkoxy, alkylthio, Alkylamino or dialkylamino each having 1 to 6 carbon atoms
  • R 3 is hydrogen, halogen or each optionally halogen-substituted alkyl, alkoxy, alkylthio, alkylamino or dialkylamino each having 1 to 6 carbon atoms
  • R 4 - R 7 are independently hydrogen , Halogen, cyano, thiocyanato or each optionally halogen-substituted alkyl, alkoxy, alkylthio, alkylsulfinyl, alkylsulf
  • A is nitrogen or a CH group
  • R 1 is hydrogen or an optionally halogen-substituted radical from the series alkyl, alkoxy, alkoxyalkyl, alkenyl and alkynyl, each with up to
  • R 2 is hydrogen, halogen or each optionally substituted by halogen alkyl, alkoxy, alkylthio, alkylamino or dialkylamino with in each case
  • R 3 is hydrogen, halogen or each optionally halogen-substituted alkyl, alkoxy, alkylthio, alkylamino or dialkylamino with in each case
  • R 4 - R 7 are each independently hydrogen, halogen, cyano, thiocyanato or each optionally halogen-substituted alkyl, alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, alkylamino, alkylcarbonyl, alkoxycarbonyl or alkylaminocarbonyl each having 1 to 3 carbon atoms in the alkyl radicals
  • R 8 represents hydrogen, halogen, cyano, thiocyanato or each optionally halogen-substituted alkyl, alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, alkylamino, alkylcarbonyl, alkoxycarbonyl or alkylaminocarbonyl each having 1 to 3 Carbon atoms in the alkyl radicals.
  • salts which are obtained from compounds of the formula (I) and bases, such as, for example, sodium, potassium or calcium hydroxide, hydride, amide and carbonate, Sodium or potassium-CrC 4 -alkanolaten, ammonia, Ci-C 4 -alkylamines, di (CrC 4 - alkyl) -amines or tri- (CrC 4 -alkyl) -amines, obtained by conventional methods.
  • bases such as, for example, sodium, potassium or calcium hydroxide, hydride, amide and carbonate, Sodium or potassium-CrC 4 -alkanolaten, ammonia, Ci-C 4 -alkylamines, di (CrC 4 - alkyl) -amines or tri- (CrC 4 -alkyl) -amines, obtained by conventional methods.
  • A is nitrogen or a CH group
  • R 1 is hydrogen, methyl, ethyl, methoxy, methoxymethyl or ethoxy,
  • R 2 is hydrogen, chlorine, methyl, ethyl, trifluoromethyl, methoxy, ethoxy,
  • R 3 is hydrogen, chlorine, methyl, ethyl, trifluoromethyl, methoxy, ethoxy,
  • R 4 - R 7 are independently hydrogen, fluorine, chlorine, cyano, or each optionally substituted by chlorine or fluorine methyl, methylthio, methylsulfinyl, methylsulfonyl, methoxycarbonyl and ethoxycarbonyl, preferably hydrogen .
  • R 8 represents hydrogen, fluorine, chlorine, bromine, cyano or represents in each case optionally substituted by chlorine or fluorine methyl, methoxy, ethoxy, methylthio, ethylthio, methylsulfinyl, ethylsulfinyl, methylsulfonyl, ethylsulfonyl, methyl or dimethylamino, preferably hydrogen.
  • R 1 is hydrogen or methyl
  • R 2 is hydrogen, chlorine, methyl, ethyl, trifluoromethyl, methoxy, ethoxy, difluoromethoxy, methylthio, methylamino or dimethylamino,
  • R 3 is hydrogen, chlorine, methyl, ethyl, trifluoromethyl, methoxy, ethoxy, difluoromethoxy, methylthio, methylamino or dimethylamino,
  • R 4 - R 7 is hydrogen
  • R 8 is hydrogen. Also particularly preferred are compounds of the formula (I) and salts thereof, in particular their alkali metal salts,
  • A is a CH group
  • R 1 is hydrogen or methyl
  • R 2 is hydrogen, chlorine, methyl, ethyl, trifluoromethyl, methoxy, ethoxy,
  • R 3 is hydrogen, chlorine, methyl, ethyl, trifluoromethyl, methoxy, ethoxy, difluoromethoxy, methylthio, methylamino or dimethylamino,
  • R 4 - R 7 is hydrogen
  • R 8 is hydrogen
  • hydrocarbon radicals mentioned in the radical definitions such as alkyl, alkenyl or alkynyl, also in combinations with heteroatoms, such as in alkoxy, alkylthio, haloalkyl or alkylamino, are also straight-chain or branched, even if not expressly stated.
  • the pyridylsulfonylureas may also be present as salts, e.g. as metal salts such as alkali (e.g., Na, K) salts or as alkaline earth (e.g., Ca, Mg) salts or as ammonium or organic amine salts.
  • metal salts such as alkali (e.g., Na, K) salts or as alkaline earth (e.g., Ca, Mg) salts or as ammonium or organic amine salts.
  • Such salts are readily obtained by conventional salt formation techniques, for example, by dissolving or dispersing a pyridylsulfonylurea, e.g. of the formula (I), in a suitable diluent, e.g. Methylene chloride, acetone, tert-butyl methyl ether or toluene, and addition of a suitable base.
  • the salts can then - be isolated by concentration or suction
  • (+) The indicated melting point (mp) refers in each case to the corresponding sodium salt, ie the corresponding compound in which the hydrogen of the -S ⁇ 2 -NH group has been replaced by sodium.
  • the herbicidal active compounds from the series of pyridyl-sulfonylureas are in the oil suspension concentrates according to the invention generally in amounts of 0.01 to 50% by weight, preferably 0.1 to 30% by weight, the term "% by weight” here and throughout the specification, unless otherwise defined, refers to the relative weight of the respective component on the total weight of the formulation.
  • Alkoxyphenoxysulfonylureas as e.g. in EP-A 0 342 569, preferably those of the formula
  • E is CH or N, preferably CH
  • R 27 is ethoxy, propoxy or isopropoxy
  • R 28 is halogen, NO 2, CF 3, CN, (Ci-C 4) -alkyl, (C 1 -C -alkoxy, (C r C4) -alkylthio or (CrC 3) alkoxy-carbonyl, preferably in 6-position on the phenyl ring, n is 0, 1, 2 or 3, preferably 0 or 1, R 29 is hydrogen, (C r C4) alkyl or (C 3 -C 4) alkenyl,
  • R 30, R 31 independently of one another are halogen, (dC 2) alkyl, (Ci-C 2) alkoxy, (Ci-C 2) - haloalkyl, (dC 2) -haloalkoxy or (Ci-C 2) alkoxy (C 1 -C 2 ) -alkyl, preferably OCH 3 or CH 3 , for example 3- (4,6-dimethoxypyrimidin-2-yl) -1- (2-ethoxyphenoxy) sulfonylurea, or salts thereof;
  • imidazolylsulfonylureas e.g.
  • MON 37500 sulfosulfuron (see Brighton Crop Prot. Conf., Weeds', 1995, p. 57), and other related sulfonylurea derivatives and mixtures thereof;
  • Typical representatives of these active ingredients include the following compounds: amidosulfuron, azimsulfuron, Bensulfuron-methyl, chlorimuron-ethyl, chlorosulfuron, cinosulfuron, Cyclosulfamuron, ethametsulfuron-methyl, ethoxysulfuron, flazasulfuron, Flupyrsulfuron-methyl-sodium, halosulfuron-methyl, imazosulfuron , Metsulfuron-methyl, nicosulfuron, oxasulfuron, primisulfuron-methyl, prosulfuron, pyrazosulfuron-ethyl, rimsulfuron, sulfometuron Methyl, sulfosulfuron, thifensulfuron-methyl, triasulfuron, tribenuron-methyl, triflusulfuron-methyl, iodosulfuron-methyl and its sodium salt (WO
  • Examples of compounds from the group of the phenylsulfonylaminocarbonyl-triazolinones are e.g. Flucarbazone or propoxycarbazone and / or salts thereof.
  • Q 1 is O (oxygen) or S (sulfur),
  • Q 2 is O (oxygen) or S (sulfur),
  • R 1 is optionally substituted by cyano, halogen or -C 4 -alkoxy-substituted alkyl having 1 to 6 carbon atoms, represents optionally cyano- or halogen-substituted alkenyl or alkinyl each having 2 to 6 carbon atoms, represents in each case optionally cyano-, halogen or CIC t Alkyl-substituted cycloalkyl or cycloalkylalkyl having in each case 3 to 6 carbon atoms in the cycloalkyl group and optionally 1 to 4 carbon atoms in the alkyl moiety, in each case optionally by nitro, cyano,
  • R 3 is hydrogen, hydroxyl, mercapto, amino, cyano, fluorine, chlorine, bromine, iodine, optionally substituted by fluorine, chlorine, bromine, cyano, C 1 -C 4 -alkoxy, C 1 -C 4 -alkylcarbonyl or C 1 -C 4 -alkoxy-carbonyl-substituted alkyl having 1 to 6 carbon atoms, represents in each case optionally substituted by fluorine, chlorine and / or bromine-substituted alkenyl or alkinyl each having 2 to 6 carbon atoms, represents in each case optionally substituted by fluorine, chlorine, cyano, C- ⁇ -C 4 Alkoxy or C 1 -C 4 -alkoxycarbonyl-substituted alkoxy, alkylthio, alkylamino or alkylcarbonylamino having in each case 1 to 6 carbon atoms in the alkyl group, for alkenyl
  • Alkinyl group for dialkylamino having in each case 1 to 4 carbon atoms in the alkyl groups, for each optionally substituted by methyl and / or ethyl aziridino, pyrrolidino, piperidino or morpholino, each optionally substituted by fluorine, chlorine, bromine, cyano and / or dC 4 alkyl substituted cycloalkyl, cycloalkenyl, cycloalkyloxy, cycloalkylthio,
  • Cycloalkylamino, cycloalkylalkyl, cycloalkylalkoxy, cycloalkylalkylthio or cycloalkylalkylamino having in each case 3 to 6 carbon atoms in the cycloalkyl or cycloalkenyl group and optionally 1 to 4 carbon atoms in the alkyl moiety, or in each case optionally by fluorine, chlorine, bromine, cyano, nitro, C 1 -C 4 Alkyl, trifluoromethyl, C r C 4 alkoxy and / or C 1 -C 4 -
  • R 4 is hydrogen, C 1 -C 4 -alkyl, hydroxy, amino, cyano, C 2 -C -alkylamino-amino, optionally substituted by fluorine, chlorine, bromine, cyano, C 1 -C 4 -alkoxy, C 1 -C 4- alkylcarbonyl or C 1 -C 6 -alkoxy-carbonyl-substituted alkyl having 1 to 6 carbon atoms, in each case optionally substituted by fluorine, chlorine and / or bromine-substituted alkenyl or alkynyl having in each case
  • R 3 and R 4 together represent optionally branched alkanediyl having 3 to 6 carbon atoms
  • phenoxyphenoxy- and benzyloxyphenoxy-carboxylic acid derivatives e.g. Methyl 2- (4- (2,4-dichlorophenoxy) phenoxy) propionate (diclofopmethyl), 2- (4- (4-bromo-2-chlorophenoxy) phenoxy) propionate (DE-A 26 01 548) Methyl 2- (4- (4-bromo-2-fluorophenoxy) -phenoxy) -propionate (US Pat. No. 4,808,750), 2- (4- (2-chloro-4-trifluoromethylphenoxy) -phenoxy) -propionic acid methyl ester (DE-A 24 33 067),
  • thiocarbamates e.g. S-ethyl-N, N-dipropylthiocarbamate (EPTC), S-ethyl-N, N-diisobutylthiocarbamate (butylate);
  • imidazolinones e.g. Methyl 2- (4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl) -5-methylbenzoate and 2- (4-isopropyl-4-methyl-5-oxo-2-imidazoline-2 yl) -4-methylbenzoic
  • Triazolopyrimidine sulfonamide derivatives e.g. N- (2,6-Difluorophenyl) -7-methyl-1,2,4-triazolo [1,5-c] pyrimidine-2-sulfonamide
  • salts preferably acid addition salts of the compounds, for example their hydrochlorides.
  • L) phosphorus-containing herbicides e.g. one or more compounds of the formula (IV) or derivatives thereof, such as salts,
  • active compounds of the formula (IV) and (V) are the following:
  • auxins and auxin analogs e.g. 4-indole-3-butyric acid, indole-3-acetic acid, 1-naphthylacetic acid, 2- (1-naphthyl) acetamide and 2-naphthyloxyacetic acid;
  • cytokinins e.g. Kinetin and 6-benzylaminopurine
  • gibberellins e.g. Gibberillic Acid, Gibberillin A4 and A7;
  • T) ethylene precursors e.g. ethephon
  • V) ureas e.g. Chlorotoluron, dimefuron, diuron, fluometuron, isoproturon, isourone, carbutilate, linuron, methabenzthiazuron, metobenzuron, metoxuron, monolinuron, neburon, siduron and tebuthiuron and
  • hydroxybenzonitriles e.g. such as bromoxynil and loxynil and their salts and esters such as bromoxyniloctanoate and loxyniloctanoate.
  • the agrochemical active substances can also be growth regulators. Examples of these are terbufos, cyclanilides and thidiazuron.
  • herbicides plant growth regulators
  • groups A to X for example, from the above-mentioned writings and / or from "The Pesticide Manual", 12th edition (2000) and 13th edition (2003), The British Crop Protection Council, "Agricultural Chemicals Book II - Herbicides - “, by WT. Thompson, Thompson Publications, Fresno CA, USA 1990 and “Farm Chemicals Handbook '90", Meister Publishing Company, Willoughby OH, USA, 1990. safener
  • the agrochemical active substances can also be safeners. Examples include:
  • n ' is a natural number from 0 to 5, preferably 0 to 3
  • T is a (Ci or C2) alkanediyl chain which is unsubstituted or substituted by one or two (C 1 -C 6 -alkyl radicals or by [(C 1 -C 3 ) -alkoxy] carbonyl;
  • W is an unsubstituted or substituted divalent heterocyclic radical from the group of unsaturated or unsaturated five-membered ring heterocycles having 1 to 3 hetero ring N or O atoms, at least one N atom and at most one O atom in the ring, preferably a radical from the group (W1) to (W4),
  • R 17 , R 19 are the same or different halogen
  • R 18 , R 20 are identical or different OR 24 , SR 24 or NR 24 R 25 or a saturated or unsaturated 3- to 7-membered heterocycle having at least one N atom and up to 3 heteroatoms, preferably from the group O and S. which is connected via the N atom to the carbonyl group in (S-II) or (S-III) and unsubstituted or by radicals from the group (C 1 -C 4 ) alkyl,
  • R 24 is hydrogen or an unsubstituted or substituted aliphatic hydrocarbon radical, preferably having a total of 1 to 18 C atoms;
  • R 25 is hydrogen, (C 1 -C 6 ) alkyl, (C 1 -C 6 ) alkoxy or substituted or unsubstituted phenyl, R x is H 1 (C r C 8 ) alkyl, C r C 8 (haloalkyl), (C 1 -C 4 ) alkoxy (C 1 -C 8 ) alkyl, cyano or
  • R 26 is hydrogen, (Ci-C 8 ) alkyl, (C r C 8 ) haloalkyl, (C r C 4 ) alkoxy (C r C 4 ) alkyl, (Ci-C 6 ) hydroxyalkyl, (C C 3 -C 12 ) is cycloalkyl or tri (C 1 -C 4 ) alkylsilyl;
  • R 27 , R 28 , R 29 are identical or different hydrogen, (C r Cs) alkyl,
  • R 21 is (C r C 4 ) alkyl, (C r C 4 ) haloalkyl, (C 2 -C 4 ) alkenyl, (C 2 -C 4 ) haloalkenyl,
  • R 22 , R 23 is identical or different hydrogen, (C r C 4 ) alkyl, (C 2 -C 4 ) alkenyl,
  • R 30 is hydrogen, a hydrocarbon radical, a hydrocarbonoxy radical, a hydrocarbylthio radical or a heterocyclyl radical which is preferably bonded via a carbon atom, where each of the last-mentioned 4 radicals is unsubstituted or substituted by one or more identical or different radicals from the group halogen, cyano, nitro , Amino, hydroxy, carboxy, formyl, carbonamide, sulfonamide and radicals of the formula -Z a -R a is substituted, wherein each hydrocarbon moiety preferably 1 to 20 carbon atoms and a C-containing radical R 30 including substituents preferably 1 to 30 Having C atoms;
  • R 31 is hydrogen or (C 1 -C 4) alkyl, preferably hydrogen, or R 30 and R 31 together with the group of the formula -CO-N- represent the radical of a 3- to 8-membered saturated or unsaturated ring;
  • R 32 is identical or different and is halogen, cyano, nitro, amino, hydroxyl, carboxy, formyl, CONH 2 , SO 2 NH 2 or a radical of the formula -Z b -R b ;
  • R 33 is hydrogen or (C 1 -C 4 ) -alkyl, preferably H;
  • R 34 is identical or different and is halogen, cyano, nitro, amino, hydroxyl, carboxy, CHO, CONH 2 , SO 2 NH 2 or a radical of the formula -Z c -R c ;
  • R a is a hydrocarbon radical or a heterocyclyl radical, where each of the two last-mentioned radicals is unsubstituted or substituted by one or more identical or different radicals from the group halogen, cyano, nitro,
  • R b , R c are a hydrocarbon radical or a heterocyclyl radical, where each of the latter two radicals is unsubstituted or substituted by one or more identical or different radicals from the group halogen, cyano, nitro, amino, hydroxyl, phosphoryl, halogen (C 1 -C 4) alkoxy, mono- and di - [(C 1 -C 4 ) alkyl] amino, or an alkyl radical in which several, preferably 2 or 3, non-adjacent CH 2 groups are each replaced by an oxygen atom;
  • Z a is a divalent group of the formula -O-, -S-, -CO-, -CS-, -CO-O-, -CO-S-,
  • Z b , Z c independently of one another a direct bond or a divalent group of the formula -O-, -S-, -CO-, -CS-, -CO-O-, -CO-S-, -O-CO-, -S-CO-, -SO-, -SO 2 -, -NR * -, -SO 2 -NR * -, -NR * -SO 2 -, -CO-NR * - or -NR * -CO-, where the bond of the respective divalent group indicated on the right is the bond to the radical R b or R c and where the R * in the last-mentioned 5 radicals are each independently H, (C 1 -C 4 ) -alkyl or halo (C r C 4 ) -alkyl; n is an integer from 0 to 4, preferably 0, 1 or 2, in particular O or 1, and m is an integer from 0 to 5, preferably 0, 1, 2 or 3, in particular 0, 1
  • R 30 cyclopropyl
  • R 34 2-OMe is (V-3)
  • R 30 cyclopropyl
  • R 34 2-OMe-5-CI is (V-4)
  • R 30 cyclopropyl
  • R 34 2-Me is (V-5)
  • X 3 is CH or N
  • R 35 is hydrogen, heterocyclyl or a hydrocarbon radical, where the latter two radicals are optionally substituted by one or more, identical or different radicals from the group halogen, cyano, nitro, amino, hydroxy, carboxy, CHO, CONH 2 , SO 2 NH 2 and Z a -R are a substituted;
  • R 36 is hydrogen, hydroxy, (Ci-C 6) -alkyl, (C 2 -C 6) alkenyl, (C 2 -C 6) -alkynyl, (CrC 6) - alkoxy, (C 2 -C 6) - Alkenyloxy, where the five last-mentioned radicals are optionally substituted by one or more, identical or different radicals from the group halogen, hydroxy, (C 1 -C 4 -alkyl, (C 1 -C 4 -alkoxy and (C 1 -C 4 ) -alkylthio, or
  • R 35 and R 36 together with the nitrogen atom carrying them have a 3- to 8-membered saturated or unsaturated ring;
  • R 37 is halogen, cyano, nitro, amino, hydroxy, carboxy, CHO, CONH 2 , SO 2 NH 2 or Z b -R b ;
  • R 38 is hydrogen, (C r C4) alkyl, (C 2 -C 4) -alkenyl or (C 2 -C 4) alkynyl;
  • R 39 is halogen, cyano, nitro, amino, hydroxy, carboxy, phosphoryl, CHO, CONH 2 ,
  • R a is a (C 2 -C 2 0) -alkyl radical whose carbon chain is mono- or polysubstituted
  • R b, R c are identical or different and are a (C 2 -C 2 o) -alkyl radical whose carbon chain one or more times interrupted by oxygen atoms, is heterocyclyl or a hydrocarbon radical, where the last two radicals optionally substituted by one or more identical or different Radicals from the group halogen, cyano, nitro, amino, hydroxy, phosphoryl, (CrC 4 ) - haloalkoxy, mono- and di - [(Ci-C 4 ) alkyl] amino substituted;
  • Z a is a divalent unit selected from O, S, CO, CS, C (O) O, C (O) S, SO, SO 2 , NR d , C (O) NR d or SO 2 NR d ;
  • Z b , Z c identically or differently, represent a direct bond or a divalent unit from the group O 1 S, CO, CS, C (O) O, C (O) S, SO, SO 2 , NR d , SO 2 NR d or C (O) NR d ;
  • R d is hydrogen, (C r C 4 ) -alkyl or (C r C 4 ) -haloalkyl;
  • n is an integer from 0 to 4, and in the case that X is CH, an integer from 0 to 5, and in the case where X is N, an integer from 0 to 4; preferably safeners of compounds of the formula (S-VI) in which X 3 CH;
  • R 35 is hydrogen, (C r C6) alkyl, (C 3 -C 6) -cycloalkyl, (C 2 -C 6) alkenyl, (C 5 -C 6) - cycloalkenyl, phenyl or 3- to 6 hetero-cyclic heterocyclyl having up to three heteroatoms from the group of nitrogen, oxygen and sulfur, where the six last-mentioned radicals are optionally substituted by one or more, identical or different substituents from the group halogen, (C 1 -C 6 ) -
  • R 36 is hydrogen, (C r C 6 ) -alkyl, (C 2 -C 6 ) -alkenyl, (C 2 -C 6 ) -alkynyl, where the last three radicals mentioned are optionally substituted by one or more, identical or different substituents from the group Halogen, hydroxy, (C 1 -C 4 ) alkyl, (C 1 -C 4 ) alkoxy and
  • R 38 is hydrogen; R39 is halogen, nitro, (C r C4) alkyl, (C "
  • R ⁇ and R ⁇ independently of one another represent hydrogen, C 1 -C 6 -alkyl, C 5 -C 6 -cycloalkyl, C 3 -C 6 -alkenyl, C 3 -C 6 -alkynyl,
  • R ⁇ and R ß together are a C 4 -C 6 alkylene or by oxygen, sulfur, SO, SO 2, NH or -N (-C 4 alkyl) - interrupted C 4 -C 6 - alkylene bridge,
  • R ⁇ is hydrogen or C 1 -C 4 -alkyl
  • R a and R b independently of one another represent hydrogen, halogen, cyano, nitro,
  • R 9 and R h independently of one another represent hydrogen, halogen, C 1 -C 4 -alkyl, trifluoromethyl, methoxy, methylthio or -COOR ', where
  • R c is hydrogen, halogen, C 1 -C 4 -alkyl or methoxy
  • R d is hydrogen, halogen, nitro, C r C 4 alkyl, C 1 -C 4 -alkoxy, C r C 4 alkylthio, C r C 4 - alkylsulfinyl, C r C 4 alkylsulfonyl, -COOR j or -CONR k R m ,
  • R e is hydrogen, halogen, C r C 4 alkyl, -COOR j, trifluoromethyl or methoxy, or R d and R e together represent a C 3 -C 4 alkylene bridge,
  • R f is hydrogen, halogen or C 1 -C 4 -alkyl
  • R x and R ⁇ independently represent hydrogen, halogen, -C 4 alkyl, C r C 4 - alkoxy, C r C 4 alkylthio, -COOR 4, trifluoromethyl, nitro or cyano,
  • R j , R k and R m independently of one another are hydrogen or C 1 -C 4 -alkyl
  • R k and R m together are a C 4 -C 6 -alkylene bridge or an interrupted by oxygen, NH or -N (C- ⁇ -C 4 alkyl) - interrupted C 4 -C 6 alkylene, and
  • R n is C 1 -C 4 alkyl, phenyl or phenyl substituted by halogen, C 1 -C 4 alkyl, methoxy, nitro or trifluoromethyl; preferably safeners of the formula (S-VIII)
  • radicals alkyl, alkoxy, haloalkyl, haloalkoxy, alkylamino and alkylthio and the corresponding unsaturated and / or substituted radicals can each be straight-chain or branched in the carbon skeleton.
  • Alkyl radicals, even in the composite meanings such as alkoxy, haloalkyl, etc., preferably have 1 to 4 carbon atoms and, for example, methyl, ethyl, n- or i-propyl, n-, i-, t- or 2-butyl.
  • Alkenyl and alkynyl radicals have the meaning of the possible unsaturated radicals corresponding to the alkyl radicals;
  • Alkenyl is for example AlII, 1-methylprop-2-en-1-yl, 2-methyl-prop-2-en-1-yl, but-2-en-1-yl, but-3-en-1-yl , 1-methyl-but-3-en-1-yl and 1-methyl-but-2-en-1-yl.
  • Alkynyl means, for example, propargyl, but-2-yn-1-yl, but-3-yn-1-yl, 1-methylbut-3-yn-1-yl.
  • "(CrC 4 ) -Alkyr is the shorthand notation for alkyl of 1 to 4 carbon atoms, as well as other general definitions of radicals with bracketed ranges for the possible number of carbon atoms.
  • Cycloalkyl is preferably a cyclic alkyl radical having 3 to 8, preferably 3 to 7, particularly preferably 3 to 6, C atoms, for example cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl.
  • Cycloalkenyl and cycloalkynyl refer to corresponding unsaturated compounds.
  • Halogen is fluorine, chlorine, bromine or iodine.
  • Haloalkinyl mean by halogen, preferably by fluorine, chlorine and / or bromine, in particular by fluorine or chlorine, partially or fully substituted alkyl, alkenyl or alkynyl, for example CF 3 , CHF 2 , CH 2 F, CF 2 CF 3 , CH 2 CHFCI , CCI 3 , CHCl 2 , CH 2 CH 2 Cl.
  • Haloalkoxy is eg OCF 3 , OCHF 2 , OCH 2 F, OCF 2 CF 3 , OCH 2 CF 3 and OCH 2 CH 2 Cl. The same applies to other halogen-substituted radicals.
  • a hydrocarbon radical may be an aromatic or an aliphatic hydrocarbon radical, where an aliphatic hydrocarbon radical is generally a straight-chain or branched saturated or unsaturated hydrocarbon radical, preferably having 1 to 18, particularly preferably 1 to 12, carbon atoms, for example alkyl, alkenyl or alkynyl ,
  • Aryl is generally a mono-, bi- or polycyclic aromatic system having preferably 6-20 C atoms, preferably 6 to 14 C atoms, more preferably 6 to 10 C atoms, e.g. Phenyl, naphthyl, tetrahydronaphthyl, indenyl, indanyl, pentalenyl and fluorenyl, more preferably phenyl.
  • Heterocyclic ring, heterocyclic radical or heterocyclyl means a mono-, bi- or polycyclic ring system which is saturated, unsaturated and / or aromatic and one or more, preferably 1 to 4, heteroatoms, preferably from the group N, S and O, contains.
  • saturated heterocycles having 3 to 7 ring atoms and one or two heteroatoms from the group N, O and S, wherein the chalcogens are not adjacent.
  • Particularly preferred are monocyclic rings having 3 to 7 ring atoms and a heteroatom from the group N, O and S, and morpholine, dioxolane, piperazine, imidazoline and oxazolidine.
  • Very particularly preferred saturated heterocycles are oxirane, pyrrolidone, morpholine and tetrahydrofuran.
  • partially unsaturated heterocycles having 5 to 7 ring atoms and one or two heteroatoms from the group N, O and S.
  • partially unsaturated heterocycles having 5 to 6 ring atoms and one heteroatom from the group N, O and S.
  • Very particular preferred partially unsaturated heterocycles are pyrazoline, imidazoline and isoxazoline.
  • heteroaryl e.g. mono- or bicyclic aromatic heterocycles having 5 to 6 ring atoms containing one to four heteroatoms from the group N, O, S, wherein the chalcogens are not adjacent.
  • monocyclic aromatic heterocycles having 5 to 6 ring atoms which contain a heteroatom from the group, N, O and S, and pyrimidine, pyrazine, pyridazine, oxazole, thiazole, thiadiazole, oxadiazole, pyrazole, triazole and isoxazole.
  • pyrazole, thiazole, triazole and furan are particularly preferred.
  • Substituted radicals such as substituted hydrocarbon radicals, for example substituted alkyl, alkenyl, alkynyl, aryl, such as phenyl and arylalkyl, such as benzyl, or substituted heterocyclyl, represent a substituted radical derived from the unsubstituted radical, where the substituents are preferably one or more, preferably 1, 2 or 3 , in the case of Cl and F also up to the maximum possible number, substituents from the group halogen, alkoxy, haloalkoxy, alkylthio, hydroxy, amino, nitro, carboxy, cyano, azido, alkoxycarbonyl, alkylcarbonyl, formyl, carbamoyl, mono- and dialkylaminocarbonyl , substituted amino such as acylamino, mono- and dialkylamino and alkylsulfinyl, haloalkylsulfinyl, alkylsulfon
  • Substituents from the group halogen for example fluorine or chlorine, (CrC 4 ) alkyl, preferably methyl or ethyl, (CrC 4 ) haloalkyl, preferably trifluoromethyl, (CrC 4 ) AIkOXy, preferably methoxy or ethoxy, (CrC 4 ) haloalkoxy, nitro and cyano.
  • substituents methyl, methoxy and chlorine are particularly preferred.
  • Mono- or disubstituted amino means a chemically stable radical from the group of substituted amino radicals which are N-substituted by, for example, one or two identical or different radicals from the group consisting of alkyl, alkoxy, acyl and aryl; preferably monoalkylamino, dialkylamino, acylamino, arylamino, N-alkyl-N-arylamino and N-heterocycles.
  • alkyl radicals having 1 to 4 carbon atoms are preferred.
  • Aryl is preferably phenyl.
  • Substituted aryl is preferably substituted phenyl.
  • acyl the definition mentioned further below applies, preferably (CrC 4) alkanoyl.
  • substituted hydroxylamino or hydrazino is preferably (CrC 4) alkanoyl.
  • Optionally substituted phenyl is preferably phenyl which is unsubstituted or mono- or polysubstituted, preferably up to three times, in halogens such as Cl and F also up to five times, by identical or different radicals from the group halogen, (CrC 4 ) alkyl, (CrC 4 ) Alkoxy, (CrC 4 ) haloalkyl, (C r C 4 ) haloalkoxy and nitro, for example o-, m- and p-tolyl, dimethylphenols, 2-, 3- and 4-chlorophenyl, 2-, 3- and 4-trifluoro- and trichlorophenyl, 2,4-, 3,5-, 2,5- and 2,3-dichloropheny
  • An acyl group means the residue of an organic acid preferably having up to 6 C atoms, e.g. the radical of a carboxylic acid and radicals derived therefrom, such as the thiocarboxylic acid, optionally N-substituted iminocarboxylic acids, or the radical of carbonic acid monoesters, optionally N-substituted
  • Acyl is, for example, formyl, alkylcarbonyl, such as (C 1 -C 4 -alkyl) carbonyl, phenylcarbonyl, where the phenyl ring may be substituted, for example as indicated above for phenyl, or alkyloxycarbonyl, phenyloxycarbonyl, benzyloxycarbonyl, alkylsulfonyl, alkylsulfinyl or N-alkyl-1 iminoalkyl.
  • stereoisomers which have the same topological linkage of the atoms, and mixtures thereof.
  • Such compounds contain one or more asymmetric C atoms or double bonds, which are not specified separately in the general formulas are.
  • the possible defined by their specific spatial form possible stereoisomers, such as enantiomers, diastereomers, Z and E isomers can be obtained by conventional methods from mixtures of stereoisomers or prepared by stereoselective reactions in combination with the use of stereochemically pure starting materials.
  • the compounds of formula (S-II) are e.g. from EP-A-0333131 (ZA-89/1960), EP-A-0269806 (US 4,891,057), EP-A-0346620 (AU-A-89/34951), EP-A-0174562, EP-A No.
  • the compounds of formula (S-IV) are known from numerous patent applications, for example US 4,021,224 and US 4,021,229.
  • Compounds of subgroup b) are further from CN-A-87/102789, EP-A-365484 and from "The Pesticide Manual", 11th to 13th edition, British Crop Protection Council and the Royal Society of Chemistry (1997), known.
  • the compounds of subgroup c) are described in WO-A-97/45016, those of subgroup d) in WO-A-99/16744 (in particular in EP-A-365484).
  • the cited documents contain detailed information on preparation processes and starting materials and name preferred compounds. These documents are expressly referred to, they are by quotation as part of this description.
  • the safeners of the above groups a) to e) reduce or prevent the phytotoxic effects which can occur when using the herbicidal compositions according to the invention in crops without impairing the effectiveness of the herbicides against harmful plants.
  • the field of application of the herbicides can be significantly extended and in particular by the use of safeners, the use of herbicides, which have so far only limited or could be used with insufficient success, ie of combinations without Safener in low dosages with little broad effect led to insufficient control of harmful plants, possible.
  • safeners in the formulations according to the invention, inter alia: 4-dichloroacetyl-1-oxa-4-aza-spiro [4.5] -decane (AD-67), 1-dichloroacetyl-hexahydro-3,3,8a-trimethylphenyl [ 1,2-a] -pyrimidine-6 (2H) -one (dicyclonone, BAS-145138), 4-dichloroacetyl-3,4-dihydro-3-methyl-2H-1,4-benzoxazine (Benoxacor), cloquintocet, 5-Chloro-quinolin-8-oxy-acetic acid (1-methylhexyl ester) (cloquintocet-mexyl), ⁇ - (cyanomethoxyimino) -phenylacetonitrile (cyometrinil), 2,2-dichloro-N- (2-oxo-2 - (2-propenylamino) -ethyl)
  • herbicide-safener mixtures are combinations of the following compounds with one another:
  • HPPD p-hydroxyphenyl pyruvate dioxygenase
  • d) compounds which act as safeners such as AD 67 (4- (dichloroacetyl) -1-oxa-4-azaspiro [4.5] decane), benoxacor, CL 304,415 (4-carboxymethylchroman-4-carboxylic acid), cloquintocet, Cloquintocet-mexyl, cyprosulfamides, dichloromide, dicyclonon, DKA-24 (N1, N2-diallyl-N2-dichloroacetylglycine amides), fenchlorazoles, fenchlorazoles-ethyl, fenclorim, flurazoles, fluxofenim, furilazoles, isoxadifen-ethyl, mefenpyr-diethyl, MW 191 ( 2-dichloromethyl-2-methyl-1,3-dioxolane), naphthalic anhydride (naphthalene-1,8-dicarboxylic
  • herbicides are combined, e.g. Fenoxaprop-p-ethyl + loxyniloctanoate, diclofopmethyl + bromoxyniloctanoate, CMPP + bromoxyniloctanoate, MCPA + loxyniloctanoate, bromoxyniloctanoate + bromoxynil heptanoate, bromoxyniloctanoate + bromoxynilheptanoate + MCPA, bromoxynil octanoate + bromoxynil-heptanoate + 2,4-D, phenmedipham + desmedipham, phenmedipham + desmedipham + ethofumesate, metamitron + ethofumesate, phenmedipham + ethofumesate + metamitron, fenoxaprop-p-ethyl + iodosul
  • Cyprosulfamide flupyrsulfuron + cyprosulfamide, pyrazosulfuron + cyprosulfamide, azimsulfuron + cyprosulfamide, bensulfuron + cyprosulfamide, bispyribac + cyprosulfamide, rimsulfuron + cyprosulfamide, tritosulfuron + cyprosulfamide, sulcotrione + cyprosulfamide, clomazone + cyprosulfamide, mesotrione + cyprosulfamide, topramezone + cyprosulfamide, metribuzin + cyprosulfamide, Bentazone + Cyprosulfamide, Bromoxynil + Cyprosulfamide, Propanil + Cyprosulfamide, Atrazine + Cyprosulfamide, Terbuthylazine + Cyprosulfamide, EPTC +
  • Cyprosulfamides acetochlor + cyprosulfamides, S-metolachlor + cyprosulfamides, flumioxazine + cyprosulfamides, flumiclorac + cyprosulfamides, fomesafen + cyprosulfamides, sulfentrazone + cyprosulfamides, dicamba + cyprosulfamides, MCPA + cyprosulfamides, MCPB + cyprosulfamides, 2,4-D + cyprosulfamides, clopyralid + Cyprosulfamide, Fluroxypyr + Cyprosulfamide, Picloram +
  • the weight ratio safener: herbicide can vary within wide limits and is preferably in the range from 1: 100 to 100: 1, in particular from 1: 100 to 50: 1, very particularly preferably from 1:10 to 10: 1
  • Herbicide (s) and safener (s) are usually dependent on the type of herbicide and / or the safener used and on the nature of the plant stock to be treated.
  • the agrochemically active compounds may also be fungicides, for example
  • Inhibitors of the respiratory chain complex I in particular diflumetorim
  • Respiratory chain complex II particularly boscalid, carboxin, fenfuram, flutolanil, furametpyr, mepronil, oxycarboxin,
  • Azoxystrobin Cyazofamide, Dimoxystrobin, Enestrobin, Famoxadone, Fenamidon, Fluoxastrobin, Kresoximethyl, Metominostrobin, Orysastrobin, Pyraclostrobin,
  • Decoupler especially dinocap, fluazinam Inhibitors of ATP production, in particular
  • Inhibitors of signal transduction in particular fenpiclonil, fludioxonil, quinoxyfen
  • Inhibitors of fat and membrane synthesis in particular chlozolinate, iprodione, procymidone, vinclozolin
  • Inhibitors of ergosterol biosynthesis in particular fenhexamide
  • Iminoctadinalesilate iminoctadine triacetate, mancopper, mancozeb, maneb, metiram, metiram zinc, propineb, sulfur and sulfur preparations containing calcium polysulphide, thiram, tolylfluanid, zineb, ziram
  • the agrochemically active compounds may also be bactericides, for example bronopol, dichlorophen, nitrapyrin, nickel dimethyldithiocarbamate, kasugamycin, octhilinone, furancarboxylic acid, oxytetracycline, probenazole, streptomycin, tecloftalam, copper sulphate and other copper preparations.
  • bactericides for example bronopol, dichlorophen, nitrapyrin, nickel dimethyldithiocarbamate, kasugamycin, octhilinone, furancarboxylic acid, oxytetracycline, probenazole, streptomycin, tecloftalam, copper sulphate and other copper preparations.
  • the fungicides listed above are known, for example, from "The Pesticide Manual”, 12th edition (2000) and 13th edition (2003), The British Crop Protection Council or the references listed for the individual active ingredients.
  • the agrochemically active compounds may also be insecticides / acaricides and / or nematicides, for example
  • Acetylcholinesterase (AChE) inhibitors carbamates, for example alanycarb, aldicarb, aldoxycarb, allyxycarb, aminocarb, bendocarb, benfuracarb, bufencarb, butacarb, butocarboxim, butoxycarboxim, carbaryl, carbofuran, carbosulfan, cloethocarb, dimetilane, ethiofencarb, fenobucarb, fenothiocarb, formetanate, furathiocarb , Isoprocarb, metam-sodium, methiocarb, methomyl, metolcarb, oxamyl,
  • Pirimicarb promecarb, propoxur, thiodicarb, thiofanox, trimethacarb, XMC,
  • Organophosphates for example acephates, azamethiphos, azinphos (-methyl, -ethyl), bromophos-ethyl, bromfenvinfos (-methyl), butathiofos, cadusafos,
  • Sodium Channel Modulators / Voltage Dependent Sodium Channel Blockers Pyrethroids, for example, acrinathrin, allethrin (d-cis-trans, d-trans), beta-cyfluthrin, bifenthrin, bioallethrin, bioallethrin-S-cyclopentyl isomer, bioethanomethrin, biopermethrin , Bioresmethrin, chlovaporthrin, cis-cypermethrin, cis
  • Oxadiazines for example Indoxacarb Semicarbazone, for example Metaflumizone (BAS3201)
  • Acetylcholine Receptor Agonists / Antagonists Chloronicotinyls, for example acetamiprid, clothianidin, dinotefuran, imidacloprid, nitenpyram, nithiazines, thiacloprid, thiamethoxam
  • Nicotine, Bensultap, Cartap Acetylcholine receptor modulators Spinosyne, for example spinosad
  • GABA-Directed Chloride Channel Antagonists Organochlorines, for example Camphechlor, Chlordane, Endosulfan, Gamma-HCH, HCH, Heptachlor, Lindane, Methoxychlor Fiprole, for example Acetoprole, Ethiprole, Fipronil, Pyrafluprole, Pyriprole,
  • Mectins for example Abamectin, Emamectin, Emamectin benzoate, Ivermectin,
  • Juvenile hormone mimetics for example, diofenolan, epofenonans, fenoxycarb, hydroprene, kinoprenes, methoprenes, pyriproxifen, triprene
  • Diacylhydrazines for example chromafenozide, Halofenozide, Methoxyfenozide, Tebufenozide
  • Benzoylureas for example bistrifluron, chlorofluazuron, diflubenzuron, fluazuron,
  • Organotin compounds for example azocyclotin, cyhexatin, fenbutatin oxides
  • Pyrroles for example Chlorfenapyr dinitrophenols, for example binapacyrl, dinobutone, dinocap, DNOC
  • METI 1 S for example fenazaquin, fenpyroximate, pyrimidifen, pyridaben,
  • Inhibitors of fatty synthesis tetronic acids for example spirodiclofen, spiromesifen
  • Tetramic acids for example spirotetramat Carboxamides, for example flonicamide
  • Octopaminergic agonists for example, amitraz
  • Nereistoxin analogs for example thiocyclam hydrogen oxalate, thiosultap-sodium
  • Agonists of the ryanodine receptor benzoic acid dicarboxamides, for example flubendiamide
  • Anthranilamides for example DPX E2Y45 (3-bromo-N- ⁇ 4-chloro-2-methyl-6- [(methylamino) carbonyl] phenyl ⁇ -1- (3-chloropyridin-2-yl) -1H-pyrazole- 5-carboxamides)
  • Feed inhibitors for example cryolites, flonicamide, pymetrozine mite growth inhibitors, for example clofentezine, etoxazole, hexythiazox
  • insecticides listed above are e.g. known from "The Pesticide Manual", 12th edition (2000) and 13th edition (2003), The British Crop Protection Council or the references listed after the individual active ingredients.
  • a particular embodiment of the invention is the joint application of insecticides (acaricides, nematicides) as agrochemical active ingredients, either together or in succession.
  • agrochemically active compounds are used according to solubility in the present invention.
  • the criterion of water-soluble or oil-soluble can be understood by any active ingredient in the literature, e.g.
  • solubilities of agrochemicals are listed in "The Pesticide Manual", 12th edition (2000), 13th edition (2003) and 14th edition (2006), The British Crop Protection Council.
  • the sulfonylureas contained as component in the oil suspension concentrates according to the invention are always understood to mean all forms of use, such as acids, esters, salts and isomers, such as stereoisomers and optical isomers.
  • their salts are always to be understood, for example with inorganic and / or organic counterions.
  • sulfonylureas can form salts in which the hydrogen of the -S ⁇ 2 -NH group is replaced by a cation suitable for agriculture.
  • salts are, for example, metal salts, in particular alkali metal salts or alkaline earth metal salts, in particular sodium and potassium salts, or else ammonium salts or salts with organic amines.
  • salt formation can take place by addition of an acid to basic groups, such as, for example, amino and alkylamino.
  • Suitable acids for this purpose are strong inorganic and organic acids, for example HCl, HBr, H 2 SO 4 or HNO 3 .
  • Preferred esters are the alkyl esters, especially the CiC-io-alkyl esters such as methyl esters.
  • acyl radical means the radical of an organic acid which is formally formed by cleavage of an OH group from the organic acid, e.g. the radical of a carboxylic acid and radicals derived therefrom, such as the thiocarboxylic acid, optionally N-substituted iminocarboxylic acids or the radicals of carbonic acid monoesters, optionally N-substituted carbamic acids, sulfonic acids, sulfinic acids, phosphonic acids, phosphinic acids.
  • An acyl radical is preferably formyl or acyl from the group CO-R Z, CS-R Z, CO-OR 2, CS-OR 2, CS-SR 2, SOR Z or SO 2 R 2, wherein R 2 are each a C 1 -C 10 - hydrocarbon radical such as C 1 -C 10 -alkyl or C 6 -C 10 -aryl which is unsubstituted or substituted, for example by one or more substituents from the group halogen such as F, Cl, Br, I, alkoxy, haloalkoxy, Hydroxy, amino, nitro, cyano or alkylthio, or R 2 means aminocarbonyl or aminosulfonyl, where the latter two radicals are unsubstituted, N-monosubstituted or N, N-disubstituted, for example by substituents from the group alkyl or aryl.
  • Acyl is, for example, formyl, haloalkylcarbonyl,
  • alkyloxycarbonyl such as (CrC 4) alkyloxycarbonyl, phenyloxycarbonyl, benzyloxycarbonyl, alkylsulfonyl, such as (CrC 4) alkylsulfonyl,
  • a hydrocarbon radical means a straight-chain, branched or cyclic and saturated or unsaturated aliphatic or aromatic hydrocarbon radical, for example alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl or aryl.
  • a hydrocarbon radical preferably has 1 to 40 C atoms, preferably 1 to 30 C atoms; particularly preferably a hydrocarbon radical is alkyl, alkenyl or alkynyl having up to 12 C atoms or cycloalkyl having 3, 4, 5, 6 or 7 ring atoms or phenyl.
  • Aryl means a mono-, bi- or polycyclic aromatic system, for example phenyl, naphthyl, tetrahydronaphthyl, indenyl, indanyl, pentalenyl, fluorenyl and the like, preferably phenyl.
  • a heterocyclic radical or ring may be saturated, unsaturated or heteroaromatic and unsubstituted or substituted; it preferably contains one or more heteroatoms in the ring, preferably from the group N, O and S; it is preferably an aliphatic heterocyclyl radical having 3 to 7 ring atoms or a heteroaromatic radical having 5 or 6 ring atoms and contains 1, 2 or 3 heteroatoms.
  • the heterocyclic radical may be e.g. a heteroaromatic radical or ring (heteroaryl), e.g.
  • a mono-, bi- or polycyclic aromatic system in which at least one ring contains one or more heteroatoms for example pyridyl, pyrimidinyl, pyridazinyl, pyrazinyl, triazinyl, thienyl, thiazolyl, oxazolyl, furyl, pyrrolyl, pyrazolyl and imidazolyl, or is partially or fully hydrogenated radical such as oxiranyl, oxetanyl, pyrrolidyl, piperidyl, piperazinyl, triazolyl, dioxolanyl, morpholinyl, tetrahydrofuryl.
  • heteroatoms for example pyridyl, pyrimidinyl, pyridazinyl, pyrazinyl, triazinyl, thienyl, thiazolyl, oxazolyl, furyl, pyrrolyl, pyrazolyl and imi
  • Suitable substituents for a substituted heterocyclic radical are the substituents mentioned below in question, in addition also oxo.
  • the oxo group may also be attached to the hetero ring atoms, which may exist in different oxidation states, e.g. at N and S, occur.
  • Substituted radicals such as substituted hydrocarbon radicals, for example substituted alkyl, alkenyl, alkynyl, aryl, phenyl and benzyl, or substituted heterocyclyl or heteroaryl, represent, for example, a substituted radical derived from the unsubstituted radical, where the substituents are, for example, one or more, preferably 1, 2 or 3 3 radicals from the group halogen, alkoxy, haloalkoxy, alkylthio, hydroxy, amino, nitro, carboxy, cyano, azido, alkoxycarbonyl, alkylcarbonyl, formyl, carbamoyl, mono- and dialkylaminocarbonyl, substituted amino, such as acylamino, mono- and dialkylamino, and Alkylsulfinyl, haloalkylsulfinyl, alkylsulfonyl, haloalkylsulfonyl and,
  • radicals with C atoms those having 1 to 4 C atoms, in particular 1 or 2 C atoms, are preferred.
  • Preferred are in the Generally given to substituents from the group halogen, for example fluorine and chlorine, (Ci-C 4) alkyl, preferably methyl or ethyl, (CrC 4) haloalkyl, preferably trifluoromethyl, (CrC 4) -alkoxy, preferably methoxy or ethoxy, (Ci-C 4 Haloalkoxy, nitro and cyano.
  • substituents methyl, methoxy and chlorine.
  • Optionally substituted phenyl is preferably phenyl which is unsubstituted or mono- or polysubstituted, preferably up to trisubstituted, by identical or different radicals, preferably from the group comprising halogen, (CrC 4) alkyl, (Ci-C 4) alkoxy, (CrC 4) haloalkyl , (C 1 -C 4 ) -haloalkoxy and nitro, for example o-, m- and p-tolyl, dimethylphenyl, 2-, 3- and 4-chlorophenyl, 2-, 3- and 4-trifluoro- and -T ⁇ ichlorphenyl, 2,4-, 3,5-, 2,5- and 2,3-dichlorophenyl, o-, m- and p-methoxyphenyl.
  • Cycloalkyl means a carbocyclic saturated ring system preferably having 3-6 C atoms, e.g. Cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl.
  • the carbon-containing radicals such as alkyl, alkoxy, haloalkyl, haloalkoxy, alkylamino and alkylthio and the corresponding unsaturated and / or substituted radicals in the carbon skeleton in each case be straight-chain or branched. Unless specifically stated, these radicals are the lower carbon skeletons, e.g. with 1 to 6 C atoms or with unsaturated groups having 2 to 6 C atoms, preferred.
  • Alkyl radicals also in the composite meanings such as alkoxy, haloalkyl, etc., mean e.g.
  • Alkynyl means e.g. Propargyl, but-2-yn-1-yl, but-3-yn-1-yl, 1-methyl-but-3-yn-1-yl.
  • Halogen is, for example, fluorine, chlorine, bromine or iodine.
  • Haloalkyl, alkenyl and alkynyl are alkyl which is partially or completely substituted by halogen, preferably by fluorine, chlorine and / or bromine, in particular by fluorine or chlorine, Alkenyl or alkynyl, eg CF 3 , CHF 2 , CH 2 F, CF 3 CF 2 , CH 2 FCHCl, CCI 3 , CHCl 2 , CH 2 CH 2 Cl;
  • Haloalkoxy is, for example, OCF 3 , OCHF 2 , OCH 2 F, CF 3 CF 2 O, OCH 2 CF 3 and OCH 2 CH 2 Cl; the same applies to haloalkenyl and other halogen-substituted radicals.
  • compositions according to the invention contain, in addition to components a) and b), one or more auxiliaries and additives, for example:
  • auxiliaries such as defoamers, antifreeze agents, evaporation inhibitors, preservatives, fragrances, dyes, stabilizers, water scavengers or thickeners,
  • one or more surfactants may be present in the formulations according to the invention as component c). These may be monomeric or polymeric (eg, graft polymers).
  • components c) are surfactants based on silicone, such as trisiloxane surfactants, derivatives of polydimethylsiloxanes and / or silicone oils, or sugar-based surfactants, such as Atplus 309 ® F (Uniqema).
  • components c) are (C 4 -C 3 o) (poly) alkylene oxide adducts which may be branched, for example, can be linear, saturated or unsaturated, in particular of fatty alcohols and / or fatty acids or Fettklareestern.
  • (poly) alkylene oxide adducts are Soprophor CY8 ® (Rhodia), Genapol ® X-060, Genapol ® X-080, Genapol ® X-150;
  • component c) are in the continuous phase of the formulation insoluble components, for example anionogenic surfactants, such as Hostapur ® OSB (Clariant), Netzer IS ® (Clariant), Galoryl DT 201 ® (CFPI), Tamol ® (BASF) or Morwet ® D 425 (Witco) may be used.
  • anionogenic surfactants such as Hostapur ® OSB (Clariant), Netzer IS ® (Clariant), Galoryl DT 201 ® (CFPI), Tamol ® (BASF) or Morwet ® D 425 (Witco) may be used.
  • component c) also sulfosuccinates, e.g. be of the formula (III),
  • R 1, R 2 independently of one another, identically or differently an unsubstituted or substituted Ci-C 3 o-hydrocarbon radical such as -C 3 O-alkyl, or a (poly) alkylene oxide adduct, and
  • M p is a cation, for example a metal cation such as an alkali or alkaline earth metal cation, an ammonium cation such as NH 4 , alkyl, alkylaryl or poly (arylalkyl) phenylammonium cation or their (poly) alkylene oxide adducts, or an amino-terminated (poly) alkylene oxide adduct ,
  • a metal cation such as an alkali or alkaline earth metal cation
  • an ammonium cation such as NH 4
  • an amino-terminated (poly) alkylene oxide adduct for example a metal cation such as an alkali or alkaline earth metal cation, an ammonium cation such as NH 4 , alkyl, alky
  • (Poly) alkylene oxide adducts in the context of this specification are reaction products of alkoxylatable starting materials such as alcohols, amines, carboxylic acids such as fatty acids, hydroxy- or amino-functional carboxylic acid esters (for example triglycerides based on castor oil) or carboxylic acid amides with alkylene oxides, where the (poly) alkylene oxide adducts have at least one alkylene oxide unit but are generally polymeric, ie 2-200, preferably 5-150 alkylene oxide
  • alkylene oxide units ethylene oxide, propylene oxide and butylene oxide units, especially ethylene oxide units, are preferred.
  • the described (poly) alkylene oxide adducts can be made from identical or different alkylene oxides, for example from blocky or random arranged ethylene oxide and propylene oxide, so that the present application also includes such mixed alkylene oxide adducts.
  • component c) may also contain non-surfactant polymers, e.g. Polyvinyl alcohols, polyacrylates, polymalinates or polyethylene oxides.
  • non-surfactant polymers e.g. Polyvinyl alcohols, polyacrylates, polymalinates or polyethylene oxides.
  • the polymers contained as component c) may be inorganic (e.g., silicates, phosphates) or organic, cationic, anionic, or neutral, synthetic, or naturally occurring.
  • the formulations according to the invention as component d) may contain various organic solvents such as non-polar solvents, polar protic or aprotic dipolar solvents and mixtures thereof.
  • organic solvents d) are - aliphatic or aromatic hydrocarbons, for example mineral oils, paraffins or toluene, xylenes and naphthalene derivatives, in particular 1-methylnaphthalene, 2-methylnaphthalene, C ⁇ -Ci ⁇ -aromatics such as the Solvesso ® series (ESSO), for example with the types Solvesso ® 100 (bp 162-177 0 C), Solvesso ® 150 (bp 187-207 0 C) and Solvesso ® 200 (bp 219-282 0 C) and C 6 -C 2 o-aliphatic, which can be linear or cyclic, such as the products of the Shellsol ® series,
  • Esters such as triacetin (acetic acid triglyceride), butyrolactone, propylene carbonate, triethyl citrate, and phthalic acid (C 1 -C 22 ) alkyl esters, especially phthalic acid (Cr
  • Ce alkyl esters, maleic acid (Ci-C 13 ) alkyl esters, linear, branched, saturated or unsaturated C 1 -C 20 alcohols such as methanol, ethanol, n- and iso-propanol, n-, iso-, sec- and tert.
  • Alkylenglykolmonoalkyether and -dialkylether such as propylene glycol monomethyl ether, especially Dowanol ® PM (propylene glycol monomethyl ether), propylene glycol monoethyl ether, ethylene glycol monomethyl ether or - monoethyl ether, diglyme and tetraglyme, Amides such as dimethylformamide (DMF) 1 dimethylacetamide, dimethylcapryl / caprin-fatty acid amide and N-alkylpyrrolidones, ketones such as the water-soluble acetone, but also water-immiscible ketones such as cyclohexanone or isophorone, - nitriles such as acetonitrile, propionitrile, butyronitrile and benzonitrile,
  • Sulfoxides and sulfones such as dimethyl sulfoxide (DMSO) and sulfolane, as well as oils in general, such as mineral oils or vegetable-based oils such as corn oil, linseed oil and rapeseed oil.
  • DMSO dimethyl sulfoxide
  • oils in general such as mineral oils or vegetable-based oils such as corn oil, linseed oil and rapeseed oil.
  • preferred organic solvents for the purposes of the present invention are ester oils such as rapeseed oil methyl ester and aliphatic or aromatic hydrocarbons, such as Solvesso ® types, z. Solvesso ® 200,
  • polycarboxylic can act as a solvent and are z.
  • Carboxylic acids preferably with 2-20 C atoms in question. Also suitable are polymeric polycarboxylic acids, preferably having molecular weights of up to 2000 g / mol.
  • polycarboxylic acids are oxalic, malonic, succinic, glutaric, adipic, pimelic, sebacic, azelaic, suberic, maleic, phthalic, terephthalic, mellitic, trimellitic, polymaleic, polyacrylic - and polymethacrylic acid and co- or
  • alkyl alcohols preferably monofunctional alkyl alcohols having 1 - 20 C atoms in question.
  • alkyl alcohols are methyl, ethyl-n-propyl, iso-propyl, n-butyl, sec-butyl, isobutyl or tert-butyl alcohol.
  • the polycarboxylic acid alkyl esters preferably have the following formula (I)
  • R ⁇ and R p are identical or different and are H, an unsubstituted or substituted C 1 -C 20 -hydrocarbon radical such as C 1 -C 10 -alkyl or a group (CR'R'VCO-OR ''', where R' and R '' are identical or differently, H or an unsubstituted or substituted Ci-C 2 o-hydrocarbon radical, such as Ci-Cio-alkyl, y is an integer from 0 to 10 and R '"is an unsubstituted or substituted C 1 -C 20 -
  • Hydrocarbon radical such as C 1 -C 0 alkyl
  • Rv and R ⁇ are identical or different unsubstituted or substituted C1 to C 20 - hydrocarbon radical such as C1-C1 0 alkyl, and x is a whole number from 0 to 20th
  • Particularly preferred polycarboxylic acid alkyl esters are diesters of the following
  • x is an integer from 0 to 20
  • Rv and R ⁇ independently Ci-C 6 alkyl are the same or different.
  • polycarboxylic acid alkyl esters examples include oxalic acid esters, such as dimethyl oxalate, diethyl oxalate, di-n-propyl oxalate, diisopropyl oxalate and methyl ethyl oxalate, malonic esters, such as dimethyl malonate, diethyl malonate, di-n-propyl malonic acid, Malonic acid diisopropyl ester and methyl malonate, succinic esters such as succinic acid dimethyl ester, succinic acid diethyl ester, succinic di-n-propyl ester, succinic diisopropyl ester and methyl succinate, glutaric acid esters such as dimethyl glutarate, glutaric acid diethyl ester, glutaric acid di-n-propyl ester, glutaric acid di-isopropyl ester and methyl glutarate, and adipic acid esters
  • Carboxylic acids with the alcohols accessible can be obtained by the reaction of "activated" polycarboxylic acids such as polycarboxylic acid anhydrides or polycarboxylic acid (poly) chlorides with the alcohols by known esterification methods.
  • the liquid formulations according to the invention may contain as component e) various agrochemicals. These are, for example, growth regulators or fertilizers.
  • component f) may also contain customary formulation auxiliaries, such as defoamers, antifreeze agents, evaporation inhibitors, preservatives, fragrances, dyes, stabilizers, water scavengers or thickeners.
  • Preferred formulation auxiliaries are antifreeze agents and evaporation inhibitors such as glycerol, for example in an amount of 2 to 10 wt .-%, and preservatives, for example Mergal K9N ® (Riedel) or Cobate ® C.
  • Tank-mix components may also be present in the formulations according to the invention as component g). Examples of this are tank mixers
  • Adjuvants such as Telmion ® (Hoechst) or vegetable oils such as Actirob B ® (Novance) or Hasten ® (Victorian Chemicals), inorganic compounds such as fertilizers, eg. As ammonium sulfate, ammonium nitrate, ammonium hydrogen sulfate, ureas or hydrotropes.
  • the active ingredient content of the formulations according to the invention can generally be between 0.001% by weight and 80% by weight, and in individual cases, in particular when using several active substances, higher loadings are also possible.
  • auxiliaries and additives which can be used to prepare the formulations according to the invention are known in principle and are described, for example, in: McCutcheon 's "Detergents and Emulsifiers Annual", MC Publ. Corp., Ridgewood NJ; Sisley and Wood, "Encyclopedia of Surface active agents, Chem., Publ.Co.ln ⁇ , NY 1964, Schonfeldt, "Grenz vomitepte ⁇ thylenoxidaddukte", Wiss. Verlagsgesellschaft, Stuttgart 1976, Winnacker-Küchler, "Chemical Technology", Volume 7, C. Hanser Verlag, Kunststoff, 4th edition 1986.
  • the present invention thus also encompasses the processes described for the preparation of the formulations according to the invention.
  • the formulations according to the invention are physically and chemically stable formulations which, when diluted with water, give spray mixtures having physically-favorable application properties.
  • the formulations of the invention have favorable biological properties and are widely used, for. B. to combat undesirable plant growth.
  • the preparation of the microcapsules can be prepared analogously to known processes.
  • the preparation of the encapsulated aqueous solutions or suspensions are preferably prepared starting from a water-in-oil emulsion with the addition of polymerizable components, if appropriate in the presence of suitable surface-active components, see, for example, US Pat. Nos. 4,157,983 and 4,534,783.
  • formulations according to the invention can be prepared, for example, as follows (exemplary embodiment):
  • An organic phase was prepared by dissolving dodecylbenzenesulfonic acid and nonionic alkylarylphenol in kerosene as a solvent.
  • the aqueous phase was prepared by dissolving glyphosate and urea / formaldehyde prepolymers in water. The two phases were then combined to form a water-in-oil emulsion with stirring. Thereafter, the temperature was raised to 40 0 C and stirring continued for 2 or more hours. The resulting product was cooled to give a suspension of microcapsules in the organic phase, the microcapsules enclosing the aqueous medium.
  • the production of microcapsules which include dissolved or dispersed in the oil phase agrochemical active ingredients can be carried out analogously to the known methods.
  • the water-soluble and microencapsulated agrochemical active ingredients are mixed with the agrochemical active substances dissolved or dispersed in the oil phase to give the oil suspension concentrate according to the invention.
  • the preparation of the oil suspension concentrates according to the invention is also provided. These can be prepared by known methods. The grinding and mixing of the components takes place as far as this is compatible with the formation or presence of the microcapsules according to the known methods.
  • the oil suspension concentrates of the present invention may optionally be diluted in conventional manner (e.g., by water), e.g. to suspensions, emulsions, suspoemulsions or solutions, preferably to emulsions. It may be advantageous to obtain spray mixtures which contain further agrochemical active substances (for example tank mix partners in the form of corresponding formulations) and / or customary auxiliaries and additives, for example self-emulsifying oils such as vegetable oils or paraffin oils and / or fertilizers.
  • the present invention therefore also relates to such herbicidal compositions, based on the oil suspension concentrates according to the invention.
  • herbicidal compositions according to the invention have excellent herbicidal activity against a broad spectrum of economically important monocotyledonous and dicotyledonous harmful plants, including species which are resistant to herbicidal active compounds such as glyphosate, glufosinate, atrazine or imidazolinone herbicides.
  • herbicidal active compounds such as glyphosate, glufosinate, atrazine or imidazolinone herbicides.
  • the hard-to-control perennial weeds that expel from rhizomes, rhizomes or other permanent organs are well detected by the active ingredients. or post-emergence.
  • the application is preferably carried out on the accumulated harmful plants (for example, weeds or unwanted crops), in particular before emergence of the (desired) crops.
  • some representatives of the monocotyledonous and dicotyledonous weed flora can be mentioned, which can be controlled by the compounds according to the invention, without the intention of limiting them to certain
  • the spectrum of activity extends to species such as e.g. Abutilon spp., Amaranthus spp., Chenopodium spp., Chrysanthemum spp., Galium spp., Ipomoea spp., Kochia spp., Lamium spp., Matricaria spp., Pharitis spp., Polygonum spp., Sida spp., Sinapis spp , Solanum spp., Stellaria spp., Veronica spp. and Viola spp., Xanthium spp., on the annual side, as well as Convolvulus, Cirsium, Rumex, and Artemisia in perennial weeds.
  • species such as e.g. Abutilon spp., Amaranthus spp., Chenopodium spp., Chrysanthemum spp., Galium spp., Ipomoea
  • herbicidal compositions according to the invention are applied to the surface of the earth before germination, either the emergence of the weed seedlings is completely prevented or the weeds grow up to the cotyledon stage, but then cease their growth and finally die completely after three to four weeks.
  • the herbicidal compositions according to the invention are distinguished by a rapidly onset and long-lasting herbicidal action.
  • the rainfastness of the active ingredients in the combinations according to the invention is generally favorable.
  • a particular advantage is the fact that the used and effective dosages of compounds (a) can be set so low that their soil effect is optimally low. Thus, their use is not only possible in sensitive cultures, but groundwater contamination is virtually avoided.
  • the combination of active substances according to the invention enables a considerable reduction in the required application rate of the active ingredients.
  • the agents according to the invention have in some cases outstanding growth-regulatory properties in the crop plants. They regulate the plant's metabolism and can thus be used to specifically influence plant constituents and facilitate harvesting, such as be used by triggering desiccation and stunted growth. Furthermore, they are also suitable for the general control and inhibition of unwanted vegetative growth, without killing the plants. Inhibition of vegetative growth plays an important role in many monocotyledonous and dicotyledonous cultures, as storage can be reduced or completely prevented.
  • the agents for combating harmful plants can be used in known plant crops or tolerant or genetically modified crops to be developed.
  • the transgenic plants are usually characterized by particular advantageous properties, in addition to the resistance to the inventive compositions, for example, by resistance to plant diseases or pathogens of plant diseases like certain insects or microorganisms like fungi, bacteria or viruses.
  • Other special properties relate to z. B. the crop in terms of quantity, quality, shelf life, composition and special ingredients.
  • one of the oil suspension concentrates according to the invention is used in the context of a method for controlling harmful organisms, wherein the application to the harmful organisms takes place in those places where these occur.
  • the use of one of the oil suspension concentrates according to the invention for controlling harmful organisms is within the scope of the invention.
  • the sulfonylurea-containing oil suspension concentrates are e.g. to
  • Control of harmful plants in crops suitable, for example in economically important arable crops such as monocotyledonous crops such as cereals (eg wheat, barley, rye, oats), rice, corn, millet, or dicotyledonous crops such as sugar beet, oilseed rape, cotton, sunflowers and legumes such as the genera Glycine (eg Glycine max.
  • monocotyledonous crops such as cereals (eg wheat, barley, rye, oats), rice, corn, millet, or dicotyledonous crops such as sugar beet, oilseed rape, cotton, sunflowers and legumes
  • Glycine eg Glycine max.
  • Soy as non-transgenic Glycine max (eg conventional varieties such as STS varieties) or transgenic Glycine max (eg RR soy or LL soy) and their crosses), Phaseolus, Pisum, Vicia and arachis, or vegetable crops from various botanical groups such as potato, leek, cabbage, carrot, tomato, onion, as well as permanent and Plantation crops such as pome and stone fruit, soft fruit, wine, Hevea, bananas, sugarcane, coffee, tea, citrus, nut orchards, roses, palm tree and forest crops. For the application of herbicide combinations, these cultures are also preferred.
  • herbivory tolerant mutant cultures and tolerant transgenic crops preferably maize, rice, cereals, rapeseed and soybean, in particular soybean, which are resistant to imidazolinone herbicides, glufosinates or glyphosates.
  • the oil suspension concentrates may also be used non-selectively to control undesired plant growth, e.g. in permanent and plantation crops, on roadsides, squares, industrial plants, airfields or railway facilities, or for so-called burn-down application, e.g. in crops, e.g. monocotyledonous crops such as cereals (e.g., wheat, barley, rye, oats), rice, corn, millet, or dicotyledonous crops such as cereals (e.g., wheat, barley, rye, oats), rice, corn, millet, or dicotyledonous crops such as
  • Glycine eg Glycine max. (soy) as non-transgenic Glycine max (eg conventional varieties such as STS varieties) or transgenic Glycine max (eg RR soy or LL soy) and their crosses
  • Phaseolus Phaseolus
  • Pisum Phaseolus
  • Vicia Triangulose
  • Arachis or vegetable crops from various botanical groups such as potato, leek, cabbage, carrot, tomato, onion.
  • Table 1 shows the composition of an oil suspension concentrate according to the invention, wherein both a component (a) and a component (b) is encapsulated.
  • Table 2 shows a composition in which only component (a) is encapsulated.

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Plant Pathology (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • Pest Control & Pesticides (AREA)
  • Agronomy & Crop Science (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Toxicology (AREA)
  • Chemical & Material Sciences (AREA)
  • Dispersion Chemistry (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Manufacturing Of Micro-Capsules (AREA)

Abstract

The invention relates to an oil suspension concentrate, comprising (a) one or a plurality of agrochemical active ingredients in the water phase, in encapsulated form in the oil phase, and (b) one or a plurality of agrochemical active ingredients encapsulated in the oil phase, and conventional adjuvants and additives.

Description

Beschreibung description
Ölsuspensionskonzentrat mit mikrogekapselten agrochemischen WirkstoffenOil suspension concentrate with microencapsulated agrochemical active ingredients
Allgemein betrifft die Erfindung Ölsuspensionskonzentrate für den Pflanzenschutz und darin enthaltene agrochemische Wirkstoffe, die in gekapselter Form vorliegen.In general, the invention relates to oil suspension concentrates for crop protection and agrochemical active substances contained therein, which are present in encapsulated form.
Mikrokapseln zeichnen sich dadurch aus, dass die Kapselhülle eine Wand ausMicrocapsules are characterized in that the capsule shell a wall
Polymeren ist, welche die beiden Flüssigkeitsphasen außerhalb und innerhalb der Kapsel physikalisch trennt. Der Begriff „Mikrokapsel" ist daher von anderen Formulierungsformen wie z.B. Emulsion, Mikrokugel, Liposom zu unterscheiden, da diese das Merkmal der physikalischen Trennung von Flüssigkeiten durch eine aus Polymeren bestehende Wand nicht aufweisen.Polymer is which physically separates the two liquid phases outside and inside the capsule. The term "microcapsule" is therefore to be distinguished from other forms of formulations such as emulsion, microsphere, liposome, since these do not have the physical separation characteristic of liquids through a wall made of polymers.
Man unterscheidet die „Öl-in-Wasser Mikroverkapselung" und die „Wasser-in-ÖI Mikroverkapselung".A distinction is made between "oil-in-water microencapsulation" and "water-in-oil microencapsulation".
Bei der Öl-in-Wasser Mikroverkapselung liegt eine Emulsion von Öl-in-Wasser vor, d.h. das nicht mit Wasser mischbare oder nicht wasserlösliche Material ist vom Polymermaterial der Mikrokapsel umgeben. Dagegen ist bei der Wasser-in-ÖI Mikroverkapselung die wässrige Phase im Inneren der Mikrokapsel. Sie wird daher auch als „Inverse-Mikroverkapselung" bezeichnet.In oil-in-water microencapsulation, there is an oil-in-water emulsion, i. the water-immiscible or water-insoluble material is surrounded by the polymer material of the microcapsule. In contrast, in the water-in-oil microencapsulation, the aqueous phase is inside the microcapsule. It is therefore also referred to as "inverse microencapsulation".
Die vorliegende Erfindung nutzt vorwiegend die Wasser-in-ÖI Mikroverkapselung, es sei denn das Verfahren der Multi-Mikroverkapselung wird eingesetzt. Bei der MuJti- Mikroverkapselung ist zwischen der „Wasser-in-ÖI-in-Wasser-Mikroverkapselung" und der „Wasser-in-ÖI-in-ÖI-Mikroverkapselung" zu unterscheiden. Im Rahmen der Erfindung ist prinzipiell die Umsetzung beider Techniken möglich, wobei die Wasser- in-ÖI-in-ÖI-Mikroverkapselung im Vordergrund steht. Für die genannten Formen der Mikroverkapselung sind entsprechendeThe present invention predominantly uses water-in-oil microencapsulation unless the multi-microencapsulation process is employed. In the case of MuJti microencapsulation, a distinction must be made between "water-in-oil-in-water microencapsulation" and "water-in-oil-in-oil microencapsulation". In the context of the invention, in principle, the implementation of both techniques is possible, wherein the water-in-oil-in-oil microencapsulation is in the foreground. For the mentioned forms of microencapsulation are appropriate
Herstellungsverfahren bekannt. Diese werden in unterschiedlichen Bereichen, z.B. Lebensmittelproduktion, Pharmazie, Farbstoffchemie, Agrochemie usw. eingesetzt.Manufacturing process known. These are in different areas, e.g. Food production, pharmacy, dyestuff chemistry, agrochemicals, etc. used.
Bei der Öl-in-Wasser Mikroverkapselung erfolgt die Bildung der Mikrokapseln ausgehend von einer ÖI-in-Wasser-Emulsion aus den in den Öl-Tröpfchen enthalten Monomeren und Vorpolymeren unter dem Einfluss von Wärme und/oder durch pH- Änderung und/oder durch mechanisches Rühren. Die jeweilige Behandlung verursacht die Polymerisierung der Monomer bzw. der Vorpolymere. Verfahren dieser Art sind z.B. in den Patenten US 4,285,720 und US 4,956,129 offenbart.In the case of oil-in-water microencapsulation, the formation of the microcapsules, starting from an oil-in-water emulsion, takes place from the monomers and prepolymers contained in the oil droplets under the influence of heat and / or by pH change and / or by mechanical stirring. The respective treatment causes the polymerization of the monomer or the prepolymers. Methods of this kind are e.g. in US Pat. Nos. 4,285,720 and 4,956,129.
Die EP 1 282 353 B1 offenbart die Kombination von Pflanzenschutzmitteln mit organischen oder anorganischen Trägermaterialien zur kontrollierten Freisetzung der Wirkstoffe, wobei auch die Verwendung der Öl-in-Wasser Mikroverkapselung vorgesehen ist. Die offenbarten Kombinationen gestatten die Unterdrückung der Antagonisierung anderer Wirkstoffe in Mischungen mit diesen und machen gleichzeitig die Anwendung von zeit- und arbeitsintensiven Splittapplikationen überflüssig. Das Problem der chemischen Inkompatibilität zwischen Wirkstoffen ist nicht Gegenstand der EP 1 282 353 B1.EP 1 282 353 B1 discloses the combination of pesticides with organic or inorganic carrier materials for the controlled release of the active ingredients, whereby the use of the oil-in-water microencapsulation is also provided. The disclosed combinations allow for the suppression of antagonization of other drugs in admixture therewith and, at the same time, eliminate the need for time and labor intensive splinter applications. The problem of chemical incompatibility between drugs is not the subject of EP 1 282 353 B1.
Wasser-in-ÖI Mikrokapseln werden ausgehend von einer Wasser-in-ÖI Emulsion durch das „Wasser-in-ÖI Verfahren" hergestellt. Ein solches Verfahren ist im US Patent US 4,157,983 offenbart. Ein entsprechendes Verfahren unter Verwendung von zwei Monomeren und Vorpolymeren ist in dem Patent US 4,534,783 offenbart.Water-in-oil microcapsules are prepared from a water-in-oil emulsion by the "water-in-oil process." Such a process is disclosed in US Patent US 4,157,983 A corresponding process using two monomers and prepolymers is in US Pat. No. 4,534,783.
Ein Verfahren zur mehrfachen Mikroverkapselung, das so genannte kontinuierliche Multi-Mikroverkapselungsverfahren, wird in der WO 2005/058476 A1 offenbart. Dabei handelt es sich um ein kontinuierliches Verfahren zur Mikroverkapselung Wasser-in-ÖI-in-Wasser durch in situ-Grenzflächenpolymerisation der entsprechenden Emulsion. Die in den Mikrokapseln eingeschlossenen aktiven Verbindungen sind gesundheitsfördernd und für andere biologische Zwecke geeignet. Der Einsatz des Verfahrens zur Formulierung von agrochemischen Wirkstoffen bzw. zur Lösung des Problems der chemischen Inkompatibiliät zwischen agrochemischen Wirkstoffen ist dabei nicht vorgesehen. Ein weiteres besonderes Verfahren zur „Wasser-in-ÖI Mikroverkapselung" ist in WO 98/28957 A offenbart. Dabei wird die Wand der Mikrokapseln in Gegenwart eines aktiven Oberflächen-Protonen-Transfer Protonen-Katalysators durch in situ- Selbstkondensation der Vorpolymere, die sich an der Grenzfläche zwischen wässriger und organischer Phase in der wässrigen Phase befinden, durch Wärmezuführung gebildet. In der wässrigen Phase im Inneren der Mikrokapseln befindet sich die aktive Substanz, die nach der Lehre der WO 98/28975 A auch aus einem Pestizide bestehen kann. Außerdem ist, dass auch die organische Phase als ein bioaktives Material ein Pestizid enthalten kann. Als Pestizide der wässrigenA process for multiple microencapsulation, the so-called continuous multi-microencapsulation process, is disclosed in WO 2005/058476 A1. It is a continuous process for microencapsulation of water-in-oil-in-water by in situ interfacial polymerization of the corresponding emulsion. The active compounds included in the microcapsules are beneficial to health and suitable for other biological purposes. The use of the method for the formulation of agrochemical active substances or for the solution of the problem of chemical incompatibility between agrochemical active ingredients is not provided for. Another particular method for "water-in-oil microencapsulation" is disclosed in WO 98/28957 A. The wall of the microcapsules in the presence of an active surface proton transfer proton catalyst by in situ self-condensation of prepolymers, which The aqueous phase inside the microcapsules contains the active substance, which according to the teaching of WO 98/28975 A can also consist of a pesticide is that the organic phase as a bioactive material may also contain a pesticide
Phase sind in der WO 98/28957 A genannt Paraquat, Diquat, Glyphosate, Dicamba, Acifluorfen, Fomesafen, loxynil, Bromoxynil, Bentazon, Atrazine und Azoxystrobin genannt. Als öllösliche Herbizide sind EPTC, Butylate, Cycloate, Molinate, Vernolate, Acetochlor, Metolachlor, Alachlor, Butachlor, Propachlor und Trifluralin genannt. Als Insektizide werden Parathion, Malathion, lonofos, Permethin, Lambda-cyhalothrin, Deltamethrin, Tralomethrin, Cypermethrin und Tefluthrin genannt, sowie als Fungizid Azoxystrobin. Optional können auch Safener eingesetzt werden. Das Problem der chemischen Inkompatibiliät zwischen zwei oder mehreren agrochemischen Wirkstoffen ist in der WO 98/28957 A nicht angesprochen.Phase are mentioned in WO 98/28957 A called paraquat, diquat, glyphosate, dicamba, acifluorfen, fomesafen, loxynil, bromoxynil, bentazone, atrazines and azoxystrobin. Oil-soluble herbicides include EPTC, butylates, cycloates, molinates, vernolates, acetochlor, metolachlor, alachlor, butachlor, propachlor and trifluralin. As insecticides parathion, malathion, lonofos, permethine, lambda-cyhalothrin, deltamethrin, tralomethrin, cypermethrin and tefluthrin are mentioned, as well as a fungicide azoxystrobin. Optionally, safeners can also be used. The problem of chemical incompatibility between two or more agrochemical active ingredients is not addressed in WO 98/28957 A.
Der Kongressbeitrag „Reverse Phase Microcapsule Suspension of Glyphosate Isopropylamine Salt in Hydrocarbon Fluids in Combination with Herbicidal Partners" aus dem Jahr 2002 (10th IUPAC International Congress on the Chemistry of Crop Protection Basel 2002, präsentiert von P. Y. Guyomar, Exxon Mobil Chemical, Book of Abstracts Topics 1-4, Vol. 1 , 4c.19) offenbart den Einsatz des wassergelösten Herbizides Glyphosat in mikrogekapselter Form (Glyphosate Capsule Suspension (CS) in oil fluids) in Kombination mit dem neben den Mikrokapseln in der Ölphase vorliegenden öllöslichen Herbizid Lactofen. Nachgewiesen wurde die Lagerbarkeit der Glyphosate-Lactofen-Formulierung über drei Monate und, dass im Spritztank keine der Co-Herbizid-Inkompatibilität zwischen den konkret genannten Herbiziden auftrat.The Congress paper "Reverse Phase Microcapsule Suspension of Glyphosate Isopropylamine Salt in Hydrocarbon Fluids in Combination with Herbicidal Partners" from 2002 (10th IUPAC International Congress on the Chemistry of Crop Protection Basel 2002, presented by PY Guyomar, Exxon Mobil Chemical, Book of Abstracts Topics 1-4, Vol.1, 4c.19) discloses the use of the water-dissolved glyphosate glyphosate in microencapsulated form (Glyphosate Capsule Suspension (CS) in oil fluids) in combination with the oil-soluble herbicide lactofen present in addition to the microcapsules in the oil phase the shelf life of the glyphosate-lactofen formulation was over three months and that in the spray tank no co-herbicide incompatibility between the specific herbicides mentioned occurred.
Der genannte Kongressbeitrag spricht allgemein die Inkompatibilität zweier Herbizide an. Mit Lactofen wird für die Ölphase ein Co-Herbizid vorgeschlagen, das sich durch eine geringe Wasserlöslichkeit, d.h. durch eine hohe Löslichkeit in Öl und zugleich eine geringe Hydrolyseempfindlichkeit auszeichnet. Eine differenziertere Betrachtung bzw. Lösungsansätze für das vielschichtige Problem der chemischen Inkompatibilität, insbesondere beim Einsatz hydrolyseempfindlicher Co-Herbizide wird daher in dem Kongressbeitrag nicht offenbart.The above-mentioned congress contribution generally addresses the incompatibility of two herbicides. With lactofen a co-herbicide is proposed for the oil phase, the is characterized by a low water solubility, ie by a high solubility in oil and at the same time a low susceptibility to hydrolysis. A more differentiated consideration or solution approaches for the complex problem of chemical incompatibility, especially when using hydrolysis-sensitive co-herbicides is therefore not disclosed in the congress article.
Grundsätzlich gilt, dass bei der Formulierung von Wirkstoffen aus der Klasse der Sulfonylharnstoffe stets auch deren Hydrolysempfindlichkeit zu berücksichtigen ist. Sehr gut sichergestellt ist deren chemische Stabilität durch die bislang etablierten Forumulierungstechniken, sofern die Sulfonylharnstoffe als Einzelwirkstoff oder in Kombination mit anderen Sulfonylharnstoffen oder auch mit Safener eingesetzt werden. Eine Herausforderung bleibt jedoch die Formulierung von Sulfonlyharnstoffen in Kombination mit Wirk- oder Hilfstoffen, deren Struktur eine Säurefunktion und/oder freie OH-Gruppen aufweisen. Wirkstoffe die für ihr hydrolyseinduzierendes Potential gegenüber Sulfonylharnstoffen bekannt sind, sind z.B. Glufosinate und Glyphosate. Der niedrige pH von Glyphosate (< 7) ist für solche Sulfonylharnstoffe, die im basischen Bereich stabil sind, schädlich.In principle, the hydrolysis sensitivity always has to be considered when formulating active substances from the class of sulfonylureas. Their chemical stability is very well ensured by the previously established forumulation techniques, provided that the sulfonylureas are used as a single active ingredient or in combination with other sulfonylureas or with safener. However, a challenge remains the formulation of sulfonylureas in combination with active ingredients or excipients whose structure has an acid function and / or free OH groups. Agents known for their hydrolysis-inducing potential over sulfonylureas are e.g. Glufosinate and glyphosate. The low pH of glyphosate (<7) is detrimental to those sulfonylureas that are stable in the basic range.
Die chemischen Inkompatibiltät von Wirkstoffen ist ein vielschichtiges Problem. Neben der Gebindestabilität bzw. Lagerstabilität kann die Stabilität des Wirkstoffs nach der Verdünnung des Konzentrats im Spritztank ein Problem sein. Bis zur Ausbringung des Wirkstoffs durch Versprühen muss das Auskristallisieren verhindert werden und die Verteilbarkeit sowie die biologische Aktivität des Wirkstoffs gewährleistet sein.The chemical incompatibility of drugs is a complex problem. In addition to the sustained release stability or storage stability, the stability of the active ingredient after dilution of the concentrate in the spray tank can be a problem. Until the application of the active substance by spraying, the crystallization must be prevented and the distributability and the biological activity of the active ingredient must be ensured.
Die Aufgabe der vorliegenden Erfindung bestand darin, eine verbesserte, flüssige Pflanzenschutzmittelformulierung mit mindestens zwei agrochemischen Wirkstoffen zur Verfügung zu stellen, wobei jeder Wirkstoff, insbesondere die in der Formulierung enthaltenen chemisch instabilen Wirkstoffe, sowie die Formulierung insgesamt, eine hohe chemische und physikalische Stabilität sowie eine hohe biologische Effektivität und Kulturpflanzenverträglichkeit aufweisen. Hierzu gehört auch allgemein die Vermeidung von antagonistischer Minderwirkung oder Überdosierung welche die Anwendung von Splittapplikationen sonst erforderlich machen.The object of the present invention was to provide an improved, liquid crop protection agent formulation having at least two agrochemical active ingredients, wherein each active ingredient, in particular the chemically unstable active ingredients contained in the formulation, and the formulation as a whole, a high chemical and physical stability and a have high biological effectiveness and crop plant compatibility. This also generally includes the avoidance of antagonistic inactivity or overdose, which otherwise necessitates the application of splinter applications.
Überraschenderweise wurde nun gefunden, dass diese Aufgabe durch das spezielle Ölsuspensionskonzentrat der vorliegenden Erfindung gelöst wird.Surprisingly, it has now been found that this object is achieved by the special oil suspension concentrate of the present invention.
Die vorliegende Erfindung betrifft somit ein Ölsuspensionskonzentrat, enthaltendThe present invention thus relates to an oil suspension concentrate containing
(a) ein oder mehrere agrochemische Wirkstoffe in der Wasser-Phase, in verkapselter Form in der Öl-Phase vorliegend, und(A) one or more agrochemical active ingredients in the water phase, in encapsulated form in the oil phase, and
(b) ein oder mehrere agrochemische Wirkstoffe in der Öl-Phase, verkapselt, sowie übliche Hilfs- und Zusatzstoffe.(B) one or more agrochemical active ingredients in the oil phase, encapsulated, and customary auxiliaries and additives.
Als besondere Ausführungsformen der Erfindung werden drei Alternativen vorgeschlagen.As particular embodiments of the invention, three alternatives are proposed.
Der Kerngedanke besteht bei den Alternativen darin, im Falle der Kombination von Wirkstoffen den eher hydrolyseempfindlichen Wirkstoff zu schützen, indem ein anderer Wirkstoff, der möglicherweise ein hydrolyseinduzierendes Potential aufweist, in jedem Fall in mikrogekapselter Form vorliegt.The core idea of the alternatives is to protect the more hydrolysis-sensitive active ingredient in the case of a combination of active ingredients, in any case in a microencapsulated form, another active ingredient which possibly has a hydrolysis-inducing potential.
Nach der ersten Alternative werden Ölsuspensionskonzentrate vorgeschlagen, die mindestens zwei unterschiedliche agrochemische Wirkstoffe enthalten, von denen mindestens einer wasserlöslich ist und im Inneren einer Mikrokapsel vorliegt. Mindestens ein weiterer, d.h. der in (b) vorliegende, in der Ölphase dispergiert oder gelöst vorliegender Wirkstoff ist ebenfalls gekapselt.According to the first alternative, oil suspension concentrates are proposed which contain at least two different agrochemical active substances, at least one of which is water-soluble and is present inside a microcapsule. At least one other, i. the active ingredient present in (b), dispersed or dissolved in the oil phase, is also encapsulated.
D.h. bei dieser ersten Alternative sind mindestens zwei Wirkstoffe, die sich z.B. in ihrer Löslichkeit und/oder in ihrer Hydrolyseempfindlichkeit unterscheiden, mikrogekapselt. Dadurch wird der hydrolyseempfindliche Wirkstoff zusätzlich geschützt, vor dem Wirkstoff, der aufgrund seines hydrolyseinduzierenden Potentials ebenfalls in mikrogekapselter Form vorliegt. Die zusätzliche Mikroverkapselung der besser in der Ölphase dispergiert oder gelöst vorliegenden Wirkstoffe kann zudem den Vorteil haben, dass aufgrund der verzögerten Freisetzung der unterschiedlich verkapselten Wirkstoffe Splittapplikationen vermieden werden können.That is, in this first alternative, at least two active substances which differ, for example, in their solubility and / or in their hydrolysis sensitivity are microencapsulated. As a result, the hydrolysis-sensitive active ingredient is additionally protected, in front of the active ingredient, which is also present in microencapsulated form due to its hydrolysis-inducing potential. The additional microencapsulation of the active ingredients dispersed or dissolved better in the oil phase can additionally have the advantage that, due to the delayed release of the differently encapsulated active ingredients, splinter applications can be avoided.
In der zweiten Alternative wird ein Ölsuspensionskonzentrat eingesetzt, das mindestens zwei unterschiedliche agrochemische Wirkstoffe enthält, von denen mindestens einer im Inneren einer Mikrokapsel vorliegt und mindestens einer in nicht gekapselter Form in der Ölphase vorliegt, wobei der in nicht gekapselter Form in der Ölphase vorliegende Wirkstoff ein Acetolactatsynthase(ALS)-Hemmer ist. D.h. gemäß dem Ansatz der zweiten Alternative wird auf die zusätzliche Mikroverkapselung der in der Ölphase dispergiert oder gelöst vorliegende Wirkstoffe verzichtet.In the second alternative, an oil suspension concentrate is used which contains at least two different agrochemical active ingredients, at least one of which is present in the interior of a microcapsule and at least one in non-encapsulated form in the oil phase, wherein the present in non-encapsulated form in the oil phase active ingredient Acetolactate synthase (ALS) inhibitor. That According to the approach of the second alternative, the additional microencapsulation of the active substances dispersed or dissolved in the oil phase is dispensed with.
In der dritten Alternative wird ein Ölsuspensionskonzentrat eingesetzt, das mindestens zwei unterschiedliche agrochemische Wirkstoffe enthält, von denen mindestens einer im Inneren einer Mikrokapsel vorliegt und mindestens einer in nicht gekapselter Form in der Ölphase vorliegt, wobei der mikroverkapselter Wirkstoff ein Acetolactatsynthase(ALS)-Hemmer ist und der Wirkstoff mit hohem hydrolysinduzierendem Potential in nicht gekapselter Form in der Ölphase vorliegt. D.h. gemäß dem Ansatz der dritten Alternative wird auf die zusätzliche Mikroverkapselung der hydrolyseinduzierenden Wirkstoffe verzichtet.The third alternative uses an oil suspension concentrate containing at least two different agrochemically active compounds, at least one of which is present inside a microcapsule and at least one in an unencapsulated form in the oil phase, where the microencapsulated agent is an acetolactate synthase (ALS) inhibitor and the active ingredient having high hydrolysis-inducing potential is present in non-encapsulated form in the oil phase. That According to the approach of the third alternative, the additional microencapsulation of the hydrolysis-inducing active ingredients is dispensed with.
Im Rahmen der Erfindung ist auch ein Ölsuspensionkonzentrat vorgesehen, das mindestens zwei unterschiedliche agrochemische Wirkstoffe enthält, von denen mindestens einer im Inneren einer Mikrokapsel vorliegt und mindestens einer in nicht-gekapselter Form in der Ölphase vorliegt, wobei der in nicht-gekapselter Form in der Ölphase vorliegende Wirkstoff ein phosphorhaltiges Herbizid ist.In the context of the invention, an oil suspension concentrate is also provided which contains at least two different agrochemical active ingredients, at least one of which is present in the interior of a microcapsule and at least one in non-encapsulated form in the oil phase, wherein in non-encapsulated form in the oil phase present active substance is a phosphorus-containing herbicide.
Nach einem zusätzlichen unabhängigen Lösungsansatz ist vorgesehen, dass die Wirkstoffe gemäß dem Multi-Mikroverkapselungsverfahren in WO 2005/058476 A1 behandelt wurden und in entsprechender Form vorliegen. Zum Schutz des bzw. der hydrolyseempfindlichen Wirkstoffe liegen im Fall der Wasser-in-ÖI-in-ÖI- Mikroverkapselung die hydrolyseinduzierenden Wirkstoffe im Inneren des Kapselkerns vor. Der hydrolyseempfindlichste Wirkstoff liegt dagegen in der Ölphase des Ölsuspensionskonzentrates vor, weil der dort am besten geschützt ist. Somit enthält das ölsuspensionskonzentrat mindestns zwei unterschiedlich agrochemische Wirkstoffe, worin mindestens ein Wirkstoff wasserlöslich ist und mindestens ein Wirkstoff in der Ölphase dispergiert oder gelöst vorliegt und die Wirkstoffe gemäß einem Multi-Mikroverkapselungsverfahren behandelt wurden und in entsprechender Form vorliegt.According to an additional independent approach, it is provided that the active substances were treated according to the multi-microencapsulation method in WO 2005/058476 A1 and are present in appropriate form. In the case of the water-in-oil-in-oil microencapsulation, the hydrolysis-inducing active substances in the interior of the Capsule core before. The most sensitive to hydrolysis active ingredient, however, is in the oil phase of the oil suspension concentrate, because there is the best protected. Thus, the oil suspension concentrate contains at least two different agrochemical active ingredients, wherein at least one active ingredient is water-soluble and at least one active ingredient is dispersed or dissolved in the oil phase and the active ingredients have been treated according to a multi-microencapsulation method and present in appropriate form.
Die Verbindungsklasse der Sulfonylharnstoffe gehört ihrem Wirkmechanismus nach zur Gruppe der ALS-Hemmer. Diese hemmen das Enzym Acetolactatsynthase (ALS) und damit die Proteinsynthese in den Pflanzen.The class of compounds of the sulfonylureas belongs to their mode of action according to the group of ALS inhibitors. These inhibit the enzyme acetolactate synthase (ALS) and thus the protein synthesis in the plants.
Nachfolgend werden die zur Beschreibung der Erfindung verwendeten Definitionen näher erläutert.The definitions used to describe the invention are explained in more detail below.
Unter dem Begriff Ölsuspensionskonzentrat (OD, Öldispersion) wird ein Suspensionskonzentrat auf Basis organischer mit Wasser nicht mischbarer Lösungsmittel verstanden. Dabei sind ein oder mehrere Wirkstoffe oder Safener in dem organischen Lösungsmittel suspendiert. Dabei können weitere Wirkstoffe oder Safener in dem organischen Lösungsmittel gelöst sein.The term oil suspension concentrate (OD, oil dispersion) is understood to mean a suspension concentrate based on organic water-immiscible solvents. One or more active substances or safeners are suspended in the organic solvent. In this case, further active ingredients or safeners may be dissolved in the organic solvent.
Der Begriff agrochemische Wirkstoff im Sinne dieser Erfindung umfasst Herbizide, Pflanzenwuchsregulatoren, Safener. D.h. die erfindungsgemäßen Ölsuspensionskonzentrate können auch einen oder mehrere Safener enthalten, wobei neben dem Wirkstoff auch der Safener in mikrogekapselter Form vorliegen kann. Mögliche Safener sind im Zusammenhang mit den agrochemischen Wirkstoffen nachfolgend beispielhaft genannt. Weiterhin können die erfindungsgemäßen Ölsuspensionskonzentrate eines oder mehrere anorganische Salze sowie übliche Hilfs- und Zusatzstoffe enthalten.The term agrochemical active ingredient in the context of this invention includes herbicides, plant growth regulators, safeners. That The oil suspension concentrates according to the invention may also contain one or more safeners, it being possible for the safener to be present in microencapsulated form in addition to the active substance. Possible safeners are mentioned below by way of example in connection with the agrochemical active ingredients. Furthermore, the oil suspension concentrates according to the invention may contain one or more inorganic salts as well as customary auxiliaries and additives.
Beispiele für einzelne agrochemische Wirkstoffe sind: HerbizideExamples of individual agrochemical active ingredients are: herbicides
Beispiele für Herbizide sind z.B. ALS-Inhibitoren (Acetolactat-Synthetase-Inhibitoren) oder Herbizide aus der Gruppe der Carbamate, Thiocarbamate, Halogenacetanilide, substituierte Phenoxy-, Naphthoxy- und Phenoxyphenoxycarbonsäure-Derivate sowie Heteroaryloxy-phenoxyalkancarbonsäure-Derivate, wie Chinolyloxy-, Chinoxalyl-oxy-, Pyridyloxy-, Benzoxazolyloxy- und Benzthiazolyloxyphenoxyalkan- carbonsäureester, Cyclo-hexandionabkömmlinge, Imidazolinone, Phosphor-haltige Herbizide, z.B. vom Glufosinate-Typ oder vom Glyphosate-Typ, Pyrimidinyloxy- pyridincarbonsäure-Derivate, Pyrimidyloxy-benzoesäure-Derivate, Triazolo- pyrimidin-sulfonamid-Derivate sowie S-(N-Aryl-N-alkylcarbamoylmethyl)- dithiophosphorsäureester, Harnstoffe sowie Hydroxybenzonitrile. Dabei sind im Falle der vorliegenden Erfindung die Herbizide aus der Gruppe der Carbamate, Thiocarbamate, Halogenacetanilide nicht als in der Ölphase vorliegende Wirkstoffe vorgesehen. In der wässrigen Phase im Inneren der Mikrokapseln, die im Ölsuspensionskonzentrat enthalten sind, können dagegen Carbamate, Thiocarbamate, Halogenacetanilide vorliegen.Examples of herbicides are e.g. ALS inhibitors (acetolactate synthetase inhibitors) or herbicides from the group of carbamates, thiocarbamates, haloacetanilides, substituted phenoxy, naphthoxy and phenoxyphenoxycarboxylic acid derivatives and heteroaryloxy-phenoxyalkanecarboxylic acid derivatives, such as quinolyloxy, quinoxalyl-oxy, pyridyloxy , Benzoxazolyloxy- and Benzthiazolyloxyphenoxyalkan-carboxylic acid esters, cyclo-hexanedione derivatives, imidazolinones, phosphorus-containing herbicides, eg glufosinate-type or glyphosate-type, pyrimidinyloxypyridinecarboxylic acid derivatives, pyrimidyloxybenzoic acid derivatives, triazolopyrimidine-sulfonamide derivatives and S- (N-aryl-N-alkylcarbamoylmethyl) -dithiophosphoric acid esters, ureas and hydroxybenzonitriles. In the case of the present invention, the herbicides from the group of carbamates, thiocarbamates, haloacetanilides are not provided as active substances present in the oily phase. On the other hand, carbamates, thiocarbamates, haloacetanilides may be present in the aqueous phase inside the microcapsules contained in the oil suspension concentrate.
Bei den herbiziden Wirkstoffen aus der Gruppe der ALS-Inhibitoren, wie Sulfonylharnstoffe, sind im Sinne der vorliegenden Erfindung neben den neutralen Verbindungen stets auch deren Salze mit anorganischen und/oder organischen Gegenionen zu verstehen. So können z.B. Sulfonylharnstoffe z.B. Salze bilden, bei denen der Wasserstoff der -Sθ2-NH-Gruppe durch ein für die Landwirtschaft geeignetes Kation ersetzt ist. Diese Salze sind beispielsweise Metallsalze, insbesondere Alkalimetallsalze oder Erdalkalimetallsalze, insbesondere Natrium- und Kaliumsalze, oder auch Ammoniumsalze oder Salze mit organischen Aminen. Ebenso kann Salzbildung durch Anlagerung einer Säure an basischen Gruppen, wie z.B. Amino und Alkylamino, erfolgen. Geeignete Säuren hierfür sind starke anorganische und organische Säuren, beispielsweise HCl, HBr, H2SO4 oder HNO3.For the purposes of the present invention, the herbicidal active compounds from the group of ALS inhibitors, such as sulfonylureas, are always to be understood as meaning, in addition to the neutral compounds, their salts with inorganic and / or organic counterions. Thus, for example, sulfonylureas can form, for example, salts in which the hydrogen of the -Sθ2-NH group is replaced by a cation suitable for agriculture. These salts are, for example, metal salts, in particular alkali metal salts or alkaline earth metal salts, in particular sodium and potassium salts, or else ammonium salts or salts with organic amines. Likewise, salt formation can take place by addition of an acid to basic groups, such as, for example, amino and alkylamino. Suitable acids for this purpose are strong inorganic and organic acids, for example HCl, HBr, H 2 SO 4 or HNO 3 .
A) Bevorzugte ALS-Inhibitoren entstammen aus der Reihe der Sulfonylharnstoffe und/oder ihrer Salze, z.B. Pyrimidin- oder Triazinylaminocarbonyl- [benzol-, pyridin-, pyrazol-, thiophen- und (alkylsulfonyl)-alkylamino-]-sulfamide. Solche geeigneten Sulfonylharnstoffe sind beispielsweiseA) Preferred ALS inhibitors come from the series of sulfonylureas and / or their salts, for example pyrimidine or triazinylaminocarbonyl [benzene, pyridine, pyrazole, thiophene and (alkylsulfonyl) alkylamino] sulfamides. Such suitable sulfonylureas are, for example
A1 ) Phenyl- und Benzylsulfonylhamstoffe und verwandte Verbindungen, z.B.A1) phenyl and benzylsulfonylureas and related compounds, e.g.
1-(2-Chlorphenylsulfonyl)-3-(4-methoxy-6-methyl-1 ,3,5-tria2in-2-yl)-harnstoff (Chlorsulfuron),1- (2-Chlorophenylsulfonyl) -3- (4-methoxy-6-methyl-1,3,5-tria2in-2-yl) -urea (chlorosulfuron),
1-(2-Ethoxycarbonylphenylsulfonyl)-3-(4-chlor-6-methoxypyrimidin-2-yl)-harnstoff1- (2-Ethoxycarbonylphenylsulfonyl) -3- (4-chloro-6-methoxypyrimidine-2-yl) -urea
(Chlorimuron-ethyl),(Chlorimuron-ethyl),
1-(2-Methoxyphenylsulfonyl)-3-(4-methoxy-6-methyl-1 ,3,5-triazin-2-yl)-harnstoff1- (2-methoxyphenylsulfonyl) -3- (4-methoxy-6-methyl-1,3,5-triazin-2-yl) urea
(Metsulfuron-methyl), 1 -(2-Chlorethoxyphenylsulfonyl)-3-(4-methoxy-6-methyl-1 ,3,5-triazin-2-yl)-harnstoff(Metsulfuron-methyl), 1- (2-Chloroethoxyphenylsulfonyl) -3- (4-methoxy-6-methyl-1,3,5-triazin-2-yl) -urea
(Triasulfuron),(Triasulfuron),
1-(2-Methoxycarbonylphenylsulfonyl)-3-(4,6-dimethylpyrimidin-2-yl)-harnstoff1- (2-Methoxycarbonylphenylsulfonyl) -3- (4,6-dimethylpyrimidin-2-yl) -urea
(Sulfumeturon-methyl),(Sulfumeturon-methyl),
1-(2-Methoxycarbonylphenylsulfonyl)-3-(4-methoxy-6-methyl-1 ,3,5-triazin-2-yl)-3- methylharnstoff (Tribenuron-methyl),1- (2-Methoxycarbonylphenylsulfonyl) -3- (4-methoxy-6-methyl-1,3,5-triazin-2-yl) -3-methylurea (tribenuron-methyl),
1-(2-Methoxycarbonylbenzylsulfonyl)-3-(4,6-dimethoxypyrimidin-2-yl)-harnstoff1- (2-Methoxycarbonylbenzylsulfonyl) -3- (4,6-dimethoxypyrimidin-2-yl) -urea
(Bensulfuron-methyl),(Bensulfuron-methyl),
1-(2-Methoxycarbonylphenylsulfonyl)-3-(4I6-bis-(difluormethoxy)pyrimidin-2-yl)- harnstoff, (Primisulfuron-methyl), 3-(4-Ethyl-6-methoxy-1 ,3,5-triazin-2-yl)-1-(2,3-dihydro-1 ,1-dioxo-2-methylbenzo-1- (2-Methoxycarbonylphenylsulfonyl) -3- (4 I 6-bis (difluoromethoxy) pyrimidin-2-yl) - urea, (primisulfuron-methyl), 3- (4-ethyl-6-methoxy-1, 3, 5-triazin-2-yl) -1- (2,3-dihydro-1, 1-dioxo-2-methylbenzoyl)
[b]thiophen-7-sulfonyl)-harnstoff (EP-A 0 079 683),[b] thiophene-7-sulfonyl) urea (EP-A 0 079 683),
3-(4-Ethoxy-6-ethyl-1 ,3,5-triazin-2-yl)-1 -(2,3-dihydro-1 , 1 -dioxo-2-methylbenzo[b]- thiophen-7-sulfonyl)harnstoff (EP-A 0 079 683),3- (4-Ethoxy-6-ethyl-1,3,5-triazin-2-yl) -1- (2,3-dihydro-1,1-dioxo-2-methylbenzo [b] -thiophene-7 sulfonyl) urea (EP-A 0 079 683),
3-(4-Methoxy-6-methyl-1 ,3,5-triazin-2-yl)-1-(2-methoxycarbonyl-5-jod-phenyl- sulfonyl)-harnstoff (lodosulfuron-methyl und dessen Natriumsalz, WO 92/13845),3- (4-Methoxy-6-methyl-1,3,5-triazin-2-yl) -1- (2-methoxycarbonyl-5-iodo-phenylsulfonyl) -urea (iodosulfuron-methyl and its sodium salt, WO 92/13845)
DPX-66037, Triflusulfuron-methyl (s. Brighton Crop Prot. Conf. - Weeds - 1995, S.DPX-66037, triflusulfuron-methyl (see Brighton Crop Prot. Conf. - Weeds - 1995, p.
853),853),
CGA-277476, (s. Brighton Crop Prot. Conf. - Weeds - 1995, S. 79),CGA-277476, (see Brighton Crop Prot. Conf. - Weeds - 1995, p.
Methyl-2-[3-(4,6-dimethoxypyrimidin-2-yl)ureidosulfonyl]-4-methansulfon-amido- methyl-benzoat (Mesosulfuron-methyl, WO 95/10507),Methyl 2- [3- (4,6-dimethoxypyrimidin-2-yl) ureidosulfonyl] -4-methanesulfonamido-methyl-benzoate (mesosulfuron-methyl, WO 95/10507),
N,N-Dimethyl-2-[3-(4,6-dimethoxypyrimidin-2-yl)ureidosulfonyl]-4-formylamino- benzamid (Foramsulfuron, WO 95/01344); A2) Thienylsulfonylharnstoffe, z.B.N, N-dimethyl-2- [3- (4,6-dimethoxypyrimidin-2-yl) ureidosulfonyl] -4-formylaminobenzamide (foramsulfuron, WO 95/01344); A2) Thienylsulfonylureas, eg
1-(2-Methoxycarbonylthiophen-3-yl)-3-(4-methoxy-6-methyl-1 ,3,5-triazin-2- yl)hamstoff (Thifensulfuron-methyl);1- (2-Methoxycarbonylthiophen-3-yl) -3- (4-methoxy-6-methyl-1,3,5-triazin-2-yl) urea (thifensulfuron-methyl);
A3) Pyrazolylsulfonylharnstoffe, z.B.A3) pyrazolylsulfonylureas, e.g.
1-(4-Ethoxycarbonyl-1-methylpyrazol-5-yl-sulfonyl)-3-(4,6-dimethoxypyrimidin-2- yl)hamstoff (Pyrazosulfuron-methyl);1- (4-ethoxycarbonyl-1-methylpyrazol-5-yl-sulfonyl) -3- (4,6-dimethoxypyrimidin-2-yl) urea (pyrazosulfuron-methyl);
Methyl-S-chlor-δ^.β-dimethoxypyrimidin^-ylcarbarnoylsulfamoyO-i-rnethyl-pyrazol- 4-carboxylat (EP-A 0 282 613); 5-(4,6-Dimethylpyrimidin-2-yl-carbamoylsulfamoyl)-1 -(2-pyridyl)-pyrazol-4-car- bonsäuremethylester (NC-330, s. Brighton Crop Prot. Conference "Weeds1 1991 , Vol.Methyl-S-chloro-δ, β, β-dimethoxypyrimidine, γ-ylylcarbamoyl-sulfamoyl-O-methyl-pyrazole-4-carboxylate (EP-A 0 282 613); Methyl 5- (4,6-dimethylpyrimidin-2-ylcarbamoylsulfamoyl) -1- (2-pyridyl) pyrazole-4-carboxylic acid (NC-330, see Brighton Crop Prot. Conference "Weeds 1 1991, Vol.
1 , S. 45 ff.),1, p. 45 ff.),
DPX-A8947, Azimsulfuron, (s. Brighton Crop Prot. Conf. Weeds1 1995, S. 65);DPX-A8947, azimsulfuron, (see Brighton Crop Prot. Conf. Weeds 1 1995, p.
A4) Sulfondiamid-Derivate, z.B.A4) sulfone diamide derivatives, e.g.
3-(4,6-Dimethoxypyrimidin-2-yl)-1-(N-methyl-N-methylsulfonylaminosulfonyl)- harnstoff (Amidosulfuron) und dessen Strukturanaloge (EP-A 0 131 258 und Z. PfI. Krankh. PfI. Schutz, Sonderheft XII, 489-497 (1990));3- (4,6-dimethoxypyrimidin-2-yl) -1- (N-methyl-N-methylsulfonylaminosulfonyl) urea (amidosulfuron) and its structural analogs (EP-A-0 131 258 and Z. Pfi. Ill. PfI Special Edition XII, 489-497 (1990));
A5) Pyridylsulfonylhamstoffe, z.B.A5) pyridylsulfonylureas, e.g.
1-(3-N,N-Dimethylaminocarbonylpyridin-2-ylsulfonyl)-3-(4,6-dimethoxypyrimidin-2- yl)-harnstoff (Nicosulfuron),1- (3-N, N-dimethylaminocarbonylpyridin-2-ylsulfonyl) -3- (4,6-dimethoxypyrimidin-2-yl) urea (nicosulfuron),
1-(3-Ethylsulfonylpyridin-2-ylsulfonyl)-3-(-(4,6-dimethoxypyrimidin-2-yl)-harnstoff1- (3-Ethylsulfonylpyridin-2-ylsulfonyl) -3 - (- (4,6-dimethoxypyrimidin-2-yl) -urea
(Rimsulfuron), 2-[3-(4,6-Dimethoxypyrimidin-2-yl)-ureidosulfonyl]-6-trifluormethyl-3-pyridin- carbonsäuremethylester, Natriumsalz (DPX-KE 459, Flupyrsulfuron, s. Brighton Crop(Rimsulfuron), 2- [3- (4,6-Dimethoxypyrimidin-2-yl) -uridosulfonyl] -6-trifluoromethyl-3-pyridine-carboxylic acid, methyl ester, sodium salt (DPX-KE 459, Flupyrsulfuron, see Brighton Crop
Prot. Conf. Weeds, 1995, S. 49),Prot. Conf. Weeds, 1995, p. 49),
Pyridylsulfonylhamstoffe, wie sie z.B. in DE-A 40 00 503 und DE-A 40 30 577 beschrieben sind, vorzugsweise solche der FormelPyridylsulfonylureas, as described e.g. in DE-A 40 00 503 and DE-A 40 30 577 are described, preferably those of the formula
worin wherein
E CH oder N, vorzugsweise CH, R20 lod oder NR25R26,E is CH or N, preferably CH, R 20 is iodine or NR 25 R 26 ,
R21 Wasserstoff, Halogen, Cyano, (Ci-C3)-Alkyl, (Ci-C3)-Alkoxy, (CrC3)- Halogenalkyl, (d-C3)-Halogenalkoxy, (CrC3)-Alkylthio, (CrC3)-Alkoxy-(d-R 21 is hydrogen, halogen, cyano, (Ci-C 3) alkyl, (Ci-C 3) alkoxy, (CrC 3) - haloalkyl, (dC 3) -haloalkoxy, (C r C 3) alkylthio, ( C r C 3 ) -alkoxy- (d-
C3)-alkyl, (CrC^-Altoxy-carbonyl, Mono- oder Di-((Ci-C3)-alkyl)-amino, (CrC 3 ) -alkyl, (C 1 -C 4 -alkoxy-carbonyl, mono- or di- ((C 1 -C 3 ) -alkyl) -amino, (Cr
C3)-Alkylsulfinyl oder -sulfonyl, SO2-NRxRy oder CO-NRxRy, insbesondereC 3 ) -alkylsulfinyl or -sulfonyl, SO 2 -NR x R y or CO-NR x R y , in particular
Wasserstoff,Hydrogen,
Rx, Ry unabhängig voneinander Wasserstoff, (CrC3)-Alkyl, (Ci-C3)-Alkenyl, (CrC3)- Alkinyl oder zusammen -(CH2)4-, -(CH2)5- oder -(CH2)2-O-(CH2)2-, n 0,1 ,2 oder 3, vorzugsweise 0 oder 1 ist, R22 Wasserstoff oder CH3, R23 Halogen, (CrC2)-Alkyl, (CrC2)-Alkoxy, (CrC2)-Halogenalkyl, insbesondereR x, R y are independently hydrogen, (C r C 3) alkyl, (Ci-C 3) -alkenyl, (CrC 3) - alkynyl or together are - (CH 2) 4 -, - (CH 2) 5 - or - (CH 2 ) 2 -O- (CH 2 ) 2, n is 0.1, 2 or 3, preferably 0 or 1, R 22 is hydrogen or CH 3 , R 23 is halogen, (C 1 -C 2 ) -alkyl, (-C 2) alkoxy, (CrC 2) -haloalkyl, in particular
CF3, (CrC2)-Halogenalkoxy, vorzugsweise OCHF2 oder OCH2CF3, R24 (CrC2)-Alkyl, (CrC2)-Halogenalkoxy, vorzugsweise OCHF2, oder (CrC2)-CF 3, (CrC 2) -haloalkoxy, preferably OCHF2 or OCH2 CF3, R 24 (-C 2) alkyl, (CrC 2) -haloalkoxy, preferably OCHF2, or (C r C 2) -
Alkoxy,alkoxy,
R25 (CrC4)-Alkyl, R26 (CrC4)-Alkylsulfonyl oderR 25 is (C r C 4 ) alkyl, R 26 is (CrC 4 ) alkylsulfonyl or
R25 und R26 gemeinsam eine Kette der Formel -(CH2)3SO2- oder -(CH2J4SO2- bedeuten, z.B. 3-(4,6-Dimethoxypyrimiden-2-yl)-1-(3-N-methylsulfonyl-N- methyl-aminopyridin-2-yl)-sulfonylharnstoff, oder deren Salze;R 25 and R 26 together represent a chain of the formula - (CH 2 ) 3 SO 2 - or - (CH 2 J 4 SO 2 -, for example 3- (4,6-dimethoxypyrimiden-2-yl) -1- (3 -N-methylsulfonyl-N-methyl-aminopyridin-2-yl) -sulfonylurea, or salts thereof;
In einer bevorzugten Ausführungsform des erfindungsgemäßen Ölsuspensionskonzentrats liegt als Herbizider Wirkstoff Pyridyl-Sulfonylharnstoff in suspendierter Form in der organischen Phase vor. Dies bedeutet, daß derIn a preferred embodiment of the oil suspension concentrate according to the invention is present as the herbicidal active ingredient pyridyl sulfonylurea in suspended form in the organic phase. This means that the
Hauptanteil (in Gew.-%) an Pyridyl-Sulfonylharnstoff ungelöst in fein verteilter Form vorliegt, ein geringerer Teil des Pyridyl-Sulfonylhamstoffes kann gelöst vorliegen. Vorzugsweise ist der Pyridyl-Sulfonylharnstoff im organischen Lösungsmittel zu mehr als 50 Gew.-%, besonders bevorzugt zu mehr als 80 Gew.-% suspendiert, jeweils bezogen auf die Gesamtmenge an Pyridyl-Sulfonylharnstoff a) in dem erfindungsgemäßen Ölsuspensionskonzentrat.Main proportion (in wt .-%) of pyridyl-sulfonylurea undissolved in finely divided form, a minor portion of the pyridyl-Sulfonylhamstoffes may be present dissolved. Preferably, the pyridyl-sulfonylurea in the organic solvent to more than 50 wt .-%, more preferably more than 80 wt .-% suspended, each based on the total amount of pyridyl-sulfonylurea a) in the oil suspension concentrate according to the invention.
A6) Als Pyridyl-Sulfonylharnstoffe bevorzugt sind Dioxazin- Pyridylsulfonylharnstoffe, insbesondere der allgemeinen Formel (I) worinA6) Preferred pyridyl-sulfonylureas are dioxazine-pyridylsulfonylureas, in particular of the general formula (I) wherein
für Stickstoff oder eine CR 11 -Gruppierung steht,is nitrogen or a CR 11 grouping,
wobeiin which
R11 für Wasserstoff, Alkyl, Halogen und Haloalkyl steht,R 11 is hydrogen, alkyl, halogen and haloalkyl,
R1 für Wasserstoff oder einen gegebenenfalls substituierten Rest aus der Reihe Alkyl, Älkoxy, Alkoxyalkyl, Alkenyl, Alkinyl, Cycloalkyl, Cycloalkylalkyl, Aralkyl und Aryl steht, R2 für Wasserstoff, Halogen oder für jeweils gegebenenfalls durch Halogen substituiertes Alkyl, Alkoxy, Alkylthio, Alkylamino oder Dialkylamino mit jeweils 1 bis 6 Kohlenstoffatomen steht, R3 für Wasserstoff, Halogen oder für jeweils gegebenenfalls durch Halogen substituiertes Alkyl, Alkoxy, Alkylthio, Alkylamino oder Dialkylamino mit jeweils 1 bis 6 Kohlenstoffatomen steht, R4 - R7 unabhängig voneinander für Wasserstoff, Halogen, Cyano, Thiocyanato oder für jeweils gegebenenfalls durch Halogen substituiertes Alkyl, Alkoxy, Alkylthio, Alkylsulfinyl, Alkylsulfonyl, Alkylamino, Alkylcarbonyl,R 1 is hydrogen or an optionally substituted radical from the group consisting of alkyl, alkoxy, alkoxyalkyl, alkenyl, alkynyl, cycloalkyl, cycloalkylalkyl, aralkyl and aryl, R 2 is hydrogen, halogen or in each case optionally halogen-substituted alkyl, alkoxy, alkylthio, Alkylamino or dialkylamino each having 1 to 6 carbon atoms, R 3 is hydrogen, halogen or each optionally halogen-substituted alkyl, alkoxy, alkylthio, alkylamino or dialkylamino each having 1 to 6 carbon atoms, R 4 - R 7 are independently hydrogen , Halogen, cyano, thiocyanato or each optionally halogen-substituted alkyl, alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, alkylamino, alkylcarbonyl,
Alkoxycarbonyl, Alkylaminocarbonyl mit jeweils 1 bis 3 Kohlenstoffatomen stehen, R8 für Wasserstoff, Halogen, Cyano, Thiocyanato oder für jeweils gegebenenfalls durch Halogen substituiertes Alkyl, Alkoxy, Alkylthio, Alkylsulfinyl, Alkylsulfonyl, Alkylamino, Alkylcarbonyl, Alkoxycarbonyl, Alkylaminocarbonyl mit jeweils 1 bis 3 Kohlenstoffatomen steht, wobei in den vorgenannten Resten die Alkyl- und Alkylengruppen jeweils 1 bis 6 C- Atome, die Alkenyl- und Alkinylgruppen jeweils 2 bis 6 C-Atome, die Cycloalkylgaippen jeweils 3 bis 6 C-Atome und die Arylgruppen jeweils 6 bzw. 10 C- Atome enthalten können.Alkoxycarbonyl, alkylaminocarbonyl having in each case 1 to 3 carbon atoms, R 8 is hydrogen, halogen, cyano, thiocyanato or in each case optionally halogen-substituted alkyl, alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, alkylamino, alkylcarbonyl, alkoxycarbonyl, alkylaminocarbonyl each having 1 to 3 Carbon atoms, where in the abovementioned radicals the alkyl and alkylene groups each have 1 to 6 C atoms, the alkenyl and alkynyl groups each have 2 to 6 C atoms, the cycloalkyl groups each have 3 to 6 C atoms and the aryl groups each have 6 or 10 C atoms. Atoms may contain.
Die Verbindungen der Formel (I) und deren Salze sind bekannt, ebenso wie deren Herstellung, z.B. aus US 5,476,936 die hiermit in die vorliegende Beschreibung aufgenommen wird.The compounds of formula (I) and their salts are known, as well as their preparation, e.g. from US 5,476,936 which is hereby incorporated into the present specification.
Bevorzugt sind Verbindungen der Formel (I) und deren Salze, worinPreference is given to compounds of the formula (I) and their salts, in which
A für Stickstoff oder eine CH-Gruppierung steht,A is nitrogen or a CH group,
R1 für Wasserstoff oder einen gegebenenfalls durch Halogen substituierten Rest aus der Reihe Alkyl, Alkoxy, Alkoxyalkyl, Alkenyl und Alkinyl mit jeweils bis zuR 1 is hydrogen or an optionally halogen-substituted radical from the series alkyl, alkoxy, alkoxyalkyl, alkenyl and alkynyl, each with up to
3 Kohlenstoffatomen steht, R2 für Wasserstoff, Halogen oder für jeweils gegebenenfalls durch Halogen substituiertes Alkyl, Alkoxy, Alkylthio, Alkylamino oder Dialkylamino mit jeweils3 carbon atoms, R 2 is hydrogen, halogen or each optionally substituted by halogen alkyl, alkoxy, alkylthio, alkylamino or dialkylamino with in each case
1 bis 3 Kohlenstoffatomen in den Alkylresten steht, R3 für Wasserstoff, Halogen oder für jeweils gegebenenfalls durch Halogen substituiertes Alkyl, Alkoxy, Alkylthio, Alkylamino oder Dialkylamino mit jeweils1 to 3 carbon atoms in the alkyl radicals, R 3 is hydrogen, halogen or each optionally halogen-substituted alkyl, alkoxy, alkylthio, alkylamino or dialkylamino with in each case
1 bis 3 Kohlenstoffatomen in den Alkylresten steht, R4 - R7 unabhängig voneinander für Wasserstoff, Halogen, Cyano, Thiocyanato oder für jeweils gegebenenfalls durch Halogen substituiertes Alkyl, Alkoxy, Alkylthio, Alkylsulfinyl, Alkylsulfonyl, Alkylamino, Alkylcarbonyl, Alkoxy- carbonyl oder Alkylaminocarbonyl mit jeweils 1 bis 3 Kohlenstoffatomen in den Alkylresten steht, R8 für Wasserstoff, Halogen, Cyano, Thiocyanato oder für jeweils gegebenenfalls durch Halogen substituiertes Alkyl, Alkoxy, Alkylthio, Alkylsulfinyl, Alkylsulfonyl, Alkylamino, Alkylcarbonyl, Alkoxycarbonyl oder Alkylaminocarbonyl mit jeweils 1 bis 3 Kohlenstoffatomen in den Alkylresten steht.R 4 - R 7 are each independently hydrogen, halogen, cyano, thiocyanato or each optionally halogen-substituted alkyl, alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, alkylamino, alkylcarbonyl, alkoxycarbonyl or alkylaminocarbonyl each having 1 to 3 carbon atoms in the alkyl radicals, R 8 represents hydrogen, halogen, cyano, thiocyanato or each optionally halogen-substituted alkyl, alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, alkylamino, alkylcarbonyl, alkoxycarbonyl or alkylaminocarbonyl each having 1 to 3 Carbon atoms in the alkyl radicals.
Weiter bevorzugt sind Salze, die man aus Verbindungen der Formel (I) und Basen, wie z.B. Natrium-, Kalium- oder Calciumhydroxid, -hydrid, -amid und -carbonat, Natrium- oder Kalium-CrC4-alkanolaten, Ammoniak, Ci-C4-Alkylaminen, Di-(CrC4- alkyl)-aminen oder Tri-(CrC4-alkyl)-aminen, nach üblichen Verfahren erhält.Further preferred are salts which are obtained from compounds of the formula (I) and bases, such as, for example, sodium, potassium or calcium hydroxide, hydride, amide and carbonate, Sodium or potassium-CrC 4 -alkanolaten, ammonia, Ci-C 4 -alkylamines, di (CrC 4 - alkyl) -amines or tri- (CrC 4 -alkyl) -amines, obtained by conventional methods.
Insbesondere bevorzugt sind Verbindungen der Formel (I) und deren Salzen, worinParticular preference is given to compounds of the formula (I) and their salts, in which
A für Stickstoff oder eine CH-Gruppierung steht,A is nitrogen or a CH group,
R1 für Wasserstoff, Methyl, Ethyl, Methoxy, Methoxymethyl oder Ethoxy steht,R 1 is hydrogen, methyl, ethyl, methoxy, methoxymethyl or ethoxy,
R2 für Wasserstoff, Chlor, Methyl, Ethyl, Trifluoromethyl, Methoxy, Ethoxy,R 2 is hydrogen, chlorine, methyl, ethyl, trifluoromethyl, methoxy, ethoxy,
Difluoromethoxy, Methylthio, Methylamino oder Dimethylamino steht, R3 für Wasserstoff, Chlor, Methyl, Ethyl, Trifluoromethyl, Methoxy, Ethoxy,Difluoromethoxy, methylthio, methylamino or dimethylamino, R 3 is hydrogen, chlorine, methyl, ethyl, trifluoromethyl, methoxy, ethoxy,
Difluoromethoxy, Methylthio, Methylamino oder Dimethylamino steht, R4 - R7 unabhängig voneinander für Wasserstoff, Fluor, Chlor, Cyano, oder für jeweils gegebenenfalls durch Chlor oder Fluor substituiertes Methyl, Methylthio, Methylsulfinyl, Methylsulfonyl, Methoxycarbonyl und Ethoxycarbonyl steht, vorzugsweise für Wasserstoff,Difluoromethoxy, methylthio, methylamino or dimethylamino, R 4 - R 7 are independently hydrogen, fluorine, chlorine, cyano, or each optionally substituted by chlorine or fluorine methyl, methylthio, methylsulfinyl, methylsulfonyl, methoxycarbonyl and ethoxycarbonyl, preferably hydrogen .
R8 für Wasserstoff, Fluor, Chlor, Brom, Cyano oder für jeweils gegebenenfalls durch Chlor oder Fluor substituiertes Methyl, Methoxy, Ethoxy, Methylthio, Ethylthio, Methylsulfinyl, Ethylsulfinyl, Methylsulfonyl, Ethylsulfonyl, Methyloder Dimethylamino steht, vorzugsweise für Wasserstoff.R 8 represents hydrogen, fluorine, chlorine, bromine, cyano or represents in each case optionally substituted by chlorine or fluorine methyl, methoxy, ethoxy, methylthio, ethylthio, methylsulfinyl, ethylsulfinyl, methylsulfonyl, ethylsulfonyl, methyl or dimethylamino, preferably hydrogen.
Besonders bevorzugt sind Verbindungen der Formel (I) und deren Salze, insbesondere deren Alkalimetallsalze,Particular preference is given to compounds of the formula (I) and salts thereof, in particular their alkali metal salts,
worin A für Stickstoff steht,where A is nitrogen,
R1 für Wasserstoff oder Methyl steht,R 1 is hydrogen or methyl,
R2 für Wasserstoff, Chlor, Methyl, Ethyl, Trifluoromethyl, Methoxy, Ethoxy, Difluoromethoxy, Methylthio, Methylamino oder Dimethylamino steht,R 2 is hydrogen, chlorine, methyl, ethyl, trifluoromethyl, methoxy, ethoxy, difluoromethoxy, methylthio, methylamino or dimethylamino,
R3 für Wasserstoff, Chlor, Methyl, Ethyl, Trifluoromethyl, Methoxy, Ethoxy, Difluoromethoxy, Methylthio, Methylamino oder Dimethylamino steht,R 3 is hydrogen, chlorine, methyl, ethyl, trifluoromethyl, methoxy, ethoxy, difluoromethoxy, methylthio, methylamino or dimethylamino,
R4 - R7 für Wasserstoff steht,R 4 - R 7 is hydrogen,
R8 für Wasserstoff steht. Ebenfalls besonders bevorzugt sind Verbindungen der Formel (I) und deren Salze, insbesondere deren Alkalimetallsalze,R 8 is hydrogen. Also particularly preferred are compounds of the formula (I) and salts thereof, in particular their alkali metal salts,
worin A für eine CH-Gruppierung steht, R1 für Wasserstoff oder Methyl steht, R2 für Wasserstoff, Chlor, Methyl, Ethyl, Trifluoromethyl, Methoxy, Ethoxy,wherein A is a CH group, R 1 is hydrogen or methyl, R 2 is hydrogen, chlorine, methyl, ethyl, trifluoromethyl, methoxy, ethoxy,
Difluoromethoxy, Methylthio, Methylamino oder Dimethylamino steht, R3 für Wasserstoff, Chlor, Methyl, Ethyl, Trifluoromethyl, Methoxy, Ethoxy, Difluoromethoxy, Methylthio, Methylamino oder Dimethylamino steht,Difluoromethoxy, methylthio, methylamino or dimethylamino, R 3 is hydrogen, chlorine, methyl, ethyl, trifluoromethyl, methoxy, ethoxy, difluoromethoxy, methylthio, methylamino or dimethylamino,
R4 - R7 für Wasserstoff steht, R8 für Wasserstoff steht.R 4 - R 7 is hydrogen, R 8 is hydrogen.
Die oben aufgeführten allgemeinen oder in Vorzugsbereichen aufgeführten Restedefinitionen können untereinander, also auch zwischen den angegebenen bevorzugten Bereichen beliebig kombiniert werden.The general or preferred radical definitions listed above can be combined as desired among one another, ie also between the stated preferred ranges.
Die bei den Restedefinitionen genannten Kohlenwasserstoffreste, wie Alkyl, Alkenyl oder Alkinyl, auch in Kombinationen mit Heteroatomen, wie in Alkoxy, Alkylthio, Haloalkyl oder Alkylamino, sind auch dann, wenn dies nicht ausdrücklich angegeben ist, geradkettig oder verzweigt.The hydrocarbon radicals mentioned in the radical definitions, such as alkyl, alkenyl or alkynyl, also in combinations with heteroatoms, such as in alkoxy, alkylthio, haloalkyl or alkylamino, are also straight-chain or branched, even if not expressly stated.
Die Pyridylsulfonylhamstoffe, z.B. solche der allgemeinen Formel (I), können auch als Salze vorliegen, z.B. als Metallsalze wie Alkali (z.B. Na, K) -Salze oder als Erdalkali (z.B. Ca, Mg) -Salze oder als Ammonium- oder organische Aminsalze. Man erhält solche Salze in einfacher Weise nach üblichen Salzbildungsmethoden, beispielsweise durch Lösen oder Dispergieren eines Pyridylsulfonylharnstoffs, z.B. der Formel (I), in einem geeigneten Verdünnungsmittel, wie z.B. Methylenchlorid, Aceton, tert.-Butyl-methylether oder Toluol, und Zugabe einer geeigneten Base. Die Salze können dann - gegebenenfalls nach längerem Rühren - durch Einengen oder Absaugen isoliert werden.The pyridylsulfonylureas, e.g. those of the general formula (I) may also be present as salts, e.g. as metal salts such as alkali (e.g., Na, K) salts or as alkaline earth (e.g., Ca, Mg) salts or as ammonium or organic amine salts. Such salts are readily obtained by conventional salt formation techniques, for example, by dissolving or dispersing a pyridylsulfonylurea, e.g. of the formula (I), in a suitable diluent, e.g. Methylene chloride, acetone, tert-butyl methyl ether or toluene, and addition of a suitable base. The salts can then - be isolated by concentration or suction - optionally after prolonged stirring.
Erfindungsgemäß bevorzugt enthaltene herbizide Wirkstoffe a) sind in der nachfolgenden Tabelle 1 genannt, worin folgende Abkürzungen verwendet werden: Smp.: = SchmelzpunktHerbicidally active compounds preferably present according to the invention are mentioned in Table 1 below, in which the following abbreviations are used: Mp .: = melting point
(+) = Der angegebene Schmelzpunkt (Smp.) bezieht sich jeweils auf das entsprechende Natriumsalz, d.h. die entsprechende Verbindung, worin der Wasserstoff der -Sθ2-NH-Gruppe durch Natrium ersetzt ist. (+) = The indicated melting point (mp) refers in each case to the corresponding sodium salt, ie the corresponding compound in which the hydrogen of the -Sθ 2 -NH group has been replaced by sodium.
Tabelle 1 : Beispiele für Verbindungen der Formel (I) mit R4 = R5= R6= R7= R8= H:Table 1: Examples of compounds of the formula (I) where R 4 = R 5 = R 6 = R 7 = R 8 = H:
Die herbiziden Wirkstoffe aus der Reihe der Pyridyl-Sulfonylharnstoffe sind in den erfindungsgemäßen Ölsuspensionskonzentraten im allgemeinen in Mengen von 0,01 bis 50 Gew.-%, bevorzugt 0,1 bis 30 Gew.-% enthalten, dabei bezieht sich die Angabe „Gew.-%" hier und in der gesamten Beschreibung, wenn nicht anders definiert, auf das relative Gewicht der jeweiligen Komponente bezogen auf das Gesamtgewicht der Formulierung.The herbicidal active compounds from the series of pyridyl-sulfonylureas are in the oil suspension concentrates according to the invention generally in amounts of 0.01 to 50% by weight, preferably 0.1 to 30% by weight, the term "% by weight" here and throughout the specification, unless otherwise defined, refers to the relative weight of the respective component on the total weight of the formulation.
A7) Alkoxyphenoxysulfonylharnstoffe, wie sie z.B. in EP-A 0 342 569 beschrieben sind, vorzugsweise solche der FormelA7) Alkoxyphenoxysulfonylureas, as e.g. in EP-A 0 342 569, preferably those of the formula
worin E CH oder N, vorzugsweise CH, where E is CH or N, preferably CH,
R27 Ethoxy, Propoxy oder Isopropoxy,R 27 is ethoxy, propoxy or isopropoxy,
R28 Halogen, NO2, CF3, CN, (Ci-C4)-Alkyl, (C1-C^-AIkOXy, (CrC4)-Alkylthio oder (CrC3)-Alkoxy-carbonyl, vorzugsweise in 6-Position am Phenylring, n 0, 1 , 2 oder 3, vorzugsweise 0 oder 1 , R29 Wasserstoff, (CrC4)-Alkyl oder (C3-C4)-Alkenyl,R 28 is halogen, NO 2, CF 3, CN, (Ci-C 4) -alkyl, (C 1 -C -alkoxy, (C r C4) -alkylthio or (CrC 3) alkoxy-carbonyl, preferably in 6-position on the phenyl ring, n is 0, 1, 2 or 3, preferably 0 or 1, R 29 is hydrogen, (C r C4) alkyl or (C 3 -C 4) alkenyl,
R30, R31 unabhängig voneinander Halogen, (d-C2)-Alkyl, (Ci-C2)-Alkoxy, (Ci-C2)- Halogenalkyl, (d-C2)-Halogenalkoxy oder (Ci-C2)-Alkoxy-(Ci-C2)-alkyl, vorzugsweise OCH3 oder CH3, bedeuten, z.B. 3-(4,6-Dimethoxypyrimidin-2- yl)-1-(2-ethoxyphenoxy)-sulfonylharnstoff, oder deren Salze;R 30, R 31 independently of one another are halogen, (dC 2) alkyl, (Ci-C 2) alkoxy, (Ci-C 2) - haloalkyl, (dC 2) -haloalkoxy or (Ci-C 2) alkoxy (C 1 -C 2 ) -alkyl, preferably OCH 3 or CH 3 , for example 3- (4,6-dimethoxypyrimidin-2-yl) -1- (2-ethoxyphenoxy) sulfonylurea, or salts thereof;
A8) Imidazolylsulfonylhamstoffe, z.B.A8) imidazolylsulfonylureas, e.g.
MON 37500, Sulfosulfuron (s. Brighton Crop Prot. Conf. Weeds', 1995, S: 57), und andere verwandte Sulfonylharnstoff-Derivate und Mischungen daraus;MON 37500, sulfosulfuron (see Brighton Crop Prot. Conf., Weeds', 1995, p. 57), and other related sulfonylurea derivatives and mixtures thereof;
Typische Vertreter dieser Wirkstoffe sind unter anderem die nachfolgend aufgeführten Verbindungen: Amidosulf uron, Azimsulfuron, Bensulfuron-Methyl, Chlorimuron-Ethyl, Chlorsulfuron, Cinosulfuron, Cyclosulfamuron, Ethametsulfuron- Methyl, Ethoxysulfuron, Flazasulfuron, Flupyrsulfuron-Methyl-Natrium, Halosulfuron- Methyl, Imazosulfuron, Metsulfuron-Methyl, Nicosulfuron, Oxasulfuron, Primisulfuron-Methyl, Prosulfuron, Pyrazosulfuron-Ethyl, Rimsulfuron, Sulfometuron- Methyl, Sulfosulfuron, Thifensulfuron-Methyl, Triasulfuron, Tribenuron-Methyl, Triflusulfuron-Methyl, lodosulfuron-Methyl und dessen Natriumsalz (WO 92/13845), Mesosulfuron-Methyl und dessen Natriumsalz (Agrow Nr. 347, 3. März 2000, Seite 22 (PJB Publications Ltd. 2000)) und Foramsulfuron und dessen Natriumsalz (Agrow Nr. 338, 15. Oktober 1999, Seite 26 (PJB Publications Ltd. 2000)).Typical representatives of these active ingredients include the following compounds: amidosulfuron, azimsulfuron, Bensulfuron-methyl, chlorimuron-ethyl, chlorosulfuron, cinosulfuron, Cyclosulfamuron, ethametsulfuron-methyl, ethoxysulfuron, flazasulfuron, Flupyrsulfuron-methyl-sodium, halosulfuron-methyl, imazosulfuron , Metsulfuron-methyl, nicosulfuron, oxasulfuron, primisulfuron-methyl, prosulfuron, pyrazosulfuron-ethyl, rimsulfuron, sulfometuron Methyl, sulfosulfuron, thifensulfuron-methyl, triasulfuron, tribenuron-methyl, triflusulfuron-methyl, iodosulfuron-methyl and its sodium salt (WO 92/13845), mesosulfuron-methyl and its sodium salt (Agrow No. 347, March 3, 2000, page 22 (PJB Publications Ltd. 2000)) and foramsulfuron and its sodium salt (Agrow No. 338, Oct. 15, 1999, page 26 (PJB Publications Ltd. 2000)).
A9) PhenylsulfonylaminocarbonyltriazolinoneA9) Phenylsulfonylaminocarbonyltriazolinone
Beispiele für Verbindungen aus der Gruppe der Phenylsulfonylaminocarbonyl- triazolinone sind z.B. Flucarbazone oder Propoxycarbazone und/oder deren Salze.Examples of compounds from the group of the phenylsulfonylaminocarbonyl-triazolinones are e.g. Flucarbazone or propoxycarbazone and / or salts thereof.
A10) (Het)Aryl-sulfonyl-aminocarbonyl-triazolinoneA10) (Het) aryl-sulfonyl-aminocarbonyl-triazolinone
Thien-3-yl-sulfonylamino(thio)carbonyl-triazolin(thi)on der allgemeinen Formel (II)Thien-3-yl-sulfonylamino (thio) carbonyl-triazoline (thi) on the general formula (II)
in welcher in which
Q1 für O (Sauerstoff) oder S (Schwefel) steht,Q 1 is O (oxygen) or S (sulfur),
Q2 für O (Sauerstoff) oder S (Schwefel) steht,Q 2 is O (oxygen) or S (sulfur),
R1 für gegebenenfalls durch Cyano, Halogen oder CrC4-Alkoxy substituiertes Alkyl mit 1 bis 6 Kohlenstoffatomen, für jeweils gegebenenfalls durch Cyano oder Halogen substituiertes Alkenyl oder Alkinyl mit jeweils 2 bis 6 Kohlenstoffatomen, für jeweils gegebenenfalls durch Cyano, Halogen oder CiC-t-Alkyl substituiertes Cycloalkyl oder Cycloalkylalkyl mit jeweils 3 bis 6 Kohlenstoffatomen in der Cycloalkylgruppe und gegebenenfalls 1 bis 4 Kohlenstoffatomen im Alkylteil, für jeweils gegebenenfalls durch Nitro, Cyano,R 1 is optionally substituted by cyano, halogen or -C 4 -alkoxy-substituted alkyl having 1 to 6 carbon atoms, represents optionally cyano- or halogen-substituted alkenyl or alkinyl each having 2 to 6 carbon atoms, represents in each case optionally cyano-, halogen or CIC t Alkyl-substituted cycloalkyl or cycloalkylalkyl having in each case 3 to 6 carbon atoms in the cycloalkyl group and optionally 1 to 4 carbon atoms in the alkyl moiety, in each case optionally by nitro, cyano,
Halogen, CrC4-Alkyl oder CrC4-Alkoxy substituiertes Aryl oder Arylalkyl mit jeweils 6 oder 10 Kohlenstoffatomen in der Arylgruppe und gegebenenfalls 1 bis 4 Kohlenstoffatomen im Alkylteil, oder für jeweils gegebenenfalls durch Nitro, Cyano, Halogen, d-C4-Alkyl oder Ci-C4-Alkoxy substituiertes Heterocyclyl oder Heterocyclylalkyl mit jeweils bis zu 6 Kohlenstoffatomen und zusätzlich 1 bis 4 Stickstoffatomen und/oder 1 bis 2 Sauerstoff- oder Schwefelatomen in der Heterocyclylgruppe und gegebenenfalls 1 bis 4 Kohlenstoffatomen im Alkylteil steht, R2 für Wasserstoff, CrC4-Alkyl, Cyano, Nitro, Halogen, für jeweils gegebenenfalls durch Cyano, Halogen oder Ci-C4-Alkoxy substituiertes Alkyl, Alkoxy, Alkoxycarbonyl, Alkylthio, Alkylsulfinyl oder Alkylsulfonyl mit jeweils 1 bis 6 Kohlenstoffatomen in der Alkylgruppe, oder für jeweils gegebenenfalls durch Cyano oder Halogen substituiertes Alkenyl, Alkinyl, Alkenyloxy oder Alkinyloxy mit jeweils 2 bis 6 Kohlenstoffatomen in der Alkenyl- oder Alkinylgruppe steht,Halogen, C 1 -C 4 -alkyl or C 1 -C 4 -alkoxy-substituted aryl or arylalkyl having in each case 6 or 10 carbon atoms in the aryl group and optionally 1 to 4 carbon atoms in the alkyl moiety, or in each case optionally by nitro, cyano, halogen, C 1 -C 4 -alkyl or C 1 -C 4 -alkyl -C 4 -alkoxy substituted Heterocyclyl or heterocyclylalkyl having in each case up to 6 carbon atoms and additionally 1 to 4 nitrogen atoms and / or 1 to 2 oxygen or sulfur atoms in the heterocyclyl group and optionally 1 to 4 carbon atoms in the alkyl part, R 2 is hydrogen, C 1 -C 4 -alkyl, cyano, Nitro, halogen, in each case optionally substituted by cyano, halogen or Ci-C 4 alkoxy-substituted alkyl, alkoxy, alkoxycarbonyl, alkylthio, alkylsulfinyl or alkylsulfonyl each having 1 to 6 carbon atoms in the alkyl group, or for each optionally substituted by cyano or halogen alkenyl , Alkynyl, alkenyloxy or alkynyloxy having in each case 2 to 6 carbon atoms in the alkenyl or alkynyl group,
R3 für Wasserstoff, Hydroxy, Mercapto, Amino, Cyano, Fluor, Chlor, Brom, lod, für gegebenenfalls durch Fluor, Chlor, Brom, Cyano, Ci-C4-Alkoxy, CrC4- Alkylcarbonyl oder C-ι-C4-Alkoxy-carbonyl substituiertes Alkyl mit 1 bis 6 Kohlenstoffatomen, für jeweils gegebenenfalls durch Fluor, Chlor und/oder Brom substituiertes Alkenyl oder Alkinyl mit jeweils 2 bis 6 Kohlenstoffatomen, für jeweils gegebenenfalls durch Fluor, Chlor, Cyano, C-ι-C4-Alkoxy oder C-ι-C4-Alkoxy-carbonyl substituiertes Alkoxy, Alkylthio, Alkylamino oder Alkylcarbonylamino mit jeweils 1 bis 6 Kohlenstoffatomen in der Alkylgruppe, für Alkenyloxy, Alkinyloxy, Alkenylthio, Alkinylthio, Alkenylamino oder Alkinylamino mit jeweils 3 bis 6 Kohlenstoffatomen in der Alkenyl- oderR 3 is hydrogen, hydroxyl, mercapto, amino, cyano, fluorine, chlorine, bromine, iodine, optionally substituted by fluorine, chlorine, bromine, cyano, C 1 -C 4 -alkoxy, C 1 -C 4 -alkylcarbonyl or C 1 -C 4 -alkoxy-carbonyl-substituted alkyl having 1 to 6 carbon atoms, represents in each case optionally substituted by fluorine, chlorine and / or bromine-substituted alkenyl or alkinyl each having 2 to 6 carbon atoms, represents in each case optionally substituted by fluorine, chlorine, cyano, C-ι-C 4 Alkoxy or C 1 -C 4 -alkoxycarbonyl-substituted alkoxy, alkylthio, alkylamino or alkylcarbonylamino having in each case 1 to 6 carbon atoms in the alkyl group, for alkenyloxy, alkynyloxy, alkenylthio, alkynylthio, alkenylamino or alkynylamino having in each case 3 to 6 carbon atoms in the alkenyl or
Alkinylgruppe, für Dialkylamino mit jeweils 1 bis 4 Kohlenstoffatomen in den Alkylgruppen, für jeweils gegebenenfalls durch Methyl und/oder Ethyl substituiertes Aziridino, Pyrrolidino, Piperidino oder Morpholino, für jeweils gegebenenfalls durch Fluor, Chlor, Brom, Cyano und/oder d-C4-Alkyl substituiertes Cycloalkyl, Cycloalkenyl, Cycloalkyloxy, Cycloalkylthio,Alkinyl group, for dialkylamino having in each case 1 to 4 carbon atoms in the alkyl groups, for each optionally substituted by methyl and / or ethyl aziridino, pyrrolidino, piperidino or morpholino, each optionally substituted by fluorine, chlorine, bromine, cyano and / or dC 4 alkyl substituted cycloalkyl, cycloalkenyl, cycloalkyloxy, cycloalkylthio,
Cycloalkylamino, Cycloalkylalkyl, Cycloalkylalkoxy, Cycloalkylalkylthio oder Cycloalkylalkylamino mit jeweils 3 bis 6 Kohlenstoffatomen in der Cycloalkyl- bzw. Cycloalkenylgruppe und gegebenenfalls 1 bis 4 Kohlenstoffatomen im Alkylteil, oder für jeweils gegebenenfalls durch Fluor, Chlor, Brom, Cyano, Nitro, Ci-C4-Alkyl, Trifluormethyl, CrC4-Alkoxy und/oder C1-C4-Cycloalkylamino, cycloalkylalkyl, cycloalkylalkoxy, cycloalkylalkylthio or cycloalkylalkylamino having in each case 3 to 6 carbon atoms in the cycloalkyl or cycloalkenyl group and optionally 1 to 4 carbon atoms in the alkyl moiety, or in each case optionally by fluorine, chlorine, bromine, cyano, nitro, C 1 -C 4 Alkyl, trifluoromethyl, C r C 4 alkoxy and / or C 1 -C 4 -
Alkoxycarbonyl substituiertes Aryl, Arylalkyl, Aryloxy, Arylalkoxy, Arylthio, Arylalkylthio, Arylamino oder Arylalkylamino mit jeweils 6 oder 10 Kohlenstoffatomen in der Arylgruppe und gegebenenfalls 1 bis 4 Kohlenstoffatomen im Alkylteil steht, R4 für Wasserstoff, CrC4-Alkyl, Hydroxy, Amino, Cyano, für C2-C-ιo-Alkyliden- amino, für gegebenenfalls durch Fluor, Chlor, Brom, Cyano, Ci-C4-Alkoxy, C1- C4-Alkylcarbonyl oder CrC^AIkoxy-carbonyl substituiertes Alkyl mit 1 bis 6 Kohlenstoffatomen, für jeweils gegebenenfalls durch Fluor, Chlor und/oder Brom substituiertes Alkenyl oder Alkinyl mit jeweils 2 bis 6 Kohlenstoffatomen, für jeweils gegebenenfalls durch Fluor, Chlor, Brom, Cyano, CrC4-AIkOXy oder CrC4-Alkoxy-carbonyl substituiertes Alkoxy, Alkylamino oder Alkylcarbonylamino mit jeweils 1 bis 6 Kohlenstoffatomen in der Alkylgruppe, für Alkenyloxy mit 3 bis 6 Kohlenstoffatomen, für Dialkylamino mit jeweils 1 bis 4 Kohlenstoffatomen in den Alkylgruppen, für jeweils gegebenenfalls durch Fluor, Chlor, Brom, Cyano und/oder CrC4-Alkyl substituiertes Cycloalkyl, Cycloalkylamino oder Cycloalkylalkyl mit jeweils 3 bis 6 Kohlenstoffatomen in der Alkylgruppe und gegebenenfalls 1 bis 4 Kohlenstoffatomen im Alkylteil, oder für jeweils gegebenenfalls durch Fluor, Chlor, Brom, Cyano, Nitro, C1-C4- Alkyl, Trifluormethyl und/oder Ci-C4-Alkoxy substituiertes Aryl oder Arylalkyl mit jeweils 6 oder 10 Kohlenstoffatomen in der Arylgruppe und gegebenenfalls 1 bis 4 Kohlenstoffatomen im Alkylteil steht, oderAlkoxycarbonyl-substituted aryl, arylalkyl, aryloxy, arylalkoxy, arylthio, arylalkylthio, arylamino or arylalkylamino each having 6 or 10 carbon atoms in the aryl group and optionally 1 to 4 carbon atoms in the alkyl moiety, R 4 is hydrogen, C 1 -C 4 -alkyl, hydroxy, amino, cyano, C 2 -C -alkylamino-amino, optionally substituted by fluorine, chlorine, bromine, cyano, C 1 -C 4 -alkoxy, C 1 -C 4- alkylcarbonyl or C 1 -C 6 -alkoxy-carbonyl-substituted alkyl having 1 to 6 carbon atoms, in each case optionally substituted by fluorine, chlorine and / or bromine-substituted alkenyl or alkynyl having in each case 2 to 6 carbon atoms, in each case optionally by fluorine, chlorine, bromine, cyano , C 1 -C 4 -alkoxy or C 1 -C 4 -alkoxycarbonyl-substituted alkoxy, alkylamino or alkylcarbonylamino having in each case 1 to 6 carbon atoms in the alkyl group, for alkenyloxy having 3 to 6 carbon atoms, for dialkylamino having in each case 1 to 4 carbon atoms in the alkyl groups, in each case optionally substituted by fluorine, chlorine, bromine, cyano and / or C 1 -C 4 -alkyl-substituted cycloalkyl, cycloalkylamino or cycloalkylalkyl each having 3 to 6 carbon atoms in the alkyl group and optionally 1 to 4 carbon atoms in the alkyl or, in each case optionally substituted by fluorine, chlorine, bromine, cyano, nitro, C 1 -C 4 -alkyl, trifluoromethyl and / or C 1 -C 4 -alkoxy, aryl or arylalkyl each having 6 or 10 carbon atoms in the aryl group and optionally 1 to 4 carbon atoms in the alkyl part, or
R3 und R4 zusammen für gegebenenfalls verzweigtes Alkandiyl mit 3 bis 6 Kohlenstoffatomen stehen,R 3 and R 4 together represent optionally branched alkanediyl having 3 to 6 carbon atoms,
- sowie Salze der Verbindungen der Formel (II) -and salts of the compounds of the formula (II)
B) Herbizide vom Typ der Phenoxyphenoxy- und Heteroaryloxyphenoxycarbonsäure-Derivate, wieB) Phenoxyphenoxy- and heteroaryloxyphenoxycarboxylic acid-type herbicides, such as
B1 ) Phenoxyphenoxy- und Benzyloxyphenoxy-carbonsäure-Derivate, z.B. 2-(4- (2,4-Dichlθφhenoxy)-phenoxy)-propionsäuremethylester (Diclofop-methyl), 2-(4-(4-Brom-2-chlorphenoxy)-phenoxy)-propionsäuremethylester (DE-A 26 01 548), 2-(4-(4-Brom-2-fluorphenoxy)-phenoxy)-propionsäuremethylester (US-A 4,808,750), 2-(4-(2-Chlor-4-trifluormethylphenoxy)-phenoxy)-propionsäuremethylester (DE-A 24 33 067),B1) phenoxyphenoxy- and benzyloxyphenoxy-carboxylic acid derivatives, e.g. Methyl 2- (4- (2,4-dichlorophenoxy) phenoxy) propionate (diclofopmethyl), 2- (4- (4-bromo-2-chlorophenoxy) phenoxy) propionate (DE-A 26 01 548) Methyl 2- (4- (4-bromo-2-fluorophenoxy) -phenoxy) -propionate (US Pat. No. 4,808,750), 2- (4- (2-chloro-4-trifluoromethylphenoxy) -phenoxy) -propionic acid methyl ester (DE-A 24 33 067),
2-(4-(2-Fluor-4-trifluormethylphenoxy)-phenoxy)-propionsäuremethylester (US-A2- (4- (2-Fluoro-4-trifluoromethylphenoxy) -phenoxy) -propionic acid methyl ester (US Pat
4,808,750),4,808,750)
2-(4-(2,4-Dichlorbenzyl)-phenoxy)-propionsäuremethylester (DE-A 24 17 487),2- (4- (2,4-dichlorobenzyl) -phenoxy) -propionic acid methyl ester (DE-A 24 17 487),
4-(4-(4-Trifluormethylphenoxy)-phenoxy)-pent-2-en-säureethylester, 2-(4-(4-Trifluormethylphenoxy)-phenoxy)-propionsäuremethylester (DE-A 24 33 067);4- (4- (4-trifluoromethylphenoxy) -phenoxy) -pent-2-enoic acid ethyl ester, 2- (4- (4-trifluoromethylphenoxy) -phenoxy) -propionic acid methyl ester (DE-A 24 33 067);
B2) "Einkernige" Heteroaryloxyphenoxy-alkancarbonsäure-Derivate, z.B. 2-(4-(3,5-Dichlorpyridyl-2-oxy)-phenoxy)-propionsäureethylester (EP-A 0 002 925), 2-(4-(3,5-Dichloφyridyl-2-oxy)-phenoxy)-propionsäurepropargylester (EP-A 0 003 114), 2-(4-(3-Chlor-5-trifluormethyl-2-pyridyloxy)-phenoxy)-propionsäuremethylester (EP-A 0 003 890),B2) "mononuclear" heteroaryloxyphenoxyalkanecarboxylic acid derivatives, eg ethyl 2- (4- (3,5-dichloropyridyl-2-oxy) -phenoxy) -propionate (EP-A 0 002 925), 2- (4- (3, 5-Dichloropyridyl-2-oxy) -phenoxy) -propionsäurepropargylester (EP-A 0 003 114), 2- (4- (3-chloro-5-trifluoromethyl-2-pyridyloxy) -phenoxy) -propionic acid methyl ester (EP-A 0 003 890),
2-(4-(3-Chlor-5-trifluormethyl-2-pyridyloxy)-phenoxy)-propionsäureethylester (EP-A 0 003 890),2- (4- (3-chloro-5-trifluoromethyl-2-pyridyloxy) -phenoxy) -propionic acid ethyl ester (EP-A 0 003 890),
2-(4-(5-Chlor-3-fluor-2-pyridyloxy)-phenoxy)-propionsäurepropargylester (EP-A 0 191 736),2- (4- (5-chloro-3-fluoro-2-pyridyloxy) -phenoxy) -propionic acid propargyl ester (EP-A 0 191 736),
2-(4-(5-Trifluormethyl-2-pyridyloxy)-phenoxy)-propionsäurebutylester (Fluazifop-butyl);Butyl 2- (4- (5-trifluoromethyl-2-pyridyloxy) phenoxy) -propionate (fluazifop-butyl);
B3) "Zweikernige" Heteroaryloxyphenoxy-alkancarbonsäure-Derivate, z.B. 2-(4-(6-Chlor-2-chinoxalyloxy)-phenoxy)-propionsäuremethylester und -ethylesterB3) "binuclear" heteroaryloxyphenoxy-alkanecarboxylic acid derivatives, e.g. 2- (4- (6-chloro-2-quinoxalyloxy) -phenoxy) -propionic acid methyl ester and ethyl ester
(Quizalofopmethyl und Quizalofopethyl),(Quizalofopmethyl and quizalofopethyl),
2-(4-(6-Fluor-2-chinoxalyloxy)-phenoxy)-propionsäuremethylester (s. J. Pest. Sei.2- (4- (6-fluoro-2-quinoxalyloxy) -phenoxy) -propionic acid methyl ester (see J. Pest.
Vol. 10, 61 (1985)),Vol. 10, 61 (1985)),
2-(4-(6-Chlor-2-chinoxalyloxy)-phenoxy)-propionsäure-2-isopropylidenaminooxy- ethylester (Propaquizafop),2- (4- (6-chloro-2-quinoxalyloxy) -phenoxy) -propionic acid 2-isopropylideneaminooxyethyl ester (propaquizafop),
2-(4-(6-Chlorbenzoxazol-2-yl-oxy)-phenoxy)-propionsäureethylester (Fenoxaprop- ethyl), dessen D(+) Isomer (Fenoxaprop-P-ethyl) und 2-(4-(6-Chlorbenzthiazol-2- yloxy)-phenoxy)-propionsäureethylester (DE-A 26 40 730),2- (4- (6-chlorobenzoxazol-2-yl-oxy) -phenoxy) -propionic acid ethyl ester (fenoxapropethyl), its D (+) isomer (fenoxaprop-P-ethyl) and 2- (4- (6-chlorobenzthiazole -2-yloxy) -phenoxy) -propionic acid ethyl ester (DE-A 26 40 730),
2-(4-(6-Chlorchinoxalyloxy)-phenoxy)-propionsäure-tetrahydro-2-furylmethylester (EP-A 0 323 727);2- (4- (6-chloroquinoxalloxy) -phenoxy) -propionic acid tetrahydro-2-furylmethyl ester (EP-A 0 323 727);
C) Chloracetanilide, z.B.C) Chloroacetanilides, e.g.
N-Methoxymethyl-2,6-diethyl-chloracetanilid (Alachlor), N-(3-Methoxyprop-2-yl)-2-methyl-6-ethyl-chloracetanilid (Metolachlor), N-(3-Methyl-1 ,2,4-oxadiazol-5-yl-methyl)-chloressigsäure-2,6-dimethylanilid,N-methoxymethyl-2,6-diethyl-chloroacetanilide (alachlor), N- (3-methoxyprop-2-yl) -2-methyl-6-ethyl-chloroacetanilide (metolachlor), N- (3-methyl-1,2-yl , 4-oxadiazol-5-yl-methyl) -chloressigsäure-2,6-dimethylanilide,
N-(2,6-Dimethylphenyl)-N-(1-pyrazolylmethyl)-chloressigsäureamid (Metazachlor);N- (2,6-dimethylphenyl) -N- (1-pyrazolylmethyl) -chloroacetic acid amide (metazachlor);
D) Thiocarbamate, z.B. S-Ethyl-N,N-dipropylthiocarbamat (EPTC), S-Ethyl-N.N-diisobutylthiocarbamat (Butylate);D) thiocarbamates, e.g. S-ethyl-N, N-dipropylthiocarbamate (EPTC), S-ethyl-N, N-diisobutylthiocarbamate (butylate);
E) Cyclohexandionoxime, z.B.E) cyclohexanedione oximes, e.g.
3-(1-Allyloxyiminobutyl)-4-hydroxy-6,6-dimethyl-2-oxocyclohex-3-encarbon- säuremethylester, (Alloxydim), 2-(1-Ethoxyiminobutyl)-5-(2-ethylthiopropyl)-3-hydroxy-cyclohex-2-en-1-on (Sethoxydim),Methyl 3- (1-Allyloxyiminobutyl) -4-hydroxy-6,6-dimethyl-2-oxocyclohex-3-eneCarbonate, (alloxydim), 2- (1-ethoxyiminobutyl) -5- (2-ethylthiopropyl) -3-hydroxycyclohex-2-en-1-one (sethoxydim),
2-(1-Ethoxyiminobutyl)-5-(2-phenylthiopropyl)-3-hydroxy-cyclohex-2-en-1-on (Cloproxydim), 2-(1 -(3-Chlorallyloxy)-iminobutyl)-5-(2-ethylthiopropyl)-3-hydroxy-cyclohex-2-en-1 - on,2- (1-Ethoxyiminobutyl) -5- (2-phenylthiopropyl) -3-hydroxycyclohex-2-en-1-one (cloproxydim), 2- (1- (3-chloroallyloxy) -iminobutyl) -5- ( 2-ethylthiopropyl) -3-hydroxycyclohex-2-en-1-one,
2-(1-(3-Chlorallyloxy)-iminopropyl)-5-(2-ethylthiopropyl)-3-hydroxy-cyclohex-2-en-1- on (Clethodim),2- (1- (3-chloroallyloxy) -iminopropyl) -5- (2-ethylthiopropyl) -3-hydroxycyclohex-2-en-1-one (clethodim),
2-(1-Ethoxyiminobutyl)-3-hydroxy-5-(thian-3-yl)-cyclohex-2-en-on (Cycloxydim), 2-(1 -Ethoxyiminopropyl)-5-(2,4,6-trimethylphenyl)-3-hydroxy-cyclohex-2-en-1 -on (Tralkoxydim);2- (1-ethoxyiminobutyl) -3-hydroxy-5- (thian-3-yl) -cyclohex-2-enone (cycloxydim), 2- (1-ethoxyiminopropyl) -5- (2,4,6- trimethylphenyl) -3-hydroxycyclohex-2-en-1-one (tralkoxydim);
F) Imidazolinone, z.B. 2-(4-lsopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)-5-methylbenzoesäure-methylester und 2-(4-lsopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)-4-methylbenzoesäureF) imidazolinones, e.g. Methyl 2- (4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl) -5-methylbenzoate and 2- (4-isopropyl-4-methyl-5-oxo-2-imidazoline-2 yl) -4-methylbenzoic
(Imazamethabenz),(Imazamethabenz),
5-Ethyl-2-(4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)-pyridin-3-carbonsäure5-ethyl-2- (4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl) pyridine-3-carboxylic acid
(Imazethapyr),(Imazethapyr),
2-(4-lsopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)-chinolin-3-carbonsäure (Imazaquin), 2-(4-lsopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)-pyridin-3-carbonsäure (lmazapyr),2- (4-Isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl) -quinoline-3-carboxylic acid (imazaquin), 2- (4-isopropyl-4-methyl-5-oxo-2-ol imidazolin-2-yl) -pyridine-3-carboxylic acid (imazapyr),
5-Methyl-2-(4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)-pyridin-3-carbonsäure5-methyl-2- (4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl) pyridine-3-carboxylic acid
(Imazethamethapyr);(Imazethamethapyr);
G) Triazolopyrimidinsulfonamid-Derivate, z.B. N-(2,6-Difluorphenyl)-7-methyl-1 ,2,4-triazolo[1 ,5-c]pyrimidin-2-sulfonamidG) Triazolopyrimidine sulfonamide derivatives, e.g. N- (2,6-Difluorophenyl) -7-methyl-1,2,4-triazolo [1,5-c] pyrimidine-2-sulfonamide
(Flumetsulam),(Flumetsulam),
N-(2,6-Dichlor-3-methylphenyl)-5,7-dimethoxy-1 ,2,4-triazolo[1 ,5-c]pyrimidin-2-N- (2,6-dichloro-3-methylphenyl) -5,7-dimethoxy-1,2,4-triazolo [1,5-c] pyrimidine-2
Sulfonamid,sulfonamide,
N-(2,6-Difluoφhenyl)-7-fluor-5-methoxy-1,2,4-triazolo[1 ,5-c]-pyrimidin-2-sulfonamid, N-(2,6-Dichlor-3-methylphenyl)-7-chlor-5-methoxy-1 ,2,4-triazolo[1 ,5-c]-pyrimidin-2- sulfonamid,N- (2,6-Difluoro-phenyl) -7-fluoro-5-methoxy-1,2,4-triazolo [1,5-c] pyrimidine-2-sulfonamide, N- (2,6-dichloro-3-) methylphenyl) -7-chloro-5-methoxy-1,2,4-triazolo [1,5-c] pyrimidine-2-sulfonamide,
N-(2-Chlor-6-methoxycarbonyl)-5,7-dimethyl-1 ,2,4-triazolo[1 ,5-c]-pyrimidin-2- sulfonamid (EP-A 0 343 752, US-A 4,988,812); H) Benzoylcyclohexandione, z.B.N- (2-chloro-6-methoxycarbonyl) -5,7-dimethyl-1,2,4-triazolo [1,5-c] pyrimidine-2-sulfonamide (EP-A 0 343 752, US Pat. No. 4,988,812 ); H) benzoylcyclohexanediones, eg
2-(2-Chlor-4-methylsulfonylbenzoyl)-cyclohexan-1 ,3-dion (SC-0051 , EP-A 0 137 963), 2-(2-Nitrobenzoyl)-4,4-dimethyl-cyclohexan-1 ,3-dion (EP-A 0 274 634), 2-(2-Nitro-3-methylsulfonylbenzoyl)-4,4-dimethylcyclohexan-1 ,3-dion (WO 91/13548);2- (2-chloro-4-methylsulfonylbenzoyl) cyclohexane-1,3-dione (SC-0051, EP-A-0 137 963), 2- (2-nitrobenzoyl) -4,4-dimethyl-cyclohexane-1, 3-dione (EP-A 0 274 634), 2- (2-nitro-3-methylsulfonylbenzoyl) -4,4-dimethylcyclohexane-1,3-dione (WO 91/13548);
I) Pyrimidinyloxy-pyridincarbonsäure- bzw. Pyrimidinyloxybenzoesäure-I) pyrimidinyloxypyridinecarboxylic acid or pyrimidinyloxybenzoic acid
Derivate, z.B.Derivatives, e.g.
3-(4,6-Dimethoxypyrimidin-2-yl)-oxy-pyridin-2-carbonsäurebenzylester (EP-A 0 249 707),Benzyl 3- (4,6-dimethoxypyrimidin-2-yl) oxy-pyridine-2-carboxylate (EP-A 0 249 707),
3-(4,6-Dimethoxypyrimidin-2-yl)-oxy-pyridin-2-carbonsäuremethylester (EP-A 0 249Methyl 3- (4,6-dimethoxypyrimidin-2-yl) oxy-pyridine-2-carboxylate (EP-A 0 249
707),707)
2,6-Bis[(4,6-dimethoxypyrimidin-2-yl)-oxy]-benzoesäure (EP-A 0 321 846),2,6-bis [(4,6-dimethoxypyrimidin-2-yl) oxy] benzoic acid (EP-A 0 321 846),
2,6-Bis[(4,6-dimethoxypyrimidin-2-yl)-oxy]-benzoesäure-1-(ethoxycarbonyl-oxyethyl)- ester (EP-A 0472 113);2,6-Bis [(4,6-dimethoxypyrimidin-2-yl) oxy] benzoic acid 1- (ethoxycarbonyl oxyethyl) ester (EP-A 0 472 113);
J) S-(N-Aryl-N-alkyl-carbamoylmethyl)-dithiophosphonsäureester, wie S-[N-(4- Chlorphenyl)-N-isopropyl-carbamoylmethyl]-O,O-dimethyl-dithiophosphat (Anilophos).J) S- (N-aryl-N-alkyl-carbamoylmethyl) -dithiophosphonic acid esters, such as S- [N- (4-chlorophenyl) -N-isopropyl-carbamoylmethyl] -O, O-dimethyl-dithiophosphate (anilophos).
K) 2,4-Diamino-s-triazine, vorzugsweise Alkylazine.K) 2,4-diamino-s-triazines, preferably alkylazines.
Bevorzugt sind auch Salze, vorzugsweise Säureadditionssalze der Verbindungen, beispielsweise deren Hydrochloride.Also preferred are salts, preferably acid addition salts of the compounds, for example their hydrochlorides.
L) phosphorhaltige Herbizide, z.B. eine oder mehrere Verbindungen der Formel (IV) oder deren Derivate wie Salze,L) phosphorus-containing herbicides, e.g. one or more compounds of the formula (IV) or derivatives thereof, such as salts,
worin Z1 einen Rest der Formel -OM, -NHCH(CH3)CONHCH(CH3)CO2M oder -NHCH(CH3)CONHCH[CH2CH(CH3)2]CO2M und M = H oder ein Salz bildendes Kation bedeuten, und/oder eine oder mehrere Verbindungen der Formel (V) oder deren Derivate wie Salze, wherein Z 1 is a radical of the formula -OM, -NHCH (CH 3 ) CONHCH (CH 3 ) CO 2 M or -NHCH (CH 3 ) CONHCH [CH 2 CH (CH 3 ) 2 ] CO 2 M and M = H or Salt-forming cation, and / or one or more compounds of the formula (V) or derivatives thereof, such as salts,
worin wherein
Z2 einen Rest der Formel CN oder CO2R1 bedeutet, in dem R1 = Q oder ein Salz bildendes Kation ist und dabei Q = H, Alkyl, Alkenyl, Alkoxyalkyl oder Cβ-Cio- Aryl, das unsubstituiert oder substituiert ist und vorzugsweise unsubstituiert oder durch einen oder mehrere Reste aus der Gruppe Alkyl, Alkoxy, Halogen, CF3, NO2 und CN substituiert ist, und R2,R3 jeweils unabhängig voneinander H, Alkyl, Cβ-Cio-Aryl, das unsubstituiert oder substituiert ist und vorzugsweise unsubstituiert oder durch einen oder mehrere Reste aus der Gruppe Alkyl, Alkoxy, Halogen, CF3, NO2 und CN substituiert ist, oder Biphenyl oder ein Salz bildendes Kation bedeuten.Z 2 is a radical of the formula CN or CO 2 R 1 , in which R 1 = Q or a salt-forming cation and Q = H, alkyl, alkenyl, alkoxyalkyl or Cβ-Cio-aryl, which is unsubstituted or substituted, and preferably unsubstituted or substituted by one or more radicals from the group alkyl, alkoxy, halogen, CF 3 , NO 2 and CN, and R 2 , R 3 are each independently H, alkyl, Cβ-Cio-aryl which is unsubstituted or substituted is and is preferably unsubstituted or substituted by one or more radicals from the group alkyl, alkoxy, halogen, CF 3 , NO 2 and CN, or biphenyl or a salt-forming cation.
Beispiele für Wirkstoffe der Formel (IV) und (V) sind folgende:Examples of active compounds of the formula (IV) and (V) are the following:
- Glufosinate und dessen Ammoniumsalz in racemischer Form, d.h. 2-Amino-4-Glufosinate and its ammonium salt in racemic form, i. 2-Amino-4-
[hydroxy(methyl)phosphinoyl]-butansäure bzw. dessen Ammoniumsalz,[hydroxy (methyl) phosphinoyl] -butanoic acid or its ammonium salt,
- das L-Enantiomer von Glufosinate und dessen Ammoniumsalz,the L-enantiomer of glufosinate and its ammonium salt,
- Bilanafos/Bialaphos, d.h. L-2-Amino-4-[hydroxy(methyl)phosphinoyl]-butanoyl-L- alaninyl-L-alanin und dessen Natriumsalz- Bilanafos / Bialaphos, i. L-2-amino-4- [hydroxy (methyl) phosphinoyl] butanoyl-L-alaninyl-L-alanine and its sodium salt
- Glyphosate.- glyphosate.
M) Carbamate, z.B. Asulam, Carbetamide, Chloropham und Propham;M) carbamates, e.g. Asulam, Carbetamide, Chloropham and Propham;
N) Benzofurane, z.B. Benfuresate und Ethofumesate; O) Phytohormone;N) benzofurans, eg benfuresates and ethofumesates; O) phytohormones;
P) Auxine und Auxinanaloga, z.B. 4-lndol-3-buttersäure, lndol-3-essigsäure, 1- Naphthylessigsäure, 2-(1-Naphthyl)acetamid und 2-Naphthyloxyessigsäure;P) Auxins and auxin analogs, e.g. 4-indole-3-butyric acid, indole-3-acetic acid, 1-naphthylacetic acid, 2- (1-naphthyl) acetamide and 2-naphthyloxyacetic acid;
Q) Cytokinine, z.B. Kinetin und 6-Benzylaminopurin;Q) cytokinins, e.g. Kinetin and 6-benzylaminopurine;
R) Gibberelline, z.B. Gibberillinsäure, Gibberillin A4 und A7;R) gibberellins, e.g. Gibberillic Acid, Gibberillin A4 and A7;
S) Abzissinsäure- und deren Derivate;S) Abzissinsäure- and their derivatives;
T) Ethylenvorläufer, z.B. Ethephon;T) ethylene precursors, e.g. ethephon;
U) Herbizide aus der Gruppe der Fettsäuresynthetase-Inhibitoren;U) herbicides from the group of fatty acid synthetase inhibitors;
V) Harnstoffe, z.B. Chlorotoluron, Dimefuron, Diuron, Fluometuron, Isoproturon, Isouron, Karbutilate, Linuron, Methabenzthiazuron, Metobenzuron, Metoxuron, Monolinuron, Neburon, Siduron und Tebuthiuron undV) ureas, e.g. Chlorotoluron, dimefuron, diuron, fluometuron, isoproturon, isourone, carbutilate, linuron, methabenzthiazuron, metobenzuron, metoxuron, monolinuron, neburon, siduron and tebuthiuron and
W) Metamitron.W) Metamitron.
X) Hydroxybenzonitrile, z.B. wie Bromoxynil und loxynil und deren Salze und Ester, wie Bromoxyniloctanoat und loxyniloctanoat.X) hydroxybenzonitriles, e.g. such as bromoxynil and loxynil and their salts and esters such as bromoxyniloctanoate and loxyniloctanoate.
Die agrochemischen Wirkstoffe können auch Wachstumsregulatoren sein. Beispiele hierfür sind Terbufos, Cyclanilide und Thidiazuron.The agrochemical active substances can also be growth regulators. Examples of these are terbufos, cyclanilides and thidiazuron.
Die Herbizide (Pflanzenwuchsregulatoren) der Gruppen A bis X sind beispielsweise aus den oben jeweils genannten Schriften und/oder aus "The Pesticide Manual", 12. Auflage (2000) und 13. Auflage (2003), The British Crop Protection Council, "Agricultural Chemicals Book Il - Herbicides -", by WT. Thompson, Thompson Publications, Fresno CA, USA 1990 und "Farm Chemicals Handbook '90", Meister Publishing Company, Willoughby OH, USA, 1990, bekannt. SafenerThe herbicides (plant growth regulators) of groups A to X, for example, from the above-mentioned writings and / or from "The Pesticide Manual", 12th edition (2000) and 13th edition (2003), The British Crop Protection Council, "Agricultural Chemicals Book II - Herbicides - ", by WT. Thompson, Thompson Publications, Fresno CA, USA 1990 and "Farm Chemicals Handbook '90", Meister Publishing Company, Willoughby OH, USA, 1990. safener
Die agrochemischen Wirkstoffe können auch Safener sein. Beispiele hierfür sind unter anderem:The agrochemical active substances can also be safeners. Examples include:
a) Verbindungen der Formeln (S-Il) bis (S-IV),a) compounds of the formulas (S-II) to (S-IV),
(S-Il) (S-III) (S-IV)(S-II) (S-III) (S-IV)
wobei die Symbole und Indizes folgende Bedeutungen haben: n' ist eine natürliche Zahl von 0 bis 5, vorzugsweise 0 bis 3; T ist eine (Ci oder C2)-Alkandiylkette, die unsubstituiert oder mit einem oder zwei (d-C-OAlkylresten oder mit [(Ci-C3)-Alkoxy]-carbonyl substituiert ist;where the symbols and indices have the following meanings: n 'is a natural number from 0 to 5, preferably 0 to 3; T is a (Ci or C2) alkanediyl chain which is unsubstituted or substituted by one or two (C 1 -C 6 -alkyl radicals or by [(C 1 -C 3 ) -alkoxy] carbonyl;
W ist ein unsubstituierter oder substituierter divalenter heterocyclischer Rest aus der Gruppe der teilungesättigten oder aromatischen Fünfring-Heterocyclen mit 1 bis 3 Heteroringatomen des Typs N oder O, wobei mindestens ein N-Atom und höchstens ein O-Atom im Ring enthalten ist, vorzugsweise ein Rest aus der Gruppe (W1) bis (W4),W is an unsubstituted or substituted divalent heterocyclic radical from the group of unsaturated or unsaturated five-membered ring heterocycles having 1 to 3 hetero ring N or O atoms, at least one N atom and at most one O atom in the ring, preferably a radical from the group (W1) to (W4),
(W1) (W2) (W3) (W4) (W1) (W2) (W3) (W4)
m' ist 0 oder 1 ;m 'is 0 or 1;
R17, R19 sind gleich oder verschieden Halogen,R 17 , R 19 are the same or different halogen,
(CrC4)Alkyl, (C1-C4)AIkOXy, Nitro oder (C-ι-C4)Haloalkyl; R18, R20 sind gleich oder verschieden OR24, SR24 oder NR24R25 oder ein gesättigter oder ungesättigter 3- bis 7-gliedriger Heterocyclus mit mindestens einem N-Atom und bis zu 3 Heteroatomen, vorzugsweise aus der Gruppe O und S, der über das N-Atom mit der Carbonylgruppe in (S-Il) bzw. (S-III) verbunden ist und unsubstituiert oder durch Reste aus der Gruppe (Ci-C4)Alkyl,(C r C 4 ) alkyl, (C 1 -C 4 ) alkoxy, nitro or (C 1 -C 4 ) haloalkyl; R 18 , R 20 are identical or different OR 24 , SR 24 or NR 24 R 25 or a saturated or unsaturated 3- to 7-membered heterocycle having at least one N atom and up to 3 heteroatoms, preferably from the group O and S. which is connected via the N atom to the carbonyl group in (S-II) or (S-III) and unsubstituted or by radicals from the group (C 1 -C 4 ) alkyl,
(CrC4)AIkOXy oder gegebenenfalls substituiertes Phenyl substituiert ist, vorzugsweise ein Rest der Formel OR24, NHR25 oder N(CHa)2, insbesondere der Formel OR24;(C 1 -C 4 ) alkoxy or optionally substituted phenyl, preferably a radical of the formula OR 24 , NHR 25 or N (CHa) 2 , in particular of the formula OR 24 ;
R24 ist Wasserstoff oder ein unsubstituierter oder substituierter aliphatischer Kohlenwasserstoffrest, vorzugsweise mit insgesamt 1 bis 18 C-Atomen;R 24 is hydrogen or an unsubstituted or substituted aliphatic hydrocarbon radical, preferably having a total of 1 to 18 C atoms;
R25 ist Wasserstoff, (CrC6)Alkyl, (C-i-CβJAlkoxy oder substituiertes oder unsubstituiertes Phenyl; Rx ist H1 (CrC8)Alkyl, CrC8(Haloalkyl), (C1-C4)Alkoxy(C1-C8)Alkyl, Cyano oderR 25 is hydrogen, (C 1 -C 6 ) alkyl, (C 1 -C 6 ) alkoxy or substituted or unsubstituted phenyl, R x is H 1 (C r C 8 ) alkyl, C r C 8 (haloalkyl), (C 1 -C 4 ) alkoxy (C 1 -C 8 ) alkyl, cyano or
COOR26, worin R26 Wasserstoff, (Ci-C8)Alkyl, (CrC8)Haloalkyl, (CrC4)Alkoxy- (CrC4)alkyl, (Ci-C6)Hydroxyalkyl, (C3-C12)Cycloalkyl oder Tri-(Ci-C4)-alkyl- silyl ist; R27, R28, R29 sind gleich oder verschieden Wasserstoff, (CrCs)Alkyl,COOR 26 , wherein R 26 is hydrogen, (Ci-C 8 ) alkyl, (C r C 8 ) haloalkyl, (C r C 4 ) alkoxy (C r C 4 ) alkyl, (Ci-C 6 ) hydroxyalkyl, (C C 3 -C 12 ) is cycloalkyl or tri (C 1 -C 4 ) alkylsilyl; R 27 , R 28 , R 29 are identical or different hydrogen, (C r Cs) alkyl,
(Ci-C8)Haloalkyl, (C3-Ci2)Cycloalkyl oder substituiertes oder unsubstituiertes Phenyl; R21 ist (CrC4)Alkyl, (CrC4)Haloalkyl, (C2-C4)Alkenyl, (C2-C4)Haloalkenyl,(Ci-C 8) haloalkyl, (C3-Ci2) cycloalkyl or substituted or unsubstituted phenyl; R 21 is (C r C 4 ) alkyl, (C r C 4 ) haloalkyl, (C 2 -C 4 ) alkenyl, (C 2 -C 4 ) haloalkenyl,
(C3-C7)Cycloalkyl, vorzugsweise Dichlormethyl; R22, R23 ist gleich oder verschieden Wasserstoff, (CrC4)Alkyl, (C2-C4)Alkenyl,(C 3 -C 7 ) cycloalkyl, preferably dichloromethyl; R 22 , R 23 is identical or different hydrogen, (C r C 4 ) alkyl, (C 2 -C 4 ) alkenyl,
(C2-C4)Alkinyl, (Ci-C4)Haloalkyl, (C2-C4)Haloalkenyl, (Ci-C4)Alkylcarbamoyl- (Ci-C4)alkyl, (C2-C4)Alkenylcarbamoyl-(Ci-C4)alkyl, (CrC4)AIkOXy-(C1 - C4)alkyl, Dioxolanyl-(CrC4)alkyl, Thiazolyl, Furyl, Furylalkyl, Thienyl, Piperidyl, substituiertes oder unsubstituiertes Phenyl, oder R22 und R23 bilden zusammen einen substituierten oder unsubstituierten heterocyclischen Ring, vorzugsweise einen Oxazolidin-, Thiazolidin-, Piperidin-, Morpholin-, Hexahydropyrimidin- oder Benzoxazinring; vorzugsweise Safener folgender Untergruppen von Verbindungen der Formeln (S-Il) bis (S-IV):(C 2 -C 4) alkynyl, (Ci-C 4) haloalkyl, (C 2 -C 4) haloalkenyl, (Ci-C 4) alkylcarbamoyl (Ci-C4) alkyl, (C 2 -C 4) Alkenylcarbamoyl - (C 1 -C 4 ) alkyl, (C 1 -C 4 ) alkoxy- (C 1 -C 4 ) alkyl, dioxolanyl- (C 1 -C 4 ) alkyl, thiazolyl, furyl, furylalkyl, thienyl, piperidyl, substituted or unsubstituted phenyl, or R 22 and R 23 together form a substituted or unsubstituted heterocyclic ring, preferably an oxazolidine, thiazolidine, piperidine, morpholine, hexahydropyrimidine or benzoxazine ring; preferably safeners of the following subgroups of compounds of the formulas (S-II) to (S-IV):
- Verbindungen vom Typ der Dichlorphenylpyrazolin-3-carbonsäure (d.h. der Formel (S-Il), worin W = (W1) und (R17Jn- = 2,4-Cl2), vorzugsweise Verbindungen wie 1-(2,4-Dichlorphenyl)-5-(ethoxycarbonyl)-5-methyl-2-pyrazolin-3- carbonsäureethylester (ll-1 , Mefenpyr-diethyl), Mefenpyr-dimethyl und MefenpyrCompounds of the type of dichlorophenylpyrazoline-3-carboxylic acid (ie of the formula (S-II) in which W = (W1) and (R 17 J n - = 2,4-Cl 2 ), preferably compounds such as 1- (2, 4-dichlorophenyl) -5- (ethoxycarbonyl) -5-methyl-2-pyrazoline-3- carboxylic acid ethyl ester (ll-1, mefenpyr-diethyl), mefenpyr-dimethyl and mefenpyr
(H-O), und verwandte Verbindungen, wie sie in der WO-A-91/07874 beschrieben sind;(H-O), and related compounds as described in WO-A-91/07874;
- Derivate der Dichlorphenylpyrazolcarbonsäure (d.h. der Formel (S-Il), worin W = (W2) und (R17V = 2,4-Cl2 ist ), vorzugsweise Verbindungen wie 1-(2,4-Derivatives of the dichlorophenylpyrazolecarboxylic acid (ie of the formula (S-II) in which W = (W 2 ) and (R 17 V = 2,4-Cl 2 ), preferably compounds such as 1- (2,4-Cl 2 )
Dichlorphenyl)-5-methyl-pyrazol-3-carbonsäureethylester (II-2), 1 -(2,4- Dichlorphenyl)-5-isopropyl-pyrazol-3-carbonsäureethylester (II-3), 1 -(2,4- Dichloφhenyl)-5-(1 ,1-dimethyl-ethyl)pyrazol-3-carbonsäureethylester (ll-4), 1-(2,4-Dichloφhenyl)-5-phenyl-pyrazol-3-carbonsäureethylester (ll-5) und verwandte Verbindungen, wie sie in EP-A-0333131 und EP-A-0269806 beschrieben sind;Dichlorophenyl) -5-methyl-pyrazole-3-carboxylic acid ethyl ester (II-2), 1- (2,4-dichlorophenyl) -5-isopropyl-pyrazole-3-carboxylic acid ethyl ester (II-3), 1 - (2,4- Dichloφhenyl) -5- (1, 1-dimethyl-ethyl) pyrazole-3-carboxylic acid ethyl ester (II-4), 1- (2,4-Dichloo-phenyl) -5-phenyl-pyrazole-3-carboxylic acid ethyl ester (II-5) and related compounds as described in EP-A-0333131 and EP-A-0269806;
- Verbindungen vom Typ der Triazolcarbonsäuren (d.h. der Formel (S-Il), worin W = (W3) und (R17V = 2,4-Cb ist), vorzugsweise Verbindungen wie Fenchlorazol- ethyl, d.h. 1-(2,4-Dichloφhenyl)-5-trichlormethyl-(1 H)-1 ,2,4-triazol-3- carbonsäureethylester (II-6), und verwandte Verbindungen (siehe EP-A-0174562 und EP-A-0346620);Compounds of the type of the triazolecarboxylic acids (ie of the formula (S-II) in which W = (W3) and (R 17 V = 2,4-Cb), preferably compounds such as fenchlorazolethyl, ie 1- (2,4 -Dichloo-phenyl) -5-trichloromethyl- (1H) -1, 2,4-triazole-3-carboxylic acid ethyl ester (II-6), and related compounds (see EP-A-0174562 and EP-A-0346620);
- Verbindungen vom Typ der 5-Benzyl- oder 5-Phenyl-2-isoxazolin-3-carbonsäure oder der 5,5-Diphenyl-2-isoxazolin-3-carbonsäure wie Isoxadifen (11-12), (worin W = (W4) ist), vorzugsweise Verbindungen wie 5-(2,4-Dichlorbenzyl)-2-isoxazolin-3- carbonsäureethylester (II-7) oder 5-Phenyl-2-isoxazolin-3-carbonsäureethylesterCompounds of the 5-benzyl or 5-phenyl-2-isoxazoline-3-carboxylic acid type or of the 5,5-diphenyl-2-isoxazoline-3-carboxylic acid, such as isoxadifen (11-12), (wherein W = (W4 ), preferably compounds such as ethyl 5- (2,4-dichlorobenzyl) -2-isoxazoline-3-carboxylate (II-7) or ethyl 5-phenyl-2-isoxazoline-3-carboxylate
(II-8) und verwandte Verbindungen, wie sie in WO-A- 91/08202 beschrieben sind, oder der 5,5-Diphenyl-2-isoxazolin-carbonsäureethylester (II-9, Isoxadifen-ethyl) oder -n-propylester (11-10) oder der 5-(4-Fluorphenyl)-5-phenyl-2-isoxazolin-3- carbonsäureethylester (11-11), wie sie in der WO-A-95/07897 beschrieben sind. - Verbindungen vom Typ der 8-Chinolinoxyessigsäure, z.B. solche der Formel (S- III), worin (R19V = 5-CI, R20 = OR24 und T = CH2 ist, vorzugsweise die(II-8) and related compounds as described in WO-A-91/08202 or ethyl 5,5-diphenyl-2-isoxazoline-carboxylate (II-9, isoxadifen-ethyl) or n-propyl ester ( 11-10) or 5- (4-fluorophenyl) -5-phenyl-2-isoxazoline-3-carboxylic acid ethyl ester (11-11), as described in WO-A-95/07897. - Compounds of the type of 8-quinolinoxyacetic acid, for example those of the formula (S-III), wherein (R 19 V = 5-CI, R 20 = OR 24 and T = CH 2 , preferably the
Verbindungen (5-Chlor-8-chinolinoxy)essigsäure-(1 -methylhexyl)-ester (111-1 , Cloquintocet-mexyl), (5-Chlor-8-chinolinoxy)essigsäure-(1 ,3-dimethyl-but-1 -yl)- ester (III-2), (5-Chlor-8-chinolinoxy)essigsäure-4-allyl-oxy-butylester (III-3), (5- Chlor-8-chinolinoxy)essigsäure-1-allyloxy-prop-2-ylester (III-4), (5-Chlor-8- chinolinoxy)essigsäureethylester (III-5), (5-Chlor-8- chinolinoxy)essigsäuremethylester (III-6), (5-Chlor-8- chinolinoxy)essigsäureallylester (lll-7), (5-Chlor-8-chinolinoxy)essigsäure-2-(2- propyliden-iminoxy)-1-ethylester (lll-8), (5-Chlor-8-chinolinoxy)essigsäure-2-oxo- prop-1-ylester (III-9), (5-Chlor-8-chinolinoxy)essigsäure (111-10) und dessen Salze wie sie z.B. in der WO-A-02/34048 beschrieben sind, und verwandte Verbindungen, wie sie in EP-A-0860750, EP-A-0094349 und EP-A-0191736 oder EP-A-0492366 beschrieben sind.Compounds (5-chloro-8-quinolinoxy) acetic acid (1-methylhexyl) ester (111-1, cloquintocet-mexyl), (5-chloro-8-quinolinoxy) acetic acid (1, 3-dimethyl-but-1 -yl) ester (III-2), (5-chloro-8-quinolinoxy) acetic acid 4-allyl oxy-butyl ester (III-3), (5-chloro-8-quinolinoxy) acetic acid 1-allyloxy prop-2-yl-ester (III-4), (5-chloro-8-quinolinoxy) acetic acid ethyl ester (III-5), (5-chloro-8-quinolinoxy) acetic acid methyl ester (III-6), (5-chloro-8-one quinolinoxy) allyl acetate (III-7), (5-chloro-8-quinolinoxy) acetic acid 2- (2- propylidene-iminoxy) -1-ethyl ester (III-8), (5-chloro-8-quinolinoxy) -acetic acid 2-oxo-prop-1-yl ester (III-9), (5-chloro-8-quinolinoxy) acetic acid (III-10) and their salts, as described, for example, in WO-A-02/34048, and related compounds, as described in EP-A-0860750, EP-A-0094349 and EP-A-0191736 or EP-A A-0492366 are described.
- Verbindungen vom Typ der (5-Chlor-8-chinolinoxy)-malonsäure, d.h. der Formel (S-III), worin (R19)n< = 5-CI, R20= OR24, T = -CH(COO-Alkyl)- ist, vorzugsweise die- Compounds of the type of (5-chloro-8-quinolinoxy) -malonic acid, ie of the formula (S-III), wherein (R 19 ) n <= 5-CI, R 20 = OR 24 , T = -CH (COO -Alkyl) - is, preferably the
Verbindungen (5-Chlor-8-chinolinoxy)-malonsäure-diethylester (111-11 ), (5-Chlor- 8-chinolinoxy)-malonsäurediallylester, (5-Chlor-8-chinolinoxy)-malonsäure- methyl-ethylester und verwandte Verbindungen, wie sie in EP-A-0582198 beschrieben sind.Compounds (5-chloro-8-quinolinoxy) -malonic acid diethyl ester (111-11), (5-chloro-8-quinolinoxy) -malonic acid diallyl ester, (5-chloro-8-quinolinoxy) -malonic acid methyl ethyl ester and related compounds as described in EP-A-0582198.
- Verbindungen vom Typ der Dichloracetamide, d.h. der Formel (S-IV), vorzugsweise: N,N-Diallyl-2,2-dichloracetamid (Dichlormid (IV-1 ), aus US 4,137,070), 4-Dichloracetyl-3,4-dihydro-3-methyl-2H-1 ,4-benzoxazin (IV-2, Benoxacor, aus EP 0149974), N1 ,N2-Diallyl-N2-dichloracetylglycinamid (DKA-24- Dichloroacetamide type compounds, i. of the formula (S-IV), preferably: N, N-diallyl-2,2-dichloroacetamide (dichloromide (IV-1), from US 4,137,070), 4-dichloroacetyl-3,4-dihydro-3-methyl-2H- 1, 4-benzoxazine (IV-2, Benoxacor, from EP 0149974), N1, N2-diallyl-N2-dichloroacetylglycinamide (DKA-24
(IV-3), aus HU 2143821 ), 4-Dichloracetyl-1-oxa-4-aza-spiro[4,5]decan (AD-67), 2,2-Dichlor-N-(1 ,3-dioxolan-2-ylmethyl)-N-(2-propenyl)acetamid (PPG-1292), 3- Dichloracetyl-2,2,5-trimethyloxazolidin (R-29148, IV-4), 3-Dichloracetyl-2,2- dimethyl-5-phenyloxazolidin, 3-Dichloracetyl-2,2-dimethyl-5-(2-thienyl)oxazolidin, 3-Dichloracetyl-5-(2-furanyl)-2,2-dimethyloxazolidin (Furilazole (IV-5), MON(IV-3), from HU 2143821), 4-dichloroacetyl-1-oxa-4-aza-spiro [4,5] decane (AD-67), 2,2-dichloro-N- (1,3-dioxolane -2-ylmethyl) -N- (2-propenyl) acetamide (PPG-1292), 3-dichloroacetyl-2,2,5-trimethyloxazolidine (R-29148, IV-4), 3-dichloroacetyl-2,2-dimethyl 5-phenyloxazolidine, 3-dichloroacetyl-2,2-dimethyl-5- (2-thienyl) oxazolidine, 3-dichloroacetyl-5- (2-furanyl) -2,2-dimethyloxazolidine (furilazole (IV-5), MON
13900), 1 -Dichloracetyl-hexahydro-3,3,8a-trimethylpyrrolo[1 ,2-a]pyrimidin-6(2H)- on (Dicyclonon, BAS 145138),13900), 1-dichloroacetyl-hexahydro-3,3,8a-trimethylpyrrolo [1,2-a] pyrimidin-6 (2H) -one (dicyclonone, BAS 145138),
b) eine oder mehreren Verbindungen aus Gruppe: 1 ,8-Naphthalsäureanhydrid, Methyl-diphenylmethoxyacetat, 1-(2-Chlorbenzyl)-3-(1- methyl-1-phenylethyl)harnstoff (Cumyluron), O,O-Diethyl S-2-ethylthioethyl phosphordithioat (Disulfoton), 4-Chlorphenyl-methylcarbamat (Mephenate), O,O- Diethyl-O-phenylphosphorotioat (Dietholate), 4-Carboxy-3,4-dihydro-2H-1 - benzopyran-4-essigsäure (CL-304415, CAS-Regno: 31541-57-8), Cyanomethoxyimino(phenyl)acetonitril (Cyometrinil), 1 ,3-Dioxolan-2- ylmethoxyimino(phenyl)acetonitril (Oxabetrinil), 4'-Chlor-2,2,2-trifluoracetophenon-O- 1 ,3-dioxolan-2-ylmethyloxim (Fluxofenim), 4,6-Dichlor-2-phenylpyrimidin (Fenclorim), Benzyl-2-chlor-4-trifluormethyl-1 ,3-thiazol-5-carboxylat (Flurazole), 2-Dichlormethyl- 2-methyl-1 ,3-dioxolan (MG-191 ), N-(4-Methylphenyl)-N'-(1 -methyl-1 - phenylethyl)harnstoff (Dymron), (2,4-Dichlorphenoxy)essigsäure (2,4-D), (4- Chloφhenoxy)essigsäure, (R,S)-2-(4-Chlor-o-tolyloxy)propionsäure (Mecoprop), 4- (2,4-Dichloφhenoxy)buttersäure (2,4-DB), (4-Chlor-o-tolyloxy)essigsäure (MCPA), 4- (4-Chlor-o-tolyloxy)buttersäure, 4-(4-Chlθφhenoxy)buttersäure, 3,6-Dichlor-2- methoxybenzoesäure (Dicamba), 1-(Ethoxycarbonyl)ethyl 3,6-dichlor-2- methoxybenzoat (Lactidichlor) sowie deren Salze und Ester, vorzugsweise (CrCe);b) one or more compounds selected from the group consisting of: 1, 8-naphthalic anhydride, methyl-diphenylmethoxyacetate, 1- (2-chlorobenzyl) -3- (1-methyl-1-phenylethyl) urea (cumyluron), O, O-diethyl S- 2-ethylthioethyl phosphorodithioate (disulfone), 4-chlorophenyl methyl carbamate (mephenate), O, O-diethyl O-phenyl phosphorotioate (dietholate), 4-carboxy-3,4-dihydro-2H-1-benzopyran-4-acetic acid ( CL-304415, CAS Regno: 31541-57-8), cyanomethoxyimino (phenyl) acetonitrile (Cyometrinil), 1, 3-dioxolan-2-ylmethoxyimino (phenyl) acetonitrile (oxabetrinil), 4'-chloro-2,2, 2-trifluoroacetophenone O-1,3-dioxolan-2-ylmethyloxime (Fluxofenim), 4,6-dichloro-2-phenylpyrimidine (fenclorim), benzyl-2-chloro-4-trifluoromethyl-1,3-thiazole-5 carboxylate (flurazole), 2-dichloromethyl 2-methyl-1,3-dioxolane (MG-191), N- (4-methylphenyl) -N '- (1-methyl-1-phenylethyl) urea (Dymron), (2,4-dichlorophenoxy) acetic acid (2 , 4-D), (4-chlorophenoxy) acetic acid, (R, S) -2- (4-chloro-o-tolyloxy) propionic acid (mecoprop), 4- (2,4-dichlorophenoxy) butyric acid (2,4- DB), (4-chloro-o-tolyloxy) acetic acid (MCPA), 4- (4-chloro-o-tolyloxy) butyric acid, 4- (4-chloro-phenoxy) butyric acid, 3,6-dichloro-2-methoxybenzoic acid (Dicamba ), 1- (ethoxycarbonyl) ethyl 3,6-dichloro-2-methoxybenzoate (lactidichloro) and their salts and esters, preferably (CrCe);
c) N-Acylsulfonamide der Formel (S-V) und ihre Salze,c) N-acylsulfonamides of the formula (S-V) and their salts,
worinwherein
R30 Wasserstoff, einen Kohlenwasserstoffrest, einen Kohlenwasserstoffoxyrest, einen Kohlenwasserstoffthiorest oder einen Heterocyclylrest, der vorzugsweise über ein C-Atom gebunden ist, wobei jeder der letztgenannten 4 Reste unsubstituiert oder durch einen oder mehrere gleiche oder verschiedene Reste aus der Gruppe Halogen, Cyano, Nitro, Amino, Hydroxy, Carboxy, Formyl, Carbonamid, Sulfonamid und Reste der Formel -Za-Ra substituiert ist, wobei jeder Kohlenwasserstoffteil vorzugsweise 1 bis 20 C-Atome aufweist und ein C-haltiger Rest R30 inklusive Substituenten vorzugsweise 1 bis 30 C-Atome aufweist;R 30 is hydrogen, a hydrocarbon radical, a hydrocarbonoxy radical, a hydrocarbylthio radical or a heterocyclyl radical which is preferably bonded via a carbon atom, where each of the last-mentioned 4 radicals is unsubstituted or substituted by one or more identical or different radicals from the group halogen, cyano, nitro , Amino, hydroxy, carboxy, formyl, carbonamide, sulfonamide and radicals of the formula -Z a -R a is substituted, wherein each hydrocarbon moiety preferably 1 to 20 carbon atoms and a C-containing radical R 30 including substituents preferably 1 to 30 Having C atoms;
R31 Wasserstoff oder (d-C^-Alkyl, vorzugsweise Wasserstoff, oder R30 und R31 zusammen mit der Gruppe der Formel -CO-N- den Rest eines 3- bis 8-gliedrigen gesättigten oder ungesättigten Rings;R 31 is hydrogen or (C 1 -C 4) alkyl, preferably hydrogen, or R 30 and R 31 together with the group of the formula -CO-N- represent the radical of a 3- to 8-membered saturated or unsaturated ring;
R32 gleich oder verschieden Halogen, Cyano, Nitro, Amino, Hydroxy, Carboxy, Formyl, CONH2, SO2NH2 oder einen Rest der Formel -Zb-Rb ;R 32 is identical or different and is halogen, cyano, nitro, amino, hydroxyl, carboxy, formyl, CONH 2 , SO 2 NH 2 or a radical of the formula -Z b -R b ;
R33 Wasserstoff oder (Ci-C4)-Alkyl, vorzugsweise H; R34 gleich oder verschieden Halogen, Cyano, Nitro, Amino, Hydroxy, Carboxy, CHO, CONH2, SO2NH2 oder einen Rest der Formel -Zc-Rc ;R 33 is hydrogen or (C 1 -C 4 ) -alkyl, preferably H; R 34 is identical or different and is halogen, cyano, nitro, amino, hydroxyl, carboxy, CHO, CONH 2 , SO 2 NH 2 or a radical of the formula -Z c -R c ;
Ra einen Kohlenwasserstoffrest oder einen Heterocyclylrest, wobei jeder der beiden letztgenannten Reste unsubstituiert oder durch einen oder mehrere gleiche oder verschiedene Reste aus der Gruppe Halogen, Cyano, Nitro,R a is a hydrocarbon radical or a heterocyclyl radical, where each of the two last-mentioned radicals is unsubstituted or substituted by one or more identical or different radicals from the group halogen, cyano, nitro,
Amino, Hydroxy, Mono- und Di-[(CrC4)-alkyl]-amino substituiert ist, oder einen Alkylrest, in dem mehrere, vorzugsweise 2 oder 3, nicht benachbarte CH2-Gruppen jeweils durch ein Sauerstoffatom ersetzt sind;Amino, hydroxy, mono- and di- [(C 1 -C 4 ) -alkyl] -amino, or an alkyl radical in which several, preferably 2 or 3, non-adjacent CH 2 groups are each replaced by an oxygen atom;
Rb,Rc gleich oder verschieden einen Kohlenwasserstoffrest oder einen Heterocyclylrest, wobei jeder der beiden letztgenannten Reste unsubstituiert oder durch einen oder mehrere gleiche oder verschiedene Reste aus der Gruppe Halogen, Cyano, Nitro, Amino, Hydroxy, Phosphoryl, Halogen- (CrC4)-alkoxy, Mono- und Di-[(Ci-C4)-alkyl]-amino substituiert ist, oder einen Alkylrest, in dem mehrere, vorzugsweise 2 oder 3, nicht benachbarte CH2-Gruppen jeweils durch ein Sauerstoffatom ersetzt sind;R b , R c, identically or differently, are a hydrocarbon radical or a heterocyclyl radical, where each of the latter two radicals is unsubstituted or substituted by one or more identical or different radicals from the group halogen, cyano, nitro, amino, hydroxyl, phosphoryl, halogen (C 1 -C 4) alkoxy, mono- and di - [(C 1 -C 4 ) alkyl] amino, or an alkyl radical in which several, preferably 2 or 3, non-adjacent CH 2 groups are each replaced by an oxygen atom;
Za eine divalente Gruppe der Formel -O-, -S-, -CO-, -CS-, -CO-O-, -CO-S-,Z a is a divalent group of the formula -O-, -S-, -CO-, -CS-, -CO-O-, -CO-S-,
-O-CO-, -S-CO-, -SO-, -SO2-, -NR*-, -CO-NR*-, -NR*-CO-, -SO2-NR*- oder -NR*-SO2-, wobei die rechts angegebene Bindung der jeweiligen divalenten Gruppe die Bindung zum Rest Ra ist und wobei die R* in den letztgenannten 5 Resten unabhängig voneinander jeweils H, (CrC4)-Alkyl oder HaIo-(CrC4)- alkyl bedeuten;-O-CO-, -S-CO-, -SO-, -SO 2 -, -NR * -, -CO-NR * -, -NR * -CO-, -SO 2 -NR * - or -NR * -SO 2 -, where the bond of the respective divalent group indicated on the right is the bond to the radical R a and wherein the R * in the latter 5 radicals are each independently H, (C r C 4 ) -alkyl or halo (CrC 4 ) - alkyl;
Zb, Zc unabhängig voneinander eine direkte Bindung oder eine divalente Gruppe der Formel -O-, -S-, -CO-, -CS-, -CO-O-, -CO-S-, -O-CO-, -S-CO-, -SO-, -SO2-, -NR*-, -SO2-NR*-, -NR*-SO2-, -CO-NR*- oder -NR*-CO-, wobei die rechts angegebene Bindung der jeweiligen divalenten Gruppe die Bindung zum Rest Rb bzw. Rc ist und wobei die R* in den letztgenannten 5 Resten unabhängig voneinander jeweils H, (d-C4)-Alkyl oder Halo-(CrC4)-alkyl bedeuten; n eine ganze Zahl von O bis 4, vorzugsweise 0, 1 oder 2, insbesondere O oder 1 , und m eine ganze Zahl von O bis 5, vorzugsweise 0, 1 , 2 oder 3, insbesondere 0, 1 oder 2; bedeuten; vorzugsweise Safener von Verbindungen der Formel (S-V), worinZ b , Z c independently of one another a direct bond or a divalent group of the formula -O-, -S-, -CO-, -CS-, -CO-O-, -CO-S-, -O-CO-, -S-CO-, -SO-, -SO 2 -, -NR * -, -SO 2 -NR * -, -NR * -SO 2 -, -CO-NR * - or -NR * -CO-, where the bond of the respective divalent group indicated on the right is the bond to the radical R b or R c and where the R * in the last-mentioned 5 radicals are each independently H, (C 1 -C 4 ) -alkyl or halo (C r C 4 ) -alkyl; n is an integer from 0 to 4, preferably 0, 1 or 2, in particular O or 1, and m is an integer from 0 to 5, preferably 0, 1, 2 or 3, in particular 0, 1 or 2; mean; preferably safeners of compounds of formula (SV) wherein
- R30 = H3C-O-CH2-, R31 = R33 = H, R34 = 2-OMe ist (V-1 ), - R30 = H3C-O-CH2-, R31 = R33 = H, R34 = 2-OMe-5-CI ist (V-2),R 30 = H 3 CO-CH 2 -, R 31 = R 33 = H, R 34 = 2-OMe is (V-1), R 30 = H 3 CO-CH 2 -, R 31 = R 33 = H, R 34 = 2-OMe-5-CI is (V-2),
- R30 = Cyclopropyl, R31 = R33 = H, R34 = 2-OMe ist (V-3),R 30 = cyclopropyl, R 31 = R 33 = H, R 34 = 2-OMe is (V-3),
- R30 = Cyclopropyl, R31 = R33 = H, R34 = 2-OMe-5-CI ist (V-4),R 30 = cyclopropyl, R 31 = R 33 = H, R 34 = 2-OMe-5-CI is (V-4),
- R30 = Cyclopropyl, R31 = R33 = H, R34 = 2-Me ist (V-5),R 30 = cyclopropyl, R 31 = R 33 = H, R 34 = 2-Me is (V-5),
- R30 = tert. Butyl, R31 = R33 = H, R34 = 2-OMe ist (V-6).R 30 = tert. Butyl, R31 = R33 = H, R34 = 2-OMe is (V-6).
d) Acylsulfamoylbenzoesäureamide der allgemeinen Formel (S-Vl), gegebenenfalls auch in Salzform,d) Acylsulfamoylbenzoesäureamide of the general formula (S-Vl), optionally in salt form,
worin wherein
X3 CH oder N;X 3 is CH or N;
R35 Wasserstoff, Heterocyclyl oder einen Kohlenwasserstoffrest, wobei die beiden letztgenannten Reste gegebenenfalls durch einen oder mehrere, gleiche oder verschiedene Reste aus der Gruppe Halogen, Cyano, Nitro, Amino, Hydroxy, Carboxy, CHO, CONH2, SO2NH2 und Za-Ra substituiert sind;R 35 is hydrogen, heterocyclyl or a hydrocarbon radical, where the latter two radicals are optionally substituted by one or more, identical or different radicals from the group halogen, cyano, nitro, amino, hydroxy, carboxy, CHO, CONH 2 , SO 2 NH 2 and Z a -R are a substituted;
R36 Wasserstoff, Hydroxy, (Ci-C6)-Alkyl, (C2-C6)-Alkenyl, (C2-C6)-Alkinyl, (CrC6)- Alkoxy, (C2-C6)-Alkenyloxy, wobei die fünf letztgenannten Reste gegebenenfalls durch einen oder mehrere, gleiche oder verschiedene Reste aus der Gruppe Halogen, Hydroxy, (CrC-O-Alkyl, (C-i-C-O-Alkoxy und (CrC4)- Alkylthio substituiert sind, oderR 36 is hydrogen, hydroxy, (Ci-C 6) -alkyl, (C 2 -C 6) alkenyl, (C 2 -C 6) -alkynyl, (CrC 6) - alkoxy, (C 2 -C 6) - Alkenyloxy, where the five last-mentioned radicals are optionally substituted by one or more, identical or different radicals from the group halogen, hydroxy, (C 1 -C 4 -alkyl, (C 1 -C 4 -alkoxy and (C 1 -C 4 ) -alkylthio, or
R35 und R36 zusammen mit dem sie tragenden Stickstoffatom einen 3- bis 8- gliedrigen gesättigten oder ungesättigten Ring; R37 Halogen, Cyano, Nitro, Amino, Hydroxy, Carboxy, CHO, CONH2, SO2NH2 oder Zb-Rb; R38 Wasserstoff, (CrC4)-Alkyl, (C2-C4)-Alkenyl oder (C2-C4)-Alkinyl;R 35 and R 36 together with the nitrogen atom carrying them have a 3- to 8-membered saturated or unsaturated ring; R 37 is halogen, cyano, nitro, amino, hydroxy, carboxy, CHO, CONH 2 , SO 2 NH 2 or Z b -R b ; R 38 is hydrogen, (C r C4) alkyl, (C 2 -C 4) -alkenyl or (C 2 -C 4) alkynyl;
R39 Halogen, Cyano, Nitro, Amino, Hydroxy, Carboxy, Phosphoryl, CHO, CONH2,R 39 is halogen, cyano, nitro, amino, hydroxy, carboxy, phosphoryl, CHO, CONH 2 ,
SO2NH2 oder Zc-Rc; Ra einen (C2-C2o)-Alkylrest, dessen Kohlenstoffkette ein- oder mehrfach durchSO 2 NH 2 or Z c -R c ; R a is a (C 2 -C 2 0) -alkyl radical whose carbon chain is mono- or polysubstituted
Sauerstoffatome unterbrochen ist, Heterocyclyl oder einen Kohlenwasserstoffrest, wobei die zwei letztgenannten Reste gegebenenfalls durch einen oder mehrere, gleiche oder verschiedene Reste aus der Gruppe Halogen, Cyano, Nitro, Amino, Hydroxy, Mono- und Di-[(CrC4)-alkyl]-amino substituiert sind;Is interrupted oxygen atoms, heterocyclyl or a hydrocarbon radical, wherein the latter two radicals optionally are substituted by one or more, identical or different radicals from the group halogen, cyano, nitro, amino, hydroxy, mono- and di - [(CrC 4 ) alkyl] amino;
Rb, Rc gleich oder verschieden einen (C2-C2o)-Alkylrest, dessen Kohlenstoffkette ein- oder mehrfach durch Sauerstoffatome unterbrochen ist, Heterocyclyl oder einen Kohlenwasserstoffrest, wobei die zwei letztgenannten Reste gegebenenfalls durch einen oder mehrere, gleiche oder verschiedene Reste aus der Gruppe Halogen, Cyano, Nitro, Amino, Hydroxy, Phosphoryl, (CrC4)- Haloalkoxy, Mono- und Di-[(Ci-C4)-alkyl]-amino substituiert sind; Za eine divalente Einheit aus der Gruppe O, S, CO, CS, C(O)O, C(O)S, SO, SO2, NRd, C(O)NRd oder SO2NRd;R b, R c are identical or different and are a (C 2 -C 2 o) -alkyl radical whose carbon chain one or more times interrupted by oxygen atoms, is heterocyclyl or a hydrocarbon radical, where the last two radicals optionally substituted by one or more identical or different Radicals from the group halogen, cyano, nitro, amino, hydroxy, phosphoryl, (CrC 4 ) - haloalkoxy, mono- and di - [(Ci-C 4 ) alkyl] amino substituted; Z a is a divalent unit selected from O, S, CO, CS, C (O) O, C (O) S, SO, SO 2 , NR d , C (O) NR d or SO 2 NR d ;
Zb, Zc gleich oder verschieden eine direkte Bindung oder eine divalente Einheit aus der Gruppe O1 S, CO, CS, C(O)O, C(O)S, SO, SO2, NRd, SO2NRd oder C(O)NRd; Rd Wasserstoff, (CrC4)-Alkyl oder (CrC4)-Haloalkyl; n eine ganze Zahl von O bis 4, und m für den Fall, dass X für CH steht, eine ganze Zahl von O bis 5, und für den Fall, dass X für N steht, eine ganze Zahl von O bis 4 bedeuten; vorzugsweise Safener von Verbindungen der Formel (S-Vl), in der X3 CH;Z b , Z c, identically or differently, represent a direct bond or a divalent unit from the group O 1 S, CO, CS, C (O) O, C (O) S, SO, SO 2 , NR d , SO 2 NR d or C (O) NR d ; R d is hydrogen, (C r C 4 ) -alkyl or (C r C 4 ) -haloalkyl; n is an integer from 0 to 4, and in the case that X is CH, an integer from 0 to 5, and in the case where X is N, an integer from 0 to 4; preferably safeners of compounds of the formula (S-VI) in which X 3 CH;
R35 Wasserstoff, (CrC6)-Alkyl, (C3-C6)-Cycloalkyl, (C2-C6)-Alkenyl, (C5-C6)- Cycloalkenyl, Phenyl oder 3- bis 6-gliedriges Heterocyclyl mit bis zu drei Heteroatomen aus der Gruppe Stickstoff, Sauerstoff und Schwefel, wobei die sechs letztgenannten Reste gegebenenfalls durch einen oder mehrere, gleiche oder verschiedene Substituenten aus der Gruppe Halogen, (Ci-C6)-R 35 is hydrogen, (C r C6) alkyl, (C 3 -C 6) -cycloalkyl, (C 2 -C 6) alkenyl, (C 5 -C 6) - cycloalkenyl, phenyl or 3- to 6 hetero-cyclic heterocyclyl having up to three heteroatoms from the group of nitrogen, oxygen and sulfur, where the six last-mentioned radicals are optionally substituted by one or more, identical or different substituents from the group halogen, (C 1 -C 6 ) -
Alkoxy, (Ci-Ce)-Haloalkoxy, (Ci-C2)-Alkylsulfinyl, (CrC2)-Alkylsulfonyl, (C3-C6)-Cycloalkyl, (CrC4)-Alkoxycarbonyl, (C1-C4)-Alkylcarbonyl und Phenyl und im Falle cyclischer Reste auch (CrC4)-Alkyl und (Ci-C4)-Haloalkyl substituiert sind; R36 Wasserstoff, (CrC6)-Alkyl, (C2-C6)-Alkenyl, (C2-C6)-Alkinyl, wobei die drei letztgenannten Reste gegebenenfalls durch einen oder mehrere, gleiche oder verschiedene Substituenten aus der Gruppe Halogen, Hydroxy, (CrC4)- Alkyl, (d-C4)-Alkoxy und (d-C4)-Alkylthio substituiert sind; >37 Halogen, (d-C^-Haloalkyl, (CrC4)-Haloalkoxy, Nitro, (d-C^-Alkyl, (C1-C4)-Alkoxy, (Ci-Ce) haloalkoxy, (Ci-C2) alkylsulfinyl, (C r C 2) alkylsulfonyl, (C 3 -C 6) -cycloalkyl, (CrC 4) alkoxycarbonyl, (C 1 -C 4 ) -alkylcarbonyl and phenyl and in the case of cyclic radicals also (C r C 4 ) -alkyl and (Ci-C 4 ) -haloalkyl are substituted; R 36 is hydrogen, (C r C 6 ) -alkyl, (C 2 -C 6 ) -alkenyl, (C 2 -C 6 ) -alkynyl, where the last three radicals mentioned are optionally substituted by one or more, identical or different substituents from the group Halogen, hydroxy, (C 1 -C 4 ) alkyl, (C 1 -C 4 ) alkoxy and (C 1 -C 4 ) alkylthio; > 37 halogen, (dC ^ haloalkyl, (C r C 4) -haloalkoxy, nitro, (dC ^ alkyl, (C 1 -C 4) -
Alkoxy, (CrC4)-Alkylsulfonyl, (Ci-C4)-Alkoxycarbonyl oder (C1-C4)-Alkoxy, (C r C 4) alkylsulfonyl, (Ci-C 4) -alkoxycarbonyl or (C 1 -C 4) -
Alkylcarbonyl;alkylcarbonyl;
R38 Wasserstoff; R39 Halogen, Nitro, (CrC4)-Alkyl, (C«|-C4)-Haloalkyl, (CrC4)-Haloalkoxy, (C3-C6)-R 38 is hydrogen; R39 is halogen, nitro, (C r C4) alkyl, (C "| -C4) haloalkyl, (CrC 4) -haloalkoxy, (C 3 -C 6) -
Cycloalkyl, Phenyl, (d-C4)-Alkoxy, Cyano, (CrC4)-Alkylthio, (C1-C4)- Alkylsulfinyl, (CrC4)-Alkylsulfonyl, (CrCO-Alkoxycarbonyl oder (C1-C4)- Alkylcarbonyl; n 0, 1 oder 2 und m 1 oder 2 bedeuten.Cycloalkyl, phenyl, (dC 4) alkoxy, cyano, (C r C4) alkylthio, (C 1 -C 4) - alkylsulfinyl, (CrC 4) alkylsulfonyl, (CrCO-alkoxycarbonyl or (C 1 -C 4 ) - alkylcarbonyl; n is 0, 1 or 2 and m is 1 or 2.
Insbesondere Verbindungen vom Typ der Acylsulfamoylbenzoesäureamide der nachfolgenden Formel (S-VII), die z.B. bekannt sind aus WO-A-99/16744,In particular, compounds of the acylsulfamoylbenzoic acid amide type represented by the following formula (S-VII), e.g. are known from WO-A-99/16744,
worin wherein
R21 = Cyclo-Propyl und R22 = H ist (S3-1 =R 21 = cyclopropyl and R 22 = H is (S3-1 =
4-Cyclopropylaminocarbonyl-N-(2-methoxybenzoyl)benzolsulfonamid;4-cyclopropylaminocarbonyl-N- (2-methoxybenzoyl) benzenesulfonamide;
Cyprosulfamide);Cyprosulfamide);
R21 = Cyclo-Propyl und R22 = 5-CI ist (S3-2), R21 = Ethyl und R22 = H ist (S3-3), R21 = iso-Propyl und R22 = 5-CI ist (S3-4) und R21 = iso-Propyl und R22 = H ist (S3-5 =R 21 = cyclopropyl and R 22 = 5-CI is (S3-2), R 21 = ethyl and R 22 = H is (S3-3), R 21 = iso-propyl and R 22 = 5-CI (S3-4) and R 21 = isopropyl and R 22 = H (S3-5 =
4-iso-propylaminocarbonyl-N-(2-methoxybenzoyl)benzolsulfonamid); e) Verbindungen vom Typ der N-Acylsulfamoylphenylharnstoffe der Formel (S-VIII), die z.B. bekannt sind aus der EP-A-365484,4-iso-propylaminocarbonyl-N- (2-methoxybenzoyl) benzenesulfonamide); e) compounds of the type of N-acylsulfamoylphenylureas of the formula (S-VIII) which are known, for example, from EP-A-365484,
worin wherein
A für einen Rest aus der GruppeA for a rest of the group
Rα und Rß unabhängig voneinander für Wasserstoff, C-i-Cβ-Alkyl, Cs-Cβ-Cycloalkyl, C3-C6-Alkenyl, C3-C6-Alkinyl,R α and R β independently of one another represent hydrogen, C 1 -C 6 -alkyl, C 5 -C 6 -cycloalkyl, C 3 -C 6 -alkenyl, C 3 -C 6 -alkynyl,
oder durch C1-C4-AIkOXy oder or by C 1 -C 4 -alkoxy or
substituiertes C1-C4-AIkOXy, oder substituted C 1 -C 4 -alkoxy, or
Rα und Rß gemeinsam für eine C4-C6-Alkylenbrücke oder eine durch Sauerstoff, Schwefel, SO, SO2, NH oder -N(CrC4-Alkyl)- unterbrochene C4-C6- Alkylenbrücke,R α and R ß together are a C 4 -C 6 alkylene or by oxygen, sulfur, SO, SO 2, NH or -N (-C 4 alkyl) - interrupted C 4 -C 6 - alkylene bridge,
Rγ für Wasserstoff oder CrC4-Alkyl,R γ is hydrogen or C 1 -C 4 -alkyl,
Ra und Rb unabhängig voneinander für Wasserstoff, Halogen, Cyan, Nitro,R a and R b independently of one another represent hydrogen, halogen, cyano, nitro,
Trifluormethyl, CrC4-Alkyl, Ci-C4-Alkoxy, d-C4-Alkylthio, CrC4-Alkylsulfιnyl, CrC4-Alkylsulfonyl, -COORj, -CONRkRm, -COR", -SO2NRkRm oder -OSO2-C1- C4-Alkyl, oder Ra und Rb gemeinsam für eine C3-C4-Alkylenbrücke, die durch Halogen oder CrC4-Alkyl substituiert sein kann, oder eine C3-C4- Alkenylenbrücke, die durch Halogen oder CrC4-Alkyl substituiert sein kann, oder eine C4-Alkadienylenbrücke, die durch Halogen oder CrC4-Alkyl substituiert sein kann, undTrifluoromethyl, C r C 4 alkyl, Ci-C 4 alkoxy, dC 4 alkylthio, C r C 4 -Alkylsulfιnyl, C r C 4 alkylsulfonyl, -COOR j, -CONR k R m, -COR ", - SO 2 NR k R m or -OSO 2 -C 1 - C 4 alkyl, or R a and R b together represent a C 3 -C 4 alkylene bridge which may be substituted by halogen or -C 4 alkyl or C 3 alkenylene -C4-, by halogen or CrC 4 - Alkyl may be substituted, or a C 4 -Alkadienylenbrücke which may be substituted by halogen or CrC 4 alkyl, and
R9 und Rh unabhängig voneinander für Wasserstoff, Halogen, Ci-C4-Alkyl, Trifluormethyl, Methoxy, Methylthio oder -COOR' stehen, wobeiR 9 and R h independently of one another represent hydrogen, halogen, C 1 -C 4 -alkyl, trifluoromethyl, methoxy, methylthio or -COOR ', where
Rc Wasserstoff, Halogen, CrC4-Alkyl oder Methoxy,R c is hydrogen, halogen, C 1 -C 4 -alkyl or methoxy,
Rd Wasserstoff, Halogen, Nitro, CrC4-Alkyl, C1-C4-AIkOXy, CrC4-Alkylthio, CrC4- Alkylsulfinyl, CrC4-Alkylsulfonyl, -COORj oder -CONRkRm,R d is hydrogen, halogen, nitro, C r C 4 alkyl, C 1 -C 4 -alkoxy, C r C 4 alkylthio, C r C 4 - alkylsulfinyl, C r C 4 alkylsulfonyl, -COOR j or -CONR k R m ,
Re Wasserstoff, Halogen, CrC4-Alkyl, -COORj, Trifluormethyl oder Methoxy, oder Rd und Re gemeinsam für eine C3-C4-Alkylenbrücke,R e is hydrogen, halogen, C r C 4 alkyl, -COOR j, trifluoromethyl or methoxy, or R d and R e together represent a C 3 -C 4 alkylene bridge,
Rf Wasserstoff, Halogen oder d-C4-Alkyl,R f is hydrogen, halogen or C 1 -C 4 -alkyl,
Rx und Rγ unabhängig voneinander Wasserstoff, Halogen, CrC4-Alkyl, CrC4- Alkoxy, CrC4-Alkylthio, -COOR4, Trifluormethyl, Nitro oder Cyan,R x and R γ independently represent hydrogen, halogen, -C 4 alkyl, C r C 4 - alkoxy, C r C 4 alkylthio, -COOR 4, trifluoromethyl, nitro or cyano,
Rj, Rk und Rm unabhängig voneinander Wasserstoff oder CrC4-Alkyl,R j , R k and R m independently of one another are hydrogen or C 1 -C 4 -alkyl,
Rk und Rm gemeinsam eine C4-C6-Alkylenbrücke oder eine durch Sauerstoff, NH oder -N(C-ι-C4-Alkyl)- unterbrochene C4-C6-Alkylenbrücke, undR k and R m together are a C 4 -C 6 -alkylene bridge or an interrupted by oxygen, NH or -N (C-ι-C 4 alkyl) - interrupted C 4 -C 6 alkylene, and
Rn CrC4-Alkyl, Phenyl oder durch Halogen, CrC4-Alkyl, Methoxy, Nitro oder Trifluormethyl substituiertes Phenyl bedeuten; vorzugsweise Safener der Formel (S-VIII) sindR n is C 1 -C 4 alkyl, phenyl or phenyl substituted by halogen, C 1 -C 4 alkyl, methoxy, nitro or trifluoromethyl; preferably safeners of the formula (S-VIII)
1-[4-(N-2-Methoxybenzoylsulfamoyl)phenyl]-3-methylharnstoff, 1-[4-(N-2-Methoxybenzoylsulfamoyl)phenyl]-3,3-dimethylhamstoff, 1-[4-(N-4,5-Dimethylbenzoylsulfamoyl)phenyl]-3-methylharnstoff, 1 -[4-(N-Naphthoylsulfamoyl)phenyl]-3,3-dimethylharnstoff, einschließlich der Stereoisomeren und der in der Landwirtschaft gebräuchlichen1- [4- (N-2-methoxybenzoylsulfamoyl) phenyl] -3-methylurea, 1- [4- (N-2-methoxybenzoylsulfamoyl) phenyl] -3,3-dimethylurea, 1- [4- (N-4, 5-dimethylbenzoylsulfamoyl) phenyl] -3-methylurea, 1- [4- (N-naphthoylsulfamoyl) phenyl] -3,3-dimethylurea, including stereoisomers and those commonly used in agriculture
Salze.Salts.
Sofern es im Einzelnen nicht anders definiert wird, gelten für die Reste in den Formeln zu (S-Il) bis (S-VIII) im Allgemeinen die folgenden Definitionen.Unless otherwise defined in detail, the following definitions generally apply to the radicals in the formulas (S-II) to (S-VIII).
Die Reste Alkyl, Alkoxy, Haloalkyl, Haloalkoxy, Alkylamino und Alkylthio sowie die entsprechenden ungesättigten und/oder substituierten Reste können im Kohlenstoffgerüst jeweils geradkettig oder verzweigt sein. Alkylreste, auch in den zusammengesetzten Bedeutungen wie Alkoxy, Haloalkyl usw. haben vorzugsweise 1 bis 4 C-Atome und, bedeuten z.B. Methyl, Ethyl, n- oder i-Propyl, n-, i-, t- oder 2-Butyl. Alkenyl- und Alkinylreste haben die Bedeutung der den Alkylresten entsprechenden möglichen ungesättigten Reste; Alkenyl bedeutet z.B. AIIyI, 1-Methylprop-2-en-1-yl, 2-Methyl-prop-2-en-1-yl, But-2-en-1-yl, But-3-en-1- yl, 1-Methyl-but-3-en-1-yl und 1-Methyl-but-2-en-1-yl. Alkinyl bedeutet z.B. Propargyl, But-2-in-1-yl, But-3-in-1-yl, 1-Methyl-but-3-in-1-yl. "(CrC4)-Alkyr ist die Kurzschreibweise für Alkyl mit 1 bis 4 C-Atomen; entsprechendes gilt für andere allgemeine Restedefinitionen mit in Klammern angegebenen Bereichen für die mögliche Anzahl von C-Atomen.The radicals alkyl, alkoxy, haloalkyl, haloalkoxy, alkylamino and alkylthio and the corresponding unsaturated and / or substituted radicals can each be straight-chain or branched in the carbon skeleton. Alkyl radicals, even in the composite meanings such as alkoxy, haloalkyl, etc., preferably have 1 to 4 carbon atoms and, for example, methyl, ethyl, n- or i-propyl, n-, i-, t- or 2-butyl. Alkenyl and alkynyl radicals have the meaning of the possible unsaturated radicals corresponding to the alkyl radicals; Alkenyl is for example AlII, 1-methylprop-2-en-1-yl, 2-methyl-prop-2-en-1-yl, but-2-en-1-yl, but-3-en-1-yl , 1-methyl-but-3-en-1-yl and 1-methyl-but-2-en-1-yl. Alkynyl means, for example, propargyl, but-2-yn-1-yl, but-3-yn-1-yl, 1-methylbut-3-yn-1-yl. "(CrC 4 ) -Alkyr is the shorthand notation for alkyl of 1 to 4 carbon atoms, as well as other general definitions of radicals with bracketed ranges for the possible number of carbon atoms.
Cycloalkyl bedeutet bevorzugt einen cyclischen Alkylrest mit 3 bis 8, vorzugsweise 3 bis 7, besonders bevorzugt 3 bis 6 C-Atomen, beispielsweise Cyclopropyl, Cyclobutyl, Cyclopentyl und Cyclohexyl. Cycloalkenyl und Cycloalkinyl bezeichnen entsprechende ungesättigte Verbindungen. Halogen bedeutet Fluor, Chlor, Brom oder lod. Haloalkyl, Haloalkenyl undCycloalkyl is preferably a cyclic alkyl radical having 3 to 8, preferably 3 to 7, particularly preferably 3 to 6, C atoms, for example cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl. Cycloalkenyl and cycloalkynyl refer to corresponding unsaturated compounds. Halogen is fluorine, chlorine, bromine or iodine. Haloalkyl, haloalkenyl and
Haloalkinyl bedeuten durch Halogen, vorzugsweise durch Fluor, Chlor und/oder Brom, insbesondere durch Fluor oder Chlor, teilweise oder vollständig substituiertes Alkyl, Alkenyl oder Alkinyl, z.B. CF3, CHF2, CH2F, CF2CF3, CH2CHFCI, CCI3, CHCI2, CH2CH2CI. Haloalkoxy ist z.B. OCF3, OCHF2, OCH2F, OCF2CF3, OCH2CF3 und OCH2CH2CI. Entsprechendes gilt für sonstige Halogen substituierte Reste. Ein Kohlenwasserstoffrest kann ein aromatischer oder ein aliphatischer Kohlenwasserstoff rest sein, wobei ein aliphatischer Kohlenwasserstoffrest im allgemeinen ein geradkettiger oder verzweigter gesättigter oder ungesättigter Kohlenwasserstoff rest ist, vorzugsweise mit 1 bis 18, besonders bevorzugt 1 bis 12 C-Atomen, z.B. Alkyl, Alkenyl oder Alkinyl.Haloalkinyl mean by halogen, preferably by fluorine, chlorine and / or bromine, in particular by fluorine or chlorine, partially or fully substituted alkyl, alkenyl or alkynyl, for example CF 3 , CHF 2 , CH 2 F, CF 2 CF 3 , CH 2 CHFCI , CCI 3 , CHCl 2 , CH 2 CH 2 Cl. Haloalkoxy is eg OCF 3 , OCHF 2 , OCH 2 F, OCF 2 CF 3 , OCH 2 CF 3 and OCH 2 CH 2 Cl. The same applies to other halogen-substituted radicals. A hydrocarbon radical may be an aromatic or an aliphatic hydrocarbon radical, where an aliphatic hydrocarbon radical is generally a straight-chain or branched saturated or unsaturated hydrocarbon radical, preferably having 1 to 18, particularly preferably 1 to 12, carbon atoms, for example alkyl, alkenyl or alkynyl ,
Vorzugsweise bedeutet aliphatischer Kohlenwasserstoffrest Alkyl, Alkenyl oder Alkinyl mit bis zu 12 C-Atomen; entsprechendes gilt für einen aliphatischen Kohlenwasserstoffrest in einem Kohlenwasserstoffoxyrest. Aryl ist im allgemeinen ein mono-, bi- oder polycyclisches aromatisches System mit vorzugsweise 6-20 C-Atomen, bevorzugt 6 bis 14 C-Atomen, besonders bevorzugt 6 bis 10 C-Atomen, z.B. Phenyl, Naphthyl, Tetrahydronaphthyl, Indenyl, Indanyl, Pentalenyl und Fluorenyl, besonders bevorzugt Phenyl.Preferably, aliphatic hydrocarbon radical alkyl, alkenyl or alkynyl having up to 12 carbon atoms; the same applies to an aliphatic hydrocarbon radical in a Kohlenwasserstoffoxyrest. Aryl is generally a mono-, bi- or polycyclic aromatic system having preferably 6-20 C atoms, preferably 6 to 14 C atoms, more preferably 6 to 10 C atoms, e.g. Phenyl, naphthyl, tetrahydronaphthyl, indenyl, indanyl, pentalenyl and fluorenyl, more preferably phenyl.
Heterocyclischer Ring, heterocyclischer Rest oder Heterocyclyl bedeutet ein mono-, bi- oder polycyclisches Ringsystem, das gesättigt, ungesättigt und/oder aromatisch ist und eine oder mehrere, vorzugsweise 1 bis 4, Heteroatome, vorzugsweise aus der Gruppe N, S und O, enthält.Heterocyclic ring, heterocyclic radical or heterocyclyl means a mono-, bi- or polycyclic ring system which is saturated, unsaturated and / or aromatic and one or more, preferably 1 to 4, heteroatoms, preferably from the group N, S and O, contains.
Bevorzugt sind gesättigte Heterocyclen mit 3 bis 7 Ringatomen und einem oder zwei Heteroatomen aus der Gruppe N, O und S, wobei die Chalcogene nicht benachbart sind. Besonders bevorzugt sind monocyclische Ringe mit 3 bis 7 Ringatomen und einem Heteroatom aus der Gruppe N, O und S, sowie Morpholin, Dioxolan, Piperazin, Imidazolin und Oxazolidin. Ganz besonders bevorzugte gesättigte Heterocyclen sind Oxiran, Pyrrolidon, Morpholin und Tetrahydrofuran. Bevorzugt sind auch teilweise ungesättigte Heterocyclen mit 5 bis 7 Ringatomen und einem oder zwei Heteroatomen aus der Gruppe N, O und S. Besonders bevorzugt sind teilweise ungesättigte Heterocyclen mit 5 bis 6 Ringatomen und einem Heteroatom aus der Gruppe N, O und S. Ganz besonders bevorzugte teilweise ungesättigte Heterocyclen sind Pyrazolin, Imidazolin und Isoxazolin. Ebenso bevorzugt ist Heteroaryl, z.B. mono- oder bicyclische aromatische Heterocyclen mit 5 bis 6 Ringatomen, die ein bis vier Heteroatome aus der Gruppe N, O, S enthalten, wobei die Chalcogene nicht benachbart sind. Besonders bevorzugt sind monocyclische aromatische Heterocyclen mit 5 bis 6 Ringatomen, die ein Heteroatom aus der Gruppe, N, O und S enthalten, sowie Pyrimidin, Pyrazin, Pyridazin, Oxazol, Thiazol, Thiadiazol, Oxadiazol, Pyrazol, Triazol und Isoxazol. Ganz besonders bevorzugt sind Pyrazol, Thiazol, Triazol und Furan.Preferred are saturated heterocycles having 3 to 7 ring atoms and one or two heteroatoms from the group N, O and S, wherein the chalcogens are not adjacent. Particularly preferred are monocyclic rings having 3 to 7 ring atoms and a heteroatom from the group N, O and S, and morpholine, dioxolane, piperazine, imidazoline and oxazolidine. Very particularly preferred saturated heterocycles are oxirane, pyrrolidone, morpholine and tetrahydrofuran. Also preferred are partially unsaturated heterocycles having 5 to 7 ring atoms and one or two heteroatoms from the group N, O and S. Particularly preferred are partially unsaturated heterocycles having 5 to 6 ring atoms and one heteroatom from the group N, O and S. Very particular preferred partially unsaturated heterocycles are pyrazoline, imidazoline and isoxazoline. Also preferred is heteroaryl, e.g. mono- or bicyclic aromatic heterocycles having 5 to 6 ring atoms containing one to four heteroatoms from the group N, O, S, wherein the chalcogens are not adjacent. Particularly preferred are monocyclic aromatic heterocycles having 5 to 6 ring atoms which contain a heteroatom from the group, N, O and S, and pyrimidine, pyrazine, pyridazine, oxazole, thiazole, thiadiazole, oxadiazole, pyrazole, triazole and isoxazole. Very particular preference is given to pyrazole, thiazole, triazole and furan.
Substituierte Reste, wie substituierte Kohlenwasserstoffreste, z.B. substituiertes Alkyl, Alkenyl, Alkinyl, Aryl wie Phenyl und Arylalkyl wie Benzyl, oder substituiertes Heterocyclyl, bedeuten einen vom unsubstituierten Grundkörper abgeleiteten substituierten Rest, wobei die Substituenten vorzugsweise einen oder mehrere, vorzugsweise 1 , 2 oder 3, im Falle von Cl und F auch bis zur maximal möglichen Anzahl, Substituenten aus der Gruppe Halogen, Alkoxy, Haloalkoxy, Alkylthio, Hydroxy, Amino, Nitro, Carboxy, Cyano, Azido, Alkoxycarbonyl, Alkylcarbonyl, Formyl, Carbamoyl, Mono- und Dialkylaminocarbonyl, substituiertes Amino wie Acylamino, Mono- und Dialkylamino und Alkylsulfinyl, Haloalkylsulfinyl, Alkylsulfonyl, Haloalkylsulfonyl und, im Falle cyclischer Reste, auch Alkyl und Haloalkyl sowie den genannten gesättigten kohlenwasserstoffhaltigen Substituenten entsprechende ungesättigte aliphatische Substituenten, vorzugsweise Alkenyl, Alkinyl, Alkenyloxy, Alkinyloxy, bedeuten. Bei Resten mit C-Atomen sind solche mit 1 bis 4 C-Atomen, insbesondere 1 oder 2 C-Atomen, bevorzugt. Bevorzugt sind in der Regel Substituenten aus der Gruppe Halogen, z.B. Fluor oder Chlor, (CrC4)Alkyl, vorzugsweise Methyl oder Ethyl, (CrC4)Haloalkyl, vorzugsweise Trifluormethyl, (CrC4)AIkOXy, vorzugsweise Methoxy oder Ethoxy, (CrC4)HaIOaIkOXy, Nitro und Cyano. Besonders bevorzugt sind dabei die Substituenten Methyl, Methoxy und Chlor.Substituted radicals, such as substituted hydrocarbon radicals, for example substituted alkyl, alkenyl, alkynyl, aryl, such as phenyl and arylalkyl, such as benzyl, or substituted heterocyclyl, represent a substituted radical derived from the unsubstituted radical, where the substituents are preferably one or more, preferably 1, 2 or 3 , in the case of Cl and F also up to the maximum possible number, substituents from the group halogen, alkoxy, haloalkoxy, alkylthio, hydroxy, amino, nitro, carboxy, cyano, azido, alkoxycarbonyl, alkylcarbonyl, formyl, carbamoyl, mono- and dialkylaminocarbonyl , substituted amino such as acylamino, mono- and dialkylamino and alkylsulfinyl, haloalkylsulfinyl, alkylsulfonyl, haloalkylsulfonyl and, in the case of cyclic radicals, also alkyl and haloalkyl and said saturated hydrocarbon-containing substituents corresponding unsaturated aliphatic substituents, preferably alkenyl, alkynyl, alkenyloxy, alkynyloxy , For radicals with C atoms, those having 1 to 4 C atoms, in particular 1 or 2 C atoms, are preferred. Preferred are usually Substituents from the group halogen, for example fluorine or chlorine, (CrC 4 ) alkyl, preferably methyl or ethyl, (CrC 4 ) haloalkyl, preferably trifluoromethyl, (CrC 4 ) AIkOXy, preferably methoxy or ethoxy, (CrC 4 ) haloalkoxy, nitro and cyano. Particularly preferred are the substituents methyl, methoxy and chlorine.
Mono- oder disubstituiertes Amino bedeutet einen chemisch stabilen Rest aus der Gruppe der substituierten Aminoreste, welche beispielsweise durch einen oder zwei gleiche oder verschiedene Reste aus der Gruppe Alkyl, Alkoxy, Acyl und Aryl N-substituiert sind; vorzugsweise Monoalkylamino, Dialkylamino, Acylamino, Arylamino, N-Alkyl-N-Arylamino sowie N-Heterocyclen. Dabei sind Alkylreste mit 1 bis 4 C-Atomen bevorzugt. Aryl ist dabei vorzugsweise Phenyl. Substituiertes Aryl ist dabei vorzugsweise substituiertes Phenyl. Für Acyl gilt dabei die weiter unten genannte Definition, vorzugsweise (CrC4)Alkanoyl. Entsprechendes gilt für substituiertes Hydroxylamino oder Hydrazino. Gegebenenfalls substituiertes Phenyl ist vorzugsweise Phenyl, das unsubstituiert oder ein- oder mehrfach, vorzugsweise bis zu dreifach, bei Halogen wie Cl und F auch bis zu fünffach, durch gleiche oder verschiedene Reste aus der Gruppe Halogen, (CrC4)Alkyl, (CrC4)Alkoxy, (CrC4)Haloalkyl, (CrC4)Haloalkoxy und Nitro substituiert ist, z.B. o-, m- und p-Tolyl, Dimethylphenyle, 2-, 3- und 4-Chlorphenyl, 2-, 3- und 4-Trifluor- und -Trichlorphenyl, 2,4-, 3,5-, 2,5- und 2,3-Dichlorphenyl, o-, m- und p-Methoxyphenyl.Mono- or disubstituted amino means a chemically stable radical from the group of substituted amino radicals which are N-substituted by, for example, one or two identical or different radicals from the group consisting of alkyl, alkoxy, acyl and aryl; preferably monoalkylamino, dialkylamino, acylamino, arylamino, N-alkyl-N-arylamino and N-heterocycles. In this case, alkyl radicals having 1 to 4 carbon atoms are preferred. Aryl is preferably phenyl. Substituted aryl is preferably substituted phenyl. This is true for acyl the definition mentioned further below applies, preferably (CrC 4) alkanoyl. The same applies to substituted hydroxylamino or hydrazino. Optionally substituted phenyl is preferably phenyl which is unsubstituted or mono- or polysubstituted, preferably up to three times, in halogens such as Cl and F also up to five times, by identical or different radicals from the group halogen, (CrC 4 ) alkyl, (CrC 4 ) Alkoxy, (CrC 4 ) haloalkyl, (C r C 4 ) haloalkoxy and nitro, for example o-, m- and p-tolyl, dimethylphenols, 2-, 3- and 4-chlorophenyl, 2-, 3- and 4-trifluoro- and trichlorophenyl, 2,4-, 3,5-, 2,5- and 2,3-dichlorophenyl, o-, m- and p-methoxyphenyl.
Ein Acylrest bedeutet den Rest einer organischen Säure mit vorzugsweise bis zu 6 C-Atomen, z.B. den Rest einer Carbonsäure und Reste davon abgeleiteter Säuren wie der Thiocarbonsäure, gegebenenfalls N-substituierter Iminocarbonsäuren, oder der Rest von Kohlensäuremonoestern, gegebenenfalls N-substituierterAn acyl group means the residue of an organic acid preferably having up to 6 C atoms, e.g. the radical of a carboxylic acid and radicals derived therefrom, such as the thiocarboxylic acid, optionally N-substituted iminocarboxylic acids, or the radical of carbonic acid monoesters, optionally N-substituted
Carbaminsäuren, Sulfonsäuren, Sulfinsäuren, Phosphonsäuren, Phosphinsäuren. Acyl bedeutet beispielsweise Formyl, Alkylcarbonyl, wie (CrC4-Alkyl)-carbonyl, Phenylcarbonyl, wobei der Phenylring substituiert sein kann, z.B. wie oben für Phenyl angegeben, oder Alkyloxycarbonyl, Phenyloxycarbonyl, Benzyloxycarbonyl, Alkylsulfonyl, Alkylsulfinyl oder N-Alkyl-1-iminoalkyl.Carbamic acids, sulfonic acids, sulfinic acids, phosphonic acids, phosphinic acids. Acyl is, for example, formyl, alkylcarbonyl, such as (C 1 -C 4 -alkyl) carbonyl, phenylcarbonyl, where the phenyl ring may be substituted, for example as indicated above for phenyl, or alkyloxycarbonyl, phenyloxycarbonyl, benzyloxycarbonyl, alkylsulfonyl, alkylsulfinyl or N-alkyl-1 iminoalkyl.
Von den Formeln (S-Il) bis (S-VIII) umfasst sind auch alle Stereoisomeren, welche die gleiche topologische Verknüpfung der Atome aufweisen, und deren Gemische. Solche Verbindungen enthalten ein oder mehrere asymmetrische C-Atome oder auch Doppelbindungen, die in den allgemeinen Formeln nicht gesondert angegeben sind. Die durch ihre spezifische Raumform definierten möglichen Stereoisomeren, wie Enantiomere, Diastereomere, Z- und E-Isomere, können nach üblichen Methoden aus Gemischen der Stereoisomeren erhalten oder auch durch stereoselektive Reaktionen in Kombination mit dem Einsatz von stereochemisch reinen Ausgangsstoffen hergestellt werden.Also encompassed by the formulas (S-II) to (S-VIII) are all stereoisomers which have the same topological linkage of the atoms, and mixtures thereof. Such compounds contain one or more asymmetric C atoms or double bonds, which are not specified separately in the general formulas are. The possible defined by their specific spatial form possible stereoisomers, such as enantiomers, diastereomers, Z and E isomers can be obtained by conventional methods from mixtures of stereoisomers or prepared by stereoselective reactions in combination with the use of stereochemically pure starting materials.
Die Verbindungen der Formel (S-Il) sind z.B. aus EP-A-0333131 (ZA-89/1960), EP-A-0269806 (US 4,891 ,057), EP-A-0346620 (AU-A-89/34951 ), EP-A-0174562, EP-A-0346620 (WO-A-91 /08202), WO-A-91/07874 oder WO-A-95/07897 (ZA 94/7120) und der dort zitierten Literatur bekannt oder können nach oder analog den dort beschriebenen Verfahren hergestellt werden. Die Verbindungen der Formel (S- III) sind aus EP-A-0086750, EP-A-094349 (US 4,902,340), EP-A-0191736 (US 4,881 ,966) und EP-A-0492366 und dort zitierter Literatur bekannt oder können nach oder analog den dort beschriebenen Verfahren hergestellt werden. Einige Verbindungen sind ferner in EP-A-0582198 und WO-A-02/34048 beschrieben. Die Verbindungen der Formel (S-IV) sind aus zahlreichen Patentanmeldungen bekannt, beispielsweise US 4,021,224 und US 4,021 ,229. Verbindungen der Untergruppe b) sind weiterhin aus CN-A-87/102789, EP-A-365484 sowie aus "The Pesticide Manual", 11. bis 13. Auflage, British Crop Protection Council and the Royal Society of Chemistry (1997), bekannt. Die Verbindungen der Untergruppe c) sind in der WO- A-97/45016, die der Untergruppe d) in der WO-A-99/16744 (insbesondere in EP-A- 365484) beschrieben. Die zitierten Schriften enthalten ausführliche Angaben zu Herstellungsverfahren und Ausgangsmaterialien und nennen bevorzugte Verbindungen. Auf diese Schriften wird ausdrücklich Bezug genommen, sie gelten durch Zitat als Bestandteil dieser Beschreibung.The compounds of formula (S-II) are e.g. from EP-A-0333131 (ZA-89/1960), EP-A-0269806 (US 4,891,057), EP-A-0346620 (AU-A-89/34951), EP-A-0174562, EP-A No. 0346620 (WO-A-91/08202), WO-A-91/07874 or WO-A-95/07897 (ZA 94/7120) and the literature cited therein, or can be prepared by or analogously to the processes described therein , The compounds of the formula (S-III) are known from EP-A-0086750, EP-A-094349 (US 4,902,340), EP-A-0191736 (US 4,881,966) and EP-A-0492366 and literature cited therein or US Pat can be prepared according to or analogously to the methods described therein. Some compounds are further described in EP-A-0582198 and WO-A-02/34048. The compounds of formula (S-IV) are known from numerous patent applications, for example US 4,021,224 and US 4,021,229. Compounds of subgroup b) are further from CN-A-87/102789, EP-A-365484 and from "The Pesticide Manual", 11th to 13th edition, British Crop Protection Council and the Royal Society of Chemistry (1997), known. The compounds of subgroup c) are described in WO-A-97/45016, those of subgroup d) in WO-A-99/16744 (in particular in EP-A-365484). The cited documents contain detailed information on preparation processes and starting materials and name preferred compounds. These documents are expressly referred to, they are by quotation as part of this description.
Die Safener der vorstehenden Gruppen a) bis e) reduzieren oder unterbinden phytotoxische Effekte, die beim Einsatz der herbiziden Mittel gemäß der Erfindung in Nutzpflanzenkulturen auftreten können, ohne die Wirksamkeit der Herbizide gegen Schadpflanzen zu beeinträchtigen. Hierdurch kann das Einsatzgebiet der Herbizide erheblich erweitert werden und insbesondere ist durch die Verwendung von Safenern der Einsatz von Herbiziden, die bislang nur beschränkt oder mit nicht ausreichendem Erfolg eingesetzt werden konnten, d.h. von Kombinationen, die ohne Safener in niedrigen Dosierungen mit wenig Breitenwirkung zu nicht ausreichender Kontrolle der Schadpflanzen führten, möglich.The safeners of the above groups a) to e) reduce or prevent the phytotoxic effects which can occur when using the herbicidal compositions according to the invention in crops without impairing the effectiveness of the herbicides against harmful plants. As a result, the field of application of the herbicides can be significantly extended and in particular by the use of safeners, the use of herbicides, which have so far only limited or could be used with insufficient success, ie of combinations without Safener in low dosages with little broad effect led to insufficient control of harmful plants, possible.
Besonders bevorzugt sind als Safener in den erfindungsgemäßen Formulierungen unter anderem: 4-Dichloracetyl-1-oxa-4-aza-spiro[4.5]-decan (AD-67), 1- Dichloracetyl-hexahydro-3,3,8a-trimethylpyπOlo[1,2-a]-pyrimidin-6(2H)-on (Dicyclonon, BAS-145138), 4-Dichloracetyl-3,4-dihydro-3-methyl-2H-1 ,4-benzoxazin (Benoxacor), Cloquintocet, 5-Chlor-chinolin-8-oxy-essigsäure-(1 -methyl-hexylester) (Cloquintocet-mexyl), α-(Cyanomethoxyimino)-phenylacetonitril (Cyometrinil), 2,2- Dichlor-N-(2-oxo-2-(2-propenylamino)-ethyl)-N-(2-propenyl)-acetamid (DKA-24), 2,2- Dichlor-N,N-di-2-propenyl-acetamid (Dichlormid), N-(4-Methyl-phenyl)-N'-(1 -methyl- 1-phenyl-ethyl)-harnstoff (Dymron), 4,6-Dichlor-2-phenyl-pyrimidin (Fenclorim), 1- (2,4-Dichlor-phenyl)-5-trichlormethyl-1 H-1 )2,4-triazol-3-carbonsäure-ethylester (Fenchlorazol-ethyl), 2-Chlor-4-trifluormethyl-thiazol-5-carbonsäure- phenylmethylester (Flurazole), 4-Chlor-N-(1 ,3-dioxolan-2-yl-methoxy)-α-trifluor- acetophenonoxim (Fluxofenim), 3-Dichloracetyl-5-(2-furanyl)-2,2-dimethyl-oxazolidin (Furilazole, MON-13900), Ethyl-4,5-dihydro-5,5-diphenyl-3-isoxazolcarboxylat (Isoxadifen-ethyl), Diethyl-1 -(2,4-dichlorphenyl)-4,5-dihydro-5-methyl-1 H-pyrazol-3,5- dicarboxylat (Mefenpyr-diethyl), 2-Dichlormethyl-2-methyl-1 ,3-dioxolan (MG-191 ), 1 ,8-Naphthalsäureanhydrid, α-(1 ,3-Dioxolan-2-yl-methoximino)-phenylacetonitril (Oxabetrinil), 2,2-Dichlor-N-(1 ,3-dioxolan-2-yl-methyl)-N-(2-propenyl)-acetamid (PPG-1292), 3-Dichloracetyl-2,2-dimethyl-oxazolidin (R-28725), 3-Dichloracetyl- 2,2,5-trimethyl-oxazolidin (R-29148), 1-(2-Chlor-phenyl)-5-phenyl-1 H-pyrazol-3- carbonsäure-methylester, 4-Cyclopropylaminocarbonyl-N-(2- methoxybenzoyl)benzolsulfonamid (Cyprosulfamide), 4-iso-propylaminocarbonyl-N- (2-methoxybenzoyl)benzolsulfonamid und N-(2-Methoxy-benzoyl)-4-[(methylamino- carbonyl)-amino]-benzolsulfonamid.Particular preference is given as safeners in the formulations according to the invention, inter alia: 4-dichloroacetyl-1-oxa-4-aza-spiro [4.5] -decane (AD-67), 1-dichloroacetyl-hexahydro-3,3,8a-trimethylphenyl [ 1,2-a] -pyrimidine-6 (2H) -one (dicyclonone, BAS-145138), 4-dichloroacetyl-3,4-dihydro-3-methyl-2H-1,4-benzoxazine (Benoxacor), cloquintocet, 5-Chloro-quinolin-8-oxy-acetic acid (1-methylhexyl ester) (cloquintocet-mexyl), α- (cyanomethoxyimino) -phenylacetonitrile (cyometrinil), 2,2-dichloro-N- (2-oxo-2 - (2-propenylamino) -ethyl) -N- (2-propenyl) -acetamide (DKA-24), 2,2-dichloro-N, N-di-2-propenyl-acetamide (dichloromid), N- (4 Methyl-phenyl) -N '- (1-methyl-1-phenyl-ethyl) -urea (Dymron), 4,6-dichloro-2-phenyl-pyrimidine (fenclorim), 1- (2,4-dichloro) phenyl) -5-trichloromethyl-1 H-1 ) ethyl 2,4-triazole-3-carboxylate (fenchlorazole-ethyl), 2-chloro-4-trifluoromethyl-thiazole-5-carboxylic acid phenylmethyl ester (flurazole), 4- Chloro-N- (1,3-dioxolan-2-yl-methoxy) -α-trifluoroacetophenone oxime (Fluxofenim), 3-dichloro oracetyl-5- (2-furanyl) -2,2-dimethyl-oxazolidine (furilazole, MON-13900), ethyl 4,5-dihydro-5,5-diphenyl-3-isoxazolecarboxylate (isoxadifen-ethyl), diethyl 1 - (2,4-dichlorophenyl) -4,5-dihydro-5-methyl-1H-pyrazole-3,5-dicarboxylate (mefenpyr-diethyl), 2-dichloromethyl-2-methyl-1,3-dioxolane ( MG-191), 1,8-naphthalic anhydride, α- (1,3-dioxolan-2-yl-methoximino) -phenylacetonitrile (oxabetrinil), 2,2-dichloro-N- (1,3-dioxolan-2-yl -methyl) -N- (2-propenyl) -acetamide (PPG-1292), 3-dichloroacetyl-2,2-dimethyl-oxazolidine (R-28725), 3-dichloroacetyl-2,2,5-trimethyl-oxazolidine ( R-29148), methyl 1- (2-chloro-phenyl) -5-phenyl-1H-pyrazole-3-carboxylate, 4-cyclopropylaminocarbonyl-N- (2-methoxybenzoyl) benzenesulfonamide (cyprosulfamide), 4-iso propylaminocarbonyl-N- (2-methoxybenzoyl) benzenesulfonamide and N- (2-methoxybenzoyl) -4 - [(methylaminocarbonyl) amino] benzenesulfonamide.
Ganz besonders bevorzugt sind die Safenern Mefenpyr-diethyl, Cloquintocet-mexyl, Isoxadifen-ethyl, 4-Cyclopropylaminocarbonyl-N-(2- methoxybenzoyl)benzolsulfonamid (Cyprosulfamide), 4-iso-propylaminocarbonyl-N- (2-methoxybenzoyl)benzolsulfonamid oder Fenchlorazol-ethyl; insbesondere ganz besonders bevorzugt sind Mefenpyr-diethyl, Cloquintocet-mexyl oder Isoxadifen- ethyl. Bevorzugte Herbizid-Safener-Mischungen sind Kombinationen der folgenden Verbindungen miteinander:Very particular preference is given to the safeners mefenpyr-diethyl, cloquintocet-mexyl, isoxadifen-ethyl, 4-cyclopropylaminocarbonyl-N- (2-methoxybenzoyl) benzenesulfonamide (cyprosulfamide), 4-iso-propylaminocarbonyl-N- (2-methoxybenzoyl) benzenesulfonamide or fenchlorazole ethyl; Particular preference is given to mefenpyr-diethyl, cloquintocet-mexyl or isoxadifen-ethyl. Preferred herbicide-safener mixtures are combinations of the following compounds with one another:
a) Verbindungen, die als ACCase-lnhibitoren wirksam sind, wie Alloxydim,a) compounds which are effective as ACCase inhibitors, such as alloxydim,
Butroxydim, Clethodim, Clodinafop-propargyl, Cycloxydim, Cyhalofop-butyl, Diclofop- methyl, Fenoxaprop, Fenoxaprop-ethyl, Fenoxaprop-P, Fenoxaprop-P-ethyl, Fluazifop, Fluazifop-P-butyl, Fluazifop-butyl, Haloxyfop, Haloxyfop-P, Haloxyfop- etotyl, Haloxyfop-P-methyl, Metamifop, Profoxydim, Propaquizafop, Quizalofop-P- tefuryl, Quizalofop-P-ethyl, Sethoxydim, Tepraloxydim, Tralkoxydim und Isoxapyrifop,Butroxydim, clethodim, clodinafop-propargyl, cycloxydim, cyhalofop-butyl, diclofopmethyl, fenoxaprop, fenoxaprop-ethyl, fenoxaprop-P, fenoxaprop-P-ethyl, fluazifop, fluazifop-p-butyl, fluazifop-butyl, haloxyfop, haloxyfop- P, haloxyfopetotyl, haloxyfop-P-methyl, metamifop, profoxydim, propaquizafop, quizalofop-P-tefuryl, quizalofop-P-ethyl, sethoxydim, tepraloxydim, tralkoxydim and isoxapyrifop,
b) Verbindungen, die als p-Hydroxyphenyl pyruvate dioxygenase (HPPD)- Inhibitoren wirksam sind, wie Benzobicyclon, Benzofenap, Isoxaflutole und dessen Diketonitrile, Mesotrione, Pyrazolynate, Pyrazoxyfen, Sulcotrione und Isoxachlortole,b) compounds which are effective as p-hydroxyphenyl pyruvate dioxygenase (HPPD) inhibitors, such as benzobicyclone, benzofenap, isoxaflutole and its diketonitrile, mesotrione, pyrazolynate, pyrazoxyfen, sulcotrione and isoxachlortole,
c) Verbindungen verschiedener Wirkstoffgruppen, wie Atrazin, Acetochlor, Aclonifen, Alachlor, Amidochlor, Amidosulfuron, Azimsulfuron, Bentazon, Bensulfuron(-methyl), Bromoxynil(-octanoat/-heptanoat), Butachlor, Bispyribac, Chlorsulfuron, Chlorimuron, Clomazone, Clopyralid, Cinosulfuron, Cyclosulfamuron, 2,4-D-Ester, 2,4-DB-Ester, 2,4-DP-Ester, CMPP-Ester, MCPA-Ester, MCPB, EPTC, Desmedipham, Diflufenican, Dicamba, Ethoxysulfuron, Ethofumesat, Flazasulfuron, Florasulam, Flucarbazone, Flumetsulam, Flufenacet, Fluoroglykofen, Fluroxypyr, Flupyrsulfuron, Foramsulfuron, Flumioxazin, Flumiclorac, Fomesafen, Glufosinate, Glyphosate, Imazapyr, Imazosulfuron, lodosulfuron, lodosulfuron-methyl, loxynil(- octanoat), Lactofen, Halosulfuron, Imazamox, Imazapic, Imazapyr, Imazethapyr, Imazaquin, Metosulam, Mesosulfuron(-methyl), (S-)Metolachlor, Metsulfuron-methyl, Metamitron, Nicosulfuron, Oxyfluorfen, Pendimethalin, Phenmedipham, Picloram, Pinoxaden, Primisulfuron-methyl, Prosulfuron, Propanil, Propoxycarbazone, Pyrazosulfuron(-methyl), Rimsulfuron, Sulfentrazone, Sulfosulfuron, Sulfometuron, Terbuthylazin, Thifensulfuron, Triasulfuron, Tribenuron, Triclopyr, Triflusulfuron- methyl, Trifluralin, Tritosulfuron, Topramezone, Oxazinon, Oxadiargyl, Metribuzin, und deren Salze, z.B. die Natriumsalze. d) Verbindungen, die als Safener wirksam sind, wie AD 67 (4-(dichloroacetyl)-1- oxa-4-azaspiro[4.5]decane), Benoxacor, CL 304,415 (4-carboxymethylchroman-4- carboxylic acid), Cloquintocet, Cloquintocet-mexyl, Cyprosulfamide, Dichlormid, Dicyclonon, DKA-24 (N1 ,N2-diallyl-N2-dichloroacetylglycinamide), Fenchlorazole, Fenchlorazole-ethyl, Fenclorim, Flurazole, Fluxofenim, Furilazole, Isoxadifen-ethyl, Mefenpyr-diethyl, MG 191 (2-dichloromethyl-2-methyl-1 ,3-dioxolane), Naphthalsäureanhydrid (naphthalene-1 ,8-dicarboxylic anhydride), Oxabetrinil and Tl- 35 (1-dichloroacetylazepane).c) Compounds of various active ingredient groups, such as atrazine, acetochlor, aclonifen, alachlor, amidochlor, amidosulfuron, azimsulfuron, bentazone, bensulfuron (-methyl), bromoxynil (-octanoate / -heptanoate), butachlor, bispyribac, chlorosulfuron, chlorimuron, clomazone, clopyralid, Cinosulfuron, cyclosulfamuron, 2,4-D-ester, 2,4-DB-ester, 2,4-DP-ester, CMPP-ester, MCPA-ester, MCPB, EPTC, desmedipham, diflufenican, dicamba, ethoxysulfuron, ethofumesate, Flazasulfuron, florasulam, flucarbazone, flumetsulam, flufenacet, fluoroglycofen, fluroxypyr, flupyrsulfuron, foramsulfuron, flumioxazine, flumiclorac, fomesafen, glufosinate, glyphosate, imazapyr, imazosulfuron, lodosulfuron, lodosulfuron-methyl, loxynil (- octanoate), lactofen, halosulfuron, imazamox, Imazapic, imazapyr, imazethapyr, imazaquin, metosulam, mesosulfuron (-methyl), (S) -metolachlor, metsulfuron-methyl, metamitron, nicosulfuron, oxyfluorfen, pendimethalin, phenmedipham, picloram, pinoxaden, primisulfuron-methyl, prosulfuron, propanil, p ropoxycarbazone, pyrazosulfuron (-methyl), rimsulfuron, sulfentrazone, sulfosulfuron, sulfometuron, terbuthylazine, thifensulfuron, triasulfuron, tribenuron, triclopyr, triflusulfuron-methyl, trifluralin, tritosulfuron, toramezone, oxazinone, oxadiargyl, metribuzin, and their salts, for example the sodium salts. d) compounds which act as safeners, such as AD 67 (4- (dichloroacetyl) -1-oxa-4-azaspiro [4.5] decane), benoxacor, CL 304,415 (4-carboxymethylchroman-4-carboxylic acid), cloquintocet, Cloquintocet-mexyl, cyprosulfamides, dichloromide, dicyclonon, DKA-24 (N1, N2-diallyl-N2-dichloroacetylglycine amides), fenchlorazoles, fenchlorazoles-ethyl, fenclorim, flurazoles, fluxofenim, furilazoles, isoxadifen-ethyl, mefenpyr-diethyl, MW 191 ( 2-dichloromethyl-2-methyl-1,3-dioxolane), naphthalic anhydride (naphthalene-1,8-dicarboxylic anhydride), oxabetrinil and Tl-35 (1-dichloroacetylazepane).
In einer weiteren Ausführungsform können z.B. verschiedene Herbizide miteinander kombiniert werden, z.B. Fenoxaprop-p-ethyl + loxynil-octanoat, Diclofop-methyl + Bromoxynil-octanoat, CMPP + Bromoxynil-octanoat, MCPA + loxynil-octanoat, Bromoxynil-octanoat + Bromoxynil-heptanoat, Bromoxynil-octanoat + Bromoxynil- heptanoat + MCPA, Bromoxynil-octanoat + Bromoxynil-heptanoat+ 2,4-D, Phenmedipham + Desmedipham, Phenmedipham + Desmedipham + Ethofumesate, Metamitron + Ethofumesate, Phenmedipham + Ethofumesate + Metamitron, Fenoxaprop-p-ethyl + lodosulfuron-methyl-natrium, Fenoxaprop-p-ethyl + Diclofop- methyl, Fenoxaprop-p-ethyl + lodosulfuron-methyl-natrium + Diclofop-methyl.In another embodiment, e.g. different herbicides are combined, e.g. Fenoxaprop-p-ethyl + loxyniloctanoate, diclofopmethyl + bromoxyniloctanoate, CMPP + bromoxyniloctanoate, MCPA + loxyniloctanoate, bromoxyniloctanoate + bromoxynil heptanoate, bromoxyniloctanoate + bromoxynilheptanoate + MCPA, bromoxynil octanoate + bromoxynil-heptanoate + 2,4-D, phenmedipham + desmedipham, phenmedipham + desmedipham + ethofumesate, metamitron + ethofumesate, phenmedipham + ethofumesate + metamitron, fenoxaprop-p-ethyl + iodosulfuron-methyl-sodium, fenoxaprop-p-ethyl + diclofop - methyl, fenoxaprop-p-ethyl + iodosulfuron-methyl-sodium + diclofop-methyl.
Als besonders bevorzugt sind die Kombinationen aus: Foramsulfuron + lodosulfuron- methyl-sodium + Isoxadifen-ethyl, lodosulfuron-methyl-sodium + Isoxadifen-ethyl, Foramsulfuron + Isoxadifen-ethyl, Fenoxaprop-P-ethyl + Ethoxysulfuron + Isoxadifen-ethyl, Ethoxysulfuron + Isoxadifen-ethyl, Fenoxaprop-P-ethyl + Isoxadifen-ethyl, lodosulfuron-methyl-sodium + Mesosulfuron-methyl + Mefenpyr- diethyl, Mesosulfuron-methyl + Mefenpyr-diethyl, lodosulfuron-methyl-sodium + Mefenpyr-diethyl, Fenoxaprop-P-ethyl + Mefenpyr-diethyl, Fenoxaprop-P-ethyl + Diclofop-methyl + Mefenpyr-diethyl, Diclofop-methyl + Mefenpyr-diethyl, Diclofop- methyl + Sethoxydim + Mefenpyr-diethyl, Sethoxydim + Mefenpyr-diethyl, Fenoxaprop-P-ethyl + Isoproturon + Mefenpyr-diethyl, Isoproturon + Mefenpyr- diethyl, Clodinafop-propargyl + Cloquintocet-mexyl, Fenoxaprop-ethyl +The combinations of foramsulfuron + iodosulfuron-methyl-sodium + isoxadifen-ethyl, iodosulfuron-methyl-sodium + isoxadifen-ethyl, foramsulfuron + isoxadifen-ethyl, fenoxaprop-P-ethyl + ethoxysulfuron + isoxadifen-ethyl, ethoxysulfuron + are particularly preferred Isoxadifen-ethyl, fenoxaprop-P-ethyl + isoxadifen-ethyl, iodosulfuron-methyl-sodium + mesosulfuron-methyl + mefenpyr-diethyl, mesosulfuron-methyl + mefenpyr-diethyl, iodosulfuron-methyl-sodium + mefenpyr-diethyl, fenoxaprop-P ethyl + mefenpyr-diethyl, fenoxaprop-P-ethyl + diclofop-methyl + mefenpyr-diethyl, diclofop-methyl + mefenpyr-diethyl, diclofopmethyl + sethoxydim + mefenpyr-diethyl, sethoxydim + mefenpyr-diethyl, fenoxaprop-P-ethyl + Isoproturon + mefenpyr-diethyl, isoproturon + mefenpyr-diethyl, clodinafop-propargyl + cloquintocet-mexyl, fenoxaprop-ethyl +
Fenchlorazole-ethyl, Fenoxaprop-P-ethyl + Fenchlorazole-ethyl, Flucarbazone + Cyprosulfamide, Foramsulfuron + Cyprosulfamide, lodosulfuron(-methyl) + Cyprosulfamide, Metosulam + Cyprosulfamide, Metsulfuron(-methyl) + Cyprosulfamide, Nicosulfuron + Cyprosulfamide, Primisulfuron(.methyl) + Cyprosulfamide, Prosulfuron + Cyprosulfamide + Cyprosulfamide, Thifensulfuron + Cyprosulfamide, Tribenuron + Cyprosulfamide, Cloransulam-methyl + Cyprosulfamide, Chlorimuron + Cyprosulfamide, Ethoxysulfuron + Cyprosulfamide, Flazasulfuron + Cyprosulfamide, Florasulam + Cyprosulfamide, Flumetsulam + Cyprosulfamide, Halosulfuron + Cyprosulfamide, Imazamox + Cyprosulfamide, Imazapic + Cyprosulfamide, Imazapyr + Cyprosulfamide, Imazethapyr + Cyprosulfamide, Mesosulfuron + Cyprosulfamide, Propoxycarbazone + Cyprosulfamide, Sulfosulfuron + Cyprosulfamide, Amidosulfuron + Cyprosulfamide, Chlorsulfuron + Cyprosulfamide, Imazaquin + Cyprosulfamide, Triasulfuron + Cyprosulfamide, Sulfometuron + Cyprosulfamide, Cyclosulfamuron +Fenchlorazole-ethyl, fenoxaprop-P-ethyl + fenchlorazole-ethyl, flucarbazone + cyprosulfamide, foramsulfuron + cyprosulfamide, iodosulfuron (-methyl) + cyprosulfamide, metosulam + cyprosulfamide, metsulfuron (-methyl) + cyprosulfamide, nicosulfuron + cyprosulfamide, primisulfuron (.methyl ) + Cyprosulfamide, prosulfuron + cyprosulfamide + cyprosulfamide, thifensulfuron + cyprosulfamide, tribenuron + cyprosulfamide, cloransulam-methyl + cyprosulfamide, chlorimuron + cyprosulfamide, ethoxysulfuron + cyprosulfamide, flazasulfuron + cyprosulfamide, florasulam + cyprosulfamide, flumetsulam + cyprosulfamide, halosulfuron + cyprosulfamide, imazamox + cyprosulfamide, Imazapic + Cyprosulfamide, Imazapyr + Cyprosulfamide, Imazethapyr + Cyprosulfamide, Mesosulfuron + Cyprosulfamide, Propoxycarbazone + Cyprosulfamide, Sulfosulfuron + Cyprosulfamide, Amidosulfuron + Cyprosulfamide, Chlorsulfuron + Cyprosulfamide, Imazaquin + Cyprosulfamide, Triasulfuron + Cyprosulfamide, Sulfometuron + Cyprosulfamide, Cyclosulfamuron +
Cyprosulfamide, Flupyrsulfuron + Cyprosulfamide, Pyrazosulfuron + Cyprosulfamide, Azimsulfuron + Cyprosulfamide, Bensulfuron + Cyprosulfamide, Bispyribac + Cyprosulfamide, Rimsulfuron + Cyprosulfamide, Tritosulfuron + Cyprosulfamide, Sulcotrione + Cyprosulfamide, Clomazone + Cyprosulfamide, Mesotrione + Cyprosulfamide, Topramezone + Cyprosulfamide, Metribuzin + Cyprosulfamide, Bentazon + Cyprosulfamide, Bromoxynil + Cyprosulfamide, Propanil + Cyprosulfamide, Atrazin + Cyprosulfamide, Terbuthylazin + Cyprosulfamide, EPTC + Cyprosulfamide, Tepraloxydim + Cyprosulfamide, Clethodim + Cyprosulfamide, Alloyxdim + Cyprosulfamide, Sethoxydim + Cyprosulfamide, Tralkoxydim + Cyprosulfamide, Clodinafop-propargyl + Cyprosulfamide, Cyhalofop-butyl + Cyprosulfamide, Diclofop-methyl + Cyprosulfamide, Fenoxaprop-P-ethyl + Cyprosulfamide, Fluazifop-P-butyl + Cyprosulfamide, Haloxyfop-methyl + Cyprosulfamide, Haloxyfop-etotyl + Cyprosulfamide, Haloxyfop-R-methyl + Cyprosulfamide, Haloxyfop-ethoxyethyl + Cyprosulfamide, Propaquizafop + Cyprosulfamide, Quizalofop-P-tefuryl + Cyprosulfamide, Quizalofop-P-ethyl +Cyprosulfamide, flupyrsulfuron + cyprosulfamide, pyrazosulfuron + cyprosulfamide, azimsulfuron + cyprosulfamide, bensulfuron + cyprosulfamide, bispyribac + cyprosulfamide, rimsulfuron + cyprosulfamide, tritosulfuron + cyprosulfamide, sulcotrione + cyprosulfamide, clomazone + cyprosulfamide, mesotrione + cyprosulfamide, topramezone + cyprosulfamide, metribuzin + cyprosulfamide, Bentazone + Cyprosulfamide, Bromoxynil + Cyprosulfamide, Propanil + Cyprosulfamide, Atrazine + Cyprosulfamide, Terbuthylazine + Cyprosulfamide, EPTC + Cyprosulfamide, Tepraloxydim + Cyprosulfamide, Clethodim + Cyprosulfamide, Alloyxdim + Cyprosulfamide, Sethoxydim + Cyprosulfamide, Tralkoxydim + Cyprosulfamide, Clodinafop-propargyl + Cyprosulfamide, Cyhalofop-butyl + Cyprosulfamide, Diclofop-methyl + Cyprosulfamide, Fenoxaprop-P-ethyl + Cyprosulfamide, Fluazifop-P-butyl + Cyprosulfamide, Haloxyfop-methyl + Cyprosulfamide, Haloxyfop-etotyl + Cyprosulfamide, Haloxyfop-R-methyl + Cyprosulfamide, Haloxyfop- ethoxyethyl + Cyprosulfamide, Propaquizafop + Cyprosulfamide, Quizalofop-P-tefuryl + Cyprosulfamide, Quizalofop-P-ethyl +
Cyprosulfamide, Acetochlor + Cyprosulfamide, S-Metolachlor + Cyprosulfamide, Flumioxazin + Cyprosulfamide, Flumiclorac + Cyprosulfamide, Fomesafen + Cyprosulfamide, Sulfentrazone + Cyprosulfamide, Dicamba + Cyprosulfamide, MCPA + Cyprosulfamide, MCPB + Cyprosulfamide, 2,4-D + Cyprosulfamide, Clopyralid + Cyprosulfamide, Fluroxypyr + Cyprosulfamide, Picloram +Cyprosulfamides, acetochlor + cyprosulfamides, S-metolachlor + cyprosulfamides, flumioxazine + cyprosulfamides, flumiclorac + cyprosulfamides, fomesafen + cyprosulfamides, sulfentrazone + cyprosulfamides, dicamba + cyprosulfamides, MCPA + cyprosulfamides, MCPB + cyprosulfamides, 2,4-D + cyprosulfamides, clopyralid + Cyprosulfamide, Fluroxypyr + Cyprosulfamide, Picloram +
Cyprosulfamide, Triclopyr + Cyprosulfamide, Glufosinate + Cyprosulfamide, Glyphosate + Cyprosulfamide und Pendimethalin + Cyprosulfamide. Das Gewichtsverhältnis Safener : Herbizid kann innerhalb weiter Grenzen variieren und liegt vorzugsweise im Bereich von 1 : 100 bis 100 : 1 , insbesondere von 1 : 100 bis 50 : 1 , ganz besonders bevorzugt 1 : 10 bis 10 : 1. Die jeweils optimalen Mengen an Herbizid(en) und Safener(n) sind üblicherweise vom Typ des Herbizids und/oder vom verwendeten Safener sowie von der Art des zu behandelnden Pflanzenbestandes abhängig.Cyprosulfamide, triclopyr + cyprosulfamide, glufosinate + cyprosulfamide, glyphosate + cyprosulfamide and pendimethalin + cyprosulfamide. The weight ratio safener: herbicide can vary within wide limits and is preferably in the range from 1: 100 to 100: 1, in particular from 1: 100 to 50: 1, very particularly preferably from 1:10 to 10: 1 Herbicide (s) and safener (s) are usually dependent on the type of herbicide and / or the safener used and on the nature of the plant stock to be treated.
Fungizidefungicides
Die agrochemischen Wirkstoffe können auch Fungizide sein, beispielsweiseThe agrochemically active compounds may also be fungicides, for example
Inhibitoren der Nucleinsäure Synthese, insbesondereInhibitors of nucleic acid synthesis, in particular
Benalaxyl, Benalaxyl-M, Bupirimat, Chiralaxyl, Clozylacon, Dimethirimol, Ethirimol, Furalaxyl, Hymexazol, Metalaxyl, Metalaxyl-M, Ofurace, Oxadixyl, OxolinsäureBenalaxyl, benalaxyl-M, bupirimate, chiralaxyl, clozylacon, dimethirimol, ethirimol, furalaxyl, hymexazole, metalaxyl, metalaxyl-M, ofurace, oxadixyl, oxolinic acid
Inhibitoren der Mitose und Zellteilung, insbesondereInhibitors of mitosis and cell division, in particular
Benomyl, Carbendazim, Diethofencarb, Fuberidazole, Pencycuron, Thiabendazol, Thiophanat-methyl, ZoxamidBenomyl, Carbendazim, Diethofencarb, Fuberidazole, Pencycuron, Thiabendazole, Thiophanate-methyl, Zoxamide
Inhibitoren der Atmungskette Komplex I, insbesondere DiflumetorimInhibitors of the respiratory chain complex I, in particular diflumetorim
Inhibitoren der Atmungskette Komplex II, insbesondere Boscalid, Carboxin, Fenfuram, Flutolanil, Furametpyr, Mepronil, Oxycarboxin,Respiratory chain complex II, particularly boscalid, carboxin, fenfuram, flutolanil, furametpyr, mepronil, oxycarboxin,
Penthiopyrad, ThifluzamidPenthiopyrad, thifluzamide
Inhibitoren der Atmungskette Komplex III, insbesondereInhibitors of the respiratory chain complex III, in particular
Azoxystrobin, Cyazofamid, Dimoxystrobin, Enestrobin, Famoxadon, Fenamidon, Fluoxastrobin, Kresoximmethyl, Metominostrobin, Orysastrobin, Pyraclostrobin,Azoxystrobin, Cyazofamide, Dimoxystrobin, Enestrobin, Famoxadone, Fenamidon, Fluoxastrobin, Kresoximethyl, Metominostrobin, Orysastrobin, Pyraclostrobin,
Picoxystrobin, TrifloxystrobinPicoxystrobin, trifloxystrobin
Entkoppler, insbesondere Dinocap, Fluazinam Inhibitoren der ATP Produktion, insbesondereDecoupler, especially dinocap, fluazinam Inhibitors of ATP production, in particular
Fentinacetat, Fentinchlorid, Fentinhydroxid, SilthiofamFentin acetate, fentin chloride, fentin hydroxide, silthiofam
Inhibitoren der Aminosäure- und Proteinbiosynthese, insbesondereInhibitors of amino acid and protein biosynthesis, in particular
Andoprim, Blasticidin-S, Cyprodinil, Kasugamycin, Kasugamycinhydrochlorid Hydrat, Mepanipyrim, PyrimethanilAndoprim, blasticidin-S, cyprodinil, kasugamycin, kasugamycin hydrochloride hydrate, mepanipyrim, pyrimethanil
Inhibitoren der Signal-Transduktion, insbesondere Fenpiclonil, Fludioxonil, QuinoxyfenInhibitors of signal transduction, in particular fenpiclonil, fludioxonil, quinoxyfen
Inhibitoren der Fett- und Membran Synthese, insbesondere Chlozolinat, Iprodion, Procymidon, VinclozolinInhibitors of fat and membrane synthesis, in particular chlozolinate, iprodione, procymidone, vinclozolin
Ampropylfos, Kalium-Ampropylfos, Edifenphos, Iprobenfos (IBP), Isoprothiolan, PyrazophosAmpropylfos, Potassium Ampropylfos, Edifenphos, Iprobenfos (IBP), Isoprothiolane, Pyrazophos
Tolclofos-methyl, Biphenyl lodocarb, Propamocarb, Propamocarb hydrochloridTolclofos-methyl, biphenyl, iodocarb, propamocarb, propamocarb hydrochloride
Inhibitoren der Ergosterol Biosynthese, insbesondere Fenhexamid,Inhibitors of ergosterol biosynthesis, in particular fenhexamide,
Azaconazol, Bitertanol, Bromuconazol, Cyproconazol, Diclobutrazol, Difenoconazol, Diniconazol, Diniconazol-M, Epoxiconazol, Etaconazol, Fenbuconazol, Fluquinconazol, Flusilazol, Flutriafol, Furconazol, Furconazol-cis, Hexaconazol, Imibenconazol, Ipconazol, Metconazol, Myclobutanil, Paclobutrazol, Penconazol, Propiconazol, Prothioconazol, Simeconazol,Azaconazole, bitertanol, bromuconazole, cyproconazole, diclobutrazole, difenoconazole, diniconazole, diniconazole-M, epoxiconazole, etaconazole, fenbuconazole, fluquinconazole, flusilazole, flutriafol, furconazole, furconazole-cis, hexaconazole, imibenconazole, ipconazole, metconazole, myclobutanil, paclobutrazole, penconazole, Propiconazole, prothioconazole, simeconazole,
Tebuconazol, Tetraconazol, Triadimefon, Triadimenol, Triticonazol, Uniconazol, Voriconazol, Imazalil, Imazalilsulfat, Oxpoconazol, Fenarimol, Flurprimidol, Nuarimol, Pyrifenox, Triforin, Pefurazoat, Prochloraz, Triflumizol, Viniconazol, Aldimoφh, Dodemoφh, Dodemorphacetat, Fenpropimoφh, Tridemoφh, Fenpropidin, Spiroxamin,Tebuconazole, tetraconazole, triadimefon, triadiconol, uniconazole, voriconazole, imazalil, imazalil sulphate, oxpoconazole, fenarimol, flurprimidol, nuarimol, pyrifenox, triforin, pefurazoate, prochloraz, triflumizole, viniconazole, aldimoφh, dodemoφh, dodemorph acetate, fenpropimoφh, tridemoφh, fenpropidin, spiroxamine,
Naftifin, Pyributicarb, Terbinafin Inhibitoren der Zellwand Synthese, insbesondereNaftifine, pyributicarb, terbinafine Inhibitors of cell wall synthesis, in particular
Benthiavalicarb, Bialaphos, Dimethomorph, Flumorph, Iprovalicarb, Polyoxins, Polyoxorim, Validamycin ABenthiavalicarb, bialaphos, dimethomorph, flumorph, iprovalicarb, polyoxins, polyoxorim, validamycin A
Inhibitoren der Melanin Biosynthese, insbesondereInhibitors of melanin biosynthesis, in particular
Capropamid, Diclocymet, Fenoxanil, Phtalid, Pyroquilon, TricyclazolCapropamide, diclocymet, fenoxanil, phtalid, pyroquilone, tricyclazole
Resistenzinduktoren, insbesondereResistance Inductors, in particular
Acibenzolar-S-methyl, Probenazol, TiadinilAcibenzolar-S-methyl, probenazole, tiadinil
Multisite, insbesondereMultisite, in particular
Captafol, Captan, Chlorothalonil, Kupfersalze wie: Kupferhydroxid, Kupfernaphthenat, Kupferoxychlorid, Kupfersulfat, Kupferoxid, Oxin-Kupfer und Bordeaux Mischung, Dichlofluanid, Dithianon, Dodin, Dodin freie Base, Ferbam, Folpet, Fluorofolpet, Guazatin, Guazatinacetat, Iminoctadin,Captafol, captan, chlorothalonil, copper salts such as: copper hydroxide, copper naphthenate, copper oxychloride, copper sulfate, copper oxide, oxine-copper and bordeaux mixture, dichlofluanid, dithianon, dodin, dodine free base, ferbam, folpet, fluorofolpet, guazatine, guazatine acetate, iminoctadine,
Iminoctadinalbesilat, Iminoctadintriacetat, Mankupfer, Mancozeb, Maneb, Metiram, Metiram Zink, Propineb, Schwefel und Schwefelpräparate enthaltend Calciumpolysulphid, Thiram, Tolylfluanid, Zineb, ZiramIminoctadinalesilate, iminoctadine triacetate, mancopper, mancozeb, maneb, metiram, metiram zinc, propineb, sulfur and sulfur preparations containing calcium polysulphide, thiram, tolylfluanid, zineb, ziram
Fungizide mit unbekannten Mechanismus, insbesondereFungicides with unknown mechanism, in particular
Amibromdol, Benthiazol, Bethoxazin, Capsimycin, Carvon, Chinomethionat, Chloropicrin, Cufraneb, Cyflufenamid, Cymoxanil, Dazomet, Debacarb, Diclomezine, Dichlorophen, Dicloran, Difenzoquat, Difenzoquat Methylsulphat, Diphenylamin, Ethaboxam, Ferimzon, flumetover, Flusulfamid, Fluopicolid, Fluoroimid, Hexachlorobenzol, 8-Hydroxychinolinsulfat, Irumamycin,Amibromdole, benthiazole, bethoxazine, capsimycin, carvone, quinomethionate, chloropicrin, cufraneb, cyflufenamid, cymoxanil, dazomet, debacarb, diclomezine, dichlorophen, dicloran, difenzoquat, difenzoquat methylsulphate, diphenylamine, ethaboxam, ferimzone, flumetover, flusulfamide, fluopicolide, fluoroimide, hexachlorobenzene , 8-hydroxyquinoline sulfate, irumamycin,
Methasulphocarb, Metrafenon, Methyl Isothiocyanat, Mildiomycin, Natamycin, Nickel dimethyldithiocarbamat, Nitrothal-isopropyl, Octhilinon, Oxamocarb, Oxyfenthiin, Pentachlorophenol und Salze, 2-Phenylphenol und Salze, Piperalin, Propanosin -Natrium, Proquinazid, Pyrrolnitrin, Quintozen, Tecloftalam, Tecnazen, Triazoxid, Trichlamid, Zarilamid und 2,3,5,6-Tetrachlor-4-Methasulphocarb, metrafenone, methyl isothiocyanate, mildiomycin, natamycin, nickel dimethyldithiocarbamate, nitrothal isopropyl, octhilinone, oxamocarb, oxyfenthiine, pentachlorophenol and salts, 2-phenylphenol and salts, piperaline, propanosine sodium, proquinazide, pyrrolnitrin, quintozene, tecloftalam, tecnazene, Triazoxide, trichlamide, zarilamide and 2,3,5,6-tetrachloro-4-
(methylsulfonyl)-pyridin, N-(4-Chlor-2-nitrophenyl)-N-ethyl-4-methyl- benzenesulfonamid, 2-Amino-4-methyl-N-phenyl-5-thiazolecarboxamid, 2-Chlor- N-(2,3-dihydro-1 ,1 ,3-trimethyl-1 H-inden-4-yl)-3-pyridincarboxamid, 3-[5-(4- Chlorphenyl)-2,3-dimethylisoxazolidin-3-yl]pyridin, cis-1 -(4-Chbφhenyl)-2-(1 H- 1 ,2,4-triazol-1 -ylj-cycloheptanol, 2,4-Dihydro-5-rnethoxy-2-methyl-4-[[[[1 -[3- (trifluoromethyl)-pheny1]-ethyliden]-amino]HDxy]-rnethyl]-phenyl]-3H-1 ,2,3-triazol- 3-on (185336-79-2), Methyl 1-(2,3-dihydro-2,2-dimethyl-1 H-inden-1-yl)-1H- imidazole-5-carboxylat, S^.δ-Trichlor^.e-pyridindicarbonitril, Methyl 2- [[[cyclopropylK^methoxyphenyO iminolmethyllthiolmethyll-.alpha.-(methylsulfonyl) pyridine, N- (4-chloro-2-nitrophenyl) -N-ethyl-4-methylbenzenesulfonamide, 2-amino-4-methyl-N-phenyl-5-thiazolecarboxamide, 2-chloro-N- (2,3-dihydro-1,1,3-trimethyl-1H-inden-4-yl) -3-pyridinecarboxamide, 3- [5- (4-chlorophenyl) -2,3-dimethylisoxazolidin-3-yl] pyridine, cis-1 - (4-chlorophenyl) -2- (1H- 1, 2,4-triazole-1-yl-cycloheptanol, 2,4-dihydro-5-rethoxy-2-methyl-4 - [[[[1 - [3- (trifluoromethyl) -phenyl] -ethyliden] -amino ] HDxy] -rnethyl] -phenyl] -3H-1,2,3-triazol-3-one (185336-79-2), methyl 1- (2,3-dihydro-2,2-dimethyl-1H) inden-1-yl) -1H-imidazole-5-carboxylate, S ^, δ-trichloro-1-pyridinedicarbonitrile, methyl 2- [[[cyclopropylK ^ methoxyphenyO iminolmethylthiolmethyll -alpha.
(methoxymethylen)- benzacetat, 4-Chlor-alpha-propinyloxy-N-[2-[3-methoxy-4- (2-propinyloxy)phenyl]ethyl]-benzacetamide, (2S)-N-[2-[4-[[3-(4-chlorophenyl)-2- propinyl]oxy]-3-methoxyphenyl]ethyl]- 3-methyl-2-[(methylsulfonyl)amino]- butanamid, 5-Chlor-7-(4-methylpiperidin-1-yl)-6-(2,4,6- trifluorophenyl)[1 ,2,4]triazolo[1 ,5-a]pyrimidin, 5-Chlor-6-(2,4,6-trifluorophenyl)-N-(methoxymethylene) - benzoacetate, 4-chloro-alpha-propynyloxy-N- [2- [3-methoxy-4- (2-propynyloxy) phenyl] ethyl] -benzacetamide, (2S) -N- [2- [4- [[3- (4-chlorophenyl) -2-propynyl] oxy] -3-methoxyphenyl] ethyl] -3-methyl-2 - [(methylsulfonyl) amino] butanamide, 5-chloro-7- (4-methylpiperidine) 1-yl) -6- (2,4,6-trifluorophenyl) [1,2,4] triazolo [1,5-a] pyrimidine, 5-chloro-6- (2,4,6-trifluorophenyl) -N -
[(1 R)-1 ,2,2-trimethylpropyl][1 ,2,4]triazolo[1 ,5-a]pyrimidin-7-amin, 5-Chlor-N- [(1 R)-1 ,2-dimethylpropyl]-6-(2,4,6-trifluorophenyl) [1 ,2,4]triazolo[1 ,5-a]pyrimidin- 7-amine, N-[1 -(δ-Brom-S-chloropyridin^-yOethyll^^-dichloronicotinamid, N-(5- Brom-3-chloφyridin-2-yl)methyl-2,4-dichlornicx)tinamid, 2-Butoxy-6-iod-3- propyl-benzopyranon-4-on, N-{(Z)-[(cyclopropylmethoxy) imino][6-[(1R) -1,2,2-trimethylpropyl] [1,2,4] triazolo [1,5-a] pyrimidin-7-amine, 5-chloro-N- [(1R) -1, 2 -dimethylpropyl] -6- (2,4,6-trifluorophenyl) [1,2,4] triazolo [1,5-a] pyrimidine-7-amine, N- [1- (δ-bromo-S-chloropyridine) -yOethyll ^^ - dichloronicotinamide, N- (5-bromo-3-chloropyridin-2-yl) methyl-2,4-dichloronoxy) tin amide, 2-butoxy-6-iodo-3-propyl-benzopyranon-4-one, N - {(Z) - [(cyclopropylmethoxy) imino] [6-
(difluomnethoxy)-2,3-difluoφhenyl]methyl}-2-benzacetamid, N-(3-Ethyl-3,5,5- trimethyl-cyclohexyl)-3-formylamino-2-hydroxy-benzamid, 2-[[[[1 -[3(1 Fluor-2- phenylethyl)oxy] phenyl] ethyliden]amino]oxy]methyl]-alpha-(methoxyimino)-N- methyl-alphaE-benzacetamid, N-{2-[3-Chlor-5-(trifluormethyl)pyridin-2-yl]ethyl}- 2-(trifluoromethyl)benzamid, N^S'.^-dichlor-δ-fluorbiphenyl^-yl^S-(difluoromethoxy) -2,3-difluorophenyl] methyl} -2-benzacetamide, N- (3-ethyl-3,5,5-trimethylcyclohexyl) -3-formylamino-2-hydroxybenzamide, 2 - [[[ [1- [3 (1-fluoro-2-phenylethyl) oxy] phenyl] ethylidene] amino] oxy] methyl] -alpha (methoxyimino) -N-methyl-alpha-E-benzoacetamide, N- {2- [3-chloro 5- (trifluoromethyl) pyridin-2-yl] ethyl} -2- (trifluoromethyl) benzamide, N, 5'S, 3'-dichloro-6-fluoro-biphenyl-1-yl ^ S-
(difluormethyl)-1 -methyl-1 H-pyrazol-4-carboxamid, N-(6-Methoxy-3-pyridinyl)- cyclopropan carboxamid, 1-[(4-Methoxyphenoxy)methyl]-2,2-dimethylpropyl-1 H- imidazol-1 - carbonsäure, O-[1 -[(4-Methoxyphenoxy)methyl]-2,2-dimethylpropyl]- 1H-imidazol- 1- carbothioic acid, 2-(2-{[6-(3-Chlor-2-methylphenoxy)-5- fluoφyrimidin-4-yl]oxy}phenyl)-2-(methoxyimino)-N-methylacetamid(difluoromethyl) -1-methyl-1H-pyrazole-4-carboxamide, N- (6-methoxy-3-pyridinyl) -cyclopropane carboxamide, 1 - [(4-methoxyphenoxy) methyl] -2,2-dimethylpropyl-1 H-imidazole-1-carboxylic acid, O- [1 - [(4-methoxyphenoxy) methyl] -2,2-dimethylpropyl] -1H-imidazole-1-carbothioic acid, 2- (2 - {[6- (3 Chloro-2-methylphenoxy) -5-fluoropyrimidin-4-yl] oxy} phenyl) -2- (methoxyimino) -N-methylacetamide
Die agrochemischen Wirkstoffe können auch Bakterizide sein, beispielsweise Bronopol, Dichlorophen, Nitrapyrin, Nickel-Dimethyldithiocarbamat, Kasugamycin, Octhilinon, Furancarbonsäure, Oxytetracyclin, Probenazol, Streptomycin, Tecloftalam, Kupfersulfat und andere Kupfer-Zubereitungen.The agrochemically active compounds may also be bactericides, for example bronopol, dichlorophen, nitrapyrin, nickel dimethyldithiocarbamate, kasugamycin, octhilinone, furancarboxylic acid, oxytetracycline, probenazole, streptomycin, tecloftalam, copper sulphate and other copper preparations.
Die vorstehend aufgeführten Fungizide (Bakterizide) sind z.B. bekannt aus „The Pesticide Manual", 12. Auflage (2000) und 13. Auflage (2003), The British Crop Protection Council oder den nach den einzelnen Wirkstoffen aufgeführten Literaturstellen.The fungicides listed above are known, for example, from "The Pesticide Manual", 12th edition (2000) and 13th edition (2003), The British Crop Protection Council or the references listed for the individual active ingredients.
Insektizideinsecticides
Die agrochemischen Wirkstoffe können auch Insektizide / Akarizide und/oder Nematizide sein, beispielsweiseThe agrochemically active compounds may also be insecticides / acaricides and / or nematicides, for example
Acetylcholinesterase (AChE) Inhibitoren Carbamate, zum Beispiel Alanycarb, Aldicarb, Aldoxycarb, Allyxycarb, Aminocarb, Bendiocarb, Benfuracarb, Bufencarb, Butacarb, Butocarboxim, Butoxycarboxim, Carbaryl, Carbofuran, Carbosulfan, Cloethocarb, Dimetilan, Ethiofencarb, Fenobucarb, Fenothiocarb, Formetanate, Furathiocarb, Isoprocarb, Metam-sodium, Methiocarb, Methomyl, Metolcarb, Oxamyl,Acetylcholinesterase (AChE) inhibitors carbamates, for example alanycarb, aldicarb, aldoxycarb, allyxycarb, aminocarb, bendocarb, benfuracarb, bufencarb, butacarb, butocarboxim, butoxycarboxim, carbaryl, carbofuran, carbosulfan, cloethocarb, dimetilane, ethiofencarb, fenobucarb, fenothiocarb, formetanate, furathiocarb , Isoprocarb, metam-sodium, methiocarb, methomyl, metolcarb, oxamyl,
Pirimicarb, Promecarb, Propoxur, Thiodicarb, Thiofanox, Trimethacarb, XMC,Pirimicarb, promecarb, propoxur, thiodicarb, thiofanox, trimethacarb, XMC,
Xylylcarb, TriazamateXylylcarb, triazamates
Organophosphate, zum Beispiel Acephate, Azamethiphos, Azinphos (-methyl, -ethyl), Bromophos-ethyl, Bromfenvinfos (-methyl), Butathiofos, Cadusafos,Organophosphates, for example acephates, azamethiphos, azinphos (-methyl, -ethyl), bromophos-ethyl, bromfenvinfos (-methyl), butathiofos, cadusafos,
Carbophenothion, Chlorethoxyfos, Chlorfenvinphos, Chlormephos, ChlorpyrifosCarbophenothion, Chlorethoxyfos, Chlorfenvinphos, Chlormephos, Chlorpyrifos
(-methyl/-ethyl), Coumaphos, Cyanofenphos, Cyanophos, Chlorfenvinphos, Demeton-S-methyl, Demeton-S-methylsulphon, Dialifos, Diazinon, Dichlofenthion, Dichlorvos/DDVP, Dicrotophos, Dimethoate, Dimethylvinphos,(-methyl / -ethyl), coumophos, cyanofenphos, cyanophos, chlorfenvinphos, demeton-S-methyl, demeton-S-methylsulphone, dialifos, diazinon, dichlofenthione, dichlorvos / DDVP, dicrotophos, dimethoates, dimethylvinphos,
Dioxabenzofos, Disulfoton, EPN, Ethion, Ethoprophos, Etrimfos, Famphur, Fenamiphos, Fenitrothion, Fensulfothion, Fenthion, Flupyrazofos, Fonofos, Formothion, Fosmethilan, Fosthiazate, Heptenophos, lodofenphos, Iprobenfos, Isazofos, Isofenphos, Isopropyl O-salicylate, Isoxathion, Malathion, Mecarbam, Methacrifos, Methamidophos, Methidathion,Dioxabenzofos, Disulfoton, EPN, Ethion, Ethoprophos, Etrimfos, Famphur, Fenamiphos, Fenitrothion, Fensulfothion, Fenthion, Flupyrazofos, Fonofos, Formothion, Fosmethilane, Fosthiazate, Heptenophos, iodofenphos, Iprobenfos, Isazofos, Isofenphos, Isopropyl O-salicylate, Isoxathione, Malathion , Mecarbam, methacrifos, methamidophos, methidathion,
Mevinphos, Monocrotophos, Naled, Omethoate, Oxydemeton-methyl, Parathion (-methyl/Mevinphos, Monocrotophos, Naled, Omethoate, Oxydemeton-methyl, Parathion (-methyl)
-ethyl), Phenthoate, Phorate, Phosalone, Phosmet, Phosphamidon, Phosphocarb, Phoxim, Pirimiphos (-methyl/-ethyl), Profenofos, Propaphos, Propetamphos, Prothiofos, Prothoate, Pyraclofos, Pyridaphenthion, Pyridathion, Quinalphos, Sebufos, Sulfotep, Sulprofos, Tebupirimfos, Temephos, Terbufos, Tetrachlorvinphos, Thiometon, Triazophos, Triclorfon, Vamidothion-ethyl), phenthoates, phorates, phosalones, phosmet, phosphamidone, phosphocarb, phoxim, pirimiphos (-methyl / -ethyl), profenofos, propaphos, Propetamphos, Prothiofos, Prothoate, Pyraclofos, Pyridaphenthion, Pyridathion, Quinalphos, Sebufos, Sulfotep, Sulprofos, Tebupirimfos, Temephos, Terbufos, Tetrachlorvinphos, Thiometon, Triazophos, Triclorfon, Vamidothion
Natrium-Kanal-Modulatoren / Spannungsabhängige Natrium-Kanal-Blocker Pyrethroide, zum Beispiel Acrinathrin, Allethrin (d-cis-trans, d-trans), Beta-Cyfluthrin, Bifenthrin, Bioallethrin, Bioallethrin-S-cyclopentyl-isomer, Bioethanomethrin, Biopermethrin, Bioresmethrin, Chlovaporthrin, Cis-Cypermethrin, Cis-Sodium Channel Modulators / Voltage Dependent Sodium Channel Blockers Pyrethroids, for example, acrinathrin, allethrin (d-cis-trans, d-trans), beta-cyfluthrin, bifenthrin, bioallethrin, bioallethrin-S-cyclopentyl isomer, bioethanomethrin, biopermethrin , Bioresmethrin, chlovaporthrin, cis-cypermethrin, cis
Resmethrin, Cis-Permethrin, Clocythrin, Cycloprothrin, Cyfluthrin, Cyhalothrin, Cypermethrin (alpha-, beta-, theta-, zeta-), Cyphenothrin, Deltamethrin, Empenthrin (1 R-isomer), Esfenvalerate, Etofenprox, Fenfluthrin, Fenpropathrin, Fenpyrithrin, Fenvalerate, Flubrocythrinate, Flucythrinate, Flufenprox, Flumethrin, Fluvalinate, Fubfenprox, Gamma-Cyhalothrin,Resmethrin, cis-permethrin, clocthrin, cycloprothrin, cyfluthrin, cyhalothrin, cypermethrin (alpha-, beta-, theta-, zeta-), cyphenothrin, deltamethrin, empenthrin (1R-isomer), esfenvalerate, etofenprox, fenfluthrin, fenpropathrin, fenpyrithrin , Fenvalerate, flubrocythrinates, flucythrinates, flufenprox, flumethrin, fluvalinates, fubfenprox, gamma-cyhalothrin,
Imiprothrin, Kadethrin, Lambda- Cyhalothrin, Metofluthrin, Permethrin (eis-, trans-), Phenothrin (1 R-trans isomer), Prallethrin, Profluthrin, Protrifenbute, Pyresmethrin, Resmethrin, RU 15525, Silafluofen, Tau-Fluvalinate, Tefluthrin, Terallethrin, Tetramethrin (-1 R- isomer), Tralomethrin, Transfluthrin, ZXI 8901 , Pyrethrins (pyrethrum)Imiprothrin, kadethrin, lambda-cyhalothrin, metofluthrin, permethrin (cis-, trans-), phenothrin (1R-trans isomer), prallethrin, profuthrin, protrifenbute, pyresmethrin, resmethrin, RU 15525, silafluofen, tau-fluvalinate, tefluthrin, terallethrin , Tetramethrin (-1 R isomer), tralomethrin, transfluthrin, ZXI 8901, pyrethrins (pyrethrum)
DDTDDT
Oxadiazine, zum Beispiel Indoxacarb Semicarbazon, zum Beispiel Metaflumizon (BAS3201 )Oxadiazines, for example Indoxacarb Semicarbazone, for example Metaflumizone (BAS3201)
Acetylcholin-Rezeptor-Agonisten/-Antagonisten Chloronicotinyle, zum Beispiel Acetamiprid, Clothianidin, Dinotefuran, Imidacloprid, Niten- pyram, Nithiazine, Thiacloprid, ThiamethoxamAcetylcholine Receptor Agonists / Antagonists Chloronicotinyls, for example acetamiprid, clothianidin, dinotefuran, imidacloprid, nitenpyram, nithiazines, thiacloprid, thiamethoxam
Nicotine, Bensultap, Cartap Acetylcholin-Rezeptor-Modulatoren Spinosyne, zum Beispiel SpinosadNicotine, Bensultap, Cartap Acetylcholine receptor modulators Spinosyne, for example spinosad
GABA-gesteuerte Chlorid-Kanal-Antagonisten Organochlorine, zum Beispiel Camphechlor, Chlordane, Endosulfan, Gamma-HCH, HCH, Heptachlor, Lindane, Methoxychlor Fiprole, zum Beispiel Acetoprole, Ethiprole, Fipronil, Pyrafluprole, Pyriprole,GABA-Directed Chloride Channel Antagonists Organochlorines, for example Camphechlor, Chlordane, Endosulfan, Gamma-HCH, HCH, Heptachlor, Lindane, Methoxychlor Fiprole, for example Acetoprole, Ethiprole, Fipronil, Pyrafluprole, Pyriprole,
Vaniliprolevaniliprole
Chlorid-Kanal-AktivatorenChloride channel activators
Mectine, zum Beispiel Abamectin, Emamectin, Emamectin-benzoate, Ivermectin,Mectins, for example Abamectin, Emamectin, Emamectin benzoate, Ivermectin,
Lepimectin, MilbemycinLepimectin, milbemycin
Juvenilhormon-Mimetika, zum Beispiel Diofenolan, Epofenonane, Fenoxycarb, Hydroprene, Kinoprene, Methoprene, Pyriproxifen, TripreneJuvenile hormone mimetics, for example, diofenolan, epofenonans, fenoxycarb, hydroprene, kinoprenes, methoprenes, pyriproxifen, triprene
Ecdysonagonisten/disruptorenEcdysone agonists / disruptors
Diacylhydrazine, zum Beispiel Chromafenozide, Halofenozide, Methoxyfenozide, TebufenozideDiacylhydrazines, for example chromafenozide, Halofenozide, Methoxyfenozide, Tebufenozide
Inhibitoren der ChitinbiosyntheseInhibitors of chitin biosynthesis
Benzoylharnstoffe, zum Beispiel Bistrifluron, Chlofluazuron, Diflubenzuron, Fluazuron,Benzoylureas, for example bistrifluron, chlorofluazuron, diflubenzuron, fluazuron,
Flucycloxuron, Flufenoxuron, Hexaflumuron, Lufenuron, Novaluron, Noviflumuron, Penfluron, Teflubenzuron, TriflumuronFlucycloxuron, flufenoxuron, hexaflumuron, lufenuron, novaluron, noviflumuron, penfluron, teflubenzuron, triflumuron
Buprofezinbuprofezin
Cyromazine Inhibitoren der oxidativen Phosphorylierung, ATP-Disruptorencyromazine Inhibitors of oxidative phosphorylation, ATP disruptors
Diafenthiurondiafenthiuron
Organozinnverbindungen, zum Beispiel Azocyclotin, Cyhexatin, Fenbutatin-oxideOrganotin compounds, for example azocyclotin, cyhexatin, fenbutatin oxides
Entkoppler der oxidativen Phoshorylierung durch Unterbrechung des H-ProtongradientenDecoupling of oxidative phosphorylation by interruption of the H proton gradient
Pyrrole, zum Beispiel Chlorfenapyr Dinitrophenole, zum Beispiel Binapacyrl, Dinobuton, Dinocap, DNOCPyrroles, for example Chlorfenapyr dinitrophenols, for example binapacyrl, dinobutone, dinocap, DNOC
Site-I-ElektronentransportinhibitorenSite I electron transport inhibitors
METI1S, zum Beispiel Fenazaquin, Fenpyroximate, Pyrimidifen, Pyridaben,METI 1 S, for example fenazaquin, fenpyroximate, pyrimidifen, pyridaben,
Tebufenpyrad, Tolfenpyrad Hydramethylnon DicofolTebufenpyrad, Tolfenpyrad Hydramethylnon Dicofol
Site-Il-Elektronentransportinhibitoren RotenoneSite II electron transport inhibitors Rotenone
Site-Ill-ElektronentransportinhibitorenSite III electron transport inhibitors
Acequinocyl, FluacrypyrimAcequinocyl, Fluacrypyrim
Mikrowelle Disruptoren der InsektendarmmembranMicrowave disruptors of insect intestinal membrane
Bacillus thuringiensis-StämmeBacillus thuringiensis strains
Inhibitoren der Fettsynthese Tetronsäuren, zum Beispiel Spirodiclofen, SpiromesifenInhibitors of fatty synthesis tetronic acids, for example spirodiclofen, spiromesifen
Tetramsäuren, zum Beispiel Spirotetramat Carboxamide, zum Beispiel FlonicamidTetramic acids, for example spirotetramat Carboxamides, for example flonicamide
Oktopaminerge Agonisten, zum Beispiel AmitrazOctopaminergic agonists, for example, amitraz
Inhibitoren der Magnesium-stimulierten ATPase,Inhibitors of magnesium-stimulated ATPase,
Propargitepropargite
Nereistoxin-Analoge, zum Beispiel Thiocyclam hydrogen Oxalate, Thiosultap-sodiumNereistoxin analogs, for example thiocyclam hydrogen oxalate, thiosultap-sodium
Agonisten des Ryanodin-Rezeptors, Benzoesäuredicarboxamide, zum Beispiel FlubendiamidAgonists of the ryanodine receptor, benzoic acid dicarboxamides, for example flubendiamide
Anthranilamide, zum Beispiel DPX E2Y45 (3-bromo-N-{4-chloro-2-methyl-6- [(methylamino)carbonyl]phenyl}-1 -(3-chloropyridin-2-yl)-1 H-pyrazole-5- carboxamide)Anthranilamides, for example DPX E2Y45 (3-bromo-N- {4-chloro-2-methyl-6- [(methylamino) carbonyl] phenyl} -1- (3-chloropyridin-2-yl) -1H-pyrazole- 5-carboxamides)
Biologika, Hormone oder PheromoneBiologics, hormones or pheromones
Azadirachtin, Bacillus spec, Beauveria spec, Codlemone, Metarrhizium spec, Paecilomyces spec, Thuringiensin, Verticillium spec.Azadirachtin, bacillus spec, beauveria spec, codlemone, metarrhicon spec, paecilomyces spec, thuringiensin, verticillium spec.
Wirkstoffe mit unbekannten oder nicht spezifischen Wirkmechanismen Fraßhemmer, zum Beispiel Cryolite, Flonicamid, Pymetrozine Milbenwachstumsinhibitoren, zum Beispiel Clofentezine, Etoxazole, HexythiazoxActive ingredients with unknown or non-specific action mechanisms Feed inhibitors, for example cryolites, flonicamide, pymetrozine mite growth inhibitors, for example clofentezine, etoxazole, hexythiazox
Amidoflumet, Benclothiaz, Benzoximate, Bifenazate, Bromopropylate, Bupro- fezin, Chinomethionat, Chlordimeform, Chlorobenzilate, Chloropicrin, CIo- thiazoben, Cycloprene, Cyflumetofen, Dicyclanil, Fenoxacrim, Fentrifanil, Flu- benzimine, Flufenerim, Flutenzin, Gossyplure, Hydramethylnone, Japonilure, Metoxadiazone, Petroleum, Piperonyl butoxide, Potassium oleate, Pyridalyl, Sulfluramid, Tetradifon, Tetrasul, Triarathene.Verbutin.Amidoflumet, benclothiaz, benzoximate, bifenazate, bromopropylate, buprofezine, quinomethionate, chlordimeform, chlorobenzilate, chloropicrin, cinothiazoben, cycloprene, cyflumetofen, dicyclanil, fenoxacrim, fentrifanil, Benzimines, Flufenerim, Flutenzin, Gossyplure, Hydramethylnone, Japonilure, Metoxadiazone, Petroleum, Piperonyl butoxide, Potassium oleate, Pyralidyl, Sulfluramid, Tetradifon, Tetrasul, Triarathene.Verbutin.
Die vorstehend aufgeführten Insektizide (Akarizide, Nematizide) sind z.B. bekannt aus „The Pesticide Manual", 12. Auflage (2000) und 13. Auflage (2003), The British Crop Protection Council oder den nach den einzelnen Wirkstoffen aufgeführten Literaturstellen.The insecticides listed above (acaricides, nematicides) are e.g. known from "The Pesticide Manual", 12th edition (2000) and 13th edition (2003), The British Crop Protection Council or the references listed after the individual active ingredients.
Eine besondere Ausführungsform der Erfindung ist die gemeinsame Applikation von Insektiziden (Akariziden, Nematiziden) als agrochemischen Wirkstoffen, entweder zusammen oder hintereinander.A particular embodiment of the invention is the joint application of insecticides (acaricides, nematicides) as agrochemical active ingredients, either together or in succession.
Die oben genannten agrochemischen Wirkstoffe werden entsprechend über Löslichkeit in vorliegender Erfindung eingesetzt. Das Kriterium wasserlöslich bzw. öllöslich kann von jedem Wirkstoff in der Fachliteratur eingesehen werden, z.B. sind Löslichkeiten agrochemischer Wirkstoffe beispielsweise in „The Pesticide Manual", 12. Auflage (2000), 13. Auflage (2003) und 14. Auflage (2006), The British Crop Protection Council, verzeichnet.The above-mentioned agrochemically active compounds are used according to solubility in the present invention. The criterion of water-soluble or oil-soluble can be understood by any active ingredient in the literature, e.g. For example, solubilities of agrochemicals are listed in "The Pesticide Manual", 12th edition (2000), 13th edition (2003) and 14th edition (2006), The British Crop Protection Council.
Unter den in den erfindungsgemäßen Ölsuspensionskonzentraten als Komponente enthaltenen Sulfonylharnstoffen werden im Sinne der vorliegenden Erfindung stets sämtliche Anwendungsformen wie Säuren, Ester, Salze und Isomere wie Stereoisomere und optische Isomere verstanden. So sind neben den neutralen Verbindungen stets auch deren Salze, z.B. mit anorganischen und/oder organischen Gegenionen zu verstehen. So können Sulfonylharnstoffe z.B. Salze bilden, bei denen der Wasserstoff der -Sθ2-NH-Gruppe durch ein für die Landwirtschaft geeignetes Kation ersetzt ist. Diese Salze sind beispielsweise Metallsalze, insbesondere Alkalimetallsalze oder Erdalkalimetallsalze, insbesondere Natrium- und Kaliumsalze, oder auch Ammoniumsalze oder Salze mit organischen Aminen. Ebenso kann Salzbildung durch Anlagerung einer Säure an basischen Gruppen, wie z.B. Amino und Alkylamino, erfolgen. Geeignete Säuren hierfür sind starke anorganische und organische Säuren, beispielsweise HCl, HBr, H2SO4 oder HNO3. Bevorzugte Ester sind die Alkylester, insbesondere die C-i-C-io-Alkylester wie Methylester.For the purposes of the present invention, the sulfonylureas contained as component in the oil suspension concentrates according to the invention are always understood to mean all forms of use, such as acids, esters, salts and isomers, such as stereoisomers and optical isomers. Thus, besides the neutral compounds, their salts are always to be understood, for example with inorganic and / or organic counterions. For example, sulfonylureas can form salts in which the hydrogen of the -Sθ 2 -NH group is replaced by a cation suitable for agriculture. These salts are, for example, metal salts, in particular alkali metal salts or alkaline earth metal salts, in particular sodium and potassium salts, or else ammonium salts or salts with organic amines. Likewise, salt formation can take place by addition of an acid to basic groups, such as, for example, amino and alkylamino. Suitable acids for this purpose are strong inorganic and organic acids, for example HCl, HBr, H 2 SO 4 or HNO 3 . Preferred esters are the alkyl esters, especially the CiC-io-alkyl esters such as methyl esters.
Soweit in dieser Beschreibung der Begriff Acylrest verwendet wird, bedeutet dieser den Rest einer organischen Säure, der formal durch Abspaltung einer OH-Gruppe aus der organischen Säure entsteht, z.B. der Rest einer Carbonsäure und Reste davon abgeleiteter Säuren wie der Thiocarbonsäure, gegebenenfalls N-substituierten Iminocarbonsäuren oder die Reste von Kohlensäuremonoestern, gegebenenfalls N-substituierter Carbaminsäuren, Sulfonsäuren, Sulfinsäuren, Phosphonsäuren, Phosphinsäuren.Insofar as the term acyl radical is used in this specification, it means the radical of an organic acid which is formally formed by cleavage of an OH group from the organic acid, e.g. the radical of a carboxylic acid and radicals derived therefrom, such as the thiocarboxylic acid, optionally N-substituted iminocarboxylic acids or the radicals of carbonic acid monoesters, optionally N-substituted carbamic acids, sulfonic acids, sulfinic acids, phosphonic acids, phosphinic acids.
Ein Acylrest ist bevorzugt Formyl oder Acyl aus der Gruppe CO-RZ, CS-RZ, CO-OR2, CS-OR2, CS-SR2, SORZ oder SO2R2, wobei R2 jeweils einen C1-C10- Kohlenwasserstoffrest wie Ci-C10-Alkyl oder C6-Cio-Aryl bedeutet, der unsubstituiert oder substituiert ist, z.B. durch einen oder mehrere Substituenten aus der Gruppe Halogen wie F, Cl, Br, I, Alkoxy, Haloalkoxy, Hydroxy, Amino, Nitro, Cyano oder Alkylthio, oder R2 bedeutet Aminocarbonyl oder Aminosulfonyl, wobei die beiden letztgenannten Reste unsubstituiert, N-monosubstituiert oder N,N-disubstituiert sind, z.B. durch Substituenten aus der Gruppe Alkyl oder Aryl. Acyl bedeutet beispielsweise Formyl, Halogenalkylcarbonyl, Alkylcarbonyl wieAn acyl radical is preferably formyl or acyl from the group CO-R Z, CS-R Z, CO-OR 2, CS-OR 2, CS-SR 2, SOR Z or SO 2 R 2, wherein R 2 are each a C 1 -C 10 - hydrocarbon radical such as C 1 -C 10 -alkyl or C 6 -C 10 -aryl which is unsubstituted or substituted, for example by one or more substituents from the group halogen such as F, Cl, Br, I, alkoxy, haloalkoxy, Hydroxy, amino, nitro, cyano or alkylthio, or R 2 means aminocarbonyl or aminosulfonyl, where the latter two radicals are unsubstituted, N-monosubstituted or N, N-disubstituted, for example by substituents from the group alkyl or aryl. Acyl is, for example, formyl, haloalkylcarbonyl, alkylcarbonyl as
(CrC4)Alkylcarbonyl, Phenylcarbonyl, wobei der Phenylring substituiert sein kann, oder Alkyloxycarbonyl, wie (CrC4) Alkyloxycarbonyl, Phenyloxycarbonyl, Benzyloxycarbonyl, Alkylsulfonyl, wie (CrC4)Alkylsulfonyl, Alkylsulfinyl, wie C1-C4 (Alkylsulfinyl), N-Alkyl-1-iminoalkyl, wie N-(CrC4)-1-imino-(CrC4)alkyl und andere Reste von organischen Säuren.(CrC 4) alkylcarbonyl, phenylcarbonyl, wherein the phenyl ring may be substituted, or alkyloxycarbonyl, such as (CrC 4) alkyloxycarbonyl, phenyloxycarbonyl, benzyloxycarbonyl, alkylsulfonyl, such as (CrC 4) alkylsulfonyl, alkylsulfinyl, such as C1-C4 (alkylsulfinyl), N-alkyl-1-iminoalkyl such as N- (CrC 4 ) -1-imino- (C 1 -C 4 ) alkyl and other organic acid residues.
Ein Kohlenwasserstoffrest bedeutet ein geradkettiger, verzweigter oder cyclischer und gesättigter oder ungesättigter aliphatischer oder aromatischer Kohlenwasserstoffrest, z.B. Alkyl, Alkenyl, Alkinyl, Cycloalkyl, Cycloalkenyl oder Aryl. Ein Kohlenwasserstoffrest weist bevorzugt 1 bis 40 C-Atome, vorzugsweise 1 bis 30 C-Atome auf; besonders bevorzugt bedeutet ein Kohlenwasserstoffrest Alkyl, Alkenyl oder Alkinyl mit bis zu 12 C-Atomen oder Cycloalkyl mit 3, 4, 5, 6 oder 7 Ringatomen oder Phenyl. Aryl bedeutet ein mono-, bi- oder polycyclisches aromatisches System, beispielsweise Phenyl, Naphthyl, Tetrahydronaphthyl, Indenyl, Indanyl, Pentalenyl, Fluorenyl und ähnliches, vorzugsweise Phenyl.A hydrocarbon radical means a straight-chain, branched or cyclic and saturated or unsaturated aliphatic or aromatic hydrocarbon radical, for example alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl or aryl. A hydrocarbon radical preferably has 1 to 40 C atoms, preferably 1 to 30 C atoms; particularly preferably a hydrocarbon radical is alkyl, alkenyl or alkynyl having up to 12 C atoms or cycloalkyl having 3, 4, 5, 6 or 7 ring atoms or phenyl. Aryl means a mono-, bi- or polycyclic aromatic system, for example phenyl, naphthyl, tetrahydronaphthyl, indenyl, indanyl, pentalenyl, fluorenyl and the like, preferably phenyl.
Ein heterocyclischer Rest oder Ring (Heterocyclyl) kann gesättigt, ungesättigt oder heteroaromatisch und unsubstituiert oder substituiert sein; er enthält vorzugsweise ein oder mehrere Heteroatome im Ring, vorzugsweise aus der Gruppe N, O und S; vorzugsweise ist er ein aliphatischer Heterocyclyl rest mit 3 bis 7 Ringatomen oder ein heteroaromatischer Rest mit 5 oder 6 Ringatomen und enthält 1 , 2 oder 3 Heteroatome. Der heterocyclische Rest kann z.B. ein heteroaromatischer Rest oder Ring (Heteroaryl) sein, wie z.B. ein mono-, bi- oder polycyclisches aromatisches System, in dem mindestens 1 Ring ein oder mehrere Heteroatome enthält, beispielsweise Pyridyl, Pyrimidinyl, Pyridazinyl, Pyrazinyl, Triazinyl, Thienyl, Thiazolyl, Oxazolyl, Furyl, Pyrrolyl, Pyrazolyl und Imidazolyl, oder ist ein partiell oder vollständig hydrierter Rest wie Oxiranyl, Oxetanyl, Pyrrolidyl, Piperidyl, Piperazinyl, Triazolyl, Dioxolanyl, Morpholinyl, Tetrahydrofuryl. Bevorzugt sind Pyrimidinyl und Triazinyl. Als Substituenten für einen substituierten heterocyclischen Rest kommen die weiter unten genannten Substituenten in Frage, zusätzlich auch Oxo. Die Oxogruppe kann auch an den Heteroringatomen, die in verschiedenen Oxidationsstufen existieren können, z.B. bei N und S, auftreten.A heterocyclic radical or ring (heterocyclyl) may be saturated, unsaturated or heteroaromatic and unsubstituted or substituted; it preferably contains one or more heteroatoms in the ring, preferably from the group N, O and S; it is preferably an aliphatic heterocyclyl radical having 3 to 7 ring atoms or a heteroaromatic radical having 5 or 6 ring atoms and contains 1, 2 or 3 heteroatoms. The heterocyclic radical may be e.g. a heteroaromatic radical or ring (heteroaryl), e.g. a mono-, bi- or polycyclic aromatic system in which at least one ring contains one or more heteroatoms, for example pyridyl, pyrimidinyl, pyridazinyl, pyrazinyl, triazinyl, thienyl, thiazolyl, oxazolyl, furyl, pyrrolyl, pyrazolyl and imidazolyl, or is partially or fully hydrogenated radical such as oxiranyl, oxetanyl, pyrrolidyl, piperidyl, piperazinyl, triazolyl, dioxolanyl, morpholinyl, tetrahydrofuryl. Preference is given to pyrimidinyl and triazinyl. Suitable substituents for a substituted heterocyclic radical are the substituents mentioned below in question, in addition also oxo. The oxo group may also be attached to the hetero ring atoms, which may exist in different oxidation states, e.g. at N and S, occur.
Substituierte Reste, wie substituierte Kohlenwasserstoffreste, z.B. substituiertes Alkyl, Alkenyl, Alkinyl, Aryl, Phenyl und Benzyl, oder substituiertes Heterocyclyl oder Heteroaryl, bedeuten beispielsweise einen vom unsubstituierten Grundkörper abgeleiteten substituierten Rest, wobei die Substituenten beispielsweise einen oder mehrere, vorzugsweise 1 , 2 oder 3 Reste aus der Gruppe Halogen, Alkoxy, Haloalkoxy, Alkylthio, Hydroxy, Amino, Nitro, Carboxy, Cyano, Azido, Alkoxycarbonyl, Alkylcarbonyl, Formyl, Carbamoyl, Mono- und Dialkylaminocarbonyl, substituiertes Amino, wie Acylamino, Mono- und Dialkylamino, und Alkylsulfinyl, Haloalkylsulfinyl, Alkylsulfonyl, Haloalkylsulfonyl und, im Falle cyclischer Reste, auch Alkyl und Haloalkyl sowie den genannten gesättigten kohlenwasserstoffhaltigen Resten entsprechende ungesättigte aliphatische Reste, wie Alkenyl, Alkinyl, Alkenyloxy, Alkinyloxy etc. bedeuten. Bei Resten mit C-Atomen sind solche mit 1 bis 4 C-Atomen, insbesondere 1 oder 2 C-Atomen, bevorzugt. Bevorzugt sind in der Regel Substituenten aus der Gruppe Halogen, z.B. Fluor und Chlor, (Ci-C4)Alkyl, vorzugsweise Methyl oder Ethyl, (CrC4)Haloalkyl, vorzugsweise Trifluormethyl, (CrC4)AIkOXy, vorzugsweise Methoxy oder Ethoxy, (Ci-C4)Haloalkoxy, Nitro und Cyano. Besonders bevorzugt sind dabei die Substituenten Methyl, Methoxy und Chlor.Substituted radicals, such as substituted hydrocarbon radicals, for example substituted alkyl, alkenyl, alkynyl, aryl, phenyl and benzyl, or substituted heterocyclyl or heteroaryl, represent, for example, a substituted radical derived from the unsubstituted radical, where the substituents are, for example, one or more, preferably 1, 2 or 3 3 radicals from the group halogen, alkoxy, haloalkoxy, alkylthio, hydroxy, amino, nitro, carboxy, cyano, azido, alkoxycarbonyl, alkylcarbonyl, formyl, carbamoyl, mono- and dialkylaminocarbonyl, substituted amino, such as acylamino, mono- and dialkylamino, and Alkylsulfinyl, haloalkylsulfinyl, alkylsulfonyl, haloalkylsulfonyl and, in the case of cyclic radicals, also alkyl and haloalkyl and said saturated hydrocarbon-containing radicals corresponding unsaturated aliphatic radicals, such as alkenyl, alkynyl, alkenyloxy, alkynyloxy, etc. For radicals with C atoms, those having 1 to 4 C atoms, in particular 1 or 2 C atoms, are preferred. Preferred are in the Generally given to substituents from the group halogen, for example fluorine and chlorine, (Ci-C 4) alkyl, preferably methyl or ethyl, (CrC 4) haloalkyl, preferably trifluoromethyl, (CrC 4) -alkoxy, preferably methoxy or ethoxy, (Ci-C 4 Haloalkoxy, nitro and cyano. Particularly preferred are the substituents methyl, methoxy and chlorine.
Gegebenenfalls substituiertes Phenyl ist vorzugsweise Phenyl, das unsubstituiert oder ein- oder mehrfach, vorzugsweise bis zu dreifach durch gleiche oder verschiedene Reste, vorzugsweise aus der Gruppe Halogen, (CrC4)Alkyl, (Ci-C4)Alkoxy, (CrC4)Halogenalkyl, (Ci-C4)Halogenalkoxy und Nitro substituiert ist, z.B. o-, m- und p-Tolyl, Dimethylphenyl, 2-, 3- und 4-Chlorphenyl, 2-, 3- und 4-Trifluor- und -Tϊichlorphenyl, 2,4-, 3,5-, 2,5- und 2,3-Dichlorphenyl, o-, m- und p-Methoxyphenyl.Optionally substituted phenyl is preferably phenyl which is unsubstituted or mono- or polysubstituted, preferably up to trisubstituted, by identical or different radicals, preferably from the group comprising halogen, (CrC 4) alkyl, (Ci-C 4) alkoxy, (CrC 4) haloalkyl , (C 1 -C 4 ) -haloalkoxy and nitro, for example o-, m- and p-tolyl, dimethylphenyl, 2-, 3- and 4-chlorophenyl, 2-, 3- and 4-trifluoro- and -Tϊichlorphenyl, 2,4-, 3,5-, 2,5- and 2,3-dichlorophenyl, o-, m- and p-methoxyphenyl.
Cycloalkyl bedeutet ein carbocyclisches, gesättigtes Ringsystem vorzugsweise mit 3-6 C-Atomen, z.B. Cyclopropyl, Cyclobutyl, Cyclopentyl oder Cyclohexyl.Cycloalkyl means a carbocyclic saturated ring system preferably having 3-6 C atoms, e.g. Cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl.
Die kohlenstoffhaltigen Reste wie Alkyl, Alkoxy, Haloalkyl, Haloalkoxy, Alkylamino und Alkylthio sowie die entsprechenden ungesättigten und/oder substituierten Reste im Kohlenstoffgerüst jeweils geradkettig oder verzweigt sein. Wenn nicht speziell angegeben, sind bei diesen Resten die niederen Kohlenstoffgerüste, z.B. mit 1 bis 6 C-Atomen bzw. bei ungesättigten Gruppen mit 2 bis 6 C-Atomen, bevorzugt. Alkylreste, auch in den zusammengesetzten Bedeutungen wie Alkoxy, Haloalkyl usw., bedeuten z.B. Methyl, Ethyl, n- oder i-Propyl, n-, i-, t- oder 2-Butyl, Pentyle, Hexyle, wie n-Hexyl, i-Hexyl und 1 ,3-Dimethylbutyl, Heptyle, wie n-Heptyl, 1 -Methylhexyl und 1 ,4-Dimethylpentyl; Alkenyl- und Alkinylreste haben die Bedeutung der den Alkylresten entsprechenden möglichen ungesättigten Reste; Alkenyl bedeutet z.B. AIIyI, 1-Methylprop-2-en-1-yl, 2-Methyl-prop-2-en-1-yl, But-2-en-1-yl, But-3-en-1-yl, 1-Methyl-but-3-en-1-yl und 1-Methyl-but-2-en-1-yl; Alkinyl bedeutet z.B. Propargyl, But-2-in-1-yl, But-3-in-1-yl, 1-Methyl-but-3-in-1-yl.The carbon-containing radicals such as alkyl, alkoxy, haloalkyl, haloalkoxy, alkylamino and alkylthio and the corresponding unsaturated and / or substituted radicals in the carbon skeleton in each case be straight-chain or branched. Unless specifically stated, these radicals are the lower carbon skeletons, e.g. with 1 to 6 C atoms or with unsaturated groups having 2 to 6 C atoms, preferred. Alkyl radicals, also in the composite meanings such as alkoxy, haloalkyl, etc., mean e.g. Methyl, ethyl, n- or i-propyl, n-, i-, t- or 2-butyl, pentyls, hexyls, such as n-hexyl, i-hexyl and 1,3-dimethylbutyl, heptyls, such as n-heptyl, 1-methylhexyl and 1, 4-dimethylpentyl; Alkenyl and alkynyl radicals have the meaning of the possible unsaturated radicals corresponding to the alkyl radicals; Alkenyl means e.g. Allyl, 1-methylprop-2-en-1-yl, 2-methylprop-2-en-1-yl, but-2-en-1-yl, but-3-en-1-yl, 1 Methyl-but-3-en-1-yl and 1-methylbut-2-en-1-yl; Alkynyl means e.g. Propargyl, but-2-yn-1-yl, but-3-yn-1-yl, 1-methyl-but-3-yn-1-yl.
Halogen bedeutet beispielsweise Fluor, Chlor, Brom oder lod. Haloalkyl, -alkenyl und -alkinyl bedeuten durch Halogen, vorzugsweise durch Fluor, Chlor und/oder Brom, insbesondere durch Fluor oder Chlor, teilweise oder vollständig substituiertes Alkyl, Alkenyl bzw. Alkinyl, z.B. CF3, CHF2, CH2F, CF3CF2, CH2FCHCI, CCI3, CHCI2, CH2CH2CI; Haloalkoxy ist z.B. OCF3, OCHF2, OCH2F, CF3CF2O, OCH2CF3 und OCH2CH2CI; entsprechendes gilt für Haloalkenyl und andere durch Halogen substituierte Reste.Halogen is, for example, fluorine, chlorine, bromine or iodine. Haloalkyl, alkenyl and alkynyl are alkyl which is partially or completely substituted by halogen, preferably by fluorine, chlorine and / or bromine, in particular by fluorine or chlorine, Alkenyl or alkynyl, eg CF 3 , CHF 2 , CH 2 F, CF 3 CF 2 , CH 2 FCHCl, CCI 3 , CHCl 2 , CH 2 CH 2 Cl; Haloalkoxy is, for example, OCF 3 , OCHF 2 , OCH 2 F, CF 3 CF 2 O, OCH 2 CF 3 and OCH 2 CH 2 Cl; the same applies to haloalkenyl and other halogen-substituted radicals.
Die erfindungsgemäßen Formulierungen enthalten neben den Komponenten a) und b) noch einen oder mehrere Hilfs- und Zusatzstoffe, z.B.:The formulations according to the invention contain, in addition to components a) and b), one or more auxiliaries and additives, for example:
(c) Tenside und/oder nicht-tensidische Polymere,(c) surfactants and / or non-surfactant polymers,
(d) organische Lösungsmittel, (e) Agrochemikalien wie beispielsweise Düngemittel,(d) organic solvents, (e) agrochemicals such as fertilizers,
(f) übliche Formulierungshilfsmittel wie Entschäumer, Frostschutzmittel, Verdunstungshemmer, Konservierungsmittel, Riechstoffe, Farbstoffe, Stabilisatoren, Wasserfänger oder Verdicker,(f) customary formulation auxiliaries, such as defoamers, antifreeze agents, evaporation inhibitors, preservatives, fragrances, dyes, stabilizers, water scavengers or thickeners,
(g) Tankmischkomponenten.(g) Tank mix components.
So können in den erfindungsgemäß Formulierungen als Komponente c) beispielsweise eines oder mehrere Tenside, z.B. ionogene, nichtionogene oder betainische Tenside enthalten sein. Diese können monomerer oder polymerer Natur (z.B. Graft-Polymere) sein. Beispiele für Komponenten c) sind Tenside auf Silikon- Basis wie Trisiloxantenside, Derivate von Polydimethylsiloxanen und/oder Silikonöle oder zuckerbasierte Tenside wie Atplus® 309 F (Uniqema). Weitere Beispiele für Komponenten c) sind (C4-C3o) (PoIy) Alkylenoxidaddukte, die z.B. verzweigt, linear, gesättigt oder ungesättigt sein können, insbesondere von Fettalkoholen und/oder Fettsäuren bzw. Fettsäureestern. Beispiele für (PoIy) Alkylenoxidaddukte sind Soprophor® CY8 (Rhodia), Genapol® X-060, Genapol® X-080, Genapol® X-150;For example, one or more surfactants, for example ionic, nonionic or betaine surfactants, may be present in the formulations according to the invention as component c). These may be monomeric or polymeric (eg, graft polymers). Examples of components c) are surfactants based on silicone, such as trisiloxane surfactants, derivatives of polydimethylsiloxanes and / or silicone oils, or sugar-based surfactants, such as Atplus 309 ® F (Uniqema). Further examples of components c) are (C 4 -C 3 o) (poly) alkylene oxide adducts which may be branched, for example, can be linear, saturated or unsaturated, in particular of fatty alcohols and / or fatty acids or Fettsäureestern. Examples of (poly) alkylene oxide adducts are Soprophor CY8 ® (Rhodia), Genapol ® X-060, Genapol ® X-080, Genapol ® X-150;
Genapol® X-200, Sapogenat T® 300, Sapogenat T® 500, Genapol® T 200, Genapol T® 800, oder Genagen® MEE (Methylesterethoxylate, Clariant) und andere endgruppenverschlossene Tenside mit einer Methyl-, Ethyl-, n-Propyl-, i-Propyl-, n- Butyl, tert-Butyl, i-Butyl, sec-Butyl oder Acetyl-Gruppe als Endgruppierung, z.B. Genapol® X-060-Methylether oder Genapol® X-150-Methylether.Genapol ® X-200, Sapogenat T ® 300, Sapogenat T ® 500, Genapol ® T 200, Genapol T ® 800, or Genagen MEE ® (Methylesterethoxylate, Clariant) and other terminally capped surfactants having a methyl, ethyl, n-propyl -, i-propyl, n-butyl, tert-butyl, i-butyl, sec-butyl or acetyl group as end grouping, for example Genapol ® X-060 methyl ether or Genapol ® X-150 methyl ether.
Weitere Beispiele für Komponenten c) sind in der kontinuierlichen Phase der Formulierung unlösliche Komponenten, beispielsweise anionogene Tenside wie Hostapur® OSB (Clariant), Netzer® IS (Clariant), Galoryl® DT 201 (CFPI), Tamol® (BASF) oder Morwet® D 425 (Witco) eingesetzt werden. Durch Einarbeitung von in der kontinuierlichen Phase unlöslichen Komponenten oder auch unlöslicher Wirkstoffe in die Formulierungen ergeben sich Dispersionen. Daher umfaßt die vorliegende Erfindung auch Dispersionen.Further examples of component c) are in the continuous phase of the formulation insoluble components, for example anionogenic surfactants, such as Hostapur ® OSB (Clariant), Netzer IS ® (Clariant), Galoryl DT 201 ® (CFPI), Tamol ® (BASF) or Morwet ® D 425 (Witco) may be used. By incorporation of insoluble in the continuous phase components or insoluble active ingredients in the formulations dispersions arise. Therefore, the present invention also encompasses dispersions.
Als Komponente c) können auch Sulfosuccinate, z.B. der Formel (III) enthalten sein,As component c) also sulfosuccinates, e.g. be of the formula (III),
worinwherein
R1, R2 unabhängig voneinander gleich oder verschieden ein unsubstituierter oder substituierter Ci-C3o-Kohlenwasserstoffrest wie CrC3o-Alkyl, oder ein (PoIy) Alkylenoxidaddukt bedeuten undR 1, R 2 independently of one another, identically or differently an unsubstituted or substituted Ci-C 3 o-hydrocarbon radical such as -C 3 O-alkyl, or a (poly) alkylene oxide adduct, and
Mp ein Kation ist, z.B. ein Metallkation wie ein Alkali- oder Erdalkalimetallkation, ein Ammoniumkation wie NH4, Alkyl-, Alkylaryl- oder Poly(arylalkyl)phenyl-ammoniumkation oder deren (PoIy) Alkylenoxidaddukte, oder ein aminoterminiertes (PoIy) Alkylenoxidaddukt ist.M p is a cation, for example a metal cation such as an alkali or alkaline earth metal cation, an ammonium cation such as NH 4 , alkyl, alkylaryl or poly (arylalkyl) phenylammonium cation or their (poly) alkylene oxide adducts, or an amino-terminated (poly) alkylene oxide adduct ,
(Poly)alkylenoxidaddukte im Sinne dieser Beschreibung sind Umsetzungsprodukte von alkoxylierbaren Ausgangsmaterialien wie Alkoholen, Aminen, Carbonsäuren wie Fettsäuren, hydroxy- oder aminofunktionellen Carbonsäureestern (beispielsweise Triglyceriden auf Ricinusölbasis) oder Carbonsäureamiden mit Alkylenoxiden, wobei die (Poly)alkylenoxidaddukte mindestens eine Alkylenoxid-Einheit aufweisen, im allgemeinen aber polymer sind, d.h. 2-200, vorzugsweise 5-150 Alkylenoxid-(Poly) alkylene oxide adducts in the context of this specification are reaction products of alkoxylatable starting materials such as alcohols, amines, carboxylic acids such as fatty acids, hydroxy- or amino-functional carboxylic acid esters (for example triglycerides based on castor oil) or carboxylic acid amides with alkylene oxides, where the (poly) alkylene oxide adducts have at least one alkylene oxide unit but are generally polymeric, ie 2-200, preferably 5-150 alkylene oxide
Einheiten aufweisen. Bei den Alkylenoxid-Einheiten sind Ethylenoxid-, Propylenoxid- und Butylenoxid-Einheiten, insbesondere Ethylenoxid-Einheiten bevorzugt. Die beschriebenen (Poly)alkylenoxidaddukte können aus gleichen oder aus verschiedenen Alkylenoxiden, beispielsweise aus blockartig oder statistisch angeordnetem Ethylenoxid und Propylenoxid aufgebaut sein, so daß die vorliegende Anmeldung auch derartige Misch-alkylenoxidaddukte umfaßt.Have units. In the alkylene oxide units, ethylene oxide, propylene oxide and butylene oxide units, especially ethylene oxide units, are preferred. The described (poly) alkylene oxide adducts can be made from identical or different alkylene oxides, for example from blocky or random arranged ethylene oxide and propylene oxide, so that the present application also includes such mixed alkylene oxide adducts.
Außerdem können als Komponente c) auch nicht-tensidische Polymere enthalten sein, z.B. Polyvinylalkohole, Polyacrylate, Polymalinate oder Polyethylenoxide.In addition, component c) may also contain non-surfactant polymers, e.g. Polyvinyl alcohols, polyacrylates, polymalinates or polyethylene oxides.
Die als Komponente c) enthaltenen Polymere können anorganisch (z.B. Silikate, Phosphate) oder organisch, kationisch, anionisch oder neutral, synthetisch oder natürlich vorkommend sein.The polymers contained as component c) may be inorganic (e.g., silicates, phosphates) or organic, cationic, anionic, or neutral, synthetic, or naturally occurring.
Außerdem können die erfindungsgemäßen Formulierungen als Komponente d) verschiedene organische Lösungsmittel wie unpolare Lösungsmittel, polare protische oder aprotisch dipolare Lösungsmittel und deren Mischungen enthalten. Beispiele für solche organischen Lösungsmittel d) sind - aliphatische oder aromatische Kohlenwasserstoffe, z.B. Mineralöle, Paraffine oder Toluol, XyIoIe und Naphthalinderivate, insbesondere 1 -Methylnaphthalin, 2-Methylnaphthalin, Cβ-Ciβ-Aromatengemische wie die Solvesso®-Reihe (ESSO) z.B. mit den Typen Solvesso® 100 (Kp. 162-177 0C), Solvesso® 150 (Kp. 187-207 0C) und Solvesso® 200 (Kp. 219-282 0C) und C6-C2o-Aliphaten, die linear oder cyclisch sein können, wie die Produkte der Shellsol®-Reihe,In addition, the formulations according to the invention as component d) may contain various organic solvents such as non-polar solvents, polar protic or aprotic dipolar solvents and mixtures thereof. Examples of such organic solvents d) are - aliphatic or aromatic hydrocarbons, for example mineral oils, paraffins or toluene, xylenes and naphthalene derivatives, in particular 1-methylnaphthalene, 2-methylnaphthalene, Cβ-Ciβ-aromatics such as the Solvesso ® series (ESSO), for example with the types Solvesso ® 100 (bp 162-177 0 C), Solvesso ® 150 (bp 187-207 0 C) and Solvesso ® 200 (bp 219-282 0 C) and C 6 -C 2 o-aliphatic, which can be linear or cyclic, such as the products of the Shellsol ® series,
Typen T und K oder BP-n Paraffine, halogenierte aliphatische oder aromatische Kohlenwasserstoffe wie Methylenchlorid bzw. Chlorbenzol,Types T and K or BP-n paraffins, halogenated aliphatic or aromatic hydrocarbons such as methylene chloride or chlorobenzene,
Ester wie Triacetin (Essigsäuretriglycerid), Butyrolacton, Propylencarbonat, Triethylcitrat und Phthalsäure-(CrC22)alkylester, speziell Phthalsäure-(CrEsters such as triacetin (acetic acid triglyceride), butyrolactone, propylene carbonate, triethyl citrate, and phthalic acid (C 1 -C 22 ) alkyl esters, especially phthalic acid (Cr
Ce)alkylester, Maleinsäure-(Ci-C13)alkylester, Lineare, verzweigte, gesättigte oder ungesättigte C1-C20 Alkohole wie Methanol, Ethanol, n- und iso-Propanol, n-, iso-, sec- und tert.-Butanol, Tetrahydrofurfurylalkohol, sowie Pentanol, Hexanol, Heptanol - Ether wie Diethylether, Tetrahydrofuran (THF), Dioxan,Ce) alkyl esters, maleic acid (Ci-C 13 ) alkyl esters, linear, branched, saturated or unsaturated C 1 -C 20 alcohols such as methanol, ethanol, n- and iso-propanol, n-, iso-, sec- and tert. Butanol, tetrahydrofurfuryl alcohol, and pentanol, hexanol, heptanol - ethers such as diethyl ether, tetrahydrofuran (THF), dioxane,
Alkylenglykolmonoalkyether und -dialkylether wie z.B. Propylenglykolmono- methylether, speziell Dowanol® PM (Propylenglykolmonomethylether), Propylen-glykolmonoethylether, Ethylenglykolmonomethylether oder - monoethylether, Diglyme und Tetraglyme, Amide wie Dimethylformamid (DMF)1 Dimethylacetamid, Dimethylcapryl/caprin-fettsäureamid und N-Alkylpyrrolidone, Ketone wie das wasserlösliche Aceton, aber auch mit Wasser nicht mischbare Ketone wie beispielsweise Cyclohexanon oder Isophoron, - Nitrile wie Acetonitril, Propionitril, Butyronitril und Benzonitril,Alkylenglykolmonoalkyether and -dialkylether such as propylene glycol monomethyl ether, especially Dowanol ® PM (propylene glycol monomethyl ether), propylene glycol monoethyl ether, ethylene glycol monomethyl ether or - monoethyl ether, diglyme and tetraglyme, Amides such as dimethylformamide (DMF) 1 dimethylacetamide, dimethylcapryl / caprin-fatty acid amide and N-alkylpyrrolidones, ketones such as the water-soluble acetone, but also water-immiscible ketones such as cyclohexanone or isophorone, - nitriles such as acetonitrile, propionitrile, butyronitrile and benzonitrile,
Sulfoxide und Sulfone wie Dimethylsulfoxid (DMSO) und Sulfolan, sowie Öle im allgemeinen, wie Mineralöle oder Öle auf pflanzlicher Basis wie Maiskeimöl, Leinsaatöl und Rapsöl.Sulfoxides and sulfones such as dimethyl sulfoxide (DMSO) and sulfolane, as well as oils in general, such as mineral oils or vegetable-based oils such as corn oil, linseed oil and rapeseed oil.
Als Komponenten d) bevorzugte organische Lösungsmittel im Sinne der vorliegenden Erfindung sind Esteröle wie Rapsölmethylester und aliphatische oder aromatische Kohlenwasserstoffe, wie Solvesso®-Typen, z. B. Solvesso® 200,As components d) preferred organic solvents for the purposes of the present invention are ester oils such as rapeseed oil methyl ester and aliphatic or aromatic hydrocarbons, such as Solvesso ® types, z. Solvesso ® 200,
Solvesso® 150.Solvesso ® 150th
Weiterhin können Polycarbonsäurealkylester als Lösungsmittel wirken und sind z. B. Alkylester niedermolekularer di-, tri-, tetra- oder auch höherfunktionellerFurthermore, polycarboxylic can act as a solvent and are z. B. alkyl esters of low molecular weight di-, tri-, tetra or higher functional
Carbonsäuren, vorzugsweise mit 2-20 C-Atomen in Frage. Ebenso kommen polymere Polycarbonsäuren, vorzugsweise mit Molekulargewichten bis 2000 g/mol in Frage. Beispiele für Polycarbonsäuren sind Oxal-, Malon-, Bernstein-, Glutar-, Adipin-, Pimelin-, Sebacin-, Azelain-, Suberin-, Malein-, Phthal-, Terephthal-, Mellit-, Trimellit-, Polymalein-, Polyacryl- und Polymethacrylsäure sowie Co- bzw.Carboxylic acids, preferably with 2-20 C atoms in question. Also suitable are polymeric polycarboxylic acids, preferably having molecular weights of up to 2000 g / mol. Examples of polycarboxylic acids are oxalic, malonic, succinic, glutaric, adipic, pimelic, sebacic, azelaic, suberic, maleic, phthalic, terephthalic, mellitic, trimellitic, polymaleic, polyacrylic - and polymethacrylic acid and co- or
Terpolymere, die Malein-, Acryl- und/oder Methacrylsäureeinheiten enthalten.Terpolymers containing maleic, acrylic and / or methacrylic acid units.
Als Alkoholkomponente der Polycarbonsäurealkylester kommen z.B. Alkylalkohole, vorzugsweise monofunktionelle Alkylalkohole mit 1 - 20 C-Atomen in Frage. Beispiele solcher Alkylalkohole sind Methyl-, Ethyh n-Propyl-, iso-Propyl-, n-Butyl-, sec.-Butyl-, iso-Butyl- oder tert-Butylalkohol.As the alcohol component of the alkyl polycarboxylates, e.g. Alkyl alcohols, preferably monofunctional alkyl alcohols having 1 - 20 C atoms in question. Examples of such alkyl alcohols are methyl, ethyl-n-propyl, iso-propyl, n-butyl, sec-butyl, isobutyl or tert-butyl alcohol.
Die Polycarbonsäurealkylester weisen vorzugsweise die nachfolgende Formel (I) auf,The polycarboxylic acid alkyl esters preferably have the following formula (I)
R-O-OC-(CRαRß)x-CO-O-Rδ (I)RO-OC- (CR α R β ) x -CO-OR δ (I)
worin Rα und Rp gleich oder verschieden H, ein unsubstituierter oder substituierter C1-C20- Kohlenwasserstoffrest wie Ci-Cio-Alkyl oder eine Gruppe (CR'R'VCO-OR'" sind, worin R' und R" gleich oder verschieden H oder ein unsubstituierter oder substituierter Ci-C2o-Kohlenwasserstoffrest wie Ci-Cio-Alkyl sind, y eine ganze Zahl von 0 bis 10 ist und R'" ein unsubstituierter oder substituierter C1-C20-wherein R α and R p are identical or different and are H, an unsubstituted or substituted C 1 -C 20 -hydrocarbon radical such as C 1 -C 10 -alkyl or a group (CR'R'VCO-OR ''', where R' and R '' are identical or differently, H or an unsubstituted or substituted Ci-C 2 o-hydrocarbon radical, such as Ci-Cio-alkyl, y is an integer from 0 to 10 and R '"is an unsubstituted or substituted C 1 -C 20 -
Kohlenwasserstoffrest wie C1-Ci0 Alkyl ist,Hydrocarbon radical such as C 1 -C 0 alkyl,
Rv und Rδ gleich oder verschieden ein unsubstituierter oder substituierter C-1-C20- Kohlenwasserstoffrest wie C1-C10 Alkyl ist, und x eine ganze Zahl von 0 bis 20 ist.Rv and R δ are identical or different unsubstituted or substituted C1 to C 20 - hydrocarbon radical such as C1-C1 0 alkyl, and x is a whole number from 0 to 20th
Besonders bevorzugte Polycarbonsäurealkylester sind Diester der nachstehendenParticularly preferred polycarboxylic acid alkyl esters are diesters of the following
Formel (Ia)Formula (Ia)
RY-O-OC-(CH2)X-CO-O-R5 (Ia) worinRY-O-OC- (CH 2 ) X -CO-OR 5 (Ia) wherein
x eine ganze Zahl von 0 bis 20 ist, undx is an integer from 0 to 20, and
Rv und Rδ unabhängig voneinander gleich oder verschieden Ci-C6-Alkyl sind.Rv and R δ independently Ci-C 6 alkyl are the same or different.
Beispiele für Polycarbonsäurealkylester sind Oxalsäureester wie Oxalsäure- dimethylester, Oxalsäure-diethylester, Oxalsäure-di-n-propylester, Oxalsäure-di- isopropylester und Oxalsäure-methylethylester, Malonsäureester wie Malonsäure- dimethylester, Malonsäure-diethylester, Malonsäure-di-n-propylester, Malonsäure-di- isopropylester und Malonsäure-methylethylester, Bernsteinsäureester wie Bernsteinsäure-dimethylester, Bernsteinsäure-diethylester, Bernsteinsäure-di-n- propylester, Bernsteinsäure-di-isopropylester und Bernsteinsäure-methylethylester, Glutarsäureester wie Glutarsäure-dimethylester, Glutarsäure-diethylester, Glutarsäure-di-n-propylester, Glutarsäure-di-isopropylester und Glutarsäure- methylethylester, und Adipinsäureester wie Adipinsäure-dimethylester, Adipinsäure- diethylester, Adipinsäure-di-n-propylester, Adipinsäure-di-isopropylester und Adipinsäure-methylethylester. Bevorzugt sind Adipinsäureester, insbesondere Adipinsäure-dimethylester. Die Polycarbonsäurealkylester sind beispielsweise durch Umsetzung der freienExamples of polycarboxylic acid alkyl esters are oxalic acid esters, such as dimethyl oxalate, diethyl oxalate, di-n-propyl oxalate, diisopropyl oxalate and methyl ethyl oxalate, malonic esters, such as dimethyl malonate, diethyl malonate, di-n-propyl malonic acid, Malonic acid diisopropyl ester and methyl malonate, succinic esters such as succinic acid dimethyl ester, succinic acid diethyl ester, succinic di-n-propyl ester, succinic diisopropyl ester and methyl succinate, glutaric acid esters such as dimethyl glutarate, glutaric acid diethyl ester, glutaric acid di-n-propyl ester, glutaric acid di-isopropyl ester and methyl glutarate, and adipic acid esters such as dimethyl adipate, adipic acid diethyl ester, adipic acid di-n-propyl ester, adipic acid di-isopropyl ester and adipic acid methyl ethyl ester. Preference is given to adipic acid esters, in particular dimethyl adipate. The polycarboxylic acid alkyl esters are, for example, by reaction of the free
Carbonsäuren mit den Alkoholen zugänglich, wobei die Ester z.B. durch Umsetzung „aktivierter" Polycarbonsäuren wie Polycarbonsäure-Anhydriden oder Polycarbonsäure(poly)chloriden mit den Alkoholen nach bekannten Veresterungsmethoden erhalten werden können.Carboxylic acids with the alcohols accessible, the esters, e.g. can be obtained by the reaction of "activated" polycarboxylic acids such as polycarboxylic acid anhydrides or polycarboxylic acid (poly) chlorides with the alcohols by known esterification methods.
Die erfindungsgemäßen Flüssigformulierungen, können als Komponente e) verschiedene Agrochemikalien enthalten. Dies sind beispielsweise Wachstumsregulatoren oder Düngemittel.The liquid formulations according to the invention may contain as component e) various agrochemicals. These are, for example, growth regulators or fertilizers.
In den erfindungsgemäßen flüssigen Formulierungen können als Komponente f) auch übliche Formulierungshilfsmittel wie Entschäumer, Frostschutzmittel, Verdunstungshemmer, Konservierungsmittel, Riechstoffe, Farbstoffe, Stabilisatoren, Wasserfänger oder Verdicker enthalten sein. Bevorzugte Formulierungshilfsmittel sind Frostschutzmittel und Verdunstungshemmer wie Glycerin, z.B. in einer Menge von 2 bis 10 Gew.-% und Konservierungsstoffe, z.B. Mergal® K9N (Riedel) oder Cobate® C.In the liquid formulations according to the invention, component f) may also contain customary formulation auxiliaries, such as defoamers, antifreeze agents, evaporation inhibitors, preservatives, fragrances, dyes, stabilizers, water scavengers or thickeners. Preferred formulation auxiliaries are antifreeze agents and evaporation inhibitors such as glycerol, for example in an amount of 2 to 10 wt .-%, and preservatives, for example Mergal K9N ® (Riedel) or Cobate ® C.
Es können in den erfindungsgemäßen Formulierungen als Komponente g) auch Tankmisch-Komponenten enthalten sein. Beispiele hierfür sind Tankmisch-Tank-mix components may also be present in the formulations according to the invention as component g). Examples of this are tank mixers
Adjuvantien wie Telmion® (Hoechst) oder Pflanzenöle wie Actirob B® (Novance) oder Hasten® (Victorian Chemicals), anorganische Verbindungen wie Düngemittel, z. B. Ammoniumsulfat, Ammoniumnitrat, Ammoniumhydrogensulfat, Harnstoffe oder Hydrotropika.Adjuvants such as Telmion ® (Hoechst) or vegetable oils such as Actirob B ® (Novance) or Hasten ® (Victorian Chemicals), inorganic compounds such as fertilizers, eg. As ammonium sulfate, ammonium nitrate, ammonium hydrogen sulfate, ureas or hydrotropes.
Der Wirkstoffgehalt der erfindungsgemäßen Formulierungen kann im allgemeinen zwischen 0,001 Gewichtsprozent und 80 Gewichtsprozent betragen, wobei im Einzelfall, insbesondere bei Verwendung mehrerer Wirkstoffe, auch höhere Beladungen möglich sind.The active ingredient content of the formulations according to the invention can generally be between 0.001% by weight and 80% by weight, and in individual cases, in particular when using several active substances, higher loadings are also possible.
Die zur Herstellung der erfindungsgemäßen Formulierungen verwendbaren Hilfsund Zusatzstoffe wie z.B. Tenside und Lösungsmittel sind im Prinzip bekannt und werden beispielsweise beschrieben in: McCutcheon's "Detergents and Emulsifiers Annual", MC Publ. Corp., Ridgewood N.J.; Sisley and Wood, "Encyclopedia of Surface active Agents", Chem. Publ.Co.lnα, N.Y. 1964; Schönfeldt, "Grenzflächenaktive Äthylenoxidaddukte", Wiss. Verlagsgesellschaft, Stuttgart 1976; Winnacker-Küchler, "Chemische Technologie", Band 7, C.Hanser-Verlag, München, 4. Auflage 1986.The auxiliaries and additives which can be used to prepare the formulations according to the invention, such as surfactants and solvents, are known in principle and are described, for example, in: McCutcheon 's "Detergents and Emulsifiers Annual", MC Publ. Corp., Ridgewood NJ; Sisley and Wood, "Encyclopedia of Surface active agents, Chem., Publ.Co.lnα, NY 1964, Schonfeldt, "Grenzflächenaktive Äthylenoxidaddukte", Wiss. Verlagsgesellschaft, Stuttgart 1976, Winnacker-Küchler, "Chemical Technology", Volume 7, C. Hanser Verlag, Munich, 4th edition 1986.
Die vorliegende Erfindung umfaßt somit auch die zur Herstellung der erfindungsgemäßen Formulierungen beschriebenen Verfahren.The present invention thus also encompasses the processes described for the preparation of the formulations according to the invention.
Die erfindungsgemäßen Formulierungen stellen physikalisch und chemisch stabile Formulierungen dar, welche bei Verdünnung mit Wasser Spritzbrühen mit physikalisch-anwendungstechnisch günstigen Eigenschaften ergeben. Darüber hinaus weisen die erfindungsgemäßen Formulierungen günstige biologische Eigenschaften auf und sind breit einsetzbar, z. B. zur Bekämpfung von unerwünschtem Pflanzenwuchs.The formulations according to the invention are physically and chemically stable formulations which, when diluted with water, give spray mixtures having physically-favorable application properties. In addition, the formulations of the invention have favorable biological properties and are widely used, for. B. to combat undesirable plant growth.
Die Herstellung der Mikrokapseln kann analog bekannten Verfahren hergestellt werden. Die Herstellung der verkapselten wässrigen Lösungen oder Suspensionen werden bevorzugt ausgehend von einer Wasser-in-ÖI-Emulsion unter Zusatz von polymerisierbaren Komponenten, gegebenenfalls in Gegenwart von geeigneten tensidischen Komponenten, hergestellt, siehe beispielsweise US 4,157,983 und US 4,534,783.The preparation of the microcapsules can be prepared analogously to known processes. The preparation of the encapsulated aqueous solutions or suspensions are preferably prepared starting from a water-in-oil emulsion with the addition of polymerizable components, if appropriate in the presence of suitable surface-active components, see, for example, US Pat. Nos. 4,157,983 and 4,534,783.
Die erfindungsgemäßen Formulierungen lassen sich beispielsweise wie folgt herstellen (Ausführungsbeispiel):The formulations according to the invention can be prepared, for example, as follows (exemplary embodiment):
Eine organische Phase wurde vorbereitet durch das Auflösen von Dodecylbenzolsulfonsäure und nicht-ionischem Alkylarylphenol in Kerosin als Lösungsmittel. Die wässrige Phase wurde vorbereitet durch Auflösen von Glyphosat und Harnstoff/Formaldehydpräpolymeren in Wasser. Die beiden Phasen wurden dann vereinigt und bildeten unter Rühren eine Wasser-in-Ölemulsion. Danach wurde die Temperatur auf 400C erhöht und das Rühren für 2 oder mehr Stunden fortgesetzt. Das resultierende Produkt wurde gekühlt, um eine Suspension von Mikrokapseln in der organischen Phase zu ergeben, wobei die Mikrokapseln das wässrige Medium umschließen. Die Herstellung von Mikrokapseln welche in der Ölphase gelöste oder dispergierte agrochemische Wirkstoffe umschließen kann analog nach den bekannten Methoden erfolgen.An organic phase was prepared by dissolving dodecylbenzenesulfonic acid and nonionic alkylarylphenol in kerosene as a solvent. The aqueous phase was prepared by dissolving glyphosate and urea / formaldehyde prepolymers in water. The two phases were then combined to form a water-in-oil emulsion with stirring. Thereafter, the temperature was raised to 40 0 C and stirring continued for 2 or more hours. The resulting product was cooled to give a suspension of microcapsules in the organic phase, the microcapsules enclosing the aqueous medium. The production of microcapsules which include dissolved or dispersed in the oil phase agrochemical active ingredients can be carried out analogously to the known methods.
Abschließend werden die wassergelösten und mikroverkapselten agrochemischen Wirkstoffe mit den in der Ölphase gelösten oder dispergierten agrochemischen Wirkstoffen gemischt, um das erfindungsgemäße Ölsuspensionskonzentrat zu ergeben.Finally, the water-soluble and microencapsulated agrochemical active ingredients are mixed with the agrochemical active substances dissolved or dispersed in the oil phase to give the oil suspension concentrate according to the invention.
Im Rahmen der Erfindung ist auch die Herstellung der erfindungsgemäßen Ölsuspensionskonzentrate vorgesehen. Diese können durch bekannte Verfahren hergestellt werden. Das Vermählen und Vermischen der Komponenten erfolgt soweit dies mit der Bildung bzw. Anwesenheit der Mikrokapseln verträglich ist nach den bekannten Methoden.In the context of the invention, the preparation of the oil suspension concentrates according to the invention is also provided. These can be prepared by known methods. The grinding and mixing of the components takes place as far as this is compatible with the formation or presence of the microcapsules according to the known methods.
Zur Anwendung können die erfindungsgemäßen Ölsuspensionskonzentrate gegebenenfalls in üblicherweise verdünnt werden (z.B. mittels Wasser), z.B. zu Suspensionen, Emulsionen, Suspoemulsionen oder Lösungen, vorzugsweise zu Emulsionen. Es kann vorteilhaft sein, erhaltenen Spritzbrühen weitere agrochemische Wirkstoffe (z.B. Tankmischpartner in Form entsprechender Formulierungen) und/oder zur Anwendung übliche Hilfs- und Zusatzstoffe, z.B. selbstemulgierende Öle wie Pflanzenöle oder Paraffinöle und/oder Düngemittel zuzugeben. Gegenstand der vorliegenden Erfindung sind daher auch solche herbiziden Mittel, auf Basis der erfindungsgemäßen Ölsuspensionskonzentrate.For use, the oil suspension concentrates of the present invention may optionally be diluted in conventional manner (e.g., by water), e.g. to suspensions, emulsions, suspoemulsions or solutions, preferably to emulsions. It may be advantageous to obtain spray mixtures which contain further agrochemical active substances (for example tank mix partners in the form of corresponding formulations) and / or customary auxiliaries and additives, for example self-emulsifying oils such as vegetable oils or paraffin oils and / or fertilizers. The present invention therefore also relates to such herbicidal compositions, based on the oil suspension concentrates according to the invention.
Die erfindungsgemäßen Ölsuspensionskonzentrate und die daraus durch Verdünnen erhältlichen Anwendungsformen (zusammen „erfindungsgemäße herbizide Mittel") weisen eine ausgezeichnete herbizide Wirksamkeit gegen ein breites Spektrum wirtschaftlich wichtiger mono- und dikotyler Schadpflanzen auf, einschließlich Arten die resistent sind gegen herbizide Wirkstoffe wie Glyphosate, Glufosinate, Atrazin oder Imidazolinon-Herbizide. Auch schwer bekämpfbare perennierende Unkräuter, die aus Rhizomen, Wurzelstöcken oder anderen Dauerorganen austreiben, werden durch die Wirkstoffe gut erfaßt. Dabei kann die Applikation im Vorsaat-, Vorauflauf- oder Nachauflaufverfahren erfolgen. Bevorzugt erfolgt die Applikation dabei auf die aufgelaufenen Schadpflanzen (z.B. Unkräuter oder unerwünschte Kulturpflanzen), insbesondere vor dem Auflaufen der (erwünschten) Kulturpflanzen. Im einzelnen seien beispielhaft einige Vertreter der mono- und dikotylen Unkrautflora genannt, die durch die erfindungsgemäßen Verbindungen kontrolliert werden können, ohne daß durch die Nennung eine Beschränkung auf bestimmte Arten erfolgen soll.The oil suspension concentrates according to the invention and the use forms obtainable therefrom by dilution (together "herbicidal compositions according to the invention") have excellent herbicidal activity against a broad spectrum of economically important monocotyledonous and dicotyledonous harmful plants, including species which are resistant to herbicidal active compounds such as glyphosate, glufosinate, atrazine or imidazolinone herbicides.The hard-to-control perennial weeds that expel from rhizomes, rhizomes or other permanent organs are well detected by the active ingredients. or post-emergence. The application is preferably carried out on the accumulated harmful plants (for example, weeds or unwanted crops), in particular before emergence of the (desired) crops. Specifically, by way of example, some representatives of the monocotyledonous and dicotyledonous weed flora can be mentioned, which can be controlled by the compounds according to the invention, without the intention of limiting them to certain species.
Auf der Seite der monokotylen Unkrautarten werden z.B. Avena spp., Alopecurus spp., Brachiaria spp., Digitaria spp., Lolium spp., Echinochloa spp., Panicum spp., Phalaris spp., Poa spp., Setaria spp. sowie Cyperusarten aus der annuellen Gruppe und auf seiten der perennierenden Spezies Agropyron, Cynodon, Imperata sowie Sorghum und auch ausdauernde Cyperusarten gut erfaßt.On the side of the monocotyledonous weeds, e.g. Avena spp., Alopecurus spp., Brachiaria spp., Digitaria spp., Lolium spp., Echinochloa spp., Panicum spp., Phalaris spp., Poa spp., Setaria spp. and Cyperus species from the annuelle group and on the part of the perennial species Agropyron, Cynodon, Imperata and Sorghum and also perennial Cyperusarten well.
Bei dikotylen Unkrautarten erstreckt sich das Wirkungsspektrum auf Arten wie z.B. Abutilon spp., Amaranthus spp., Chenopodium spp., Chrysanthemum spp., Galium spp., Ipomoea spp., Kochia spp., Lamium spp., Matricaria spp., Pharbitis spp., Polygonum spp.,Sida spp., Sinapis spp., Solanum spp., Stellaria spp., Veronica spp. und Viola spp., Xanthium spp., auf der annuellen Seite sowie Convolvulus, Cirsium, Rumex und Artemisia bei den perennierenden Unkräutern.In dicotyledonous weed species, the spectrum of activity extends to species such as e.g. Abutilon spp., Amaranthus spp., Chenopodium spp., Chrysanthemum spp., Galium spp., Ipomoea spp., Kochia spp., Lamium spp., Matricaria spp., Pharitis spp., Polygonum spp., Sida spp., Sinapis spp , Solanum spp., Stellaria spp., Veronica spp. and Viola spp., Xanthium spp., on the annual side, as well as Convolvulus, Cirsium, Rumex, and Artemisia in perennial weeds.
Werden die erfindungsgemäßen herbiziden Mittel vor dem Keimen auf die Erdoberfläche appliziert, so wird entweder das Auflaufen der Unkrautkeimlinge vollständig verhindert oder die Unkräuter wachsen bis zum Keimblattstadium heran, stellen jedoch dann ihr Wachstum ein und sterben schließlich nach Ablauf von drei bis vier Wochen vollkommen ab.If the herbicidal compositions according to the invention are applied to the surface of the earth before germination, either the emergence of the weed seedlings is completely prevented or the weeds grow up to the cotyledon stage, but then cease their growth and finally die completely after three to four weeks.
Bei Applikation der herbiziden Mittel auf die grünen Pflanzenteile im Nachauflaufverfahren tritt ebenfalls sehr rasch nach der Behandlung ein drastischer Wachstumsstop ein und die Unkrautpflanzen bleiben in dem zumWhen the herbicidal compositions are applied to the green plant parts in the postemergence process, a drastic growth arrest also occurs very rapidly after the treatment and the weed plants remain in the
Applikationszeitpunkt vorhandenen Wachstumsstadium stehen oder sterben nach einer gewissen Zeit ganz ab, so daß auf diese Weise eine für die Kulturpflanzen schädliche Unkrautkonkurrenz sehr früh und nachhaltig beseitigt wird. Die erfindungsgemäßen herbiziden Mittel zeichnen sich durch eine schnell einsetzende und lang andauernde herbizide Wirkung aus. Die Regenfestigkeit der Wirkstoffe in den erfindungsgemäßen Kombinationen ist in der Regel günstig. Als besonderer Vorteil fällt ins Gewicht, daß die verwendeten und wirksamen Dosierungen von Verbindungen (a) so gering eingestellt werden können, daß ihre Bodenwirkung optimal niedrig ist. Somit wird deren Einsatz nicht nur in empfindlichen Kulturen erst möglich, sondern Grundwasser-Kontaminationen werden praktisch vermieden. Durch die erfindungsgemäßen Kombination von Wirkstoffen wird eine erhebliche Reduzierung der nötigen Aufwandmenge der Wirkstoffe ermöglicht.Application stage existing stage of growth or die after a certain time completely off, so that in this way harmful to the crops weed competition is eliminated very early and sustainably. The herbicidal compositions according to the invention are distinguished by a rapidly onset and long-lasting herbicidal action. The rainfastness of the active ingredients in the combinations according to the invention is generally favorable. A particular advantage is the fact that the used and effective dosages of compounds (a) can be set so low that their soil effect is optimally low. Thus, their use is not only possible in sensitive cultures, but groundwater contamination is virtually avoided. The combination of active substances according to the invention enables a considerable reduction in the required application rate of the active ingredients.
Die genannten Eigenschaften und Vorteile sind in der praktischen Unkrautbekämpfung gefordert, um landwirtschaftliche Kulturen von unerwünschten Konkurrenzpflanzen freizuhalten und damit die Erträge qualitativ und quantitativ zu sichern und/oder zu erhöhen. Der technische Standard wird durch diese neuenThe said properties and advantages are required in practical weed control in order to keep agricultural crops free of undesired competing plants and thus to secure and / or increase yields qualitatively and quantitatively. The technical standard will be through this new
Kombinationen hinsichtlich der beschriebenen Eigenschaften deutlich übertroffen.Combinations in terms of the properties described clearly exceeded.
Darüberhinaus weisen die erfindungsgemäßen Mittel teilweise hervorragende wachstumsregulatorische Eigenschaften bei den Kulturpflanzen auf. Sie greifen regulierend in den pflanzeneigenen Stoffwechsel ein und können damit zur gezielten Beeinflussung von Pflanzeninhaltsstoffen und zur Ernteerleichterung wie z.B. durch Auslösen von Desikkation und Wuchsstauchung eingesetzt werden. Desweiteren eignen sie sich auch zur generellen Steuerung und Hemmung von unerwünschtem vegetativem Wachstum, ohne dabei die Pflanzen abzutöten. Eine Hemmung des vegetativen Wachstums spielt bei vielen mono- und dikotylen Kulturen eine große Rolle, da das Lagern hierdurch verringert oder völlig verhindert werden kann.Moreover, the agents according to the invention have in some cases outstanding growth-regulatory properties in the crop plants. They regulate the plant's metabolism and can thus be used to specifically influence plant constituents and facilitate harvesting, such as be used by triggering desiccation and stunted growth. Furthermore, they are also suitable for the general control and inhibition of unwanted vegetative growth, without killing the plants. Inhibition of vegetative growth plays an important role in many monocotyledonous and dicotyledonous cultures, as storage can be reduced or completely prevented.
Aufgrund ihrer herbiziden und pflanzenwachstumsregulatorischen Eigenschaften können die Mittel zur Bekämpfung von Schadpflanzen in bekannten Pflanzenkulturen oder noch zu entwickelnden toleranten oder gentechnisch veränderten Kulturpflanzen eingesetzt werden. Die transgenen Pflanzen zeichnen sich in der Regel durch besondere vorteilhafte Eigenschaften aus, neben den Resistenzen gegenüber den erfindungsgemäßen Mitteln beispielsweise durch Resistenzen gegenüber Pflanzenkrankheiten oder Erregern von Pflanzenkrankheiten wie bestimmten Insekten oder Mikroorganismen wie Pilzen, Bakterien oder Viren. Andere besondere Eigenschaften betreffen z. B. das Erntegut hinsichtlich Menge, Qualität, Lagerfähigkeit, Zusammensetzung und spezieller Inhaltsstoffe. So sind transgene Pflanzen mit erhöhtem Stärkegehalt oder veränderter Qualität der Stärke oder solche mit anderer Fettsäurezusammensetzung des Ernteguts bekannt.Because of their herbicidal and plant growth regulatory properties, the agents for combating harmful plants can be used in known plant crops or tolerant or genetically modified crops to be developed. The transgenic plants are usually characterized by particular advantageous properties, in addition to the resistance to the inventive compositions, for example, by resistance to plant diseases or pathogens of plant diseases like certain insects or microorganisms like fungi, bacteria or viruses. Other special properties relate to z. B. the crop in terms of quantity, quality, shelf life, composition and special ingredients. Thus, transgenic plants with increased starch content or altered quality of the starch or those with other fatty acid composition of the crop are known.
Prinzipiell ist nicht ausgeschlossen, dass eines der erfindungsgemäßen Ölsuspensionskonzentrate im Rahmen eines Verfahrens zur Bekämpfung von Schadorganismen eingesetzt wird, wobei die Applikation gegenüber den Schadorganismen an jenen Orten erfolgt, an denen diese Auftreten. Allgemein liegt die Verwendung eines der erfindungsgemäßen Ölsuspensionskonzentrate zur Bekämpfung von Schadorganismen im Rahmen der Erfindung.In principle, it is not excluded that one of the oil suspension concentrates according to the invention is used in the context of a method for controlling harmful organisms, wherein the application to the harmful organisms takes place in those places where these occur. In general, the use of one of the oil suspension concentrates according to the invention for controlling harmful organisms is within the scope of the invention.
Die Aufwandmenge der Herbizide, z.B. im Fall der Pyridyl-Sulfonylharnstoffe, kann in einem weiten Bereich variieren, beispielsweise zwischen 0,001 g und 500 g AS/ha (AS/ha bedeutet dabei im Folgenden „Aktivsubstanz pro Hektar" = bezogen auf 100%igen Wirkstoff). Bei Anwendungen mit Aufwandmengen von 0,01 g bis 200 g AS/ha der Herbizide, wird im Vor- und Nachauflaufverfahren ein relativ breites Spektrum an Schadpflanzen bekämpft, z.B. an annuellen und perennierenden mono- oder dikotylen Unkräutern sowie an unerwünschten Kulturpflanzen. Bei den erfindungsgemäßen Kombinationen liegen die Aufwandmengen in der Regel niedriger, z. B. im Bereich von 0,001 g bis 100 g AS/ha, vorzugsweise 0,005 g bis 50 g AS/ha, besonders bevorzugt 0,01 g bis 9 g AS/ha.The application rate of the herbicides, e.g. in the case of the pyridyl-sulfonylureas, can vary within a wide range, for example between 0.001 g and 500 g of AS / ha (AS / ha in the following refers to "active substance per hectare" = based on 100% active ingredient) from 0.01 g to 200 g of AS / ha of the herbicides, a relatively broad spectrum of harmful plants is combated in the pre-emergence and postemergence processes, for example on annual and perennial monocotyledonous or dicotyledonous weeds as well as on undesired crop plants generally lower, for example in the range of 0.001 g to 100 g AS / ha, preferably 0.005 g to 50 g AS / ha, particularly preferably 0.01 g to 9 g AS / ha.
Die Sulfonylharnstoff enthaltenden Ölsuspensionskonzentrate, sind z.B. zurThe sulfonylurea-containing oil suspension concentrates are e.g. to
Bekämpfung von Schadpflanzen in Pflanzenkulturen geeignet, beispielsweise in wirtschaftlich bedeutenden Ackerbaukulturen z.B. monokotylen Ackerbaukulturen wie Getreide (z.B. Weizen, Gerste, Roggen, Hafer), Reis, Mais, Hirse, oder dikotylen Ackerbaukulturen wie Zuckerrübe, Raps, Baumwolle, Sonnenblumen und Leguminosen z.B. der Gattungen Glycine (z.B. Glycine max. (Soja) wie nicht- transgene Glycine max. (z.B. konventionelle Sorten wie STS-Sorten) oder transgene Glycine max. (z.B. RR-Soja oder LL-Soja) und deren Kreuzungen), Phaseolus, Pisum, Vicia und Arachis, oder Gemüsekulturen aus verschiedenen botanischen Gruppen wie Kartoffel, Lauch, Kohl, Karotte, Tomate, Zwiebel, sowie Dauer- und Plantagenkulturen wie Kern- und Steinobst, Beerenobst, Wein, Hevea, Bananen, Zuckerrohr, Kaffee, Tee, Citrus, Nussplantagen, Rosen, Palmenkulturen und Forstkulturen. Für die Anwendung von Herbizid-Kombinationen sind diese Kulturen ebenfalls bevorzugt. Für die Herbizid-Kombinationen sind vor allem gegenüber den Herbiziden tolerante Mutantenkulturen und tolerante transgene Kulturen von besonderem Interesse, vorzugsweise Mais, Reis, Getreide, Raps und Soja, insbesondere Soja, die gegen Imidazolinon-Herbizide, Glufosinate oder Glyphosate resistent sind.Control of harmful plants in crops suitable, for example in economically important arable crops such as monocotyledonous crops such as cereals (eg wheat, barley, rye, oats), rice, corn, millet, or dicotyledonous crops such as sugar beet, oilseed rape, cotton, sunflowers and legumes such as the genera Glycine (eg Glycine max. (Soy) as non-transgenic Glycine max (eg conventional varieties such as STS varieties) or transgenic Glycine max (eg RR soy or LL soy) and their crosses), Phaseolus, Pisum, Vicia and arachis, or vegetable crops from various botanical groups such as potato, leek, cabbage, carrot, tomato, onion, as well as permanent and Plantation crops such as pome and stone fruit, soft fruit, wine, Hevea, bananas, sugarcane, coffee, tea, citrus, nut orchards, roses, palm tree and forest crops. For the application of herbicide combinations, these cultures are also preferred. Of particular interest to the herbicidal combinations are, in particular, herbivory tolerant mutant cultures and tolerant transgenic crops, preferably maize, rice, cereals, rapeseed and soybean, in particular soybean, which are resistant to imidazolinone herbicides, glufosinates or glyphosates.
Die Ölsuspensionskonzentrate können auch nicht-selektiv zur Bekämpfung unerwünschten Pflanzenwuchses eingesetzt werden, z.B. in Dauer- und Plantagenkulturen, an Wegrändern, Plätzen, Industrieanlagen, Flugplätzen oder Eisenbahnanlagen, oder zur sogenannten Burn-Down-Anwendung, z.B. in Ackerbaukulturen z.B. monokotylen Ackerbaukulturen wie Getreide (z.B. Weizen, Gerste, Roggen, Hafer), Reis, Mais, Hirse, oder dikotylen Ackerbaukulturen wieThe oil suspension concentrates may also be used non-selectively to control undesired plant growth, e.g. in permanent and plantation crops, on roadsides, squares, industrial plants, airfields or railway facilities, or for so-called burn-down application, e.g. in crops, e.g. monocotyledonous crops such as cereals (e.g., wheat, barley, rye, oats), rice, corn, millet, or dicotyledonous crops such as
Zuckerrübe, Raps, Baumwolle, Sonnenblumen und Leguminosen z.B. der Gattungen Glycine (z.B. Glycine max. (Soja) wie nicht-transgene Glycine max. (z.B. konventionelle Sorten wie STS-Sorten) oder transgene Glycine max. (z.B. RR-Soja oder LL-Soja) und deren Kreuzungen), Phaseolus, Pisum, Vicia und Arachis, oder Gemüsekulturen aus verschiedenen botanischen Gruppen wie Kartoffel, Lauch, Kohl, Karotte, Tomate, Zwiebel.Sugar beet, oilseed rape, cotton, sunflowers and legumes, e.g. of the genera Glycine (eg Glycine max. (soy) as non-transgenic Glycine max (eg conventional varieties such as STS varieties) or transgenic Glycine max (eg RR soy or LL soy) and their crosses), Phaseolus, Pisum , Vicia and Arachis, or vegetable crops from various botanical groups such as potato, leek, cabbage, carrot, tomato, onion.
Die Erfindung wird durch Beispiele näher erläutert, ohne sie dadurch einzuschränken.The invention will be explained in more detail by examples, without thereby restricting them.
Beispiel 1 :Example 1 :
Tabelle 1 zeigt die Zusammensetzung eines erfindungsgemäßen Ölsuspensionskonzentrates, wobei sowohl eine Komponente (a) als auch eine Kompenente (b) verkapselt ist. Tabelle 1Table 1 shows the composition of an oil suspension concentrate according to the invention, wherein both a component (a) and a component (b) is encapsulated. Table 1
Beispiel 2:Example 2:
Tabelle 2 zeigt eine Zusammensetzung in der nur Komponente (a) verkapselt ist.Table 2 shows a composition in which only component (a) is encapsulated.
Tabelle 2Table 2

Claims

Patentansprüche: claims:
1. Ölsuspensionskonzentrat, enthaltend1. Oil suspension concentrate containing
(a) ein oder mehrere agrochemische Wirkstoffe in der Wasser-Phase, in verkapselter Form in der Öl-Phase vorliegend, und(A) one or more agrochemical active ingredients in the water phase, in encapsulated form in the oil phase, and
(b) ein oder mehrere agrochemische Wirkstoffe in der Öl-Phase, verkapselt vorliegend, sowie übliche Hilfs- und Zusatzstoffe.(B) one or more agrochemical active ingredients in the oil phase, encapsulated in the present case, and customary auxiliaries and additives.
2. Ölsuspensionskonzentrat gemäß Anspruch 1 , worin mindestens einer der in (b) vorliegenden Wirkstoffe ein Sulfonylharnstoff, insbesondere ein Phenylsulfonylharnstoff, ein Heteroarylsulfonharnstoff, ein (Het)Aryl- sulfonylaminocarbonyltriazolinon, oder ein Pyridyl-sulfonylharnstoff ist.2. An oil suspension concentrate according to claim 1, wherein at least one of the active ingredients present in (b) is a sulfonylurea, in particular a phenylsulfonylurea, a heteroarylsulfoneurea, a (Het) arylsulfonylaminocarbonyltriazolinone, or a pyridylsulfonylurea.
3. Ölsuspensionskonzentrat gemäß Anspruch 1 , worin mindestens einer der in (b) vorliegenden Wirkstoffe ein Thien-3-yl-sulfonylamin(thio)carbonyltriazolin(thi)on und/oder dessen Salz ist.3. An oil suspension concentrate according to claim 1, wherein at least one of the active ingredients present in (b) is a thien-3-yl-sulfonylamine (thio) carbonyltriazoline (thi) on and / or its salt.
4. Ölsuspensionskonzentrat gemäß Anspruch 1 , worin mindestens einer der in (b) vorliegenden Wirkstoffe ein Phenylsulfonylharnstoff ist.4. An oil suspension concentrate according to claim 1, wherein at least one of the active ingredients present in (b) is a phenylsulfonylurea.
5. Ölsuspensionskonzentrat gemäß Anspruch 1 , worin mindestens einer der in (b) vorliegenden Wirkstoffe ein Dioxazin-Pyridylsulfonylharnstoff und/oder dessen Salz ist.5. An oil suspension concentrate according to claim 1, wherein at least one of the active ingredients present in (b) is a dioxazine pyridylsulfonylurea and / or its salt.
6. Ölsuspensionskonzentrat gemäß Anspruch 1 , worin mindestens einer der in (b) vorliegenden Wirkstoffe ein Phenylsulfonylaminocarbonyltriazolinon ist.6. An oil suspension concentrate according to claim 1, wherein at least one of the active ingredients present in (b) is a phenylsulfonylaminocarbonyltriazolinone.
7. Ölsuspensionskonzentrat gemäß Anspruch 1 , worin mindestens einer der in (b) vorliegenden Wirkstoffe ein Propoxycarbazon und/oder dessen Salz ist. 7. An oil suspension concentrate according to claim 1, wherein at least one of the active ingredients present in (b) is a propoxycarbazone and / or its salt.
8. Ölsuspensionskonzentrat gemäß einem der vorliegenden Ansprüche, wobei sich die Mikrokapseln, welche die in der Ölphase dispergiert oder gelöst vorliegenden Wirkstoffe enthalten, in ihren Freisetzungseigenschaften von den Mikrokapseln, welche die wasserlöslichen Wirkstoffe enthalten, unterscheiden.8. An oil suspension concentrate according to any one of the preceding claims, wherein the microcapsules containing the active substances dispersed or dissolved in the oil phase differ in their release properties from the microcapsules containing the water-soluble active substances.
9. Ölsuspensionskonzentrat gemäß einem der vorhergehenden Ansprüche, wobei sich die in der Ölphase vorliegenden Wirkstoffe in ihren chemischen Eigenschaften von den wasserlöslichen Wirkstoffen unterscheiden.9. Oil suspension concentrate according to one of the preceding claims, wherein the active substances present in the oil phase differ in their chemical properties from the water-soluble active ingredients.
10. Ölsuspensionskonzentrat gemäß Anspruch 9, wobei sich die in der Ölphase vorliegenden Wirkstoffe in ihrer Hydrolyseempfindlichkeit unterscheiden.10. The oil suspension concentrate according to claim 9, wherein the active substances present in the oil phase differ in their hydrolysis sensitivity.
11. Ölsuspensionskonzentrat gemäß einem der vorhergehenden Ansprüche, wobei sich in der Ölphase vorliegenden Wirkstoffe in ihrem Schmelzpunkt, von den wasserlöslichen Wirkstoffen unterscheiden.11. Oil suspension concentrate according to one of the preceding claims, wherein present in the oil phase active ingredients differ in their melting point, from the water-soluble active ingredients.
12. Ölsuspensionskonzentrat gemäß einem der vorhergehenden Ansprüche, wobei die in gekapselter Form vorliegenden Wirkstoffe einen Schmelzpunkt > 120 °C aufweisen.12. Oil suspension concentrate according to one of the preceding claims, wherein the active ingredients present in encapsulated form have a melting point> 120 ° C.
13. Verwendung eines Ölsuspensionskonzentrats nach einem oder mehreren der Ansprüche 1 bis 12 zur Verhinderung oder zur Verzögerung des chemischen Abbaus, insbesondere der Hydrolyse von Wirkstoffen in agrochemischer Formulierungen.13. Use of an oil suspension concentrate according to one or more of claims 1 to 12 for preventing or delaying the chemical degradation, in particular the hydrolysis of active ingredients in agrochemical formulations.
14. Verfahren zur Bekämpfung von Schadpflanzen, wobei eine wirksame Menge eines Ölsuspensionskonzentrats nach einem oder mehreren der Ansprüche 1 bis 12, auf die Schad pflanzen, Teile der Pflanzen, Pflanzensamen oder die Flächen an denen die Pflanzen wachsen appliziert wird.14. A method of controlling harmful plants, wherein an effective amount of an oil suspension concentrate according to one or more of claims 1 to 12, plant on the Schad, parts of the plants, plant seeds or the areas where the plants grow.
15. Verwendung eines Ölsuspensionskonzentrats nach einem oder mehreren der Ansprüche 1 bis 12, zur Bekämpfung von Schad pflanzen. 15. Use of an oil suspension concentrate according to one or more of claims 1 to 12, plants for controlling harmful plants.
16. Verwendung eines Ölsuspensionskonzentrats nach einem oder mehreren der Ansprüche 1 bis 12, zur Herstellung von Wirkstoff-Formulierungen. 16. Use of an oil suspension concentrate according to one or more of claims 1 to 12, for the preparation of active ingredient formulations.
EP08701053A 2007-01-23 2008-01-10 Oil suspension concentrate with micro-encapsulated agrochemical active ingredients Withdrawn EP2111104A2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP08701053A EP2111104A2 (en) 2007-01-23 2008-01-10 Oil suspension concentrate with micro-encapsulated agrochemical active ingredients

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP07001380A EP1952688A1 (en) 2007-01-23 2007-01-23 Oil suspension concentrate with microencapsulated and with non-microencapsulated agrochemical agents
EP08701053A EP2111104A2 (en) 2007-01-23 2008-01-10 Oil suspension concentrate with micro-encapsulated agrochemical active ingredients
PCT/EP2008/000126 WO2008089890A2 (en) 2007-01-23 2008-01-10 Oil suspension concentrate with micro-encapsulated agrochemical active ingredients

Publications (1)

Publication Number Publication Date
EP2111104A2 true EP2111104A2 (en) 2009-10-28

Family

ID=38564578

Family Applications (2)

Application Number Title Priority Date Filing Date
EP07001380A Withdrawn EP1952688A1 (en) 2007-01-23 2007-01-23 Oil suspension concentrate with microencapsulated and with non-microencapsulated agrochemical agents
EP08701053A Withdrawn EP2111104A2 (en) 2007-01-23 2008-01-10 Oil suspension concentrate with micro-encapsulated agrochemical active ingredients

Family Applications Before (1)

Application Number Title Priority Date Filing Date
EP07001380A Withdrawn EP1952688A1 (en) 2007-01-23 2007-01-23 Oil suspension concentrate with microencapsulated and with non-microencapsulated agrochemical agents

Country Status (15)

Country Link
US (1) US20080176746A1 (en)
EP (2) EP1952688A1 (en)
JP (1) JP2010516720A (en)
KR (1) KR20090113864A (en)
CN (1) CN101621924A (en)
AR (1) AR064982A1 (en)
AU (1) AU2008209129A1 (en)
BR (1) BRPI0807401A2 (en)
CA (1) CA2676210A1 (en)
EA (1) EA013316B1 (en)
EC (1) ECSP099527A (en)
IL (1) IL199960A0 (en)
MX (1) MX2009007824A (en)
UA (1) UA96009C2 (en)
WO (1) WO2008089890A2 (en)

Families Citing this family (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2323399B2 (en) * 2007-06-19 2010-02-26 Gat Microencapsulation Ag SUSPENSIONS IN AGRICULTURAL SULFONILE AND COMBINATIONS OILS.
US20110053776A1 (en) * 2009-09-01 2011-03-03 Bahr James T Blends of micro-encapsulated pesticide formulations
CN101715778A (en) * 2009-12-08 2010-06-02 安徽丰乐农化有限责任公司 Fenoxaprop.Flucarbazone composite herbicide
GB2483050B (en) * 2010-08-17 2012-12-19 Rotam Agrochem Int Co Ltd Herbicidal compositions
BR112013006341A2 (en) * 2010-09-17 2016-06-21 Dow Agrosciences Llc liquid agricultural formulations with improved stability
CN102057900B (en) * 2011-01-26 2013-05-01 河北博嘉农业有限公司 Thidiazuron suspension agent
RU2460296C1 (en) * 2011-05-03 2012-09-10 Михаил Аркадьевич Ершов Method of stimulation of seed germination
RU2504154C2 (en) * 2011-05-12 2014-01-20 Федеральное государственное бюджетное образовательное учреждение высшего профессионального образования "Чувашский государственный педагогический университет им. И.Я. Яковлева" Stimulant for presowing treatment of grain crop seeds
GB201109239D0 (en) * 2011-06-01 2011-07-13 Syngenta Participations Ag Herbicidal compositions
RU2462034C1 (en) * 2011-08-12 2012-09-27 Михаил Аркадьевич Ершов Method of obtaining stimulator of grain crops
CN103102307A (en) * 2013-03-04 2013-05-15 黑龙江大学 Method for synthesizing tolfenpyrad
EP3081550A4 (en) * 2013-12-11 2017-04-26 Oxiteno S.A. Industria e Comercio Polycarboxilic acid alkyl ester derived from branched and linear alcohol of plant origin, and use of an alkyl ester in agrochemical formulations
GB201501793D0 (en) * 2015-02-03 2015-03-18 Eden Research Plc Encapsulation of high potency active agents
CR20180248A (en) * 2016-01-21 2018-07-31 Upl Ltd AN IMPROVED HERBICIAL FORMULATION
US12004509B2 (en) * 2016-11-18 2024-06-11 Indorama Ventures Oxides Australia Pty Limited Co-formulation comprising a plant growth regulator and an oil, and methods of preparing and using said co-formulation
CN108575993A (en) * 2018-04-19 2018-09-28 河北威远生物化工有限公司 A kind of dispersible micro-capsule oil-suspending agent of glufosinate-ammonium and preparation method thereof
CN112437606B (en) 2018-06-05 2025-03-28 孟山都技术公司 Herbicide composition
JP2021527035A (en) * 2018-06-05 2021-10-11 モンサント テクノロジー エルエルシー Herbicide composition
CN109497057B (en) * 2019-01-02 2020-02-21 中国农业大学 Abamectin B2 microcapsule suspension for controlling root-knot nematode and preparation method thereof
WO2022034533A1 (en) * 2020-08-13 2022-02-17 Coromandel International Limited Insecticidal composition

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4285720A (en) * 1972-03-15 1981-08-25 Stauffer Chemical Company Encapsulation process and capsules produced thereby
US4157983A (en) * 1977-07-28 1979-06-12 Champion International Corporation Process for production of encapsulated water-dispersible materials
US4956129A (en) * 1984-03-30 1990-09-11 Ici Americas Inc. Microencapsulation process
US4534783A (en) * 1984-01-03 1985-08-13 Monsanto Co. High concentration encapsulation of water soluble-materials
US5700475A (en) * 1995-12-29 1997-12-23 Monsanto Company Stabilized pesticidal compositions and their use
DE69713885D1 (en) * 1996-04-16 2002-08-14 Du Pont HERBICIDAL MIXTURES
ATE251839T1 (en) * 1996-12-31 2003-11-15 Syngenta Ltd NEW PROCESS FOR WATER-IN-OIL MICRO-ENCAPSULATION AND THE MICRO-CAPSULES AVAILABLE AFTER IT
DE10022989A1 (en) * 2000-05-11 2001-11-22 Aventis Cropscience Gmbh Use of enveloped agrochemical, especially herbicide, safener, growth regulator, insecticide or fungicide, for suppression of antagonistic interactions in agrochemical mixtures
ES2235642B2 (en) * 2003-12-18 2006-03-01 Gat Formulation Gmbh CONTINUOUS MULTI-MICROENCAPSULATION PROCESS FOR THE IMPROVEMENT OF STABILITY AND STORAGE OF BIOLOGICALLY ACTIVE INGREDIENTS.
EP1844653B1 (en) * 2006-03-30 2017-07-26 GAT Microencapsulation GmbH Novel agrochemical formulations containing microcapsules

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO2008089890A2 *

Also Published As

Publication number Publication date
AU2008209129A1 (en) 2008-07-31
KR20090113864A (en) 2009-11-02
EP1952688A1 (en) 2008-08-06
BRPI0807401A2 (en) 2014-05-27
UA96009C2 (en) 2011-09-26
MX2009007824A (en) 2009-07-30
AR064982A1 (en) 2009-05-06
US20080176746A1 (en) 2008-07-24
IL199960A0 (en) 2010-04-15
WO2008089890A2 (en) 2008-07-31
EA200900855A1 (en) 2009-12-30
JP2010516720A (en) 2010-05-20
WO2008089890A3 (en) 2009-05-22
CA2676210A1 (en) 2008-07-31
CN101621924A (en) 2010-01-06
EA013316B1 (en) 2010-04-30
ECSP099527A (en) 2009-08-28

Similar Documents

Publication Publication Date Title
EP2111104A2 (en) Oil suspension concentrate with micro-encapsulated agrochemical active ingredients
EP2048945A2 (en) New microemulsifiable concentrates
EP1096855B1 (en) Herbicides with substituted phenylsulfonylureas for controlling weeds in rice
EP1415537B1 (en) Combinations of herbicides and safeners
EP1926379A2 (en) Novel sulfonamide-containing solid formulations
JP5188974B2 (en) Use of lactate esters to improve the effectiveness of pesticides
WO2001097615A2 (en) Herbicidal agent
EP1523235A1 (en) Liquid adjuvants
EP2117317A2 (en) Penetration enhancer for herbicides and safeners
EP1926378A1 (en) Storage-stable sulphonamide formulations
DE10231615A1 (en) Fixed adjuvants
WO2008017377A2 (en) New microemulsion concentrates
EP1844654A1 (en) Penetration enhancer for agrochemicals
DE10258856A1 (en) Liquid agrochemical adjuvant comprising alkoxylated polyalkyl-phenol derivative surfactant(s) and fatty acid ester(s), having synergistic effect in improving effect of active agents, especially herbicides
EP1836894A1 (en) Novel sulfonamide-containing solid formulations
BR122016002407B1 (en) Herbicidal compositions including diflufenican, flurtamone and flufenacet, process for combating unwanted plant growth and use

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Kind code of ref document: A2

Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MT NL NO PL PT RO SE SI SK TR

17P Request for examination filed

Effective date: 20091123

RBV Designated contracting states (corrected)

Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MT NL NO PL PT RO SE SI SK TR

DAX Request for extension of the european patent (deleted)
STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN

18D Application deemed to be withdrawn

Effective date: 20120801