DE4019362A1 - HERBICIDE COMPOSITIONS BASED ON N-PHOSPHONOMETHYL GLYCIN AND THEIR USE - Google Patents
HERBICIDE COMPOSITIONS BASED ON N-PHOSPHONOMETHYL GLYCIN AND THEIR USEInfo
- Publication number
- DE4019362A1 DE4019362A1 DE4019362A DE4019362A DE4019362A1 DE 4019362 A1 DE4019362 A1 DE 4019362A1 DE 4019362 A DE4019362 A DE 4019362A DE 4019362 A DE4019362 A DE 4019362A DE 4019362 A1 DE4019362 A1 DE 4019362A1
- Authority
- DE
- Germany
- Prior art keywords
- glyphosate
- compositions according
- amount
- phosphonomethylglycine
- active
- 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- Withdrawn
Links
- 239000000203 mixture Substances 0.000 title claims description 47
- 239000004009 herbicide Substances 0.000 title claims description 13
- 230000002363 herbicidal effect Effects 0.000 title claims description 11
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 title 2
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 claims description 68
- 239000005562 Glyphosate Substances 0.000 claims description 36
- 229940097068 glyphosate Drugs 0.000 claims description 36
- 239000004094 surface-active agent Substances 0.000 claims description 25
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 9
- 239000004480 active ingredient Substances 0.000 claims description 8
- 239000013543 active substance Substances 0.000 claims description 7
- 150000003863 ammonium salts Chemical class 0.000 claims description 7
- NUFNQYOELLVIPL-UHFFFAOYSA-N acifluorfen Chemical compound C1=C([N+]([O-])=O)C(C(=O)O)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 NUFNQYOELLVIPL-UHFFFAOYSA-N 0.000 claims description 6
- 239000000243 solution Substances 0.000 claims description 6
- 239000012190 activator Substances 0.000 claims description 5
- 239000007788 liquid Substances 0.000 claims description 5
- 239000007921 spray Substances 0.000 claims description 5
- 239000000080 wetting agent Substances 0.000 claims description 5
- XMTQQYYKAHVGBJ-UHFFFAOYSA-N 3-(3,4-DICHLOROPHENYL)-1,1-DIMETHYLUREA Chemical compound CN(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 XMTQQYYKAHVGBJ-UHFFFAOYSA-N 0.000 claims description 4
- 239000002890 Aclonifen Substances 0.000 claims description 4
- 239000005484 Bifenox Substances 0.000 claims description 4
- 239000005507 Diflufenican Substances 0.000 claims description 4
- 239000005510 Diuron Substances 0.000 claims description 4
- SUSRORUBZHMPCO-UHFFFAOYSA-N MC-4379 Chemical compound C1=C([N+]([O-])=O)C(C(=O)OC)=CC(OC=2C(=CC(Cl)=CC=2)Cl)=C1 SUSRORUBZHMPCO-UHFFFAOYSA-N 0.000 claims description 4
- CHNUNORXWHYHNE-UHFFFAOYSA-N Oxadiazon Chemical compound C1=C(Cl)C(OC(C)C)=CC(N2C(OC(=N2)C(C)(C)C)=O)=C1Cl CHNUNORXWHYHNE-UHFFFAOYSA-N 0.000 claims description 4
- 229940100389 Sulfonylurea Drugs 0.000 claims description 4
- DDBMQDADIHOWIC-UHFFFAOYSA-N aclonifen Chemical compound C1=C([N+]([O-])=O)C(N)=C(Cl)C(OC=2C=CC=CC=2)=C1 DDBMQDADIHOWIC-UHFFFAOYSA-N 0.000 claims description 4
- 239000000654 additive Substances 0.000 claims description 4
- VGPYEHKOIGNJKV-UHFFFAOYSA-N asulam Chemical compound COC(=O)NS(=O)(=O)C1=CC=C(N)C=C1 VGPYEHKOIGNJKV-UHFFFAOYSA-N 0.000 claims description 4
- WYEHFWKAOXOVJD-UHFFFAOYSA-N diflufenican Chemical compound FC1=CC(F)=CC=C1NC(=O)C1=CC=CN=C1OC1=CC=CC(C(F)(F)F)=C1 WYEHFWKAOXOVJD-UHFFFAOYSA-N 0.000 claims description 4
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 4
- 159000000000 sodium salts Chemical class 0.000 claims description 4
- CHZCERSEMVWNHL-UHFFFAOYSA-N 2-hydroxybenzonitrile Chemical compound OC1=CC=CC=C1C#N CHZCERSEMVWNHL-UHFFFAOYSA-N 0.000 claims description 3
- CAAMSDWKXXPUJR-UHFFFAOYSA-N 3,5-dihydro-4H-imidazol-4-one Chemical compound O=C1CNC=N1 CAAMSDWKXXPUJR-UHFFFAOYSA-N 0.000 claims description 3
- 241000196324 Embryophyta Species 0.000 claims description 3
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 3
- 239000005977 Ethylene Substances 0.000 claims description 3
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 3
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims description 3
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 3
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 claims description 2
- 239000002794 2,4-DB Substances 0.000 claims description 2
- 239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 claims description 2
- PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 claims description 2
- UWHURBUBIHUHSU-UHFFFAOYSA-N 2-[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamoylsulfamoyl]benzoic acid Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 UWHURBUBIHUHSU-UHFFFAOYSA-N 0.000 claims description 2
- CABMTIJINOIHOD-UHFFFAOYSA-N 2-[4-methyl-5-oxo-4-(propan-2-yl)-4,5-dihydro-1H-imidazol-2-yl]quinoline-3-carboxylic acid Chemical compound N1C(=O)C(C(C)C)(C)N=C1C1=NC2=CC=CC=C2C=C1C(O)=O CABMTIJINOIHOD-UHFFFAOYSA-N 0.000 claims description 2
- UPMXNNIRAGDFEH-UHFFFAOYSA-N 3,5-dibromo-4-hydroxybenzonitrile Chemical compound OC1=C(Br)C=C(C#N)C=C1Br UPMXNNIRAGDFEH-UHFFFAOYSA-N 0.000 claims description 2
- 239000004254 Ammonium phosphate Substances 0.000 claims description 2
- 101000742062 Bos taurus Protein phosphatase 1G Proteins 0.000 claims description 2
- 239000005489 Bromoxynil Substances 0.000 claims description 2
- 239000005981 Imazaquin Substances 0.000 claims description 2
- 125000002252 acyl group Chemical group 0.000 claims description 2
- 239000000853 adhesive Substances 0.000 claims description 2
- 230000001070 adhesive effect Effects 0.000 claims description 2
- 125000002947 alkylene group Chemical group 0.000 claims description 2
- -1 ammo niumsulfamat Chemical compound 0.000 claims description 2
- 229910000148 ammonium phosphate Inorganic materials 0.000 claims description 2
- 235000019289 ammonium phosphates Nutrition 0.000 claims description 2
- SOIFLUNRINLCBN-UHFFFAOYSA-N ammonium thiocyanate Chemical compound [NH4+].[S-]C#N SOIFLUNRINLCBN-UHFFFAOYSA-N 0.000 claims description 2
- 239000002518 antifoaming agent Substances 0.000 claims description 2
- 239000007864 aqueous solution Substances 0.000 claims description 2
- MXWJVTOOROXGIU-UHFFFAOYSA-N atrazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)C)=N1 MXWJVTOOROXGIU-UHFFFAOYSA-N 0.000 claims description 2
- 239000008139 complexing agent Substances 0.000 claims description 2
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 claims description 2
- 239000012895 dilution Substances 0.000 claims description 2
- 238000010790 dilution Methods 0.000 claims description 2
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims description 2
- 239000005556 hormone Substances 0.000 claims description 2
- 229940088597 hormone Drugs 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 239000003112 inhibitor Substances 0.000 claims description 2
- NRXQIUSYPAHGNM-UHFFFAOYSA-N ioxynil Chemical compound OC1=C(I)C=C(C#N)C=C1I NRXQIUSYPAHGNM-UHFFFAOYSA-N 0.000 claims description 2
- 125000001325 propanoyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 2
- ODCWYMIRDDJXKW-UHFFFAOYSA-N simazine Chemical compound CCNC1=NC(Cl)=NC(NCC)=N1 ODCWYMIRDDJXKW-UHFFFAOYSA-N 0.000 claims description 2
- 239000002904 solvent Substances 0.000 claims description 2
- 239000003381 stabilizer Substances 0.000 claims description 2
- YROXIXLRRCOBKF-UHFFFAOYSA-N sulfonylurea Chemical class OC(=N)N=S(=O)=O YROXIXLRRCOBKF-UHFFFAOYSA-N 0.000 claims description 2
- 150000003918 triazines Chemical class 0.000 claims description 2
- 238000000034 method Methods 0.000 claims 2
- 239000005588 Oxadiazon Substances 0.000 claims 1
- 230000000996 additive effect Effects 0.000 claims 1
- VJYIFXVZLXQVHO-UHFFFAOYSA-N chlorsulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)Cl)=N1 VJYIFXVZLXQVHO-UHFFFAOYSA-N 0.000 claims 1
- 238000005260 corrosion Methods 0.000 claims 1
- 230000007797 corrosion Effects 0.000 claims 1
- 150000003839 salts Chemical class 0.000 description 10
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 7
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 7
- 235000011130 ammonium sulphate Nutrition 0.000 description 7
- 239000012141 concentrate Substances 0.000 description 7
- JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical class CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 7
- 150000001412 amines Chemical class 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 238000009472 formulation Methods 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- ZTMKADLOSYKWCA-UHFFFAOYSA-N lenacil Chemical compound O=C1NC=2CCCC=2C(=O)N1C1CCCCC1 ZTMKADLOSYKWCA-UHFFFAOYSA-N 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- 240000006995 Abutilon theophrasti Species 0.000 description 1
- GEHMBYLTCISYNY-UHFFFAOYSA-N Ammonium sulfamate Chemical compound [NH4+].NS([O-])(=O)=O GEHMBYLTCISYNY-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 241000207783 Ipomoea Species 0.000 description 1
- 235000021506 Ipomoea Nutrition 0.000 description 1
- 235000001855 Portulaca oleracea Nutrition 0.000 description 1
- 241000219304 Portulacaceae Species 0.000 description 1
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000001166 ammonium sulphate Substances 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 125000004437 phosphorous atom Chemical group 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000007928 solubilization Effects 0.000 description 1
- 238000005063 solubilization Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- 150000003456 sulfonamides Chemical class 0.000 description 1
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical class NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 description 1
- 210000002105 tongue Anatomy 0.000 description 1
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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
- A01N57/20—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing acyclic or cycloaliphatic radicals
-
- 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
Landscapes
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Dispersion Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Toxicology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
Die Erfindung betrifft neue konzentrierte Formulierungen auf der Basis von N-Phosphonomethylglycin und/oder Verbindungen mit N-Phosphonomethylglycylgruppen.The invention relates to novel concentrated formulations the base of N-phosphonomethylglycine and / or compounds with N-phosphonomethylglycyl groups.
N-Phosphonomethylglycin, das auch als Glyphosat bezeichnet wird, sowie dessen analoge Verbindungen, ihre herbiciden Eigenschaften und diese Verbindungen enthaltende Formulie rungen sind insbesondere in US 37 99 758 A beschrieben. Obwohl zahlreiche wasserlösliche und nicht wasserlösliche Glyphosatderivate bekannt sind, verwendet man im allgemeinen vorzugsweise die wasserlöslichen Derivate; aus diesem Grund wurden generell die Salze des N-Phosphonomethylglycins und speziell das Isopropylammoniumsalz entwickelt und kommerzia lisiert.N-phosphonomethylglycine, also referred to as glyphosate and their analogous compounds, their herbicides Properties and formulations containing these compounds ments are described in particular in US 37 99 758 A. Although numerous water-soluble and not water-soluble Glyphosate derivatives are known, are used in general preferably the water-soluble derivatives; for this reason were generally the salts of N-phosphonomethylglycine and specifically, the isopropylammonium salt is developed and commercially lisiert.
Aus EP 2 90 416 A sind Konzentrate auf der Basis von Salzen des N-Phosphonomethylglycins bekannt, die das N-Phosphono methylglycin in der Säureform enthalten, wobei dieses N-Phosphonomethylglycin und/oder seine Derivate jedoch in allen Fällen in löslicher oder solubilisierter Form enthal ten sind; diese Konzentrate sind gekennzeichnet durch die Anwesenheit eines alkoxylierten Amins speziellen Typs. Die ses alkoxylierte Amin darf höchstens 12 Alkoxygruppen im Molekül aufweisen, muß die Eigenschaften eines grenzflächen aktiven Mittels besitzen und muß die herbicide Wirksamkeit der N-Phosphonomethylglycin-Derivate begünstigen. Es kann in herkömmlichen N-Phosphonomethylglyin-Formulierungen in ge ringerer Menge als die herkömmlichen grenzflächenaktiven Mittel eingesetzt werden, zumindest im Fall der Konzentrate, die zur Freilandanwendung in Form verdünnter Spritzbrühen in einer Ausbringmenge von 100 bis 600 l/ha bestimmt sind. Wenn die Zusammensetzungen auf der Basis von N-Phosphonomethyl glycin ein Ammoniumsalz wie Ammoniumsulfat enthalten, ist das gemäß EP 2 90 416 A eingesetzte alkoxylierte Amin ein ethoxyliertes Amin, das nur 2 Ethoxygruppen im Molekül auf weist.From EP 2 90 416 A are concentrates based on salts of N-phosphonomethylglycine known as the N-phosphono methylglycine contained in the acid form, this being N-phosphonomethylglycine and / or its derivatives, however, in all cases in soluble or solubilized form are; These concentrates are characterized by Presence of an alkoxylated amine of a specific type. the This alkoxylated amine may contain at most 12 alkoxy groups in the Having molecules must have the properties of an interface active agent and must have the herbicidal activity favoring the N-phosphonomethylglycine derivatives. It can be in conventional N-phosphonomethylglyin formulations in ge lower amount than the conventional surfactant Be used, at least in the case of concentrates, for field application in the form of dilute spray mixtures in an application rate of 100 to 600 l / ha are determined. If the compositions based on N-phosphonomethyl Glycine containing an ammonium salt such as ammonium sulfate is the alkoxylated amine used according to EP 2 90 416 A ethoxylated amine containing only 2 ethoxy groups in the molecule has.
Der Erfindung liegt die Aufgabe zugrunde, konzentrierte Zu sammensetzungen bzw. Formulierungen, d.h. Konzentrate, auf der Basis von N-Phosphonomethylglycin oder Derivaten davon und insbesondere auf der Basis entsprechender wasserlösli cher Salze anzugeben. Ferner sollen Konzentrate auf der Ba sis von N-Phosphonomethylglycin oder seinen Derivaten ange geben werden, mit denen verdünnte Spritzbrühen mit guter herbicider Wirksamkeit hergestellt werden können. Die Kon zentrate auf der Basis von Salzen des N-Phosphonomethylgly cins sollen ferner auch neuartige grenzflächenaktive Mittel enthalten, welche die biologische Wirksamkeit begünstigen. Darüber hinaus sollen Konzentrate auf der Basis von Salzen des N-Phosphonomethylglycins angegeben werden, die grenz flächenaktive Mittel mit verbesserter Solubilisierungswir kung enthalten. Schließlich sollen Konzentrate auf der Basis von Salzen des N-Phosphonomethylglycins angegeben werden, die neuartige grenzflächenaktive Mittel enthalten, die in konzentrierten Lösungen mit bestimmten anorganischen Salzen und insbesondere mit Ammoniumsulfat verträglich sind. The invention is based on the object, concentrated Zu Compositions or formulations, i. Concentrates, on the base of N-phosphonomethylglycine or derivatives thereof and in particular based on corresponding water-soluble specify salts. Furthermore, concentrates on the Ba sis of N-phosphonomethylglycine or its derivatives will give, with which dilute spray liquors with good herbicidal activity can be produced. The Kon based on salts of N-phosphonomethylgly cins are also thought to be novel surfactants contain, which favor the biological effectiveness. In addition, concentrates based on salts of N-phosphonomethylglycine, the limit surfactants with improved solubilization properties kung contained. Finally, concentrates are based on salts of N-phosphonomethylglycine, contain the novel surfactants that are used in concentrated solutions with certain inorganic salts and especially compatible with ammonium sulphate.
Die Aufgabe wird anspruchsgemäß gelöst. Die Unteransprüche betreffen vorteilhafte Ausführungsformen.The task is solved according to the claim. The dependent claims relate to advantageous embodiments.
Die erfindungsgemäßen Zusammensetzungen sind flüssig und be stehen aus wäßrigen Lösungen, die enthalten:The compositions of the invention are liquid and be consist of aqueous solutions containing:
- a) N-Phosphonomethylglycin und/oder eines oder mehrere Deri vate davon in einer Menge von mindestens 40 g Glyphosat- Aquivalent/l unda) N-phosphonomethylglycine and / or one or more deri of which at least 40 g glyphosate Equivalent / l and
-
b) ein grenzflächenaktives Mittel mit Aktivatoreigenschaften
der Formel
in der bedeuten:
R geradkettiges oder verzweigtes C8-22-Alkyl oder C8-22-Alkenyl,
A Alkylen, vorzugsweise Ethylen oder Propylen,
R¹ Wasserstoff oder Acyl, wie Formyl, Acetyl und Propanoyl (CH₃-CH₂-CO) und
n, n′ und n′′ ganze Zahlen derart, daß die Summe n+n′+n′′ 1 bis 15 und vorzugsweise 3 bis 12 beträgt.b) a surfactant having activator properties of the formula in which mean
R is straight-chain or branched C 8-22 -alkyl or C 8-22 -alkenyl,
A is alkylene, preferably ethylene or propylene,
R¹ is hydrogen or acyl, such as formyl, acetyl and propanoyl (CH₃-CH₂-CO) and
n, n 'and n''are integers such that the sum n + n' + n '' is 1 to 15 and preferably 3 to 12.
Anstelle eines einzigen grenzflächenaktiven Mittels b) kön nen im Rahmen der Erfindung auch entsprechende Gemische ein gesetzt werden, bei denen im Mittel R, n, n′ und n′′ den obi gen Definitionen entsprechen. Instead of a single surfactant b) kön NEN in the context of the invention also corresponding mixtures are set, in which on average R, n, n 'and n' 'the obi correspond to definitions.
Unter Derivaten des N-Phosphonomethylglycins werden Verbin dungen verstanden, welche die GruppierungAmong derivatives of N-phosphonomethylglycine be verbin understood the grouping
enthalten, wobei das Stickstoffatom eine freie Valenz und das Phosphoratom zwei freie Valenzen aufweist, vorzugsweise als Salze, Ester oder Amide, wobei diese Definitionen weit auszulegen sind, beispielsweise derart, daß die Sulfonamide mit umfaßt sind.contain, wherein the nitrogen atom a free valence and the phosphorus atom has two free valences, preferably as salts, esters or amides, these definitions being far are interpreted, for example, such that the sulfonamides with are included.
Die angegebenen Prozentwerte sind, falls nichts anderes er wähnt ist, massebezogen (Masse-%). Unter Glyphosat-Äquiva lent wird ferner die entsprechende Menge Produkt verstanden, als ob das gesamte Derivat des N-Phosphonomethylglycins in Form von N-Phosphonomethylglycin selbst vorläge.The percentages given are, if not otherwise mentions is mass related (mass%). Under glyphosate equivalents lent is also understood to mean the corresponding amount of product, as if the entire derivative of N-phosphonomethylglycine in Form of N-phosphonomethylglycine itself.
Besonders vorteilhafte erfindungsgemäße konzentrierte Zusam mensetzungen sind die oben beschriebenen Zusammensetzungen, die ferner durch eines oder mehrere der nachstehend angege benen Merkmale gekennzeichnet sind:Particularly advantageous concentrated Zusam invention Compositions are the compositions described above, further characterized by one or more of the following characteristics are marked:
- a) Die Menge an N-Phosphonomethylglycin oder Derivaten davon überschreitet die Löslichkeitsgrenze im betreffenden Me dium nicht und liegt vorzugsweise im Bereich von 60 bis 200 g/l und noch bevorzugter im Bereich von 90 bis 150 g/l.a) The amount of N-phosphonomethylglycine or derivatives thereof exceeds the solubility limit in the Me in question dium not and is preferably in the range of 60 to 200 g / l and more preferably in the range of 90 to 150 g / l.
- b) die konzentrierte Lösung enthält ein Ammoniumsalz (NH4- Salz), wie Ammoniumnitrat, Ammoniumphosphat, Ammoniumsul famat, Ammoniumthiocyanat oder vorzugsweise das Sulfat, in einer Menge von 50 bis 400 g/l und vorzugsweise in einer Menge von 100 bis 300 g/l;b) the concentrated solution contains an ammonium salt (NH 4 salt), such as ammonium nitrate, ammonium phosphate, ammonium sulphamate, ammonium thiocyanate or preferably the sulphate, in an amount of 50 to 400 g / l and preferably in an amount of 100 to 300 g / l;
- c) die konzentrierten Zusammensetzungen sind zur Verdünnung durch den Anwender, besonders in der Landwirtschaft, be stimmt, wobei diese Zusammensetzungen in Wasser enthal tende Behälter in einer Menge eingebracht werden, daß Spritzbrühen resultieren, die in einer Ausbringmenge von 100 bis 600 l/ha angewandt werden können, was einer Aus bringmenge an Wirkstoff von 0,125 bis 4,5 kg/ha ent spricht;c) the concentrated compositions are for dilution by the user, especially in agriculture, be true, these compositions contained in water tende container are introduced in an amount that Spray mixtures result in an application rate of 100 to 600 l / ha can be applied, which is an off bring amount of active ingredient from 0.125 to 4.5 kg / ha ent speaks;
- d) das Massenverhältnis von Glyphosat-Äquivalent zu grenz flächenaktivem Mittel liegt im Bereich von 0,6 bis 6 und vorzugsweise im Bereich von 1 bis 3;d) the mass ratio of glyphosate equivalent to limit Areal active agent is in the range of 0.6 to 6 and preferably in the range of 1 to 3;
- e) das Lösungsmittel ist Wasser.e) the solvent is water.
Die oben angegebene relativ hohe Menge an grenzflächenakti vem Mittel betrifft das grenzflächenaktive Mittel mit Akti vatoreigenschaften bezüglich der biologischen bzw. herbici den Wirksamkeit entsprechender Zusammensetzungen; die erfin dungsgemäßen Zusammensetzungen können darüber hinaus, wie im folgenden näher erläutert ist, beliebige weitere Bestand teile enthalten, insbesondere grenzflächenaktive Mittel ver schiedenster Art mit Netzmitteleigenschaften; diese grenz flächenaktiven Mittel werden ferner in Mengen eingesetzt, die erheblich kleiner sind als die Aktivatordosis.The above indicated relatively high amount of surface active agent From the mean, the surfactant relates to Akti vatoreigenschaften concerning the biological or herbici the effectiveness of corresponding compositions; the inventor In addition, compositions according to the invention can, as in The following is explained in more detail, any further stock parts, in particular surfactants ver most diverse type with wetting agent properties; this border surfactants are also used in quantities which are considerably smaller than the activator dose.
Die erfindungsgemäßen flüssigen konzentrierten Zusammenset zungen werden gewöhnlich durch einfaches Mischen der Be standteile hergestellt.The liquid concentrated compositions according to the invention Tongues are usually prepared by simply mixing the Be manufactured components.
Die erfindungsgemäßen Zusammensetzungen enthalten gewöhnlich 5 bis 25% und vorzugsweise 7 bis 20% Wirkstoffe (Herbici de), 0,5 bis 40% und vorzugsweise 10 bis 20% eines oder mehrerer grenzflächenaktiver Mittel mit Aktivatoreigenschaf ten, 10 bis 50 und vorzugsweise 20 bis 30% eines Ammonium salzes als Hilfsmittel und 0,1 bis 10% eines oder mehrerer grenzflächenaktiver Mittel mit Netzmitteleigenschaften sowie 0 bis 30% geeignete Zusätze wie Antischaummittel, Korro sionsinhibitoren, Komplexbildner, Stabilisierungsmittel, Penetrationsmittel, Adhäsive und dergl. Die erfindungs gemäßen Zusammensetzungen können ferner beliebige feste oder flüssige Additive enthalten, wie sie herkömmlicherweise bei entsprechenden Formulierungen zur Anwendung kommen.The compositions of the invention usually contain 5 to 25% and preferably 7 to 20% active ingredients (Herbici de), 0.5 to 40% and preferably 10 to 20% of one or several surfactants with Aktivatoreigenschaf 10 to 50 and preferably 20 to 30% of an ammonium salts as auxiliaries and 0.1 to 10% of one or more Surfactant with wetting agent properties as well 0 to 30% suitable additives such as antifoam, Korro anion inhibitors, complexing agents, stabilizers, Penetrating agents, adhesives and the like. The Invention Compositions according to the invention can furthermore be any solid or contain liquid additives, as they are commonly used in corresponding formulations are used.
Wie erwähnt, können die erfindungsgemäßen konzentrierten Zu sammensetzungen neben dem oben definierten grenzflächenakti ven Mittel mit Aktivatoreigenschaften ferner noch ein oder mehrere andere grenzflächenaktive Mittel enthalten. Als grenzflächenaktive Mittel können Netzmittel ionischen oder nichtionischen Typs sowie Gemische solcher grenzflächenakti ver Mittel eingesetzt werden. Hierzu gehören beispielsweise Polykondensationsprodukte von Ethylenoxid mit Fettalkoholen, Fettsäuren, Fettaminen oder substituierten Phenolen, insbe sondere Alkylphenolen oder Arylphenolen, Salze von Sulfo bernsteinsäureestern, Taurinderivate, insbesondere Alkyltau rate, Phosphorsäureester polyethoxylierter Alkohole oder Phenole, Ester von Fettsäuren und Polyolen sowie etwa Deri vate der oben genannten Verbindungen mit Sulfatgruppen, Sul fonatgruppen und Phosphatgruppen.As mentioned, the concentrated Zu Compositions in addition to the surface area defined above Furthermore, agents with activator properties are still on or contain several other surfactants. When Surfactants can be ionic or wetting agents nonionic type as well as mixtures of such surface active agents ver means are used. These include, for example Polycondensation products of ethylene oxide with fatty alcohols, Fatty acids, fatty amines or substituted phenols, esp special alkylphenols or arylphenols, salts of sulfo succinic acid esters, taurine derivatives, especially alkyltau rate, phosphoric acid esters of polyethoxylated alcohols or Phenols, esters of fatty acids and polyols, and about Deri vate of the above compounds with sulfate groups, Sul fonate groups and phosphate groups.
Neben dem N-Phosphonomethylglycin und/oder seinen Derivaten können die erfindungsgemäßen Zusammensetzungen ferner auch andere, bekannte Wirkstoffe mit herbiciden Eigenschaften oder pflanzenwachstumsregulierender Wirkung enthalten.In addition to the N-phosphonomethylglycine and / or its derivatives the compositions according to the invention may also be used other known active ingredients with herbicidal properties or plant growth regulating activity.
Herbicide Wirkstoffe, die im Gemisch mit Glyphosat-Derivaten in den erfindungsgemäßen Zusammensetzungen vorliegen können, sind beispielsweise Acifluorfen oder das Natriumsalz davon, Aclonifen, Bifenox, Diflufenican, Asulam, Triazine, insbe sondere Simazin und Atrazin, Diuron sowie Oxadiazon, Herbi cide vom Hormontyp oder vom Phenoxytyp, insbesondere 2,4-D, 2,4-DB und MCPP, Hydroxybenzonitrile, insbesondere Bromoxy nil und Ioxynil, Imidazolinone, insbesondere Imazaquin und Imazapur, sowie etwa Sulfonylharnstoffe, insbesondere Chlor sulfuron und Metsulfuron. Die angegebenen Namen entsprechen den genormten chemischen Kurzbezeichnungen für diese Herbi cide.Herbicide active ingredients mixed with glyphosate derivatives may be present in the compositions according to the invention, are, for example, acifluorfen or the sodium salt thereof, Aclonifen, Bifenox, Diflufenican, Asulam, Triazines, esp especially simazine and atrazine, diuron and oxadiazone, Herbi cide of the hormone type or of the phenoxy type, in particular 2,4-D, 2,4-DB and MCPP, hydroxybenzonitriles, especially bromoxy nil and ioxynil, imidazolinones, in particular imazaquin and Imazapur, as well as sulfonylureas, especially chlorine sulfurone and metsulfuron. The specified names correspond the standardized chemical abbreviations for these Herbi cide.
Diese Herbicide werden zumeist in einer Menge von 1 bis 400 Masseteilen auf 100 Masseteile Glyphosat bzw. Glyphosat- Aquivalente eingesetzt. Durch den Bezug auf die Glyphosat- Äquivalentmenge wird die Berechnung der entsprechenden Men genanteile so vorgenommen, als ob sämtliche Derivate des Glyphosats in Form von N-Phosphonomethylglycin selbst vor lägen.These herbicides are mostly in the range of 1 to 400 Parts by weight per 100 parts by weight of glyphosate or glyphosate Used equivalents. By referring to the glyphosate Equivalent amount will be the calculation of the corresponding menu genanteile made as if all derivatives of the Glyphosats in the form of N-phosphonomethylglycine itself before BE REDUCED.
Im einzelnen werden, wenn von Glyphosat verschiedene Wirk stoffe eingesetzt und mit Glyphosat gemischt werden, folgen de Mengenverhältnisse im allgemeinen angewandt, wobei das Massenverhältnis rp definiert ist alsSpecifically, when different from glyphosate action used and mixed with glyphosate, follow de proportions generally applied, the Mass ratio rp is defined as
Allgemein enthalten die erfindungsgemäßen herbiciden Zusam mensetzungen gewöhnlich etwa 0,05 bis etwa 95% eines oder mehrerer herbicider Wirkstoffe, ungefähr 1 bis ungefähr 95% eines oder mehrerer flüssiger Träger und ggf. etwa 0,1 bis etwa 50% eines oder mehrerer grenzflächenaktiver Mittel.In general, the inventive herbicidal Zusam contain usually about 0.05 to about 95% of one or more several herbicidal agents, from about 1 to about 95% one or more liquid carriers and possibly about 0.1 to about 50% of one or more surfactants.
Die folgenden Beispiele erläutern die Erfindung und insbe sondere erfindungsgemäße Lösungen und ihre Anwendung. In den Beispielen ist der Wirkstoff N-Phosphonomethylglycin in Form des Isopropylammoniumsalzes.The following examples illustrate the invention and esp special solutions according to the invention and their application. In the Examples are the active ingredient N-phosphonomethylglycine in the form of the isopropylammonium salt.
Das bei diesem Beispiel eingesetzte grenzflächenaktive Mit tel war eine Verbindung der FormelThe interfacial agent used in this example tel was a compound of the formula
mit n+n′+n′′ = 3.with n + n '+ n' '= 3.
Diese Lösungen werden in einer Menge von 2,5 und 5 l in 300 l Wasser verdünnt; die so erhaltenen Spritzbrühen werden durch Spritzen auf verschiedene Unkräuter angewandt. These solutions are in an amount of 2.5 and 5 l in Diluted 300 liters of water; become the spray mixtures thus obtained applied by spraying on different weeds.
Die Zusammensetzungen der Beispiele 1 bis 4 besitzen bei einer angewandten Wirkstoffdosis von 250 g/l, bezogen auf N- Phosphonomethylglycin, gegenüber verschiedenen Unkräutern, insbesondere Ipomoea, Portulak und Abutilon theophrasti, eine deutlich höhere Wirksamkeit als Handelsprodukte und insbesondere das unter der Bezeichnung Round-up im Handel befindliche Produkt, das den gleichen Wirkstoff enthält, je doch zusammen mit gewöhnlichen grenzflächenaktiven Wirkstof fen.The compositions of Examples 1 to 4 have at an applied active substance dose of 250 g / l, based on N- Phosphonomethylglycine, against various weeds, especially Ipomoea, purslane and Abutilon theophrasti, a much higher effectiveness than commercial products and in particular that under the designation Round-up in the trade product containing the same active ingredient, each but together with ordinary surfactant fen.
Claims (19)
- a) N-Phosphonomethylglycin und/oder eines oder mehrere Derivate davon in einer Menge von mindestens 40 g Glyphosat-Äquivalent/l und
- b) ein grenzflächenaktives Mittel mit Aktivatoreigen
schaften der Formel
in der bedeuten:
R geradkettiges oder verzweigtes C8-22-Alkyl oder C8-22-Alkenyl,
A Alkylen, vorzugsweise Ethylen oder Propylen,
R¹ Wasserstoff oder Acyl, wie Formyl, Acetyl und Propanoyl und
n, n′ und n′′ ganze Zahlen derart, daß die Summe n+n′+n′′ 1 bis 15 beträgt.
- a) N-phosphonomethylglycine and / or one or more derivatives thereof in an amount of at least 40 g glyphosate equivalent / l and
- b) a surfactant having Aktivatoreigen properties of the formula in which mean
R is straight-chain or branched C 8-22 -alkyl or C 8-22 -alkenyl,
A is alkylene, preferably ethylene or propylene,
R¹ is hydrogen or acyl, such as formyl, acetyl and propanoyl and
n, n 'and n''are integers such that the sum n + n' + n '' is 1 to 15.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR8908433A FR2648316A1 (en) | 1989-06-20 | 1989-06-20 | HERBICIDE COMPOSITIONS BASED ON N-PHOSPHONOMETHYLGLYCIN AND THEIR USE |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE4019362A1 true DE4019362A1 (en) | 1991-01-03 |
Family
ID=9383094
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE4019362A Withdrawn DE4019362A1 (en) | 1989-06-20 | 1990-06-18 | HERBICIDE COMPOSITIONS BASED ON N-PHOSPHONOMETHYL GLYCIN AND THEIR USE |
Country Status (18)
| Country | Link |
|---|---|
| JP (1) | JPH0334901A (en) |
| KR (1) | KR910000016A (en) |
| AU (1) | AU5756590A (en) |
| BR (1) | BR9002986A (en) |
| CA (1) | CA2019087A1 (en) |
| DE (1) | DE4019362A1 (en) |
| DK (1) | DK149390A (en) |
| FR (1) | FR2648316A1 (en) |
| GB (1) | GB2233229B (en) |
| GR (1) | GR900100459A (en) |
| HU (1) | HUT54023A (en) |
| IE (1) | IE902130A1 (en) |
| IT (1) | IT1248734B (en) |
| LU (1) | LU87747A1 (en) |
| NL (1) | NL9001407A (en) |
| PT (1) | PT94414A (en) |
| SE (1) | SE9002166L (en) |
| ZA (1) | ZA904785B (en) |
Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1996025043A1 (en) * | 1995-02-13 | 1996-08-22 | Novartis Ag | Herbicidal composition and method of controlling weeds |
| WO1998024313A1 (en) * | 1996-12-06 | 1998-06-11 | Huntsman Surfactants Technology Corporation | Herbicidal compositions |
| WO1999013723A1 (en) * | 1997-09-17 | 1999-03-25 | American Cyanamid Company | Synergistic herbicidal methods and compositions |
| WO1999052367A1 (en) * | 1998-04-08 | 1999-10-21 | Aventis Cropscience Gmbh | Synergistic herbicidal agents based on leaf herbicides containing phosphorus, imidazolinones and hormone weed-killers |
| WO2001011957A1 (en) * | 1999-08-18 | 2001-02-22 | Huntsman Petrochemical Corporation | Polyether diamine-based surfactant adjuvants and compositions thereof |
| WO2002098221A1 (en) * | 2001-06-01 | 2002-12-12 | Huntsman Petrochemical Corporation | Adjuvant compositions and pesticides |
| WO2002102153A3 (en) * | 2001-05-21 | 2003-11-13 | Monsanto Technology Llc | Pesticide concentrates containing etheramine surfactants |
| WO2004039153A1 (en) * | 2002-10-30 | 2004-05-13 | Clariant Gmbh | Pesticide formulations containing alkoxylated amines |
| WO2004039154A1 (en) * | 2002-10-30 | 2004-05-13 | Clariant Gmbh | Pesticide formulations containing alkoxylated amines |
| US6992045B2 (en) | 2000-05-19 | 2006-01-31 | Monsanto Technology Llc | Pesticide compositions containing oxalic acid |
| US7049270B2 (en) | 2000-05-19 | 2006-05-23 | Monsanto Technology Llc | Potassium glyphosate formulations |
| US7135437B2 (en) | 2000-05-19 | 2006-11-14 | Monsanto Technology Llc | Stable liquid pesticide compositions |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DK169734B1 (en) * | 1993-03-09 | 1995-01-30 | Kvk Agro As | Herbicide preparation, method of preparation thereof and activating additive for admixture with herbicide preparations |
| FI933374A7 (en) * | 1993-07-28 | 1995-01-29 | Kemira Oy | Weed control composition, adjuvant for improving weed control efficacy and method for treating crops |
| FR2737390B1 (en) * | 1995-08-04 | 1997-09-19 | Rhone Poulenc Chimie | WATER-SOLUBLE PHYTOSANITARY COMPOSITION COMPRISING AT LEAST POLYACOXYLATED AMIDOAMINES |
| US6586367B2 (en) | 1996-09-05 | 2003-07-01 | Syngenta Crop Protection, Inc. | Process for the control of weeds |
| US6133199A (en) * | 1997-07-30 | 2000-10-17 | Monsanto Company | Process and compositions promoting biological effectiveness of exogenous chemical substances in plants |
| FR2766669B1 (en) * | 1997-07-30 | 1999-10-29 | Flamel Tech Sa | GLYPHOSATE EMULSION, ONE OF ITS PREPARATION METHODS, AND PHYTO-TOXIC COMPOSITION CONTAINING THE SAME |
| US6127317A (en) * | 1997-09-17 | 2000-10-03 | American Cyanamid Company | Concentrated, aqueous herbicidal compositions containing an imidazolinyl acid salt and a glyphosate salt |
| BR9908694A (en) * | 1998-03-09 | 2000-11-21 | Monsanto Co | Mixtures for weed control in glyphosate-tolerant soybeans |
| DE19836684A1 (en) * | 1998-08-13 | 2000-02-17 | Hoechst Schering Agrevo Gmbh | Use of a synergistic herbicidal combination including a glufosinate- or glyphosate-type, imidazolinone or protoporphyrinogen oxidase to control weeds in rice |
| US6277787B1 (en) | 1998-09-14 | 2001-08-21 | American Cyanamid Co. | Synergistic herbicidal methods and compositions |
| US6214768B1 (en) | 1998-09-14 | 2001-04-10 | American Cyanamid Co. | Synergistic herbicidal methods and compositions |
| AU2007329024B2 (en) | 2006-12-06 | 2013-04-11 | Akzo Nobel Chemicals International B.V. | Alkylamidopropyl dialkylamine surfactants as adjuvants |
| WO2008069826A1 (en) | 2006-12-06 | 2008-06-12 | Akzo Nobel N.V. | Compatibility agents for herbicidal formulations comprising 2,4-(dichlorophenoxy) acetic acid salts |
| AR077768A1 (en) | 2009-07-22 | 2011-09-21 | Huntsman Corp Australia Pty Ltd | COCOALQUILPOLIAMINE ALCOXYLATES AS AGENTS FOR HIGH-POWER HERBICIDE COMPOSITIONS |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4528023A (en) * | 1983-07-25 | 1985-07-09 | Stauffer Chemical Company | Enhancement of herbicidal activity of tetraaluminum salts of N-phosphonomethylglycine |
| ES2058337T5 (en) * | 1987-04-29 | 2005-10-01 | Monsanto Europe S.A. | IMPROVED FORMULATIONS OF GLYPHOSATE. |
-
1989
- 1989-06-20 FR FR8908433A patent/FR2648316A1/en not_active Withdrawn
-
1990
- 1990-06-13 IE IE213090A patent/IE902130A1/en unknown
- 1990-06-15 CA CA002019087A patent/CA2019087A1/en not_active Abandoned
- 1990-06-18 SE SE9002166A patent/SE9002166L/en not_active Application Discontinuation
- 1990-06-18 DE DE4019362A patent/DE4019362A1/en not_active Withdrawn
- 1990-06-19 GR GR900100459A patent/GR900100459A/en unknown
- 1990-06-19 LU LU87747A patent/LU87747A1/en unknown
- 1990-06-19 AU AU57565/90A patent/AU5756590A/en not_active Abandoned
- 1990-06-19 DK DK149390A patent/DK149390A/en not_active IP Right Cessation
- 1990-06-19 PT PT94414A patent/PT94414A/en not_active Application Discontinuation
- 1990-06-20 JP JP2162548A patent/JPH0334901A/en active Pending
- 1990-06-20 KR KR1019900009081A patent/KR910000016A/en not_active Withdrawn
- 1990-06-20 HU HU903921A patent/HUT54023A/en unknown
- 1990-06-20 GB GB9013692A patent/GB2233229B/en not_active Expired - Lifetime
- 1990-06-20 IT IT02070190A patent/IT1248734B/en active IP Right Grant
- 1990-06-20 ZA ZA904785A patent/ZA904785B/en unknown
- 1990-06-20 NL NL9001407A patent/NL9001407A/en not_active Application Discontinuation
- 1990-06-20 BR BR909002986A patent/BR9002986A/en unknown
Cited By (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1996025043A1 (en) * | 1995-02-13 | 1996-08-22 | Novartis Ag | Herbicidal composition and method of controlling weeds |
| WO1998024313A1 (en) * | 1996-12-06 | 1998-06-11 | Huntsman Surfactants Technology Corporation | Herbicidal compositions |
| US6248695B1 (en) | 1996-12-06 | 2001-06-19 | Huntsman Surfactants Technology Corporation | Herbicidal compositions |
| WO1999013723A1 (en) * | 1997-09-17 | 1999-03-25 | American Cyanamid Company | Synergistic herbicidal methods and compositions |
| AU744073B2 (en) * | 1997-09-17 | 2002-02-14 | American Cyanamid Company | Synergistic herbicidal methods and compositions |
| CZ302186B6 (en) * | 1997-09-17 | 2010-12-08 | American Cyanamid Company | Method for synergistic control of undesirable plants, concentrated, aqueous, synergistic, herbicidal composition and process for the preparation thereof |
| WO1999052367A1 (en) * | 1998-04-08 | 1999-10-21 | Aventis Cropscience Gmbh | Synergistic herbicidal agents based on leaf herbicides containing phosphorus, imidazolinones and hormone weed-killers |
| US6436874B1 (en) | 1998-04-08 | 2002-08-20 | Aventis Cropscience Gmbh | Synergistic herbicidal agents based on leaf herbicides containing phosphorus, imidazolinones and hormone weed killers |
| AU763130B2 (en) * | 1998-04-08 | 2003-07-17 | Bayer Cropscience Ag | Synergistic herbicidal compositions based on phosphorus containing foliar herbicides, imidazolinones and growth promoting herbicides |
| WO2001011957A1 (en) * | 1999-08-18 | 2001-02-22 | Huntsman Petrochemical Corporation | Polyether diamine-based surfactant adjuvants and compositions thereof |
| US6992045B2 (en) | 2000-05-19 | 2006-01-31 | Monsanto Technology Llc | Pesticide compositions containing oxalic acid |
| US7049270B2 (en) | 2000-05-19 | 2006-05-23 | Monsanto Technology Llc | Potassium glyphosate formulations |
| US7135437B2 (en) | 2000-05-19 | 2006-11-14 | Monsanto Technology Llc | Stable liquid pesticide compositions |
| US7723265B2 (en) | 2000-05-19 | 2010-05-25 | Monsanto Technology | Pesticide compositions containing oxalic acid |
| US10736325B2 (en) | 2000-05-19 | 2020-08-11 | Monsanto Technology Llc | Surfactants and formulations |
| WO2002102153A3 (en) * | 2001-05-21 | 2003-11-13 | Monsanto Technology Llc | Pesticide concentrates containing etheramine surfactants |
| WO2002098221A1 (en) * | 2001-06-01 | 2002-12-12 | Huntsman Petrochemical Corporation | Adjuvant compositions and pesticides |
| WO2004039153A1 (en) * | 2002-10-30 | 2004-05-13 | Clariant Gmbh | Pesticide formulations containing alkoxylated amines |
| WO2004039154A1 (en) * | 2002-10-30 | 2004-05-13 | Clariant Gmbh | Pesticide formulations containing alkoxylated amines |
| DE10250552A1 (en) * | 2002-10-30 | 2004-05-19 | Clariant Gmbh | Pesticide formulations containing alkoxylated amines |
| DE10250551A1 (en) * | 2002-10-30 | 2004-05-19 | Clariant Gmbh | Pesticide formulations containing alkoxylated amines |
Also Published As
| Publication number | Publication date |
|---|---|
| IE902130A1 (en) | 1991-01-02 |
| IT9020701A0 (en) | 1990-06-20 |
| PT94414A (en) | 1991-02-08 |
| CA2019087A1 (en) | 1990-12-20 |
| KR910000016A (en) | 1991-01-29 |
| AU5756590A (en) | 1991-01-03 |
| IT1248734B (en) | 1995-01-26 |
| FR2648316A1 (en) | 1990-12-21 |
| GB9013692D0 (en) | 1990-08-08 |
| IT9020701A1 (en) | 1991-12-20 |
| GB2233229B (en) | 1992-05-06 |
| SE9002166L (en) | 1990-12-21 |
| DK149390D0 (en) | 1990-06-19 |
| DK149390A (en) | 1990-12-21 |
| IE902130L (en) | 1990-12-20 |
| HUT54023A (en) | 1991-01-28 |
| SE9002166D0 (en) | 1990-06-18 |
| HU903921D0 (en) | 1990-11-28 |
| ZA904785B (en) | 1991-04-24 |
| GB2233229A (en) | 1991-01-09 |
| JPH0334901A (en) | 1991-02-14 |
| GR900100459A (en) | 1991-11-15 |
| LU87747A1 (en) | 1991-02-18 |
| BR9002986A (en) | 1991-08-20 |
| NL9001407A (en) | 1991-01-16 |
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