FR2537395A1 - FUNGICIDAL COMPOSITIONS BASED ON PHOSPHITE - Google Patents
FUNGICIDAL COMPOSITIONS BASED ON PHOSPHITE Download PDFInfo
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- FR2537395A1 FR2537395A1 FR8220995A FR8220995A FR2537395A1 FR 2537395 A1 FR2537395 A1 FR 2537395A1 FR 8220995 A FR8220995 A FR 8220995A FR 8220995 A FR8220995 A FR 8220995A FR 2537395 A1 FR2537395 A1 FR 2537395A1
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- 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
- A01N57/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
- A01N57/12—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur 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
- 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<
- A01N47/34—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the groups, e.g. biuret; Thio analogues thereof; Urea-aldehyde condensation products
-
- 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
- A01N59/00—Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds
- A01N59/26—Phosphorus; Compounds thereof
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- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
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- Engineering & Computer Science (AREA)
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- General Health & Medical Sciences (AREA)
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- Environmental Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
1. COMPOSITION FONGICIDE. 2. ELLE EST A BASE D'UN MELANGE SYNERGIQUE DE MATIERES ACTIVES COMPRENANT AU MOINS : - UN COMPOSE DE FORMULE : (CF DESSIN DANS BOPI) AVEC R OH, ALCOYLE (C-C), ALCOXYLE (C-C), M H (SI R OH), METAL ALCALIN, ALCALINOTERREUX OU ALUMINIUM, N 1 A 3 - LE CYMOXANIL. 3. CETTE COMPOSITION EST UTILISABLE POUR LA PROTECTION DES PLANTES CONTRE LES MALADIES, EN TRAITEMENT PREVENTIF OU CURATIF.1. FUNGICIDE COMPOSITION. 2. IT IS BASED ON A SYNERGIC MIXTURE OF ACTIVE MATERIALS INCLUDING AT LEAST: - A COMPOUND OF FORMULA: (CF DRAWING IN BOPI) WITH R OH, ALCOHOL (CC), ALCOXYL (CC), MH (SI R OH) , ALKALINE, ALKALINOTERREOUS METAL OR ALUMINUM, N 1 TO 3 - CYMOXANIL. 3. THIS COMPOSITION CAN BE USED FOR THE PROTECTION OF PLANTS AGAINST DISEASES, AS A PREVENTIVE OR CURATIVE TREATMENT.
Description
La présente invention concerne de-nouvelles compositions pour laThe present invention relates to novel compositions for
protection des plantes contre les maladies fongiques et en particulier des compositions contenant comme matières actives un fongicide du type phosphite et la l( 2-cyano-2 méthoxyiminoacétyl)-3-éthyl urée. Il est connu d'utiliser des fongicides systémiques pour protéger les plantes contre les maladies fongiques Il existe notamment le phoséthyl-Al, nonm commun pour le tris 0-éthylphosphonate d'aluminium ou éthyl phosphite d'aluminium, utilisé pour la protection de la vigne et d'autres plantes contre les Phycomycètes Ce produit a une action remarquable en traitement préventif et une activité curative secondaire à sa dose normale d'utilisation Il est habituellement utilisé en mélange avec des fongicides de contact. Par ailleurs, on utilise un autre fongicide, la 1- ( 2-cyano-2-méthoxyiminoacétyl)-3-éthylurée ou cymoxanil d'action systémique limitée et présentant une action curative secondaire Ce produit est généralement utilisé sur Phycomycètes en mélange avec un fongicide contact pour plant protection against fungal diseases and in particular compositions containing as active ingredients a phosphite fungicide and 1 (2-cyano-2-methoxyiminoacetyl) -3-ethyl urea. It is known to use systemic fungicides to protect plants against fungal diseases. In particular, there is phosethyl-Al, a nonmal for aluminum tris-0-ethylphosphonate or aluminum ethylphosphite, used for the protection of the vine. and other plants against Phycomycetes This product has a remarkable action in preventive treatment and a secondary healing activity at its normal dose of use It is usually used in mixture with contact fungicides. In addition, another fungicide, 1- (2-cyano-2-methoxyiminoacetyl) -3-ethylurea or cymoxanil of limited systemic action and with a secondary curative action is used. This product is generally used on Phycomycetes mixed with a fungicide. contact for
améliorer sa rémanence.improve its persistence.
On a maintenant trouvé de manière surprenante que si on associe le phoséthyl A 1 ou certains de ses dérivés homologues avec le cymoxanil, les mélanges ont une action synergique remarquable notamment curative qui permet une It has now been found, surprisingly, that if phosethyl A 1 or certain of its homologous derivatives are combined with cymoxanil, the mixtures have a remarkable synergistic action, notably a curative action which allows
nouvelle application de ces matières actives. new application of these active ingredients.
Plus particulièrement l'invention concerne une c OM position fongicide à base d'un mélange de matières actives dont l'une est du type phosphite caractérisée en ce qu'elle contient au moins: -A) un composé de formule: h n vn O dans laquelle s R est un OH ou un alcoyle de 2 A 4 atomes de More particularly, the invention relates to a fungicidal agent based on a mixture of active ingredients, one of which is of the phosphite type, characterized in that it contains at least: -A) a compound of formula: ## STR2 ## in which which R is an OH or an alkyl of 2 to 4 carbon atoms
carbone, ou un alcoxyle de 2 A 4 atonies de carbone. carbon, or an alkoxyl of 2 to 4 carbon atoms.
M est un atome d'hydrogène (seulement lorsque R est lui-même un radical hydroxyle) ou un atome de métal alcalin ou alcalinoterreux ou d'aluminium, M is a hydrogen atom (only when R is itself a hydroxyl radical) or an alkali metal or alkaline earth metal or aluminum atom,
-et B) la 1 ( 2-cyano-2-méthoxyiminoacétyl)-3-éthylurée. and B) 1 (2-cyano-2-methoxyiminoacetyl) -3-ethylurea.
Parmi les composés A les phosphites mono et disodique, les éthyl phosphites de sodium, de calcium et d'aluminium sont préférés De plus, le rapport pondéral B/A est avantageusemient compris entre 1/100 et 20/100 et de préférence entre 2/100 et 10/100; les compositions selon l'invention peuvent en outre comprendre d'autres matières actives, en général de un A trois fongicides de contact choisis dans le groupe comprenant des antimildiou tels que le captafol, le folpel, le manébe, le zinèbe, le mancozèbe, le miétirame zinc (complexe de zinèbe et de disulfure de polyéthylène thiurame) ou encore des fongicides actifs contre d'autres maladies comme le botrytis, l'excoriose etc Les mélanges selon l'invention peuvent être préparés en formule prête A l'emploi ou mélangés extemporanénent. L'exemple suivant donné A titre non limitatif illustre l'invention et montre comment elle peut être mise Among the compounds A mono and disodium phosphites, ethyl phosphites of sodium, calcium and aluminum are preferred In addition, the weight ratio B / A is preferably between 1/100 and 20/100 and preferably between 2/100 and 20/100. 100 and 10/100; the compositions according to the invention may further comprise other active ingredients, generally from one to three contact fungicides selected from the group consisting of antimildiou such as captafol, folpel, manebe, zineb, mancozeb, Zinc metiram (complex of zineb and polyethylene thiuram disulfide) or fungicides active against other diseases such as botrytis, excoriosis etc. The mixtures according to the invention can be prepared ready-to-use formula or mixed extemporaneously . The following example given by way of non-limiting example illustrates the invention and shows how it can be put
en pratique.in practice.
ExempleExample
On prépare un mélange de phoséthyl-Al et de cymoxanil dans un rapport E/A 6/100 Ce mélange ainsi formulé est utilisé in vivo sur Plasmooara viticola sur plants de vigne en serre A mixture of phosethyl-Al and cymoxanil in an E / A ratio of 6/100 is prepared. This mixture thus formulated is used in vivo on Plasmooara viticola on greenhouse vine plants.
(traitement curatif).(cure).
Des plants de vigne (céi age Chardonay), cultivés en pots sont traités sur les deux faces de leurs feuilles ar pulvérisation d'une suspension aqueuse, A la dilution Vine plants (Chardonay) grown in pots are treated on both sides of their leaves by spraying with an aqueous suspension.
2 '5373952 '537395
désirée, contenant des matières actives à tester, respectivemilt le phoséthyl-Al seul, sous forme de poulre mouillabie à 80 % en poids de mat ière active, cyuoxanil seul en poudre mnouillable, prête à l'cmploi, a 30 % en poids de matière active, et le mélange des deux poudres mrouillables. Cette suspension ainsi constituée est diluée, respectivement une et deux fois, à l'aide d'eau pour obtenir trois émulsions à pulvériser de concentration désirée en matières actives à tester La pulvérisation est effectuée anns des conditions telles que la pulvérisation d'une suspension de concentration égale à 1 g/l correspond à l'application d'environ 2 microgrammes de matières desired, containing active ingredients to be tested, respectivemilt the phoséthyl-Al only, in the form of wetland poultry 80% by weight of active material, cyuoxanil only in dry powder, ready for use, 30% by weight of material active, and mixing the two lockable powders. This suspension thus constituted is diluted, respectively one and two times, with water to obtain three emulsions to be sprayed with the desired concentration of active ingredients to be tested. Spraying is carried out under conditions such as the spraying of a suspension of concentration equal to 1 g / l corresponds to the application of approximately 2 micrograms of
actives par cm de surface de feuille de la plante. active per cm of leaf area of the plant.
On prépare de la même façon dans chaque cas deux suspensions contenant chacune l'une des matières actives A et B à la concentration à laquelle elles se trouvent dans In the same way, two suspensions each containing one of the active ingredients A and B at the concentration at which they are found in each case are prepared in the same way.
le mélange.The mixture.
Quelques (n à 1 à 3 jours) jours avant la pulvérisation de matières actives, la contamination des plantes a été effectuée par pulvérisation, sur la face inférieure des feuilles,-d'une suspension aqueuse de 80 000 unités/cm environ de spores de Plasmopara viticola responsable du mildiou de la vigne Ensuite, les pots ont été placés pendant 48 heures en cellule d'incubation à 100 A few (n to 1 to 3 days) days before the spraying of active ingredients, the contamination of the plants was carried out by spraying, on the underside of the leaves, an aqueous suspension of 80 000 units / cm of Plasmopara viticola responsible for the downy mildew of the vine Then, the pots were placed for 48 hours in incubation cell at 100
d'humidité relative et à 20 C.relative humidity and at 20 C.
On effectue le contrôle des plants-9 jours après la contamination Le contrôle est effectué par mesure des surfaces sporulées en pourcentage par rapport au témoin, The control of the plants is carried out-9 days after the contamination The control is carried out by measuring the sporulated surfaces in percentage relative to the control,
dont la surface est totalement sporulée. whose surface is totally sporulated.
Les résultats sont consignés dans le tableau suivant: The results are recorded in the following table:
EFFICACITE CURATIVE AVF C TRAIT 151 EZJT CURATIVE EFFICIENCY AVF C TRAIT 151 EZJT
PRODUIT DOSE N JOU Rts) APRES C O NTAIMINATION s i 2 3 PHOSETHYL i O O PRODUCT DOSE N JOU Rts) AFTER C O NTAIMINATION s i 2 3 PHOSETHYL i O O
2 70 35 O2 70 35 O
0,03 15 15 O0.03 15 15 O
CYM 4 OXANIL 0,06 75 75 OCYM 4 OXANIL 0.06 75 75 O
eeee
9,12 100 80 259.12 100 80 25
0,50.5
PHOSETHYL + 0,03 90 75 75.PHOSETHYL + 0.03 90 75 75.
CYM 4 OXANIL i + 0,06 97 95 e 5 e e e CYM 4 OXANIL i + 0.06 97 95 th 5 th th
22
0.12 100 97 850.12 100 97 85
Ce tableau montre clairement que l'activit 6 curative des mélanges à trois doses distinctes est supérieure à tres supérieure à la somme de celle du phoséthyl Ai et'du cymoxanil pris 54 parément On obtient une protection quasi totale encor e au bout de 2 jours et encore bonne au bout de 3 jours, les constituants étant dan cc Crnier caz lnci orsqu' ils sont u-tili sés This table clearly shows that the curative activity of the mixtures with three distinct doses is greater than the sum of that of phosethyl Al and cymoxanil taken by a factor. Almost complete protection is obtained after 2 days and still good after 3 days, the constituents being in Crnier caz lnci where they are used
sépar 4 ne nt.4 separate nt.
Cet exemple montre l'excellente activité fongicide des compositions selon l'invention qui peuvent être utilisés sur dililérentes famille_ de champignons phytouathog 9 nes telles que par exemple les Phyconycètes, en traitement préventif ou curatif. Pour leur emploi dans la pratique, les composés This example shows the excellent fungicidal activity of the compositions according to the invention which can be used on the following families of phytouathogenic fungi such as, for example, Phyconycetes, as preventive or curative treatment. For their use in practice, the compounds
selon l'invention ne sont généralement pas utilisés seuls. according to the invention are generally not used alone.
Le plus souvent ils sont utilisés dans des compositions qui comprennent en général, en plus de la matière active, ur support (ou diluant) inerte et/ou un agent tensioactif Most often they are used in compositions which generally comprise, in addition to the active ingredient, an inert carrier (or diluent) and / or a surfactant.
compatibles avec la matière active. compatible with the active ingredient.
Ces compositions font également partie de la présente invention Elles contiennent habituellement de 0,001 à 95 % en poids de matière active Leur teneur en agent tensioactif est en général comprise entre 0,1 % et 20 These compositions are also part of the present invention. They usually contain from 0.001 to 95% by weight of active material. Their surfactant content is in general between 0.1% and 20% by weight.
% en poids.% in weight.
Par le terme 'support", dans le présent exposé, on désigne une matière organique ou minérale, naturelle ou synthétique, avec laquelle la matière active est associée pour faciliter son application sur la plante, sur des graines ou sur le sol Ce support est donc généralement inerte et il doit être acceptable en agriculture, notamment sur la plante traitée Le support peut être solide; (argiles, silicates naturels ou synthétiques, silice, craies, résines, cires, engrais solides, etc) ou liquide (eau, alcools, cétones, fractions de pétrole, hydrocarbures aromatiques ou paraffiniques, hydrocarbures chlorés, gaz By the term "support", in the present description, denotes an organic or inorganic material, natural or synthetic, with which the active ingredient is associated to facilitate its application to the plant, on seeds or on the ground This support is therefore generally inert and must be acceptable in agriculture, especially on the treated plant The support can be solid (clays, natural or synthetic silicates, silica, chalks, resins, waxes, solid fertilizers, etc.) or liquid (water, alcohols, ketones , petroleum fractions, aromatic or paraffinic hydrocarbons, chlorinated hydrocarbons, gases
liquéfiés, etc).liquefied, etc.).
L'agent tensioactif peut être un agent énul- The surfactant may be an enor-
sionnant, dispersant ou mouillant de type'ionique ou non ionique On peut citer par exemple des sels d'acides polyacryliques; des sels d'acides lignosulfoniques, des sels d'acides phénolsulfoniques ou naphtalènesulfoniques, des polycondensats d'oxyde d'éthylène sur des alcools gras ou sur des acides aras ou sur d a mine Ls dra u phénols substitués (notamment des alkylphénols ou des arylphénols ou le styrylph nol); des sels d'esters d'aciees sulfosucciniques; des 7 'riv 5 S de la taurine (notamment des alkyltaurates); des esters phosphoriques d'alcools au ce p;: nu Lis olyoxy 6thylés La présence d'au moins un ajent tensioactif est genéralement indispensable surtout lorsque le sups ort inerte n'est pas soluble uans For example, salts of polyacrylic acids may be mentioned, for example, ionic or nonionic dispersants or wetting agents; lignosulfonic acid salts, salts of phenolsulphonic or naphthalenesulphonic acids, polycondensates of ethylene oxide with fatty alcohols or aromatic acids or with substituted phenols (especially alkylphenols or arylphenols or styrylphenol); salts of sulfosuccinic acid esters; 7% rivals of taurine (especially alkyltaurates); The presence of at least one surfactant additive is generally essential, especially when the inert sulphoxide is not soluble in water.
l'eau, et que l'agent vecteur de l'application est l'eau. water, and that the agent vector of the application is water.
Les co Jpositions utilisées dans l'invention peuvent The compositions used in the invention can
être sous des forues assez diverses, solides ou liquides. to be under quite diverse, solid or liquid forests.
Comme formes de compositions solides, on peut citer les poudres pour poudrage ou dispersion (à teneur en As forms of solid compositions, mention may be made of powders for dusting or dispersion (with a content of
Iiatières actives pouvant aller jusqu'à 100 %). Active ingredients up to 100%).
Comme formes de compositions liquides ou destin 6 es A constituer des compositions liquides lors de l'application, on peut citer les solutions, en particulier As forms of liquid compositions or intended to constitute liquid compositions during application, mention may be made of the solutions, in particular
les concentres solubles dans l'eau, les concentrés émul- water-soluble concentrates, emulsion concentrates
sionnables, les émulsions, les suspensions concentrées, les aérosols, les poudres mouillables (ou poudre à pulvérisers, Emulsions, concentrated suspensions, aerosols, wettable powders (or spray powder,
les pâtes.pasta.
Les concentrés émulsionnables ou solubles comprennent le plus souvent 10 à 80 % de matière active, les émulsions ou solutions prêtes à l'application The emulsifiable or soluble concentrates most often comprise 10 to 80% active ingredient, the emulsions or solutions ready for application.
contenant, quant à elles, 0,001 à 20 % de matière active. containing, for their part, 0.001 to 20% of active ingredient.
En plus du solvant, les concentrés émulsionnables peuvent contenir, quand c'est nécessaire, 2 à 20 % d'additifs appropriés, comme des stabilisants, des agents tensioactifs, des agents de pénétration, des inhibiteurs de In addition to the solvent, the emulsifiable concentrates may contain, when necessary, 2 to 20% of suitable additives, such as stabilizers, surfactants, penetration agents,
corrosion, des colorants, des adhésifs. corrosion, dyes, adhesives.
A partir de ces concentres, on peut obtenir par dilution avec de l'eau des émulsions de toute concentration désirée, qui conviennent particulièrement à l'application From these concentrates, it is possible to obtain, by dilution with water, emulsions of any desired concentration, which are particularly suitable for application
sur les feuilles.on the leaves.
Les suspensions concentrées, également applicables en pulvérisation, sont préparées de manière à obtenir un produit fluide stable ne se déposant pas et elles contiennent habituellement de 10 à 75 % de matières 7. actives, ûe 3,5 à 15 % d'agents tonsioactifs, de 0,1 à 10 deagjents thixotropes, de O à -30 % d'additifs ai,-iopriés, C 0.1 ime des anti-Im Iousses, des inhibiteurs 4 e corrosion, des stabilisants, des ac;ents de p 6 nétration e e JL t co Mi Ye support, de l' eau ou un liquide or janiqlue -1 ans lequel la matière activeÄ est peu ou pa 5 olubl e cetaine Cs matières solides organiques ou de-, sels ninéraux peuvent etre dissous lans le support pour aider à een cher la The concentrated suspensions, which are also applicable as sprays, are prepared in such a way as to obtain a stable fluid product which does not settle and usually contain from 10 to 75% of active materials, and from 3.5 to 15% of toning agents. from 0.1 to 10 thixotropic agents, from 0 to 30% of suitable additives, C 0.1, anti-foils, corrosion inhibitors, stabilizers, p-acetylation acetates; In the case of water or liquid, the active substance is little or less soluble. Organic solids or inorganic salts may be dissolved in the support to een dear
sédimentatiorn ou comme antigels pour l'eau. sedimentatiorn or as antifreeze for water.
Les poudres naouillablus <ou poudre à% pulvériser) The powders naouillablus <or powder to% spray)
sont habituellement préparées de'manière qu'elles- are usually prepared in such a way that
contiennent 20 à 95 % de matières actives, et 21 les contiennent habituellement, en plus du support solide, de (J à 5 % d'un agent ifouillant, de 3 à 10 % d'un ar 9 ent dispersant* et, quand c'est nécessaire, de u J Io 1 % d'un ou Pduzieurs stabilisants et/ou autres additi'fu, commie des agents de pénétration, des adhésifs, ou des agents afitimottants, co 1 orants#'etc* A titre d'exemple, voici diverses compositions de poudres mouillables: miatière active (mélange B/A à 6, 5/100 > 50 % alcool gras éthoxylé (agent mouillant) 2,5 % styrylphinol éthoxyl 4 <agent dispersant> '5 craie <support inerte) 42,5 % Un autre exemple de poudre mouîllable a la composition suivante: -matièr e active (mélange B/A à 6,6/100 > phoséthyl-Al 50 I cyinoxanil 3,3 % folpel 25 alcool gras éthoxylé <agent'mouillant) 5,7 % *-styrylphénol éthoxylé <agent dispersant) 6 % Pour'obtenir ces poudres 'à pulvériser ou poudres mouillanles, on rtélange intimement la matiàre active dans des mélangeurs appropri 6 S avec les substances additionnelles et on broie avec des moulins ou autres broyeurs appropriés On obtient par là des poudres à pulvériser dont la nouillabilité et la mise en suspension sont avantageuses; on peut les mettre en suspension avec de l'eau à toute concentration désirée et cette suspension est utilisable très avantageusement en particulier pour contain 20 to 95% of active ingredients, and usually contain, in addition to the solid carrier, from 5% of a bleaching agent, from 3 to 10% of an dispersant, and when It is necessary to use one or more stabilizing agents and / or other additives, such as penetrating agents, adhesives, or cosurfactants, coaters, etc, by way of example. here are various wettable powder compositions: active ingredient (6: 5/100> 50% alcohol / ethoxylated fatty alcohol mixture (wetting agent) 2.5% styrylphinol ethoxyl 4 <dispersing agent> chalk <inert carrier) 42 Another example of a wettable powder has the following composition: - active material (B / A mixture at 6.6 / 100> phosethyl-Al 50 I cyinoxanil 3.3% folpel ethoxylated fatty alcohol <wetting agent) 5.7% * - ethoxylated styrylphenol <dispersing agent) 6% To obtain these powders for spraying or for wettable powders, the active ingredient is intimately mixed in melts. Suitable abrasives 6 S with the additional substances and grinded with mills or other suitable grinders. Thereby obtain powders for spraying whose nvibability and suspension are advantageous; they can be suspended with water at any desired concentration and this suspension can be used very advantageously especially for
l'application sur les feuilles des végétaux. the application on the leaves of the plants.
Comme cela a déjà été dit, les dispersions et emulsions aqueuses, par exemple des compositions obtenues en diluant à l'aide d'eau une poudre mouillable ou un concentré 6 mulsionnable selon l'invention, sont comprises dans le cadre général de la présente invention Les énulsions peuvent être du type eau-dans-l'huile ou huile-dans-l'eau et elles peuvent avoir une consistance As already mentioned, aqueous dispersions and emulsions, for example compositions obtained by diluting with water a wettable powder or a multivolvable concentrate according to the invention, are included in the general scope of the present invention. The enzers can be of the water-in-oil or oil-in-water type and they can have a consistency
épaisse comme celle d'une "mayonnaise". thick like that of a "mayonnaise".
Les granulés destinés a être disposés sur le sol sont habituellement préparés de manière qu'ils aient des dimensions comprises entre 0,1 et 2 mm et ils peuvent être fabriqués par agglomération ou imprégnation En général, les granulés contiennent 0,5 3 25 % de matière active et O à 10 % d'additifs comme stabilisants, des agents de The granules intended to be placed on the ground are usually prepared so that they have dimensions of between 0.1 and 2 mm and they can be manufactured by agglomeration or impregnation In general, the granules contain 0.5 to 25% of active ingredient and from 0 to 10% of additives as stabilizers,
modification à libération lente, des liants et des solvants. slow release modification, binders and solvents.
Les composés de formule (II) peuvent encore être utilisés sous forme de poudre pour poudrage, on peut ainsi utiliser une composition comprenant 50 g de matière active et 950 g de talc I on peut aussi utiliser une composition comprenant 20 g de matière active, 10 g de silice finement divisée et 970 g de talc; on mélange et broie ces The compounds of formula (II) can also be used in the form of a dusting powder, it is thus possible to use a composition comprising 50 g of active material and 950 g of talc. It is also possible to use a composition comprising 20 g of active substance, g of finely divided silica and 970 g of talc; we mix and grind these
constituants et on applique le mélange par poudrage. components and apply the mixture by dusting.
L'invention concerne de plus un procédé de traitement des végétaux contre les champignons phytopathogènes Ce procédé est caractérisé en ce qu'il consiste à appliquer sur ces végétaux une quantité efficace d'une composition contenant comme matière active un composé selon la formule (II) Par "quantité efficace* on entend une quantité suffisante pour permettre le contrôle et la destruction des champignons préF-nts sur ces vég 6 étaux Les doses d'utilisation peuvent toutefois varier dans de larges limites selon le char,pignon a comnbattre, le type de culture, et les conditions climatiques. S F Lv ENDICATIONS 1) Composition fongicic e a r&se d'un zélange de iratière active dont l'une est du type phosphite caracti-é 4 sé en ce qu'elle contient au moins in A) un composé de formule a (R p >n dans laquelle a R est un DE ou un alcoyle de 2 à 4 atomes de carbone, ou un alcoxyle de 2 à 4 atomes de carbone. M est un atome d'hydrogène (seulement lorque-A est lui mime un radical hydroxyle) ou un atome The invention also relates to a method for treating plants against phytopathogenic fungi This method is characterized in that it consists in applying to these plants an effective amount of a composition containing as active ingredient a compound according to formula (II) By "effective amount" is meant an amount sufficient to allow the control and destruction of pre-fungi on these 6-veal plants. Doses of use may, however, vary within wide limits depending on the tank, the gear to be combated, the type of cultivation, and climatic conditions SF LV ENDICATIONS 1) Fungicidal composition consisting of a mixture of active irate material, one of which is of the phosphite type, characterized in that it contains at least one of wherein R is DE or an alkyl of 2 to 4 carbon atoms, or an alkoxyl of 2 to 4 carbon atoms M is a hydrogen atom (only lorque-A is it mime one hydroxyl radical) or an atom
2 G O de métal alcalin ou alcalinoterreux ou d'aluminium. 2 G O of alkaline or alkaline earth metal or aluminum.
n est un entier de 1 à 3 et B) le 1 < 2-cyano-2-méthoxyinincac 4 tyl)-3ethylu Zee 2) Composition selon la revendication lu caractérisée en ce gue le rapport pondéral de B/A est compris entre 1/100 n is an integer of 1 to 3 and B) 1 <2-cyano-2-methoxyinincac 4 tyl) -3-ethyl Zee 2) Composition according to claim 1, characterized in that the weight ratio of B / A is between 1 / 100
et 20/100.and 20/100.
3) Composition selon l'une des revendications 1 et 2, 3) Composition according to one of claims 1 and 2,
caractérisée en ce que-le rapport B/A est con-pris entre characterized in that the B / A ratio is between
2/100 et 10/ 100.2/100 and 10/100.
4 > Corpos-ition selon la revendication 1, caractérisée en ce 4> Corpos-ition according to claim 1, characterized in that
3 ue le cor-posé A est le tris-O-éthylphosphonate d'aluminium. The corpuscle A is aluminum tris-O-ethylphosphonate.
54) Conzositien súei'on l'une des revendications 1 à 4 54) Conzositien súei'on one of claims 1 to 4
caràctlêrîsee en ce qu 'elle comprend en outre un fon- in that it also comprises a foun-
gicide c e contact antimildiou.gicide and antimyroid contact.
6) Composition selon la revendication 5, caractérisoée en ce 6) Composition according to claim 5, characterized in that
que le fongicide de contact est le folpel. that the contact fungicide is the folpel.
7) Composition selon la revendication 5, caractérisaée en ce 7) Composition according to claim 5, characterized in that
que le fongicide de contact est le captafol. that the contact fungicide is captafol.
8) Composition selon la revendication 5, caractérisée en ce 8) Composition according to claim 5, characterized in that
que le fongicide de contact est le mancozèbe. that the contact fungicide is mancozeb.
9) Composition selon la revendication 5, caracterisée en 9) Composition according to claim 5, characterized in
ce que le fongicide de contact est à base de cuivre. what the contact fungicide is copper-based.
) Procédé de traitement des plantes contre les maladies fongiques, caractérisée en ce qu'on leur applique une ) A method of treating plants against fungal diseases, characterized in that they are applied to them
composition selon l'une des revendications 1 à 9. Composition according to one of Claims 1 to 9.
11) Procédé de traitement selon la revendication 10), caractérisée en ce qu'il est appliqué après la 11) Treatment method according to claim 10, characterized in that it is applied after the
contamination des plantes par le ou les champignons. contamination of the plants by the fungus (s).
Priority Applications (26)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR8220995A FR2537395A1 (en) | 1982-12-10 | 1982-12-10 | FUNGICIDAL COMPOSITIONS BASED ON PHOSPHITE |
| IT23919/83A IT1167274B (en) | 1982-12-10 | 1983-11-28 | MIXTURE OF PHOSETHYL A1 + CYMOXANIL FUNGICIDES |
| RO83112704A RO88470A (en) | 1982-12-10 | 1983-11-30 | FUNGICIDE SINERGETICS COMPOSITION |
| KR1019830005673A KR920003209B1 (en) | 1982-12-10 | 1983-11-30 | Fungicidal composition |
| BG063301A BG41998A3 (en) | 1982-12-10 | 1983-12-02 | Fungicide means and method for prevention from fungi on plants |
| BR8306675A BR8306675A (en) | 1982-12-10 | 1983-12-05 | FUNGICIDE COMPOSITION AND PROCESS FOR TREATING PLANTS AGAINST FUNGIC DISEASES |
| AT0426783A AT390167B (en) | 1982-12-10 | 1983-12-06 | PHOSPHITE-BASED FUNGICIDAL COMPOSITIONS |
| ZA839154A ZA839154B (en) | 1982-12-10 | 1983-12-08 | Fungicidal compositions |
| AU22198/83A AU554252B2 (en) | 1982-12-10 | 1983-12-08 | Phosphites and cymoxanil fungicides |
| PL1983244975A PL138023B1 (en) | 1982-12-10 | 1983-12-08 | Fungicide |
| JP58232219A JPS59112907A (en) | 1982-12-10 | 1983-12-08 | Fungicidal composition |
| NZ206522A NZ206522A (en) | 1982-12-10 | 1983-12-08 | Fungicidal compositions containing a phosphite compound and a urea derivative |
| DE3344433A DE3344433C2 (en) | 1982-12-10 | 1983-12-08 | Phosphitic based fungicidal compositions and their use |
| GB08332801A GB2131296B (en) | 1982-12-10 | 1983-12-08 | Fungicidal compositions |
| HU834217A HU196550B (en) | 1982-12-10 | 1983-12-09 | Sinergetic fungicides containing as active substance aluminium-tris /0-ethil-phosphonate/ and 1-/2-cyan-2-metoxi-imino-acethil/-3-ethil-carbamide |
| BE0/212024A BE898428A (en) | 1982-12-10 | 1983-12-09 | FUNGICIDAL COMPOSITIONS AND THEIR USE. |
| PT77799A PT77799B (en) | 1982-12-10 | 1983-12-09 | PROCESS FOR THE PREPARATION OF FUNGICIDAL COMPOSITIONS BASED ON PHOSETHYL AL AND CYNOXANIL |
| DD83257729A DD219658A5 (en) | 1982-12-10 | 1983-12-09 | FUNGICIDAL COMPOSITIONS AT PHOSPHIT BASIS |
| CH6607/83A CH657505A5 (en) | 1982-12-10 | 1983-12-09 | FUNGICIDAL COMPOSITION BASED ON A MIXTURE OF ACTIVE MATERIAL. |
| DK566783A DK566783A (en) | 1982-12-10 | 1983-12-09 | FUNGICIDE PREPARATION BASED ON A MIXTURE OF A PHOSPHITE TYPE FUNGICIDE AND 1- (2-CYANO-2-METHOXYIMINOACETYL) -3-ETHYLURINE |
| NL8304258A NL8304258A (en) | 1982-12-10 | 1983-12-09 | FUNGICIDE PREPARATIONS, METHOD FOR MANUFACTURING THEM AND METHOD FOR TREATING CROPS FOR PROTECTION AGAINST FUNGI. |
| IE2890/83A IE56329B1 (en) | 1982-12-10 | 1983-12-09 | Fungicidal compositions |
| LU85123A LU85123A1 (en) | 1982-12-10 | 1983-12-09 | PHOSPHITE-BASED FUNGICIDAL COMPOSITIONS |
| SE8306811A SE8306811L (en) | 1982-12-10 | 1983-12-09 | FUNGICIDA COMPOSITIONS BASED ON PHOSPHITE |
| CA000442941A CA1227750A (en) | 1982-12-10 | 1983-12-09 | Fungicidal compositions |
| CS839267A CS241143B2 (en) | 1982-12-10 | 1983-12-09 | Fungicide |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR8220995A FR2537395A1 (en) | 1982-12-10 | 1982-12-10 | FUNGICIDAL COMPOSITIONS BASED ON PHOSPHITE |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| FR2537395A1 true FR2537395A1 (en) | 1984-06-15 |
| FR2537395B1 FR2537395B1 (en) | 1985-03-29 |
Family
ID=9280107
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FR8220995A Granted FR2537395A1 (en) | 1982-12-10 | 1982-12-10 | FUNGICIDAL COMPOSITIONS BASED ON PHOSPHITE |
Country Status (26)
| Country | Link |
|---|---|
| JP (1) | JPS59112907A (en) |
| KR (1) | KR920003209B1 (en) |
| AT (1) | AT390167B (en) |
| AU (1) | AU554252B2 (en) |
| BE (1) | BE898428A (en) |
| BG (1) | BG41998A3 (en) |
| BR (1) | BR8306675A (en) |
| CA (1) | CA1227750A (en) |
| CH (1) | CH657505A5 (en) |
| CS (1) | CS241143B2 (en) |
| DD (1) | DD219658A5 (en) |
| DE (1) | DE3344433C2 (en) |
| DK (1) | DK566783A (en) |
| FR (1) | FR2537395A1 (en) |
| GB (1) | GB2131296B (en) |
| HU (1) | HU196550B (en) |
| IE (1) | IE56329B1 (en) |
| IT (1) | IT1167274B (en) |
| LU (1) | LU85123A1 (en) |
| NL (1) | NL8304258A (en) |
| NZ (1) | NZ206522A (en) |
| PL (1) | PL138023B1 (en) |
| PT (1) | PT77799B (en) |
| RO (1) | RO88470A (en) |
| SE (1) | SE8306811L (en) |
| ZA (1) | ZA839154B (en) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2840847B2 (en) * | 1989-01-23 | 1998-12-24 | ローヌ・プーランアグロ株式会社 | Stabilized pesticide composition |
| FR2655816B1 (en) * | 1989-12-14 | 1994-04-29 | Rhone Poulenc Agrochimie | DISPERSABLE GRANULES OF FUNGICIDE PRODUCTS. |
| DE4142974C2 (en) * | 1991-12-24 | 1996-05-30 | Alexander Burkhart Gross Und E | Fungicidal compositions |
| FR2738112B1 (en) * | 1995-09-05 | 1997-09-26 | Rhone Poulenc Agrochimie | METHOD FOR IMPROVING BANANA FRUIT YIELDS |
| FR2771898B1 (en) * | 1997-12-04 | 2000-01-07 | Rhone Poulenc Agrochimie | FUNGICIDE AND / OR SYNERGISTIC BACTERICIDE COMPOSITION |
| TW200306155A (en) * | 2002-03-19 | 2003-11-16 | Du Pont | Benzamides and advantageous compositions thereof for use as fungicides |
| ITMI20022516A1 (en) * | 2002-11-27 | 2004-05-28 | Isagro Spa | FUNGICIDAL COMPOSITIONS. |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2333440A2 (en) * | 1975-12-04 | 1977-07-01 | Du Pont | Fungicide compsn. - contg. (2)-cyano-(N)-ethyl-carbamoyl-(2)-methoxy-imino-acetamide |
| FR2377155A1 (en) * | 1977-01-14 | 1978-08-11 | Philagro Sa | FUNGICIDE COMPOSITIONS BASED ON ALCOYLPHOSPHITES |
-
1982
- 1982-12-10 FR FR8220995A patent/FR2537395A1/en active Granted
-
1983
- 1983-11-28 IT IT23919/83A patent/IT1167274B/en active
- 1983-11-30 KR KR1019830005673A patent/KR920003209B1/en not_active Expired
- 1983-11-30 RO RO83112704A patent/RO88470A/en unknown
- 1983-12-02 BG BG063301A patent/BG41998A3/en unknown
- 1983-12-05 BR BR8306675A patent/BR8306675A/en not_active IP Right Cessation
- 1983-12-06 AT AT0426783A patent/AT390167B/en not_active IP Right Cessation
- 1983-12-08 DE DE3344433A patent/DE3344433C2/en not_active Expired - Lifetime
- 1983-12-08 ZA ZA839154A patent/ZA839154B/en unknown
- 1983-12-08 AU AU22198/83A patent/AU554252B2/en not_active Expired
- 1983-12-08 PL PL1983244975A patent/PL138023B1/en unknown
- 1983-12-08 JP JP58232219A patent/JPS59112907A/en active Pending
- 1983-12-08 GB GB08332801A patent/GB2131296B/en not_active Expired
- 1983-12-08 NZ NZ206522A patent/NZ206522A/en unknown
- 1983-12-09 DD DD83257729A patent/DD219658A5/en unknown
- 1983-12-09 SE SE8306811A patent/SE8306811L/en not_active Application Discontinuation
- 1983-12-09 PT PT77799A patent/PT77799B/en unknown
- 1983-12-09 CA CA000442941A patent/CA1227750A/en not_active Expired
- 1983-12-09 HU HU834217A patent/HU196550B/en unknown
- 1983-12-09 CS CS839267A patent/CS241143B2/en unknown
- 1983-12-09 DK DK566783A patent/DK566783A/en not_active Application Discontinuation
- 1983-12-09 LU LU85123A patent/LU85123A1/en unknown
- 1983-12-09 IE IE2890/83A patent/IE56329B1/en not_active IP Right Cessation
- 1983-12-09 BE BE0/212024A patent/BE898428A/en not_active IP Right Cessation
- 1983-12-09 NL NL8304258A patent/NL8304258A/en not_active Application Discontinuation
- 1983-12-09 CH CH6607/83A patent/CH657505A5/en not_active IP Right Cessation
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2333440A2 (en) * | 1975-12-04 | 1977-07-01 | Du Pont | Fungicide compsn. - contg. (2)-cyano-(N)-ethyl-carbamoyl-(2)-methoxy-imino-acetamide |
| FR2377155A1 (en) * | 1977-01-14 | 1978-08-11 | Philagro Sa | FUNGICIDE COMPOSITIONS BASED ON ALCOYLPHOSPHITES |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| CP | Supplementary protection certificate (spc) filed |
Free format text: PRODUCT NAME: CYMOXANIL; MANCOZEBE; PHOSETYL-ALUMINIUM; NAT. REGISTRATION NO/DATE: 8800060 19880929; FIRST REGISTRATION: FR - 8800060 19880929 Spc suppl protection certif: 97C0073 Filing date: 19970805 |
|
| C1 | Application for supplementary protection certificate (spc) for plant protection laid open to the public |
Free format text: 97C0073, 970805 |
|
| CP | Supplementary protection certificate (spc) filed |
Free format text: 97C0073, 970805 |
|
| CP | Supplementary protection certificate (spc) filed | ||
| C2 | Application for supplementary protection certificate (spc) for plant protection granted |
Free format text: 97C0073, 19970805, EXPIRES: 20030929 |