US20100035840A1 - Pesticidal composition comprising fosetyl-aluminium, propamocarb-hcl and an insecticide substance - Google Patents

Pesticidal composition comprising fosetyl-aluminium, propamocarb-hcl and an insecticide substance Download PDF

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Publication number
US20100035840A1
US20100035840A1 US12/520,565 US52056507A US2010035840A1 US 20100035840 A1 US20100035840 A1 US 20100035840A1 US 52056507 A US52056507 A US 52056507A US 2010035840 A1 US2010035840 A1 US 2010035840A1
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United States
Prior art keywords
propamocarb
fosetyl
composition according
hcl
weight ratio
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US12/520,565
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English (en)
Inventor
Heike Hungenberg
Wolfgang Thielert
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Bayer Intellectual Property GmbH
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Bayer CropScience AG
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Publication of US20100035840A1 publication Critical patent/US20100035840A1/en
Assigned to BAYER INTELLECTUAL PROPERTY GMBH reassignment BAYER INTELLECTUAL PROPERTY GMBH ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: BAYER CROPSCIENCE AG
Assigned to BAYER INTELLECTUAL PROPERTY GMBH reassignment BAYER INTELLECTUAL PROPERTY GMBH CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNEE ADDRESS PREVIOUSLY RECORDED AT REEL: 034891 FRAME: 0140. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Assignors: BAYER CROPSCIENCE AG
Abandoned legal-status Critical Current

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    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N57/00Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
    • A01N57/10Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
    • A01N57/12Biocides, 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
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N47/00Biocides, 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
    • A01N47/08Biocides, 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
    • A01N47/10Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
    • A01N47/12Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, neither directly attached to a ring nor the nitrogen atom being a member of a heterocyclic ring

Definitions

  • the present invention relates to a pesticide composition intended for protecting plants, crops or seeds against fungal diseases or insect damages, and the corresponding methods of protection by application of the said composition. More precisely, the subject of the present invention is a pesticide composition based on fosetyl-Al, propamocarb-HCl and an insecticide active substance or compound and optionally a further fungicide active substance or compound.
  • the present invention provides a pesticide composition which can be used, in particular by the farmer, for controlling the pest infesting crops and in particular for controlling insects or diseases of corn, beet, cotton, canola, beans, peanuts vegetables, lucerne, soybean, market garden crops, turf, wood, tree and horticultural plants, for example Pythium on corn.
  • the pesticide compounds useful for the protection of plants must be endowed with an ecotoxicity which is reduced to the minimum. As far as possible, they should not be dangerous or toxic to the operator during use. The economic factor should of course not be overlooked in the search for novel pesticide agents.
  • Fosetyl-aluminium or fosetyl-Al is a known compound having as chemical name aluminium ethylhydrogenphosphonate-fosetyl-Al is described in British patent GB-1449394- and which is represented by the following formula:
  • Propamocarb-hydrochloride or propamocarb-HCl is a known compound having as chemical name propyl [3-(dimethylamino)propyl]carbamate hydrochloride-propamocarb is described in British patent GB-1212708- and which is represented by the following formula:
  • the present invention provides a composition comprising:
  • composition according to the invention as herein-described fosetyl-Al can be replaced by a phosphorous acid derivative such as metal phosphites like fosetyl-sodium, and phosphorous acid itself and its alkali metal or alkaline earth metal salts.
  • phosphorous acid itself is the preferred substitute of fosetyl-Al, any composition comprising phosphorous acid is part of the present invention.
  • propamocarb-HCl and propamocarb can be used in the same manner. Both forms are part of the present invention in its various aspects or preferences.
  • the present invention advantageously provides a pesticide composition which is completely high-performing in particular as regards its efficacy against pests and the perenniallity of this efficacy so as to be able to reduce the doses of chemical products spread in the environment for combating pest damages or attacks of plants or crops.
  • the invention provides a pesticide composition capable to be more active and active for longer, and which therefore has a lower dose, but which is also less toxic, in particular in the treatment of plants and particularly the foliar and seed treatments of fungal diseases or the control of insects, for example, of cereals, cotton, peanut, bean, beet, canola, Solanaceae , grapevine, vegetables, lucerne, soybean, market garden crops, turf, wood or horticultural plants.
  • the composition according to the invention allows controlling a broad variety of insects or fungi.
  • the pesticide composition according to the invention exhibits an improved efficacy against fungus like Plasmodiophoromycetes, Oomycetes, Chytridiomycetes, Zygomycetes, Basidiomycetes, Deuteromycetes and Ascomycetes.
  • a pesticide composition comprising fosetyl-Al, propamocarb-HCl; an insecticide compound and optionally a further fungicide compound.
  • a composition surprisingly and unexpectedly allows a very high and perennial insecticide or anti-fungal efficacy against a broad spectrum of insects or fungi and in particular against those responsible for diseases or damages of corn for example to Oomycetes.
  • Other insect pests or diseases of corn can be controlled with the pesticide composition according to the invention, in particular the control of Ascomycetes or Basidiomycetes.
  • the pesticide composition according to the invention may also be used for the treatment of bacterial or virus diseases.
  • Insects or nematodes that can be controlled with the pesticide composition according to the invention include a broad variety of these damaging organisms.
  • insecticide compound B is preferably selected in the list consisting of:
  • the composition according to the invention comprises fosetyl-Al, propamocarb-HCl and abamectin; fosetyl-Al, propamocarb-HCl and acephate; fosetyl-Al, propamocarb-HCl and acetamiprid; fosetyl-Al, propamocarb-HCl and acrinathrin; fosetyl-Al, propamocarb-HCl and aldicarb; fosetyl-Al, propamocarb-HCl and alpha-cypermethrin; fosetyl-Al, propamocarb-HCl and beta-cyfluthrin; fosetyl-Al, propamocarb-HCl and bifenthrin; fosetyl-Al, propamocarb-HCl and carbaryl; fosetyl-Al, propamocarb-HCl and carbofuran; foset
  • the composition according to the invention comprises fosetyl-Al, propamocarb-HCl and abamectin; fosetyl-Al, propamocarb-HCl and acetamiprid; fosetyl-Al, propamocarb-HCl and aldicarb; fosetyl-Al, propamocarb-HCl and beta-cyfluthrin; fosetyl-Al, propamocarb-HCl and carbofuran; fosetyl-Al, propamocarb-HCl and chlorpyrifos-E; fosetyl-Al, propamocarb-HCl and clothianidin; fosetyl-Al, propamocarb-HCl and cypermethrin; fosetyl-Al, propamocarb-HCl and cyromazine; fosetyl-Al, propamocarb-HCl and deltamethrin; fosetyl-Al,
  • the composition according to the invention comprises fosetyl-Al, propamocarb-HCl and abamectin; fosetyl-Al, propamocarb-HCl and aldicarb; fosetyl-Al, propamocarb-HCl and beta-cyfluthrin; fosetyl-Al, propamocarb-HCl and chlorpyrifos-E; fosetyl-Al, propamocarb-HCl and clothianidin; fosetyl-Al, propamocarb-HCl and cyromazine; fosetyl-Al, propamocarb-HCl and deltamethrin; fosetyl-Al, propamocarb-HCl and diflubenzuron; fosetyl-Al, propamocarb-HCl and emamectin-benzoate; fosetyl-Al, propamocarb-HCl and fipronil
  • the A1/A2 weight ratio preferably ranges from 1/3 to 3/1; more preferably is equal to 1.
  • the A/B weight ratio preferably ranges from 1/125 to 125/1; more preferably from 1/25 to 25/1.
  • the compound ratio A/B in the pesticide composition according to the invention, can be advantageously selected so as to produce a synergistic effect.
  • synergistic effect is understood to mean in particular that defined by Colby in an article entitled “Calculation of the synergistic and antagonistic responses of herbicide combinations” Weeds, (1967), 15, pages 20-22.
  • E represents the expected percentage of inhibition of the pest for the combination of the two compounds at defined doses (for example equal to x and y respectively)
  • X is the percentage of inhibition observed for the pest by compound A at a defined dose (equal to x)
  • Y is the percentage of inhibition observed for the pest by compound B at a defined dose (equal to y).
  • the present invention provides a composition comprising:
  • composition according to the invention can comprise a further fungicide compound C preferably selected in the list consisting of:
  • Most preferred compounds C in the composition according to the invention can be selected in the list consisting of benalaxyl, benalaxyl-M, benthiavalicarb, carboxin, chlorothalonil, cyazofamid, cymoxanil, dimetomorph, fluazinam, fludioxonil, fluoxastrobin, fluquinconazole, flutriafol, hexaconazole, hymexazol, ipconazole, mancozeb, mandipropamid, maneb, mefenoxam, metalaxyl, metiram, penconazole, penthiopyrad, phosphorous acid, propamocarb-fosetylate, propineb, prothioconazole, tebuconazole, thiram, triadimenol, trifloxystrobin, triticonazole and N-[2-(1,3-dimethyl-but
  • composition according to the invention preferably comprises
  • the A/B/C weight ratio preferably ranges from 1/100/100 to 1/0.01/0.01; more preferably from Jan. 80, 1980 to 1/0.05/0.05; even more preferably from 1/50/100 to 1/1.5/2.5; still even more preferably from 1/12/25 to 1/6/12.
  • the compound ratio A/B/C can be advantageously selected so as to produce a synergistic effect.
  • synergistic effect is understood to mean in particular that defined by Colby in an article entitled “Calculation of the synergistic and antagonistic responses of herbicide combinations” Weeds, (1967), 15, pages 20-22.
  • E represents the expected percentage of inhibition of the pest for the combination of the three compounds at defined doses (for example equal to x, y and z respectively)
  • Y is the percentage of inhibition observed for the pest by compound B at a defined dose (equal to y)
  • Z is the percentage of inhibition observed for the pest by compound C at a defined dose (equal to z).
  • the pesticide composition according to the invention may comprise from 0.00001 to 100%, preferably from 0.001 to 80%, of active compounds, whether these compounds are combined, or whether they are in the form of two or more active ingredients used separately.
  • the pesticide composition according to the invention may eventually also comprise one or more other active substances selected from fungicide, herbicide, insecticide or plant growth regulator active compounds.
  • the pesticide composition according to the invention may also comprise any other adjuvants or auxiliary agent useful in plant protection formulations such as, for example, an agriculturally suitable inert carrier and optionally an agriculturally suitable surfactant.
  • the pesticide composition according to the invention can be used alone or in formulations containing one or the other of the active ingredients or alternatively both of them together, in combination or association with one or more other compatible components which are, for example, solid or liquid fillers or diluents, adjuvants, surfactants or equivalents, which are suitable for the desired use and which are acceptable for uses in agriculture.
  • the formulations can be of any type known in the sector that is suitable for application onto all types of cultures or crops. These formulations, which can be prepared in any manner known by the skilled person, also form part of the invention.
  • the formulations may also contain ingredients of other types, such as protective colloids, adhesives, thickeners, thixotropic agents, penetrating agents, oils for spraying, stabilisers, preserving agents (in particular mould-proofing or biocide agents), sequestering or chelating agents or the like. More generally, the compounds used in the invention can be combined with any solid or liquid additives corresponding to the usual formulation techniques.
  • filler means an organic or inorganic, natural or synthetic component with which the active components are combined to facilitate its application, for example, onto the plants, the seeds or the soil.
  • This filler is consequently generally inert and it must be acceptable (for example acceptable for agronomic uses, in particular for treating plants).
  • the filler can be solid, for example clays, natural or synthetic silicates, silica, resins, waxes, solid fertilizers (for example ammonium salts), natural soil minerals, such as kaolins, clays, talc, lime, quartz, attapulgite, montmorillonite, bentonite or diatomaceous earths, or synthetic minerals, such as silica, alumina or silicates, in particular aluminium or magnesium silicates.
  • the solid fillers which are suitable for granules are as follows: natural, crushed or broken rocks, such as calcite, marble, pumice, sepiolite and dolomite; synthetic granules of inorganic or organic flours; granules of organic material such as sawdust, coconut shell, corn ear or envelope, or tobacco stem; kieselguhr, tricalcium phosphate, powdered cork or adsorbent carbon black; water-soluble polymers, resins, waxes; or solid fertilizers.
  • Such composition may, if so desired, contain one or more compatible agents such as wetting agents, dispersing agents, emulsifiers or colourings which, when they are solid, may also act as diluents.
  • the fillers may also be liquid, for example: water, alcohols, in particular butanol or glycol, as well as ethers or esters thereof, in particular methyl glycol acetate; ketones, in particular acetone, cyclohexanone, methyl ethyl ketone, methyl isobutyl ketone or isophorone; petroleum fractions such as paraffinic or aromatic hydrocarbons, in particular xylenes or alkylnaphthalenes; mineral or plant oils; aliphatic chlorohydrocarbons, in particular trichloroethane or methylene chloride; aromatic chlorohydrocarbons, in particular chlorobenzenes; water-soluble or highly polar solvents such as dimethylformamide, dimethyl sulphoxide, N,N-dimethyl-acetamide or N-methylpyrrolidone; N-octylpyrrolidone, liquefied gases; or the like, whether they are taken separately or as a mixture.
  • the surfactant can be an emulsifier, a dispersing agent or a wetting agent, of ionic or nonionic type or a mixture of these surfactants.
  • surfactants there are used, for example, polyacrylic acid salts, lignosulphonic acid salts, phenolsulphonic or naphthalenesulphonic acid salts, polycondensates of ethylene oxide with fatty alcohols or fatty acids or fatty esters or fatty amines, substituted phenols (in particular alkylphenols or arylphenols), ester-salts of sulphosuccinic acid, taurine derivatives (in particular alkyl taurates), phosphoric esters of alcohols or of polycondensates of ethylene oxide with phenols, fatty acid esters with polyols, or sulphate, sulphonate or phosphate functional derivatives of the compounds described above.
  • the presence of at least one surfactant is generally essential when the active ingredients and/or the
  • the formulations may also contain other additives such as adhesives or dyes.
  • Adhesives such as carboxymethylcellulose or natural or synthetic polymers in the form of powders, granules or matrices, such as gum arabic, latex, polyvinylpyrrolidone, polyvinyl alcohol or polyvinyl acetate, natural phospholipids, such as cephalins or lecithins, or synthetic phospholipids can be used in the formulations.
  • colourings such as inorganic pigments, such as, for example: iron oxides, titanium oxides, Prussian blue; organic colouring stuffs, such as those of the alizarin, azo or metal phthalocyanin type; or of trace elements such as iron, manganese, boron, copper, cobalt, molybdenum or zinc salts.
  • inorganic pigments such as, for example: iron oxides, titanium oxides, Prussian blue
  • organic colouring stuffs such as those of the alizarin, azo or metal phthalocyanin type
  • trace elements such as iron, manganese, boron, copper, cobalt, molybdenum or zinc salts.
  • the pesticide composition according to the present invention covers not only the compositions which are ready to be applied to the crop by means of a suitable device, such as a spraying device, but also the commercial concentrated composition which have to be diluted before application to the crop.
  • the pesticide composition herein described is used in general for application to growing plants, or to sites where crops are grown or intended to grow, or for the treatment, coating or film-coating of seeds.
  • seeds may comprise any propagation materials, like for example seeds, fruit, tubers, grains, roots, rhizomes, parts of plants.
  • the pesticide composition according to the invention may also be applied to the vegetation and in particular to the leaves infested or capable of being infested with the phytopathogenic fungi or damaged by insects.
  • Another method of applying the pesticide composition according to the invention is to add a formulation containing the active ingredients to the irrigation water.
  • a method for controlling the phytopathogenic fungi or damaging insects of plants, crops or seeds characterized in that an agronomically effective and substantially non-phytotoxic quantity of a pesticide composition according to the invention is applied as seed treatment, foliar application, stem application, drench or drip application (chemigation) to the seed, the plant or to the fruit of the plant or to soil or to inert substrate (e.g. inorganic substrates like sand, rockwool, glasswool; expanded minerals like perlite, vermiculite, zeolite or expanded clay), Pumice, Pyroclastic materials or stuff, synthetic organic substrates (e.g. polyurethane), organic substrates (e.g.
  • peat e.g. peat, composts, tree waste products like coir, wood fibre or chips, tree bark
  • a liquid substrate e.g. floating hydroponic systems, Nutrient Film Technique, Aeroponics
  • the method according to the invention may either be a curing, preventing or eradicating method.
  • a composition used can be prepared beforehand by mixing the two or more active compounds according to the invention.
  • a lower dose may offer adequate protection.
  • the optimum dose usually depends on several factors, for example on the type of phytopathogenic fungus to be treated or insect to control, on the type or level of development of the infested plant, on the density of vegetation, or alternatively on the method of application.
  • the crop treated with the pesticide composition or combination according to the invention is, for example, grapevine, but this could be cereals, vegetables, lucerne, soybean, market garden crops, turf, wood, tree or horticultural plants.
  • the method of treatment according to the invention may also be useful to treat propagation material such as tubers or rhizomes, but also seeds, seedlings or seedlings pricking out and plants or plants pricking out. This method of treatment may also be useful to treat roots.
  • the method of treatment according to the invention may also be useful to treat the over-ground parts of the plant such as trunks, stems or stalks, leaves, flowers and fruit of the concerned plant.
  • cotton Among the plants that can be protected by the method according to the invention, mention can be made of cotton; flax; vine; fruit or vegetable crops such as Rosaceae sp. (for instance pip fruit such as apples and pears, but also stone fruit such as apricots, almonds and peaches), Ribesioidae sp., Juglandaceae sp., Betulaceae sp., Anacardiaceae sp., Fagaceae sp., Moraceae sp., Oleaceae sp., Actimidaceae sp., Lauraceae sp., Musaceae sp.
  • Rosaceae sp. for instance pip fruit such as apples and pears, but also stone fruit such as apricots, almonds and peaches
  • Rosaceae sp. for instance pip fruit such as apples and pears, but also stone fruit such as apricots, almonds and peaches
  • Rubiaceae sp. for instance banana trees and plantins
  • Rubiaceae sp. Theaceae sp., Sterculiceae sp., Rutaceae sp. (for instance lemons, oranges and grapefruit); Solanaceae sp. (for instance tomatoes), Liliaceae sp., Asteraceae sp. (for instance lettuces), Umbelliferae sp., Cruciferae sp., Chenopodiaceae sp., Cucurbitaceae sp., Papilionaceae sp. (for instance peas), Rosaceae sp. (for instance strawberries); major crops such as Graminae sp.
  • Asteraceae sp. for instance sunflower
  • Cruciferae sp. for instance colza
  • Fabacae sp. for instance peanuts
  • Papilionaceae sp. for instance soybean
  • Solanaceae sp. for instance potatoes
  • Chenopodiaceae sp. for instance beetroots
  • horticultural and forest crops as well as genetically modified homologues of these crops.
  • composition according to the invention may also be used in the treatment of genetically modified organisms with the compounds according to the invention or the agrochemical compositions according to the invention.
  • Genetically modified plants are plants into genome of which a heterologous gene encoding a protein of interest has been stably integrated.
  • the expression “heterologous gene encoding a protein of interest” essentially means genes which give the transformed plant new agronomic properties, or genes for improving the agronomic quality of the modified plant.
  • the composition according to the invention may also be used against fungal diseases liable to grow on or inside timber.
  • the term “timber” means all types of species of wood, and all types of working of this wood intended for construction, for example solid wood, high-density wood, laminated wood, and plywood.
  • the method for treating timber according to the invention mainly consists in contacting one or more compounds according to the invention, or a composition according to the invention; this includes for example direct application, spraying, dipping, injection or any other suitable means.
  • Powdery mildew diseases such as:
  • the damaging insects of crops which can be controlled at any development stage by using the pesticide composition according to the invention include:
  • the present invention provides a product comprising compounds (A1 and A2) and a compound (B) and optionally a compound (C), as herein defined, as a combined preparation for simultaneous, separate or sequential use in controlling the phytopathogenic fungi or damaging insects of plants, crops or seeds at a site.
  • the pesticide composition according to the invention can be prepared immediately before use by using a kit-of-parts for controlling, curatively or preventively, the phytopathogenic fungi of crops, such a kit-of-parts may comprise at least compounds (A1 and A2) and at least one compound (B) and optionally compound (C) intended to be combined or used simultaneously, separately or sequentially in controlling the phytopathogenic fungi of crops at a site.
  • ingredients which comprise in particular the active agents (A1 and A2) and (B) and optionally compound (C) and which are packaged separately, are provided in the form of a powder or in the form of a liquid which is concentrated to a greater or lesser degree.
  • the user simply has to mix in the prescribed doses and to add the quantities of liquid, for example of water, necessary to obtain a formulation which is ready to use and which can be applied to the crops.
  • active compound 1 part by weight of active compound is mixed with the stated amount of solvent and emulsifier, and the concentrate is diluted with emulsifier-containing water to the desired concentration.
  • Cabbage leaves Brassica oleracea
  • Cabbage leaves Brassica oleracea
  • active compound 1 part by weight of active compound is mixed with the stated amount of solvent and emulsifier, and the concentrate is diluted with emulsifier-containing water to the desired concentration.
  • Cabbage leaves Brassica oleracea
  • Cabbage leaves Brassica oleracea
  • the mortality is determined. 100% means that all the caterpillars have been killed; 0% means that none of the caterpillars have been killed.
  • active compound 1 part by weight of active compound is mixed with the stated amount of solvent and emulsifier, and the concentrate is diluted with emulsifier-containing water to the desired concentration.
  • Cabbage leaves Brassica oleracea
  • Cabbage leaves Brassica oleracea
  • the mortality is determined. 100% means that all the caterpillars have been killed; 0% means that none of the caterpillars have been killed.

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  • Life Sciences & Earth Sciences (AREA)
  • Dentistry (AREA)
  • Wood Science & Technology (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Agronomy & Crop Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Pest Control & Pesticides (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Pretreatment Of Seeds And Plants (AREA)
  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
US12/520,565 2006-12-22 2007-12-21 Pesticidal composition comprising fosetyl-aluminium, propamocarb-hcl and an insecticide substance Abandoned US20100035840A1 (en)

Applications Claiming Priority (3)

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EP06127178.9 2006-12-22
EP06127178 2006-12-22
PCT/EP2007/064430 WO2008077931A2 (en) 2006-12-22 2007-12-21 Pesticide composition comprising fosetyl-aluminium, propamocarb-hcl and an insecticide active substance

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PCT/EP2007/064430 A-371-Of-International WO2008077931A2 (en) 2006-12-22 2007-12-21 Pesticide composition comprising fosetyl-aluminium, propamocarb-hcl and an insecticide active substance

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US13/781,228 Expired - Fee Related US9125417B2 (en) 2006-12-22 2013-02-28 Pesticide composition comprising fosetyl-aluminium, propamocarb-HCl and an insecticide active substance
US14/803,468 Expired - Fee Related US9210935B2 (en) 2006-12-22 2015-07-20 Pesticide composition comprising fosetyl-aluminium, propamocarb-HCl and an insecticide active substance

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US (3) US20100035840A1 (ja)
EP (3) EP2111111A2 (ja)
JP (2) JP5563828B2 (ja)
KR (3) KR20150041169A (ja)
CN (1) CN101562982B (ja)
AR (1) AR064663A1 (ja)
AU (1) AU2007337969B8 (ja)
BR (1) BRPI0719452A2 (ja)
CA (1) CA2673374C (ja)
CL (1) CL2007003748A1 (ja)
CO (1) CO6220915A2 (ja)
EA (3) EA023723B1 (ja)
IL (1) IL198635A0 (ja)
MA (1) MA31104B1 (ja)
MX (1) MX2009006604A (ja)
UA (1) UA95499C2 (ja)
WO (1) WO2008077931A2 (ja)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20090318386A1 (en) * 2000-03-28 2009-12-24 Reiner Fischer Active compound combinations having insecticidal and acaricidal properties
US20110071220A1 (en) * 2008-03-27 2011-03-24 Bayer Cropscience Ag Use of Tetronic Acid Derivatives for Fighting Insects and Red Spider Mites by Watering on the Ground, Droplet Application or Immersion Application
US8846568B2 (en) 2009-03-25 2014-09-30 Bayer Cropscience Ag Active compound combinations having insecticidal and acaricidal properties

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CL2007003746A1 (es) 2006-12-22 2008-07-18 Bayer Cropscience Ag Composicion pesticida que comprende propamocarb-hcl y un compuesto insecticida; y metodo para controlar hongos fitopatogenos o insecticidas daninos de las plantas, cultivos o semillas que comprende aplicar dicha composicion.
EP2119362A1 (en) * 2008-05-15 2009-11-18 Bayer CropScience AG Method for improving the tolerance of crops to chilling temperatures and/or frost
CN101658177B (zh) * 2009-07-22 2013-06-12 深圳诺普信农化股份有限公司 一种含有氰霜唑的复配杀菌组合物
BR112012013536A2 (pt) * 2009-12-10 2015-09-15 Basf Se "misturas, composição pesticida, método para controlar pragas, método para a proteção de material de propagação de planta de pragas e material de propagação de planta"
CN101984825A (zh) * 2010-07-15 2011-03-16 江阴苏利科技有限公司 一种含有氟啶胺和三乙膦酸铝的杀菌组合物及其用途
CN101999392A (zh) * 2010-12-28 2011-04-06 青岛瀚生生物科技股份有限公司 一种含吡蚜酮复配组合物
CN102017991A (zh) * 2010-12-31 2011-04-20 陕西美邦农药有限公司 一种含有三乙膦酸铝与三唑类化合物的杀菌组合物
CN103651539B (zh) * 2012-09-11 2015-09-09 陕西美邦农药有限公司 一种含吡噻菌胺的农药组合物
CN103262851A (zh) * 2013-05-30 2013-08-28 南宁市德丰富化工有限责任公司 一种含霜霉威的杀虫杀菌复配剂
CN114467965B (zh) * 2020-11-13 2024-02-09 山东潍坊润丰化工股份有限公司 一种含霜霉威与三乙膦酸铝的可溶性粒剂及其应用
CN114467964B (zh) * 2020-11-13 2024-02-02 山东潍坊润丰化工股份有限公司 一种含霜霉威与三乙膦酸铝的可湿性粉剂及其应用

Family Cites Families (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL157191C (nl) 1966-12-17 Schering Ag Werkwijze voor het bereiden van een preparaat met fungicide en fungistatische werking.
DE2463046C2 (de) 1973-12-14 1984-05-03 PEPRO - Société pour le Développement et la Vente de Spécialités Chimiques, Lyon Fungizide Mittel auf Ammoniumphosphonatbasis
DE4216814A1 (de) * 1991-07-16 1993-01-21 Bayer Ag 3-aryl-4-hydroxy-(delta)(pfeil hoch)3(pfeil hoch)-dihydrofuranon- und 3-aryl-4-hydroxy-(delta)(pfeil hoch)3(pfeil hoch)-dihydrothiophenon-derivate
PL201168B1 (pl) * 1996-08-05 2009-03-31 Bayer Ag Podstawione fenyloketoenole, sposób wytwarzania tych związków, związki pośrednie, pestycydy i zastosowanie związków
FR2761577B1 (fr) * 1997-04-04 1999-05-14 Rhone Poulenc Agrochimie Composition fongicide synergique a base de propacarbe et de derives de l'acide phosphoreux
WO1999042468A1 (en) * 1998-02-20 1999-08-26 Aventis Cropscience Uk Limited Fungicides
CZ299375B6 (cs) * 1998-11-30 2008-07-09 Nihon Nohyaku Co., Ltd. Ftalamidové deriváty nebo jejich soli, zemedelsko-zahradnický insekticid je obsahující a jeho použití
FR2821719B1 (fr) * 2001-03-08 2003-06-13 Aventis Cropscience Sa Nouvelles compositions fongicides a base de derive de pyridylmethylbenzamide et de propamocarbe
DE10231333A1 (de) * 2002-07-11 2004-01-22 Bayer Cropscience Ag Cis-Alkoxysubstituierte spirocyclische 1-H-Pyrrolidin-2,4-dion-Derivate
DE10310906A1 (de) * 2003-03-13 2004-09-23 Bayer Cropscience Ag Synergistische Wirkstoffkombinationen
WO2006024333A2 (en) * 2004-08-17 2006-03-09 Syngenta Participations Ag Aqueous neonicotinoid compositions for seed treatment
WO2006022225A1 (ja) 2004-08-23 2006-03-02 Nihon Nohyaku Co., Ltd. 光学活性フタルアミド誘導体及び農園芸用殺虫剤並びにその使用方法
MX2007012214A (es) * 2005-04-08 2007-12-10 Syngenta Participations Ag Mezclas pesticidas.
JP5020238B2 (ja) * 2005-06-21 2012-09-05 バイエル・クロップサイエンス・アーゲー 亜リン酸誘導体、マンデルアミド類の化合物及びさらなる殺菌性化合物を含んでいる殺菌剤組成物
KR101422552B1 (ko) * 2006-07-06 2014-07-24 바이엘 크롭사이언스 아게 피리딜에틸벤즈아미드 유도체 및 살충성 화합물을 포함하는농약 조성물
KR20090057126A (ko) * 2006-09-18 2009-06-03 바스프 에스이 안트라닐아미드 살충제 및 살진균제를 포함하는 살충 혼합물
CL2007003747A1 (es) * 2006-12-22 2008-07-18 Bayer Cropscience Ag Composicion pesticida que comprende fosetil-al y un compuesto insecticida; y metodo para controlar hongos fitopatogenos o insecticidas daninos de las plantas, cultivos o semillas que comprende aplicar dicha composicion.

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20090318386A1 (en) * 2000-03-28 2009-12-24 Reiner Fischer Active compound combinations having insecticidal and acaricidal properties
US20110071220A1 (en) * 2008-03-27 2011-03-24 Bayer Cropscience Ag Use of Tetronic Acid Derivatives for Fighting Insects and Red Spider Mites by Watering on the Ground, Droplet Application or Immersion Application
US8846568B2 (en) 2009-03-25 2014-09-30 Bayer Cropscience Ag Active compound combinations having insecticidal and acaricidal properties

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EA023723B1 (ru) 2016-07-29
EP2319322A2 (en) 2011-05-11
US20150320047A1 (en) 2015-11-12
BRPI0719452A2 (pt) 2013-12-10
EP2319323A3 (en) 2011-12-21
AU2007337969A1 (en) 2008-07-03
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CL2007003748A1 (es) 2008-07-18
US9125417B2 (en) 2015-09-08
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US20130178447A1 (en) 2013-07-11
EP2111111A2 (en) 2009-10-28
CO6220915A2 (es) 2010-11-19
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US9210935B2 (en) 2015-12-15
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AR064663A1 (es) 2009-04-15
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