WO2012029893A1 - Method for producing agricultural crop - Google Patents

Method for producing agricultural crop Download PDF

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Publication number
WO2012029893A1
WO2012029893A1 PCT/JP2011/069863 JP2011069863W WO2012029893A1 WO 2012029893 A1 WO2012029893 A1 WO 2012029893A1 JP 2011069863 W JP2011069863 W JP 2011069863W WO 2012029893 A1 WO2012029893 A1 WO 2012029893A1
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Prior art keywords
compound
group
composition
carbon atoms
agrochemical
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PCT/JP2011/069863
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French (fr)
Japanese (ja)
Inventor
亀井昌敏
水島洋泉
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花王株式会社
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Priority claimed from JP2011047410A external-priority patent/JP5763370B2/en
Priority claimed from JP2011047411A external-priority patent/JP5763371B2/en
Application filed by 花王株式会社 filed Critical 花王株式会社
Priority to BR112013004493A priority Critical patent/BR112013004493A2/en
Priority to CN201180052202.5A priority patent/CN103209588B/en
Priority to US13/820,352 priority patent/US10188101B2/en
Publication of WO2012029893A1 publication Critical patent/WO2012029893A1/en

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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
    • A01N25/00Biocides, 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
    • A01N25/30Biocides, 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 characterised by the surfactants
    • 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
    • A01N25/00Biocides, 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
    • A01N25/02Biocides, 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
    • A01N25/04Dispersions, emulsions, suspoemulsions, suspension concentrates or gels

Definitions

  • the present invention relates to an agrochemical efficacy enhancer composition and an agrochemical composition.
  • agrochemical-containing compositions have been used in order to sufficiently bring out the effects of agrochemicals.
  • an agrochemical-containing composition that is highly effective for bipyridinium herbicides can be obtained by combining an anionic surfactant and a chelating agent (see, for example, International Publication No. 95/31903).
  • an agrochemical-containing composition having a high agrochemical effect can be obtained by adding a chelating agent to a cationic surfactant and adding another surfactant (for example, International Publication No. 95). / 17817).
  • non-aqueous spreading agent prepared by dissolving sorbitan fatty acid ester, polyoxyethylene alkyl ether and polyether-modified silicone in isopropyl alcohol has been proposed in order to improve wettability (Japanese Patent Laid-Open No. 2000-001404). See claims and others)).
  • Japanese Patent Application Laid-Open No. 2006-248994 discloses a non-aqueous pesticide spreading agent composition containing a surfactant, a water-soluble organic solvent having a flash point of 70 ° C. or higher, an antifoaming agent, or a defoaming agent. Yes.
  • JP 2006-257072 discloses a herbicidal composition containing a polyoxyalkylene fatty acid ester and another nonionic surfactant.
  • Japanese Patent Application Laid-Open No. 2008-184455 discloses a specific nonionic surfactant, an anionic surfactant, a specific ether selected from the group consisting of hydrophobic agrochemical active compounds, polyoxyethylene polyoxypropylene block copolymers, and the like.
  • An agrochemical solution containing a predetermined amount of a compound and 1,3-dimethyl-2-imidazolidinone is disclosed.
  • Japanese Patent Laid-Open No. 2002-249403 discloses an agrochemical efficacy enhancer containing at least one of a specific alcohol compound, a specific ether compound and a specific ester compound as an active ingredient. Summary of invention
  • the present invention includes one or more compounds (A) selected from the following (A1) to (A5), one or more compounds (B) selected from the following (B1) to (B2), a fungicide, an insecticide, A method for producing agricultural crops, comprising a step of applying a pesticide composition containing any one of a pesticide active ingredient selected from active ingredients of each of an acaricide, a herbicide, and a plant growth regulator to an object of the pesticide active ingredient.
  • the present invention provides an efficacy enhancer composition for agricultural chemicals that improves the wettability (easiness of spreading) of agricultural chemicals and can effectively enhance the efficacy of agricultural chemicals.
  • an agrochemical efficacy enhancer composition and an agrochemical composition that can improve the wettability of an agrochemical and effectively enhance the efficacy of the agrochemical.
  • the present invention includes the following aspects.
  • the present invention relates to a method for producing agricultural crops, comprising a step of applying an agrochemical composition containing any of the agrochemical ingredients to a target of the agrochemical substance.
  • the present invention relates to an efficacy enhancer composition for agricultural chemicals containing the above compound (A) [hereinafter referred to as compound (A)] and the above compound (B) [hereinafter referred to as compound (B)].
  • Agrochemical composition comprising compound (A), compound (B), and an agrochemical base selected from active ingredients of fungicides, insecticides, acaricides, herbicides and plant growth regulators About.
  • a plant comprising the agrochemical efficacy enhancer composition of the present invention described above and any pesticide active ingredient selected from active ingredients of fungicides, insecticides, acaricides, herbicides and plant growth regulators. It is related with the production method of a plant including the process given to.
  • the present invention relates to a plant production method including a step of applying the agrochemical composition of the present invention to a plant.
  • the efficacy enhancer composition for agricultural chemicals of the present invention contains a compound (A) and a compound (B).
  • the reason why the wettability (easiness of wetting and spreading) of the pesticide is improved by using the compound (A) and the compound (B) in combination is not clear, but it is adsorbed at the interface between the droplet and the leaf and decreases the interfacial tension. It is estimated that the compound (B) to be reduced and the compound (A) to reduce the surface tension of the droplet itself interact with each other by structural similarity, and the wettability of the agricultural chemical is drastically improved. is doing.
  • the efficacy enhancer composition for agricultural chemicals of the present invention contains one or more compounds (A) selected from the following (A1) to (A5) from the viewpoint of improving wettability and enhancing efficacy of agricultural chemicals.
  • (B) is (B1), among the following compounds (A1) to (A5), (A1), (A4) and (A5) are preferable from the viewpoint of improving wettability and enhancing the efficacy of agricultural chemicals.
  • (A1) and (A5) are more preferable.
  • (B) is (B2), among the following compounds (A1) to (A5), (A1), (A2), (A4) are from the viewpoint of improving the wettability and enhancing the efficacy of the agricultural chemical.
  • (A1) and (A4) are more preferable.
  • the compound (A1) is represented by the following general formula (A1).
  • R 1a is a linear or branched alkyl or alkenyl group having 10 to 16 carbon atoms, preferably 10 to 10 carbon atoms, from the viewpoints of improving wetability and enhancing the efficacy of agricultural chemicals.
  • 14 linear or branched alkyl group or alkenyl group, more preferably a linear or branched alkyl group or alkenyl group having 10 to 12 carbon atoms, and still more preferably a linear or branched group having 12 carbon atoms.
  • l is the average number of moles of ethyleneoxy group (EO) added, and is 3 to 40, preferably 4 to 30, more preferably 4 to 4 from the viewpoint of improving wettability and enhancing the efficacy of agricultural chemicals. 25, more preferably 5-20, even more preferably 5-15, even more preferably 5-12, and even more preferably 5-10.
  • R 2a is a hydrogen atom or a methyl group, preferably a hydrogen atom, from the viewpoint of improving wettability and enhancing the efficacy of agricultural chemicals.
  • Compound (A2) is a polyoxyethylene fatty acid ester.
  • the fatty acid has 8 to 16 carbon atoms, preferably 10 to 14 and more preferably 10 to 12 from the viewpoint of improving wettability and enhancing the efficacy of the agricultural chemical.
  • the fatty acid in the compound (A2) preferably has a linear or branched alkyl group or alkenyl group, and more preferably a linear alkyl group.
  • Examples of the fatty acid in the compound (A2) include caprylic acid, capric acid, lauric acid, myristic acid, palmitic acid and the like.
  • the average number of moles of ethylene oxide added is 5 to 40, preferably 5 to 20, and more preferably 6 to 15 from the viewpoints of improving wettability and enhancing the efficacy of agricultural chemicals.
  • the ester is preferably a monoester.
  • Compound (A3) is polyoxyethylene sorbitan fatty acid ester.
  • the number of carbon atoms of the fatty acid is from 8 to 16, preferably from 10 to 14, and more preferably from 10 to 12, from the viewpoint of improving the wettability and enhancing the efficacy of the agricultural chemical.
  • the fatty acid in the compound (A3) preferably has a linear or branched alkyl group or alkenyl group, and more preferably a linear alkyl group.
  • Examples of the fatty acid in the compound (A3) include caprylic acid, capric acid, lauric acid, myristic acid, palmitic acid and the like.
  • the average added mole number of ethylene oxide is 5 to 40, preferably 5 to 20, and more preferably 6 to 15.
  • the esterification degree is preferably 1.
  • Compound (A4) is a (poly) glycerin fatty acid ester.
  • “(poly) glycerin” means “glycerin or polyglycerin”.
  • the number of carbon atoms of the fatty acid is from 8 to 16, preferably from 8 to 12, more preferably from 10 to 12, and even more preferably from the viewpoint of improving wetability and enhancing the efficacy of the agricultural chemical.
  • the fatty acid in the compound (A4) preferably has a linear or branched alkyl group or alkenyl group, and more preferably a linear alkyl group.
  • Examples of the fatty acid in the compound (A4) include caprylic acid, capric acid, lauric acid, myristic acid, palmitic acid and the like.
  • the average degree of condensation of glycerin is 1 to 3, preferably 1 to 2, and more preferably 2 from the viewpoint of improving wetability and enhancing the efficacy of agricultural chemicals.
  • the compound (A5) is an alkyl saccharide represented by the following general formula (A5).
  • R 3a —O— (G) p (A5)
  • R 3a is an alkyl group having 8 to 16 carbon atoms, preferably 10 to 14 carbon atoms, from the viewpoint of improving wettability and enhancing the efficacy of agricultural chemicals.
  • G represents a reducing sugar having 5 to 6 carbon atoms, such as ribose, arabinose, xylose, allose, altrose, glucose, mannose, fructose, gulose, idose, galactose, talose, etc., preferably glucose, mannose, fructose, galactose More preferably, it is glucose.
  • p represents a number of 1 to 10, preferably 1 to 5, from the viewpoints of improving wettability and enhancing the efficacy of agricultural chemicals.
  • R 1b O — [(PO) m / (EO) n ] —R 2b (B1)
  • R 1b is a linear or branched alkyl group or alkenyl group having 6 to 12 carbon atoms, preferably 8 to 8 carbon atoms, from the viewpoints of improving wetability and enhancing the efficacy of agricultural chemicals. 12 straight-chain or branched alkyl groups or alkenyl groups, more preferably straight-chain or branched alkyl groups or alkenyl groups having 8 to 10 carbon atoms, and even more preferably straight-chain chains having 8 to 10 carbon atoms.
  • M is the average number of moles of propyleneoxy group (PO) added, and is 1 to 25, preferably 2 to 20, more preferably 2 to 20 from the viewpoint of improving the wettability and enhancing the efficacy of the agricultural chemical. More preferably, it is 2 to 18, still more preferably 2 to 16, even more preferably 2 to 12, and still more preferably 2 to 10.
  • N is the average number of added moles of ethyleneoxy group (EO), and is 0 to 4, preferably 0 to 3, more preferably 0 to 2 from the viewpoint of improving wettability and enhancing the efficacy of agricultural chemicals. More preferably, it is 0 to 1, and still more preferably 0.
  • the ratio of m in the general formula (B1) to the total of m and n is preferably m / (m + n).
  • R 2b is a hydrogen atom or a methyl group, preferably a hydrogen atom, from the viewpoint of improving wettability and enhancing the efficacy of agricultural chemicals.
  • the arrangement of PO and EO, from the viewpoint of ductility improvement and pesticide efficacy potentiating humidity is preferably a block sequence, the R 1b O- -More preferably, the blocks are arranged in the order of EO.
  • R 3b is a linear or branched alkyl group having 8 to 14 carbon atoms, preferably a straight chain having 8 to 12 carbon atoms, from the viewpoints of improving wetability and enhancing the effectiveness of agricultural chemicals. It is a chain or branched alkyl group, more preferably a linear or branched alkyl group having 8 to 10 carbon atoms, and still more preferably a linear alkyl group having 10 carbon atoms.
  • the weight ratio of the compound (A) to the compound (B) is (A) / (B), preferably 0.03 to 30, more preferably 0.05 to 20, more preferably 0.1-10, even more preferably 0.2-9, even more preferably 0.2-8, even more preferably 0.3-8, even more preferably 0.5-2 It is. If (A) / (B) weight ratio is the said range, the wettability of the spray liquid with respect to a plant and the permeability
  • the total amount of the compound (A) and the compound (B) is preferably 5% by weight or more, more preferably 10% by weight or more, still more preferably 20% by weight or more. Preferably, it contains 40% by weight or more, still more preferably 60% by weight or more, still more preferably 80% by weight or more, and even more preferably 90% by weight or more.
  • the upper limit that can be taken is 100% by weight.
  • the concentration of the compound (A) and the compound (B) is sufficient when used with dilution with an agricultural chemical, and a good agricultural chemical efficacy enhancing effect Is obtained. Therefore, in order to obtain the effect of enhancing the effectiveness of agricultural chemicals, it can be used at the same dilution ratio of agricultural chemicals as usual, which is preferable in terms of cost and workability.
  • a surfactant other than the compound (A) and the compound (B) can be used in combination as long as the effects of the compound (A) and the compound (B) are not hindered.
  • surfactants include compound (A), nonionic surfactants other than compound (B), anionic surfactants, cationic surfactants and amphoteric surfactants, or mixtures thereof.
  • the content can be appropriately selected as long as the effects of the compound (A) and the compound (B) are not hindered.
  • the proportion of compound (A) and compound (B) in the total surfactant of the agricultural chemical efficacy enhancing agent composition is preferably 50% by weight or more, and 70% by weight. More preferably, it is more preferably 90% by weight or more.
  • Nonionic surfactants include polyoxyethylene alkyl ethers (however, those not corresponding to the general formulas (A1) and (B1)), polyoxyethylene alkyl aryl ethers, polyoxyethylene alkyl aryl ether formaldehyde condensates, Polyoxyalkylene aryl ether, polyoxyalkylene alkyl sorbitol ester, polyoxyalkylene alkyl glycerol ester, polyoxyalkylene block copolymer, polyoxyalkylene block copolymer alkyl glycerol ester, polyoxyalkylene alkyl sulfonamide, polyoxypropylene block Copolymer, polyoxyethylene oleyl ether, polyoxyalkylene alkylphenol, polyoxyalkylene alkyl poly Such glycosidic, and the like a mixture of two or more of these.
  • Examples of cationic surfactants include alkylamine ethylene oxide adducts, alkylamine propylene oxide adducts such as tallow amine ethylene oxide adducts, oleylamine ethylene oxide adducts, soyamine ethylene oxide adducts, cocoamine ethylene oxide adducts, Examples include synthetic alkylamine ethylene oxide adducts, octylamine ethylene oxide adducts, dialkylamine derivatives, and the like, and mixtures thereof.
  • dialkylamine derivative examples include dialkylmonomethylhydroxyethylammonium propionate, dialkylmonomethylbenzalkonium chloride, dialkylmonomethylethylammonium ethyl sulfate, dialkylmonomethylamine oxide, dialkylmonomethylaminocarboxybetaine, and dialkylmonomethylhydroxysulfobetaine.
  • the cationic surfactant is preferably an alkylamine ethylene oxide adduct, an alkylamine propylene oxide adduct, or a dialkylamine derivative from the viewpoint of improving wettability and enhancing the effectiveness of agricultural chemicals, and a tallow amine ethylene oxide adduct or dilauryl.
  • Monomethylbenzalkonium chloride is more preferred.
  • anionic surfactants typical ones can be obtained in aqueous solution or in the solid state, examples of which are sodium mono- and di-alkylnaphthalene sulfonates, sodium alpha-olefin sulfonates, alkane sulfonic acids.
  • the anionic surfactant is preferably a fatty acid salt, more preferably a sodium salt or potassium salt of a higher fatty acid such as oleic acid or castor oil fatty acid, and more preferably potassium oleate, from the viewpoint of improving emulsification dispersibility.
  • Amphoteric surfactants include lauryl dimethylamine oxide, Armox C / 12, amine oxide, monaterics, miranols, betaine, Lonzaines, other amine oxides, There is a mixture.
  • the efficacy enhancer composition for agricultural chemicals of the present invention may be composed of the compound (A) and the compound (B), but when it contains components other than the compound (A) and the compound (B), the balance is water. And / or organic solvents are preferred.
  • the composition containing water and / or an organic solvent is excellent in low-temperature or high-temperature stability of the composition, and further excellent in long-term storage stability.
  • the composition containing water or an organic solvent facilitates dispersion and dissolution of the compound (A) and the compound (B) in the dilution medium (water and / or organic solvent) at the time of dilution. The effect can be enhanced.
  • Preferred organic solvents include isobutanol, isopropanol, ethanol, diethylene glycol, ethyl lactic acid, butyl cellosolve, polyethylene glycol (weight average molecular weight 200 to 400), dimethyl sulfoxide, N-butyl carbitol, 1,3-butylene glycol, di Examples thereof include propylene glycol 2- (2-methoxyethoxy) ethanol and ethyl carbitol, and ethyl lactic acid and diethylene glycol are preferable and diethylene glycol is more preferable from the viewpoint of improving the wettability of the agricultural chemical and enhancing the efficacy of the agricultural chemical.
  • the content of water and / or organic solvent in the efficacy enhancer composition for agricultural chemicals of the present invention is not particularly limited, but 50% of the compound (A) and compound (B) in the efficacy enhancer composition for agricultural chemicals are used. It is preferably used in an amount of at least wt%, more preferably at least 70 wt%, and even more preferably at least 90 wt%.
  • the content of water and / or organic solvent in the composition is preferably less than 50% by weight, for example, 1 to less than 50% by weight, and more preferably 5 to 30% by weight.
  • the agrochemical composition of this invention contains the said compound (A), a compound (B), and an agrochemical raw material.
  • the active ingredient of an agrochemical means an active ingredient of an agrochemical.
  • the agrochemical composition of the present invention is any one selected from the active ingredients of the agrochemical efficacy enhancer composition of the present invention and each of the fungicides, insecticides, acaricides, herbicides, and plant growth regulators. The thing containing an agrochemical raw material is mentioned.
  • the agrochemical composition of the present invention comprises (i) a compound that releases hydrogen peroxide and hydrogen peroxide in water, and (ii) hypochlorous acid, hypochlorite, and water.
  • the content of one or more compounds selected from compounds that release hypochlorous acid is low, for example, 0.1% by weight or less in the composition as hypochlorous acid or hydrogen peroxide, and further 0.01% by weight % Or less, particularly those not contained are preferred.
  • the weight ratio of the total of the compound (A) and the compound (B) to the active ingredient of the agrochemical is from the viewpoint of improving wettability and enhancing the efficacy of the agrochemical
  • the total weight of the compound (B) / the weight of the agrochemical base is preferably 0.1 to 100, more preferably 0.2 to 40, and still more preferably 0.2 to 20.
  • the formulation type of the agrochemical composition of the present invention may be any of emulsion, solution, wettable powder, granule, powder, flowable formulation, etc., and the formulation type is not limited. Therefore, it may contain other additives according to the formulation type, such as emulsifiers, solvents, dispersants, carriers and the like.
  • the method of using the agrochemical efficacy enhancer composition according to the present invention includes a method of using the various agrochemical compositions containing the agrochemical efficacy enhancer composition, and a pesticide (the agrochemical efficacy enhancer of the present invention). There is a method of using an attached agrochemical efficacy enhancer composition at the time of dilution use, and any of these methods can provide the effect of enhancing the efficacy of the present invention.
  • a chelating agent In the preparation of the agricultural chemical composition of the present invention, a chelating agent, a pH adjuster, inorganic salts, and a thickener may be added as necessary.
  • chelating agents examples include aminopolycarboxylic acid chelating agents, aromatic and aliphatic carboxylic acid chelating agents, amino acid chelating agents, ether polycarboxylic acid chelating agents, and phosphonic acid chelating agents (for example, Iminodimethylphosphonic acid (IDP), alkyldiphosphonic acid (ADPA), etc.), or dimethylglyoxime (DG), hydroxycarboxylic acid chelating agent, polymer electrolyte (including oligomer) chelating agent, etc. May be in the form of an acid or a salt of sodium, potassium, ammonium or the like.
  • the chelating agent is preferably blended at a ratio of 0.01 to 30-fold mol with respect to the component (B) in the efficacy enhancer composition for agricultural chemicals.
  • RNX type 2 compound b) NX type 3 compound c) R-NX-CH 2 CH 2 -NX-R type compound d) R-NX-CH 2 CH 2 -NX type 2 compound and e) X 2 N- All R'-NX type 2 compounds can be used.
  • X represents —CH 2 COOH or —CH 2 CH 2 COOH
  • R represents a hydrogen atom, an alkyl group, a hydroxyl group, a hydroxyalkyl group or a substituent representing a known chelate compound of this type
  • R ′ represents It represents a group representing an alkylene group, a cycloalkylene group, and a known chelate compound of this type.
  • Typical examples of these include ethylenediaminetetraacetic acid (EDTA), cyclohexanediaminetetraacetic acid (CDTA), nitrilotriacetic acid (NTA), iminodiacetic acid (IDA), N- (2-hydroxyethyl) iminodiacetic acid (HIMDA), diethylenetriaminepenta
  • EDTA ethylenediaminetetraacetic acid
  • CDTA cyclohexanediaminetetraacetic acid
  • NTA nitrilotriacetic acid
  • IDA iminodiacetic acid
  • HAMDA iminodiacetic acid
  • diethylenetriaminepenta examples include acetic acid (DTPA), N- (2-hydroxyethyl) ethylenediamine triacetic acid (EDTA-OH), glycol ether diamine tetraacetic acid (GEDTA), and salts thereof.
  • DTPA N- (2-hydroxyethyl) ethylenediamine triacetic acid
  • Aromatic and aliphatic carboxylic acid chelating agents that can be used in the present invention are oxalic acid, succinic acid, pyruvic acid or anthranilic acid and salts thereof.
  • Amino acid chelating agents that can be used in the present invention include glycine, serine, alanine, lysine, cystine, cysteine, ethionine, tyrosine, methionine, and salts and derivatives thereof.
  • Examples of the hydroxycarboxylic acid chelating agent that can be used in the present invention include glycolic acid, malic acid, citric acid, gluconic acid, heptonic acid, acetic acid, and salts thereof.
  • examples of the ether polycarboxylic acid-based chelating agent that can be used in the present invention include compounds represented by the following formula and similar compounds and salts thereof (particularly Na salts).
  • polymer electrolyte (containing oligomer) chelating agent examples include acrylic acid polymer, maleic anhydride polymer, ⁇ -hydroxyacrylic acid polymer, itaconic acid polymer and copolymers thereof, epoxy Examples thereof include succinic acid polymers.
  • the pH adjuster that can be used in the present invention is citric acid, phosphoric acid (pyrophosphoric acid), gluconic acid or the like, or a salt thereof.
  • inorganic salts examples include inorganic mineral salts such as inorganic salt clay, talc, bentonite, zeolite, calcium carbonate, diatomaceous earth, and white carbon.
  • inorganic ammonium salts include ammonium sulfate, ammonium nitrate, and phosphoric acid. Examples include ammonium, ammonium thiocyanate, ammonium chloride, and ammonium sulfamate.
  • any of natural, semi-synthetic and synthetic water-soluble thickeners can be used.
  • natural mucilage xanthan gum derived from microorganisms, xanthan gum, pectin derived from plants, gum arabic , Guar gum, etc.
  • semi-synthetic mucilage cellulose or starch derivative methylated product, carboxyalkylated product, hydroxyalkylated product (including methylcellulose, carboxymethylcellulose, hydroxymethylcellulose etc.), sorbitol, etc.
  • Specific examples include acrylates, polymaleates, polyvinylpyrrolidones, pentaerythritol ethylene oxide adducts, and the like.
  • examples of the agrochemical base used in the agrochemical composition of the present invention include those described in the Agricultural Handbook 2001 edition (Japan Plant Protection Association), but are not limited thereto.
  • the efficacy enhancer composition for agricultural chemicals of the present invention can be safely used with no phytotoxicity to various crops.
  • Bactericides include sulfur-based dinebu (zinc ethylene bisdithiocarbamate), manneb (manganese ethylene bisdithiocarbamate), manzeb (zinc ion coordinated manganese ethylene bisdithiocarbamate), polycarbamate (bisdimethyldithiocarbamoyl zinc ethylene bis Dithiocarbamate), benzimidazole as benomyl (methyl-1- (butylcarbamoyl) -2-benzimidazolecarbamate), thiophanate methyl (1,2-bis (3-methoxycarbonyl 2-thioureido) benzene), dicarboximide Vinclozolin (3- (3,5-dichlorophenyl) -5-methyl-5-vinyl-1,3-oxazolidine-2,4-dione), iprodione (3- (3,5-dichlorophenyl) -N-isopropyl -2,4-D
  • examples of natural insecticides include pyrethrins derived from pesticide chrysanthemums, piperonyl butoxides, rotenones derived from leguminous shrubs, nicotine (3- (1-methyl-2-pyrrolidinyl) pyridine sulfate), and the like. .
  • IGR agents include diflubenzuron (1- (4 chlorophenyl) -3- (2,6-difluorobenzoyl) urea), teflubenzuron (1- (3,5-dichloro-2,4-difluorophenyl) ) -3- (2,6-difluorobenzoyl) urea), chlorfluazuron (1- [3,5-dichloro-4- (3-chloro-5-trifluoromethyl-2-pyridyloxy) phenyl]- Examples include 3- (2,6-difluorobenzoyl) urea.
  • CPCBS parachlorophenyl parachlorobenzene sulfonate
  • phenisobromolate isopropyl 4,4′-dibromobenzylate
  • tetradiphone (2,4,5,4′-tetrachlorodiphenyl sulfone
  • Fluacinam (3-chloro-N- (3-chloro-5-trifluoromethyl-2-pyridyl) - ⁇ , ⁇ , ⁇ -trifluoro-2,6-dinitro-p-toluidine
  • fenbutasin oxide hexakis ( ⁇ , ⁇ -dimethylphen
  • Sobromolate isopropyl 4,4'-dibromobenzylate
  • amitraz (3-methyl-1,5-bis (2,4-xylyl) -1,3,5-triazapenta-1,4-diene)
  • Examples of the herbicide include acid amide type herbicides such as stam (3,4-dichloropropionanilide, DCPA).
  • Examples of the urea herbicide include DCMU (3- (3,4-dichlorophenyl) -1,1-dimethylurea).
  • Bipyridylium herbicides include, for example, paraquat (1,1'-dimethyl-4,4'-bipyridinium dichloride), diquat (6,7-dihydrodipyrido [1,2-a: 2 ', 1'c] pyrazine And dium dibromide).
  • Examples of diazine herbicides include bromacil (5-bromo-3-sec-butyl-6-methyluracil) and the like.
  • Examples of the triazine herbicide include simazine (2-chloro-4,6-bis (ethylamino) -1,3,5-triazine).
  • Examples of the nitrile herbicide include DBN (2,6-dichlorobenzonitrile).
  • Examples of the dinitroaniline herbicide include trifluralin ( ⁇ , ⁇ , ⁇ -trifluoro-2,6-dinitro-N, N-dipropyl-p-toluidine).
  • Examples of carbamate herbicides include bencho curve (Saturn) (Sp-chlorobenzyl-N, N-diethylthiocarbamate).
  • Examples of the diphenyl ether herbicide include NIP (2,4-dichlorophenyl-p-nitrophenyl ether).
  • Examples of phenolic herbicides include PCP (sodium pentachlorophenoxide).
  • Examples of the benzoic acid herbicide include MDBA (dimethylamine-3,6-dichloro-o-anisate).
  • Examples of the phenoxy herbicide include 2,4-D sodium salt (sodium 2,4-dichlorophenoxyacetate).
  • Examples of the amino acid herbicide include glyphosate (N- (phosphonomethyl) glycine or a salt thereof) glyphosate (ammonium-DL-homoalanin-4-yl (methyl) phosphinate).
  • Examples of the aliphatic herbicide include TCA sodium salt (sodium trichloroacetate), and preferable examples include DBN (2,6-dichlorobenzonitrile), DCMU (3- (3,4-dichlorophenyl)- 1,1-dimethylurea), paraquat (1,1'-dimethyl-4,4'-bipyridium dichloride), diquat (6,7-dihydrodipyrido [1,2-a: 2 ', 1'c] pyrazine Dium dibromide).
  • TCA sodium salt sodium trichloroacetate
  • preferable examples include DBN (2,6-dichlorobenzonitrile), DCMU (3- (3,4-dichlorophenyl)- 1,1-dimethylurea), paraquat (1,1'-dimethyl-4,4'-bipyridium dichloride), diquat (6,7-dihydrodipyrido [1,2-a: 2 ', 1'c] pyra
  • plant growth regulators such as fertilizers, preservatives and the like other than those described above can be mixed and used in the agricultural chemical composition of the present invention.
  • Plant growth regulators include indole butyric acid, ethiclozate (ethyl 5-chloro-3 (1H) indazoline acetate), benzylaminopurine (6- (N-benzylamino) purine), forchlorphenuron (1- (2 -Chloro-4-pyridyl) -3-phenylurea), gibberellin, decyl alcohol, ethephone (2-chloroethylphosphonic acid) and the like.
  • indole butyric acid include indole butyric acid, ethiclozate (ethyl 5-chloro-3 (1H) indazoline acetate), benzylaminopurine (6- (N-benzylamino) purine), forchlorphenuron (1- (2 -Chloro-4-pyridyl) -3-phenylurea), gibberellin, decyl alcohol, ethephone (2-chloroethylphosphonic acid) and the
  • the present invention for the purpose of bactericidal, insecticidal, acaricidal, herbicidal or plant growth regulation, it contains the agrochemical efficacy enhancer composition of the present invention, and the agrochemical efficacy enhancer composition is used on a weight basis for the agrochemical active ingredient.
  • An agrochemical composition containing 0.03 to 50 times, preferably 0.1 to 50 times, more preferably 0.3 to 35 times is used.
  • the total content of compound (A) and compound (B) in the agricultural chemical formulation for spraying is preferably 30 ppm to 50000 ppm, more preferably 50 ppm to 25000 ppm, and even more preferably. 100 ppm to 20000 ppm, even more preferably 300 to 15000 ppm, even more preferably 500 to 12000 ppm, and even more preferably 600 to 10,000 ppm. If the content is at least the lower limit, the wettability of the droplets on the plant surface and the penetration of the agricultural chemical into the plant will be good, and an excellent agricultural chemical efficacy enhancing effect will be obtained. Further, if the content is less than or equal to the upper limit value, the wettability of the droplets becomes appropriate, and the droplets adhere to the plant body and become difficult to flow down.
  • the balance of the agrochemical formulation is preferably water.
  • the total content of the compound (A) and the compound (B) in the agricultural chemical formulation for spraying is within the above range, preferably 1 L to 500 L / 10a, more preferably 1L to 300L / 10a, more preferably 5L to 200L / 10a, even more preferably 1L to 150L / 10a, even more preferably 5L to 100L / 10a, even more preferably 5L to 50L / 10a, even more preferably 5L It can be sprayed at a rate of ⁇ 30 L / 10a. If the spraying amount is equal to or greater than the lower limit, sufficient wettability can be obtained, and a good effect of enhancing agricultural chemical efficacy can be obtained.
  • the present invention there is also provided a method for spraying an agricultural chemical composition or a method for cultivating agricultural crops, in which the agricultural chemical composition of the present invention (the agricultural chemical formulation prepared from the agricultural chemical composition of the present invention) is sprayed at the above ratio. .
  • Examples of the agrochemical formulation using the efficacy enhancer composition for agricultural chemicals of the present invention include an agricultural chemical formulation comprising a packaging package of the efficacy enhancing agent composition for agricultural chemicals of the present invention and a packaging package of agricultural chemical ingredients. .
  • a pesticide comprising a package of the compound (A) and the compound (B), a package of a surfactant other than the compound (A) and the compound (B), and a package of the agrochemical component It can also be made into a preparation.
  • the agrochemical component to be a packaged package means an emulsion, a wettable powder, or the like that may contain an agrochemical base and an optional component in an arbitrary ratio.
  • the form in each package is not limited and is prepared according to the use and purpose.
  • compound (A), compound (B), and any pesticidal active ingredient selected from active ingredients of fungicides, insecticides, acaricides, herbicides and plant growth regulators are mixed.
  • a method for producing an agrochemical composition can be provided. In this production method, it is preferable to use the compound (A), the compound (B), and the agrochemical raw material at the ratio described in the efficacy enhancer composition for agrochemicals or the agrochemical composition.
  • the production method of the agricultural product of the present invention uses the agricultural chemical composition of the present invention in the scene where the agricultural chemical is used.
  • the target of the method of the present invention is a fungicide as a fungus, an insecticide as a pest (insect), an acaricide as a mite, a herbicide as a weed (a plant that does not correspond to a crop), a plant growth regulator as a crop (for cultivation purposes).
  • these methods can be carried out as a method of applying the agrochemical composition to an object selected from plants, pests and fungi (for example, spraying on a crop cultivation area, etc.). And / or weeds.
  • the production method of the agricultural product of the present invention is any one selected from the active ingredient of each of the efficacy enhancer composition for agricultural chemicals of the present invention and a fungicide, insecticide, acaricide, herbicide and plant growth regulator.
  • the method of producing the agricultural product of the present invention may be a method including a step of applying the agrochemical composition of the present invention to an object of an agrochemical raw material.
  • the method for applying the agrochemical efficacy enhancer composition, the agrochemical active ingredient, or the agrochemical composition to the target of the agrochemical active substance is not particularly limited, and includes the agrochemical efficacy enhancer composition of the present invention as described above.
  • the efficacy enhancer composition for agricultural chemicals or the agricultural chemical composition is used for the active ingredient of agricultural chemicals.
  • the efficacy enhancer composition for agricultural chemicals of this invention and an agricultural chemical raw material can also be separately applied to the target of an agricultural chemical raw material by the above-mentioned method.
  • an efficacy enhancer composition for agricultural chemicals including a spray preparation containing the composition and water
  • an agricultural chemical active ingredient including a spraying preparation containing the active ingredient and water
  • an agricultural chemical A composition including a preparation for spraying prepared from an agrochemical composition
  • the plant surface is generally covered with epicuticular wax, cuticular wax, cutin and the like and has a hydrophobic property.
  • the water contact angle is an indicator of the hydrophobicity of the plant surface.
  • the contact angle of a plant that exhibits the effect of enhancing the effectiveness of the agricultural chemical of the present invention is preferably 50 to 180 degrees, more preferably 70 to 180 degrees, and still more preferably 90 to 180 degrees.
  • the contact angle is measured by dropping 5 ⁇ L of water onto the surface of the plant to be applied (for example, the surface of the third leaf) at 25 ° C., and photographing the state of the liquid droplet 10 seconds after dropping with a microscope from the side. Then, the contact angle between the target surface and the water droplet is measured by image processing.
  • the representative plants having a portion showing a contact angle in the above range are as follows, but are not limited thereto.
  • Examples of the weeds to which the method of the present invention is applied include gypsy moth, seahorse moth, kobimee, dogbier, hoshishiba, hinokishiba, chigaya, taiwan ashiki, azegaya, hiki, napiergrass, tsunoia ashi, kobukkinenokoro, tamagayatsuri, tamagotsugatsu, , Kusanem, Cuckoo Thistle, Crane Thistle, Aubiyu, Maruyu Yusa, Himalayan Clover, Water Hyacinth, Cyprus, Nanban Ruri, Nioigagusa, Nangoku Denji Sou, Ogigi, Konagi, Subuhigi Preferred weeds that exhibit the effect of enhancing the agrochemical efficacy of the present invention
  • the crops to which the method of the present invention is applied include barley, peas, rice, wheat, cabbage, taro, strawberry, melon, eggplant, tomato, leek, rape, soybean, kidney bean, sweet potato, cucumber, Chinese cabbage, apple, Examples include pears, peaches, oysters, and citrus.
  • Preferred crops that exhibit the effect of enhancing the effectiveness of the agricultural chemical of the present invention are barley, peas, rice, wheat, cabbage, Chinese cabbage, taro, strawberry, melon, eggplant, tomato, leek, rape, soybean, cucumber, and kidney bean. More preferred are rice, wheat, cabbage, Chinese cabbage, soybean, leek, kidney bean and cucumber.
  • the efficacy enhancer composition for agricultural chemicals and the compound (A) and compound (B) contained in the agricultural chemical composition are separated by gas chromatography even after the preparation of the composition, and are detected by an FID detector. Can be detected. For example, after diluting a pesticide efficacy enhancer composition or a pesticide composition with a suitable solvent such as ethanol, and measuring under the following conditions, the pesticide efficacy enhancer composition or the compound in the pesticide composition (A ) And compound (B) can be quantitatively confirmed.
  • Example 1 and Comparative Example 1 show the compounds (A) and (B) and comparative compounds used in the following Examples and Comparative Examples.
  • Inhibibies were used as test plants. Inhibibies were grown in advance in a 12 cm pot, and plants in the 8-leaf stage were used for the test. A test solution obtained by collecting the fifth leaf of the lobster and mixing it with water so that the concentrations of the compound (A) and the compound (B) are the concentrations in the pesticide spray solution shown in Tables 3 and 4. 5 ⁇ L of (no pesticide) was dropped on the center of the leaf. In addition, the contact angle with respect to the water of the leaf surface of Inbiebi was 130 degrees.
  • the contact angle with respect to the water of the leaf surface of Inbiebi was 130 degrees.
  • the evaluation of the herbicidal efficacy was carried out on the 14th day after spraying, and the ground part weight was measured, and the herbicidal rate based on the raw part raw weight in the untreated area was calculated based on the following formula. The higher the value of the herbicidal rate, the higher the pesticide efficacy (the herbicidal effect).
  • the non-treated section is a section where a diluted mixture (pesticidal spray solution) with an agrochemical and an agrochemical efficacy enhancer composition is not sprayed (the same applies to other tests).
  • Herbicide rate (%) (weight of above-ground part of untreated area-above-ground part weight of treated area) / above-ground part weight of untreated area x 100 From the results of Tables 3 and 4, it was confirmed that the herbicidal effect can be improved according to the agrochemical composition of the present invention.
  • Insecticidal rate (%) (Number of living insects in untreated group ⁇ Number of living insects in treated group) / Number of living insects in untreated group ⁇ 100 From the results of Tables 3 and 4, it was confirmed that according to the agrochemical composition of the present invention, the insecticidal effect can be improved.
  • Kidney beans were grown in a 12 cm pot until the fifth leaf stage. Thirty Kanzawa spider mites per strain were applied in 3 iterations. Composition of a potentiating agent for agricultural chemicals in an amount of 0.3 g of Nissoran wettable powder (Nippon Soda Co., Ltd. acaricide; 10% by weight effective as hexithiazox) in 1 L of water and the concentration when sprayed as shown in Tables 3 and 4 The product [compound (A) and compound (B)] was mixed to prepare an agrochemical spray liquid (agrochemical composition). The pesticide spray solution was sprayed onto the kidney beans with the spray amount shown in Tables 3 and 4.
  • the contact angle with respect to the water of a kidney bean leaf surface was 100 degree
  • a wire mesh cylinder was covered, and the number of surviving mites was measured after 3 days, and the acaricidal rate was calculated by the following formula.
  • Mite kill rate (%) (number of surviving mites in untreated group ⁇ number of surviving mites in treated group) / number of surviving mites in untreated group ⁇ 100 From the results of Tables 3 and 4, it was confirmed that the acaricidal effect can be improved according to the agrochemical composition of the present invention.
  • Botrytis cinerea is a fungicide resistant fungus (Botrytis cinerea) (number of bacteria 10 7 / mL), were applied at an application rate of 50 mL / 10a cucumber. Then, it left still under 25 degreeC and 90% relative humidity, and infected the microbe.
  • Control value (%) ⁇ 1 ⁇ (number of lesions in treated area / number of lesions in untreated area) ⁇ ⁇ 100 From the results of Tables 3 and 4, it was confirmed that the bactericidal effect can be improved according to the agrochemical composition of the present invention.
  • Example 2 and Comparative Example 2 Table 5 shows the compounds (A) and comparative compounds used in the following Examples and Comparative Examples.
  • Compound (A) in Table 5 [some of which also uses Compound (A) in Table 1 of Example 1] and Compound (B) in Table 2 of Example 1 in combination of Table 6
  • the effect enhancer composition for agricultural chemicals shown in Table 6 (one containing 100% by weight of the compounds shown in Tables 5 and 2 or containing the compounds shown in Tables 5 and 2 and a solvent) was prepared, and the same as in Example 1.
  • a wettability test, a herbicidal test, an insecticidal test, an acaricidal test, and a bactericidal test were conducted. The results are shown in Table 6.
  • Example 3 and Comparative Example 3 show the compounds (A) and (B2) and comparative compounds used in the following Examples and Comparative Examples.
  • the efficacy enhancer composition for agricultural chemicals in Tables 9 and 10 And a solvent containing the solvent] were prepared, and a wettability test, a herbicidal test, an insecticidal test, an acaricidal test, and a bactericidal test were conducted by the following methods.
  • compounds other than A-2-11, A-2-12, A′-2-7 and all the compounds in Table 8 were manufactured by Kao Corporation, and A-2-11 in Table 7 A-2-12 and A′-2-7 are manufactured by Taiyo Kagaku Co., Ltd.
  • compounds not corresponding to the compound (A) and the compound (B) are also shown in the respective columns for convenience.
  • Example 1-233 contains 10% by weight of water
  • Example 1-234 uses 10% by weight of ethyl lactic acid
  • Example 1-235 uses 10% by weight of diethylene glycol, respectively. Used as solvent.

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Abstract

Provided is a pesticide potentiator composition which comprises: one or more kinds of compounds (A) selected from among a specific ethoxylate compound, a specific polyoxyethylene fatty acid ester, a specific polyoxyethylene sorbitan fatty acid ester, a specific (poly)glycerol fatty acid ester and a specific alkyl saccharide; and one or more kinds of compounds (B) selected from among a specific polyoxyalkylene alkyl ether and a specific aliphatic alcohol.

Description

農作物の生産方法Crop production method
 本発明は、農薬用効力増強剤組成物及び農薬組成物に関する。
背景技術
The present invention relates to an agrochemical efficacy enhancer composition and an agrochemical composition.
Background art
 従来、農薬の効果を十分引き出すために、農薬含有組成物に各種界面活性剤が利用されている。例えば、陰イオン界面活性剤とキレート剤とを組み合わせることでビピリジニウム系除草剤に効果の高い農薬含有組成物が得られることが知られている(例えば国際公開第95/31903参照)。また、陽イオン界面活性剤にキレート剤を配合し、更に別の界面活性剤を添加することで、農薬の効果の高い農薬含有組成物が得られることも知られている(例えば国際公開第95/17817参照)。更に、濡れ性を向上させるためソルビタン脂肪酸エステル、ポリオキシエチレンアルキルエーテル及びポリエーテル変性シリコーンをイソプロピルアルコールに溶解してなる非水系の展着剤が提案されている(特開2000-001404号公報(特許請求の範囲その他)参照)。また、特開2006-248994号公報には、界面活性剤、引火点70℃以上の水溶性有機溶剤、消泡剤又は破泡剤を含有する非水系農薬用展着剤組成物が開示されている。また、特開2006-257072号公報には、ポリオキシアルキレン脂肪酸エステルと他の非イオン性界面活性剤とを含有する除草剤組成物が開示されている。また、特開2008-184455号公報には、疎水性農薬活性化合物、ポリオキシエチレンポリオキシプロピレンブロックコポリマー等からなる群より選ばれる特定のノニオン性界面活性剤、アニオン性界面活性剤、特定のエーテル化合物、及び1,3-ジメチル-2-イミダゾリジノンを、それぞれ所定量含有する農薬液剤が開示されている。また、特開2002-249403号公報には、特定のアルコール化合物、特定のエーテル化合物及び特定のエステル化合物の少なくとも一種を有効成分として含有する農薬用効力増強剤が開示されている。
発明の要約
Conventionally, various surfactants have been used in agrochemical-containing compositions in order to sufficiently bring out the effects of agrochemicals. For example, it is known that an agrochemical-containing composition that is highly effective for bipyridinium herbicides can be obtained by combining an anionic surfactant and a chelating agent (see, for example, International Publication No. 95/31903). It is also known that an agrochemical-containing composition having a high agrochemical effect can be obtained by adding a chelating agent to a cationic surfactant and adding another surfactant (for example, International Publication No. 95). / 17817). Furthermore, a non-aqueous spreading agent prepared by dissolving sorbitan fatty acid ester, polyoxyethylene alkyl ether and polyether-modified silicone in isopropyl alcohol has been proposed in order to improve wettability (Japanese Patent Laid-Open No. 2000-001404). See claims and others)). Japanese Patent Application Laid-Open No. 2006-248994 discloses a non-aqueous pesticide spreading agent composition containing a surfactant, a water-soluble organic solvent having a flash point of 70 ° C. or higher, an antifoaming agent, or a defoaming agent. Yes. JP 2006-257072 discloses a herbicidal composition containing a polyoxyalkylene fatty acid ester and another nonionic surfactant. Japanese Patent Application Laid-Open No. 2008-184455 discloses a specific nonionic surfactant, an anionic surfactant, a specific ether selected from the group consisting of hydrophobic agrochemical active compounds, polyoxyethylene polyoxypropylene block copolymers, and the like. An agrochemical solution containing a predetermined amount of a compound and 1,3-dimethyl-2-imidazolidinone is disclosed. Japanese Patent Laid-Open No. 2002-249403 discloses an agrochemical efficacy enhancer containing at least one of a specific alcohol compound, a specific ether compound and a specific ester compound as an active ingredient.
Summary of invention
 本発明は、下記(A1)~(A5)から選ばれる一種以上の化合物(A)と、下記(B1)~(B2)から選ばれる一種以上の化合物(B)と、殺菌剤、殺虫剤、殺ダニ剤、除草剤及び植物成長調節剤各々の有効成分から選択される何れかの農薬原体とを含有する農薬組成物を農薬原体の対象物に施す工程を含む、農作物の生産方法。
(A1):下記一般式(A1)で示されるポリオキシエチレンアルキルエーテル
   R1aO-(EO)l-R2a (A1)
 (式中、R1aは炭素数10~16の直鎖又は分岐鎖のアルキル基又はアルケニル基を示し、EOはエチレンオキシ基を示し、lはエチレンオキシ基の平均付加モル数であり、3~40の数を示し、R2aは水素原子又はメチル基を示す。)
(A2):ポリオキシエチレン脂肪酸エステル
(ただし、脂肪酸の炭素数は8~16であり、エチレンオキシドの平均付加モル数は5~40である。)
(A3):ポリオキシエチレンソルビタン脂肪酸エステル
(ただし、脂肪酸の炭素数は8~16であり、エチレンオキシドの平均付加モル数は5~40である。)
(A4):(ポリ)グリセリン脂肪酸エステル
(ただし、脂肪酸の炭素数は8~16であり、グリセリンの平均縮合度は1~3である。)
(A5):下記一般式(A5)で示されるアルキルサッカライド
 R3a-O-(G)p   (A5)
 (式中、R3aは炭素数8~16のアルキル基、Gは炭素数5~6の還元糖を示し、pは1~10の数を示す。)
(B1)下記一般式(B1)で示されるポリオキシアルキレンアルキルエーテル
      R1bO-[(PO)m/(EO)n]-R2b (B1)
(式中、R1bは炭素数6~12の直鎖又は分岐鎖のアルキル基又はアルケニル基を示し、POはプロピレンオキシ基を示し、EOはエチレンオキシ基を示し、m、nはそれぞれ、プロピレンオキシ基、エチレンオキシ基の平均付加モル数であり、mは1~25の数、nは0~4の数を示し、R2bは水素原子又はメチル基を示す。“/”はPOとEOの配列がランダムでもブロックでもよいことを意味する。) 
(B2):下記一般式(B2)で示される脂肪族アルコール
     R3b-OH (B2)
 (式中、R3bは炭素数8~14の直鎖又は分岐鎖のアルキル基を示す。) 
 さらに、本発明は、上記化合物(A)と、上記化合物(B)を含有する組成物の農薬用展着剤組成物としての用途を提供する。
 さらに、上記化合物(A)と、上記化合物(B)と、殺菌剤、殺虫剤、殺ダニ剤、除草剤及び植物成長調節剤各々の有効成分から選択される何れかの農薬原体と混合することを含む農薬の効力を増強する方法を提供する。
The present invention includes one or more compounds (A) selected from the following (A1) to (A5), one or more compounds (B) selected from the following (B1) to (B2), a fungicide, an insecticide, A method for producing agricultural crops, comprising a step of applying a pesticide composition containing any one of a pesticide active ingredient selected from active ingredients of each of an acaricide, a herbicide, and a plant growth regulator to an object of the pesticide active ingredient.
(A1): Polyoxyethylene alkyl ether represented by the following general formula (A1) R 1a O— (EO) 1 —R 2a (A1)
(Wherein R 1a represents a linear or branched alkyl group or alkenyl group having 10 to 16 carbon atoms, EO represents an ethyleneoxy group, l represents the average number of moles of the ethyleneoxy group, 3 to 40 represents the number, and R 2a represents a hydrogen atom or a methyl group.)
(A2): Polyoxyethylene fatty acid ester (wherein the fatty acid has 8 to 16 carbon atoms and the average added mole number of ethylene oxide is 5 to 40)
(A3): Polyoxyethylene sorbitan fatty acid ester (wherein the fatty acid has 8 to 16 carbon atoms and the average added mole number of ethylene oxide is 5 to 40)
(A4): (Poly) glycerin fatty acid ester (wherein the fatty acid has 8 to 16 carbon atoms, and the average condensation degree of glycerin is 1 to 3)
(A5): alkyl saccharide represented by the following general formula (A5) R 3a —O— (G) p (A5)
(Wherein R 3a represents an alkyl group having 8 to 16 carbon atoms, G represents a reducing sugar having 5 to 6 carbon atoms, and p represents a number of 1 to 10)
(B1) Polyoxyalkylene alkyl ether represented by the following general formula (B1) R 1b O — [(PO) m / (EO) n] —R 2b (B1)
(Wherein R 1b represents a linear or branched alkyl group or alkenyl group having 6 to 12 carbon atoms, PO represents a propyleneoxy group, EO represents an ethyleneoxy group, and m and n represent propylene. The average number of added moles of oxy group and ethyleneoxy group, m is a number from 1 to 25, n is a number from 0 to 4, R 2b is a hydrogen atom or a methyl group, “/” is PO and EO (This means that the arrangement may be random or block.)
(B2): aliphatic alcohol represented by the following general formula (B2) R 3b —OH (B2)
(In the formula, R 3b represents a linear or branched alkyl group having 8 to 14 carbon atoms.)
Furthermore, this invention provides the use as a spreading agent composition for agricultural chemicals of the composition containing the said compound (A) and the said compound (B).
Further, the compound (A), the compound (B), and any of the active ingredients of the fungicides, insecticides, acaricides, herbicides and plant growth regulators are mixed. A method for enhancing the efficacy of pesticides is provided.
発明の詳細な説明
 上記文献では、例えば、農薬の葉面散布において、植物の葉面上において液滴が十分に濡れ広がらない事により、その結果農薬の効果が十分に発揮されない場合があった。
Detailed description of the invention In the above-mentioned literature, for example, in spraying foliage on a pesticide, the droplets do not sufficiently wet and spread on the foliage of the plant, and as a result, the effect of the pesticide may not be sufficiently exhibited.
 本発明は、農薬の湿展性(濡れ広がりやすさ)を向上させ、農薬の効力を効果的に増強できる農薬用効力増強剤組成物を提供する。 The present invention provides an efficacy enhancer composition for agricultural chemicals that improves the wettability (easiness of spreading) of agricultural chemicals and can effectively enhance the efficacy of agricultural chemicals.
 本発明によれば、農薬の湿展性を向上させ、農薬の効力を効果的に増強できる農薬用効力増強剤組成物及び農薬組成物が提供される。 According to the present invention, there are provided an agrochemical efficacy enhancer composition and an agrochemical composition that can improve the wettability of an agrochemical and effectively enhance the efficacy of the agrochemical.
 本発明は次の態様を含む。 (1)上記化合物(A)と、上記(B1)又は(B2)である化合物(B)と、殺菌剤、殺虫剤、殺ダニ剤、除草剤及び植物成長調節剤各々の有効成分から選択される何れかの農薬原体とを含有する農薬組成物を農薬原体の対象物に施す工程を含む、農作物の生産方法に関する。 (2)上記化合物(A)〔以下、化合物(A)という〕、及び上記化合物(B)〔以下、化合物(B)という〕を含有する農薬用効力増強剤組成物に関する。 (3)化合物(A)と、化合物(B)と、殺菌剤、殺虫剤、殺ダニ剤、除草剤及び植物成長調節剤各々の有効成分から選択される農薬原体とを含有する農薬組成物に関する。 (4)上記本発明の農薬用効力増強剤組成物と、殺菌剤、殺虫剤、殺ダニ剤、除草剤及び植物成長調節剤各々の有効成分から選択される何れかの農薬原体とを植物に施す工程を含む、植物の生産方法に関する。 (5)上記本発明の農薬組成物を植物に施す工程を含む、植物の生産方法に関する。(6)一般式(A1)で示される化合物(A)、及び一般式(B1)で示される化合物(B)を含有する農薬用効力増強剤組成物に関する。 (7)上記化合物(A)及び上記化合物(B)として(B1)を含有する農薬用効力増強剤組成物に関する。  The present invention includes the following aspects. (1) The compound (A), the compound (B) which is the above (B1) or (B2), and an active ingredient of each of a fungicide, an insecticide, an acaricide, a herbicide and a plant growth regulator. The present invention relates to a method for producing agricultural crops, comprising a step of applying an agrochemical composition containing any of the agrochemical ingredients to a target of the agrochemical substance. (2) The present invention relates to an efficacy enhancer composition for agricultural chemicals containing the above compound (A) [hereinafter referred to as compound (A)] and the above compound (B) [hereinafter referred to as compound (B)]. (3) Agrochemical composition comprising compound (A), compound (B), and an agrochemical base selected from active ingredients of fungicides, insecticides, acaricides, herbicides and plant growth regulators About. (4) A plant comprising the agrochemical efficacy enhancer composition of the present invention described above and any pesticide active ingredient selected from active ingredients of fungicides, insecticides, acaricides, herbicides and plant growth regulators. It is related with the production method of a plant including the process given to. (5) The present invention relates to a plant production method including a step of applying the agrochemical composition of the present invention to a plant. (6) It relates to an efficacy enhancer composition for agricultural chemicals containing the compound (A) represented by the general formula (A1) and the compound (B) represented by the general formula (B1). (7) The present invention relates to an efficacy enhancer composition for agricultural chemicals containing (B1) as the compound (A) and the compound (B). *
 本発明の農薬用効力増強剤組成物は、化合物(A)と化合物(B)とを含有する。化合物(A)と化合物(B)とを併用することにより、農薬の湿展性(濡れ広がりやすさ)が向上する理由は明らかではないが、液滴と葉の界面に吸着し界面張力を低下させる化合物(B)と、液滴自体の表面張力を低下させる化合物(A)とが、構造的に類似することで相互作用を及ぼしあい、飛躍的に農薬の湿展性が向上するものと推定している。 The efficacy enhancer composition for agricultural chemicals of the present invention contains a compound (A) and a compound (B). The reason why the wettability (easiness of wetting and spreading) of the pesticide is improved by using the compound (A) and the compound (B) in combination is not clear, but it is adsorbed at the interface between the droplet and the leaf and decreases the interfacial tension. It is estimated that the compound (B) to be reduced and the compound (A) to reduce the surface tension of the droplet itself interact with each other by structural similarity, and the wettability of the agricultural chemical is drastically improved. is doing.
<化合物(A)>
 本発明の農薬用効力増強剤組成物は、湿展性向上及び農薬の効力増強の観点から、下記(A1)~(A5)から選ばれる一種以上の化合物(A)を含有する。(B)が(B1)であるとき、下記化合物(A1)~(A5)のうち、湿展性向上及び農薬の効力増強の観点から、(A1)、(A4)、(A5)が好ましく、(A1)、(A5)がより好ましい。 また、(B)が(B2)であるとき、下記化合物(A1)~(A5)のうち、湿展性向上及び農薬の効力増強の観点から、(A1)、(A2)、(A4)が好ましく、(A1)、(A4)がより好ましい。
<Compound (A)>
The efficacy enhancer composition for agricultural chemicals of the present invention contains one or more compounds (A) selected from the following (A1) to (A5) from the viewpoint of improving wettability and enhancing efficacy of agricultural chemicals. When (B) is (B1), among the following compounds (A1) to (A5), (A1), (A4) and (A5) are preferable from the viewpoint of improving wettability and enhancing the efficacy of agricultural chemicals. (A1) and (A5) are more preferable. When (B) is (B2), among the following compounds (A1) to (A5), (A1), (A2), (A4) are from the viewpoint of improving the wettability and enhancing the efficacy of the agricultural chemical. (A1) and (A4) are more preferable.
 化合物(A1)は下記一般式(A1)で表される。
  R1aO-(EO)l-R2a   (A1)
 一般式(A1)において、R1aは、湿展性向上及び農薬の効力増強の観点から、炭素数10~16の直鎖又は分岐鎖のアルキル基又はアルケニル基であり、好ましくは炭素数10~14の直鎖又は分岐鎖のアルキル基又はアルケニル基であり、より好ましくは炭素数10~12の直鎖又は分岐鎖のアルキル基又はアルケニル基であり、さらに好ましくは炭素数12の直鎖又は分岐鎖のアルキル基又はアルケニル基であり、さらにより好ましくは炭素数12の直鎖アルキル基である。また、lは、エチレンオキシ基(EO)の平均付加モル数であり、湿展性を向上し、農薬の効力を増強する観点から、3~40、好ましくは4~30、より好ましくは4~25、さらに好ましくは5~20、さらにより好ましくは5~15、さらにより好ましくは5~12、さらにより好ましくは5~10である。また、R2aは、湿展性向上及び農薬の効力増強の観点から、水素原子又はメチル基であり、好ましくは水素原子である。
The compound (A1) is represented by the following general formula (A1).
R 1a O— (EO) 1 —R 2a (A1)
In the general formula (A1), R 1a is a linear or branched alkyl or alkenyl group having 10 to 16 carbon atoms, preferably 10 to 10 carbon atoms, from the viewpoints of improving wetability and enhancing the efficacy of agricultural chemicals. 14 linear or branched alkyl group or alkenyl group, more preferably a linear or branched alkyl group or alkenyl group having 10 to 12 carbon atoms, and still more preferably a linear or branched group having 12 carbon atoms. A chain alkyl group or an alkenyl group, and even more preferably a linear alkyl group having 12 carbon atoms. Further, l is the average number of moles of ethyleneoxy group (EO) added, and is 3 to 40, preferably 4 to 30, more preferably 4 to 4 from the viewpoint of improving wettability and enhancing the efficacy of agricultural chemicals. 25, more preferably 5-20, even more preferably 5-15, even more preferably 5-12, and even more preferably 5-10. R 2a is a hydrogen atom or a methyl group, preferably a hydrogen atom, from the viewpoint of improving wettability and enhancing the efficacy of agricultural chemicals.
 化合物(A2)は、ポリオキシエチレン脂肪酸エステルである。化合物(A2)では、湿展性向上及び農薬の効力増強の観点から、脂肪酸の炭素数は8~16であり、10~14が好ましく、10~12がより好ましい。化合物(A2)における脂肪酸は直鎖又は分岐鎖のアルキル基又はアルケニル基を有するものが好ましく、直鎖のアルキル基がより好ましい。化合物(A2)における脂肪酸としては、カプリル酸、カプリン酸、ラウリン酸、ミリスチン酸、パルミチン酸等が挙げられる。また、化合物(A2)では、湿展性向上及び農薬の効力増強の観点から、エチレンオキシドの平均付加モル数は5~40であり、5~20が好ましく、6~15がより好ましい。また、エステルはモノエステルが好ましい。 Compound (A2) is a polyoxyethylene fatty acid ester. In the compound (A2), the fatty acid has 8 to 16 carbon atoms, preferably 10 to 14 and more preferably 10 to 12 from the viewpoint of improving wettability and enhancing the efficacy of the agricultural chemical. The fatty acid in the compound (A2) preferably has a linear or branched alkyl group or alkenyl group, and more preferably a linear alkyl group. Examples of the fatty acid in the compound (A2) include caprylic acid, capric acid, lauric acid, myristic acid, palmitic acid and the like. In the compound (A2), the average number of moles of ethylene oxide added is 5 to 40, preferably 5 to 20, and more preferably 6 to 15 from the viewpoints of improving wettability and enhancing the efficacy of agricultural chemicals. The ester is preferably a monoester.
 化合物(A3)は、ポリオキシエチレンソルビタン脂肪酸エステルである。化合物(A3)では、湿展性向上及び農薬の効力増強の観点から、脂肪酸の炭素数は8~16であり、10~14が好ましく、10~12がより好ましい。化合物(A3)における脂肪酸は直鎖又は分岐鎖のアルキル基又はアルケニル基を有するものが好ましく、直鎖のアルキル基がより好ましい。化合物(A3)における脂肪酸としては、カプリル酸、カプリン酸、ラウリン酸、ミリスチン酸、パルミチン酸等が挙げられる。また、化合物(A3)では、湿展性向上及び農薬の効力増強の観点から、エチレンオキシドの平均付加モル数は5~40であり、5~20が好ましく、6~15がより好ましい。また、エステル化度は1が好ましい。 Compound (A3) is polyoxyethylene sorbitan fatty acid ester. In the compound (A3), the number of carbon atoms of the fatty acid is from 8 to 16, preferably from 10 to 14, and more preferably from 10 to 12, from the viewpoint of improving the wettability and enhancing the efficacy of the agricultural chemical. The fatty acid in the compound (A3) preferably has a linear or branched alkyl group or alkenyl group, and more preferably a linear alkyl group. Examples of the fatty acid in the compound (A3) include caprylic acid, capric acid, lauric acid, myristic acid, palmitic acid and the like. In the compound (A3), from the viewpoint of improving wettability and enhancing the efficacy of the agricultural chemical, the average added mole number of ethylene oxide is 5 to 40, preferably 5 to 20, and more preferably 6 to 15. The esterification degree is preferably 1.
 化合物(A4)は、(ポリ)グリセリン脂肪酸エステルである。ここで、「(ポリ)グリセリン」は、「グリセリン又はポリグリセリン」の意味である。化合物(A4)では、湿展性向上及び農薬の効力増強の観点から、脂肪酸の炭素数は8~16であり、8~12が好ましく、10~12がより好ましく、12がさらに好ましい。化合物(A4)における脂肪酸は直鎖又は分岐鎖のアルキル基又はアルケニル基を有するものが好ましく、直鎖のアルキル基がより好ましい。化合物(A4)における脂肪酸としては、カプリル酸、カプリン酸、ラウリン酸、ミリスチン酸、パルミチン酸等が挙げられる。また、化合物(A4)では、湿展性向上及び農薬の効力増強の観点から、グリセリンの平均縮合度は1~3であり、好ましくは1~2、より好ましくは2である。 Compound (A4) is a (poly) glycerin fatty acid ester. Here, “(poly) glycerin” means “glycerin or polyglycerin”. In the compound (A4), the number of carbon atoms of the fatty acid is from 8 to 16, preferably from 8 to 12, more preferably from 10 to 12, and even more preferably from the viewpoint of improving wetability and enhancing the efficacy of the agricultural chemical. The fatty acid in the compound (A4) preferably has a linear or branched alkyl group or alkenyl group, and more preferably a linear alkyl group. Examples of the fatty acid in the compound (A4) include caprylic acid, capric acid, lauric acid, myristic acid, palmitic acid and the like. In the compound (A4), the average degree of condensation of glycerin is 1 to 3, preferably 1 to 2, and more preferably 2 from the viewpoint of improving wetability and enhancing the efficacy of agricultural chemicals.
 化合物(A5)は、下記一般式(A5)で示されるアルキルサッカライドである。
  R3a-O-(G)p        (A5)
 式中、R3aは、湿展性向上及び農薬の効力増強の観点から、炭素数8~16であり、好ましくは10~14のアルキル基である。Gは、炭素数5~6の還元糖、例えばリボース、アラビノース、キシロース、アロース、アルトロース、グルコース、マンノース、フルクトース、グロース、イドース、ガラクトース、タロース等を示し、好ましくはグルコース、マンノース、フルクトース、ガラクトース、より好ましくはグルコースである。pは湿展性向上及び農薬の効力増強の観点から、1~10、好ましくは1~5の数を示す。
The compound (A5) is an alkyl saccharide represented by the following general formula (A5).
R 3a —O— (G) p (A5)
In the formula, R 3a is an alkyl group having 8 to 16 carbon atoms, preferably 10 to 14 carbon atoms, from the viewpoint of improving wettability and enhancing the efficacy of agricultural chemicals. G represents a reducing sugar having 5 to 6 carbon atoms, such as ribose, arabinose, xylose, allose, altrose, glucose, mannose, fructose, gulose, idose, galactose, talose, etc., preferably glucose, mannose, fructose, galactose More preferably, it is glucose. p represents a number of 1 to 10, preferably 1 to 5, from the viewpoints of improving wettability and enhancing the efficacy of agricultural chemicals.
<化合物(B1)>
 化合物(B1)は下記一般式(B1)で表される。
  R1bO-[(PO)m/(EO)n]-R2b   (B1)
 一般式(B1)において、R1bは、湿展性向上及び農薬の効力増強の観点から、炭素数6~12の直鎖又は分岐鎖のアルキル基又はアルケニル基であり、好ましくは炭素数8~12の直鎖又は分岐鎖のアルキル基又はアルケニル基であり、より好ましくは炭素数8~10の直鎖又は分岐鎖のアルキル基又はアルケニル基であり、さらに好ましくは炭素数8~10の直鎖アルキル基である。また、mは、プロピレンオキシ基(PO)の平均付加モル数であり、湿展性向上び農薬の効力増強の観点から、1~25であり、好ましくは2~20、より好ましくは2~20、さらに好ましくは2~18、さらにより好ましくは2~16、さらにより好ましくは2~12、さらにより好ましくは2~10である。また、nは、エチレンオキシ基(EO)の平均付加モル数であり、湿展性向上及び農薬の効力増強の観点から、0~4であり、好ましくは0~3、より好ましくは0~2、さらに好ましくは0~1、さらにより好ましくは0である。また、化合物(B)は、湿展性向上及び農薬の効力増強の観点から、一般式(B1)中のmと、m及びnの合計との比が、m/(m+n)で、好ましくは0.5~1.0、より好ましくは0.6~1.0、さらに好ましくは0.7~1.0、さらにより好ましくは0.8~1.0、さらにより好ましくは0.9~1.0、さらにより好ましくは1.0である。また、R2bは、湿展性向上及び農薬の効力増強の観点から、水素原子又はメチル基であり、好ましくは水素原子である。また、化合物(B1)において、POとEOが共存する場合、POとEOの配列は、湿展性向上及び農薬の効力増強の観点から、ブロック配列であることが好ましく、R1bO-にPO・EOの順にブロック配列していることがさらに好ましい。
<Compound (B1)>
The compound (B1) is represented by the following general formula (B1).
R 1b O — [(PO) m / (EO) n ] —R 2b (B1)
In the general formula (B1), R 1b is a linear or branched alkyl group or alkenyl group having 6 to 12 carbon atoms, preferably 8 to 8 carbon atoms, from the viewpoints of improving wetability and enhancing the efficacy of agricultural chemicals. 12 straight-chain or branched alkyl groups or alkenyl groups, more preferably straight-chain or branched alkyl groups or alkenyl groups having 8 to 10 carbon atoms, and even more preferably straight-chain chains having 8 to 10 carbon atoms. It is an alkyl group. M is the average number of moles of propyleneoxy group (PO) added, and is 1 to 25, preferably 2 to 20, more preferably 2 to 20 from the viewpoint of improving the wettability and enhancing the efficacy of the agricultural chemical. More preferably, it is 2 to 18, still more preferably 2 to 16, even more preferably 2 to 12, and still more preferably 2 to 10. N is the average number of added moles of ethyleneoxy group (EO), and is 0 to 4, preferably 0 to 3, more preferably 0 to 2 from the viewpoint of improving wettability and enhancing the efficacy of agricultural chemicals. More preferably, it is 0 to 1, and still more preferably 0. Further, in the compound (B), from the viewpoint of improving the wettability and enhancing the efficacy of the agricultural chemical, the ratio of m in the general formula (B1) to the total of m and n is preferably m / (m + n). 0.5-1.0, more preferably 0.6-1.0, even more preferably 0.7-1.0, even more preferably 0.8-1.0, and even more preferably 0.9- 1.0, even more preferably 1.0. R 2b is a hydrogen atom or a methyl group, preferably a hydrogen atom, from the viewpoint of improving wettability and enhancing the efficacy of agricultural chemicals. Also, PO in the compound (B1), if the PO and EO coexist, the arrangement of PO and EO, from the viewpoint of ductility improvement and pesticide efficacy potentiating humidity is preferably a block sequence, the R 1b O- -More preferably, the blocks are arranged in the order of EO.
<化合物(B2)>
 化合物(B2)は下記一般式(B2)で表される。
   R3b-OH    (B2)
 一般式(B2)において、R3bは、湿展性向上及び農薬の効力増強の観点から、炭素数8~14の直鎖又は分岐鎖のアルキル基であり、好ましくは炭素数8~12の直鎖又は分岐鎖のアルキル基であり、より好ましくは炭素数8~10の直鎖又は分岐鎖のアルキル基であり、さらに好ましくは炭素数10の直鎖のアルキル基である。
<Compound (B2)>
The compound (B2) is represented by the following general formula (B2).
R 3b —OH (B2)
In the general formula (B2), R 3b is a linear or branched alkyl group having 8 to 14 carbon atoms, preferably a straight chain having 8 to 12 carbon atoms, from the viewpoints of improving wetability and enhancing the effectiveness of agricultural chemicals. It is a chain or branched alkyl group, more preferably a linear or branched alkyl group having 8 to 10 carbon atoms, and still more preferably a linear alkyl group having 10 carbon atoms.
<農薬用効力増強剤組成物の組成等>
 本発明の農薬用効力増強剤組成物において、化合物(A)と化合物(B)の重量比は、(A)/(B)で、好ましくは0.03~30、より好ましくは0.05~20、更に好ましくは0.1~10、さらにより好ましくは0.2~9、さらにより好ましくは0.2~8、さらにより好ましくは0.3~8、さらにより好ましくは0.5~2である。(A)/(B)重量比が前記範囲であれば、植物に対する散布液の湿展性及び農薬成分の浸透性が良好となり、優れた農薬効力増強効果が得られる。
<Composition etc. of agricultural chemical efficacy enhancer composition>
In the efficacy enhancer composition for agricultural chemicals of the present invention, the weight ratio of the compound (A) to the compound (B) is (A) / (B), preferably 0.03 to 30, more preferably 0.05 to 20, more preferably 0.1-10, even more preferably 0.2-9, even more preferably 0.2-8, even more preferably 0.3-8, even more preferably 0.5-2 It is. If (A) / (B) weight ratio is the said range, the wettability of the spray liquid with respect to a plant and the permeability | transmittance of an agrochemical component will become favorable, and the outstanding agrochemical efficacy enhancement effect will be acquired.
 本発明の農薬用効力増強剤組成物は、化合物(A)と化合物(B)とを合計で好ましくは5重量%以上、より好ましくは10重量%以上、さらに好ましくは20重量%以上、さらにより好ましくは40重量%以上、さらにより好ましくは60重量%以上、さらにより好ましくは80重量%以上、さらにより好ましくは90重量%以上含有する。取り得る上限値は100重量%である。化合物(A)と化合物(B)の合計含有量が前記範囲であれば、農薬と共に希釈して用いられる際に化合物(A)と化合物(B)の濃度が十分となり、良好な農薬効力増強効果が得られる。従って、農薬効力増強効果を得るために、通常と同様の農薬の希釈倍率で使用でき、費用及び作業性の面でも好ましいものとなる。 In the agrochemical efficacy enhancer composition of the present invention, the total amount of the compound (A) and the compound (B) is preferably 5% by weight or more, more preferably 10% by weight or more, still more preferably 20% by weight or more. Preferably, it contains 40% by weight or more, still more preferably 60% by weight or more, still more preferably 80% by weight or more, and even more preferably 90% by weight or more. The upper limit that can be taken is 100% by weight. When the total content of the compound (A) and the compound (B) is within the above range, the concentration of the compound (A) and the compound (B) is sufficient when used with dilution with an agricultural chemical, and a good agricultural chemical efficacy enhancing effect Is obtained. Therefore, in order to obtain the effect of enhancing the effectiveness of agricultural chemicals, it can be used at the same dilution ratio of agricultural chemicals as usual, which is preferable in terms of cost and workability.
 更に、本発明では、化合物(A)、化合物(B)による効果を妨げない範囲で、化合物(A)、化合物(B)以外の界面活性剤を併用することもできる。そのような界面活性剤としては、化合物(A)、化合物(B)以外の非イオン界面活性剤、陰イオン界面活性剤、陽イオン界面活性剤及び両性界面活性剤、或いはそれらの混合物が挙げられる。 Furthermore, in the present invention, a surfactant other than the compound (A) and the compound (B) can be used in combination as long as the effects of the compound (A) and the compound (B) are not hindered. Examples of such surfactants include compound (A), nonionic surfactants other than compound (B), anionic surfactants, cationic surfactants and amphoteric surfactants, or mixtures thereof. .
 化合物(A)、化合物(B)以外の界面活性剤を併用する場合、その含有量は、化合物(A)、化合物(B)による効果を妨げない範囲で適宜選択可能であるが、湿展性向上及び農薬の効力増強の観点から、農薬用効力増強剤組成物の全界面活性剤中に占める化合物(A)及び化合物(B)の割合が50重量%以上であることが好ましく、70重量%以上であることがより好ましく90重量%以上であることがさらに好ましい。 When a surfactant other than the compound (A) and the compound (B) is used in combination, the content can be appropriately selected as long as the effects of the compound (A) and the compound (B) are not hindered. From the viewpoint of improving and enhancing the efficacy of agricultural chemicals, the proportion of compound (A) and compound (B) in the total surfactant of the agricultural chemical efficacy enhancing agent composition is preferably 50% by weight or more, and 70% by weight. More preferably, it is more preferably 90% by weight or more.
 非イオン界面活性剤としては、ポリオキシエチレンアルキルエーテル〔但し、一般式(A1)及び一般式(B1)に該当しないもの〕、ポリオキシエチレンアルキルアリールエーテル、ポリオキシエチレンアルキルアリールエーテルホルムアルデヒド縮合物、ポリオキシアルキレンアリールエーテル、ポリオキシアルキレンアルキルソルビトールエステル、ポリオキシアルキレンアルキルグリセロールエステル、ポリオキシアルキレンブロック共重合体、ポリオキシアルキレンブロック共重合体アルキルグリセロールエステル、ポリオキシアルキレンアルキルスルホンアミド、ポリオキシプロピレンブロック共重合体、ポリオキシエチレンオレイルエーテル、ポリオキシアルキレンアルキルフェノール、ポリオキシアルキレンアルキルポリグリコシドなど、及びこれらのうちの2種以上の混合物などが挙げられる。 Nonionic surfactants include polyoxyethylene alkyl ethers (however, those not corresponding to the general formulas (A1) and (B1)), polyoxyethylene alkyl aryl ethers, polyoxyethylene alkyl aryl ether formaldehyde condensates, Polyoxyalkylene aryl ether, polyoxyalkylene alkyl sorbitol ester, polyoxyalkylene alkyl glycerol ester, polyoxyalkylene block copolymer, polyoxyalkylene block copolymer alkyl glycerol ester, polyoxyalkylene alkyl sulfonamide, polyoxypropylene block Copolymer, polyoxyethylene oleyl ether, polyoxyalkylene alkylphenol, polyoxyalkylene alkyl poly Such glycosidic, and the like a mixture of two or more of these.
 陽イオン界面活性剤としては、アルキルアミンエチレンオキサイド付加物、アルキルアミンプロピレンオキサイド付加物、例えばタローアミンエチレンオキサイド付加物、オレイルアミンエチレンオキサイド付加物、ソイアミンエチレンオキサイド付加物、ココアミンエチレンオキサイド付加物、合成アルキルアミンエチレンオキサイド付加物、オクチルアミンエチレンオキサイド付加物、ジアルキルアミン誘導体など及びそれらの混合物が挙げられる。前記ジアルキルアミン誘導体としては、ジアルキルモノメチルヒドロキシエチルアンモニウムプロピオネート、ジアルキルモノメチルベンザルコニウムクロライド、ジアルキルモノメチルエチルアンモニウムエチルサルフェート、ジアルキルモノメチルアミンオキサイド、ジアルキルモノメチルアミノカルボキシベタイン、ジアルキルモノメチルヒドロキシスルホベタインなどがある。 Examples of cationic surfactants include alkylamine ethylene oxide adducts, alkylamine propylene oxide adducts such as tallow amine ethylene oxide adducts, oleylamine ethylene oxide adducts, soyamine ethylene oxide adducts, cocoamine ethylene oxide adducts, Examples include synthetic alkylamine ethylene oxide adducts, octylamine ethylene oxide adducts, dialkylamine derivatives, and the like, and mixtures thereof. Examples of the dialkylamine derivative include dialkylmonomethylhydroxyethylammonium propionate, dialkylmonomethylbenzalkonium chloride, dialkylmonomethylethylammonium ethyl sulfate, dialkylmonomethylamine oxide, dialkylmonomethylaminocarboxybetaine, and dialkylmonomethylhydroxysulfobetaine.
 陽イオン界面活性剤としては、湿展性向上及び農薬の効力増強の観点から、アルキルアミンエチレンオキサイド付加物、アルキルアミンプロピレンオキサイド付加物、ジアルキルアミン誘導体が好ましく、タローアミンエチレンオキサイド付加物、ジラウリルモノメチルベンザルコニウムクロライドがより好ましい。 The cationic surfactant is preferably an alkylamine ethylene oxide adduct, an alkylamine propylene oxide adduct, or a dialkylamine derivative from the viewpoint of improving wettability and enhancing the effectiveness of agricultural chemicals, and a tallow amine ethylene oxide adduct or dilauryl. Monomethylbenzalkonium chloride is more preferred.
 陰イオン界面活性剤のうち、典型的なものは、水溶液或いは固体状態で入手され得るが、その例としては、モノ-及びジ-アルキルナフタレンスルホン酸ナトリウム、アルファ-オレフィンスルホン酸ナトリウム、アルカンスルホン酸ナトリウム、アルキルスルホコハク酸塩、アルキル硫酸塩、ポリオキシアルキレンアルキルエーテル硫酸塩、ポリオキシアルキレンアルキルアリールエーテル硫酸塩、ポリオキシアルキレンスチリルフェニルエーテル硫酸塩、モノ-及びジ-アルキルベンゼンスルホン酸塩、アルキルナフタレンスルホン酸塩、アルキルナフタレンスルホネートのホルムアルデヒド縮合物、アルキルジフェニルエーテルスルホン酸塩、オレフィニックスルホン酸塩、モノ及びジアルキルリン酸塩、ポリオキシアルキレンモノ及びジアルキルリン酸塩、ポリオキシアルキレンモノ及びジフェニルエーテルリン酸塩、ポリオキシアルキレンモノ及びジアルキルフェニルエーテルリン酸塩、ポリカルボン酸塩、脂肪酸塩、直鎖及び分岐アルキルポリオキシアルキレンエーテル酢酸又はその塩、アルケニルポリオキシアルキレンエーテル酢酸又はその塩、直鎖及び分岐アルキルアミドポリオキシアルキレンエーテル酢酸又はその塩、ステアリン酸及びその塩、オレイン酸及びその塩、N-メチル脂肪酸タウリド(taurides)、これらのうちの2種以上の混合物など(ナトリウム、カリウム、アンモニウム及びアミン塩を含む)が挙げられる。陰イオン界面活性剤としては、乳化分散性向上の観点から、脂肪酸塩が好ましく、オレイン酸、ヒマシ油脂肪酸等の高級脂肪酸のナトリウム塩、カリウム塩がより好ましく、オレイン酸カリウムがより好ましい。 Among the anionic surfactants, typical ones can be obtained in aqueous solution or in the solid state, examples of which are sodium mono- and di-alkylnaphthalene sulfonates, sodium alpha-olefin sulfonates, alkane sulfonic acids. Sodium, alkyl sulfosuccinate, alkyl sulfate, polyoxyalkylene alkyl ether sulfate, polyoxyalkylene alkyl aryl ether sulfate, polyoxyalkylene styryl phenyl ether sulfate, mono- and di-alkyl benzene sulfonate, alkyl naphthalene sulfone Acid salt, formaldehyde condensate of alkyl naphthalene sulfonate, alkyl diphenyl ether sulfonate, olefinic sulfonate, mono and dialkyl phosphate, polyoxyalkylene mono And dialkyl phosphates, polyoxyalkylene mono and diphenyl ether phosphates, polyoxyalkylene mono and dialkyl phenyl ether phosphates, polycarboxylates, fatty acid salts, linear and branched alkyl polyoxyalkylene ether acetic acids or salts thereof, Alkenyl polyoxyalkylene ether acetic acid or its salt, linear and branched alkylamide polyoxyalkylene ether acetic acid or its salt, stearic acid and its salt, oleic acid and its salt, N-methyl fatty acid taurides, of these A mixture of two or more kinds (including sodium, potassium, ammonium and amine salts) can be mentioned. The anionic surfactant is preferably a fatty acid salt, more preferably a sodium salt or potassium salt of a higher fatty acid such as oleic acid or castor oil fatty acid, and more preferably potassium oleate, from the viewpoint of improving emulsification dispersibility.
 また、両性界面活性剤としては、ラウリルジメチルアミンオキサイド、アルモックス(Armox)C/12、アミンオキサイド、モナテリックス(Monaterics)、ミラノール(Miranols)、ベタイン、ロンザイン(Lonzaines)、他のアミンオキサイド、これらの混合物などがある。 Amphoteric surfactants include lauryl dimethylamine oxide, Armox C / 12, amine oxide, monaterics, miranols, betaine, Lonzaines, other amine oxides, There is a mixture.
 本発明の農薬用効力増強剤組成物は、化合物(A)及び化合物(B)からなるものであってもよいが、化合物(A)及び化合物(B)以外の成分を含む場合、残部は水及び/又は有機溶媒が好ましい。水及び/又は有機溶媒を含有する該組成物は、該組成物の低温又は高温安定性に優れ、更に長期保存安定性に優れる。また、水又は有機溶媒を含有する組成物は、希釈時の化合物(A)及び化合物(B)の希釈媒体(水及び/又は有機溶媒)への分散及び溶解が容易となるため、農薬効力増強効果を高めることができる。好ましい有機溶媒としては、イソブタノール、イソプロパノール、エタノール、ジエチレングリコール、エチル乳酸、ブチルセルソルブ、ポリエチレングリコール(重量平均分子量200~400)、ジメチルスルホキシド、N-ブチルカルビトール、1,3-ブチレングリコール、ジプロピレングリコール2-(2-メトキシエトキシ)エタノール、エチルカルビトールが挙げられるが、農薬の湿展性向上及び農薬の効力増強の観点から、エチル乳酸、ジエチレングリコールが好ましく、ジエチレングリコールがより好ましい。 The efficacy enhancer composition for agricultural chemicals of the present invention may be composed of the compound (A) and the compound (B), but when it contains components other than the compound (A) and the compound (B), the balance is water. And / or organic solvents are preferred. The composition containing water and / or an organic solvent is excellent in low-temperature or high-temperature stability of the composition, and further excellent in long-term storage stability. In addition, the composition containing water or an organic solvent facilitates dispersion and dissolution of the compound (A) and the compound (B) in the dilution medium (water and / or organic solvent) at the time of dilution. The effect can be enhanced. Preferred organic solvents include isobutanol, isopropanol, ethanol, diethylene glycol, ethyl lactic acid, butyl cellosolve, polyethylene glycol (weight average molecular weight 200 to 400), dimethyl sulfoxide, N-butyl carbitol, 1,3-butylene glycol, di Examples thereof include propylene glycol 2- (2-methoxyethoxy) ethanol and ethyl carbitol, and ethyl lactic acid and diethylene glycol are preferable and diethylene glycol is more preferable from the viewpoint of improving the wettability of the agricultural chemical and enhancing the efficacy of the agricultural chemical.
 本発明の農薬用効力増強剤組成物中に占める水及び又は有機溶媒の含有量は、特に制限されないが、農薬用効力増強剤組成物中に占める化合物(A)及び化合物(B)が、50重量%以上となる量で使用することが好ましく、より好ましくは70重量%以上、さらに好ましくは90重量%以上となるよう使用することが好ましい。水及び/又は有機溶媒の含有量は、組成物中、50重量%未満、例えば1~50重量%未満、更に5~30重量%が好ましい。 The content of water and / or organic solvent in the efficacy enhancer composition for agricultural chemicals of the present invention is not particularly limited, but 50% of the compound (A) and compound (B) in the efficacy enhancer composition for agricultural chemicals are used. It is preferably used in an amount of at least wt%, more preferably at least 70 wt%, and even more preferably at least 90 wt%. The content of water and / or organic solvent in the composition is preferably less than 50% by weight, for example, 1 to less than 50% by weight, and more preferably 5 to 30% by weight.
<農薬組成物>
 本発明の農薬組成物は、上記化合物(A)と、化合物(B)と、農薬原体とを含有するものである。ここで、農薬原体とは農薬の有効成分をいう。本発明の農薬組成物としては、本発明の農薬用効力増強剤組成物と、殺菌剤、殺虫剤、殺ダニ剤、除草剤、及び植物成長調節剤各々の有効成分から選択される何れかの農薬原体とを含有するものが挙げられる。なお、農作物への影響を考慮すると、本発明の農薬組成物は、(i)酸化水素及び水中で過酸化水素を放出する化合物、並びに(ii)次亜塩素酸、次亜塩素酸塩及び水中で次亜塩素酸を放出する化合物、から選ばれる1種以上の化合物の含有量が少ない、例えば、次亜塩素酸又は過酸化水素として組成物中0.1重量%以下、更に0.01重量%以下であるもの、特には含有しないものが好ましい。これは、後述する農薬製剤や散布用の農薬製剤などにおいても同様である。
<Agricultural chemical composition>
The agrochemical composition of this invention contains the said compound (A), a compound (B), and an agrochemical raw material. Here, the active ingredient of an agrochemical means an active ingredient of an agrochemical. The agrochemical composition of the present invention is any one selected from the active ingredients of the agrochemical efficacy enhancer composition of the present invention and each of the fungicides, insecticides, acaricides, herbicides, and plant growth regulators. The thing containing an agrochemical raw material is mentioned. In consideration of the effects on agricultural products, the agrochemical composition of the present invention comprises (i) a compound that releases hydrogen peroxide and hydrogen peroxide in water, and (ii) hypochlorous acid, hypochlorite, and water. The content of one or more compounds selected from compounds that release hypochlorous acid is low, for example, 0.1% by weight or less in the composition as hypochlorous acid or hydrogen peroxide, and further 0.01% by weight % Or less, particularly those not contained are preferred. The same applies to the agrochemical formulations described later and the agricultural chemical formulations for spraying.
 本発明の農薬組成物において、化合物(A)と農薬原体との重量比は、農薬の湿展性向上及び農薬の効力増強の観点から、化合物(A)/農薬原体=0.05~50であることが好ましく、0.1~10であることがより好ましい。 In the agrochemical composition of the present invention, the weight ratio of the compound (A) to the pesticide raw material is compound (A) / pesticide raw material = 0.05- 50 is preferable, and 0.1 to 10 is more preferable.
 また、本発明の農薬組成物において、化合物(B)と農薬原体との重量比は、農薬の湿展性向上及び農薬の効力増強の観点から、化合物(B)/農薬原体=0.05~50であることが好ましく、0.1~20であることがより好ましい。0.1~10であることがさらにより好ましい。 In the agricultural chemical composition of the present invention, the weight ratio of the compound (B) and the agricultural chemical raw material is such that the compound (B) / the agricultural chemical raw material = 0. It is preferably from 05 to 50, more preferably from 0.1 to 20. Even more preferably, it is 0.1-10.
 さらに、本発明の農薬組成物において、化合物(A)及び化合物(B)の合計と、農薬原体との重量比は、湿展性向上及び農薬の効力増強の観点から、化合物(A)及び化合物(B)の合計重量/農薬原体の重量=0.1~100であることが好ましく、0.2~40であることがより好ましく、0.2~20であることがさらにより好ましい。 Furthermore, in the agrochemical composition of the present invention, the weight ratio of the total of the compound (A) and the compound (B) to the active ingredient of the agrochemical is from the viewpoint of improving wettability and enhancing the efficacy of the agrochemical, The total weight of the compound (B) / the weight of the agrochemical base is preferably 0.1 to 100, more preferably 0.2 to 40, and still more preferably 0.2 to 20.
 また、本発明の農薬組成物の製剤型は、乳剤、液剤、水和剤、粒剤、粉剤、フロアブル製剤等いずれでもよく、製剤型は問わない。従って、その製剤型に応じた他の添加剤、例えば乳化剤、溶剤、分散剤、担体等を含有するものであってもよい。本発明に係わる農薬用効力増強剤組成物の使用方法は、農薬用効力増強剤組成物を含有する上記各種剤型の農薬組成物を使用する方法と、農薬(本発明の農薬用効力増強剤組成物を含有しないもの)希釈使用時に別添の農薬用効力増強剤組成物を使用する方法があるが、どちらの方法にても本発明の目的とする効力増強作用が得られる。 Further, the formulation type of the agrochemical composition of the present invention may be any of emulsion, solution, wettable powder, granule, powder, flowable formulation, etc., and the formulation type is not limited. Therefore, it may contain other additives according to the formulation type, such as emulsifiers, solvents, dispersants, carriers and the like. The method of using the agrochemical efficacy enhancer composition according to the present invention includes a method of using the various agrochemical compositions containing the agrochemical efficacy enhancer composition, and a pesticide (the agrochemical efficacy enhancer of the present invention). There is a method of using an attached agrochemical efficacy enhancer composition at the time of dilution use, and any of these methods can provide the effect of enhancing the efficacy of the present invention.
 本発明の農薬組成物の製剤中に必要に応じてキレート剤、pH調節剤、無機塩類、増粘剤を加えてもよい。 In the preparation of the agricultural chemical composition of the present invention, a chelating agent, a pH adjuster, inorganic salts, and a thickener may be added as necessary.
 本発明に使用し得るキレート剤としては、アミノポリカルボン酸系キレート剤、芳香族及び脂肪族カルボン酸系キレート剤、アミノ酸系キレート剤、エーテルポリカルボン酸系キレート剤、ホスホン酸系キレート剤(例えばイミノジメチルホスホン酸(IDP)、アルキルジホスホン酸(ADPA)等である)、又はジメチルグリオキシム(DG)、ヒドロキシカルボン酸系キレート剤、高分子電解質系(含オリゴマー)キレート剤等であり、これらは酸のまま或いはナトリウム、カリウム、アンモニウム等の塩の形のものであってもよい。キレート剤は農薬用効力増強剤組成物中の(B)成分に対して、0.01~30倍モルの割合で配合されるのが好ましい。 Examples of chelating agents that can be used in the present invention include aminopolycarboxylic acid chelating agents, aromatic and aliphatic carboxylic acid chelating agents, amino acid chelating agents, ether polycarboxylic acid chelating agents, and phosphonic acid chelating agents (for example, Iminodimethylphosphonic acid (IDP), alkyldiphosphonic acid (ADPA), etc.), or dimethylglyoxime (DG), hydroxycarboxylic acid chelating agent, polymer electrolyte (including oligomer) chelating agent, etc. May be in the form of an acid or a salt of sodium, potassium, ammonium or the like. The chelating agent is preferably blended at a ratio of 0.01 to 30-fold mol with respect to the component (B) in the efficacy enhancer composition for agricultural chemicals.
 アミノポリカルボン酸系キレート剤としては、
a)RNX2型化合物
b)NX3型化合物
c)R-NX-CH2CH2-NX-R型化合物
d)R-NX-CH2CH2-NX2型化合物及び
e)X2N-R'-NX2型化合物
の全てが使用できる。上記式中Xは-CH2COOH又は-CH2CH2COOHを表し、Rは水素原子、アルキル基、水酸基、ヒドロキシアルキル基又はこの種の公知のキレート化合物を表す置換基を表し、R'はアルキレン基、シクロアルキレン基及びこの種の公知のキレート化合物を表す基を表す。これらの代表例としては、エチレンジアミンテトラ酢酸(EDTA)、シクロヘキサンジアミンテトラ酢酸(CDTA)、ニトリロトリ酢酸(NTA)、イミノジ酢酸(IDA)、N-(2-ヒドロキシエチル)イミノジ酢酸(HIMDA)、ジエチレントリアミンペンタ酢酸(DTPA)、N-(2-ヒドロキシエチル)エチレンジアミン三酢酸(EDTA-OH)及びグリコールエーテルジアミンテトラ酢酸(GEDTA)並びにこれらの塩等が挙げられる。
As aminopolycarboxylic acid chelating agent,
a) RNX type 2 compound b) NX type 3 compound c) R-NX-CH 2 CH 2 -NX-R type compound d) R-NX-CH 2 CH 2 -NX type 2 compound and e) X 2 N- All R'-NX type 2 compounds can be used. In the above formula, X represents —CH 2 COOH or —CH 2 CH 2 COOH, R represents a hydrogen atom, an alkyl group, a hydroxyl group, a hydroxyalkyl group or a substituent representing a known chelate compound of this type, and R ′ represents It represents a group representing an alkylene group, a cycloalkylene group, and a known chelate compound of this type. Typical examples of these include ethylenediaminetetraacetic acid (EDTA), cyclohexanediaminetetraacetic acid (CDTA), nitrilotriacetic acid (NTA), iminodiacetic acid (IDA), N- (2-hydroxyethyl) iminodiacetic acid (HIMDA), diethylenetriaminepenta Examples include acetic acid (DTPA), N- (2-hydroxyethyl) ethylenediamine triacetic acid (EDTA-OH), glycol ether diamine tetraacetic acid (GEDTA), and salts thereof.
 本発明に使用し得る芳香族及び脂肪族カルボン酸系キレート剤は、シュウ酸、コハク酸、ピルビン酸又はアントラニル酸及びこれらの塩等である。また、本発明に使用し得るアミノ酸系キレート剤はグリシン、セリン、アラニン、リジン、シスチン、システイン、エチオニン、チロシン又はメチオニン及びこれらの塩及び誘導体等である。また、本発明に使用し得るヒドロキシカルボン酸系キレート剤としては、グリコール酸、リンゴ酸、クエン酸、グルコン酸、ヘプトン酸、酢酸及びこれらの塩等である。更に、本発明に使用し得るエーテルポリカルボン酸系キレート剤としては、例えば次式で表される化合物並びにその類似化合物及びその塩(特にNa塩等)が挙げられる。 Aromatic and aliphatic carboxylic acid chelating agents that can be used in the present invention are oxalic acid, succinic acid, pyruvic acid or anthranilic acid and salts thereof. Amino acid chelating agents that can be used in the present invention include glycine, serine, alanine, lysine, cystine, cysteine, ethionine, tyrosine, methionine, and salts and derivatives thereof. Examples of the hydroxycarboxylic acid chelating agent that can be used in the present invention include glycolic acid, malic acid, citric acid, gluconic acid, heptonic acid, acetic acid, and salts thereof. Furthermore, examples of the ether polycarboxylic acid-based chelating agent that can be used in the present invention include compounds represented by the following formula and similar compounds and salts thereof (particularly Na salts).
Figure JPOXMLDOC01-appb-C000001
Figure JPOXMLDOC01-appb-C000001
 本発明に使用し得る高分子電解質系(含オリゴマー)キレート剤としては、アクリル酸重合体、無水マレイン酸重合体、α-ヒドロキシアクリル酸重合体、イタコン酸重合体及びこれらの共重合体、エポキシコハク酸重合体等が挙げられる。 Examples of the polymer electrolyte (containing oligomer) chelating agent that can be used in the present invention include acrylic acid polymer, maleic anhydride polymer, α-hydroxyacrylic acid polymer, itaconic acid polymer and copolymers thereof, epoxy Examples thereof include succinic acid polymers.
 本発明に使用し得るpH調節剤としてはクエン酸、リン酸(ピロリン酸)、グルコン酸等或いはこれらの塩である。 The pH adjuster that can be used in the present invention is citric acid, phosphoric acid (pyrophosphoric acid), gluconic acid or the like, or a salt thereof.
 本発明に使用し得る無機塩類としては、無機鉱物塩として例えば無機塩クレー、タルク、ベントナイト、ゼオライト、炭酸カルシウム、ケイソウ土、ホワイトカーボン等が挙げられ、無機アンモニウム塩として例えば硫酸アンモニウム、硝酸アンモニウム、リン酸アンモニウム、チオシアン酸アンモニウム、塩化アンモニウム、スルファミン酸アンモニウム等が挙げられる。 Examples of inorganic salts that can be used in the present invention include inorganic mineral salts such as inorganic salt clay, talc, bentonite, zeolite, calcium carbonate, diatomaceous earth, and white carbon. Examples of inorganic ammonium salts include ammonium sulfate, ammonium nitrate, and phosphoric acid. Examples include ammonium, ammonium thiocyanate, ammonium chloride, and ammonium sulfamate.
 また本発明に使用し得る増粘剤としては、天然、半合成及び合成の水溶性増粘剤は何れも使用でき、天然粘質物では、微生物由来のキサンタンガム、ザンフロー、植物由来のペクチン、アラビアガム、グアーガムなどが、半合成粘質物では、セルロース又はでんぷん誘導体のメチル化物、カルボキシアルキル化物、ヒドロキシアルキル化物(メチルセルロース、カルボキシメチルセルロース、ヒドロキシメチルセルロースなどを含む)、ソルビトールなどが、また合成粘質物では、ポリアクリル酸塩、ポリマレイン酸塩、ポリビニルピロリドン、ペンタエリスリトールエチレンオキサイド付加物などが具体例として挙げられる。 As the thickener that can be used in the present invention, any of natural, semi-synthetic and synthetic water-soluble thickeners can be used. In natural mucilage, xanthan gum derived from microorganisms, xanthan gum, pectin derived from plants, gum arabic , Guar gum, etc., semi-synthetic mucilage, cellulose or starch derivative methylated product, carboxyalkylated product, hydroxyalkylated product (including methylcellulose, carboxymethylcellulose, hydroxymethylcellulose etc.), sorbitol, etc. Specific examples include acrylates, polymaleates, polyvinylpyrrolidones, pentaerythritol ethylene oxide adducts, and the like.
 次に本発明の農薬組成物に用いられる農薬原体としては、例えば、農薬ハンドブック2001年度版(社団法人 日本植物防疫協会)に記載のものが挙げられるが、これらに限定されるものではない。また、本発明の農薬用効力増強剤組成物は種々の作物に対して薬害はなく安全に使用できるものである。 Next, examples of the agrochemical base used in the agrochemical composition of the present invention include those described in the Agricultural Handbook 2001 edition (Japan Plant Protection Association), but are not limited thereto. Moreover, the efficacy enhancer composition for agricultural chemicals of the present invention can be safely used with no phytotoxicity to various crops.
 殺菌剤としては、硫黄系のジネブ(亜鉛エチレンビスジチオカーバメート)、マンネブ(マンガンエチレンビスジチオカーバメート)、マンゼブ(亜鉛イオン配位マンガニーズエチレンビスジチオカーバメート) 、ポリカーバメート(ビスジメチルジチオカルバモイル亜鉛エチレンビスジチオカーバメート)、ベンズイミダゾール系としてはベノミル(メチル-1-(ブチルカルバモイル)-2-ベンズイミダゾールカーバメート) 、チオファネートメチル(1,2-ビス(3-メトキシカルボニル・2-チオウレイド)ベンゼン)、ジカルボキシイミド系のビンクロゾリン(3-(3,5-ジクロロフェニル)-5-メチル-5-ビニル-1,3-オキサゾリジン-2,4-ジオン)、イプロジオン(3-(3,5-ジクロロフェニル)-N-イソプロピル-2,4-ジオキソイミダゾリジン-1-カルボキサミド)、プロシミドン(N-(3,5-ジクロロフェニル)-1,2-ジメチルシクロプロパン-1,2-ジカルボキシイミド)、他にトリアジン(2,4-ジクロロ-6-(2-クロロアニリノ)-1,3,5-トリアジン)、トリフミゾール((E)-4-クロロ-α,α,α-トリフルオロ-N-(1-イミダゾール-1-イル-2-プロポキシエチリダン)-o-トルイジン)、イミノクタジン酢酸塩(1,1-イミニオディ(オクタメチレン)ジグアニジウムトリアセテート)、有機銅(Oxine-copper)、水酸化第二銅(コサイドボルドー等)、抗生物質系殺菌剤(ストレプトマイシン系、テトラサイクリン系、ポリオキシ系、ブラストサイジンS、カスガマイシン系、バリダマイシン系)、トリアジメホン(1-(4-クロロフェノキシ)-3,3-ジメチル-1-(1,2,4-トリアゾール-1-イル)-2-ブタノン)、イソプロチオラン(ジイソプロピル-1,3-ジチオラン-2-イリデンマロネート)、TPN(テトラクロルイソフタロニトリル)等があり、好適なものとしては、有機銅(Oxine-copper)、水酸化第二銅、トリフミゾール((E)-4-クロロ-α,α,α-トリフルオロ-N-(1-イミダゾール-1-イル-2-プロポキシエチリダン)-o-トルイジン),イプロジオン(3-(3,5-ジクロロフェニル)-N-イソプロピル-2,4-ジオキソイミダゾリジン-1-カルボキサミド)が挙げられる。 Bactericides include sulfur-based dinebu (zinc ethylene bisdithiocarbamate), manneb (manganese ethylene bisdithiocarbamate), manzeb (zinc ion coordinated manganese ethylene bisdithiocarbamate), polycarbamate (bisdimethyldithiocarbamoyl zinc ethylene bis Dithiocarbamate), benzimidazole as benomyl (methyl-1- (butylcarbamoyl) -2-benzimidazolecarbamate), thiophanate methyl (1,2-bis (3-methoxycarbonyl 2-thioureido) benzene), dicarboximide Vinclozolin (3- (3,5-dichlorophenyl) -5-methyl-5-vinyl-1,3-oxazolidine-2,4-dione), iprodione (3- (3,5-dichlorophenyl) -N-isopropyl -2,4-Dioxoimi Zolidine-1-carboxamide), procymidone (N- (3,5-dichlorophenyl) -1,2-dimethylcyclopropane-1,2-dicarboximide), and triazine (2,4-dichloro-6- (2 -Chloroanilino) -1,3,5-triazine), trifumizole ((E) -4-chloro-α, α, α-trifluoro-N- (1-imidazol-1-yl-2-propoxyethylidan)- o-toluidine), iminotadine acetate (1,1-iminiodi (octamethylene) diguanidinium triacetate), organic copper (Oxine-copper), cupric hydroxide (such as cocide Bordeaux), antibiotic fungicides ( Streptomycin, tetracycline, polyoxy, blasticidin S, kasugamycin, validamycin), triazimephone (1- (4-chlorophenoxy) -3,3-dimethyl-1- (1,2, 4-triazol-1-yl) -2-butanone), isoprothiolane (diisopropyl-1,3-dithiolane-2-ylidene malonate), TPN (tetrachloroisophthalonitrile), and the like. Organic copper, cupric hydroxide, trifumisol ((E) -4-chloro-α, α, α-trifluoro-N- (1-imidazol-1-yl-2-propoxyethylidan) -O-toluidine), iprodione (3- (3,5-dichlorophenyl) -N-isopropyl-2,4-dioxoimidazolidine-1-carboxamide).
 殺虫剤の場合、ピレスロイド系殺虫剤としては、ペルメトリン((3-フェノキシベンジル=(1RS,3RS)-(1RS,3RS)-3-(2,2-ジクロロビニル)-2,2-ジメチルシクロプロパンカルボキシラート)、シベルメトリン((RS)-α-シアノ-3-フェノキシベンジル=(1RS,3RS)-(1RS,3RS)-3-(2,2-ジクロロビニル)-2,2-ジメチルシクロプロパンカルボキシラート)、フェンバレレエート(α-シアノ-3-フェノキシベンジル-2-(4-クロロフェニル)-3-メチルブタノエート)、有機リン系殺虫剤としては、DDVP(ジメチル2,2-ジクロルビニルホスフェート)、スミチオン(MEP) (O,O-ジメチル-O-(3-メチル-4-ニトロフェニル)チオフォスフェート)、マラソン(S-〔1,2,-ビス(エトキシカルボニル)エチル〕ジメチルホスホロチオールチオネート)、ジメトエート(ジメチルS-(N-メチルカルバモイルメチル)ジチオホスフェート)、エルサン(S-〔α-(エトキシカルボニル)ベンジル〕ジメチルホスホロチオールチオネート) 、バイジット(O,O-ジメチル-O-(3-メチル-4-メチルチオフェニルチオホスフェート))、カーバメート系殺虫剤としては、バッサ(O-sec-ブチルフェニルメチルカーバメート)、MTMC(m-トリルメチルカーバメート)、メオパール(3,4-ジメチルフェニル-N -メチルカーバメート)、メソミル(S メチル-N 〔(メチルカルバモイル)オキシ〕チオアセトイミド)等があり、好適なものとしては、ペルメトリン,DDVP(ジメチル2,2-ジクロルビニルホスフェート)、メソミル(Sメチル-N〔(メチルカルバモイル)オキシ〕チオアセトイミド)が挙げられる。 In the case of insecticides, pyrethroid insecticides include permethrin ((3-phenoxybenzyl = (1RS, 3RS)-(1RS, 3RS) -3- (2,2-dichlorovinyl) -2,2-dimethylcyclopropane). Carboxylate), cybermethrin ((RS) -α-cyano-3-phenoxybenzyl = (1RS, 3RS)-(1RS, 3RS) -3- (2,2-dichlorovinyl) -2,2-dimethylcyclopropanecarboxyl Rat), fenvalerate (α-cyano-3-phenoxybenzyl-2- (4-chlorophenyl) -3-methylbutanoate), and organophosphorus insecticides such as DDVP (dimethyl 2,2-dichlorovinyl) Phosphate), sumithione (MEP) (O, O-dimethyl-O- (3-methyl-4-nitrophenyl) thiophosphate), marathon (S- [1,2, -bis (ethoxycarbonyl) ethyl] dimethylphosphoro) Thiolthionate), dimethoate (dimethyl S- (N-methyl) Rubamoylmethyl) dithiophosphate), ersan (S- [α- (ethoxycarbonyl) benzyl] dimethylphosphorothiolthionate), visit (O, O-dimethyl-O- (3-methyl-4-methylthiophenylthiophosphate)) Carbamate insecticides include bassa (O-sec-butylphenylmethylcarbamate), MTMC (m-tolylmethylcarbamate), meopal (3,4-dimethylphenyl-N -methylcarbamate), mesomil (S methyl-N [(Methylcarbamoyl) oxy] thioacetimide) and the like are preferably permethrin, DDVP (dimethyl 2,2-dichlorovinyl phosphate), and mesomil (S methyl-N [(methylcarbamoyl) oxy] thioacetimide). Can be mentioned.
 更に、天然系殺虫剤としては、除虫菊由来のピレトリン剤、ピペロニルブトキシド剤、マメ科のかん木デリス由来のロテノン剤、ニコチン剤(3-(1-メチル-2-ピルロリジニル)ピリジンサルフェート)等が挙げられる。昆虫成長制御剤(IGR剤)としては、ジフルベンズロン(1-(4クロロフェニル)-3-(2,6-ジフルオロベンゾイル)尿素)、テフルベンズロン(1-(3,5-ジクロロ-2,4-ジフルオロフェニル)-3-(2,6-ジフルオロベンゾイル)尿素)、クロルフルアズロン(1-〔3,5-ジクロロ-4-(3-クロロ-5-トリフルオロメチル-2-ピリジルオキシ)フェニル〕-3-(2,6-ジフルオロベンゾイル)尿素等が挙げられる。 Furthermore, examples of natural insecticides include pyrethrins derived from pesticide chrysanthemums, piperonyl butoxides, rotenones derived from leguminous shrubs, nicotine (3- (1-methyl-2-pyrrolidinyl) pyridine sulfate), and the like. . Insect growth regulators (IGR agents) include diflubenzuron (1- (4 chlorophenyl) -3- (2,6-difluorobenzoyl) urea), teflubenzuron (1- (3,5-dichloro-2,4-difluorophenyl) ) -3- (2,6-difluorobenzoyl) urea), chlorfluazuron (1- [3,5-dichloro-4- (3-chloro-5-trifluoromethyl-2-pyridyloxy) phenyl]- Examples include 3- (2,6-difluorobenzoyl) urea.
 また殺ダニ剤としては、CPCBS(パラクロロフェニルパラクロロベンゼンスルホネート)、フェニソブロモレート(4,4'-ジブロムベンジル酸イソプロピル)、テトラジホン(2,4,5,4'-テトラクロロジフェニルスルホン) 、フェノチオカルブ(S-4-フェノキシブチル=ジメチルチオカーバメート)、フェンピロキシメート(tert-ブチル=(E)-α-(1,3-ジメチル-5-フェノキシピラゾール-4-イルメチレンアミノオキシ)-p-トルアート)、フルアシナム(3-クロロ-N-(3-クロロ-5-トリフルオロメチル-2-ピリジル)-α,α,α-トリフルオロ-2,6-ジニトロ-p-トルイジン)、酸化フェンブタスズ(ヘキサキス(β,β-ジメチルフェニルエチル)ジスタンノキサン)、ヘキシチアゾクス(トランス-5-(4-クロロフェニル)-N -シクロヘキシル-4-メチル-2-オキソチアゾリジン-3-カルボキサミド)、アミトラスズ(3-メチル-1,5-ビス(2,4-キシリル)-1,3,5-トリアザペンタ-1,4-ジエン)等があり、好適なものとしては、フェニソブロモレート(4,4'-ジブロムベンジル酸イソプロピル),アミトラスズ(3-メチル-1,5-ビス(2,4-キシリル)-1,3,5-トリアザペンタ-1,4-ジエン),フェンピロキシメート(tert-ブチル=(E)-α-(1,3-ジメチル-5-フェノキシピラゾール-4-イルメチレンアミノオキシ)-p-トルアート)が挙げられる。 Moreover, as an acaricide, CPCBS (parachlorophenyl parachlorobenzene sulfonate), phenisobromolate (isopropyl 4,4′-dibromobenzylate), tetradiphone (2,4,5,4′-tetrachlorodiphenyl sulfone), Phenothiocarb (S-4-phenoxybutyl = dimethylthiocarbamate), fenpyroximate (tert-butyl = (E) -α- (1,3-dimethyl-5-phenoxypyrazol-4-ylmethyleneaminooxy) -p-toluate) , Fluacinam (3-chloro-N- (3-chloro-5-trifluoromethyl-2-pyridyl) -α, α, α-trifluoro-2,6-dinitro-p-toluidine), fenbutasin oxide (hexakis ( β, β-dimethylphenylethyl) distannoxane), hexythiazox (trans-5- (4-chlorophenyl) -N -cyclohexyl-4-methyl-2-oxothiazolid -3-carboxamide), amitraz (3-methyl-1,5-bis (2,4-xylyl) -1,3,5-triazapenta-1,4-diene), and the like. Sobromolate (isopropyl 4,4'-dibromobenzylate), amitraz (3-methyl-1,5-bis (2,4-xylyl) -1,3,5-triazapenta-1,4-diene), And fenpyroximate (tert-butyl = (E) -α- (1,3-dimethyl-5-phenoxypyrazol-4-ylmethyleneaminooxy) -p-toluate).
 除草剤としては、酸アミド系除草剤として、例えばスタム(3,4-ジクロルプロピオンアニリド、DCPA)等が挙げられる。尿素系除草剤として、例えば、DCMU(3-(3,4-ジクロロフェニル)-1,1-ジメチルウレア)等が挙げられる。ビピリジリウム系除草剤としては、例えばパラコート(1,1'-ジメチル-4,4'-ビピリジウムジクロライド)、ジクワット(6,7-ジヒドロジピリド[1,2-a:2',1'c]ピラジンディウムジブロマイド)等が挙げられる。ダイアジン系除草剤としては、例えばブロマシル(5-ブロモ-3-sec-ブチル-6-メチルウラシル)等が挙げられる。トリアジン系除草剤としては、例えばシマジン(2-クロロ-4,6-ビス(エチルアミノ)-1,3,5-トリアジン)等が挙げられる。ニトリル系除草剤としては、例えばDBN(2,6-ジクロロベンゾニトリル)等が挙げられる。ジニトロアニリン系除草剤としては、例えばトリフルラリン(α,α,α-トリフルオロ-2,6-ジニトロ-N,N-ジプロピル-p-トルイジン)等が挙げられる。カーバメート系除草剤としては、例えばベンチオカーブ(サターン)(S-p-クロロベンジル-N,N-ジエチルチオカーバメート)等が挙げられる。ジフェニルエーテル系除草剤としては、例えばNIP(2,4-ジクロロフェニル-p-ニトロフェニルエーテル)等が挙げられる。フェノール系除草剤としては、例えばPCP(ソディウムペンタクロロフェノキシド)等が挙げられる。安息香酸系除草剤としては、例えばMDBA(ジメチルアミン-3,6-ジクロロ-o-アニセート)等が挙げられる。フェノキシ系除草剤としては、例えば2,4-Dナトリウム塩(ソディウム2,4-ジクロロフェノキシアセテート)等が挙げられる。アミノ酸除草剤としては、例えばグリホセート(N-(ホスホノメチル)グリシン又はその塩)グリホシネート(アンモニウム-DL-ホモアラニン-4-イル(メチル)ホスフィネート)等が挙げられる。また脂肪族系除草剤としては、例えばTCAナトリウム塩(ソディウム・トリクロロアセテート)あり、好適なものとしては、DBN(2,6-ジクロロベンゾニトリル),DCMU(3-(3,4-ジクロロフェニル)-1,1-ジメチルウレア),パラコート(1,1'-ジメチル-4,4'-ビピリジウムジクロライド)、ジクワット(6,7-ジヒドロジピリド[1,2-a:2',1'c]ピラジンディウムジブロマイド)が挙げられる。 Examples of the herbicide include acid amide type herbicides such as stam (3,4-dichloropropionanilide, DCPA). Examples of the urea herbicide include DCMU (3- (3,4-dichlorophenyl) -1,1-dimethylurea). Bipyridylium herbicides include, for example, paraquat (1,1'-dimethyl-4,4'-bipyridinium dichloride), diquat (6,7-dihydrodipyrido [1,2-a: 2 ', 1'c] pyrazine And dium dibromide). Examples of diazine herbicides include bromacil (5-bromo-3-sec-butyl-6-methyluracil) and the like. Examples of the triazine herbicide include simazine (2-chloro-4,6-bis (ethylamino) -1,3,5-triazine). Examples of the nitrile herbicide include DBN (2,6-dichlorobenzonitrile). Examples of the dinitroaniline herbicide include trifluralin (α, α, α-trifluoro-2,6-dinitro-N, N-dipropyl-p-toluidine). Examples of carbamate herbicides include bencho curve (Saturn) (Sp-chlorobenzyl-N, N-diethylthiocarbamate). Examples of the diphenyl ether herbicide include NIP (2,4-dichlorophenyl-p-nitrophenyl ether). Examples of phenolic herbicides include PCP (sodium pentachlorophenoxide). Examples of the benzoic acid herbicide include MDBA (dimethylamine-3,6-dichloro-o-anisate). Examples of the phenoxy herbicide include 2,4-D sodium salt (sodium 2,4-dichlorophenoxyacetate). Examples of the amino acid herbicide include glyphosate (N- (phosphonomethyl) glycine or a salt thereof) glyphosate (ammonium-DL-homoalanin-4-yl (methyl) phosphinate). Examples of the aliphatic herbicide include TCA sodium salt (sodium trichloroacetate), and preferable examples include DBN (2,6-dichlorobenzonitrile), DCMU (3- (3,4-dichlorophenyl)- 1,1-dimethylurea), paraquat (1,1'-dimethyl-4,4'-bipyridium dichloride), diquat (6,7-dihydrodipyrido [1,2-a: 2 ', 1'c] pyrazine Dium dibromide).
 更に、本発明の農薬組成物には上記以外の植物成長調節剤、肥料、防腐剤等の1種以上を混合して用いることもできる。 Furthermore, one or more kinds of plant growth regulators, fertilizers, preservatives and the like other than those described above can be mixed and used in the agricultural chemical composition of the present invention.
 植物成長調節剤としては、インドール酪酸、エチクロゼート(5-クロロ-3(1H)インダゾリン酢酸エチル)、ベンジルアミノプリン(6-(N-ベンジルアミノ)プリン)、ホルクロルフェニュロン(1-(2-クロロ-4-ピリジル)-3-フェニル尿素)、ジベレリン、デシルアルコール、エテホン(2-クロロエチルホスホン酸)等が挙げられる。 Plant growth regulators include indole butyric acid, ethiclozate (ethyl 5-chloro-3 (1H) indazoline acetate), benzylaminopurine (6- (N-benzylamino) purine), forchlorphenuron (1- (2 -Chloro-4-pyridyl) -3-phenylurea), gibberellin, decyl alcohol, ethephone (2-chloroethylphosphonic acid) and the like.
 本発明では、殺菌、殺虫、殺ダニ、除草又は植物成長調節を目的として、本発明の農薬用効力増強剤組成物を含有し、該農薬用効力増強剤組成物を重量基準で農薬原体の0.03~50倍、好ましくは0.1~50倍、更に好ましくは0.3~35倍含有する農薬組成物を用いる。 In the present invention, for the purpose of bactericidal, insecticidal, acaricidal, herbicidal or plant growth regulation, it contains the agrochemical efficacy enhancer composition of the present invention, and the agrochemical efficacy enhancer composition is used on a weight basis for the agrochemical active ingredient. An agrochemical composition containing 0.03 to 50 times, preferably 0.1 to 50 times, more preferably 0.3 to 35 times is used.
 本発明の農薬組成物を散布する場合、散布用の農薬製剤中の化合物(A)及び化合物(B)の含有量の合計は、好ましくは30ppm~50000ppm、より好ましくは50ppm~25000ppm、更に好ましくは100ppm~20000ppm、更により好ましくは300~15000ppm、更により好ましくは500~12000ppm、更により好ましくは600~10000ppmである。含有量が下限値以上であれば、植物表面への液滴の湿展性及び農薬の植物への浸透性が良好となり、優れた農薬効力増強効果が得られる。また、含有量が上限値以下であれば、液滴の湿展性が適切となり植物体へ液滴が付着して流れ落ち難くなるため農薬効力増強効果を十分に発揮できる。なお、前記農薬製剤の残部は水が好ましい。 When spraying the agricultural chemical composition of the present invention, the total content of compound (A) and compound (B) in the agricultural chemical formulation for spraying is preferably 30 ppm to 50000 ppm, more preferably 50 ppm to 25000 ppm, and even more preferably. 100 ppm to 20000 ppm, even more preferably 300 to 15000 ppm, even more preferably 500 to 12000 ppm, and even more preferably 600 to 10,000 ppm. If the content is at least the lower limit, the wettability of the droplets on the plant surface and the penetration of the agricultural chemical into the plant will be good, and an excellent agricultural chemical efficacy enhancing effect will be obtained. Further, if the content is less than or equal to the upper limit value, the wettability of the droplets becomes appropriate, and the droplets adhere to the plant body and become difficult to flow down. The balance of the agrochemical formulation is preferably water.
 本発明の農薬組成物を散布する場合、散布用の農薬製剤中の化合物(A)及び化合物(B)の含有量の合計が前記範囲にあれば、好ましくは1L~500L/10a、より好ましくは1L~300L/10a、更に好ましくは5L~200L/10a、更により好ましくは1L~150L/10a、更により好ましくは5L~100L/10a、さらにより好ましくは5L~50L/10a、さらにより好ましくは5L~30L/10aの割合で散布することができる。散布量が下限値以上であれば十分な濡れ性を得ることができ良好な農薬効力増強効果が得られ、また、上限値以下であれば適度な濡れが実現でき、液滴が葉面上より流れ落ち難くなる。すなわち、本発明によれば、本発明の農薬組成物(本発明の農薬組成物から調製した農薬製剤)を上記の割合で散布する、農薬組成物の散布方法もしくは農作物の栽培方法も提供される。 When spraying the agricultural chemical composition of the present invention, if the total content of the compound (A) and the compound (B) in the agricultural chemical formulation for spraying is within the above range, preferably 1 L to 500 L / 10a, more preferably 1L to 300L / 10a, more preferably 5L to 200L / 10a, even more preferably 1L to 150L / 10a, even more preferably 5L to 100L / 10a, even more preferably 5L to 50L / 10a, even more preferably 5L It can be sprayed at a rate of ˜30 L / 10a. If the spraying amount is equal to or greater than the lower limit, sufficient wettability can be obtained, and a good effect of enhancing agricultural chemical efficacy can be obtained. It becomes difficult to flow down. That is, according to the present invention, there is also provided a method for spraying an agricultural chemical composition or a method for cultivating agricultural crops, in which the agricultural chemical composition of the present invention (the agricultural chemical formulation prepared from the agricultural chemical composition of the present invention) is sprayed at the above ratio. .
 本発明の農薬用効力増強剤組成物を用いた農薬製剤としては、本発明の農薬用効力増強剤組成物の分包包装体と、農薬成分の分包包装体とからなる農薬製剤が挙げられる。また、化合物(A)と化合物(B)の分包包装体と、化合物(A)と化合物(B)以外の界面活性剤の分包包装体と、農薬成分の分包包装体とからなる農薬製剤とすることも可能である。尚、ここで、分包包装体となる農薬成分とは、農薬原体と任意成分とを任意の割合で含んでいてもよい、乳剤、水和剤等の形態のものを意味する。各分包包装体中の形態は限定されず、用途、目的に応じて調製される。 Examples of the agrochemical formulation using the efficacy enhancer composition for agricultural chemicals of the present invention include an agricultural chemical formulation comprising a packaging package of the efficacy enhancing agent composition for agricultural chemicals of the present invention and a packaging package of agricultural chemical ingredients. . Further, a pesticide comprising a package of the compound (A) and the compound (B), a package of a surfactant other than the compound (A) and the compound (B), and a package of the agrochemical component It can also be made into a preparation. Here, the agrochemical component to be a packaged package means an emulsion, a wettable powder, or the like that may contain an agrochemical base and an optional component in an arbitrary ratio. The form in each package is not limited and is prepared according to the use and purpose.
 本発明により、化合物(A)と、化合物(B)と、殺菌剤、殺虫剤、殺ダニ剤、除草剤及び植物成長調節剤各々の有効成分から選択される何れかの農薬原体とを混合する、農薬組成物の製造方法を提供することができる。この製造方法では、農薬用効力増強剤組成物や農薬組成物で説明した割合で化合物(A)、化合物(B)及び農薬原体を用いることが好ましい。 According to the present invention, compound (A), compound (B), and any pesticidal active ingredient selected from active ingredients of fungicides, insecticides, acaricides, herbicides and plant growth regulators are mixed. A method for producing an agrochemical composition can be provided. In this production method, it is preferable to use the compound (A), the compound (B), and the agrochemical raw material at the ratio described in the efficacy enhancer composition for agrochemicals or the agrochemical composition.
 本発明の農作物の生産方法は、農薬の使用場面で本発明の農薬組成物を用いる。 本発明方法の対象物は、殺菌剤は菌、殺虫剤は病害虫(昆虫)、殺ダニ剤はダニ、除草剤は雑草(農作物に該当しない植物)、植物成長調節剤は農作物(栽培目的となる植物)であり、これらの複数が対象物となってもよい。また、これらの方法は、前記農薬組成物を、植物、病害虫及び菌から選ばれる対象物に適用(例えば、農作物の栽培地に散布する等)する方法として実施でき、この場合、植物は、農作物及び/又は雑草類である。 The production method of the agricultural product of the present invention uses the agricultural chemical composition of the present invention in the scene where the agricultural chemical is used. The target of the method of the present invention is a fungicide as a fungus, an insecticide as a pest (insect), an acaricide as a mite, a herbicide as a weed (a plant that does not correspond to a crop), a plant growth regulator as a crop (for cultivation purposes These may be a target object. In addition, these methods can be carried out as a method of applying the agrochemical composition to an object selected from plants, pests and fungi (for example, spraying on a crop cultivation area, etc.). And / or weeds.
 また、本発明の農作物の生産方法は、本発明の農薬用効力増強剤組成物と、殺菌剤、殺虫剤、殺ダニ剤、除草剤及び植物成長調節剤各々の有効成分から選択される何れかの農薬原体とを農薬原体の対象物に施す工程を含む。また、本発明の農作物の生産方法は、前記本発明の農薬組成物を農薬原体の対象物に施す工程を含む方法であってもよい。農薬用効力増強剤組成物、農薬原体、又は農薬組成物を農薬原体の対象物に施す方法は、特に限定されず、前述したように、本発明の農薬用効力増強剤組成物を含む農薬用組成物を葉面、茎、果実等に直接散布したり、水耕栽培やロックウールのように根に接触している水耕液や供給水に希釈混合して根表面等に供給(塗布)する方法が挙げられる。本発明の農薬用効力増強剤組成物の効果(有効成分の植物への付着性を向上させる効果)を有効に発揮させるには、農薬用効力増強剤組成物又は農薬組成物を農薬原体の対象物に施す方法として、植物の地上部へ散布する方法が好ましく、葉面に散布する方法がより好ましい。また、本発明の農薬用効力増強剤組成物と農薬原体とを、前記した方法で別々に農薬原体の対象物に施すこともできる。 Further, the production method of the agricultural product of the present invention is any one selected from the active ingredient of each of the efficacy enhancer composition for agricultural chemicals of the present invention and a fungicide, insecticide, acaricide, herbicide and plant growth regulator. A step of applying a pesticide active ingredient to an object of the pesticide active ingredient. Moreover, the method of producing the agricultural product of the present invention may be a method including a step of applying the agrochemical composition of the present invention to an object of an agrochemical raw material. The method for applying the agrochemical efficacy enhancer composition, the agrochemical active ingredient, or the agrochemical composition to the target of the agrochemical active substance is not particularly limited, and includes the agrochemical efficacy enhancer composition of the present invention as described above. Directly spray the composition for pesticides on the foliage, stems, fruits, etc., or dilute and mix with hydroponics or feed water that is in contact with the roots, such as hydroponics or rock wool. Application). In order to effectively demonstrate the effect of the efficacy enhancer composition for agricultural chemicals of the present invention (the effect of improving the adhesion of active ingredients to plants), the efficacy enhancer composition for agricultural chemicals or the agricultural chemical composition is used for the active ingredient of agricultural chemicals. As a method of applying to the object, a method of spraying on the above-ground part of the plant is preferable, and a method of spraying on the leaf surface is more preferable. Moreover, the efficacy enhancer composition for agricultural chemicals of this invention and an agricultural chemical raw material can also be separately applied to the target of an agricultural chemical raw material by the above-mentioned method.
 本発明では、農薬用効力増強剤組成物(該組成物と水を含有する散布用製剤も含む)と農薬原体(農薬原体と水を含有する散布用製剤も含む)とを、又は農薬組成物(農薬組成物から調製した散布用製剤も含む)を、植物の水に対する接触角が50~180度である部分、例えば葉、茎などに、滴下する、散布する等により接触させることが好ましい。植物表面は一般的にエピクチクラワックス、クチクラワックス、クチンなどに覆われ疎水性の特性を有する。それ故、農薬を含有した水溶液を植物へ散布した際、散布水滴が疎水性表面にはじかれ濡れないことにより、農薬が付着せずまたは浸透せず、除草剤、殺虫剤、殺菌剤等の効果を低下させることが問題となっている。本発明の農薬用効力増強剤組成物と農薬原体とを又は農薬組成物を、植物の疎水性が高い部分に散布して接触、付着させることで、高い農薬増強効果を示す。 In the present invention, an efficacy enhancer composition for agricultural chemicals (including a spray preparation containing the composition and water) and an agricultural chemical active ingredient (including a spraying preparation containing the active ingredient and water), or an agricultural chemical A composition (including a preparation for spraying prepared from an agrochemical composition) can be brought into contact with a part of a plant having a contact angle with water of 50 to 180 degrees, for example, a leaf, a stem, or the like by dropping or spraying. preferable. The plant surface is generally covered with epicuticular wax, cuticular wax, cutin and the like and has a hydrophobic property. Therefore, when an aqueous solution containing pesticides is sprayed on plants, the sprayed water droplets are not repelled on the hydrophobic surface and do not get wet, so that the pesticides do not adhere or penetrate and the effects of herbicides, insecticides, fungicides, etc. It has become a problem to lower. A high agrochemical enhancement effect is exhibited by spraying the pesticide efficacy enhancer composition of the present invention and a pesticide active ingredient or a pesticide composition on a portion of a plant that is highly hydrophobic to contact and adhere thereto.
 植物表面の疎水性を示す指標として水の接触角がある。本発明の農薬効力増強効果がより発揮される植物の接触角として、50度~180度が好ましく、より好ましくは70度~180度、さらにより好ましくは90度~180度である。接触角測定方法は、25℃において、水5μLを施用対象となる植物の表面(例えば、第3葉の表面)に滴下し、横からマイクロスコープにより滴下10秒後の液滴の状態を撮影し、画像処理により対象面と水滴との接触角を測定する。 The water contact angle is an indicator of the hydrophobicity of the plant surface. The contact angle of a plant that exhibits the effect of enhancing the effectiveness of the agricultural chemical of the present invention is preferably 50 to 180 degrees, more preferably 70 to 180 degrees, and still more preferably 90 to 180 degrees. The contact angle is measured by dropping 5 μL of water onto the surface of the plant to be applied (for example, the surface of the third leaf) at 25 ° C., and photographing the state of the liquid droplet 10 seconds after dropping with a microscope from the side. Then, the contact angle between the target surface and the water droplet is measured by image processing.
 上記範囲の接触角を示す部分を有する代表的な植物は以下のとおりであるが、これらに限定されるものではない。本発明方法の適用対象である雑草としては、ギョウギシバ、タツノツメガヤ、コヒメビエ、イヌビエ、オヒシバ、メヒシバ、チガヤ、タイワンアシカキ、アゼガヤ、ハイキビ、ネピアグラス、ツノアイアシ、コツブキンエノコロ、タマガヤツリ、コゴメガヤツリ、ハマスゲ、クロタマガヤツリ、クサネム、カッコウアザミ、ツルノゲイトウ、アオビユ、マルバツユクサ、シマツユクサ、ホテイアオイ、シマニシキソウ、ナンバンルリソウ、ニオイニガグサ、ナンゴクデンジソウ、オジギソウ、コナギ、スベリヒユ、コトブキギク、ベルベットリーフ、スギナなどが挙げられる。本発明の農薬効力増強効果がより発揮される好ましい雑草としては、ギョウギシバ、コヒメビエ、イヌビエ、オヒシバ、メヒシバ、チガヤ、タイワンアシカキ、アゼガヤ、ハイキビ、コツブキンエノコロ、クサネム、ナンゴクデンジソウ、オジギソウ、ベルベットリーフ、スギナが挙げられ、より好ましくは、ギョウギシバ、コヒメビエ、イヌビエ、オヒシバ、メヒシバ、チガヤ、クサネム、ベルベットリーフ、スギナが挙げられる。 The representative plants having a portion showing a contact angle in the above range are as follows, but are not limited thereto. Examples of the weeds to which the method of the present invention is applied include gypsy moth, seahorse moth, kobimee, dogbier, hoshishiba, hinokishiba, chigaya, taiwan ashiki, azegaya, hiki, napiergrass, tsunoia ashi, kobukkinenokoro, tamagayatsuri, tamagotsugatsu, , Kusanem, Cuckoo Thistle, Crane Thistle, Aubiyu, Maruyu Yusa, Himalayan Clover, Water Hyacinth, Cyprus, Nanban Ruri, Nioigagusa, Nangoku Denji Sou, Ogigi, Konagi, Subuhigi Preferred weeds that exhibit the effect of enhancing the agrochemical efficacy of the present invention include gypsy moth, kohibibie, dogfish, hoshiba, hinokishiba, chigaya, taiwan ashiki, azegaya, hiki, kotsubukinenokoro, kusanem, rangokudenjio, ogigi, velvet leaf, More preferred are cedar, and more preferred are C. cerevisiae, Kobimee, Inubie, Oshiba, Agaricus, Chigaya, Kusanem, velvet leaf, and Sugina.
 また、本発明方法の適用対象である農作物としては、オオムギ、エンドウ、イネ、コムギ、キャベツ、サトイモ、イチゴ、メロン、ナス、トマト、ネギ、アブラナ、ダイズ、インゲンマメ、サツマイモ、キュウリ、ハクサイ、リンゴ、ナシ、モモ、カキ、カンキツなどが挙げられる。本発明の農薬効力増強効果がより発揮される好ましい作物としては、オオムギ、エンドウ、イネ、コムギ、キャベツ、ハクサイ、サトイモ、イチゴ、メロン、ナス、トマト、ネギ、アブラナ、ダイズ、キュウリ、インゲンマメであり、より好ましくは、イネ、コムギ、キャベツ、ハクサイ、ダイズ、ネギ、インゲンマメ、キュウリである。 Further, the crops to which the method of the present invention is applied include barley, peas, rice, wheat, cabbage, taro, strawberry, melon, eggplant, tomato, leek, rape, soybean, kidney bean, sweet potato, cucumber, Chinese cabbage, apple, Examples include pears, peaches, oysters, and citrus. Preferred crops that exhibit the effect of enhancing the effectiveness of the agricultural chemical of the present invention are barley, peas, rice, wheat, cabbage, Chinese cabbage, taro, strawberry, melon, eggplant, tomato, leek, rape, soybean, cucumber, and kidney bean. More preferred are rice, wheat, cabbage, Chinese cabbage, soybean, leek, kidney bean and cucumber.
 なお、農薬用効力増強剤組成物ならびに農薬組成物に含有される化合物(A)及び化合物(B)は、組成物の調製後であっても、ガスクロマトグラフィーにより分離し、FID検出器にて検出することができる。例えば、農薬用効力増強剤組成物又は農薬組成物をエタノール等の適当な溶媒で希釈した後、以下の条件で測定することにより、農薬用効力増強剤組成物又は農薬組成物中の化合物(A)及び化合物(B)の存否を定量的に確認することができる。
装置:ガスクロマトグラフィー分析システム(Agilent Technologies 6850 Series II)
カラム:DB5((5%-Phenyl)-Methylpolysiloxane)
カラムサイズ:12m×200μm×0.33μm、
ヘリウムガス流量:1.0mL/min、圧力:85.0kPa、
カラム温度条件(初期カラム温度:60℃、2minホールド→10℃/min昇温→300℃、14minホールド)
実施例
In addition, the efficacy enhancer composition for agricultural chemicals and the compound (A) and compound (B) contained in the agricultural chemical composition are separated by gas chromatography even after the preparation of the composition, and are detected by an FID detector. Can be detected. For example, after diluting a pesticide efficacy enhancer composition or a pesticide composition with a suitable solvent such as ethanol, and measuring under the following conditions, the pesticide efficacy enhancer composition or the compound in the pesticide composition (A ) And compound (B) can be quantitatively confirmed.
Equipment: Gas Chromatography Analysis System (Agilent Technologies 6850 Series II)
Column: DB5 ((5% -Phenyl) -Methylpolysiloxane)
Column size: 12m × 200μm × 0.33μm,
Helium gas flow rate: 1.0mL / min, pressure: 85.0kPa,
Column temperature conditions (Initial column temperature: 60 ° C, hold for 2 min → 10 ° C / min temperature rise → 300 ° C, hold for 14 min)
Example
 次の実施例は本発明の実施について述べる。 実施例は本発明の例示について述べるものであり、 本発明を限定するためではない。 The following examples describe the implementation of the present invention. The examples are for illustration of the present invention and are not intended to limit the present invention.
実施例1及び比較例1
 表1、2に、以下の実施例、比較例で用いた化合物(A)及び化合物(B)、並びに比較化合物を示す。
Example 1 and Comparative Example 1
Tables 1 and 2 show the compounds (A) and (B) and comparative compounds used in the following Examples and Comparative Examples.
 表1、2の化合物を表3、4の組み合わせで用いて表3、4の農薬用効力増強剤組成物〔表1、2の化合物が100重量%を占めるもの〕を調製し、以下の方法で湿展性試験、殺草試験、殺虫試験、殺ダニ試験、及び殺菌試験を行った。表1中の全ての化合物及び表2中のB’-3、B’-4以外の全ての化合物は花王(株)製であり、表2のB’-3、B’-4はいずれも和光純薬工業(株)製である。なお、表3、4では、化合物(A)、化合物(B)に該当しない化合物も便宜的にそれぞれの欄に示した。 Using the compounds shown in Tables 1 and 2 in the combinations shown in Tables 3 and 4 to prepare the efficacy enhancer composition for agricultural chemicals shown in Tables 3 and 4 (in which the compounds shown in Tables 1 and 2 occupy 100% by weight), the following method The wettability test, the herbicidal test, the insecticidal test, the acaricidal test, and the bactericidal test were conducted. All compounds in Table 1 and all compounds other than B′-3 and B′-4 in Table 2 are manufactured by Kao Corporation, and both B′-3 and B′-4 in Table 2 are Wako Pure Chemical Industries, Ltd. In Tables 3 and 4, compounds not corresponding to the compound (A) and the compound (B) are also shown in the respective columns for convenience.
[湿展性試験]
 試験植物としてイヌビエを用いた。予め12cmポットにイヌビエを生育させ、8葉期の植物体を試験に供した。イヌビエの第5葉を採取し、農薬用効力増強剤組成物を化合物(A)及び化合物(B)の濃度が表3、4に示す農薬散布液中の濃度になるよう水と混合した試験液(農薬を含まないもの)を葉の中央部に5μL滴下した。なお、イヌビエ葉面の水に対する接触角は130度であった。滴下1分後、液滴の長径と短径をノギスで計測し、長方形として液滴の広がった面積を計測することで、液滴の疎水葉面における湿展性を評価した。反復は5反復である。その結果、表3、4に示すように本発明の農薬用効力増強剤組成物によれば、その湿展性を飛躍的に向上できることが確認された。
[Wetability test]
Inhibibies were used as test plants. Inhibibies were grown in advance in a 12 cm pot, and plants in the 8-leaf stage were used for the test. A test solution obtained by collecting the fifth leaf of the lobster and mixing it with water so that the concentrations of the compound (A) and the compound (B) are the concentrations in the pesticide spray solution shown in Tables 3 and 4. 5 μL of (no pesticide) was dropped on the center of the leaf. In addition, the contact angle with respect to the water of the leaf surface of Inbiebi was 130 degrees. One minute after the dropping, the major and minor diameters of the droplets were measured with calipers, and the area where the droplets spread as a rectangle was measured to evaluate the wettability of the droplets on the hydrophobic leaf surface. The iteration is 5 iterations. As a result, as shown in Tables 3 and 4, it was confirmed that the wettability can be remarkably improved according to the efficacy enhancer composition for agricultural chemicals of the present invention.
[殺草試験]
 12cmポットにイヌビエを生育させ、草丈が18cm程度の植物体を試験に供した。水1Lにラウンドアップ液剤(日産化学工業社製除草剤;グリホサートイソプロピルアミン塩として有効分41重量%)を4.8gと、散布時の濃度が表3、4に示す通りとなる量の農薬用効力増強剤組成物〔化合物(A)及び化合物(B)〕とを混合し、農薬散布液(農薬組成物)を作製した。農薬散布液を、表3、4に示す散布量で前記植物体全体にかかるように葉面散布し、殺草効力を評価した。なお、イヌビエ葉面の水に対する接触角は130度であった。殺草効力の評価は散布後14日目に地上部重量を量り、無処理区の地上部生重量を基準とした殺草率を下記式に基づき算出した。殺草率の数値が高いほど、農薬効力(殺草効果)が高いことを示す。ここで無処理区とは農薬及び農薬効力増強剤組成物との希釈混合物(農薬散布液)を散布していない区のことである(他の試験でも同様)。
 殺草率(%)=(無処理区の地上部重量-処理区の地上部重量)/無処理区の地上部重量×100
 表3、4の結果から、本発明の農薬組成物によれば、その殺草効果を向上できることが確認された。
[Weed killing test]
Inobie was grown in a 12 cm pot, and a plant having a plant height of about 18 cm was used for the test. 4.8g of a round-up solution (herbicide manufactured by Nissan Chemical Industries; 41% by weight effective as glyphosate isopropylamine salt) in 1 liter of water, and for agricultural chemicals in such an amount that the concentration during spraying is as shown in Tables 3 and 4 The efficacy enhancer composition [compound (A) and compound (B)] was mixed to prepare an agrochemical spray liquid (agrochemical composition). The pesticide spray solution was sprayed on the surface of the plant so as to cover the whole plant at the spray amount shown in Tables 3 and 4, and the herbicidal efficacy was evaluated. In addition, the contact angle with respect to the water of the leaf surface of Inbiebi was 130 degrees. The evaluation of the herbicidal efficacy was carried out on the 14th day after spraying, and the ground part weight was measured, and the herbicidal rate based on the raw part raw weight in the untreated area was calculated based on the following formula. The higher the value of the herbicidal rate, the higher the pesticide efficacy (the herbicidal effect). Here, the non-treated section is a section where a diluted mixture (pesticidal spray solution) with an agrochemical and an agrochemical efficacy enhancer composition is not sprayed (the same applies to other tests).
Herbicide rate (%) = (weight of above-ground part of untreated area-above-ground part weight of treated area) / above-ground part weight of untreated area x 100
From the results of Tables 3 and 4, it was confirmed that the herbicidal effect can be improved according to the agrochemical composition of the present invention.
[殺虫試験]
 12cmポットに草丈15cmになるまでイネ苗を生育させた。イネ1株に、羽化後3~5日経過したウンカを10個体、3反復にて供試し培養した。水1Lにスミチオン乳剤(住友化学社製殺虫剤;フェニトロチオンとして有効分50重量%)0.3gと、散布時の濃度が表3、4に示す通りとなる量の農薬用効力増強剤組成物〔化合物(A)及び化合物(B)〕とを混合し、農薬散布液(農薬組成物)を作製した。農薬散布液を、表3、4に示す散布量でウンカが付着したイネ苗へ葉面散布した。なお、イネ苗葉面の水に対する接触角は135度であった。風乾後、金網円筒をかぶせ、その3日後、生存虫数を測定し、下記式により殺虫率を算出した。殺虫率の数値が高いほど、農薬効力(殺虫効果)が高いことを示す。
 殺虫率(%)=(無処理区の生存虫数-処理区の生存虫数)/無処理区の生存虫数×100
 表3、4の結果から、本発明の農薬組成物によれば、その殺虫効果を向上できることが確認された。
[Insecticide test]
Rice seedlings were grown in a 12 cm pot until the plant height was 15 cm. Ten rice plants, 3 to 5 days after emergence, were tested and cultured in 3 repeats on one rice strain. Sumition emulsion (Sumitomo Chemical Co., Ltd. insecticide; effective 50% by weight as fenitrothion) 0.3 g in 1 liter of water and an agrochemical efficacy enhancer composition in an amount as shown in Tables 3 and 4 when sprayed [ Compound (A) and Compound (B)] were mixed to prepare an agrochemical spray liquid (agrochemical composition). The pesticide spray solution was sprayed onto the rice seedlings to which the planthopper had adhered in the amounts shown in Tables 3 and 4. In addition, the contact angle with respect to the water of a rice seedling leaf surface was 135 degree | times. After air-drying, a wire mesh cylinder was covered, and 3 days later, the number of live insects was measured, and the insecticidal rate was calculated by the following formula. The higher the insecticidal rate, the higher the pesticide efficacy (insecticidal effect).
Insecticidal rate (%) = (Number of living insects in untreated group−Number of living insects in treated group) / Number of living insects in untreated group × 100
From the results of Tables 3 and 4, it was confirmed that according to the agrochemical composition of the present invention, the insecticidal effect can be improved.
[殺ダニ試験]
 12cmポットに5葉期になるまでインゲンマメを生育させた。1株あたりカンザワハダニ30匹を3反復にてうえつけた。水1Lにニッソラン水和剤(日本曹達社殺ダニ剤;ヘキシチアゾクスとして有効分10重量%)0.3gと、散布時の濃度が表3、4に示す通りとなる量の農薬用効力増強剤組成物〔化合物(A)及び化合物(B)〕とを混合し、農薬散布液(農薬組成物)を作製した。農薬散布液を、表3、4に示す散布量でインゲンマメへ葉面散布した。なお、インゲンマメ葉面の水に対する接触角は100度であった。風乾後、金網円筒をかぶせ、3日後に生存ダニ数を測定し、下記式により殺ダニ率を算出した。殺ダニ率の数値が高いほど、農薬効力(殺ダニ効果)が高いことを示す。
 殺ダニ率(%)=(無処理区の生存ダニ数-処理区の生存ダニ数)/無処理区の生存ダニ数×100
 表3、4の結果から、本発明の農薬組成物によれば、その殺ダニ効果を向上できることが確認された。
[Micidal test]
Kidney beans were grown in a 12 cm pot until the fifth leaf stage. Thirty Kanzawa spider mites per strain were applied in 3 iterations. Composition of a potentiating agent for agricultural chemicals in an amount of 0.3 g of Nissoran wettable powder (Nippon Soda Co., Ltd. acaricide; 10% by weight effective as hexithiazox) in 1 L of water and the concentration when sprayed as shown in Tables 3 and 4 The product [compound (A) and compound (B)] was mixed to prepare an agrochemical spray liquid (agrochemical composition). The pesticide spray solution was sprayed onto the kidney beans with the spray amount shown in Tables 3 and 4. In addition, the contact angle with respect to the water of a kidney bean leaf surface was 100 degree | times. After air-drying, a wire mesh cylinder was covered, and the number of surviving mites was measured after 3 days, and the acaricidal rate was calculated by the following formula. The higher the mite killing rate, the higher the pesticide efficacy (miticidal effect).
Mite kill rate (%) = (number of surviving mites in untreated group−number of surviving mites in treated group) / number of surviving mites in untreated group × 100
From the results of Tables 3 and 4, it was confirmed that the acaricidal effect can be improved according to the agrochemical composition of the present invention.
[殺菌試験]
 12cmポットに3葉期になるまでキュウリを栽培した。殺菌剤抵抗性菌であるキュウリ灰色カビ病菌(Botrytis cinerea)の胞子懸濁液(菌数は107個/mL)を、キュウリに50mL/10aの散布量で散布した。その後、25℃、90%相対湿度下に静置し、菌を感染させた。3日後、水1Lにベンレート水和剤(住友化学社製殺菌剤;ベノミルとして有効分50重量%)0.5gと、散布時の濃度が表3、4に示す通りとなる量の農薬用効力増強剤組成物〔化合物(A)及び化合物(B)〕とを混合し、農薬散布液(農薬組成物)を作製した。農薬散布液を、表3、4に示す散布量でキュウリに葉面散布した。なお、キュウリ葉面の水に対する接触角は90度であった。次いで、ポットを25℃、85%相対湿度下に静置し、一週間後、病斑数を数え、以下の式を用いて防除価を算出した。防除価の数値が高いほど、農薬効力(殺菌効果)が高いことを示す。
 防除価(%)={1-(処理区の病斑数/無処理区の病斑数)}×100
 表3、4の結果から、本発明の農薬組成物によれば、その殺菌効果を向上できることが確認された。
[Sterilization test]
Cucumbers were grown in 12 cm pots until the third leaf stage. Spore suspension of cucumber Botrytis cinerea is a fungicide resistant fungus (Botrytis cinerea) (number of bacteria 10 7 / mL), were applied at an application rate of 50 mL / 10a cucumber. Then, it left still under 25 degreeC and 90% relative humidity, and infected the microbe. After 3 days, 0.5 g of benrate wettable powder (Sumitomo Chemical's fungicide; 50% by weight effective as benomyl) in 1 liter of water, and the efficacy for agricultural chemicals in the amount when sprayed as shown in Tables 3 and 4 The enhancer composition [compound (A) and compound (B)] was mixed to prepare an agrochemical spray liquid (agrochemical composition). The pesticide spray solution was sprayed onto the cucumber with the spray amount shown in Tables 3 and 4. In addition, the contact angle with respect to the water of a cucumber leaf surface was 90 degree | times. Next, the pot was allowed to stand at 25 ° C. and 85% relative humidity, and after one week, the number of lesions was counted, and the control value was calculated using the following formula. The higher the control value, the higher the pesticide efficacy (bactericidal effect).
Control value (%) = {1− (number of lesions in treated area / number of lesions in untreated area)} × 100
From the results of Tables 3 and 4, it was confirmed that the bactericidal effect can be improved according to the agrochemical composition of the present invention.
Figure JPOXMLDOC01-appb-T000002
Figure JPOXMLDOC01-appb-T000002
Figure JPOXMLDOC01-appb-T000003
Figure JPOXMLDOC01-appb-T000003
Figure JPOXMLDOC01-appb-T000004
Figure JPOXMLDOC01-appb-T000004
Figure JPOXMLDOC01-appb-T000005
Figure JPOXMLDOC01-appb-T000005
実施例2及び比較例2
 表5に、以下の実施例、比較例で用いた化合物(A)及び比較化合物を示す。表5の化合物(A)〔一部は実施例1の表1の化合物(A)も用いている〕と、実施例1の表2の化合物(B)とを、表6の組み合わせで用いて表6の農薬用効力増強剤組成物(表5、表2の化合物が100重量%を占めるもの、又は表5、表2の化合物と溶媒を含有するもの)を調製し、実施例1と同様に湿展性試験、殺草試験、殺虫試験、殺ダニ試験、及び殺菌試験を行った。結果を表6に示す。なお、表6では、化合物(A)、化合物(B)に該当しない化合物も便宜的にそれぞれの欄に示した。また、表6中、実施例2-17では水10重量%を、実施例2-18ではエチル乳酸10重量%を、実施例2-19ではジエチレングリコール10重量%を、それぞれ溶媒として使用した。
Example 2 and Comparative Example 2
Table 5 shows the compounds (A) and comparative compounds used in the following Examples and Comparative Examples. Compound (A) in Table 5 [some of which also uses Compound (A) in Table 1 of Example 1] and Compound (B) in Table 2 of Example 1 in combination of Table 6 The effect enhancer composition for agricultural chemicals shown in Table 6 (one containing 100% by weight of the compounds shown in Tables 5 and 2 or containing the compounds shown in Tables 5 and 2 and a solvent) was prepared, and the same as in Example 1. A wettability test, a herbicidal test, an insecticidal test, an acaricidal test, and a bactericidal test were conducted. The results are shown in Table 6. In Table 6, compounds not corresponding to the compound (A) and the compound (B) are also shown in the respective columns for convenience. In Table 6, 10% by weight of water was used in Example 2-17, 10% by weight of ethyl lactic acid in Example 2-18, and 10% by weight of diethylene glycol in Example 2-19, respectively.
 表6の結果から、本発明の農薬用効力増強剤組成物によれば、その湿展性を飛躍的に向上できることが確認された。また、本発明の農薬組成物によれば、その殺草効果を向上できることが確認された。また、本発明の農薬組成物によれば、その殺虫効果を向上できることが確認された。また、本発明の農薬組成物によれば、その殺ダニ効果を向上できることが確認された。また、本発明の農薬組成物によれば、その殺菌効果を向上できることが確認された。 From the results of Table 6, it was confirmed that the wettability can be remarkably improved according to the efficacy enhancer composition for agricultural chemicals of the present invention. Moreover, according to the agrochemical composition of this invention, it was confirmed that the herbicidal effect can be improved. Moreover, according to the agrochemical composition of this invention, it was confirmed that the insecticidal effect can be improved. Moreover, according to the agrochemical composition of this invention, it was confirmed that the miticide effect can be improved. Moreover, according to the agrochemical composition of this invention, it was confirmed that the bactericidal effect can be improved.
Figure JPOXMLDOC01-appb-T000006
Figure JPOXMLDOC01-appb-T000006
Figure JPOXMLDOC01-appb-T000007
Figure JPOXMLDOC01-appb-T000007
実施例3及び比較例3
 表7、8に、以下の実施例、比較例で用いた化合物(A)及び化合物(B2)、並びに比較化合物を示す。
Example 3 and Comparative Example 3
Tables 7 and 8 show the compounds (A) and (B2) and comparative compounds used in the following Examples and Comparative Examples.
 表7、8の化合物を表9、10の組み合わせで用いて表9、10の農薬用効力増強剤組成物〔表7、8の化合物が100重量%を占めるもの、又は表7、8の化合物と溶媒を含有するもの〕を調製し、以下の方法で湿展性試験、殺草試験、殺虫試験、殺ダニ試験、及び殺菌試験を行った。表7中A-2-11、A-2-12、A’-2-7以外の化合物及び表8中の全ての化合物は花王(株)製であり、表7中のA-2-11、A-2-12、A’-2-7は太陽化学(株)製である。なお、表10では、化合物(A)、化合物(B)に該当しない化合物も便宜的にそれぞれの欄に示した。また、表10中、実施例1-2-33では水10重量%を、実施例1-2-34ではエチル乳酸10重量%を、実施例1-2-35ではジエチレングリコール10重量%を、それぞれ溶媒として使用した。 Using the compounds in Tables 7 and 8 in combinations of Tables 9 and 10, the efficacy enhancer composition for agricultural chemicals in Tables 9 and 10 And a solvent containing the solvent] were prepared, and a wettability test, a herbicidal test, an insecticidal test, an acaricidal test, and a bactericidal test were conducted by the following methods. In Table 7, compounds other than A-2-11, A-2-12, A′-2-7 and all the compounds in Table 8 were manufactured by Kao Corporation, and A-2-11 in Table 7 A-2-12 and A′-2-7 are manufactured by Taiyo Kagaku Co., Ltd. In Table 10, compounds not corresponding to the compound (A) and the compound (B) are also shown in the respective columns for convenience. In Table 10, Example 1-233 contains 10% by weight of water, Example 1-234 uses 10% by weight of ethyl lactic acid, Example 1-235 uses 10% by weight of diethylene glycol, respectively. Used as solvent.
Figure JPOXMLDOC01-appb-T000008
Figure JPOXMLDOC01-appb-T000008
Figure JPOXMLDOC01-appb-T000009
Figure JPOXMLDOC01-appb-T000009
Figure JPOXMLDOC01-appb-T000010
Figure JPOXMLDOC01-appb-T000010
Figure JPOXMLDOC01-appb-T000011
Figure JPOXMLDOC01-appb-T000011

Claims (10)

  1.  下記(A1)~(A5)から選ばれる一種以上の化合物(A)と、下記(B1)~(B2)から選ばれる一種以上の化合物(B)と、殺菌剤、殺虫剤、殺ダニ剤、除草剤及び植物成長調節剤各々の有効成分から選択される何れかの農薬原体とを含有する農薬組成物を農薬原体の対象物に施す工程を含む、農作物の生産方法。
     (A1):下記一般式(A1)で示されるポリオキシエチレンアルキルエーテル
       R1aO-(EO)l-R2a (A1)
     (式中、R1aは炭素数10~16の直鎖又は分岐鎖のアルキル基又はアルケニル基を示し、EOはエチレンオキシ基を示し、lはエチレンオキシ基の平均付加モル数であり、3~40の数を示し、R2aは水素原子又はメチル基を示す。)
     (A2):ポリオキシエチレン脂肪酸エステル
    (ただし、脂肪酸の炭素数は8~16であり、エチレンオキシドの平均付加モル数は5~40である。)
     (A3):ポリオキシエチレンソルビタン脂肪酸エステル
    (ただし、脂肪酸の炭素数は8~16であり、エチレンオキシドの平均付加モル数は5~40である。)
     (A4):(ポリ)グリセリン脂肪酸エステル
    (ただし、脂肪酸の炭素数は8~16であり、グリセリンの平均縮合度は1~3である。)
     (A5):下記一般式(A5)で示されるアルキルサッカライド
      R3a-O-(G)p    (A5)
     (式中、R3aは炭素数8~16のアルキル基、Gは炭素数5~6の還元糖を示し、pは1~10の数を示す。)
     (B1)下記一般式(B1)で示されるポリオキシアルキレンアルキルエーテル
          R1bO-[(PO)m/(EO)n]-R2b (B1)
     (式中、R1bは炭素数6~12の直鎖又は分岐鎖のアルキル基又はアルケニル基を示し、POはプロピレンオキシ基を示し、EOはエチレンオキシ基を示し、m、nはそれぞれ、プロピレンオキシ基、エチレンオキシ基の平均付加モル数であり、mは1~25の数、nは0~4の数を示し、R2bは水素原子又はメチル基を示す。“/”はPOとEOの配列がランダムでもブロックでもよいことを意味する。)
     (B2):下記一般式(B2)で示される脂肪族アルコール
         R3b-OH (B2)
     (式中、R3bは炭素数8~14の直鎖又は分岐鎖のアルキル基を示す。)
    One or more compounds (A) selected from the following (A1) to (A5), one or more compounds (B) selected from the following (B1) to (B2), a fungicide, an insecticide, an acaricide, A method for producing agricultural crops, comprising a step of applying a pesticide composition containing any one of the pesticide active ingredients selected from the active ingredients of each of the herbicide and the plant growth regulator to the target of the pesticide active ingredient.
    (A1): Polyoxyethylene alkyl ether represented by the following general formula (A1) R 1a O— (EO) 1 —R 2a (A1)
    (Wherein R 1a represents a linear or branched alkyl group or alkenyl group having 10 to 16 carbon atoms, EO represents an ethyleneoxy group, l represents the average number of moles of the ethyleneoxy group, 3 to 40 represents the number, and R 2a represents a hydrogen atom or a methyl group.)
    (A2): Polyoxyethylene fatty acid ester (wherein the fatty acid has 8 to 16 carbon atoms and the average added mole number of ethylene oxide is 5 to 40)
    (A3): Polyoxyethylene sorbitan fatty acid ester (wherein the fatty acid has 8 to 16 carbon atoms and the average added mole number of ethylene oxide is 5 to 40)
    (A4): (Poly) glycerin fatty acid ester (wherein the fatty acid has 8 to 16 carbon atoms, and the average condensation degree of glycerin is 1 to 3)
    (A5): alkyl saccharide represented by the following general formula (A5) R 3a —O— (G) p (A5)
    (Wherein R 3a represents an alkyl group having 8 to 16 carbon atoms, G represents a reducing sugar having 5 to 6 carbon atoms, and p represents a number of 1 to 10)
    (B1) Polyoxyalkylene alkyl ether represented by the following general formula (B1) R 1b O — [(PO) m / (EO) n] —R 2b (B1)
    (Wherein R 1b represents a linear or branched alkyl group or alkenyl group having 6 to 12 carbon atoms, PO represents a propyleneoxy group, EO represents an ethyleneoxy group, and m and n represent propylene. The average number of added moles of oxy group and ethyleneoxy group, m is a number from 1 to 25, n is a number from 0 to 4, R 2b is a hydrogen atom or a methyl group, “/” is PO and EO (This means that the arrangement may be random or block.)
    (B2): aliphatic alcohol represented by the following general formula (B2) R 3b —OH (B2)
    (In the formula, R 3b represents a linear or branched alkyl group having 8 to 14 carbon atoms.)
  2.  化合物(A)及び化合物(B)の重量比が(A)/(B)で0.03~30である、請求項1記載の農作物の生産方法。 The method for producing a crop according to claim 1, wherein the weight ratio of the compound (A) and the compound (B) is 0.03 to 30 in terms of (A) / (B).
  3.  化合物(B)の一般式(B1)においてm/(m+n)が0.5~1である、請求項1又は2記載の農作物の生産方法。 3. The method for producing a crop according to claim 1, wherein m / (m + n) is 0.5 to 1 in the general formula (B1) of the compound (B).
  4.  化合物(A)及び化合物(B)の合計重量/農薬原体の重量が0.1~100である請求項1~3の何れか1項記載の農作物の生産方法。 The method for producing a crop according to any one of claims 1 to 3, wherein the total weight of the compound (A) and the compound (B) / the weight of the agrochemical base is 0.1 to 100.
  5.  水及び/又は有機溶媒を含有する請求項1~3の何れか1項記載の農作物の生産方法。 The method for producing a crop according to any one of claims 1 to 3, comprising water and / or an organic solvent.
  6.  農薬組成物を、植物の水に対する接触角が50~180度である部分に接触させる、請求項1~4何れか1項記載の農作物の生産方法。 The method for producing an agricultural crop according to any one of claims 1 to 4, wherein the agricultural chemical composition is brought into contact with a portion having a contact angle of 50 to 180 degrees with respect to water of the plant.
  7.  散布用の農薬製剤中の化合物(A)及び化合物(B)の含有量の合計は、30ppm~50000ppmである、請求項1~4何れか1項記載の農作物の生産方法。 The method for producing a crop according to any one of claims 1 to 4, wherein the total content of the compound (A) and the compound (B) in the agricultural chemical preparation for spraying is 30 ppm to 50000 ppm.
  8.  散布用農薬製剤を1L~500L/10aで散布する、請求項1~4何れか1項記載の農作物の生産方法。 The method for producing a crop according to any one of claims 1 to 4, wherein the agricultural chemical formulation for spraying is sprayed at 1 L to 500 L / 10a.
  9.  下記(A1)~(A5)から選ばれる一種以上の化合物(A)と、下記(B1)~(B2)から選ばれる一種以上の化合物(B)を含有する組成物の農薬用展着剤組成物としての用途。 A composition for agricultural chemicals comprising one or more compounds (A) selected from the following (A1) to (A5) and one or more compounds (B) selected from the following (B1) to (B2): Use as a thing.
  10.  請求項1に記載した化合物(A)と、請求項1に記載した化合物(B)と、殺菌剤、殺虫剤、殺ダニ剤、除草剤及び植物成長調節剤各々の有効成分から選択される何れかの農薬原体と混合することを含む農薬の効力を増強する方法。 Any one selected from the active ingredients of the compound (A) according to claim 1, the compound (B) according to claim 1, and a fungicide, insecticide, acaricide, herbicide and plant growth regulator. A method of enhancing the efficacy of a pesticide, including mixing with the pesticide active ingredient.
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CN114097778A (en) * 2021-11-24 2022-03-01 中化化工科学技术研究总院有限公司 Low-temperature-resistant tank mix synergist containing vegetable oil and preparation method thereof
CN114097778B (en) * 2021-11-24 2023-02-24 中化化工科学技术研究总院有限公司 Low-temperature-resistant tank mix synergist containing vegetable oil and preparation method of low-temperature-resistant tank mix synergist

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