WO2012029893A1 - Method for producing agricultural crop - Google Patents
Method for producing agricultural crop Download PDFInfo
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- 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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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/30—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests characterised by the surfactants
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
- A01N25/04—Dispersions, emulsions, suspoemulsions, suspension concentrates or gels
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
Description
背景技術 The present invention relates to an agrochemical efficacy enhancer composition and an agrochemical composition.
Background art
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
(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.
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.
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.
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)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)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.
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.
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.
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
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.
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.
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.
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.
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.
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.
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.
Claims (10)
- 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.) - 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).
- 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).
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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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CN201180052202.5A CN103209588B (en) | 2010-09-03 | 2011-09-01 | The production method of crops |
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