WO2009119072A1 - 植物病害防除剤 - Google Patents
植物病害防除剤 Download PDFInfo
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- WO2009119072A1 WO2009119072A1 PCT/JP2009/001302 JP2009001302W WO2009119072A1 WO 2009119072 A1 WO2009119072 A1 WO 2009119072A1 JP 2009001302 W JP2009001302 W JP 2009001302W WO 2009119072 A1 WO2009119072 A1 WO 2009119072A1
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- plant disease
- disease control
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Classifications
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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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/713—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with four or more nitrogen atoms as the only ring hetero atoms
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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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/88—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms six-membered rings with three ring hetero atoms
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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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/18—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, directly attached to a heterocyclic or cycloaliphatic ring
Definitions
- the present invention relates to a plant disease control agent comprising a tetrazoyloxime derivative or the like and other agricultural and horticultural bactericidal active ingredients as active ingredients.
- the present invention was made as part of a study on a plant disease control agent containing a tetrazoyl oxime derivative and / or a salt thereof as an active ingredient described in Patent Document 1, and is effective for plant diseases at a low dose.
- Another object of the present invention is to provide a plant disease control agent that exhibits a better control effect.
- X is a hydrogen atom, an unsubstituted or substituted C1-6 alkyl group, an unsubstituted or substituted C1-6 alkoxy group, a halogen atom, a nitro group, a cyano group, an unsubstituted or substituted group Or an unsubstituted or substituted C1-6 alkylsulfonyl group, and q represents an integer of 0-5.
- A is the formula (2) or (3)
- Z is a hydrogen atom, an amino group, or a formula: —NHC ( ⁇ O) —Q (where Q is a hydrogen atom, a C1-8 alkyl group, a C1-6 haloalkyl group, a C3-6 cycloalkyl group) C1-8 alkoxy group, C3-6 cycloalkyloxy group, C7-20 aralkyloxy group, C1-4 alkylthio C1-8 alkyl group, C1-4 alkoxy C1-2 alkyl group, C1-4 acylamino C1-6 alkyl And a C1-4 acylamino C1-6 alkoxy group, a C1-8 alkylamino group, a C2-6 alkenyl group, a C7-20 aralkyl group, or a C6-10 aryl group).
- R represents a hydrogen atom or a halogen atom.
- the plant disease control agent of the present invention exhibits an excellent control effect on plant diseases at a very low dose, and is free from worry about phytotoxicity on useful plants.
- the plant disease control agent of the present invention comprises at least one of the tetrazoyl oxime derivative represented by the formula (1) and a salt thereof, and at least one of other agricultural and horticultural bactericidal active ingredients. .
- X represents a hydrogen atom, an unsubstituted or substituted C1-6 alkyl group, an unsubstituted or substituted C1-6 alkoxy group, a halogen It represents an atom, a nitro group, a cyano group, an aryl group having an unsubstituted or substituted group, or a C1-6 alkylsulfonyl group having an unsubstituted or substituted group.
- Examples of the C1-6 alkyl group of the unsubstituted or substituted C1-6 alkyl group for X include a methyl group, an ethyl group, an n-propyl group, an i-propyl group, an n-butyl group, an s-butyl group, Examples include i-butyl group, t-butyl group, n-pentyl group, n-hexyl group and the like.
- C1-6 alkoxy group of the unsubstituted or substituted C1-6 alkoxy group of X a methoxy group, an ethoxy group, an n-propoxy group, an i-propoxy group, an n-butoxy group, an s-butoxy group
- Examples include i-butoxy group and t-butoxy group.
- the substituent of the C1-6 alkyl group and C1-6 alkoxy group is not particularly limited as long as it is chemically acceptable, but halogen atoms such as fluorine atom, chlorine atom, bromine atom, iodine atom; Group, ethoxy group, n-propoxy group, i-propoxy group, n-butoxy group, s-butoxy group, i-butoxy group, t-butoxy group and the like C1-6 alkoxy groups; phenyl group, 4-methylphenyl group A phenyl group having an unsubstituted or substituted group such as 2-chlorophenyl group; a nitro group; a cyano group; an unsubstituted or substituted group such as an amino group, a methylamino group, a dimethylamino group, an acetylamino group, or a benzoylamino group Amino group; and the like.
- halogen atoms such as fluorine
- halogen atom for X examples include a fluorine atom, a chlorine atom, a bromine atom, and an iodine atom.
- the aryl group of the unsubstituted or substituted aryl group for X is not particularly limited, but is preferably a C6-10 aryl group. More specifically, a phenyl group, 1-naphthyl group, 2-naphthyl group and the like can be mentioned.
- the substituent for the aryl group is not particularly limited as long as it is chemically acceptable.
- halogen atoms such as fluorine atom, chlorine atom, bromine atom, iodine atom; methyl group, ethyl group, n-propyl group, i-propyl group, n-butyl group, s-butyl group, i-butyl group, t
- a C1-6 alkyl group such as a butyl group, an n-pentyl group, an n-hexyl group; Vinyl group, 1-propenyl group, 2-propenyl group, 1-butenyl group, 2-butenyl group, 3-butenyl group, 1-pentenyl group, 2-pentenyl group, 3-pentenyl group, 4-pentenyl group, 1- A C2-6 alkenyl group such as a hexenyl group, a 2-hexenyl group, a 3-hexenyl group,
- alkynyl groups Up to 6 alkynyl groups; C1-6 alkoxy groups such as methoxy group, ethoxy group, n-propoxy group, i-propoxy group, n-butoxy group, s-butoxy group, i-butoxy group, t-butoxy group; Nitro group; cyano group; and the like.
- Examples of the C1-6 alkylsulfonyl group of the unsubstituted C1-6 alkylsulfonyl group of X include a methylsulfonyl group, an ethylsulfonyl group, an n-propylsulfonyl group, an i-propylsulfonyl group, and the like.
- the substituent for the C1-6 alkylsulfonyl group is not particularly limited as long as it is chemically acceptable, and examples thereof include those exemplified as the substituent for the C1-6 alkyl group of X. .
- q represents an integer of 0 to 5, preferably 0 or 1, and more preferably 0.
- Xs may be the same or different.
- A represents a tetrazoyl group represented by the formula (2) or the formula (3).
- Y represents a methyl group, an ethyl group, an n-propyl group, an i-propyl group, an n-butyl group, an s-butyl group, an i-butyl group, a t-butyl group, An alkyl group such as n-pentyl group and n-hexyl group is shown.
- D represents a group represented by Formula (4) or Formula (5).
- Z represents a hydrogen atom, an amino group, or a group represented by the formula: —NHC ( ⁇ O) —Q.
- Q is a hydrogen atom, C1-8 alkyl group, C1-6 haloalkyl group, C3-6 cycloalkyl group, C1-8 alkoxy group, C3-6 cycloalkyloxy group, C7-20 aralkyloxy group, C1-4 alkylthio C1 8 to 8 alkyl groups, C1 to 4 alkoxy C1 to 2 alkyl groups, C1 to 4 acylamino C1 to 6 alkyl groups, C1 to 4 acylamino C1 to 6 alkoxy groups, C1 to 8 alkylamino groups, C2 to 6 alkenyl groups, aralkyl groups Or an aryl group is shown.
- C1-8 alkyl group of Q methyl group, ethyl group, n-propyl group, isopropyl group, 1,1-dimethylpropyl group, n-butyl group, isobutyl group, sec-butyl group, t-butyl group, Examples include isoamyl group, 1-methylbutyl group, 2-methylbutyl group, neopentyl group, 1-ethylpropyl group, n-pentyl group, n-hexyl group, n-heptyl group, n-octyl group and the like.
- the C1-6 haloalkyl group of Q includes chloromethyl group, difluoromethyl group, trifluoromethyl group, difluorochloromethyl group, pentafluoroethyl group, 3,3,3-trifluoro-n-propyl group, 1-chloro group A hexyl group etc. are mentioned.
- Examples of the C3-6 cycloalkyl group of Q include a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, a cyclohexyl group, and the like.
- methoxy group, ethoxy group, propoxy group isopropoxy group, 1,1-dimethylpropoxy group, butoxy group, isobutoxy group, s-butoxy group, t-butoxy group, i-pentyl Oxy group, 1-methylbutoxy group, 2-methylbutoxy group, neopentyloxy group, 1-ethylpropoxy group, n-pentyloxy group, n-hexyloxy group, n-heptyloxy group, n-octyloxy group, etc. Is mentioned.
- Examples of the C3-6 cycloalkyloxy group of Q include a cyclopropyloxy group, a cyclobutyloxy group, a cyclopentyloxy group, a cyclohexyloxy group, and the like.
- Examples of the C7-20 aralkyloxy group for Q include a benzyloxy group and a phenethyloxy group.
- Examples of the C1-4 alkylthio C1-8 alkyl group of Q include a methylthiomethyl group, a 2-methylthioethyl group, an ethylthiomethyl group, a butylthiomethyl group, and the like.
- Examples of the C1-4 alkoxy C1-2 alkyl group of Q include a methoxymethyl group, an ethoxymethyl group, a 2-methoxyethyl group, a 2-ethoxyethyl group, and an n-butoxymethyl group.
- the C1-4 acylamino C1-6 alkyl group of Q includes an acetylaminomethyl group, 2- (propionylamino) ethyl group, 3- (acetylamino) propyl group, 3- (propionylamino) propyl group, 3- (pivaloylamino) ) Propyl group, 4- (acetylamino) butyl group, 5- (acetylamino) pentyl group, 6- (acetylamino) hexyl group and the like.
- the C1-4 acylamino C1-6 alkoxy group of Q includes an acetylaminomethoxy group, 2- (propionylamino) ethoxy group, 3- (acetylamino) propoxy group, 3- (propionylamino) propoxy group, 3- (pivaloylamino) ) Propoxy group and the like.
- the C1-8 alkylamino group of Q includes methylamino group, ethylamino group, n-propylamino group, i-propylamino group, n-butylamino group, i-butylamino group, s-butylamino group, t -Butylamino group, neopentylamino group, 1-ethylpropylamino group, n-pentylamino group, n-hexylamino group, n-heptylamino group, n-octylamino group and the like.
- Examples of the C2-6 alkenyl group of Q include allyl group, i-propenyl group, 1-butenyl group, 2-butenyl group, 2-pentenyl group, 5-hexenyl group and the like.
- Examples of the C7-20 aralkyl group of Q include a benzyl group, a phenethyl group, a 3-phenylpropyl group, a 1-naphthylmethyl group, a 2-naphthylmethyl group, and the like.
- Examples of the C6-10 aryl group for Q include a phenyl group, a 1-naphthyl group, and a 2-naphthyl group.
- R represents a hydrogen atom; or a halogen atom such as a fluorine atom, a chlorine atom, or a bromine atom.
- the salt of the tetrazoyl oxime derivative represented by the above formula (1) is not particularly limited as long as it is a salt acceptable in agriculture and horticulture.
- salts of inorganic acids such as hydrochloride, nitrate, sulfate and phosphate
- salts of organic acids such as acetate, lactate, propionate and benzoate
- the tetrazoyl oxime derivative represented by the above formula (1) has (E) and (Z) stereoisomers based on a carbon-nitrogen double bond. Both of these two stereoisomers and mixtures thereof are included in the present invention. Usually, the synthesized product is obtained only as the (Z) isomer or as a mixture of the (E) isomer and the (Z) isomer. Two isomers can be isolated by separating and purifying a mixture of the (E) isomer and the (Z) isomer by a known method such as silica gel column chromatography.
- the (Z) isomer is generally more effective in controlling plant diseases than the (E) isomer.
- the (Z) body also tends to be stabilized at a certain ratio as a mixture of the (E) body and the (Z) body due to the action of light or the like in the natural environment and partly changed to the (E) body. Both compounds and mixtures thereof are also useful.
- the stable ratio of (E) body and (Z) body changes with each compound, it cannot be specified unconditionally.
- the tetrazoyl oxime derivative represented by the formula (1) and a salt thereof can be produced by, for example, a method described in WO03 / 016303 pamphlet.
- Examples of the tetrazoyloxime derivative represented by the formula (1) used in the present invention include compounds described in WO03 / 016303 pamphlet.
- the plant disease control agent of the present invention includes fosetyl in addition to the above-described tetrazoyl oxime derivatives and salts thereof (hereinafter sometimes referred to as "tetrazoyl oxime derivatives"). At least one selected from the group consisting of propamocarb, basic copper chloride, chlorothalonil, manzeb, simoxanyl, phorpet, iminotazine, cyazofamide, metalaxyl, fludioxonil, tebuconazole, prothioconazole, thiamethoxam, azoxystrobin, and salts thereof contains.
- tetrazoyl oxime derivatives At least one selected from the group consisting of propamocarb, basic copper chloride, chlorothalonil, manzeb, simoxanyl, phorpet, iminotazine, cyazofamide, metalaxyl, fludioxonil, te
- the active ingredient compound includes the optically active compound. Specifically, it is like metalaxyl M with respect to metalaxyl.
- other pesticidal active ingredients can be used as appropriate in the plant control agent of the present invention, and specific examples include the active ingredients shown below.
- an active ingredient is described by the common name (including some pending applications) of active ingredient compound names.
- Active ingredient compound of fungicide generator name; including some pending applications
- Anilinopyrimidine compounds such as mepanipyrim, pyrimethanil, cyprodinil
- Pyridinamine compounds such as fluazinam;
- Triadimefon Tritermizole, triflumizole, etaconazole, propiconazole, penconazole, luconilole, flusilazole, flusilazole, penconazole, flusilazole.
- cycloconazole hexaconazole, furconazole-cis, prochloraz, metconazole, epoxiconazole, tetraconazole, tetraconazole le), oxpoconazole fumarate, sipconazole, triadimenol, flutriafol, difenoconazole, difenoconazole fluconazole (Fenbuconazole), bromuconazole, diniconazole, tricyclazole, probenazole, simeconazole, pefuracone ole), imibenconazole (imibenconazole), azole compounds such as imazalil (imazalil);
- Quinoxaline-based compounds such as quinomethionate; manneb, zineb, polycarbamate, methylram, propineb, febam, abam, nab ), Thiram, ziram and the like dithiocarbamate compounds;
- Organochlorine compounds such as fthalide and quintozen; Imidazole compounds such as benomyl, thiophanate-methyl, carbendazim, thiabendazole, and fuberazole.
- Mefenoxam (mefenoxam), oxadixyl (ofaxyl), off-race (ofurace), benalaxyl (benalaxyl), benalaxyl-M (benalaxyl-M), furalaxyl (furalaxyl), cyprofuramide (cyprofuramide, etc.)
- Sulfenic acid-based compounds such as dichlorfluanid
- Nitrophenyl compounds such as dinocap
- Copper-based compounds such as cupric hydroxide and organic copper
- Isoxazole compounds such as hymexazole
- Organophosphorus compounds such as turcophos-methyl, S-benzyl O, O-diisopropyl
- N-halogenothioalkyl compounds such as captan, captafol, etc .
- Dicarboximide compounds such as procymidone, iprodione, vinclozolin
- Benzanilide compounds such as flutolanil, mepronil, zoxamide, thiadinyl
- carboxin, oxycarboxin, thifluzamide, thifluzamide, thifluzamide anilide compounds such as boscalid, fluopicolide, fluopyram, bixafen;
- Piperazine-based compounds such as triforine; Pyridine compounds such as pyrifenox; Carbinol compounds such as fenarimol and flutriafol; Piperidine-based compounds such as fenpropidine; Morpholine-based compounds such as fenpropimorph and tridemorph; Organotin compounds such as fentin hydroxide and fentin acetate; Urea compounds such as pencycuron; Synamic acid compounds such as dimethomorph, flumorph and flumetober; Phenyl carbamate compounds such as dietofencarb;
- Cyanopyrrole compounds such as fenpiclonil; cresoxime-methyl, methminophen, methminostrobin, trifloxystrobin, boxyxtrobin strobilurin-based compounds such as oryzatrobin, dimoxystrobin, pyraclostrobin, fluoxastrobin; Oxazolidinone compounds such as famoxadone; Thiazole carboxamide-based compounds such as ethaboxam; Silylamide compounds such as silthiopham; Amino acid amide carbamate compounds such as iprovalivalb, benchavaricarb-isopropyl;
- Imidazolidine compounds such as fenamidone; Hydroxyanilide compounds such as fenhexamide; Benzenesulfonamide-based compounds such as flusulfamide; Oxime ether compounds such as cyflufenamide; Phenoxyamide compounds such as phenoxanil; Antibiotics such as validamycin, kasugamycin, polyoxins;
- Examples of other compounds include trifluanid, isoprothiolane, pyroquilon, dichromezine, quinoxyfen, spiroxamine, chlorpamine, chlorpamine, and chlorpamine. Salt (metam-sodium), nicobifen, metraphenone, UBF-307, diclocymet, proquinazid, amisulbrom, ribib carb Lopamide, 5-chlor-7- (4-methyl-piperidin-1-yl) -6- (2,4,6-trifluor-phenyl)-[1,2,4] triazolo [1,5- a] pyrimidin, OK-5203 and the like.
- Insecticide, acaricide, nematicide or soil pesticide active compound (generic name; including some pending applications) Profenofos, dichlorvos, fenamifos, fenitrothion, EPN, diazinon, chlorpyrifos methyl, phos, thiphos Phosphocarb, cadusafos, disulfoton, chlorpyrifos, demethon-S-methyl, dimethoate, methamidophos (methamido) hos), isoxathion (isoxathion), isofenphos (ethofenphos), ethifos (ethionfos), quinalphos (quinalphos), dimethylvinphos (sulprofos), thioprofoth (sulprofos), thiomethone (thimidone) Pyraclofos, pyridafenthion, pyrimiphos-methyl, propapho
- Nereistoxin derivatives such as cartap, thiocyclam, bensultap, sodium thiosultap-sodium;
- Organochlorine compounds such as dicophor, tetradiphon, endosulfan, dienochlor, dieldrin;
- Organometallic compounds such as fenbutatin oxide and cyhexatin;
- Fenvalerate permethrin, cypermethrin, deltamethrin, cyhalothrin, tefluthrin, etofenprothrin , Bifenthrin, flucitrinate, fluvalinate, cycloprotorin, lambda-cyhalothrin, pyrethrins, esphethrins Valenate (esfenvalerate), tetramethrin, resmethrin, protrifenbute, zeta-cyperthrin, acrinathrin, alpha cyperthrin, alpha cyperthrin , Gamma-cyhalothrin, theta-permethrin, tau-fluvalinate, tralomethrin, profluthrin, beta-cypermethrin cypermethrin), beta-cyfluthrin (beta-c
- Pyridazinone compounds such as pyridaben; Fenpyroximate, fipronil, tebufenpyrad, ethiprole, tolfenpyrad, acetoprole, acetoprole, pyrafluprol Imidacloprid, nitenpyram, acetamiprid, thiacloprid, clothianidin, dinotefuran, nicotinefurnith, nithiazinoid Hydrazine compounds such as tebufenozide, methoxyphenozide, chromafenozide, halofenozide;
- Other compounds include flonicamid, buprofezin, hexythiazox, amitraz, chlordiform, silaflufen, silafluofine, silaflufen, Chlorfenapyr, indoxacarb, acequinosyl, etoxazole, cyromazine, 1,3-dichloropropene, 1,3-dichloropropene Dithiophenon, benclothiaz, flufenrim, pyridalyl, spirodiclofen, bifenazite, spiromethiphen, spiromethiphen , Clofentezine, fluacrylpyrim, metaflumizone, flubenamide, cyflumethofen, chloranthranylpyrrole (chlorantr) niliprole, cienopyrafen, pyrifluquinazone, phenazaquin, amidoflumet, methanoyl, methanoid compounds
- Bacillus thuringienses aizawai, Bacillus thuringienses kurstaki, Bacillus thuringienses israelensis, Bacillus thuringienses japonensis, Bacillus thuringienses tenebrionis, crystal protein toxin Bacillus Thuringienses generated, entomopathogenic viral agents, entomopathogenic fungus agent, nematode pathogenic fungi agents such as Microbial pesticides, avermectin, emamectin-benzoate, milbemectin, spinosad, iverme Chin (ivermectin), antibiotics or semisynthetic antibiotics such as lepimectin (lepimectin), etc.; Natural products such as azadirachtin, rotenone, etc .; Synergists such as piperonyl butoxide; Repellents such as dee
- Plant disease control agent of the present invention comprises at least one of the tetrazoyl oxime derivatives and at least one of the other agricultural and horticultural bactericidal active ingredients, and uses both components in combination.
- a remarkable plant disease control effect that cannot be predicted from the plant disease control effect obtained by using each single agent alone can be obtained.
- the blending ratio of the tetrazoyl oxime derivative and other agricultural and horticultural active ingredients is not particularly limited, and the tetrazoyl oxime derivative and other agricultural and horticultural active ingredients are used in combination.
- a synergistic effect can be obtained by simply doing this, but the weight ratio of (tetrazoyl oxime derivative etc.) :( other agricultural and horticultural bactericidal active ingredients) is usually 1: 10,000,000 to 10,000,000: 1.
- a preparation containing a tetrazoyloxime derivative and a preparation containing another agricultural and horticultural bactericidal active ingredient are mixed at a predetermined ratio.
- a method for making a disease control agent (b) a method for making a plant disease control agent by mixing a tetrazoyl oxime derivative and other agricultural and horticultural bactericidal active ingredients at a predetermined ratio, and (c) containing a tetrazoyl oxime derivative, etc. And a method of diluting a predetermined amount of a preparation containing a preservative active ingredient for other agricultural and horticultural use with water to obtain a water-diluted solution of a plant disease control agent.
- the plant disease control agent to be used can be used in the form of general pesticides for the purpose of use as a pesticide, that is, in the form of wettable powder, granule, powder, emulsion, aqueous solvent, suspension, flowable, etc. it can.
- vegetable powder such as soybean flour and wheat flour, diatomaceous earth, apatite, gypsum, talc, bentonite, pyrophyllite, clay, etc.
- Organic or inorganic compounds such as mineral fine powder, sodium benzoate, urea, and sodium sulfate are used.
- petroleum fractions such as kerosene, xylene and solvent naphtha, cyclohexane, cyclohexanone, dimethylformamide, dimethyl sulfoxide, alcohol, acetone, trichloroethylene, methyl isobutyl ketone, mineral oil, vegetable oil, water Etc. are used.
- a surfactant can be added if necessary.
- the surfactant is not particularly limited.
- alkylphenyl ether added with polyoxyethylene alkyl ether added with polyoxyethylene, higher fatty acid ester added with polyoxyethylene, sorbitan added with polyoxyethylene Higher fatty acid esters, nonionic surfactants such as tristyryl phenyl ether added with polyoxyethylene, sulfates of alkyl phenyl ether added with polyoxyethylene, alkylnaphthalene sulfonate, polycarboxylate, lignin sulfone Acid salt, formaldehyde condensate of alkyl naphthalene sulfonate, and isobutylene-maleic anhydride copolymer.
- the active ingredient concentration in the plant disease control agent of the present invention is not particularly limited, and various concentrations may be used depending on the form of the preparation described above as necessary. Can be changed. For example, in a wettable powder, it is usually 5 to 90% by weight, preferably 10 to 85% by weight; in an emulsion, usually 3 to 70% by weight, preferably 5 to 60% by weight; In general, it can be 0.01 to 50% by weight, preferably 0.05 to 40% by weight.
- the wettable powders, emulsions and flowables obtained in this way are diluted with water to a predetermined concentration to form suspensions or emulsions, and the granules and powders are sprayed on the soil as they are before or after germination of weeds. Processed or mixed. For example, when applying the plant disease control agent of the present invention, an appropriate amount of 0.1 g or more of active ingredient per hectare is applied.
- Additives such as rapeseed oil, soybean oil, sunflower oil, castor oil, pine oil, cottonseed oil, derivatives of these oils; and oil concentrates thereof are added to the plant disease control agent of the present invention. You can also.
- the plant disease control agent of the present invention can be used in combination with known insecticides, acaricides, herbicides, plant growth regulators, fertilizers, etc. to reduce the amount used and save labor. May be able to bring.
- Example 1 to 29 Drug I
- a suspension (SC agent) containing the compound represented by the formula (1) was prepared by the following procedure.
- the compound represented by the formula (1) the compounds described in Table 3 of the WO03 / 016303 pamphlet (compound numbers (3) to (8)) were used.
- Tomato Blight Control Test Tomato seedlings (variety “Regina”, 4-5 leaf stage) cultivated in an unglazed pot were treated with the plant disease control agent obtained in the examples shown in Table 1 with an active ingredient of 50 ppm. Sprayed at a concentration of. After spraying, it was air-dried at room temperature, sprayed and inoculated with a zoospore susceptor suspension of Phytophthora infestans, and kept for 4 days in a high-humidity constant temperature room (20 ° C.) repeating light and dark every 12 hours. The lesion appearance on the leaves was compared with no treatment, and the control value was determined. The results are shown in Table 1 together with the expected values calculated as follows.
- E M + N ⁇ MN / 100.
- E represents an expected control value (%)
- M represents a control value (%) when the drug I is used alone
- N represents a control value (%) when the drug II is used alone.
- Test Example 2 Cucumber downy mildew control test Cucumber (variety “Sagamihanjiro”) cultivated in an unglazed pot with the plant disease control agent obtained in the examples shown in Table 2 at the concentrations shown in the table Scattered. After spraying, it was air-dried at room temperature, sprayed with a spore suspension of Pseudoperonospora cubensis, and kept in a temperature-controlled room (25 ° C.) repeating light and darkness and dryness every 12 hours for 4 days. The lesion appearance on the leaves was compared with no treatment to determine the control value. The results are shown in Table 2 together with the expected values calculated using the above Colby equation.
- medical agent II was larger than the control value at the time of non-processing. Therefore, the synergistic effect by using the medicine I and the medicine II together was recognized.
- the plant disease control agent of the present invention exhibits an excellent control effect against plant diseases at a very low dose, and is not industrially useful because it is free from fear of phytotoxicity against useful plants.
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Abstract
Description
本願は、2008年3月24日に、日本に出願された特願2008-075748号に基づき優先権を主張し、その内容をここに援用する。
かくして、本発明によれば、式(1)
本発明の植物病害防除剤は、前記式(1)で表されるテトラゾイルオキシム誘導体及びその塩の少なくとも一種、並びに、他の農園芸用殺菌活性成分の少なくとも一種を含有することを特徴とする。
前記式(1)中、Xは、水素原子、無置換若しくは置換基を有するC1~6アルキル基、無置換若しくは置換基を有するC1~6アルコキシ基、ハロゲン原子、ニトロ基、シアノ基、無置換若しくは置換基を有するアリール基、又は無置換若しくは置換基を有するC1~6アルキルスルホニル基を表す。
Xの、無置換若しくは置換基を有するアリール基のアリール基としては、特に限定されないが、C6~10アリール基が好ましい。より具体的には、フェニル基、1-ナフチル基、2-ナフチル基等が挙げられる。
ビニル基、1-プロペニル基、2-プロペニル基、1-ブテニル基、2-ブテニル基、3-ブテニル基、1-ペンテニル基、2-ペンテニル基、3-ペンテニル基、4-ペンテニル基、1-ヘキセニル基、2-ヘキセニル基、3-ヘキセニル基、4-ヘキセニル基、5-ヘキセニル基等のC2~6アルケニル基;
エチニル基、1-プロピニル基、2-プロピニル基、1-ブチニル基、2-ブチニル基、3-ブチニル基、1-ペンチニル基、2-ペンチニル基、3-ペンチニル基、4-ペンチニル基等のC2~6アルキニル基;
メトキシ基、エトキシ基、n-プロポキシ基、i-プロポキシ基、n-ブトキシ基、s-ブトキシ基、i-ブトキシ基、t-ブトキシ基等のC1~6アルコキシ基;
ニトロ基;シアノ基;等が挙げられる。
qが2以上のとき、X同士は、同一であっても相異なっていてもよい。
式(2)又は式(3)中、Yは、メチル基、エチル基、n-プロピル基、i-プロピル基、n-ブチル基、s-ブチル基、i-ブチル基、t-ブチル基、n-ペンチル基、n-ヘキシル基等のアルキル基を示す。
Zは水素原子、アミノ基、又は式:-NHC(=O)-Qで示される基を表す。
Qは水素原子、C1~8アルキル基、C1~6ハロアルキル基、C3~6シクロアルキル基、C1~8アルコキシ基、C3~6シクロアルキルオキシ基、C7~20アラルキルオキシ基、C1~4アルキルチオC1~8アルキル基、C1~4アルコキシC1~2アルキル基、C1~4アシルアミノC1~6アルキル基、C1~4アシルアミノC1~6アルコキシ基、C1~8アルキルアミノ基、C2~6アルケニル基、アラルキル基又はアリール基を示す。
QのC7~20アラルキルオキシ基としては、ベンジルオキシ基、フェネチルオキシ基等が挙げられる。
QのC1~4アルコキシC1~2アルキル基としては、メトキシメチル基、エトキシメチル基、2-メトキシエチル基、2-エトキシエチル基、n-ブトキシメチル基等が挙げられる。
QのC7~20アラルキル基としては、べンジル基、フェネチル基、3-フェニルプロピル基、1-ナフチルメチル基、2-ナフチルメチル基等が挙げられる。
QのC6~10アリール基としては、フェニル基、1-ナフチル基、2-ナフチル基等が挙げられる。
Rは、水素原子;又は、フッ素原子、塩素原子、臭素原子等のハロゲン原子:を表す。
本発明の植物病害防除剤は、上述のテトラゾイルオキシム誘導体及びその塩(以下、「テトラゾイルオキシム誘導体等」ということがある。)に加えて、ホセチル、プロパモカルブ、塩基性塩化銅、クロロタロニル、マンゼブ、シモキサニル、フォルペット、イミノクタジン、シアゾファミド、メタラキシル、フルジオキソニル、テブコナゾール、プロチオコナゾール、チアメトキサム、アゾキシストロビン、及びその塩からなる群から選ばれる少なくとも一種を含有する。
なお、前記有効成分化合物には、その光学活性化合物も含むものとする。具体的には、メタラキシルに対するメタラキシルMのごとくである。
本発明の植物防除剤には、上記農薬活性成分以外にも適宜他の農薬活性成分を混用することができ、具体的には下記に示す活性成分を例示することができる。
なお、活性成分は、有効成分化合物名の一般名(一部申請中を含む)で記す。
殺菌剤の有効成分化合物(一般名;一部申請中を含む)
メパニピリム(mepanipyrim)、ピリメタニル(pyrimethanil)、シプロジニル(cyprodinil)などのアニリノピリミジン系化合物;
フルアジナム(fluazinam)などのピリジナミン系化合物;
ベノミル(benomyl)、チオファネートメチル(thiophanate‐methyl)、カルベンダジム(carbendazim)、チアベンダゾール(thiabendazole)、フベリアゾール(fuberiazole)、などのイミダゾール系化合物;
メフェノキサム(mefenoxam)、オキサジキシル(oxadixyl)、オフレース(ofurace)、ベナラキシル(benalaxyl)、ベナラキシル-M(benalaxyl-M)、フララキシル(furalaxyl)、シプロフラム(cyprofuram)などのフェニルアミド系化合物;
ジクロフルアニド(dichlofluanid)のようなスルフェン酸系化合物;
ジノキャップ(dinocap)などのニトロフェニル系化合物;
水酸化第二銅(cupric hydroxide)、有機銅(oxine copper)などの銅系化合物;
ヒメキサゾール(hymexazol)などのイソキサゾール系化合物;
トルコホスメチル(tolcofos‐methyl)、S-ベンジル O,O-ジイソプロピルホスホロチオエート、O-エチル S,S-ジフェニルホスホロジチオエート、アルミニウムエチルハイドロゲンホスホネートなどの有機リン系化合物;
プロシミドン(procymidone)、イプロジオン(iprodione)、ビンクロゾリン(vinclozolin)などのジカルボキシイミド系化合物;
フルトラニル(flutolanil)、メプロニル(mepronil)、ゾキサミド(zoxamid)、チアジニル(tiadinil)などのベンズアニリド系化合物;カルボキシン(carboxin)、オキシカルボキシン(oxycarboxin)、チフルザミド(thifluzamide)、ペンチオピラド(penthiopyrad)、ボスカリド(boscalid)、フルオピコリド(fluopicolide)、フルオピラム(fluopyram)、ビキサフェン(bixafen)などのアニリド系化合物;
ピリフェノックス(pyrifenox)などのピリジン系化合物;
フェナリモル(fenarimol)、フルトリアフォル(flutriafol)などのカルビノール系化合物;
フェンプロピディン(fenpropidine)などのピペリジン系化合物;
フェンプロピモルフ(fenpropimorph)、トリデモルフ(tridemorph)などのモルフォリン系化合物;
フェンチンヒドロキシド(fentin hydroxide)、フェンチンアセテート(fentin acetate)などの有機スズ系化合物;
ペンシキュロン(pencycuron)などの尿素系化合物;
ジメトモルフ(dimethomorph)、フルモルフ(flumorph)フルメトーバー(flumetover)などのシンナミック酸系化合物;
ジエトフェンカルブ(diethofencarb)などのフェニルカーバメート系化合物;
ファモキサドン(famoxadone)などのオキサゾリジノン系化合物;
エタボキサム(ethaboxam)などのチアゾールカルボキサミド系化合物;
シルチオファム(silthiopham)などのシリルアミド系化合物;
イプロバリカルブ(iprovalicarb)、ベンチアバリカルブ-イソプロピル(benthiavalicarb-isopropyl)などのアミノアシッドアミドカーバメート系化合物;
フェンヘキサミド(fenhexamid)などのハイドロキシアニリド系化合物;
フルスルファミド(flusulfamide)などのベンゼンスルホンアミド系化合物;
シフルフェナミド(cyflufenamid)などのオキシムエーテル系化合物;
フェノキサニル(fenoxanil)などのフェノキシアミド系化合物;
バリダマイシン(validamycin)、カスガマイシン(kasugamycin)、ポリオキシン(polyoxins)などの抗生物質;
プロフェノホス(profenofos)、ジクロルボス(dichlorvos)、フェナミホス(fenamiphos)、フェニトロチオン(fenitrothion)、EPN、ダイアジノン(diazinon)、クロルピリホスメチル(chlorpyrifos-methyl)、アセフェート(acephate)、プロチオホス(prothiofos)、ホスチアゼート(fosthiazate)、ホスホカルブ(phosphocarb)、カズサホス(cadusafos)、ジスルホトン(dislufoton)、クロルピリホス(chlorpyrifos)、デメトン-S-メチル(demeton-S-methyl)、ジメトエート(dimethoate)、メタミドホス(methamidophos)、イソキサチオン(isoxathion)、イソフェンホス(isofenphos)、エチオン(ethion)、エトリムホス(etrimfos)、キナルホス(quinalphos)、ジメチルビンホス(dimethylvinphos)、スルプロホス(sulprofos)、チオメトン(thiometon)、バミドチオン(vamidothion)、ピラクロホス(pyraclofos)、ピリダフェンチオン (pyridaphenthion)、ピリミホスメチル(pirimiphos-methyl)、プロパホス(propaphos)、ホサロン(phosalone)、ホルモチオン(formothion)、マラチオン(malathion)、テトラクロルビンホス(tetrachlovinphos)、クロルフェンビンホス(chlorfenvinphos)、シアノホス(cyanophos)、トリクロルホン(trichlorfon)、メチダチオン(methidathion)、フェントエート(phenthoate)、ESP、アジンホスメチル(azinphos-methyl)、フェンチオン(fenthion)、ヘプテノホス(heptenophos)、メトキシクロル(methoxychlor)、パラチオン(paration)、モノクロトホス(monocrotophos)、イミシアホス(imicyafos)、パラチオン-メチル(parathion-methyl)、テルブホス(terbufos)、ホスファミドン(phospamidon)、ホスメット(phosmet)、ホレート(phorate)などの有機リン酸エステル系化合物;
ジコホル(dicofol)、テトラジホン(tetradifon)、エンドスルファン(endosulufan)、ジエノクロル(dienochlor)、ディルドリン(dieldrin)のような有機塩素系化合物;
酸化フェンブタスズ(fenbutatin oxide)、シヘキサチン(cyhexatin)などの有機金属系化合物;
メトプレン(methoprene)、ピリプロキシフェン(pyriproxyfen)、フェノキシカルブ(fenoxycarb)、ジオフェノラン(diofenolan)などの幼若ホルモン様化合物;
フェンピロキシメート(fenpyroximate)、フィプロニル(fipronil)、テブフェンピラド(tebufenpyrad)、エチプロール(ethiprole)、トルフェンピラド(tolfenpyrad)、アセトプロール(acetoprole)、ピラフルプロール(pyrafluprole)、ピリプロール(pyriprole)のようなピラゾール系化合物;
イミダクロプリド(imidacloprid)、ニテンピラム(nitenpyram)、アセタミプリド(acetamiprid)、チアクロプリド(thiacloprid)、クロチアニジン(clothianidin)、ジノテフラン(dinotefuran)、ニチアジン(nithiazine)などのネオニコチノイド;
テブフェノジド(tebufenozide)、メトキシフェノジド(methoxyfenozide)、クロマフェノジド(chromafenozide)、ハロフェノジド(halofenozide)などのヒドラジン系化合物;
アザディラクチン(azadirachtin)、ロテノン(rotenone)などのような天然物;
ピペロニルブトキシド(piperonyl butoxide)のような協力剤;
ディート(deet)のような忌避剤等。
本発明の植物病害防除剤は、前記テトラゾイルオキシム誘導体等の少なくとも一種と、前記他の農園芸用殺菌活性成分の少なくとも一種とを含有し、両成分を併用することにより、各単剤のみの使用で得られる植物病害防除効果からでは予想できない顕著な植物病害防除効果(相乗効果)を得ることができる。
(1)薬剤I
薬剤Iとして、以下の手順にて、前記式(1)で表される化合物を含有する懸濁剤(SC剤)を調製した。式(1)で表される化合物としては、WO03/016303号パンフレットの表3に記載の化合物(化合物番号(3)-(8))を用いた。
ポリオキシエチレンアリールフェニルエーテルエーテル 2部
ジアルキルスルホサクシネートナトリウム塩 0.5部
グリセリン 5部
キサンタンガム 0.3部
水 82.2部
以上を混合し、粒度が3ミクロン以下になるまで湿式粉砕して、有効成分10%のSC剤を得た。
薬剤IIとして、以下の(A)~(O)を、他の農園芸用殺菌活性成分として含有する製剤を用いた。
(A)日曹アリエッティ水和剤(有効成分:ホセチル、有効成分量:80%、日本曹達社製)
(B)ドイツボルドーA(塩基性塩化銅、有効成分量:銅として50%、北興化学社製)
(C)フォルペット簡易乳剤〔市販のフォルペット(フォルペット標準品、和光純薬社製)を用いて、簡易乳剤としたもの〕
(D)日曹プレビクールN液剤(プロパモカルブ塩酸塩、有効成分量:64%、日本曹達社製)
(E)武田ダコニール1000(主成分:TPN(クロロタロニル)、有効成分量:40%、住化武田農薬社製)
(F)ジマンダイセンWP(主成分:マンゼブ、有効成分量:75%、ダウケミカル日本(株)製)
(G)カーゼートWP(有効成分:シモキサニル、有効成分量:50%、デュポン社製)
(H)ベルクートWP(有効成分:イミノクタジンアルベシル酸塩、有効成分:40%、日本曹達(株)製)
(I)ランマンフロアブル(有効成分:シアゾファミド、有効成分量:9.4%、石原産業製)
(J)サブデューマックス液剤(有効成分:メタラキシルM、有効成分量:22.0%、シンジェンタ社製)
(K)セイビアーフロアブル20(有効成分:フルジオキソニル、有効成分量:20%、シンジェンタ社製)
(L)シルバキュアフロアブル(有効成分:テブコナゾール、有効成分量:40%、バイエル社製)
(M)JOAO EC(有効成分:プロチオコナゾール、有効成分量:25%、バイエル社製)
(N)アクタラ顆粒水和剤(有効成分:チアメトキサム、有効成分量:10%、シンジェンタ社製)
(O)アミスター20FL(有効成分:アゾキシストロビン、有効成分量:20%、シンジェンタ製)
薬剤Iと薬剤IIとを、第1表~第2表に示す割合でタンクミックスして実施例1~13の植物病害防除剤を調整した。
また、薬剤Iと薬剤IIとを、第3表~第5表に示す割合になるように滅菌水で溶かして実施例14~29の薬液を作成した。
(比較例1~45)
薬剤Iのみ、又は薬剤IIのみを第1表~第5表に示す濃度になるように調整し、比較例の植物病害防除剤とした。なお、比較例8、19、29、35及び45においては、薬剤Iまたは薬剤IIを含む植物病害防除剤を使用していない。
なお、第1表~第5表における濃度は、薬剤I及び薬剤IIの有効成分の濃度である。
この調製した植物病害防除剤を用いて、下記に示す試験を行った。
素焼きポットで栽培したトマト幼苗(品種「レジナ」、4~5葉期)に、第1表に示す実施例で得られた植物病害防除剤を、有効成分50ppmの濃度で散布した。散布後、室温で自然乾燥し、トマト疫病菌(Phytophthora infestans)の遊走子嚢懸濁液を噴霧接種し、明暗を12時間毎に繰り返す高湿度の恒温室(20℃)に4日間保持した。葉上の病斑出現状態を無処理と比較調査し、防除価を求めた。その結果を、下記のようにして算出した期待値と共に、第1表に示す。
ここで、Eは防除価期待値(%)、Mは薬剤I単独使用時の防除価(%)、Nは薬剤II単独使用時の防除価(%)を表す。
素焼きポットで栽培したキュウリ(品種「相模半白」)幼苗に、第2表に示す実施例で得られた植物病害防除剤を表に記載の濃度で散布した。散布後、室温で自然乾燥し、キュウリべと病菌(Pseudoperonospora cubensis)の胞子懸濁液を噴霧接種し、明暗及び乾湿を12時間毎に繰り返す恒温室(25℃)に4日間保持した。葉上の病斑出現状態を無処理と比較調査し防除価を求めた。その結果を、上記コルビーの式を用いて計算した期待値と共に、第2表に示す。
(試験例3)Pythium aphanidermatum又はPythium ultimum菌防除試験
第3表~第5表に示す実施例で得られた薬液を、表3~5に示す濃度となるようにPDA培地に、培地量の1%分添加して寒天平板を作成した。この寒天平板にPythium aphanidermatumもしくはPythium ultimumの菌叢ディスク(直径5mm)を置床した。20℃で3~4日間静置後、菌叢直径を測定し、無処理区に対する菌糸伸長阻害率を求め、防除価とした。その結果を、上記コルビーの式を用いて計算した期待値と共に、第3表~第5表に示す。
ここで、菌糸伸長阻害率(%)は、下記式から求められる。
菌糸伸長阻害率(%)(防除価)=(1-(薬剤処理区の菌叢直径)/(無処理区の菌叢直径))×100%
また、第3表及び第4表は、Pythium aphanidermatumの菌叢ディスクを使用した試験例の結果を示し、第5表は、Pythium ultimumの菌叢ディスクを使用した試験例の結果を示す。
なお、前記実施例で得られた薬液の代わりに、薬剤Iのみを用いた場合(比較例20~21、比較例30~31、比較例36~37)、薬剤IIのみを用いた場合(比較例22~28、比較例32~34、比較例38~44)、無処理の場合(比較例29、比較例35、比較例45)についても同様に試験した。その結果を第3表~第5表に示す。
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EP (2) | EP2258192A4 (ja) |
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CY (1) | CY1119250T1 (ja) |
DK (1) | DK2649880T3 (ja) |
ES (1) | ES2637396T3 (ja) |
HR (1) | HRP20171210T1 (ja) |
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LT (1) | LT2649880T (ja) |
ME (1) | ME02931B (ja) |
PL (1) | PL2649880T3 (ja) |
PT (1) | PT2649880T (ja) |
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WO (1) | WO2009119072A1 (ja) |
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WO2011105239A1 (ja) * | 2010-02-26 | 2011-09-01 | 日本曹達株式会社 | テトラゾリルオキシム誘導体またはその塩、ならびに殺菌剤 |
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Cited By (17)
Publication number | Priority date | Publication date | Assignee | Title |
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JP2011509971A (ja) * | 2008-01-15 | 2011-03-31 | バイエル・クロツプサイエンス・アクチエンゲゼルシヤフト | テトラゾリルオキシム誘導体と殺菌剤活性物質又は殺虫剤活性物質を含んでいる殺有害生物剤組成物 |
EP3262940A1 (en) * | 2008-01-15 | 2018-01-03 | Bayer Intellectual Property GmbH | Pesticide composition comprising a tetrazolyloxime derivative and an insecticide active substance |
US9060518B2 (en) | 2008-01-15 | 2015-06-23 | Pierre-Yves Coqueron | Pesticide composition comprising a tetrazolyloxime derivative and a fungicide or an insecticide active substance |
JP2011515369A (ja) * | 2008-03-19 | 2011-05-19 | バイエル・クロツプサイエンス・アクチエンゲゼルシヤフト | 殺菌剤ヒドロキシモイル−テトラゾール誘導体 |
JP2011515368A (ja) * | 2008-03-19 | 2011-05-19 | バイエル・クロツプサイエンス・アクチエンゲゼルシヤフト | 殺菌剤ヒドロキシモイル−テトラゾール誘導体 |
WO2011105239A1 (ja) * | 2010-02-26 | 2011-09-01 | 日本曹達株式会社 | テトラゾリルオキシム誘導体またはその塩、ならびに殺菌剤 |
US9156816B2 (en) | 2010-02-26 | 2015-10-13 | Nippon Soda Co., Ltd. | Tetrazolyloxime derivative or salt thereof and fungicide |
JP5587970B2 (ja) * | 2010-02-26 | 2014-09-10 | 日本曹達株式会社 | テトラゾリルオキシム誘導体またはその塩、ならびに殺菌剤 |
JP5512794B2 (ja) * | 2010-03-16 | 2014-06-04 | 日本曹達株式会社 | 植物病害防除剤 |
US9034835B2 (en) | 2010-03-16 | 2015-05-19 | Nippon Soda Co., Ltd. | Plant disease control agent with a tetrazolyl oxime derivative and either triflumizole or hydroxy-isoxazole as the active ingredients |
WO2011131602A2 (en) | 2010-04-20 | 2011-10-27 | Basf Se | Fungicidal mixtures based on azolopyrimmidinylamines |
JP2013542934A (ja) * | 2010-10-07 | 2013-11-28 | バイエル・クロップサイエンス・アーゲー | テトラゾリルオキシム誘導体とチアゾリルピペリジン誘導体を含んでいる殺菌剤組成物 |
WO2012045798A1 (en) | 2010-10-07 | 2012-04-12 | Bayer Cropscience Ag | Fungicide composition comprising a tetrazolyloxime derivative and a thiazolylpiperidine derivative |
JP2016188221A (ja) * | 2010-10-07 | 2016-11-04 | バイエル・クロップサイエンス・アクチェンゲゼルシャフト | テトラゾリルオキシム誘導体とチアゾリルピペリジン誘導体を含んでいる殺菌剤組成物 |
JP2013173733A (ja) * | 2012-01-24 | 2013-09-05 | Sumitomo Chemical Co Ltd | 植物病害防除組成物及び植物病害の防除方法 |
JP2016079140A (ja) * | 2014-10-20 | 2016-05-16 | 日本曹達株式会社 | 農園芸用殺菌剤 |
KR20230131834A (ko) | 2021-01-19 | 2023-09-14 | 닛뽕소다 가부시키가이샤 | 혼합제 |
Also Published As
Publication number | Publication date |
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RS56116B1 (sr) | 2017-10-31 |
LT2649880T (lt) | 2017-09-25 |
KR101259242B1 (ko) | 2013-04-29 |
EP2258192A4 (en) | 2012-12-19 |
EP2258192A1 (en) | 2010-12-08 |
HUE033290T2 (en) | 2017-11-28 |
US8592461B2 (en) | 2013-11-26 |
JP5373766B2 (ja) | 2013-12-18 |
SI2649880T1 (sl) | 2017-10-30 |
US8592412B1 (en) | 2013-11-26 |
JPWO2009119072A1 (ja) | 2011-07-21 |
JP2013139486A (ja) | 2013-07-18 |
EP2649880A1 (en) | 2013-10-16 |
HRP20171210T1 (hr) | 2017-10-20 |
EP2649880B1 (en) | 2017-06-21 |
ME02931B (me) | 2018-04-20 |
CY1119250T1 (el) | 2018-02-14 |
US20110159110A1 (en) | 2011-06-30 |
KR20100120215A (ko) | 2010-11-12 |
PL2649880T3 (pl) | 2017-10-31 |
PT2649880T (pt) | 2017-08-24 |
US20130296313A1 (en) | 2013-11-07 |
DK2649880T3 (en) | 2017-07-31 |
ES2637396T3 (es) | 2017-10-13 |
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