WO2010055909A1 - Pest control agent composition for agricultural and horticultural use - Google Patents
Pest control agent composition for agricultural and horticultural use Download PDFInfo
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- WO2010055909A1 WO2010055909A1 PCT/JP2009/069348 JP2009069348W WO2010055909A1 WO 2010055909 A1 WO2010055909 A1 WO 2010055909A1 JP 2009069348 W JP2009069348 W JP 2009069348W WO 2010055909 A1 WO2010055909 A1 WO 2010055909A1
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- pest control
- horticultural
- control composition
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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
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/24—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms
- A01N43/32—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms six-membered rings
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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
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
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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
- A01N43/82—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 five-membered rings with three ring hetero atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D285/00—Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
- C07D285/01—Five-membered rings
- C07D285/02—Thiadiazoles; Hydrogenated thiadiazoles
- C07D285/04—Thiadiazoles; Hydrogenated thiadiazoles not condensed with other rings
- C07D285/06—1,2,3-Thiadiazoles; Hydrogenated 1,2,3-thiadiazoles
Definitions
- the present invention includes a 4-cyclopropyl-1,2,3-thiadiazole derivative or a salt thereof, and one or more compounds having fungicidal or insecticidal activity as active ingredients.
- the present invention relates to a pest control composition for use.
- the pesticide composition for agricultural and horticultural use containing as an active ingredient one or more compounds having an antibacterial and / or insecticidal activity as well as an extremely broad bactericidal and insecticidal effect It has been found that it has a spectrum, and the present invention has been completed.
- R 1 , R 2 , R 3 , R 4 and R 5 may be the same or different and each represents a hydrogen atom; a halogen atom or a (C 1 -C 3 ) alkyl group.
- R 6 is a hydrogen atom; (C 1 -C 8 ) alkyl group; (C 3 -C 6 ) cycloalkyl group; phenyl (C 1 -C 6 ) alkyl group; halogen atom, cyano group, (C 1 -C 6 ) Alkyl group, halo (C 1 -C 6 ) alkyl group, (C 3 -C 6 ) cycloalkyl group, halo (C 3 -C 6 ) cycloalkyl group, (C 1 -C 6 ) alkoxy group, halo ( A substituted phenyl having one or more substituents which may be the same or different, selected from the group consisting of a C 1 -C 6 ) alk
- Y represents an oxygen atom or —N (R 7 ) — (wherein R 7 represents a hydrogen atom, a (C 1 -C 6 ) alkyl group or a (C 3 -C 6 ) cycloalkyl group).
- W represents an oxygen atom or a sulfur atom.
- Agro-horticultural pest control composition [2] Compounds having bactericidal activity are vitertanol, bromconazole, cyproconazole, difenoconazole, diniconazole, enilconazole, epoxiconazole, fluquinconazole, fenbuconazole, flusilazole, flutriahol, hexaconazole, imi Benconazole, ipconazole, metconazole, microbutanyl, penconazole, propiconazole, prothioconazole, cimeconazole, triadimethone, triadimenol, tebuconazole, tetraconazole, triticonazole, prochloraz, pefrazate, imazalyl, triflumizole, ciazofamide, miazofamide
- the agricultural and horticultural pest control composition of the present invention has a broad spectrum with respect to various plant diseases and pests compared to the prior art, and exhibits an excellent pest control effect at a low dose. Since the agricultural and horticultural pest control composition of the present invention effectively controls various diseases and pests with a small amount of application, the burden on the global environment can be reduced.
- the agricultural and horticultural pest control composition of the present invention is effective for 4-cyclopropyl-1,2,3-thiadiazole derivatives or salts thereof and one or more compounds having fungicidal activity and / or insecticidal activity. It is contained as a component.
- the 4-cyclopropyl-1,2,3-thiadiazole derivative or a salt thereof used in the present invention is represented by the following general formula (I).
- halogen atom refers to a chlorine atom, a bromine atom, an iodine atom or a fluorine atom.
- (C 1 -C 6 ) alkyl group means, for example, methyl group, ethyl group, normal propyl group, isopropyl group, normal butyl group, isobutyl group, secondary butyl group, tertiary butyl group, normal pentyl group, neopentyl group A straight-chain or branched alkyl group having 1 to 6 carbon atoms such as a normal group or a normal hexyl group;
- halo (C 1 -C 6 ) alkyl group refers to a linear or branched alkyl group having 1 to 6 carbon atoms substituted with one or more halogen atoms which may be the same or different, Examples thereof include a trifluoromethyl group, a difluoromethyl group, a perfluoroethyl group, a perfluoroisopropyl group, a chloromethyl group, a bromomethyl group, a 1-bromoethyl group, and a 2,3-dibromopropyl group.
- (C 3 -C 6 ) cycloalkyl group means, for example, 3 to 6 carbon atoms such as cyclopropyl group, cyclobutyl group, cyclopentyl group, cyclohexyl group, 2-methylcyclopropyl group, 2-methylcyclopentyl group, etc.
- An alicyclic alkyl group is shown.
- halo (C 3 -C 6 ) cycloalkyl group refers to a cycloalkyl group having 3 to 6 carbon atoms substituted with one or more halogen atoms which may be the same or different, for example, a fluorocyclopropyl group , Dichlorocyclobutyl group, bromocyclopentyl group and the like.
- (C 1 -C 6 ) alkoxy group means, for example, methoxy group, ethoxy group, normal propoxy group, isopropoxy group, normal butoxy group, secondary butoxy group, tertiary butoxy group, normal pentyloxy group, isopentyloxy group A straight-chain or branched alkoxy group having 1 to 6 carbon atoms such as a group, a neopentyloxy group, and a normal hexyloxy group;
- the “halo (C 1 -C 6 ) alkoxy group” is an alkoxy having a linear or branched alkyl group having 1 to 6 carbon atoms substituted with one or more halogen atoms which may be the same or different. Group, for example, a difluoromethoxy group, a trifluoromethoxy group, a 2,2,2-trifluoroethoxy group or the like.
- (C 1 -C 6 ) alkoxycarbonyl group means, for example, linear or branched such as methoxycarbonyl group, ethoxycarbonyl group, normal propoxycarbonyl group, isopropoxycarbonyl group, normal butoxycarbonyl group, tertiary butoxycarbonyl group, etc.
- a chain-like alkoxycarbonyl group having 1 to 6 carbon atoms is shown.
- Examples of the salt of the 4-cyclopropyl-1,2,3-thiadiazole derivative represented by the general formula (I) used in the present invention include inorganic acid salts such as hydrochloride, sulfate, nitrate and phosphate; Organic salts such as salts, fumarate, maleate, oxalate, methanesulfonate, benzenesulfonate, paratoluenesulfonate; salts with bases such as sodium ion, potassium ion, calcium ion It can be illustrated.
- inorganic acid salts such as hydrochloride, sulfate, nitrate and phosphate
- Organic salts such as salts, fumarate, maleate, oxalate, methanesulfonate, benzenesulfonate, paratoluenesulfonate
- salts with bases such as sodium ion, potassium ion, calcium ion It can be illustrated.
- the 4-cyclopropyl-4-cyclopropyl-1,2,3-thiadiazole derivative represented by the general formula (I) used in the present invention contains one or more asymmetric centers in the structural formula. In some cases, two or more optical isomers and diastereomers may exist, but the present invention includes all of the optical isomers and a mixture containing them in an arbitrary ratio.
- R 1 , R 2 , R 3 , R 4 and R 5 are preferably a hydrogen atom or a (C 1 -C 6 ) alkyl group, Each may be the same or different.
- R 1 is most preferably a hydrogen atom.
- R 2 , R 3 , R 4 and R 5 are more preferably a hydrogen atom or a (C 1 -C 3 ) alkyl group, and each may be the same or different.
- R 2 , R 3 , R 4 and R 5 are most preferably hydrogen atoms.
- R 6 is preferably a hydrogen atom; a halogen atom, a cyano group, a (C 1 -C 6 ) alkyl group, or a halo (C 1 -C 6 ).
- the compound represented by the general formula (I) disclosed in the present invention can be produced according to the method described in JP 2007-99749 A, but the compound used in the present invention is not limited to these. It is not something.
- Table 1 shows 1 H-NMR data of some of the 4-cyclopropyl-1,2,3-thiadiazole derivatives exemplified in Table 1.
- the compound numbers in Table 2 indicate the numbers described in Table 1 above.
- Examples of the compound having fungicidal activity used in the agricultural and horticultural pest control composition of the present invention include, for example, vitertanol, bromconazole, cyproconazole, difenoconazole, diniconazole, enilconazole, epoxiconazole, and fluquinconazole.
- Fenbuconazole flusilazole, flutriazole, hexaconazole, imibenconazole, ipconazole, metconazole, microbutanyl, penconazole, propiconazole, prothioconazole, cimeconazole, triadimethone, triadimenol, tebuconazole, tetraconazole, tri Ticonazole, prochloraz, pefrazoate, imazalyl, triflumizole, cyazofamide, benomyl, carbendazim, thiabendazole, fuberidazole, Taboxam, etridiazole, oxpoconazole fumaric acid, hymexazole, azoxystrobin, dimoxystrobin, enestrobrin, fluoxastrobin, cresoxime methyl, methinostrobin, orizastrobin, picoxystrobin, pyraclostrobin
- insecticidal compound used in the agricultural and horticultural pest control composition of the present invention include, for example, acetamiprid, pymetrozine, fenitrothion, acephate, carbaryl, mesomil, cartap, cyhalothrin, etofenprox, teflubenzuron, fulbenzamide , Flufenoxuron, tebufenozide, fenpyroximate, pyridaben, imidacloprid, buprofezin, BPMC, MIPC, malathion, methidathion, fenthion, diazinon, oxydeprophos, bamidthione, ethiophene carb, pirimicurve, permethrin, cypermethalfen fenproline, bifenthrin Nitenpyram, Chlorfluazuron, Methoxyphenozide, Tebufenpyrad, Piri Diphen,
- the agricultural and horticultural pest control composition of the present invention has a broad spectrum and is synergistic compared to the case where compounds having bactericidal activity and / or insecticidal activity against various plant diseases and pests are used alone. Has a control effect. It is particularly suitable for controlling plant diseases and pests in paddy rice, barley, wheat and other crops.
- plant diseases and pests can be exemplified as the application targets of the agricultural and horticultural pest control composition of the present invention.
- plant diseases include filamentous fungal diseases, bacterial diseases, and viral diseases, such as diseases of the genus Botrytis, diseases of the genus Helmintosporium, diseases of the genus Fusarium, septoria ( Diseases of the genus Septoria, diseases of the genus Sarcospora, diseases of the genus Pseudocercosporella, diseases of the genus Rhynchosporium, diseases of the genus Pyricularia, diseases of the genus Alternaria
- diseases of the genus Hemilia, genus Rhizoctonia, Ustilago Basidiomycetous diseases such as genus diseases, Typula diseases, Puccinia diseases, Phakopsora diseases; for example, Venturia diseases, Podosphaera genus diseases, Diseases of the genus Leptosphaeria,
- Individual plant diseases include, for example, rice blast (Priculararia oryzae); rice rot (Rhizoctonia solani); rice sesame leaf blight (Cochiobulus miabialusius, Rhizominuspisumus, Rhizominuspissumis, Rhizominuspissum) Fusarium roseum, Mucor sp., Poma sp., Tricoderma sp.); Rice idiot (Gibberella fujikuroi); Barley and wheat and other powdery mildew (Blumeria grami sul); And other host plants Powdery mildew (Erysiphe cichoracoacorum); Barley and wheat rhinoceros (Pseudocercosporella herpotrichoides); Wheat etc.
- rice blast Primaryculararia oryzae
- rice rot Rhizoctonia solani
- rice sesame leaf blight Cochiobulus miabialusius, Rhizominuspisumus, Rhizominuspissumis, Rhizo
- apple black spot disease Venturia inaequalis
- apple spotted leaf disease Alternaria mary
- pear black spot disease Alternaria kikuchiana
- citrus black spot disease Diaporthe citri
- Cercospora beticola peanut black spot
- Leafy leaf disease Pyrenoph
- ra graminea barley cloud scab
- wheat naked scab Ustilago nudia
- wheat wheat scab (Tillletia cariole); Pseudomonas phytopathies such as Pseudomonas syringae pv.
- insects examples include Hemoptera, for example, Megacopta punctatissimum, Oysarcoris lewisi, Egysarcorus varvae, and (Platia stali), Coleus puntigger, Spider helicopter (Leptocorisa chinensis), Cyprus cavatus (Riptortus clavatus), Kobanei tsunagushi tsugehit Tephantitis pyrioides), Apolygus spinolai, Akasujimekuragame, Stenotus rubrovititalus, Trigonoticlus cotertialum Green leafhoppers (Epoasca onukii), Green leafhoppers (Nephotettix cinticesps), Thai whitefin leafhoppers (Nepotettix virescens), Green leafhoppers (Laodelphax straitellarus vulva) ns), Sejirounka (Sogatella furcifera), Diaphorina
- Lepidoptera includes, for example, apple wolfberry (Adoxophyes orana fascita), tea wolfberry monk (Adoxophyces honmai), nippon cynosphincumopampusu cinopus cinopus cympopuscopupuscupopushisopumusu Chamonaki (Homona magnanima), Chanohosoga (Caloptilia theivora), Artemisia dasak (Ascotis selenaria), Grapeberry moss (Endopizia viteana), Codling moth (Lasprey mons) (Phyllonorycter ringoniella), Gin Mont leafminer (Lyonetia prunifoliella malinella), mandarin orange leafminer (Phyllocnistis citrella), diamondback moth (Plutella xylostella), pink bollworm (Pectinophora gossypiella), peach fruit moth (Carposina niponensis
- the Coleoptera (Coleoptera), for example, cupreous chafer (Anomala cuprea), Japanese beetle (Popillia japonica), Hirata beetle (Lyctus brunneus), Hirata red flour beetle (Tribolium confusum), beetle, Epilachna vigintioctopunctata (Epilachna vigintioctopunctata), Gomadarakamikiri (Anoplophora malasiaca ), Pinewood beetle (Monochamus alternatus), azuki beetle (Callosobrchuchus chinensis), cucumber beetle (Alacophora femorialis), rootworm species (Diabrotica spp.), Cotton Umushi (Anthonomus gradis grandis), Mexican beetle (Epilachna varivestis), Colorado potato beetle (Leptinotarsa decemlineata),
- Diptera for example, Agromyza oryzae, Emius eu (s), citrus (Eri), citrus (Eri), citrus (Eri), citrus (Eri), citrus (Eri), citrus (Eri), citrus (Epi), citrus
- thrips include, for example, Shiratotrips dorsalis, Thripspalmipalm, and Thripspalmipalmis.
- Examples of the termites include, but are not limited to, the termites (Coptothermes formosanus), the Yamato termites (Reticulitermes spatras), and Examples of the eyes (Oroptoptera) include, for example, Oxya yezoensis, Kera (Gryllotalpa sp.), Cockroach (Periplaneta americana), German cockroach (Blatella germanica) and the like.
- mites examples include, for example, citrus spider mite (Pananychus citri), apple spider mite (Pananychus urticae), spider mite (Tetanychus kantawai), tick mite (Tetanichus kantawai), Rabbit mite (Aculops pelekassi), Scarlet mite mite (Eriophys chibaensis), Butter mite (Polyphagotarsonemus latus), Robin mite (Rhizoglyphus robini), Kenagarona phragmite Scentiae, etc.
- examples of the order of Tylenchida include Pratylenchus coffeae, Pratylenchus penetran, and Potato sect.
- Examples of the larvae include, for example, longi nematode (Longidorus sp.), And examples of the mollusc gastropoda (Gastropoda) include, for example, slugs (Inciliaria bilineta). It is done.
- Examples of the plant that can be used for the agricultural and horticultural pest control composition of the present invention include grains such as rice, barley, wheat, rye, oats, corn, and Takatsuki; soybeans, red beans, broad beans, peas, peanuts, etc. Beans; apples, citrus fruits, pears, grapes, peaches, plums, cherry peaches, walnuts, almonds, bananas, strawberries and other fruit trees or fruits; cabbage, tomatoes, eggplant, spinach, broccoli, lettuce, onion, leek, peppers, etc.
- Root vegetables such as carrots, potatoes, sweet potatoes, radishes, lotus roots, turnips; for processing cotton, hemp, mulberry, mitsumata, rapeseed, beet, hops, sugar cane, sugar beet, olives, rubber, coffee, tobacco, tea, etc.
- Crops; potatoes such as pumpkin, cucumber, watermelon, melon; orchardgrass, sorghum, timothy, clover, alfalfa, etc.
- Grasses grasses such as Korean turf, bentgrass; crops for fragrances such as lavender, rosemary, thyme, parsley, pepper, ginger, etc .; It is not something.
- the pest control composition for agricultural and horticultural use of the present invention is a target plant, the seed of the target plant, the seed of the target plant, the cultivation carrier for sowing, or the soil, which is expected to generate the disease / pest with an effective amount of the composition effective for control.
- the target plant can be protected by treating the etc.
- the treatment of the target plant, the seed of the target plant, the cultivation carrier or the soil for sowing includes the application and application of the agricultural and horticultural pest control composition, application to the soil where the target crop is grown, irrigation, etc. included.
- the agricultural and horticultural pest control composition of the present invention may be used as it is, or appropriately diluted or suspended in water or the like, for controlling various diseases and pests.
- rice nursery box application seed treatment, seed dressing application method, seed disinfection method, planting hole treatment, plant head treatment, cropping Application methods such as treatment and soil mixing can be suitably used.
- seed treatment such as dressing and soaking, soaking treatment of seedling roots, cropping at the time of sowing, cultivation container and planting hole for raising seedlings, plant origin, etc.
- seed treatment such as dressing and soaking, soaking treatment of seedling roots, cropping at the time of sowing, cultivation container and planting hole for raising seedlings, plant origin, etc.
- the “cultivation carrier” or “soil” in carrying out the method of use of the present invention refers to a support for cultivating a plant, and the material is not particularly limited, but may be a material on which a plant can grow. For example, it includes so-called various soils, seedling mats, water, etc., sand, vermiculite, cotton, paper, diatomaceous earth, agar, gel-like substances, polymer substances, rock wool, glass wool, wood chips, bark, Pumice can also be included.
- Examples of the method of spraying on the foliage of plants include, for example, a method of diluting a liquid preparation such as an emulsion or a flowable agent or a solid preparation such as a wettable powder or a granular wettable powder with water or spraying without diluting, or a powder. Or a method of spraying smoke.
- Examples of application methods to the soil include, for example, a method in which a liquid or solid preparation is diluted or not diluted with water and applied to the vicinity of a plant installation place or a nursery bed for raising seedlings, etc. The method of spraying in the vicinity or nursery, the method of spraying powder, wettable powder, wettable granule powder, granule etc.
- the dosage form may vary depending on the time of application such as application at seeding, application at greening period, application at transplantation, etc., but agents such as powder, granule wettable powder, granules, etc. Apply with a mold. It can also be applied by mixing with soil, and it can be mixed with soil and powder, granulated wettable powder or granules, for example, mixed with ground soil, mixed with soil covering, mixed with the entire soil. Simply, the soil and various preparations may be applied alternately in layers.
- the time of application at the time of sowing may be before sowing, at the same time, after sowing, or after soil covering.
- seed treatment such as dressing and soaking on seeds or treatment on a cultivation carrier close to a plant body is preferable from sowing to raising seedling.
- treatment on a cultivation carrier in the vicinity of the plant being cultivated is suitable. It is possible to perform spraying treatment using a granule or irrigation treatment in a liquid of a drug diluted or not diluted in water.
- the irrigation treatment of the liquid drug or the granule spraying treatment to the nursery seedling bed is preferable.
- a granule is processed into a planting hole at the time of planting or is mixed with a cultivation carrier in the vicinity of the transplantation site.
- the agricultural and horticultural pest control composition of the present invention is generally used in a form convenient for use according to a conventional method for agricultural chemical preparations. That is, the 4-cyclopropyl-1,2,3-thiadiazole derivative represented by the general formula (I) or a salt thereof is suitable for use with a suitable inert carrier or with an auxiliary agent as necessary.
- dissolved, separated, suspended, mixed, impregnated, adsorbed or adhered to appropriate dosage forms such as suspensions, emulsions, solutions, wettable powders, granules, powders, tablets, seed coatings, etc. In that case, it may be used after being formulated into a suspension or liquid suitable for treatment such as spraying, coating, and immersion.
- the inert carrier that can be used in the agricultural and horticultural pest control composition used in the present invention may be either solid or liquid.
- materials that can be used as the solid carrier include soybean flour, cereal flour, and wood. Powder, bark powder, saw powder, tobacco stem powder, walnut shell powder, bran, fiber powder, residues after extraction of plant extracts, synthetic polymers such as ground synthetic resin, clays (eg kaolin, bentonite, acid clay) , Talc (eg, talc, pyrophyllite, etc.), silica (eg, diatomaceous earth, silica sand, mica, white carbon (synthetic highly dispersed silicic acid, also called hydrous finely divided silicon, hydrous silicic acid, and some products contain calcium silicate as the main component) .) ⁇ , Inorganic mineral powders such as activated carbon, sulfur powder, pumice, calcined diatomaceous earth, brick ground, fly ash, sand, calcium carbonate, calcium phosphate Ammonium
- the material that can be used as a liquid carrier is not particularly limited as long as it has a solvent ability, but can also disperse an active ingredient compound with the aid of an auxiliary agent without having a solvent ability.
- a liquid carrier for example, water, alcohol (Eg, methanol, ethanol, isopropanol, butanol, ethylene glycol, etc.), ketones (eg, acetone, methyl ethyl ketone, methyl isobutyl ketone, diisobutyl ketone, cyclohexanone, etc.), ethers (eg, ethyl ether, dioxane, cellosolve, dipropyl ether, Tetrahydrofuran, etc.), aliphatic hydrocarbons (eg kerosene, mineral oil, etc.), aromatic hydrocarbons (eg benzene, toluene, xylene, solvent naphtha, alkylnaphthalene, etc.), hal
- adjuvants can be used depending on the purpose. These adjuvants may be used alone, in some cases, two or more kinds of adjuvants may be used in combination, and in some cases, no adjuvant may be used.
- a surfactant is used as an auxiliary agent for the purpose of emulsifying, dispersing, solubilizing and / or wetting the active ingredient compound, for example, polyoxyethylene alkyl ether, polyoxyethylene alkyl aryl ether.
- Polyoxyethylene higher fatty acid ester Polyoxyethylene resin acid ester, polyoxyethylene sorbitan monolaurate, polyoxyethylene sorbitan monooleate, alkyl aryl sulfonate, naphthalene sulfonic acid condensate, lignin sulfonate, higher Surfactants such as alcohol sulfates are listed.
- auxiliary agents for example, casein, gelatin, starch, methylcellulose, carboxymethylcellulose, gum arabic,
- adjuvants such as polyvinyl alcohol, pine oil, coconut oil, bentonite, and lignin sulfonate.
- the following adjuvants may be used, and for example, adjuvants such as waxes, stearates and alkyl phosphates may be used.
- adjuvants such as waxes, stearates and alkyl phosphates
- auxiliary agents such as naphthalenesulfonic acid condensate and condensed phosphate can be used.
- an auxiliary agent such as silicone oil can be used.
- the pesticide composition for agricultural and horticultural use used in the present invention further includes other pesticides for agricultural and horticultural use for the purpose of controlling the target pests to be controlled, the appropriate control period, or reducing the dose and synergistic effects. It can be used in combination with herbicides, nematicides, fungicides, biological pesticides, etc., and can be used in combination with herbicides, plant growth regulators, fertilizers, etc. Is possible.
- the agricultural and horticultural pest control composition used in the method of use of the present invention can be mixed or used in combination with other components as necessary.
- Repellents include, for example, odorous compounds such as naphthalene compounds, contact inhibitors such as castor oil, pine resin, polybutane, diphenylamine pentachlorophenol, quinone, zinc oxide, aromatic solvents, N- (trichloromethylthio) -4-cyclohexene- Bitter substances such as 1,2-carboximide, anthraquinone, copper oxalate, terpene oil, paradichlorobenzene, aryl isothiocyanate, amyl acetate, anethole, citrus oil, cresols, geranium oil or lavender oil, Menthol, methyl salicylate, nicotine, pentanethiol, pyridines, tribut
- toxic substances or growth inhibitory substances include, for example, 3-chloro-4-toluidine hydrochloride, strychnine, 20,25-diazacholesterol hydrochloride (code name: SC-12937), etc. Can be illustrated.
- the sum of the content of the compound having insecticidal activity may be appropriately selected from the range of about 0.01 to about 80 parts by mass in 100 parts by mass of the agricultural and horticultural pest control composition.
- about 0.01 to about 50 parts by mass is appropriate, preferably Is preferably about 1 to about 50 parts by weight.
- the compounding ratio of the compound having bactericidal activity and / or insecticidal activity with respect to 1 part by mass of the 4-cyclopropyl-1,2,3-thiadiazole derivative represented by the general formula (I) or a salt thereof is about 0. It is blended in the range of 01 to about 1000 parts by weight, and is preferably in the range of about 0.05 to about 100 parts by weight, more preferably about 0. It is in the range of 1 to about 100 parts by weight.
- the application rate of the agricultural and horticultural pest control composition varies depending on the compounding ratio of the active ingredient compound, meteorological conditions, formulation form, application time, application method, application location, target disease, target crop, etc.
- an active ingredient compound it may be applied by appropriately selecting from about 0.1 g to about 1000 g per are, and preferably in the range of about 1 to about 100 g.
- the seed treatment agent is usually selected from the range of about 0.1 to about 1000 g as an active ingredient compound per 100 kg of seed weight, and is preferably applied in the range of about 1 to about 300 g.
- the 4-cyclopropyl-1,2,3-thiadiazole derivative represented by the general formula (I) or a salt thereof, which is an active ingredient of the agricultural and horticultural pest control composition of the present invention bactericidal activity and / or
- bactericidal activity an active ingredient of the agricultural and horticultural pest control composition of the present invention
- a synergistic effect of a propyl-1,2,3-thiadiazole derivative or a salt thereof and a compound having bactericidal activity and / or insecticidal activity can be exhibited.
- a 4-cyclopropyl-1,2,3-thiadiazole derivative represented by the general formula (I) or a salt thereof and a compound having a bactericidal activity and / or an insecticidal activity alone, or a dilution thereof The liquid may be mixed and applied at the time of treatment at the site of use, and further, the plant foliage, seeds, cultivation carrier and the like may be treated separately at the same time.
- each when each is applied separately separately, it may be applied at the same time, and an interval of about 7 days may be provided, but at the time when any one of the active ingredients remains in the plant or the cultivation carrier, the other.
- the above-mentioned “simultaneous period” is a concept including that at least a part of the period during which both are treated as described above, and the application work is not necessarily performed at the same time. There is no need.
- One or more effective compounds of such a 4-cyclopropyl-1,2,3-thiadiazole derivative represented by the general formula (I) or a salt thereof and a compound having fungicidal activity and / or insecticidal activity are each independently used in the plant foliage, seeds or cultivation carrier.
- a method for controlling plant diseases to be treated is also one aspect of the present invention.
- the above-mentioned agricultural and horticultural pest control composition It is the same as in the product.
- each compound number represents a compound number described in Table 1, and “part” represents “part by mass”.
- Test Example 1 Wheat powdery mildew control effect test by mixing seed treatment agent 0.1 g of water is applied to 5 g of wheat (variety: Chihoku wheat) seeds (dried state), and the water treatment with the treatment dosage shown in the table is applied to the water. The seeds were treated so as to adhere uniformly. The treated seeds were air-dried and then sown in a plastic pot having a diameter of 10 cm and cultivated in a greenhouse. When the wheat grew at the 6th leaf stage / parting stage (after about 70 days), the wheat was inoculated with spores of powdery mildew (Blumeria graminis). Seven days after the inoculation, the disease index and the control value (%) of the developed leaves were calculated according to the following criteria. At this time, the disease index of the untreated section was 5.0. The results are shown in Tables 3 and 4.
- “ga.i./100 Kg seed” means the amount (g) of active ingredient (Active Ingredient) used per 100 kg seed (hereinafter, Tables 4 to 6 are also the same).
- Test Example 2 Wheat red rust control effect test by mixed seed treatment (greenhouse test) According to the method described in Test Example 1, wheat (variety: chihoku wheat) seeds (dried state) were treated and cultivated. At the time when the wheat grew at the 6-leaf stage / parting stage (about 70 days after sowing), the wheat was spray-inoculated with a spore suspension of Puccinia recondita. Seven days after the inoculation, the disease index and the control value (%) of the developed leaves were calculated according to the criteria of Test 1. The results are shown in Tables 5 and 6.
- Test Example 3 Wheat powdery mildew control effect test by mixing seed treatment agent (field test) Compound 1-93 and the control compound were mixed so as to have the treatment doses shown in the table, and treated so as to uniformly adhere to the dried seeds of wheat (variety: Chihoku wheat).
- the seeding amount was equivalent to 120 kg / ha, and the above seeds were sown in a 2 m 2 (1 m ⁇ 2 m) section.
- the incidence index of the naturally occurring powdery mildew (Blumeria graminis) on the following leaves and leaves according to the criteria of Test Example 1 was calculated. Investigation was made and the control value (%) was calculated.
- Test Example 4 Wheat red rust control effect test by mixing seed treatment agent (field test) Compound 1-93 and the control compound were mixed so as to have the treatment doses shown in the table, and treated so as to uniformly adhere to the dried seeds of wheat (variety: Hokushin). The seeding amount was equivalent to 120 kg / ha, and the above seeds were sown in a 2 m 2 (1 m ⁇ 2 m) section. In the next year when wheat emerges (around BBCH 51-59, approximately 190 to 200 days after sowing), the incidence index of naturally occurring red rust fungus (Puccinia recondita) is determined for the following leaves and leaves in accordance with the criteria of Test Example 1. Investigation was made and the control value (%) was calculated.
- the compound of the present invention is intended to control a disease for a very long period from the growing season to the late stage of the plant only by applying it to the seed of the target plant or a carrier for seeding the target plant. .
- the compound of the present invention combines all of these elements.
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Abstract
A pest control agent composition for agricultural and horticultural use, which has a broad bactericidal/pesticidal spectrum with respect to various plant diseases/pests, and exhibits excellent control effect with a small amount. The pest control agent composition for agricultural and horticultural use is characterized by containing, as active ingredients, a 4-cyclopropyl-1,2,3-thiadiazole derivative represented by general formula (I) or a salt thereof, and one or more compounds having a bactericidal activity and/or a pesticidal activity.
Description
本発明は4-シクロプロピル-1,2,3-チアジアゾール誘導体又はその塩類と、殺菌活性又は殺虫活性を有する化合物の1種又は2種以上とを有効成分として含有することを特徴とする農園芸用病害虫防除剤組成物に関する。
The present invention includes a 4-cyclopropyl-1,2,3-thiadiazole derivative or a salt thereof, and one or more compounds having fungicidal or insecticidal activity as active ingredients. The present invention relates to a pest control composition for use.
農業及び園芸等の作物生産は病害並びに害虫等による被害が今なお大きく、また既存薬に対する微生物、菌類又は害虫の薬剤抵抗性の要因から新規な農園芸用殺菌殺虫防除剤組成物の開発が望まれている。このため、これまで数多くの農園芸用病害虫防除剤組成物がそれぞれの薬剤の性質に応じて研究、開発されている。近年就農者の老齢化等により各種の省力的な施用方法や地球環境保全の目的から使用薬量の低減が求められており、これらの目的に適した農園芸用殺菌殺虫防除剤組成物の創出が強く求められている。
Agricultural and horticultural crop production is still severely affected by diseases and pests, and the development of a new agricultural and horticultural fungicidal insecticide control composition is desired due to factors such as the resistance of microorganisms, fungi or pests to existing drugs. It is rare. For this reason, many agricultural and horticultural pest control compositions have been researched and developed according to the properties of the respective drugs. In recent years, due to the aging of farmers, etc., it has been required to reduce the amount of drugs used for various labor-saving application methods and the purpose of global environmental protection, and creation of agricultural and horticultural fungicidal insecticide control compositions suitable for these purposes Is strongly demanded.
このような状況下、農園芸用殺菌防除剤としては、ある種の1,2,3-チアジアゾール誘導体が有用であることが知られている(例えば、特許文献1参照。)。しかしながら、本発明の一般式(I)で表される4-シクロプロピル-1,2,3-チアジアゾール誘導体と他の殺菌防除剤又は殺虫防除剤とを組み合わせた組成物に関する記載は無く、示唆もされていない。
Under such circumstances, it is known that certain 1,2,3-thiadiazole derivatives are useful as agricultural and horticultural fungicides (see, for example, Patent Document 1). However, there is no description or suggestion regarding a composition in which the 4-cyclopropyl-1,2,3-thiadiazole derivative represented by the general formula (I) of the present invention is combined with other fungicides or insecticides. It has not been.
従来技術の化合物は単独では農園芸用殺菌剤・殺虫剤(殺菌剤及び/又は殺虫剤を意味する。以下同じ。)として、その効力や防除スペクトラムの点で必ずしも十分ではなかった。近年、地球環境保護の観点から、投下薬剤量の低減や効率的な植物病害・害虫(植物病害及び/又は害虫を意味する。以下同じ。)の防除を目的として、殺菌・殺虫(殺菌及び/又は殺虫を意味する。以下同じ。)スペクトラムの補完や相乗効果を有する混合剤の組合せが報告されている。しかしながら、混合する種類によっては拮抗作用を生じ、相加効果程度の効果しか得られない場合もあり、最適な組合せを見出すには試行錯誤を繰り返すしかないのが現状である。従って、種々の植物病害・害虫に対して広い殺菌・殺虫スペクトラムを有し、低薬量で優れた防除効果を示す農園芸用病害虫防除剤組成物の開発が望まれていた。
本発明は種々の植物病害及び/又は害虫に対して広い殺菌及び/又は殺虫スペクトラムを有し、低薬量で優れた防除効果を示す農園芸用病害虫防除剤組成物を提供することを目的とする。 Prior art compounds alone are not necessarily sufficient in terms of their efficacy and control spectrum as agricultural and horticultural fungicides and insecticides (meaning fungicides and / or insecticides; the same shall apply hereinafter). In recent years, from the viewpoint of protecting the global environment, sterilization and insecticide (sterilization and / or pesticides) are aimed at reducing the amount of drugs to be dropped and controlling plant diseases and pests (meaning plant diseases and / or pests; the same shall apply hereinafter). (This also applies to insecticides. The same shall apply hereinafter.) Combinations of admixtures that have spectrum complementation and synergistic effects have been reported. However, depending on the type of mixing, an antagonistic action may be produced, and only an effect of an additive effect may be obtained. At present, trial and error must be repeated to find an optimal combination. Therefore, it has been desired to develop a pest control composition for agricultural and horticultural use that has a broad bactericidal and insecticidal spectrum against various plant diseases and pests and exhibits an excellent control effect at a low dose.
It is an object of the present invention to provide a pest control composition for agricultural and horticultural use having a broad bactericidal and / or insecticidal spectrum against various plant diseases and / or pests and exhibiting an excellent control effect at a low dose. To do.
本発明は種々の植物病害及び/又は害虫に対して広い殺菌及び/又は殺虫スペクトラムを有し、低薬量で優れた防除効果を示す農園芸用病害虫防除剤組成物を提供することを目的とする。 Prior art compounds alone are not necessarily sufficient in terms of their efficacy and control spectrum as agricultural and horticultural fungicides and insecticides (meaning fungicides and / or insecticides; the same shall apply hereinafter). In recent years, from the viewpoint of protecting the global environment, sterilization and insecticide (sterilization and / or pesticides) are aimed at reducing the amount of drugs to be dropped and controlling plant diseases and pests (meaning plant diseases and / or pests; the same shall apply hereinafter). (This also applies to insecticides. The same shall apply hereinafter.) Combinations of admixtures that have spectrum complementation and synergistic effects have been reported. However, depending on the type of mixing, an antagonistic action may be produced, and only an effect of an additive effect may be obtained. At present, trial and error must be repeated to find an optimal combination. Therefore, it has been desired to develop a pest control composition for agricultural and horticultural use that has a broad bactericidal and insecticidal spectrum against various plant diseases and pests and exhibits an excellent control effect at a low dose.
It is an object of the present invention to provide a pest control composition for agricultural and horticultural use having a broad bactericidal and / or insecticidal spectrum against various plant diseases and / or pests and exhibiting an excellent control effect at a low dose. To do.
本発明者等は上記課題に対処すべく、鋭意研究を重ねた結果、本発明の一般式(I)で表される4-シクロプロピル-1,2,3-チアジアゾール誘導体又はその塩類と、他の殺菌及び/又は殺虫活性を有する化合物の1種又は2種以上とを有効成分として含有する農園芸用病害虫防除剤組成物が相加的な防除効果を示すのみならず、極めて広い殺菌・殺虫スペクトラムを有することを見出し、本発明を完成させるに至った。
As a result of intensive studies to address the above problems, the present inventors have found that the 4-cyclopropyl-1,2,3-thiadiazole derivative represented by the general formula (I) of the present invention or a salt thereof, and the like The pesticide composition for agricultural and horticultural use containing as an active ingredient one or more compounds having an antibacterial and / or insecticidal activity as well as an extremely broad bactericidal and insecticidal effect It has been found that it has a spectrum, and the present invention has been completed.
即ち、本発明は
[1]一般式(I): That is, the present invention
[1] General formula (I):
[1]一般式(I): That is, the present invention
[1] General formula (I):
{式中、R1、R2、R3、R4及びR5はそれぞれ同一又は異なっても良く、水素原子;ハロゲン原子又は(C1-C3)アルキル基を示す。
R6は水素原子;(C1-C8)アルキル基;(C3-C6)シクロアルキル基;フェニル(C1-C6)アルキル基;ハロゲン原子、シアノ基、(C1-C6)アルキル基、ハロ(C1-C6)アルキル基、(C3-C6)シクロアルキル基、ハロ(C3-C6)シクロアルキル基、(C1-C6)アルコキシ基、ハロ(C1-C6)アルコキシ基、カルボキシル基及び(C1-C6)アルコキシカルボニル基からなる群より選択される1または同一もしくは異なっても良い2以上の置換基を有する置換フェニル(C1-C6)アルキル基;フェニル基又はハロゲン原子、シアノ基、(C1-C6)アルキル基、ハロ(C1-C6)アルキル基、(C3-C6)シクロアルキル基、ハロ(C3-C6)シクロアルキル基、(C1-C6)アルコキシ基、ハロ(C1-C6)アルコキシ基、カルボキシル基及び(C1-C6)アルコキシカルボニル基からなる群より選択される1または同一もしくは異なっても良い2以上の置換基を有する置換フェニル基を示す。
Yは酸素原子又は-N(R7)-(式中、R7は水素原子、(C1-C6)アルキル基又は(C3-C6)シクロアルキル基を示す。)
Wは酸素原子又は硫黄原子を示す。}で表される4-シクロプロピル-1,2,3-チアジアゾール誘導体若しくはその塩類と、殺菌活性及び/又は殺虫活性を有する化合物の1種又は2種以上とを有効成分として含有することを特徴とする農園芸用病害虫防除剤組成物、
[2]殺菌活性を有する化合物がビテルタノール、ブロムコナゾール、シプロコナゾール、ジフェノコナゾール、ジニコナゾール、エニルコナゾール、エポキシコナゾール、フルキンコナゾール、フェンブコナゾール、フルシラゾール、フルトリアホール、ヘキサコナゾール、イミベンコナゾール、イプコナゾール、メトコナゾール、ミクロブタニル、ペンコナゾール、プロピコナゾール、プロチオコナゾール、シメコナゾール、トリアジメホン、トリアジメノール、テブコナゾール、テトラコナゾール、トリチコナゾール、プロクロラズ、ペフラゾエート、イマザリル、トリフルミゾール、シアゾファミド、ベノミル、カルベンダジム、チアベンダゾール、フベリダゾール、エタボキサム、エトリジアゾール、オキスポコナゾールフマル酸、ヒメキサゾール、アゾキシストロビン、ジモキシストロビン、エネストロブリン、フルオキサストロビン、クレソキシムメチル、メトミノストロビン、オリザストロビン、ピコキシストロビン、ピラクロストロビン、トリフロキシストロビン、カルボキシン、ベナラキシル、ボスカリド、ビキサフェン、フェンヘキサミド、フルトラニル、フラメトピル、メプロニル、メタラキシル、メフェノキサム、オフラセ、オキサジキシル、オキシカルボキシン、ペンチオピラド、チフルザミド、チアジニル、ジメトモルフ、フルモルフ、フルメトベル、フルオピコリド、カルプロパミド、ジクロシメット、マンジプロパミド、フルアジナム、ピリフェノックス、ブピリメート、シプロジニル、フェナリモル、フェリムゾン、メパニピリム、ヌアリモール、ピリメタニル、トリホリン、フェンピクロニル、フルジオキソニル、アルジモルフ、ドデモルフ、フェンプロピモルフ、トリデモルフ、フェンプロピジン、イプロジオン、プロシミドン、ビンクロゾリン、ファモキサドン、フェナミドン、オクチリノン、プロベナゾール、アニラジン、ジクロメジン、ピロキロン、プロキナジド、トリシクラゾール、カプタホル、キャプタン、ダゾメット、ホルペット、フェノキサニル、キノキシフェン、アミスルブロム、マンゼブ、マンネブ、メタム、メチラム、ファーバム、プロピネブ、チウラム、ジネブ、ジラム、ジエトフェンカルブ、イプロバリカルブ、ベンチアバリカルブイソプロピル、プロパモカルブ塩酸塩、チオファネートメチル、ピリベンカルブ、ボルドー液、塩基性塩化銅、塩基性硫酸銅、水酸化第二銅、8-ヒドロキシキノリン銅、ドジン、イミノクタジンアルベシル酸塩、イミノクタジン酢酸塩、グアザチン、カスガマイシン、ストレプトマイシン、ポリオキシン、オキシテトラサイクリン、バリダマイシンA、ビナパクリル、ジノカップ、ジノブトン、ジチアノン、イソプロチオラン、エジフェンホス、イプロベンホス、ホセチル、ホセチルアルミニウム、ピラゾホス、トルクロホスメチル、クロロタロニル、ジクロフルアニド、フルスルファミド、ヘキサクロロベンゼン、フサライド、ペンシクロン、キントゼン、シフルフェナミド、シモキサニル、ジメチリモール、エチリモール、フララキシル、メトラフェノン、スピロキサミン、アンバム、硫黄、石灰硫黄合剤、エクロメゾール、炭酸水素カリウム、炭酸水素カルシウム、チアジアジン、テクロフタラム、トリアジン、ノニルフェノールスルホン酸銅、ヒドロキシイソキサゾール、フルオルイミド、ポリカーバメート、メタスルホカルブ、EDDP、IBP、トルフェンピラド、フルオピラム、イソチアニル又はイソピラザムより選択される1種又は2種以上である[1]に記載の農園芸用殺菌防除剤組成物、
[3]殺虫活性を有する化合物が、アセタミプリド、ピメトロジン、フェニトロチオン、アセフェート、カルバリル、メソミル、カルタップ、シハロトリン、エトフェンプロックス、テフルベンズロン、フルベンジアミド、フルフェノクスロン、テブフェノジド、フェンピロキシメート、ピリダベン、イミダクロプリド、ブプロフェジン、BPMC、MIPC、マラチオン、メチダチオン、フェンチオン、ダイアジノン、オキシデプロホス、バミドチオン、エチオフェンカルブ、ピリミカーブ、ペルメトリン、シペルメトリン、ビフェントリン、ハルフェンプロックス、シラフルオフェン、ニテンピラム、クロルフルアズロン、メトキシフェノジド、テブフェンピラド、ピリミジフェン、ケルセン、プロパルギット、ヘキシチアゾクス、クロフェンテジン、スピノサド、ミルベメクチン、BT(Bacillus thuringiensis)、インドキサカルブ、メタフルミゾン、クロルフェナピル、フィプロニル、エトキサゾール、アセキノシル、ピリミホスメチル、アクリナトリン、キノメチオネート、クロルピリホス、アバメクチン、エマメクチン安息香酸塩、酸化フェンブタスズ、テルブホス、エトプロホス、カズサホス、フェナミフォス、フェンスルフォチオン、DSP、ジクロフェンチオン、ホスチアゼート、オキサミル、イサミドホス、ホスチエタン、イサゾホス、チオナジン、ベンフラカルブ、スピロジクロフェン、エチオフェンカルブ、アジンホス・メチル、ジスルホトン、メチオカルブ、オキシジメトン・メチル、パラチオン、シフルトリン、ベータ・シフルトリン、テブピリムホス、スピロメシフェン、エンドスルファン、アミトラズ、トラロメトリン、アセトプロール、エチプロール、エチオン、トリクロルホン、メタミドホス、ジクロルボス、メビンホス、モノクロトホス、ジメトエート、フォルメタネート、ホルモチオン、メカルバム、チオメトン、ジスルホトン、ナレッド、メチルパラチオン、シアノホス、ジアミダホス、アルベンダゾール、オキシベンダゾール、フェンベンダゾール、オクスフェンダゾール、プロパホス、スルプロホス、プロチオホス、プロフェノホス、イソフェンホス、テメホス、フェントエート、ジメチルビンホス、クロルフェビンホス、テトラクロルビンホス、ホキシム、イソキサチオン、ピラクロホス、クロルピリホス、ピリダフェンチオン、ホサロン、ホスメット、ジオキサベンゾホス、キナルホス、ピレトリン、アレスリン、プラレトリン、レスメトリン、ペルメトリン、テフルトリン、フェンプロパトリン、アルファシペルメトリン、ラムダ・シハルトリン、デルタメトリン、フェンバレレート、エスフェンバレレート、フルシトリネート、フルバリネート、シクロプロトリン、チオジカルブ、アルジカルブ、アラニカルブ、メトルカルブ、キシリカルブ、プロポキスル、フェノキシカルブ、フェノチオカルブ、ビフェナゼート、カルボフラン、カルボスルファン、硫黄、ピリフルキナゾン、フラチオカルブ、ジアフェンチウロン、ジフルベンズロン、ヘキサフルムロン、ノバルロン、ルフェヌロン、クロルフルアズロン、水酸化トリシクロヘキシルスズ、オレイン酸ナトリウム、オレイン酸カリウム、メトプレン、ハイドロプレン、ビナパクリル、アミトラズ、クロルベンジレート、フェニソブロモレート、テトラジホン、ベンスルタップ、ベンゾメート、クロマフェノジド、ハロフェノジド、エンドスルファン、ジオフェノラン、トルフェンピラド、トリアザメート、硫酸ニコチン、チアクロプリド、チアメトキサム、クロチアニジン、ジノテフラン、フルアジナム、ピリプロキシフェン、フルアクリピリム、ヒドラメチルノン、シロマジン、TPIC、チオシクラム、フェナザキン、ポリナクチン複合体、アザディラクチン、ロテノン、ヒドロキシプロピルデンプン、メスルフェンホス、ホスホカルブ、イソアミドホス、アルドキシカルブ、メタム・ナトリウム、酒石酸モランテル、ダゾメット、塩酸レバミゾール、トリクラミド、トルフェンピラド、ピリダリル、クロラントラニリプロール、シエノピラフェン又はシフルメトフェンより選択される1種又は2種以上である[1]に記載の農園芸用病害虫防除剤組成物、
[4] [1]~[3]に記載の農園芸用病害虫防除剤組成物の有効量で当該病害及び/または害虫の発生が予測される対象植物、対象植物の種子、種子を播種するための栽培担体又は土壌を処理することを特徴とする農園芸用病害虫防除剤組成物の使用方法、及び
[5]処理が農園芸用病害虫防除剤組成物溶液への対象植物の種子の浸漬又は農園芸用病害虫防除剤組成物による種子の粉衣等の種子処理又は植物体に近接する土壌もしくは栽培担体の処理である[4]に記載の農園芸用病害虫防除剤組成物の使用方法に関する。 {Wherein R 1 , R 2 , R 3 , R 4 and R 5 may be the same or different and each represents a hydrogen atom; a halogen atom or a (C 1 -C 3 ) alkyl group.
R 6 is a hydrogen atom; (C 1 -C 8 ) alkyl group; (C 3 -C 6 ) cycloalkyl group; phenyl (C 1 -C 6 ) alkyl group; halogen atom, cyano group, (C 1 -C 6 ) Alkyl group, halo (C 1 -C 6 ) alkyl group, (C 3 -C 6 ) cycloalkyl group, halo (C 3 -C 6 ) cycloalkyl group, (C 1 -C 6 ) alkoxy group, halo ( A substituted phenyl having one or more substituents which may be the same or different, selected from the group consisting of a C 1 -C 6 ) alkoxy group, a carboxyl group and a (C 1 -C 6 ) alkoxycarbonyl group (C 1- C 6 ) alkyl group; phenyl group or halogen atom, cyano group, (C 1 -C 6 ) alkyl group, halo (C 1 -C 6 ) alkyl group, (C 3 -C 6 ) cycloalkyl group, halo (C 3 - 6) cycloalkyl, (C 1 -C 6) alkoxy groups, halo (C 1 -C 6) alkoxy groups, 1 or the same is selected from a carboxyl group and (C 1 -C 6) alkoxy group consisting of a carbonyl group Or the substituted phenyl group which has two or more substituents which may differ may be shown.
Y represents an oxygen atom or —N (R 7 ) — (wherein R 7 represents a hydrogen atom, a (C 1 -C 6 ) alkyl group or a (C 3 -C 6 ) cycloalkyl group).
W represents an oxygen atom or a sulfur atom. And a salt thereof and one or more compounds having bactericidal activity and / or insecticidal activity as active ingredients Agro-horticultural pest control composition,
[2] Compounds having bactericidal activity are vitertanol, bromconazole, cyproconazole, difenoconazole, diniconazole, enilconazole, epoxiconazole, fluquinconazole, fenbuconazole, flusilazole, flutriahol, hexaconazole, imi Benconazole, ipconazole, metconazole, microbutanyl, penconazole, propiconazole, prothioconazole, cimeconazole, triadimethone, triadimenol, tebuconazole, tetraconazole, triticonazole, prochloraz, pefrazate, imazalyl, triflumizole, ciazofamide, miazofamide , Carbendazim, thiabendazole, fuberidazole, ethaboxam, etridiazole, oxpoconazole fumarate, Mexazole, azoxystrobin, dimoxystrobin, enestrobrin, floxastrobin, cresoxime methyl, metminostrobin, orizastrobin, picoxystrobin, pyraclostrobin, trifloxystrobin, carboxin, benalaxyl, Boscalid, bixafen, fenhexamide, flutolanil, furametopyr, mepronil, metalaxyl, mefenoxam, ofrase, oxadixyl, oxycarboxyl, pentiopyrad, tifluzamide, thiazinyl, dimethomorph, flumorph, flumetober, flupicoride, carpropamide, diclopimeflumman Knox, bupirimate, cyprodinil, phenalimol, ferrimzone, mepanipyrim, nuarimol , Pyrimethanil, triphorine, fenpicuronyl, fludioxonil, aldimorph, dodemorph, fenpropimorph, tridemorph, fenpropidin, iprodione, procymidone, vinclozoline, famoxadone, fenamidone, octyrinone, probenazole, anilazine, diclomedine, pyroxidan , Dazomet, Holpet, Phenoxanyl, Quinoxifene, Amisulbrom, Manzeb, Manneb, Metam, Methylam, Farbum, Propineb, Thiuram, Dinebu, Zyram, Dietofencarb, Iprovalicarb, Benchavalicarb isopropyl, Propamocarb hydrochloride, Thiophanate methyl, Pyricarb solution Copper chloride, basic sulfuric acid , Cupric hydroxide, 8-hydroxyquinoline copper, dodine, iminotadine albecylate, iminotadine acetate, guazatine, kasugamycin, streptomycin, polyoxin, oxytetracycline, validamycin A, vinapacryl, dinocup, dinobutone, dithianone, isoprothiolane, edifenphos , Iprobenfos, fosetyl, fosetylaluminum, pyrazophos, tolcrofosmethyl, chlorothalonil, diclofluuride, fursulfamide, hexachlorobenzene, fusaride, pencyclon, quintozen, cyflufenamide, simoxanyl, dimethylmethylol, ethylimole, flaxyl, metolaphenone, spiroxamine, sulfur, lime, sulfur Mixture, echromesole, potassium bicarbonate, bicarbonate One or more selected from the group consisting of sium, thiadiazine, teclophthalam, triazine, copper nonylphenol sulfonate, hydroxyisoxazole, fluoroimide, polycarbamate, metasulfocarb, EDDP, IBP, tolfenpyrad, fluopyram, isothianyl or isopyrazam The agricultural and horticultural fungicidal composition according to [1],
[3] Compounds having insecticidal activity include acetamiprid, pymetrozine, fenitrothion, acephate, carbaryl, mesomil, cartap, cyhalothrin, etofenprox, teflubenzuron, fulvendiamide, flufenoxuron, tebufenozide, fenpyroximate, pyridaben, imidacloprid, MC , MIPC, malathion, methidathion, fenthion, diazinon, oxydeprophos, bamidthione, ethiophene carb, pirimicurve, permethrin, cypermethrin, bifenthrin, halfenprox, silafluophene, nitenpyram, chlorfluazuron, methoxyphenozide, tebufenpyrazel, pyrimidifen , Hexythiazox, kurofu Ntedine, spinosad, milbemectin, BT (Bacillus thuringiensis), indoxacarb, metaflumizone, chlorfenapyr, fipronil, etoxazole, acequinosyl, pirimiphosmethyl, acrinathrin, quinomethionate, chlorpyrifos, abamectin benzoate, emamectinphosate Fenamifos, Fencerfothion, DSP, Diclofenthion, Phosthiazate, Oxamyl, Isamidophos, Phoschietane, Isazofos, Thionazine, Benfuracarb, Spirodroclofen, Ethiophene Carb, Azinphos methyl, Disulfotone, Methiocarb, Oxydimethone methyl, Parathion, Cyfluthrin, Beta Phosphorus, Tebupyrimphos, Spiromesifene, Endosulfan, Amitraz, Tralomethrin, Acetoprole, Ethiprole, Ethion, Trichlorphone, Metamidophos, Dichlorvos, Mevinphos, Monocrotophos, Dimethoate, Formethanate, Formothione, Mecarbam, Thiometone, Disulfotone, Nared, Methylparathion Cyanophos, diamidazos, albendazole, oxybendazole, fenbendazole, oxfendazole, propaphos, sulprophos, prothiophos, profenofos, isofenphos, temefos, phentoate, dimethylvinphos, chlorfevinphos, tetrachlorvinphos, foxime, isoxathione , Pyracrofos, chlorpyrifos, pyridafenthione, hosalon, phosme , Dioxabenzophos, quinalphos, pyrethrin, allethrin, praretrin, resmethrin, permethrin, tefluthrin, phenpropatoline, alpha cypermethrin, lambda cycharthrin, deltamethrin, fenvalerate, esfenvalerate, flucitrinate, fulvalinate, Cycloprotonline, Thiodicarb, Aldicarb, Alanicarb, Metorcarb, Xilicarb, Propoxyl, Phenoxycarb, Fenothiocarb, Bifenazate, Carbofuran, Carbosulfan, Sulfur, Pyrifluquinazone, Furatiocarb, Difenthuron, Diflubenzuron, Hexaflumulone, Novaluron Chlorfluazuron, tricyclohexyltin hydroxide, sodium oleate, potassium oleate Um, metoprene, hydroprene, binapacryl, amitraz, chlorbenzilate, phenisobromolate, tetradiphone, bensultap, benzomate, chromafenozide, halophenozide, endosulfan, diophenolan, tolfenpyrad, triazamate, nicotine sulfate, thiacloprid, thiamethoxam, crothianidane , Pyriproxyfen, fluacrylpyrim, hydramethylnon, cyromazine, TPIC, thiocyclam, phenazaquin, polynactin complex, azadirachtin, rotenone, hydroxypropyl starch, mesulfenphos, phosphocarb, isoamidophos, aldoxycarb, metam sodium, morantel tartrate, Dazomet, levamisole hydrochloride, trichlami , Tolfenpyrad, pyridalyl, chlorantraniliprole, Shienopirafen or is one or more selected from cyflumetofen agricultural or horticultural pest control composition according to [1],
[4] To plant the target plant, the seed of the target plant, the seed of which the occurrence of the disease and / or the pest is predicted with an effective amount of the agricultural and horticultural pest control composition according to [1] to [3] A method for using a pest control composition for agricultural and horticultural use, characterized by treating a cultivation carrier or soil of
[5] Soil or cultivating carrier in which the treatment is soaking the seed of the target plant in the agricultural / horticultural pest control composition solution, seed treatment such as seed dressing with the agricultural / horticultural pest control composition, or the plant body It is related with the usage method of the agricultural and horticultural pest control composition as described in [4].
R6は水素原子;(C1-C8)アルキル基;(C3-C6)シクロアルキル基;フェニル(C1-C6)アルキル基;ハロゲン原子、シアノ基、(C1-C6)アルキル基、ハロ(C1-C6)アルキル基、(C3-C6)シクロアルキル基、ハロ(C3-C6)シクロアルキル基、(C1-C6)アルコキシ基、ハロ(C1-C6)アルコキシ基、カルボキシル基及び(C1-C6)アルコキシカルボニル基からなる群より選択される1または同一もしくは異なっても良い2以上の置換基を有する置換フェニル(C1-C6)アルキル基;フェニル基又はハロゲン原子、シアノ基、(C1-C6)アルキル基、ハロ(C1-C6)アルキル基、(C3-C6)シクロアルキル基、ハロ(C3-C6)シクロアルキル基、(C1-C6)アルコキシ基、ハロ(C1-C6)アルコキシ基、カルボキシル基及び(C1-C6)アルコキシカルボニル基からなる群より選択される1または同一もしくは異なっても良い2以上の置換基を有する置換フェニル基を示す。
Yは酸素原子又は-N(R7)-(式中、R7は水素原子、(C1-C6)アルキル基又は(C3-C6)シクロアルキル基を示す。)
Wは酸素原子又は硫黄原子を示す。}で表される4-シクロプロピル-1,2,3-チアジアゾール誘導体若しくはその塩類と、殺菌活性及び/又は殺虫活性を有する化合物の1種又は2種以上とを有効成分として含有することを特徴とする農園芸用病害虫防除剤組成物、
[2]殺菌活性を有する化合物がビテルタノール、ブロムコナゾール、シプロコナゾール、ジフェノコナゾール、ジニコナゾール、エニルコナゾール、エポキシコナゾール、フルキンコナゾール、フェンブコナゾール、フルシラゾール、フルトリアホール、ヘキサコナゾール、イミベンコナゾール、イプコナゾール、メトコナゾール、ミクロブタニル、ペンコナゾール、プロピコナゾール、プロチオコナゾール、シメコナゾール、トリアジメホン、トリアジメノール、テブコナゾール、テトラコナゾール、トリチコナゾール、プロクロラズ、ペフラゾエート、イマザリル、トリフルミゾール、シアゾファミド、ベノミル、カルベンダジム、チアベンダゾール、フベリダゾール、エタボキサム、エトリジアゾール、オキスポコナゾールフマル酸、ヒメキサゾール、アゾキシストロビン、ジモキシストロビン、エネストロブリン、フルオキサストロビン、クレソキシムメチル、メトミノストロビン、オリザストロビン、ピコキシストロビン、ピラクロストロビン、トリフロキシストロビン、カルボキシン、ベナラキシル、ボスカリド、ビキサフェン、フェンヘキサミド、フルトラニル、フラメトピル、メプロニル、メタラキシル、メフェノキサム、オフラセ、オキサジキシル、オキシカルボキシン、ペンチオピラド、チフルザミド、チアジニル、ジメトモルフ、フルモルフ、フルメトベル、フルオピコリド、カルプロパミド、ジクロシメット、マンジプロパミド、フルアジナム、ピリフェノックス、ブピリメート、シプロジニル、フェナリモル、フェリムゾン、メパニピリム、ヌアリモール、ピリメタニル、トリホリン、フェンピクロニル、フルジオキソニル、アルジモルフ、ドデモルフ、フェンプロピモルフ、トリデモルフ、フェンプロピジン、イプロジオン、プロシミドン、ビンクロゾリン、ファモキサドン、フェナミドン、オクチリノン、プロベナゾール、アニラジン、ジクロメジン、ピロキロン、プロキナジド、トリシクラゾール、カプタホル、キャプタン、ダゾメット、ホルペット、フェノキサニル、キノキシフェン、アミスルブロム、マンゼブ、マンネブ、メタム、メチラム、ファーバム、プロピネブ、チウラム、ジネブ、ジラム、ジエトフェンカルブ、イプロバリカルブ、ベンチアバリカルブイソプロピル、プロパモカルブ塩酸塩、チオファネートメチル、ピリベンカルブ、ボルドー液、塩基性塩化銅、塩基性硫酸銅、水酸化第二銅、8-ヒドロキシキノリン銅、ドジン、イミノクタジンアルベシル酸塩、イミノクタジン酢酸塩、グアザチン、カスガマイシン、ストレプトマイシン、ポリオキシン、オキシテトラサイクリン、バリダマイシンA、ビナパクリル、ジノカップ、ジノブトン、ジチアノン、イソプロチオラン、エジフェンホス、イプロベンホス、ホセチル、ホセチルアルミニウム、ピラゾホス、トルクロホスメチル、クロロタロニル、ジクロフルアニド、フルスルファミド、ヘキサクロロベンゼン、フサライド、ペンシクロン、キントゼン、シフルフェナミド、シモキサニル、ジメチリモール、エチリモール、フララキシル、メトラフェノン、スピロキサミン、アンバム、硫黄、石灰硫黄合剤、エクロメゾール、炭酸水素カリウム、炭酸水素カルシウム、チアジアジン、テクロフタラム、トリアジン、ノニルフェノールスルホン酸銅、ヒドロキシイソキサゾール、フルオルイミド、ポリカーバメート、メタスルホカルブ、EDDP、IBP、トルフェンピラド、フルオピラム、イソチアニル又はイソピラザムより選択される1種又は2種以上である[1]に記載の農園芸用殺菌防除剤組成物、
[3]殺虫活性を有する化合物が、アセタミプリド、ピメトロジン、フェニトロチオン、アセフェート、カルバリル、メソミル、カルタップ、シハロトリン、エトフェンプロックス、テフルベンズロン、フルベンジアミド、フルフェノクスロン、テブフェノジド、フェンピロキシメート、ピリダベン、イミダクロプリド、ブプロフェジン、BPMC、MIPC、マラチオン、メチダチオン、フェンチオン、ダイアジノン、オキシデプロホス、バミドチオン、エチオフェンカルブ、ピリミカーブ、ペルメトリン、シペルメトリン、ビフェントリン、ハルフェンプロックス、シラフルオフェン、ニテンピラム、クロルフルアズロン、メトキシフェノジド、テブフェンピラド、ピリミジフェン、ケルセン、プロパルギット、ヘキシチアゾクス、クロフェンテジン、スピノサド、ミルベメクチン、BT(Bacillus thuringiensis)、インドキサカルブ、メタフルミゾン、クロルフェナピル、フィプロニル、エトキサゾール、アセキノシル、ピリミホスメチル、アクリナトリン、キノメチオネート、クロルピリホス、アバメクチン、エマメクチン安息香酸塩、酸化フェンブタスズ、テルブホス、エトプロホス、カズサホス、フェナミフォス、フェンスルフォチオン、DSP、ジクロフェンチオン、ホスチアゼート、オキサミル、イサミドホス、ホスチエタン、イサゾホス、チオナジン、ベンフラカルブ、スピロジクロフェン、エチオフェンカルブ、アジンホス・メチル、ジスルホトン、メチオカルブ、オキシジメトン・メチル、パラチオン、シフルトリン、ベータ・シフルトリン、テブピリムホス、スピロメシフェン、エンドスルファン、アミトラズ、トラロメトリン、アセトプロール、エチプロール、エチオン、トリクロルホン、メタミドホス、ジクロルボス、メビンホス、モノクロトホス、ジメトエート、フォルメタネート、ホルモチオン、メカルバム、チオメトン、ジスルホトン、ナレッド、メチルパラチオン、シアノホス、ジアミダホス、アルベンダゾール、オキシベンダゾール、フェンベンダゾール、オクスフェンダゾール、プロパホス、スルプロホス、プロチオホス、プロフェノホス、イソフェンホス、テメホス、フェントエート、ジメチルビンホス、クロルフェビンホス、テトラクロルビンホス、ホキシム、イソキサチオン、ピラクロホス、クロルピリホス、ピリダフェンチオン、ホサロン、ホスメット、ジオキサベンゾホス、キナルホス、ピレトリン、アレスリン、プラレトリン、レスメトリン、ペルメトリン、テフルトリン、フェンプロパトリン、アルファシペルメトリン、ラムダ・シハルトリン、デルタメトリン、フェンバレレート、エスフェンバレレート、フルシトリネート、フルバリネート、シクロプロトリン、チオジカルブ、アルジカルブ、アラニカルブ、メトルカルブ、キシリカルブ、プロポキスル、フェノキシカルブ、フェノチオカルブ、ビフェナゼート、カルボフラン、カルボスルファン、硫黄、ピリフルキナゾン、フラチオカルブ、ジアフェンチウロン、ジフルベンズロン、ヘキサフルムロン、ノバルロン、ルフェヌロン、クロルフルアズロン、水酸化トリシクロヘキシルスズ、オレイン酸ナトリウム、オレイン酸カリウム、メトプレン、ハイドロプレン、ビナパクリル、アミトラズ、クロルベンジレート、フェニソブロモレート、テトラジホン、ベンスルタップ、ベンゾメート、クロマフェノジド、ハロフェノジド、エンドスルファン、ジオフェノラン、トルフェンピラド、トリアザメート、硫酸ニコチン、チアクロプリド、チアメトキサム、クロチアニジン、ジノテフラン、フルアジナム、ピリプロキシフェン、フルアクリピリム、ヒドラメチルノン、シロマジン、TPIC、チオシクラム、フェナザキン、ポリナクチン複合体、アザディラクチン、ロテノン、ヒドロキシプロピルデンプン、メスルフェンホス、ホスホカルブ、イソアミドホス、アルドキシカルブ、メタム・ナトリウム、酒石酸モランテル、ダゾメット、塩酸レバミゾール、トリクラミド、トルフェンピラド、ピリダリル、クロラントラニリプロール、シエノピラフェン又はシフルメトフェンより選択される1種又は2種以上である[1]に記載の農園芸用病害虫防除剤組成物、
[4] [1]~[3]に記載の農園芸用病害虫防除剤組成物の有効量で当該病害及び/または害虫の発生が予測される対象植物、対象植物の種子、種子を播種するための栽培担体又は土壌を処理することを特徴とする農園芸用病害虫防除剤組成物の使用方法、及び
[5]処理が農園芸用病害虫防除剤組成物溶液への対象植物の種子の浸漬又は農園芸用病害虫防除剤組成物による種子の粉衣等の種子処理又は植物体に近接する土壌もしくは栽培担体の処理である[4]に記載の農園芸用病害虫防除剤組成物の使用方法に関する。 {Wherein R 1 , R 2 , R 3 , R 4 and R 5 may be the same or different and each represents a hydrogen atom; a halogen atom or a (C 1 -C 3 ) alkyl group.
R 6 is a hydrogen atom; (C 1 -C 8 ) alkyl group; (C 3 -C 6 ) cycloalkyl group; phenyl (C 1 -C 6 ) alkyl group; halogen atom, cyano group, (C 1 -C 6 ) Alkyl group, halo (C 1 -C 6 ) alkyl group, (C 3 -C 6 ) cycloalkyl group, halo (C 3 -C 6 ) cycloalkyl group, (C 1 -C 6 ) alkoxy group, halo ( A substituted phenyl having one or more substituents which may be the same or different, selected from the group consisting of a C 1 -C 6 ) alkoxy group, a carboxyl group and a (C 1 -C 6 ) alkoxycarbonyl group (C 1- C 6 ) alkyl group; phenyl group or halogen atom, cyano group, (C 1 -C 6 ) alkyl group, halo (C 1 -C 6 ) alkyl group, (C 3 -C 6 ) cycloalkyl group, halo (C 3 - 6) cycloalkyl, (C 1 -C 6) alkoxy groups, halo (C 1 -C 6) alkoxy groups, 1 or the same is selected from a carboxyl group and (C 1 -C 6) alkoxy group consisting of a carbonyl group Or the substituted phenyl group which has two or more substituents which may differ may be shown.
Y represents an oxygen atom or —N (R 7 ) — (wherein R 7 represents a hydrogen atom, a (C 1 -C 6 ) alkyl group or a (C 3 -C 6 ) cycloalkyl group).
W represents an oxygen atom or a sulfur atom. And a salt thereof and one or more compounds having bactericidal activity and / or insecticidal activity as active ingredients Agro-horticultural pest control composition,
[2] Compounds having bactericidal activity are vitertanol, bromconazole, cyproconazole, difenoconazole, diniconazole, enilconazole, epoxiconazole, fluquinconazole, fenbuconazole, flusilazole, flutriahol, hexaconazole, imi Benconazole, ipconazole, metconazole, microbutanyl, penconazole, propiconazole, prothioconazole, cimeconazole, triadimethone, triadimenol, tebuconazole, tetraconazole, triticonazole, prochloraz, pefrazate, imazalyl, triflumizole, ciazofamide, miazofamide , Carbendazim, thiabendazole, fuberidazole, ethaboxam, etridiazole, oxpoconazole fumarate, Mexazole, azoxystrobin, dimoxystrobin, enestrobrin, floxastrobin, cresoxime methyl, metminostrobin, orizastrobin, picoxystrobin, pyraclostrobin, trifloxystrobin, carboxin, benalaxyl, Boscalid, bixafen, fenhexamide, flutolanil, furametopyr, mepronil, metalaxyl, mefenoxam, ofrase, oxadixyl, oxycarboxyl, pentiopyrad, tifluzamide, thiazinyl, dimethomorph, flumorph, flumetober, flupicoride, carpropamide, diclopimeflumman Knox, bupirimate, cyprodinil, phenalimol, ferrimzone, mepanipyrim, nuarimol , Pyrimethanil, triphorine, fenpicuronyl, fludioxonil, aldimorph, dodemorph, fenpropimorph, tridemorph, fenpropidin, iprodione, procymidone, vinclozoline, famoxadone, fenamidone, octyrinone, probenazole, anilazine, diclomedine, pyroxidan , Dazomet, Holpet, Phenoxanyl, Quinoxifene, Amisulbrom, Manzeb, Manneb, Metam, Methylam, Farbum, Propineb, Thiuram, Dinebu, Zyram, Dietofencarb, Iprovalicarb, Benchavalicarb isopropyl, Propamocarb hydrochloride, Thiophanate methyl, Pyricarb solution Copper chloride, basic sulfuric acid , Cupric hydroxide, 8-hydroxyquinoline copper, dodine, iminotadine albecylate, iminotadine acetate, guazatine, kasugamycin, streptomycin, polyoxin, oxytetracycline, validamycin A, vinapacryl, dinocup, dinobutone, dithianone, isoprothiolane, edifenphos , Iprobenfos, fosetyl, fosetylaluminum, pyrazophos, tolcrofosmethyl, chlorothalonil, diclofluuride, fursulfamide, hexachlorobenzene, fusaride, pencyclon, quintozen, cyflufenamide, simoxanyl, dimethylmethylol, ethylimole, flaxyl, metolaphenone, spiroxamine, sulfur, lime, sulfur Mixture, echromesole, potassium bicarbonate, bicarbonate One or more selected from the group consisting of sium, thiadiazine, teclophthalam, triazine, copper nonylphenol sulfonate, hydroxyisoxazole, fluoroimide, polycarbamate, metasulfocarb, EDDP, IBP, tolfenpyrad, fluopyram, isothianyl or isopyrazam The agricultural and horticultural fungicidal composition according to [1],
[3] Compounds having insecticidal activity include acetamiprid, pymetrozine, fenitrothion, acephate, carbaryl, mesomil, cartap, cyhalothrin, etofenprox, teflubenzuron, fulvendiamide, flufenoxuron, tebufenozide, fenpyroximate, pyridaben, imidacloprid, MC , MIPC, malathion, methidathion, fenthion, diazinon, oxydeprophos, bamidthione, ethiophene carb, pirimicurve, permethrin, cypermethrin, bifenthrin, halfenprox, silafluophene, nitenpyram, chlorfluazuron, methoxyphenozide, tebufenpyrazel, pyrimidifen , Hexythiazox, kurofu Ntedine, spinosad, milbemectin, BT (Bacillus thuringiensis), indoxacarb, metaflumizone, chlorfenapyr, fipronil, etoxazole, acequinosyl, pirimiphosmethyl, acrinathrin, quinomethionate, chlorpyrifos, abamectin benzoate, emamectinphosate Fenamifos, Fencerfothion, DSP, Diclofenthion, Phosthiazate, Oxamyl, Isamidophos, Phoschietane, Isazofos, Thionazine, Benfuracarb, Spirodroclofen, Ethiophene Carb, Azinphos methyl, Disulfotone, Methiocarb, Oxydimethone methyl, Parathion, Cyfluthrin, Beta Phosphorus, Tebupyrimphos, Spiromesifene, Endosulfan, Amitraz, Tralomethrin, Acetoprole, Ethiprole, Ethion, Trichlorphone, Metamidophos, Dichlorvos, Mevinphos, Monocrotophos, Dimethoate, Formethanate, Formothione, Mecarbam, Thiometone, Disulfotone, Nared, Methylparathion Cyanophos, diamidazos, albendazole, oxybendazole, fenbendazole, oxfendazole, propaphos, sulprophos, prothiophos, profenofos, isofenphos, temefos, phentoate, dimethylvinphos, chlorfevinphos, tetrachlorvinphos, foxime, isoxathione , Pyracrofos, chlorpyrifos, pyridafenthione, hosalon, phosme , Dioxabenzophos, quinalphos, pyrethrin, allethrin, praretrin, resmethrin, permethrin, tefluthrin, phenpropatoline, alpha cypermethrin, lambda cycharthrin, deltamethrin, fenvalerate, esfenvalerate, flucitrinate, fulvalinate, Cycloprotonline, Thiodicarb, Aldicarb, Alanicarb, Metorcarb, Xilicarb, Propoxyl, Phenoxycarb, Fenothiocarb, Bifenazate, Carbofuran, Carbosulfan, Sulfur, Pyrifluquinazone, Furatiocarb, Difenthuron, Diflubenzuron, Hexaflumulone, Novaluron Chlorfluazuron, tricyclohexyltin hydroxide, sodium oleate, potassium oleate Um, metoprene, hydroprene, binapacryl, amitraz, chlorbenzilate, phenisobromolate, tetradiphone, bensultap, benzomate, chromafenozide, halophenozide, endosulfan, diophenolan, tolfenpyrad, triazamate, nicotine sulfate, thiacloprid, thiamethoxam, crothianidane , Pyriproxyfen, fluacrylpyrim, hydramethylnon, cyromazine, TPIC, thiocyclam, phenazaquin, polynactin complex, azadirachtin, rotenone, hydroxypropyl starch, mesulfenphos, phosphocarb, isoamidophos, aldoxycarb, metam sodium, morantel tartrate, Dazomet, levamisole hydrochloride, trichlami , Tolfenpyrad, pyridalyl, chlorantraniliprole, Shienopirafen or is one or more selected from cyflumetofen agricultural or horticultural pest control composition according to [1],
[4] To plant the target plant, the seed of the target plant, the seed of which the occurrence of the disease and / or the pest is predicted with an effective amount of the agricultural and horticultural pest control composition according to [1] to [3] A method for using a pest control composition for agricultural and horticultural use, characterized by treating a cultivation carrier or soil of
[5] Soil or cultivating carrier in which the treatment is soaking the seed of the target plant in the agricultural / horticultural pest control composition solution, seed treatment such as seed dressing with the agricultural / horticultural pest control composition, or the plant body It is related with the usage method of the agricultural and horticultural pest control composition as described in [4].
本発明の農園芸用病害虫防除剤組成物は、従来技術に比べて種々の植物病害・害虫に対して広いスペクトラムを有し、かつ低薬量で優れた病害虫防除効果を示す。本発明の農園芸用病害虫防除剤組成物は少ない散布量で種々の病害・害虫を効果的に防除するため、地球環境への負荷が少なくて済む。
The agricultural and horticultural pest control composition of the present invention has a broad spectrum with respect to various plant diseases and pests compared to the prior art, and exhibits an excellent pest control effect at a low dose. Since the agricultural and horticultural pest control composition of the present invention effectively controls various diseases and pests with a small amount of application, the burden on the global environment can be reduced.
本発明の農園芸用病害虫防除剤組成物は4-シクロプロピル-1,2,3-チアジアゾール誘導体又はその塩類と、殺菌活性及び/又は殺虫活性を有する化合物の1種又は2種以上とを有効成分として含有することを特徴とする。本発明に用いられる4-シクロプロピル-1,2,3-チアジアゾール誘導体又はその塩類は下記一般式(I)で表される。
The agricultural and horticultural pest control composition of the present invention is effective for 4-cyclopropyl-1,2,3-thiadiazole derivatives or salts thereof and one or more compounds having fungicidal activity and / or insecticidal activity. It is contained as a component. The 4-cyclopropyl-1,2,3-thiadiazole derivative or a salt thereof used in the present invention is represented by the following general formula (I).
上記一般式(I)の定義において、「ハロゲン原子」とは塩素原子、臭素原子、沃素原子又はフッ素原子を示す。
「(C1-C6)アルキル基」とは、例えば、メチル基、エチル基、ノルマルプロピル基、イソプロピル基、ノルマルブチル基、イソブチル基、セカンダリーブチル基、ターシャリーブチル基、ノルマルペンチル基、ネオペンチル基、ノルマルヘキシル基等の直鎖又は分鎖状の炭素原子数1~6個のアルキル基を示す。 In the definition of the general formula (I), the “halogen atom” refers to a chlorine atom, a bromine atom, an iodine atom or a fluorine atom.
“(C 1 -C 6 ) alkyl group” means, for example, methyl group, ethyl group, normal propyl group, isopropyl group, normal butyl group, isobutyl group, secondary butyl group, tertiary butyl group, normal pentyl group, neopentyl group A straight-chain or branched alkyl group having 1 to 6 carbon atoms such as a normal group or a normal hexyl group;
「(C1-C6)アルキル基」とは、例えば、メチル基、エチル基、ノルマルプロピル基、イソプロピル基、ノルマルブチル基、イソブチル基、セカンダリーブチル基、ターシャリーブチル基、ノルマルペンチル基、ネオペンチル基、ノルマルヘキシル基等の直鎖又は分鎖状の炭素原子数1~6個のアルキル基を示す。 In the definition of the general formula (I), the “halogen atom” refers to a chlorine atom, a bromine atom, an iodine atom or a fluorine atom.
“(C 1 -C 6 ) alkyl group” means, for example, methyl group, ethyl group, normal propyl group, isopropyl group, normal butyl group, isobutyl group, secondary butyl group, tertiary butyl group, normal pentyl group, neopentyl group A straight-chain or branched alkyl group having 1 to 6 carbon atoms such as a normal group or a normal hexyl group;
「ハロ(C1-C6)アルキル基」とは、同一又は異なっても良い1以上のハロゲン原子により置換された直鎖又は分岐鎖状の炭素原子数1~6個のアルキル基を示し、例えばトリフルオロメチル基、ジフルオロメチル基、パーフルオロエチル基、パーフルオロイソプロピル基、クロロメチル基、ブロモメチル基、1-ブロモエチル基、2,3-ジブロモプロピル基等を示す。
The “halo (C 1 -C 6 ) alkyl group” refers to a linear or branched alkyl group having 1 to 6 carbon atoms substituted with one or more halogen atoms which may be the same or different, Examples thereof include a trifluoromethyl group, a difluoromethyl group, a perfluoroethyl group, a perfluoroisopropyl group, a chloromethyl group, a bromomethyl group, a 1-bromoethyl group, and a 2,3-dibromopropyl group.
「(C3-C6)シクロアルキル基」とは、例えば、シクロプロピル基、シクロブチル基、シクロペンチル基、シクロヘキシル基、2-メチルシクロプロピル基、2-メチルシクロペンチル基等の炭素原子数3~6個の脂環式アルキル基等を示す。
「ハロ(C3-C6)シクロアルキル基」とは、同一又は異なっても良い1以上のハロゲン原子により置換された炭素原子数3~6個のシクロアルキル基を示し、例えばフルオロシクロプロピル基、ジクロロシクロブチル基、ブロモシクロペンチル基等を示す。 “(C 3 -C 6 ) cycloalkyl group” means, for example, 3 to 6 carbon atoms such as cyclopropyl group, cyclobutyl group, cyclopentyl group, cyclohexyl group, 2-methylcyclopropyl group, 2-methylcyclopentyl group, etc. An alicyclic alkyl group is shown.
The “halo (C 3 -C 6 ) cycloalkyl group” refers to a cycloalkyl group having 3 to 6 carbon atoms substituted with one or more halogen atoms which may be the same or different, for example, a fluorocyclopropyl group , Dichlorocyclobutyl group, bromocyclopentyl group and the like.
「ハロ(C3-C6)シクロアルキル基」とは、同一又は異なっても良い1以上のハロゲン原子により置換された炭素原子数3~6個のシクロアルキル基を示し、例えばフルオロシクロプロピル基、ジクロロシクロブチル基、ブロモシクロペンチル基等を示す。 “(C 3 -C 6 ) cycloalkyl group” means, for example, 3 to 6 carbon atoms such as cyclopropyl group, cyclobutyl group, cyclopentyl group, cyclohexyl group, 2-methylcyclopropyl group, 2-methylcyclopentyl group, etc. An alicyclic alkyl group is shown.
The “halo (C 3 -C 6 ) cycloalkyl group” refers to a cycloalkyl group having 3 to 6 carbon atoms substituted with one or more halogen atoms which may be the same or different, for example, a fluorocyclopropyl group , Dichlorocyclobutyl group, bromocyclopentyl group and the like.
「(C1-C6)アルコキシ基」とは、例えばメトキシ基、エトキシ基、ノルマルプロポキシ基、イソプロポキシ基、ノルマルブトキシ基、セカンダリーブトキシ基、ターシャリーブトキシ基、ノルマルペンチルオキシ基、イソペンチルオキシ基、ネオペンチルオキシ基、ノルマルヘキシルオキシ基等の直鎖又は分岐鎖状の炭素原子数1~6個のアルコキシ基を示す。
「ハロ(C1-C6)アルコキシ基」とは、同一又は異なっても良い1以上のハロゲン原子により置換された直鎖又は分岐鎖状の炭素原子数1~6個のアルキル基を有するアルコキシ基を示し、例えばジフルオロメトキシ基、トリフルオロメトキシ基、2,2,2-トリフルオロエトキシ基等を示す。 “(C 1 -C 6 ) alkoxy group” means, for example, methoxy group, ethoxy group, normal propoxy group, isopropoxy group, normal butoxy group, secondary butoxy group, tertiary butoxy group, normal pentyloxy group, isopentyloxy group A straight-chain or branched alkoxy group having 1 to 6 carbon atoms such as a group, a neopentyloxy group, and a normal hexyloxy group;
The “halo (C 1 -C 6 ) alkoxy group” is an alkoxy having a linear or branched alkyl group having 1 to 6 carbon atoms substituted with one or more halogen atoms which may be the same or different. Group, for example, a difluoromethoxy group, a trifluoromethoxy group, a 2,2,2-trifluoroethoxy group or the like.
「ハロ(C1-C6)アルコキシ基」とは、同一又は異なっても良い1以上のハロゲン原子により置換された直鎖又は分岐鎖状の炭素原子数1~6個のアルキル基を有するアルコキシ基を示し、例えばジフルオロメトキシ基、トリフルオロメトキシ基、2,2,2-トリフルオロエトキシ基等を示す。 “(C 1 -C 6 ) alkoxy group” means, for example, methoxy group, ethoxy group, normal propoxy group, isopropoxy group, normal butoxy group, secondary butoxy group, tertiary butoxy group, normal pentyloxy group, isopentyloxy group A straight-chain or branched alkoxy group having 1 to 6 carbon atoms such as a group, a neopentyloxy group, and a normal hexyloxy group;
The “halo (C 1 -C 6 ) alkoxy group” is an alkoxy having a linear or branched alkyl group having 1 to 6 carbon atoms substituted with one or more halogen atoms which may be the same or different. Group, for example, a difluoromethoxy group, a trifluoromethoxy group, a 2,2,2-trifluoroethoxy group or the like.
「(C1-C6)アルコキシカルボニル基」とは、例えばメトキシカルボニル基、エトキシカルボニル基、ノルマルプロポキシカルボニル基、イソプロポキシカルボニル基、ノルマルブトキシカルボニル基、ターシャリーブトキシカルボニル基等の直鎖又は分岐鎖状の炭素原子数1~6個のアルコキシカルボニル基を示す。
“(C 1 -C 6 ) alkoxycarbonyl group” means, for example, linear or branched such as methoxycarbonyl group, ethoxycarbonyl group, normal propoxycarbonyl group, isopropoxycarbonyl group, normal butoxycarbonyl group, tertiary butoxycarbonyl group, etc. A chain-like alkoxycarbonyl group having 1 to 6 carbon atoms is shown.
本発明に用いられる一般式(I)で表される4-シクロプロピル-1,2,3-チアジアゾール誘導体の塩類としては、例えば塩酸塩、硫酸塩、硝酸塩、燐酸塩等の無機酸塩類;酢酸塩、フマル酸塩、マレイン酸塩、シュウ酸塩、メタンスルホン酸塩、ベンゼンスルホン酸塩、パラトルエンスルホン酸塩等の有機酸塩類;ナトリウムイオン、カリウムイオン、カルシウムイオン等の塩基との塩類を例示することができる。
Examples of the salt of the 4-cyclopropyl-1,2,3-thiadiazole derivative represented by the general formula (I) used in the present invention include inorganic acid salts such as hydrochloride, sulfate, nitrate and phosphate; Organic salts such as salts, fumarate, maleate, oxalate, methanesulfonate, benzenesulfonate, paratoluenesulfonate; salts with bases such as sodium ion, potassium ion, calcium ion It can be illustrated.
本発明に用いられる一般式(I)で表される4-シクロプロピル-4-シクロプロピル-1,2,3-チアジアゾール誘導体は、その構造式中に1つ又は複数個の不斉中心を含む場合があり、2種以上の光学異性体及びジアステレオマーが存在する場合もあるが、本発明は各々の光学異性体及びそれらが任意の割合で含まれる混合物をも全て包含するものである。
The 4-cyclopropyl-4-cyclopropyl-1,2,3-thiadiazole derivative represented by the general formula (I) used in the present invention contains one or more asymmetric centers in the structural formula. In some cases, two or more optical isomers and diastereomers may exist, but the present invention includes all of the optical isomers and a mixture containing them in an arbitrary ratio.
本発明に用いられる一般式(I)で表される化合物において、R1、R2、R3、R4及びR5として好ましくは、水素原子又は(C1-C6)アルキル基であり、それぞれが同一でも良いし、異なっても良い。R1として最も好ましくは水素原子である。R2、R3、R4及びR5として更に好ましくは、水素原子又は(C1-C3)アルキル基であり、それぞれが同一でも良いし、異なっても良い。中でも、R2、R3、R4及びR5として最も好ましくは水素原子である。
In the compound represented by the general formula (I) used in the present invention, R 1 , R 2 , R 3 , R 4 and R 5 are preferably a hydrogen atom or a (C 1 -C 6 ) alkyl group, Each may be the same or different. R 1 is most preferably a hydrogen atom. R 2 , R 3 , R 4 and R 5 are more preferably a hydrogen atom or a (C 1 -C 3 ) alkyl group, and each may be the same or different. Among them, R 2 , R 3 , R 4 and R 5 are most preferably hydrogen atoms.
本発明に用いられる一般式(I)で表される化合物において、R6として好ましくは、水素原子;ハロゲン原子、シアノ基、(C1-C6)アルキル基、ハロ(C1-C6)アルキル基、(C3-C6)シクロアルキル基、ハロ(C3-C6)シクロアルキル基、(C1-C6)アルコキシ基、ハロ(C1-C6)アルコキシ基、カルボキシル基及び(C1-C6)アルコキシカルボニル基からなる群より選択される1または同一もしくは異なっても良い2以上の置換基を有する置換フェニル(C1-C6)アルキル基;フェニル基;ハロゲン原子、シアノ基、(C1-C6)アルキル基、ハロ(C1-C6)アルキル基、(C3-C6)シクロアルキル基、ハロ(C3-C6)シクロアルキル基、(C1-C6)アルコキシ基、ハロ(C1-C6)アルコキシ基、カルボキシル基及び(C1-C6)アルコキシカルボニル基からなる群より選択される1または同一もしくは異なっても良い2以上の置換基を有する置換フェニル基を示す。
Yとして好ましくは酸素原子又は-NH-であり、Wとして好ましくは酸素原子又は硫黄原子である。 In the compound represented by the general formula (I) used in the present invention, R 6 is preferably a hydrogen atom; a halogen atom, a cyano group, a (C 1 -C 6 ) alkyl group, or a halo (C 1 -C 6 ). Alkyl groups, (C 3 -C 6 ) cycloalkyl groups, halo (C 3 -C 6 ) cycloalkyl groups, (C 1 -C 6 ) alkoxy groups, halo (C 1 -C 6 ) alkoxy groups, carboxyl groups and (C 1 -C 6) alkoxycarbonyl 1 or substituted phenyl having the same or different and may be 2 or more substituents selected from the group consisting of group (C 1 -C 6) alkyl group; a phenyl group; a halogen atom, cyano, (C 1 -C 6) alkyl group, halo (C 1 -C 6) alkyl group, (C 3 -C 6) cycloalkyl group, halo (C 3 -C 6) cycloalkyl group, (C -C 6) alkoxy groups, halo (C 1 -C 6) alkoxy group, carboxyl group and (C 1 -C 6) alkoxy 1 or the same or different and may be two or more substituents selected from the group consisting of a carbonyl group A substituted phenyl group having a group is shown.
Y is preferably an oxygen atom or —NH—, and W is preferably an oxygen atom or a sulfur atom.
Yとして好ましくは酸素原子又は-NH-であり、Wとして好ましくは酸素原子又は硫黄原子である。 In the compound represented by the general formula (I) used in the present invention, R 6 is preferably a hydrogen atom; a halogen atom, a cyano group, a (C 1 -C 6 ) alkyl group, or a halo (C 1 -C 6 ). Alkyl groups, (C 3 -C 6 ) cycloalkyl groups, halo (C 3 -C 6 ) cycloalkyl groups, (C 1 -C 6 ) alkoxy groups, halo (C 1 -C 6 ) alkoxy groups, carboxyl groups and (C 1 -C 6) alkoxycarbonyl 1 or substituted phenyl having the same or different and may be 2 or more substituents selected from the group consisting of group (C 1 -C 6) alkyl group; a phenyl group; a halogen atom, cyano, (C 1 -C 6) alkyl group, halo (C 1 -C 6) alkyl group, (C 3 -C 6) cycloalkyl group, halo (C 3 -C 6) cycloalkyl group, (C -C 6) alkoxy groups, halo (C 1 -C 6) alkoxy group, carboxyl group and (C 1 -C 6) alkoxy 1 or the same or different and may be two or more substituents selected from the group consisting of a carbonyl group A substituted phenyl group having a group is shown.
Y is preferably an oxygen atom or —NH—, and W is preferably an oxygen atom or a sulfur atom.
本発明で開示されている一般式(I)で表される化合物は、特開2007-99749号公報に記載された方法に従って製造することができるが、本発明に用いられる化合物はこれらに限定されるものではない。
The compound represented by the general formula (I) disclosed in the present invention can be produced according to the method described in JP 2007-99749 A, but the compound used in the present invention is not limited to these. It is not something.
以下の第1表に、一般式(I)で表される4-シクロプロピル-4-シクロプロピル-1,2,3-チアジアゾール誘導体の具体例を列挙するが、本発明はこれらに限定されるものではない。なお、第1表において、「Me」はメチル基を、「Et」はエチル基を、「Ph」はフェニル基を、「Bu」はブチル基を、「n-Pr」はノルマルプロピル基を、「i-Pr」はイソプロピル基を、「n-Bu」はノルマルブチル基を、「i-Bu」はイソブチル基を、「s-Bu」はセカンダリーブチル基を、「t-Bu」はターシャリーブチル基を表す。また、「nD(℃)」は化合物の屈折率を示す。
Specific examples of the 4-cyclopropyl-4-cyclopropyl-1,2,3-thiadiazole derivative represented by the general formula (I) are listed in Table 1 below, but the present invention is limited to these. It is not a thing. In Table 1, “Me” represents a methyl group, “Et” represents an ethyl group, “Ph” represents a phenyl group, “Bu” represents a butyl group, “n-Pr” represents a normal propyl group, “I-Pr” is an isopropyl group, “n-Bu” is a normal butyl group, “i-Bu” is an isobutyl group, “s-Bu” is a secondary butyl group, and “t-Bu” is tertiary. Represents a butyl group. “N D (° C.)” indicates the refractive index of the compound.
第1表に例示した4-シクロプロピル-1,2,3-チアジアゾール誘導体のうち、一部の化合物の1H-NMRデータを第2表に示す。第2表中の化合物番号は上記第1表に記載の番号を示す。
Table 1 shows 1 H-NMR data of some of the 4-cyclopropyl-1,2,3-thiadiazole derivatives exemplified in Table 1. The compound numbers in Table 2 indicate the numbers described in Table 1 above.
本発明の農園芸用病害虫防除剤組成物で使用される殺菌活性を有する化合物としては、例えば、ビテルタノール、ブロムコナゾール、シプロコナゾール、ジフェノコナゾール、ジニコナゾール、エニルコナゾール、エポキシコナゾール、フルキンコナゾール、フェンブコナゾール、フルシラゾール、フルトリアホール、ヘキサコナゾール、イミベンコナゾール、イプコナゾール、メトコナゾール、ミクロブタニル、ペンコナゾール、プロピコナゾール、プロチオコナゾール、シメコナゾール、トリアジメホン、トリアジメノール、テブコナゾール、テトラコナゾール、トリチコナゾール、プロクロラズ、ペフラゾエート、イマザリル、トリフルミゾール、シアゾファミド、ベノミル、カルベンダジム、チアベンダゾール、フベリダゾール、エタボキサム、エトリジアゾール、オキスポコナゾールフマル酸、ヒメキサゾール、アゾキシストロビン、ジモキシストロビン、エネストロブリン、フルオキサストロビン、クレソキシムメチル、メトミノストロビン、オリザストロビン、ピコキシストロビン、ピラクロストロビン、トリフロキシストロビン、カルボキシン、ベナラキシル、ボスカリド、ビキサフェン、フェンヘキサミド、フルトラニル、フラメトピル、メプロニル、メタラキシル、メフェノキサム、オフラセ、オキサジキシル、オキシカルボキシン、ペンチオピラド、チフルザミド、チアジニル、ジメトモルフ、フルモルフ、フルメトベル、フルオピコリド、カルプロパミド、ジクロシメット、マンジプロパミド、フルアジナム、ピリフェノックス、ブピリメート、シプロジニル、フェナリモル、フェリムゾン、メパニピリム、ヌアリモール、ピリメタニル、トリホリン、フェンピクロニル、フルジオキソニル、アルジモルフ、ドデモルフ、フェンプロピモルフ、トリデモルフ、フェンプロピジン、イプロジオン、プロシミドン、ビンクロゾリン、ファモキサドン、フェナミドン、オクチリノン、プロベナゾール、アニラジン、ジクロメジン、ピロキロン、プロキナジド、トリシクラゾール、カプタホル、キャプタン、ダゾメット、ホルペット、フェノキサニル、キノキシフェン、アミスルブロム、マンゼブ、マンネブ、メタム、メチラム、ファーバム、プロピネブ、チウラム、ジネブ、ジラム、ジエトフェンカルブ、イプロバリカルブ、ベンチアバリカルブイソプロピル、プロパモカルブ塩酸塩、チオファネートメチル、ピリベンカルブ、ボルドー液、塩基性塩化銅、塩基性硫酸銅、水酸化第二銅、8-ヒドロキシキノリン銅、ドジン、イミノクタジンアルベシル酸塩、イミノクタジン酢酸塩、グアザチン、カスガマイシン、ストレプトマイシン、ポリオキシン、オキシテトラサイクリン、バリダマイシンA、ビナパクリル、ジノカップ、ジノブトン、ジチアノン、イソプロチオラン、エジフェンホス、イプロベンホス、ホセチル、ホセチルアルミニウム、ピラゾホス、トルクロホスメチル、クロロタロニル、ジクロフルアニド、フルスルファミド、ヘキサクロロベンゼン、フサライド、ペンシクロン、キントゼン、シフルフェナミド、シモキサニル、ジメチリモール、エチリモール、フララキシル、メトラフェノン、スピロキサミン、アンバム、硫黄、石灰硫黄合剤、エクロメゾール、炭酸水素カリウム、炭酸水素カルシウム、チアジアジン、テクロフタラム、トリアジン、ノニルフェノールスルホン酸銅、ヒドロキシイソキサゾール、フルオルイミド、ポリカーバメート、メタスルホカルブ、EDDP、IBP、トルフェンピラド、フルオピラム、イソチアニル、又はイソピラザムが挙げられるが、これらに限定されるものではない。
Examples of the compound having fungicidal activity used in the agricultural and horticultural pest control composition of the present invention include, for example, vitertanol, bromconazole, cyproconazole, difenoconazole, diniconazole, enilconazole, epoxiconazole, and fluquinconazole. , Fenbuconazole, flusilazole, flutriazole, hexaconazole, imibenconazole, ipconazole, metconazole, microbutanyl, penconazole, propiconazole, prothioconazole, cimeconazole, triadimethone, triadimenol, tebuconazole, tetraconazole, tri Ticonazole, prochloraz, pefrazoate, imazalyl, triflumizole, cyazofamide, benomyl, carbendazim, thiabendazole, fuberidazole, Taboxam, etridiazole, oxpoconazole fumaric acid, hymexazole, azoxystrobin, dimoxystrobin, enestrobrin, fluoxastrobin, cresoxime methyl, methinostrobin, orizastrobin, picoxystrobin, pyraclostrobin , Trifloxystrobin, carboxin, benalaxyl, boscalid, bixaphene, fenhexamide, flutolanil, furametopyr, mepronil, metalaxyl, mefenoxam, oflase, oxadixyl, oxycarboxyl, penthiopyrad, tifluzamide, thiazinyl, dimethomorph, flucolide, flucolide , Carpropamide, Diclocimet, Mandipropamide, Fluazinam, Pyriphenox, Bupirimate, Cypro Nil, phenalimol, ferrimzone, mepanipyrim, nuarimol, pyrimethanil, triphorin, fenpicuronyl, fludioxonil, aldimorph, dodemorph, fenpropimorph, tridemorph, fenpropidin, iprodione, procymidone, vinclozoline, famoxadone, fenamidone, octiziridine, octiziridine, octiziridine Pyroxylone, proquinazide, tricyclazole, captafor, captan, dazomet, holpet, phenoxanyl, quinoxyphene, amisulbrom, manzeb, manneb, metam, methylam, farbum, propineb, thiuram, dinebu, ziram, dietofencarb, provalimocarb ib Salt, thiophanate Methyl, pyribencarb, Bordeaux, basic copper chloride, basic copper sulfate, cupric hydroxide, 8-hydroxyquinoline copper, dodine, iminoctadine albecylate, iminoctadine acetate, guazatine, kasugamycin, streptomycin, polyoxin, oxytetracycline , Validamycin A, binapacryl, dinocup, dinobutone, dithianon, isoprothiolane, edifenephos, iprobenphos, fosetyl, fosetylaluminum, pyrazophos, tolcrofosmethyl, chlorothalonil, diclofuranide, fursulfamide, hexachlorobenzene, fusalide, pencyclon, quintozene, cyflufenamide, cyflufenamide , Ethymol, Flaxil, Metraphenone, Spiroxamine, Ambam, Sulfur Lime-sulfur mixture, echromezol, potassium hydrogen carbonate, calcium hydrogen carbonate, thiadiazine, teclophthalam, triazine, copper nonylphenol sulfonate, hydroxyisoxazole, fluorimide, polycarbamate, metasulfocarb, EDDP, IBP, tolfenpyrad, fluopyram, isothianyl, Or isopyrazam, but is not limited thereto.
また本発明の農園芸用病害虫防除剤組成物で使用される殺虫活性を有する化合物としては、例えば、アセタミプリド、ピメトロジン、フェニトロチオン、アセフェート、カルバリル、メソミル、カルタップ、シハロトリン、エトフェンプロックス、テフルベンズロン、フルベンジアミド、フルフェノクスロン、テブフェノジド、フェンピロキシメート、ピリダベン、イミダクロプリド、ブプロフェジン、BPMC、MIPC、マラチオン、メチダチオン、フェンチオン、ダイアジノン、オキシデプロホス、バミドチオン、エチオフェンカルブ、ピリミカーブ、ペルメトリン、シペルメトリン、ビフェントリン、ハルフェンプロックス、シラフルオフェン、ニテンピラム、クロルフルアズロン、メトキシフェノジド、テブフェンピラド、ピリミジフェン、ケルセン、プロパルギット、ヘキシチアゾクス、クロフェンテジン、スピノサド、ミルベメクチン、BT(Bacillus thuringiensis)、インドキサカルブ、メタフルミゾン、クロルフェナピル、フィプロニル、エトキサゾール、アセキノシル、ピリミホスメチル、アクリナトリン、キノメチオネート、クロルピリホス、アバメクチン、エマメクチン安息香酸塩、酸化フェンブタスズ、テルブホス、エトプロホス、カズサホス、フェナミフォス、フェンスルフォチオン、DSP、ジクロフェンチオン、ホスチアゼート、オキサミル、イサミドホス、ホスチエタン、イサゾホス、チオナジン、ベンフラカルブ、スピロジクロフェン、エチオフェンカルブ、アジンホス・メチル、ジスルホトン、メチオカルブ、オキシジメトン・メチル、パラチオン、シフルトリン、ベータ・シフルトリン、テブピリムホス、スピロメシフェン、エンドスルファン、アミトラズ、トラロメトリン、アセトプロール、エチプロール、エチオン、トリクロルホン、メタミドホス、ジクロルボス、メビンホス、モノクロトホス、ジメトエート、フォルメタネート、ホルモチオン、メカルバム、チオメトン、ジスルホトン、ナレッド、メチルパラチオン、シアノホス、ジアミダホス、アルベンダゾール、オキシベンダゾール、フェンベンダゾール、オクスフェンダゾール、プロパホス、スルプロホス、プロチオホス、プロフェノホス、イソフェンホス、テメホス、フェントエート、ジメチルビンホス、クロルフェビンホス、テトラクロルビンホス、ホキシム、イソキサチオン、ピラクロホス、クロルピリホス、ピリダフェンチオン、ホサロン、ホスメット、ジオキサベンゾホス、キナルホス、ピレトリン、アレスリン、プラレトリン、レスメトリン、ペルメトリン、テフルトリン、フェンプロパトリン、アルファシペルメトリン、ラムダ・シハルトリン、デルタメトリン、フェンバレレート、エスフェンバレレート、フルシトリネート、フルバリネート、シクロプロトリン、チオジカルブ、アルジカルブ、アラニカルブ、メトルカルブ、キシリカルブ、プロポキスル、フェノキシカルブ、フェノチオカルブ、ビフェナゼート、カルボフラン、カルボスルファン、硫黄、ピリフルキナゾン、フラチオカルブ、ジアフェンチウロン、ジフルベンズロン、ヘキサフルムロン、ノバルロン、ルフェヌロン、クロルフルアズロン、水酸化トリシクロヘキシルスズ、オレイン酸ナトリウム、オレイン酸カリウム、メトプレン、ハイドロプレン、ビナパクリル、アミトラズ、クロルベンジレート、フェニソブロモレート、テトラジホン、ベンスルタップ、ベンゾメート、クロマフェノジド、ハロフェノジド、エンドスルファン、ジオフェノラン、トルフェンピラド、トリアザメート、硫酸ニコチン、チアクロプリド、チアメトキサム、クロチアニジン、ジノテフラン、フルアジナム、ピリプロキシフェン、フルアクリピリム、ヒドラメチルノン、シロマジン、TPIC、チオシクラム、フェナザキン、ポリナクチン複合体、アザディラクチン、ロテノン、ヒドロキシプロピルデンプン、メスルフェンホス、ホスホカルブ、イソアミドホス、アルドキシカルブ、メタム・ナトリウム、酒石酸モランテル、ダゾメット、塩酸レバミゾール、トリクラミド、トルフェンピラド、ピリダリル、クロラントラニリプロール、シエノピラフェン又はシフルメトフェンが挙げられるが、これらに限定されるものではない。
Examples of the insecticidal compound used in the agricultural and horticultural pest control composition of the present invention include, for example, acetamiprid, pymetrozine, fenitrothion, acephate, carbaryl, mesomil, cartap, cyhalothrin, etofenprox, teflubenzuron, fulbenzamide , Flufenoxuron, tebufenozide, fenpyroximate, pyridaben, imidacloprid, buprofezin, BPMC, MIPC, malathion, methidathion, fenthion, diazinon, oxydeprophos, bamidthione, ethiophene carb, pirimicurve, permethrin, cypermethalfen fenproline, bifenthrin Nitenpyram, Chlorfluazuron, Methoxyphenozide, Tebufenpyrad, Piri Diphen, Kelsen, Propargit, Hexithiazox, Clofentedine, Spinosad, Milbemectin, BT (Bacillus thuringiensis), Indoxacarb, Metaflumizone, Chlorphenapyr, Fipronil, Etoxazole, Acequinosyl, Pirimiphosmethyl, Acrinathine, Acrinato Fenbutasin oxide, terbufos, teprofos, etoprofos, kazusafos, fenamifos, fencerfothione, DSP, diclofenthione, phosthiazete, oxamyl, isamidophos, phostietane, isazophos, thionadine, benfuracarb, spirodiclofen, etiophencarb, azinephos methyl, disulfotone, Xidimeton methyl, parathion, cyfluthrin, beta cyfluthrin, tebupyrimfos, spiromesifen, endosulfan, amitraz, tralomethrin, acetoprole, ethiprole, ethion, trichlorfone, methamidophos, dichlorvos, mevinphos, monocrotophos, dimethoate, formethione, formothion Mecarbam, thiomethone, disulfoton, nared, methyl parathion, cyanophos, diamidafos, albendazole, oxybendazole, fenbendazole, oxfendazole, propaphos, sulprophos, prothiophos, profenofos, isofenphos, temefos, phentoate, dimethylbinphos, chlorfevin Phos, tetrachlorvinphos, phoxime, isoxathione, pi Crofos, Chlorpyrifos, Pyridafenthion, Hosalon, Phosmet, Dioxabenzophos, Quinalfos, Pyrethrin, Allethrin, Praretrin, Resmethrin, Permethrin, Tefluthrin, Fenpropatoline, Alpha cypermethrin, Lambda siharthrin, Deltamethrin, Fenvalerate, Esfenvalerate, Flucitrinate, fulvalinate, cycloprotorin, thiodicarb, aldicarb, alanib, metorcarb, xilicarb, propoxyl, phenoxycarb, phenothiocarb, bifenazate, carbofuran, carbosulfan, sulfur, pyrifluquinazone, furthiocarb, difenbenzuron, diflubenzuron Flumuron, Novallon, Lufenuron, Chlorfluazuron, Tricyclohexyltin oxide, sodium oleate, potassium oleate, methoprene, hydroprene, binapacryl, amitraz, chlorbenzilate, phenisobromolate, tetradiphone, bensultap, benzomate, chromafenozide, halophenozide, endosulfan, diophenolane, tolfenpyrad, triazamate, sulfuric acid Nicotine, thiacloprid, thiamethoxam, clothianidin, dinotefuran, fluazinam, pyriproxyfen, fluacrylpyrim, hydramethylnon, cyromazine, TPIC, thiocyclam, phenazaquin, polynactin complex, azadilactin, rotenone, hydroxypropyl starch, mesulfenphos, phosphocarb, isoamidophos, Aldoxycarb, Metam Natuliu , Morantel tartrate, dazomet, levamisole hydrochloride, trichlamide, tolfenpyrad, pyridalyl, chlorantraniliprole, sienopyrafen, or cyflumetofene.
本発明の農園芸用病害虫防除剤組成物は、種々の植物病害・害虫に対して殺菌活性及び/又は殺虫活性を有する化合物を各々単独で使用する場合に比べて幅広いスペクトラムを有するとともに相乗的な防除効果を有する。特に水稲、大麦、小麦及びその他作物の植物病害・害虫の防除に適している。
The agricultural and horticultural pest control composition of the present invention has a broad spectrum and is synergistic compared to the case where compounds having bactericidal activity and / or insecticidal activity against various plant diseases and pests are used alone. Has a control effect. It is particularly suitable for controlling plant diseases and pests in paddy rice, barley, wheat and other crops.
本発明の農園芸用病害虫防除剤組成物の使用対象としては、下記の植物病害・害虫を例示することができる。
植物病害としては、糸状菌類病害、細菌類病害、ウイルス病病害を含むものであり、例えば、ボトリチス(Botrytis)属病害、ヘルミントスポリウム(Helminthosporium)属病害、フザリウム(Fusarium)属病害、セプトリア(Septoria)属病害、サルコスポラ(Cercospora)属病害、シュードサルコスポレラ(Pseudocercosporella)属病害、リンコスポリウム(Rhynchosporium)属病害、ピリキュラリア(Pyricularia)属病害、アルタナリア(Alternaria)属病害等の不完全菌類病害;例えば、ヘミレリア(Hemilelia)属病害、リゾクトニア(Rhizoctonia)属病害、ウスティラゴ(Ustilago)属病害、ティフラ(Typhula)属病害、プッキニア(Puccinia)属病害、ファコプソラ(Phakopsora)属病害等の担子菌類病害;例えば、ベンチュリア(Venturia)属病害、ポドスフェラ(Podosphaera)属病害、レプトスファエリア(Leptosphaeria)属病害、ブルメリア(Blumeria)属病害、エリシフェ(Erysiphe)属病害、ミクロドキュウム(Microdochium)属病害、スクレロチニア(Sclerotinia)属病害、ゲウマノマイセス(Gaeumannomyces)属病害、モニリニア(Monilinia)属病害、ウンシヌラ(Unsinula)属病害等の子のう菌類病害;例えば、アスコクイタ(Ascochyta)属病害、フォマ(Phoma)属病害、ピシウム(Pythium)属病害、コルティシウム(Corticium)属病害、ピレノフォラ(Pyrenophora)属病害等のその他の菌類病害;例えば、シュードモナス(Pseudomonas)属病害、ザントモナス(Xanthomonas)属病害、エルヴィニア(Erwinia)属病害等の細菌類による病害;例えば、タバコモザイクウイルス等のウイルス類による病害等を含むものである。 The following plant diseases and pests can be exemplified as the application targets of the agricultural and horticultural pest control composition of the present invention.
Examples of plant diseases include filamentous fungal diseases, bacterial diseases, and viral diseases, such as diseases of the genus Botrytis, diseases of the genus Helmintosporium, diseases of the genus Fusarium, septoria ( Diseases of the genus Septoria, diseases of the genus Sarcospora, diseases of the genus Pseudocercosporella, diseases of the genus Rhynchosporium, diseases of the genus Pyricularia, diseases of the genus Alternaria For example, diseases of the genus Hemilia, genus Rhizoctonia, Ustilago Basidiomycetous diseases such as genus diseases, Typula diseases, Puccinia diseases, Phakopsora diseases; for example, Venturia diseases, Podosphaera genus diseases, Diseases of the genus Leptosphaeria, diseases of the genus Blumeria, diseases of the genus Erysiphe, diseases of the genus Microdocium, diseases of the genus Sclerotinia, diseases of the genus Geumonimonia Aspergillus disease such as (Unsinula) genus disease; for example, Ascochita genus Other fungal diseases such as Pseudomonas, Xanthomonas, Xanthomonas, Xanthomonas, Xanthomonas, Xanthomonas, Xanthomonas, Xanthomonas, Xanthomonas, Xanthomonas, Xanthomonas, Xanthomonas, Xanthomonas, Xanthomonas, Xanthomonas Diseases caused by bacteria such as genus diseases and diseases of the genus Erwinia; for example, diseases caused by viruses such as tobacco mosaic virus.
植物病害としては、糸状菌類病害、細菌類病害、ウイルス病病害を含むものであり、例えば、ボトリチス(Botrytis)属病害、ヘルミントスポリウム(Helminthosporium)属病害、フザリウム(Fusarium)属病害、セプトリア(Septoria)属病害、サルコスポラ(Cercospora)属病害、シュードサルコスポレラ(Pseudocercosporella)属病害、リンコスポリウム(Rhynchosporium)属病害、ピリキュラリア(Pyricularia)属病害、アルタナリア(Alternaria)属病害等の不完全菌類病害;例えば、ヘミレリア(Hemilelia)属病害、リゾクトニア(Rhizoctonia)属病害、ウスティラゴ(Ustilago)属病害、ティフラ(Typhula)属病害、プッキニア(Puccinia)属病害、ファコプソラ(Phakopsora)属病害等の担子菌類病害;例えば、ベンチュリア(Venturia)属病害、ポドスフェラ(Podosphaera)属病害、レプトスファエリア(Leptosphaeria)属病害、ブルメリア(Blumeria)属病害、エリシフェ(Erysiphe)属病害、ミクロドキュウム(Microdochium)属病害、スクレロチニア(Sclerotinia)属病害、ゲウマノマイセス(Gaeumannomyces)属病害、モニリニア(Monilinia)属病害、ウンシヌラ(Unsinula)属病害等の子のう菌類病害;例えば、アスコクイタ(Ascochyta)属病害、フォマ(Phoma)属病害、ピシウム(Pythium)属病害、コルティシウム(Corticium)属病害、ピレノフォラ(Pyrenophora)属病害等のその他の菌類病害;例えば、シュードモナス(Pseudomonas)属病害、ザントモナス(Xanthomonas)属病害、エルヴィニア(Erwinia)属病害等の細菌類による病害;例えば、タバコモザイクウイルス等のウイルス類による病害等を含むものである。 The following plant diseases and pests can be exemplified as the application targets of the agricultural and horticultural pest control composition of the present invention.
Examples of plant diseases include filamentous fungal diseases, bacterial diseases, and viral diseases, such as diseases of the genus Botrytis, diseases of the genus Helmintosporium, diseases of the genus Fusarium, septoria ( Diseases of the genus Septoria, diseases of the genus Sarcospora, diseases of the genus Pseudocercosporella, diseases of the genus Rhynchosporium, diseases of the genus Pyricularia, diseases of the genus Alternaria For example, diseases of the genus Hemilia, genus Rhizoctonia, Ustilago Basidiomycetous diseases such as genus diseases, Typula diseases, Puccinia diseases, Phakopsora diseases; for example, Venturia diseases, Podosphaera genus diseases, Diseases of the genus Leptosphaeria, diseases of the genus Blumeria, diseases of the genus Erysiphe, diseases of the genus Microdocium, diseases of the genus Sclerotinia, diseases of the genus Geumonimonia Aspergillus disease such as (Unsinula) genus disease; for example, Ascochita genus Other fungal diseases such as Pseudomonas, Xanthomonas, Xanthomonas, Xanthomonas, Xanthomonas, Xanthomonas, Xanthomonas, Xanthomonas, Xanthomonas, Xanthomonas, Xanthomonas, Xanthomonas, Xanthomonas, Xanthomonas, Xanthomonas Diseases caused by bacteria such as genus diseases and diseases of the genus Erwinia; for example, diseases caused by viruses such as tobacco mosaic virus.
個々の植物病害としては、例えば、イネいもち病(Pyricularia oryze);イネ紋枯病(Rhizoctonia solani);イネごま葉枯病(Cochiobolus miyabeanus);イネ苗立ち枯れ病(Rhizopus chinensis、Pythium graminicola、Fusarium graminicola、Fusarium roseum、Mucor sp.、Phoma sp.、Tricoderma sp.);イネ馬鹿苗病(Gibberella fujikuroi);オオムギ及びコムギ等のうどんこ病(Blumeria graminis);キュウリ等のうどんこ病(Sphaerotheca fuliginea);ナス及び他の宿主植物のうどんこ病(Erysiphe cichoracoarum);オオムギ及びコムギ等の眼紋病(Pseudocercosporella herpotrichoides);コムギ等の黒穂病(Urocystis tritici);オオムギ及びコムギ等の雪腐病(Microdochium nivalis、Pythium iwayamai、Typhla ishikariensis、Typhla incarnata、Sclerotinia borealis);オオムギ及びコムギ等の赤かび病(Fusarium graminearum、Fusarium avenaceum、Fusarium culmorum、Microdochium nivalis);ダイズさび病(Phakopsora pachyrhizi);他の植物のさび病;オオムギ及びコムギ等のさび病(Puccinia hodei、Puccinia recondita、Puccinia striiformis);オオムギ及びコムギ等の立枯病(Gaeumannomyces graminis);エンバク及び他の植物の冠さび病(Puccinia coronata);キュウリ、イチゴ等の灰色かび病(Botrytis cinerea);トマト、キャベツ等の菌核病(Sclerotinia sclerotiorum);ジャガイモまたはトマト及び他の植物の疫病(Phytophthora infestans);キュウリべと病(Pseudoperonospora cubensis);ブドウ及び種々の植物のべと病(Plasmopara viticola)等;トウモロコシごま葉枯病(Cochliobolus heterostrophus);その他の植物の各種葉枯病等が挙げられる。
Individual plant diseases include, for example, rice blast (Priculararia oryzae); rice rot (Rhizoctonia solani); rice sesame leaf blight (Cochiobulus miabialusius, Rhizominuspisumus, Rhizominuspissumis, Rhizominuspissum) Fusarium roseum, Mucor sp., Poma sp., Tricoderma sp.); Rice idiot (Gibberella fujikuroi); Barley and wheat and other powdery mildew (Blumeria grami sul); And other host plants Powdery mildew (Erysiphe cichoracoacorum); Barley and wheat rhinoceros (Pseudocercosporella herpotrichoides); Wheat etc. incarnata, Sclerotinia borealis); Fusarium graminearum, Fusarium avenaceum, Fusarium culmorum, Microdochium nivalis); soybean rust disease P ora pachyrhizi); rust disease of other plants; rust disease of barley and wheat (Puccinia hodei, Puccinia recondita, Puccinia striiformis); wilt disease of barley and wheat, etc .; Diseases (Puccinia coronata); Gray mold diseases such as cucumbers and strawberries (Botrytis cinerea); Mycorrhizal diseases such as tomatoes and cabbages (Sclerotinia sclerotiorum); Potato or other plant plagues (Phytophthora infectious diseases; (Pseudoperonospora cubensis); grapes and various Plants of downy mildew (Plasmopara viticola) and the like; Southern Corn Leaf Blight (Cochliobolus heterostrophus); various blight like other plants and the like.
また、リンゴ黒星病(Venturia inaequalis);リンゴ斑点落葉病(Alternaria mali);ナシ黒斑病(Alternaria kikuchiana);カンキツ黒点病(Diaporthe citri);カンキツそうか病(Elsinoe fawcetti);テンサイ褐斑病(Cercospora beticola);ラッカセイ褐斑病(Cercospora arachidicola);ラッカセイ黒渋病(Cercospora personata);コムギ葉枯れ病(Septoria tritici);コムギふ枯れ病(Leptosphaeria nodorum);オオムギ網斑病(Pyrenophora teres);オオムギ斑葉病(Pyrenophora graminea);オオムギ雲形病(Rhynchosporium secalis);コムギ裸黒穂病(Ustilago nuda);、コムギなまぐさ黒穂病(Tilletia caries);シバの葉腐病(Rhizoctonia solani);シバのダラースポット病(Sclerotinia homoeocarpa);例えば、キュウリ斑点細菌病(Pseudomonas syringae pv.lachrymans)、トマト青枯病(Pseudomonas solanacearum)又はイネ籾枯細菌病(Pseudomonas glumae)等のPsuedomonas属による病害;例えば、キャベツ黒腐病(Xanthomonas campestris)、イネ白葉枯病(Xanthomonas oryzae)又はカンキツかいよう病(Xanthomonas citri)等のXanthomonas属による病害;例えば、キャベツ軟腐病(Erwinia carotovora)等のErwinia属による細菌病;タバコモザイク病(Tobacco mosaic virus)等のウイルス病等に対しても、顕著な防除効果を有するものである。
In addition, apple black spot disease (Venturia inaequalis); apple spotted leaf disease (Alternaria mary); pear black spot disease (Alternaria kikuchiana); citrus black spot disease (Diaporthe citri); Cercospora beticola; peanut black spot (Cercospora perzonata); Leafy leaf disease (Pyrenoph) ra graminea); barley cloud scab (Rhynchosporia secalis); wheat naked scab (Ustilago nudia); wheat wheat scab (Tillletia cariole); Pseudomonas phytopathies such as Pseudomonas syringae pv. Rice white leaf Diseases caused by the genus Xanthomonas such as Xanthomonas oryzae or citrus canker disease (Xanthomonas citri); for example, bacterial diseases caused by Erwinia genus such as cabbage soft rot (Erwinia carotovora); tobacco mosaic disease (Tobacco disease) In contrast, it has a remarkable control effect.
害虫としては、半翅目(Hemiptera)としては、例えば、マルカメムシ(Megacopta punctatissimum)、オオトゲシラホシカメムシ(Eysarcoris lewisi)、トゲシラホシカメムシ(Eysarcoris parvus)、ミナミアオカメムシ(Nezara viridula)、チャバネアオカメムシ(Plautia stali)、ホソハリカメムシ(Cletus punctiger)、クモヘリカメムシ(Leptocorisa chinensis)、ホソヘリカメムシ(Riptortus clavatus)、コバネヒョウタンナガカメムシ(Togo hemipterus)、ナシグンバイ(Stephanitis nashi)、ツツジグンバイ(Stephanitis pyrioides)、ウスミドリメクラガメ(Apolygus spinolai)、アカスジメクラガメ(Stenotus rubrovittalus)、アカヒゲホソミドリメクラガメ(Trigonotylus coelestialium)等の異翅類(Heteroptera);フタテンヒメヨコバイ(Arboridia apicalis)、チャノミドリヒメヨコバイ(Empoasca onukii)、ツマグロヨコバイ(Nephotettix cincticeps)、タイワンツマグロヨコバイ(Nephotettix virescens)、ヒメトビウンカ(Laodelphax striatellus)、トビイロウンカ(Nilaparvata lugens)、セジロウンカ(Sogatella furcifera)、ミカンキジラミ(Diaphorina citri)、ミカントゲコナジラミ(Aleurocanthus spiniferus)、シルバーリーフコナジラミ(Bemisia argentifolii)、タバココナジラミ(Bemisia tabaci)、ミカンコナジラミ(Dialeurodes citri)、オンシツコナジラミ(Trialeurodes vaporariorum)、ブドウネアブラムシ(Viteus vitifolii)、リンゴワタムシ(Eriosoma lanigerum)、ユキヤナギアブラムシ(Aphis citricola)、マメアブラムシ(Aphis craccivora)、ワタアブラムシ(Aphis gossypii)、ジャガイモヒゲナガアブラムシ(Aulacorthum solani)、ダイコンアブラムシ(Brevicoryne brassicae)、チューリップヒゲナガアブラムシ(Macrosiphum euphorbiae)、モモアカアブラムシ(Myzus persicae)、ムギクビレアブラムシ(Rhopalosiphum padi)、ムギヒゲナガアブラムシ(Sitobion akebiae)、クワコナカイガラムシ(Pseudococcus comstocki)、ツノロウムシ(Ceroplastes ceriferus)、アカマルカイガラムシ(Aonidiella aurantii)、ナシマルカイガラムシ(Comstockaspis perniciosa)、クワシロカイガラムシ(Pseudaulacaspis pentagoa)、ヤノネカイガラムシ(Unaspis yanonensis)等の同翅類(Homoptera)が挙げられる。
Examples of the pests include Hemoptera, for example, Megacopta punctatissimum, Oysarcoris lewisi, Egysarcorus varvae, and (Platia stali), Coleus puntigger, Spider helicopter (Leptocorisa chinensis), Cyprus cavatus (Riptortus clavatus), Kobanei tsunagushi tsugehit Tephantitis pyrioides), Apolygus spinolai, Akasujimekuragame, Stenotus rubrovititalus, Trigonoticlus cotertialum Green leafhoppers (Epoasca onukii), Green leafhoppers (Nephotettix cinticesps), Thai whitefin leafhoppers (Nepotettix virescens), Green leafhoppers (Laodelphax straitellarus vulva) ns), Sejirounka (Sogatella furcifera), Diaphorina citri (Diaphorina citri), mandarin orange spiny whitefly (Aleurocanthus spiniferus), silverleaf whitefly (Bemisia argentifolii), tobacco whitefly (Bemisia tabaci), mandarin orange whitefly (Dialeurodes citri), greenhouse whitefly (Trialeurodes vaporariorum) , Grape aphids (Viteus vififolii), apple beetles (Eriosoma lanigerum), snowy aphids (Aphis citricola), bean aphids (Aphis cracivovora), cotton Aphis gossypii, potato beetle aphids (Aulacorthum solani), radish aphids (Brevicoryne brassicae), tulip beetle aphids (Macrosiphum euphorbiae), peach zebra aphids akebiae), stag beetle (Pseudococcus commtocci), horned beetle (Ceroplasts ceriferus), red beetle (Aonidiella aurantiii), pear worm (Comtocka) pis perniciosa), white peach scale (Pseudaulacaspis pentagoa), Yano yanonensis (Unaspis yanonensis) same Orthoptera such as (Homoptera), and the like.
鱗翅目(Lepidoptera)としては、例えば、リンゴコカクモンハマキ(Adoxophyes orana fasciata)、チャノコカクモンハマキ(Adoxophyes honmai)、ミダレカクモンハマキ(Archips fuscocupreanus)、モモシンクイガ(Carposina niponensis)、ナシヒメシンクイ(Grapholita molesta)、チャハマキ(Homona magnanima)、チャノホソガ(Caloptilia theivora)、ヨモギエダシャク(Ascotis selenaria)、グレイプベリーモス(Endopiza viteana)、コドリンガ(Laspeyresia pomonella)、キンモンホソガ(Phyllonorycter ringoniella)、ギンモンハモグリガ(Lyonetia prunifoliella malinella)、ミカンハモグリガ(Phyllocnistis citrella)、コナガ(Plutella xylostella)、ワタアカミムシ(Pectinophora gossypiella)、モモシンクイガ(Carposina niponensis)、ニカメイガ(Chilo suppressalis)、サンカメイガ(Scirpophaga incertulas)、コブノメイガ(Cnaphalocrocis medinalis)、ハイマダラノメイガ(Hellulla undalis)、アゲハ(Papilio xuthus)、モンシロチョウ(Pieris rapae crucivora)、オビカレハ(Malacosoma neustria testacea)、アメリカシロヒトリ(Hyphantria cunea)、シバツトガ(Parapediasia teterrella)、オオタバコガ(Helicoverpa armigera)、ヘリオチス種(Heliothis spp.)、カブラヤガ(Agrotis segetum)、タマナギンウワバ(Autographa nigrisigna)、ヨトウガ(Mamestra brassicae)、シロイチモジヨトウ(Spodoptera exigua)、ハスモンヨトウ(Spodoptera litura)等が挙げられる。
Lepidoptera includes, for example, apple wolfberry (Adoxophyes orana fascita), tea wolfberry monk (Adoxophyces honmai), nippon cynosphincumopampusu cinopus cinopus cympopuscopupuscupopushisopumusu Chamonaki (Homona magnanima), Chanohosoga (Caloptilia theivora), Artemisia dasak (Ascotis selenaria), Grapeberry moss (Endopizia viteana), Codling moth (Lasprey mons) (Phyllonorycter ringoniella), Gin Mont leafminer (Lyonetia prunifoliella malinella), mandarin orange leafminer (Phyllocnistis citrella), diamondback moth (Plutella xylostella), pink bollworm (Pectinophora gossypiella), peach fruit moth (Carposina niponensis), rice stem borer (Chilo suppressalis), Sankameiga (Scirpophaga incertulas) , Cnaphalocrosis medinalis, Hamelula undalis, Papilio xutus Cabbage butterfly (Pieris rapae crucivora), lackey moth (Malacosoma neustria testacea), the United States white Arctiidae (Hyphantria cunea), Shibatsutoga (Parapediasia teterrella), cotton bollworm (Helicoverpa armigera), Heliothis species (Heliothis spp.), Kaburayaga (Agrotis segetum), Tamanagin'uwaba (Autographa nigrisigna), mushroom brassicae, Spodoptera exigua, Spodoptera litra, and the like.
鞘翅目(Coleoptera)としては、例えば、ドウガネブイブイ(Anomala cuprea)、マメコガネ(Popillia japonica)、ヒラタキクイムシ(Lyctus brunneus)、ヒラタコクヌストモドキ(Tribolium confusum)、ニジュウヤホシテントウ(Epilachna vigintioctopunctata)、ゴマダラカミキリ(Anoplophora malasiaca)、マツノマダラカミキリ(Monochamus alternatus)、アズキゾウムシ(Callosobruchus chinensis)、ウリハムシ(Aulacophora femoralis)、ルートワーム種(Diabrotica spp.)、ワタミゾウムシ(Anthonomus gradis grandis)、メキシカンビートル(Epilachna varivestis)、コロラドハムシ(Leptinotarsa decemlineata)、イネミズゾウムシ(Lissorhoptrus oryzophilus)、イネドロオイムシ(Oulema oryzae)、シバオサゾウムシ(Sphenophrus venatus vestitus)等が挙げられ、膜翅目(Hymenoptera)としては、例えば、カブラハバチ(Athalia rosae ruficornis)、チュウレンジハバチ(Arge pagana)、クロヤマアリ(Formica japonica)等が挙げられる。
The Coleoptera (Coleoptera), for example, cupreous chafer (Anomala cuprea), Japanese beetle (Popillia japonica), Hirata beetle (Lyctus brunneus), Hirata red flour beetle (Tribolium confusum), beetle, Epilachna vigintioctopunctata (Epilachna vigintioctopunctata), Gomadarakamikiri (Anoplophora malasiaca ), Pinewood beetle (Monochamus alternatus), azuki beetle (Callosobrchuchus chinensis), cucumber beetle (Alacophora femorialis), rootworm species (Diabrotica spp.), Cotton Umushi (Anthonomus gradis grandis), Mexican beetle (Epilachna varivestis), Colorado potato beetle (Leptinotarsa decemlineata), rice water weevil (Lissorhoptrus oryzophilus), Inedorooimushi (Oulema oryzae), grass reed weevil (Sphenophrus venatus vestitus), and the like, Hymenoptera ( As Hymenoptera, for example, bee (Athalia rosae ruficornis), horn range bee (Arge pagana), black ant (Formica japonica) and the like can be mentioned.
双翅目(Diptera)としては、例えば、イネハモグリバエ(Agromyza oryzae)、イネミギワバエ(Hydrellia griseola)、マメハモグリバエ(Liriomyza trifolii)、タマネギバエ(Delia antiqua)、イエバエ(Musca domestica)、チカイエカ(Culex pipiens molestus)、アカイエカ(Culex pipiens pallens)等が挙げられ、アザミウマ目(Thysanoptera)としては、例えば、チャノキイロアザミウマ(Scirtothrips dorsalis)、ミナミキイロアザミウマ(Thrips palmi)、ネギアザミウマ(Thrips tabaci)、ミカンキイロアザミウマ(Frankliniella occidentalis)が挙げられ、シロアリ目(Isoptera)としては、例えば、イエシロアリ(Coptotermes formosanus)、ヤマトシロアリ(Reticulitermes speratus)、チャタテムシ(Psocoptera)、ヒラタチャタテ(Liposcelis bostrychophilus)等が挙げられ、直翅目(Orthoptera)としては、例えば、コバネイナゴ(Oxya yezoensis)、ケラ(Gryllotalpa sp.)、ワモンゴキブリ(Periplaneta americana)、チャバネゴキブリ(Blattella germanica)等が挙げられる。
As Diptera, for example, Agromyza oryzae, Emius eu (s), citrus (Eri), citrus (Eri), citrus (Eri), citrus (Eri), citrus (Eri), citrus (Eri), citrus (Epi), citrus Examples of the thrips (Thysanoptera) include, for example, Shiratotrips dorsalis, Thripspalmipalm, and Thripspalmipalmis. Examples of the termites (Isoptera) include, but are not limited to, the termites (Coptothermes formosanus), the Yamato termites (Reticulitermes spatras), and Examples of the eyes (Oroptoptera) include, for example, Oxya yezoensis, Kera (Gryllotalpa sp.), Cockroach (Periplaneta americana), German cockroach (Blatella germanica) and the like.
ダニ目(Acarina)としては、例えば、ミカンハダニ(Panonychus citri)、リンゴハダニ(Panonychus ulmi)、ナミハダニ(Tetranychus urticae)、カンザワハダニ(Tetranychus kanzawai)、ミナミヒメハダニ(Brevipalpus phoenicis)、クローバーハダニ(Bryobia praetiosa)、ミカンサビダニ(Aculops pelekassi)、ニセナシサビダニ(Eriophyes chibaensis)、チャノホコリダニ(Polyphagotarsonemus latus)、ロビンネダニ(Rhizoglyphus robini)、ケナガコナダニ(Tyrophagus putrescentiae)等が挙げられ、ハリセンチュウ目(Tylenchida)としては、例えば、ミナミネグサレセンチュウ(Pratylenchus coffeae)、キタネグサレセンチュウ(Pratylenchus penetrans)、ジャガイモシストセンチュウ(Globodera rostochiensis)、サツマイモネコブセンチュウ(Meloidogyne incognita)等が挙げられ、ニセハリセンチュウ目(Dorylaimida)としては、例えば、ナガハリセンチュウ(Longidorus sp.)が挙げられ、軟体動物門腹足綱(Gastropoda)としては、例えば、ナメクジ(Incilaria bilineata)等が挙げられる。
Examples of the mites (Acarina) include, for example, citrus spider mite (Pananychus citri), apple spider mite (Pananychus urticae), spider mite (Tetanychus kantawai), tick mite (Tetanichus kantawai), Rabbit mite (Aculops pelekassi), Scarlet mite mite (Eriophys chibaensis), Butter mite (Polyphagotarsonemus latus), Robin mite (Rhizoglyphus robini), Kenagarona phragmite Scentiae, etc., and examples of the order of Tylenchida include Pratylenchus coffeae, Pratylenchus penetran, and Potato sect. Examples of the larvae (Dorilamida) include, for example, longi nematode (Longidorus sp.), And examples of the mollusc gastropoda (Gastropoda) include, for example, slugs (Inciliaria bilineta). It is done.
本発明の農園芸用病害虫防除剤組成物を使用できる植物としては、例えば、稲、大麦、小麦、ライ麦、オート麦、トウモロコシ、高粱等の穀類;大豆、小豆、そら豆、えんどう豆、落花生等の豆類;リンゴ、柑橘類、梨、ブドウ、桃、梅、桜桃、クルミ、アーモンド、バナナ、イチゴ等の果樹又は果実類;キャベツ、トマト、ナス、ほうれん草、ブロッコリー、レタス、タマネギ、ネギ、ピーマン等の野菜類;ニンジン、馬鈴薯、サツマイモ、大根、蓮根、かぶ等の根菜類;綿、麻、コウゾ、ミツマタ、菜種、ビート、ホップ、サトウキビ、テンサイ、オリーブ、ゴム、コーヒー、タバコ、茶等の加工用作物類;カボチャ、キュウリ、スイカ、メロン等の瓜類;オーチャードグラス、ソルガム、チモシー、クローバー、アルファルファ等の牧草類;高麗芝、ベントグラス等の芝類;ラベンダー、ローズマリー、タイム、パセリ、胡椒、しょうが等の香料等用作物類;キク、バラ、蘭等の花卉類等が挙げられるがこれらに限定されるものではない。
Examples of the plant that can be used for the agricultural and horticultural pest control composition of the present invention include grains such as rice, barley, wheat, rye, oats, corn, and Takatsuki; soybeans, red beans, broad beans, peas, peanuts, etc. Beans; apples, citrus fruits, pears, grapes, peaches, plums, cherry peaches, walnuts, almonds, bananas, strawberries and other fruit trees or fruits; cabbage, tomatoes, eggplant, spinach, broccoli, lettuce, onion, leek, peppers, etc. Vegetables: Root vegetables such as carrots, potatoes, sweet potatoes, radishes, lotus roots, turnips; for processing cotton, hemp, mulberry, mitsumata, rapeseed, beet, hops, sugar cane, sugar beet, olives, rubber, coffee, tobacco, tea, etc. Crops; potatoes such as pumpkin, cucumber, watermelon, melon; orchardgrass, sorghum, timothy, clover, alfalfa, etc. Grasses; grasses such as Korean turf, bentgrass; crops for fragrances such as lavender, rosemary, thyme, parsley, pepper, ginger, etc .; It is not something.
本発明の農園芸用病害虫防除剤組成物は、防除に有効な当該組成物の有効量で当該病害・害虫の発生が予測される対象植物、対象植物の種子、播種するための栽培担体又は土壌等を処理することによって対象植物を保護することができる。対象植物、対象植物の種子、播種するための栽培担体又は土壌等の処理とは、当該農園芸用病害虫防除剤組成物の散布、塗布、対象作物が生育している土壌に対する散布、灌注等が含まれる。具体的には、本発明の農園芸用病害虫防除剤組成物は、各種病害・害虫を防除するためにそのまま、又は水等で適宜希釈し、若しくは懸濁させた形で使用すれば良く、対象作物において発生する病害・害虫に対して植物の茎葉部に散布するほかに、稲育苗箱施用、種子処理、種子粉衣等の施用方法、種子消毒法、植穴処理、株元処理、作条処理、土壌混和等の施用方法を好適に用いることができる。果樹、穀類、野菜等の畑作において発生する病害に対しては粉衣や浸漬等の種子処理、苗根の浸漬処理、播種時等の作条、育苗用の栽培容器や植え穴、株元等の育苗担体等への潅注、表面散布、混和処理等の後潅水等して植物に吸収させて使用する方法を好適に用いることができる。加えて水耕栽培における水耕液への処理、くん煙或いは樹幹注入等に使用しても良い。
The pest control composition for agricultural and horticultural use of the present invention is a target plant, the seed of the target plant, the seed of the target plant, the cultivation carrier for sowing, or the soil, which is expected to generate the disease / pest with an effective amount of the composition effective for control. The target plant can be protected by treating the etc. The treatment of the target plant, the seed of the target plant, the cultivation carrier or the soil for sowing includes the application and application of the agricultural and horticultural pest control composition, application to the soil where the target crop is grown, irrigation, etc. included. Specifically, the agricultural and horticultural pest control composition of the present invention may be used as it is, or appropriately diluted or suspended in water or the like, for controlling various diseases and pests. In addition to spraying on plant foliage for diseases and pests that occur in crops, rice nursery box application, seed treatment, seed dressing application method, seed disinfection method, planting hole treatment, plant head treatment, cropping Application methods such as treatment and soil mixing can be suitably used. For diseases that occur in field crops such as fruit trees, cereals, and vegetables, seed treatment such as dressing and soaking, soaking treatment of seedling roots, cropping at the time of sowing, cultivation container and planting hole for raising seedlings, plant origin, etc. It is possible to suitably use a method in which the plant is absorbed by a plant by post-irrigation such as irrigation of a seedling carrier, surface spraying, mixing treatment, etc. In addition, you may use for the treatment to the hydroponic liquid in hydroponics, smoking, or trunk injection.
本発明の使用方法を実施する場合の「栽培担体」又は「土壌」とは、植物を栽培するための支持体を示すものであり、材質は特に制限されないが、植物が生育しうる材質であれば良く、例えば、いわゆる各種土壌、育苗マット、水等を含むものであり、砂、バーミキュライト、綿、紙、珪藻土、寒天、ゲル状物質、高分子物質、ロックウール、グラスウール、木材チップ、バーク、軽石等を含むこともできる。
The “cultivation carrier” or “soil” in carrying out the method of use of the present invention refers to a support for cultivating a plant, and the material is not particularly limited, but may be a material on which a plant can grow. For example, it includes so-called various soils, seedling mats, water, etc., sand, vermiculite, cotton, paper, diatomaceous earth, agar, gel-like substances, polymer substances, rock wool, glass wool, wood chips, bark, Pumice can also be included.
植物の茎葉部に散布する方法としては、例えば、乳剤、フロアブル剤等の液体製剤又は水和剤若しくは顆粒水和剤等の固形製剤を水で希釈し、又は希釈せずに散布する方法、粉剤を散布する方法又はくん煙等が挙げられる。土壌への施用方法としては、例えば、液体又は固体製剤を水に希釈又は希釈せずして植物体の設置場所近辺又は育苗のための苗床等に施用する方法、粒剤を植物体の設置場所近辺又は苗床に散布する方法、播種前又は移植前に粉剤、水和剤、顆粒水和剤、粒剤等を散布し土壌全体と混和する方法、播種前又は植物体を植える前に植え穴、作条等に粉剤、水和剤、顆粒水和剤、粒剤等を散布する方法などが挙げられる。水稲の育苗箱への施用方法としては、剤型は、例えば、播種時施用、緑化期施用、移植時施用など施用時期により異なる場合もあるが、粉剤、顆粒水和剤、粒剤等の剤型で施用すれば良い。培土との混和によっても施用することができ、培土と粉剤、顆粒水和剤又は粒剤等との混和、例えば、床土混和、覆土混和、培土全体への混和等することができる。単に、培土と各種製剤を交互に層状にして施用しても良い。播種時の施用の時期は播種の前、同時、播種後いずれでも良く、覆土後に施用しても良い。
Examples of the method of spraying on the foliage of plants include, for example, a method of diluting a liquid preparation such as an emulsion or a flowable agent or a solid preparation such as a wettable powder or a granular wettable powder with water or spraying without diluting, or a powder. Or a method of spraying smoke. Examples of application methods to the soil include, for example, a method in which a liquid or solid preparation is diluted or not diluted with water and applied to the vicinity of a plant installation place or a nursery bed for raising seedlings, etc. The method of spraying in the vicinity or nursery, the method of spraying powder, wettable powder, wettable granule powder, granule etc. before sowing or transplanting and mixing with the whole soil, the planting hole before sowing or before planting the plant, Examples include a method of spraying powder, wettable powder, wettable powder, granule, etc. on the strip. As a method for applying paddy rice to a seedling box, the dosage form may vary depending on the time of application such as application at seeding, application at greening period, application at transplantation, etc., but agents such as powder, granule wettable powder, granules, etc. Apply with a mold. It can also be applied by mixing with soil, and it can be mixed with soil and powder, granulated wettable powder or granules, for example, mixed with ground soil, mixed with soil covering, mixed with the entire soil. Simply, the soil and various preparations may be applied alternately in layers. The time of application at the time of sowing may be before sowing, at the same time, after sowing, or after soil covering.
畑作物、例えば麦等においては、播種から育苗期において、種子への粉衣や浸漬等の種子処理又は植物体に近接する栽培担体等への処理が好ましい。畑へ直接播種する植物においては、種子への直接の処理の他、栽培中の植物に近接する栽培担体等への処理が好適である。粒剤を用いて散布処理又は水に希釈又は希釈しない薬剤を液状にて潅注処理を行うこと等ができる。
移植を行う栽培植物の播種、育苗期の処理としては、種子への直接の処理の他、育苗用の苗床への液状とした薬剤の潅注処理又は粒剤の散布処理が好ましい。又、定植時に粒剤を植え穴に処理したり、移植場所近辺の栽培担体に混和することも好ましい態様である。
本発明の農園芸用病害虫防除剤組成物は、農薬製剤上の常法に従い、使用上都合の良い形状に製剤して使用するのが一般的である。即ち、一般式(I)で表される4-シクロプロピル-1,2,3-チアジアゾール誘導体又はその塩類は、これを適当な不活性担体に、又は必要に応じて補助剤と一緒に適当な割合に配合して溶解、分離、懸濁、混合、含浸、吸着若しくは付着させ、適宜の剤形、例えば懸濁剤、乳剤、液剤、水和剤、粒剤、粉剤、錠剤、種子コーティング等にあっては、噴霧、塗布、浸漬等の処理に適した懸濁液や液剤等に製剤して使用すれば良い。 In field crops such as wheat, seed treatment such as dressing and soaking on seeds or treatment on a cultivation carrier close to a plant body is preferable from sowing to raising seedling. In plants that are sown directly in a field, in addition to direct treatment on seeds, treatment on a cultivation carrier in the vicinity of the plant being cultivated is suitable. It is possible to perform spraying treatment using a granule or irrigation treatment in a liquid of a drug diluted or not diluted in water.
As the seeding of the cultivated plant to be transplanted and the treatment at the seedling raising stage, in addition to the direct treatment to the seed, the irrigation treatment of the liquid drug or the granule spraying treatment to the nursery seedling bed is preferable. Moreover, it is also a preferable aspect that a granule is processed into a planting hole at the time of planting or is mixed with a cultivation carrier in the vicinity of the transplantation site.
The agricultural and horticultural pest control composition of the present invention is generally used in a form convenient for use according to a conventional method for agricultural chemical preparations. That is, the 4-cyclopropyl-1,2,3-thiadiazole derivative represented by the general formula (I) or a salt thereof is suitable for use with a suitable inert carrier or with an auxiliary agent as necessary. Combined in proportion, dissolved, separated, suspended, mixed, impregnated, adsorbed or adhered to appropriate dosage forms such as suspensions, emulsions, solutions, wettable powders, granules, powders, tablets, seed coatings, etc. In that case, it may be used after being formulated into a suspension or liquid suitable for treatment such as spraying, coating, and immersion.
移植を行う栽培植物の播種、育苗期の処理としては、種子への直接の処理の他、育苗用の苗床への液状とした薬剤の潅注処理又は粒剤の散布処理が好ましい。又、定植時に粒剤を植え穴に処理したり、移植場所近辺の栽培担体に混和することも好ましい態様である。
本発明の農園芸用病害虫防除剤組成物は、農薬製剤上の常法に従い、使用上都合の良い形状に製剤して使用するのが一般的である。即ち、一般式(I)で表される4-シクロプロピル-1,2,3-チアジアゾール誘導体又はその塩類は、これを適当な不活性担体に、又は必要に応じて補助剤と一緒に適当な割合に配合して溶解、分離、懸濁、混合、含浸、吸着若しくは付着させ、適宜の剤形、例えば懸濁剤、乳剤、液剤、水和剤、粒剤、粉剤、錠剤、種子コーティング等にあっては、噴霧、塗布、浸漬等の処理に適した懸濁液や液剤等に製剤して使用すれば良い。 In field crops such as wheat, seed treatment such as dressing and soaking on seeds or treatment on a cultivation carrier close to a plant body is preferable from sowing to raising seedling. In plants that are sown directly in a field, in addition to direct treatment on seeds, treatment on a cultivation carrier in the vicinity of the plant being cultivated is suitable. It is possible to perform spraying treatment using a granule or irrigation treatment in a liquid of a drug diluted or not diluted in water.
As the seeding of the cultivated plant to be transplanted and the treatment at the seedling raising stage, in addition to the direct treatment to the seed, the irrigation treatment of the liquid drug or the granule spraying treatment to the nursery seedling bed is preferable. Moreover, it is also a preferable aspect that a granule is processed into a planting hole at the time of planting or is mixed with a cultivation carrier in the vicinity of the transplantation site.
The agricultural and horticultural pest control composition of the present invention is generally used in a form convenient for use according to a conventional method for agricultural chemical preparations. That is, the 4-cyclopropyl-1,2,3-thiadiazole derivative represented by the general formula (I) or a salt thereof is suitable for use with a suitable inert carrier or with an auxiliary agent as necessary. Combined in proportion, dissolved, separated, suspended, mixed, impregnated, adsorbed or adhered to appropriate dosage forms such as suspensions, emulsions, solutions, wettable powders, granules, powders, tablets, seed coatings, etc. In that case, it may be used after being formulated into a suspension or liquid suitable for treatment such as spraying, coating, and immersion.
本発明で用いられる農園芸用病害虫防除剤組成物に使用できる不活性担体としては固体又は液体の何れであっても良く、固体の担体になりうる材料としては、例えばダイズ粉、穀物粉、木粉、樹皮粉、鋸粉、タバコ茎粉、クルミ殻粉、ふすま、繊維素粉末、植物エキス抽出後の残渣、粉砕合成樹脂等の合成重合体、粘土類(例えばカオリン、ベントナイト、酸性白土等)、タルク類(例えばタルク、ピロフィライト等)、シリカ類{例えば珪藻土、珪砂、雲母、ホワイトカーボン(含水微粉珪素、含水珪酸ともいわれる合成高分散珪酸で、製品により珪酸カルシウムを主成分として含むものもある。)}、活性炭、イオウ粉末、軽石、焼成珪藻土、レンガ粉砕物、フライアッシュ、砂、炭酸カルシウム、燐酸カルシウム等の無機鉱物性粉末、硫安、燐安、硝安、尿素、塩安等の化学肥料、堆肥等が挙げられる。これらは単独で若しくは二種以上の混合物の形で使用することもできる。
The inert carrier that can be used in the agricultural and horticultural pest control composition used in the present invention may be either solid or liquid. Examples of materials that can be used as the solid carrier include soybean flour, cereal flour, and wood. Powder, bark powder, saw powder, tobacco stem powder, walnut shell powder, bran, fiber powder, residues after extraction of plant extracts, synthetic polymers such as ground synthetic resin, clays (eg kaolin, bentonite, acid clay) , Talc (eg, talc, pyrophyllite, etc.), silica (eg, diatomaceous earth, silica sand, mica, white carbon (synthetic highly dispersed silicic acid, also called hydrous finely divided silicon, hydrous silicic acid, and some products contain calcium silicate as the main component) .)}, Inorganic mineral powders such as activated carbon, sulfur powder, pumice, calcined diatomaceous earth, brick ground, fly ash, sand, calcium carbonate, calcium phosphate Ammonium sulfate, ammonium phosphate, ammonium nitrate, urea, fertilizer salts depreciation etc., compost and the like. These may be used alone or in the form of a mixture of two or more.
液体の担体になりうる材料としては、それ自体溶媒能を有するものの他、溶媒能を有さずとも補助剤の助けにより有効成分化合物を分散させうるものなら特に限定されず、例えば、水、アルコール類(例えばメタノール、エタノール、イソプロパノール、ブタノール、エチレングリコール等)、ケトン類(例えばアセトン、メチルエチルケトン、メチルイソブチルケトン、ジイソブチルケトン、シクロヘキサノン等)、エーテル類(例えばエチルエーテル、ジオキサン、セロソルブ、ジプロピルエ-テル、テトラヒドロフラン等)、脂肪族炭化水素類(例えばケロシン、鉱油等)、芳香族炭化水素類(例えばベンゼン、トルエン、キシレン、ソルベントナフサ、アルキルナフタレン等)、ハロゲン化炭化水素類(例えばジクロロエタン、クロロホルム、四塩化炭素、塩素化ベンゼン等)、エステル類(例えば酢酸エチル、ジイソプピルフタレ-ト、ジブチルフタレート、ジオクチルフタレート等)、アミド類(例えばジメチルホルムアミド、ジエチルホルムアミド、ジメチルアセトアミド等)、ニトリル類(例えばアセトニトリル等)、ジメチルスルホキシド類が挙げられる。これらは単独で若しくは二種以上の混合物の形で使用することもできる。
The material that can be used as a liquid carrier is not particularly limited as long as it has a solvent ability, but can also disperse an active ingredient compound with the aid of an auxiliary agent without having a solvent ability. For example, water, alcohol (Eg, methanol, ethanol, isopropanol, butanol, ethylene glycol, etc.), ketones (eg, acetone, methyl ethyl ketone, methyl isobutyl ketone, diisobutyl ketone, cyclohexanone, etc.), ethers (eg, ethyl ether, dioxane, cellosolve, dipropyl ether, Tetrahydrofuran, etc.), aliphatic hydrocarbons (eg kerosene, mineral oil, etc.), aromatic hydrocarbons (eg benzene, toluene, xylene, solvent naphtha, alkylnaphthalene, etc.), halogenated hydrocarbons (eg dichloroethane, Roform, carbon tetrachloride, chlorinated benzene, etc.), esters (eg, ethyl acetate, diisopropyl phthalate, dibutyl phthalate, dioctyl phthalate, etc.), amides (eg, dimethylformamide, diethylformamide, dimethylacetamide, etc.), Nitriles (for example, acetonitrile etc.) and dimethyl sulfoxides are mentioned. These may be used alone or in the form of a mixture of two or more.
さらに、目的に応じて他の補助剤を使用することもできる。これらの補助剤は単独で、ある場合は二種以上の補助剤を併用することもできるし、又ある場合には全く補助剤を使用しないことも可能である。これらの補助剤として具体的には、有効成分化合物の乳化、分散、可溶化及び/又は湿潤の目的のために界面活性剤が使用され、例えば、ポリオキシエチレンアルキルエーテル、ポリオキシエチレンアルキルアリールエーテル、ポリオキシエチレン高級脂肪酸エステル、ポリオキシエチレン樹脂酸エステル、ポリオキシエチレンソルビタンモノラウレート、ポリオキシエチレンソルビタンモノオレエート、アルキルアリ-ルスルホン酸塩、ナフタレンスルホン酸縮合物、リグニンスルホン酸塩、高級アルコール硫酸エステル等の界面活性剤が挙げられる。又、有効成分化合物の分散安定化、粘着及び/又は結合の目的のために、次に例示する補助剤を使用することもでき、例えば、カゼイン、ゼラチン、澱粉、メチルセルロース、カルボキシメチルセルロース、アラビアゴム、ポリビニルアルコール、松根油、糠油、ベントナイト、リグニンスルホン酸塩等の補助剤が挙げられる。
Furthermore, other adjuvants can be used depending on the purpose. These adjuvants may be used alone, in some cases, two or more kinds of adjuvants may be used in combination, and in some cases, no adjuvant may be used. Specifically, a surfactant is used as an auxiliary agent for the purpose of emulsifying, dispersing, solubilizing and / or wetting the active ingredient compound, for example, polyoxyethylene alkyl ether, polyoxyethylene alkyl aryl ether. , Polyoxyethylene higher fatty acid ester, polyoxyethylene resin acid ester, polyoxyethylene sorbitan monolaurate, polyoxyethylene sorbitan monooleate, alkyl aryl sulfonate, naphthalene sulfonic acid condensate, lignin sulfonate, higher Surfactants such as alcohol sulfates are listed. Further, for the purpose of stabilizing the dispersion of the active ingredient compound, sticking and / or binding, the following auxiliary agents can be used, for example, casein, gelatin, starch, methylcellulose, carboxymethylcellulose, gum arabic, Examples include adjuvants such as polyvinyl alcohol, pine oil, coconut oil, bentonite, and lignin sulfonate.
固体製品の流動性改良のために次に挙げる補助剤を使用することもでき、例えばワックス、ステアリン酸塩、燐酸アルキルエステル等の補助剤を使用できる。懸濁性製品の解こう剤として、例えばナフタレンスルホン酸縮合物、縮合燐酸塩等の補助剤を使用することもできる。消泡剤としては、例えばシリコーン油等の補助剤を使用することもできる。
本発明に用いられる農園芸用病害虫防除剤組成物には、更に防除対象病害虫、防除適期の拡大のため、或いは薬量の低減、相乗効果を図る目的で他の農園芸用殺虫剤、殺ダニ剤、殺線虫剤、殺菌剤、生物農薬等と混合して使用することも可能であり、又、使用場面に応じて除草剤、植物成長調節剤、肥料等と混合して使用することも可能である。 In order to improve the fluidity of solid products, the following adjuvants may be used, and for example, adjuvants such as waxes, stearates and alkyl phosphates may be used. As a peptizer for the suspension product, for example, auxiliary agents such as naphthalenesulfonic acid condensate and condensed phosphate can be used. As the antifoaming agent, for example, an auxiliary agent such as silicone oil can be used.
The pesticide composition for agricultural and horticultural use used in the present invention further includes other pesticides for agricultural and horticultural use for the purpose of controlling the target pests to be controlled, the appropriate control period, or reducing the dose and synergistic effects. It can be used in combination with herbicides, nematicides, fungicides, biological pesticides, etc., and can be used in combination with herbicides, plant growth regulators, fertilizers, etc. Is possible.
本発明に用いられる農園芸用病害虫防除剤組成物には、更に防除対象病害虫、防除適期の拡大のため、或いは薬量の低減、相乗効果を図る目的で他の農園芸用殺虫剤、殺ダニ剤、殺線虫剤、殺菌剤、生物農薬等と混合して使用することも可能であり、又、使用場面に応じて除草剤、植物成長調節剤、肥料等と混合して使用することも可能である。 In order to improve the fluidity of solid products, the following adjuvants may be used, and for example, adjuvants such as waxes, stearates and alkyl phosphates may be used. As a peptizer for the suspension product, for example, auxiliary agents such as naphthalenesulfonic acid condensate and condensed phosphate can be used. As the antifoaming agent, for example, an auxiliary agent such as silicone oil can be used.
The pesticide composition for agricultural and horticultural use used in the present invention further includes other pesticides for agricultural and horticultural use for the purpose of controlling the target pests to be controlled, the appropriate control period, or reducing the dose and synergistic effects. It can be used in combination with herbicides, nematicides, fungicides, biological pesticides, etc., and can be used in combination with herbicides, plant growth regulators, fertilizers, etc. Is possible.
本発明の使用方法に用いられる農園芸用病害虫防除剤組成物には、必要に応じて他の成分を混合又は併用することができ、例えば種子処理に際して、鳥類をはじめとする動物類による摂取(誤飲を含む)を避けるために忌避剤や他の成分を含有せしめることもできる。忌避剤としては、例えばナフタレン化合物等の臭気性化合物、ひまし油、松脂、ポリブタン、ジフェニルアミンペンタクロロフェノール、キノン、酸化亜鉛、芳香族溶媒等の接触阻害剤、N-(トリクロロメチルチオ)-4-シクロヘキセン-1,2-カルボキシイミド、アントラキノン、蓚酸銅、テルペン油等の苦味物質類、パラジクロルベンゼン、アリールイソチオシアナート、酢酸アミル、アネトール、柑橘油、クレゾール類、ゼラニウム油又はラベンダー油等のハーブ油、メントール、サリチル酸メチル、ニコチン、ペンタンチオール、ピリジン類、塩化トリブチルスズ、チラム、ジラム、カーバメート系殺虫剤(例えばメチオカルブ等)、グアザチン、塩素化シクロジエン系殺虫剤(例えばエンドリン等)、有機リン系殺虫剤(例えばフェンチオン等)等を例示することができる。他の成分として、毒性物質又は増殖抑制物質(不妊化剤)としては、例えば3-クロロ-4-トルイジン塩酸塩、ストリキニーネ、20,25-ジアザコレステロール塩酸塩(コード名:SC-12937)等を例示することができる。
The agricultural and horticultural pest control composition used in the method of use of the present invention can be mixed or used in combination with other components as necessary. For example, during seed treatment, ingestion by animals including birds ( Repellents and other ingredients can be included to avoid accidental ingestion). Repellents include, for example, odorous compounds such as naphthalene compounds, contact inhibitors such as castor oil, pine resin, polybutane, diphenylamine pentachlorophenol, quinone, zinc oxide, aromatic solvents, N- (trichloromethylthio) -4-cyclohexene- Bitter substances such as 1,2-carboximide, anthraquinone, copper oxalate, terpene oil, paradichlorobenzene, aryl isothiocyanate, amyl acetate, anethole, citrus oil, cresols, geranium oil or lavender oil, Menthol, methyl salicylate, nicotine, pentanethiol, pyridines, tributyltin chloride, thiram, ziram, carbamate insecticides (such as methiocarb), guazatine, chlorinated cyclodiene insecticides (such as endrin), organophosphorus insecticides (such as endrin) Example If it is possible to illustrate the fenthion, etc.) and the like. As other components, toxic substances or growth inhibitory substances (fertility agents) include, for example, 3-chloro-4-toluidine hydrochloride, strychnine, 20,25-diazacholesterol hydrochloride (code name: SC-12937), etc. Can be illustrated.
本発明に用いられる農園芸用病害虫防除剤組成物の有効成分である一般式(I)で表される4-シクロプロピル-1,2,3-チアジアゾール誘導体又はその塩類の含有量と、殺菌活性若しくは殺虫活性を有する化合物の含有量との和としては、農園芸用病害虫防除剤組成物100質量部中、約0.01~約80質量部の範囲から適宜選択して使用すれば良く、例えば、農園芸分野で使用される各種製剤(乳剤、粉剤、水和剤、粒剤、顆粒水和剤、フロアブル剤等)とする場合は約0.01~約50質量部が適当であり、好ましくは、約1~約50質量部が良い。その配合比としては一般式(I)で表される4-シクロプロピル-1,2,3-チアジアゾール誘導体又はその塩類1質量部に対して殺菌活性及び/又は殺虫活性を有する化合物が約0.01~約1000質量部の範囲で配合され、殺菌及び/又は殺虫活性の拡大や相乗効果を引き出すために、好ましくは約0.05~約100質量部の範囲であり、より好ましくは約0.1~約100質量部の範囲である。
Content of 4-cyclopropyl-1,2,3-thiadiazole derivative represented by general formula (I) or a salt thereof, which is an active ingredient of the agricultural and horticultural pest control composition used in the present invention, and bactericidal activity Alternatively, the sum of the content of the compound having insecticidal activity may be appropriately selected from the range of about 0.01 to about 80 parts by mass in 100 parts by mass of the agricultural and horticultural pest control composition. In the case of various preparations used in the agricultural and horticultural fields (emulsions, powders, wettable powders, granules, wettable powders, flowables, etc.), about 0.01 to about 50 parts by mass is appropriate, preferably Is preferably about 1 to about 50 parts by weight. The compounding ratio of the compound having bactericidal activity and / or insecticidal activity with respect to 1 part by mass of the 4-cyclopropyl-1,2,3-thiadiazole derivative represented by the general formula (I) or a salt thereof is about 0. It is blended in the range of 01 to about 1000 parts by weight, and is preferably in the range of about 0.05 to about 100 parts by weight, more preferably about 0. It is in the range of 1 to about 100 parts by weight.
農園芸用病害虫防除剤組成物の施用量は、有効成分化合物の配合割合、気象条件、製剤形態、施用時期、施用方法、施用場所、防除対象病害、対象作物等により異なるが、通常の散布剤としては、有効成分化合物として1アール当たり約0.1g~約1000g範囲から適宜選択して施用すれば良く、好ましくは約1~約100gの範囲が良い。種子処理剤としては、通常種子重量100kg当たり有効成分化合物として約0.1~約1000gの範囲から適宜選択して施用すれば良く、好ましくは約1~約300gの範囲が良い。
The application rate of the agricultural and horticultural pest control composition varies depending on the compounding ratio of the active ingredient compound, meteorological conditions, formulation form, application time, application method, application location, target disease, target crop, etc. As an active ingredient compound, it may be applied by appropriately selecting from about 0.1 g to about 1000 g per are, and preferably in the range of about 1 to about 100 g. The seed treatment agent is usually selected from the range of about 0.1 to about 1000 g as an active ingredient compound per 100 kg of seed weight, and is preferably applied in the range of about 1 to about 300 g.
また、本発明の農園芸用病害虫防除剤組成物の有効成分である一般式(I)で表される4-シクロプロピル-1,2,3-チアジアゾール誘導体又はその塩類と、殺菌活性及び/又は殺虫活性を有する化合物とは各々単独で同時期に使用することにより、予め有効成分が混合された農園芸用病害虫防除剤組成物と同様の殺菌・殺虫スペクトラムの拡大効果が期待でき、4-シクロプロピル-1,2,3-チアジアゾール誘導体又はその塩類と、殺菌活性及び/又は殺虫活性を有する化合物との相乗効果を発揮させることができる。即ち、一般式(I)で表される4-シクロプロピル-1,2,3-チアジアゾール誘導体又はその塩類と、殺菌活性及び/又は殺虫活性を有する化合物を各々単独で製剤化したものやその希釈液を、使用の現場において処理時に混用して施用してもよく、更に、別々に同時期にこれらを用いて植物の茎葉部、種子、栽培担体等を処理してもよい。なお、各々単独で別々に施用する場合、同時に施用してもよく、約7日程度の間隔を設けてもよいが、いずれか一方の有効成分が植物又は栽培担体に残存している時期に他方の有効成分を施用することが好ましく、上記の「同時期」とは、そのように両者が処理されている時期の少なくとも一部が重複することを含む概念であり、必ずしも全く同時に施用作業を行う必要はない。このような、一般式(I)で表される4-シクロプロピル-1,2,3-チアジアゾール誘導体又はその塩類と、殺菌活性及び/又は殺虫活性を有する化合物の1種又は2種以上の有効量を用いて、当該4-シクロプロピル-1,2,3-チアジアゾール誘導体又はその塩類と、殺菌活性及び/又は殺虫活性を有する化合物を各々単独で植物の茎葉部、種子又は栽培担体に同時期に処理する植物病害の防除方法も、本発明の1つである。一般式(I)で表される4-シクロプロピル-1,2,3-チアジアゾール誘導体又はその塩類と、殺菌活性若しくは殺虫活性を有する化合物の有効量としては、上述した農園芸用病害虫防除剤組成物におけるのと同様である。
Further, the 4-cyclopropyl-1,2,3-thiadiazole derivative represented by the general formula (I) or a salt thereof, which is an active ingredient of the agricultural and horticultural pest control composition of the present invention, bactericidal activity and / or By using each of the compounds having insecticidal activity alone at the same time, it can be expected to have the same effect of expanding the bactericidal and insecticidal spectrum as the agricultural and horticultural pesticide composition pre-mixed with active ingredients. A synergistic effect of a propyl-1,2,3-thiadiazole derivative or a salt thereof and a compound having bactericidal activity and / or insecticidal activity can be exhibited. That is, a 4-cyclopropyl-1,2,3-thiadiazole derivative represented by the general formula (I) or a salt thereof and a compound having a bactericidal activity and / or an insecticidal activity alone, or a dilution thereof The liquid may be mixed and applied at the time of treatment at the site of use, and further, the plant foliage, seeds, cultivation carrier and the like may be treated separately at the same time. In addition, when each is applied separately separately, it may be applied at the same time, and an interval of about 7 days may be provided, but at the time when any one of the active ingredients remains in the plant or the cultivation carrier, the other The above-mentioned “simultaneous period” is a concept including that at least a part of the period during which both are treated as described above, and the application work is not necessarily performed at the same time. There is no need. One or more effective compounds of such a 4-cyclopropyl-1,2,3-thiadiazole derivative represented by the general formula (I) or a salt thereof and a compound having fungicidal activity and / or insecticidal activity The 4-cyclopropyl-1,2,3-thiadiazole derivative or a salt thereof and the compound having bactericidal activity and / or insecticidal activity are each independently used in the plant foliage, seeds or cultivation carrier. A method for controlling plant diseases to be treated is also one aspect of the present invention. As the effective amount of the 4-cyclopropyl-1,2,3-thiadiazole derivative represented by the general formula (I) or a salt thereof and the compound having bactericidal activity or insecticidal activity, the above-mentioned agricultural and horticultural pest control composition It is the same as in the product.
次に実施例を挙げて具体的に説明するが発明の要旨を超えない限りそれらに限定されるものではない。以下において、各化合物番号は第1表に記載の化合物番号を示し、「部」は「質量部」を表す。
Next, the present invention will be specifically described with reference to examples, but the present invention is not limited to these examples unless it exceeds the gist of the invention. In the following, each compound number represents a compound number described in Table 1, and “part” represents “part by mass”.
[製剤例1]
化合物番号1-12 5部
チアメトキサム 5部
キシレン 70部
N-メチルピロリドン 10部
ポリオキシエチレンノニルフェニルエーテルと
アルキルベンゼンスルホン酸カルシウムとの混合物 10部
以上を均一に混合溶解して乳剤とする。 [Formulation Example 1]
Compound No. 1-12 5 parts thiamethoxam 5 parts xylene 70 parts N-methylpyrrolidone 10 parts Mixture of polyoxyethylene nonylphenyl ether and calcium alkylbenzenesulfonate 10 parts or more are mixed and dissolved uniformly to give an emulsion.
化合物番号1-12 5部
チアメトキサム 5部
キシレン 70部
N-メチルピロリドン 10部
ポリオキシエチレンノニルフェニルエーテルと
アルキルベンゼンスルホン酸カルシウムとの混合物 10部
以上を均一に混合溶解して乳剤とする。 [Formulation Example 1]
Compound No. 1-12 5 parts thiamethoxam 5 parts xylene 70 parts N-methylpyrrolidone 10 parts Mixture of polyoxyethylene nonylphenyl ether and calcium alkylbenzenesulfonate 10 parts or more are mixed and dissolved uniformly to give an emulsion.
[製剤例2]
化合物番号1-93 1部
フルジオキソニル 2部
クレー粉末 82部
珪藻土粉末 15部
以上を均一に混合粉砕して粉剤とする。 [Formulation Example 2]
Compound No. 1-93 1 part fludioxonil 2 parts clay powder 82 parts diatomaceous earth powder 15 parts or more are mixed and ground uniformly to form a powder.
化合物番号1-93 1部
フルジオキソニル 2部
クレー粉末 82部
珪藻土粉末 15部
以上を均一に混合粉砕して粉剤とする。 [Formulation Example 2]
Compound No. 1-93 1 part fludioxonil 2 parts clay powder 82 parts diatomaceous earth powder 15 parts or more are mixed and ground uniformly to form a powder.
[製剤例3]
化合物番号1-12 2部
フルキンコナゾール 3部
ベントナイトとクレーの混合粉末 90部
リグニンスルホン酸カルシウム 5部
以上を均一に混合し、適量の水を加えて混練し、造粒、乾燥して粒剤とする。 [Formulation Example 3]
Compound No. 1-12 2 parts fluquinconazole 3 parts bentonite and clay mixed powder 90 parts calcium lignin sulfonate 5 parts or more uniformly mixed, kneaded with an appropriate amount of water, granulated and dried to give granules And
化合物番号1-12 2部
フルキンコナゾール 3部
ベントナイトとクレーの混合粉末 90部
リグニンスルホン酸カルシウム 5部
以上を均一に混合し、適量の水を加えて混練し、造粒、乾燥して粒剤とする。 [Formulation Example 3]
Compound No. 1-12 2 parts fluquinconazole 3 parts bentonite and clay mixed powder 90 parts calcium lignin sulfonate 5 parts or more uniformly mixed, kneaded with an appropriate amount of water, granulated and dried to give granules And
[製剤例4]
化合物1-93 10部
イミダクロプリド 10部
カオリンと合成高分散珪酸 75部
ポリオキシエチレンノニルフェニルエーテルと
アルキルベンゼンスルホン酸カルシウムとの混合物 5部
以上を均一に混合粉砕して水和剤とする。 [Formulation Example 4]
Compound 1-93 10 parts Imidacloprid 10 parts Kaolin, synthetic highly dispersed silicic acid 75 parts Mixture of polyoxyethylene nonylphenyl ether and calcium alkylbenzenesulfonate 5 parts or more are uniformly mixed and ground to obtain a wettable powder.
化合物1-93 10部
イミダクロプリド 10部
カオリンと合成高分散珪酸 75部
ポリオキシエチレンノニルフェニルエーテルと
アルキルベンゼンスルホン酸カルシウムとの混合物 5部
以上を均一に混合粉砕して水和剤とする。 [Formulation Example 4]
Compound 1-93 10 parts Imidacloprid 10 parts Kaolin, synthetic highly dispersed silicic acid 75 parts Mixture of polyoxyethylene nonylphenyl ether and calcium alkylbenzenesulfonate 5 parts or more are uniformly mixed and ground to obtain a wettable powder.
試験例1.種子処理剤混用によるコムギうどんこ病防除効果試験
5gのコムギ(品種:チホクコムギ)種子(乾燥状態)に0.1gの水を塗し、表中記載の処理薬量の水和剤を当該水処理した種子に均一に付着するように処理した。処理した種子を風乾後、直径10cmのプラスチックポットに播種し温室内で栽培した。コムギが6葉期/分けつ期に生育した時点(約70日後)で、そのコムギにうどんこ病菌(Blumeria graminis)の胞子をふりかけ接種した。接種7日後に、下記の基準に従って、展開葉の発病指数及び防除価(%)を算出した。このとき無処理区の発病指数は5.0であった。結果を第3表、及び第4表に示す。 Test Example 1 Wheat powdery mildew control effect test by mixing seed treatment agent 0.1 g of water is applied to 5 g of wheat (variety: Chihoku wheat) seeds (dried state), and the water treatment with the treatment dosage shown in the table is applied to the water. The seeds were treated so as to adhere uniformly. The treated seeds were air-dried and then sown in a plastic pot having a diameter of 10 cm and cultivated in a greenhouse. When the wheat grew at the 6th leaf stage / parting stage (after about 70 days), the wheat was inoculated with spores of powdery mildew (Blumeria graminis). Seven days after the inoculation, the disease index and the control value (%) of the developed leaves were calculated according to the following criteria. At this time, the disease index of the untreated section was 5.0. The results are shown in Tables 3 and 4.
5gのコムギ(品種:チホクコムギ)種子(乾燥状態)に0.1gの水を塗し、表中記載の処理薬量の水和剤を当該水処理した種子に均一に付着するように処理した。処理した種子を風乾後、直径10cmのプラスチックポットに播種し温室内で栽培した。コムギが6葉期/分けつ期に生育した時点(約70日後)で、そのコムギにうどんこ病菌(Blumeria graminis)の胞子をふりかけ接種した。接種7日後に、下記の基準に従って、展開葉の発病指数及び防除価(%)を算出した。このとき無処理区の発病指数は5.0であった。結果を第3表、及び第4表に示す。 Test Example 1 Wheat powdery mildew control effect test by mixing seed treatment agent 0.1 g of water is applied to 5 g of wheat (variety: Chihoku wheat) seeds (dried state), and the water treatment with the treatment dosage shown in the table is applied to the water. The seeds were treated so as to adhere uniformly. The treated seeds were air-dried and then sown in a plastic pot having a diameter of 10 cm and cultivated in a greenhouse. When the wheat grew at the 6th leaf stage / parting stage (after about 70 days), the wheat was inoculated with spores of powdery mildew (Blumeria graminis). Seven days after the inoculation, the disease index and the control value (%) of the developed leaves were calculated according to the following criteria. At this time, the disease index of the untreated section was 5.0. The results are shown in Tables 3 and 4.
[発病指数]
0 : 発病なし
0.5: 病斑面積率 10%未満
1 : 病斑面積率 10~20%未満
2 : 病斑面積率 20~30%未満
3 : 病斑面積率 30~40%未満
4 : 病斑面積率 40~50%未満
5 : 病斑面積率 50~60%未満
6 : 病斑面積率 60~70%未満
7 : 病斑面積率 70~80%未満
8 : 病斑面積率 80~90%未満
9 : 病斑面積率 90~100%未満
10 : 病斑面積率 100%
[数式-1]
防除価(%)=(1-{処理区の発病指数÷無処理区の発病指数})×100 [Disease index]
0: No disease occurrence 0.5: Spot area ratio less than 10% 1: Spot lesion area ratio 10 to less than 20% 2: Spot lesion area ratio 20 to less than 30% 3: Spot lesion area ratio 30 to less than 40% 4: Spot area ratio 40 to less than 50% 5: Spot area ratio 50 to less than 60% 6: Spot area ratio 60 to less than 70% 7: Spot area ratio 70 to less than 80% 8: Spot area ratio 80 to Less than 90% 9: lesion area ratio 90 to less than 100% 10: lesion area ratio 100%
[Formula-1]
Control value (%) = (1- {Disease index in treated area ÷ Disease index in untreated area}) × 100
0 : 発病なし
0.5: 病斑面積率 10%未満
1 : 病斑面積率 10~20%未満
2 : 病斑面積率 20~30%未満
3 : 病斑面積率 30~40%未満
4 : 病斑面積率 40~50%未満
5 : 病斑面積率 50~60%未満
6 : 病斑面積率 60~70%未満
7 : 病斑面積率 70~80%未満
8 : 病斑面積率 80~90%未満
9 : 病斑面積率 90~100%未満
10 : 病斑面積率 100%
[数式-1]
防除価(%)=(1-{処理区の発病指数÷無処理区の発病指数})×100 [Disease index]
0: No disease occurrence 0.5: Spot area ratio less than 10% 1: Spot lesion area ratio 10 to less than 20% 2: Spot lesion area ratio 20 to less than 30% 3: Spot lesion area ratio 30 to less than 40% 4: Spot area ratio 40 to less than 50% 5: Spot area ratio 50 to less than 60% 6: Spot area ratio 60 to less than 70% 7: Spot area ratio 70 to less than 80% 8: Spot area ratio 80 to Less than 90% 9: lesion area ratio 90 to less than 100% 10: lesion area ratio 100%
[Formula-1]
Control value (%) = (1- {Disease index in treated area ÷ Disease index in untreated area}) × 100
殺菌活性を有する対照化合物としては、以下の物質を用いた。
化合物A:フルジオキソニル(fludioxonil)
化合物B:ビテルタノール(bitertanol)
化合物C:フベリダゾール(fuberidazole)
化合物D:トリアジメノール(triadimenol)
化合物E:トリチコナゾール(triticonazole)
化合物F:グアザチン(guazatine)
化合物G:フルキンコナゾール(fluquinconazole)
化合物H:プロクロラズ(prochloraz)
化合物I:カルボキシン(carboxin)
化合物J:チウラム(thiram) The following substances were used as control compounds having bactericidal activity.
Compound A: fludioxonil
Compound B: bittertanol
Compound C: fuberidazole
Compound D: triadimenol
Compound E: triticonazole
Compound F: guazatine
Compound G: fluquinconazole
Compound H: prochloraz
Compound I: Carboxin
Compound J: thiuram
化合物A:フルジオキソニル(fludioxonil)
化合物B:ビテルタノール(bitertanol)
化合物C:フベリダゾール(fuberidazole)
化合物D:トリアジメノール(triadimenol)
化合物E:トリチコナゾール(triticonazole)
化合物F:グアザチン(guazatine)
化合物G:フルキンコナゾール(fluquinconazole)
化合物H:プロクロラズ(prochloraz)
化合物I:カルボキシン(carboxin)
化合物J:チウラム(thiram) The following substances were used as control compounds having bactericidal activity.
Compound A: fludioxonil
Compound B: bittertanol
Compound C: fuberidazole
Compound D: triadimenol
Compound E: triticonazole
Compound F: guazatine
Compound G: fluquinconazole
Compound H: prochloraz
Compound I: Carboxin
Compound J: thiuram
試験例2.種子処理剤混用によるコムギ赤さび病防除効果試験(温室内試験)
試験例1に記載の方法に従って、コムギ(品種:チホクコムギ)種子(乾燥状態)を処理、栽培した。コムギが6葉期/分けつ期に生育した時点(播種後約70日)で、そのコムギに赤さび病菌(Puccinia recondita)の胞子懸濁液を噴霧接種した。接種7日後に、試験1の基準に従って、展開葉の発病指数及び防除価(%)を算出した。結果を第5表及び第6表に示す。 Test Example 2 Wheat red rust control effect test by mixed seed treatment (greenhouse test)
According to the method described in Test Example 1, wheat (variety: chihoku wheat) seeds (dried state) were treated and cultivated. At the time when the wheat grew at the 6-leaf stage / parting stage (about 70 days after sowing), the wheat was spray-inoculated with a spore suspension of Puccinia recondita. Seven days after the inoculation, the disease index and the control value (%) of the developed leaves were calculated according to the criteria of Test 1. The results are shown in Tables 5 and 6.
試験例1に記載の方法に従って、コムギ(品種:チホクコムギ)種子(乾燥状態)を処理、栽培した。コムギが6葉期/分けつ期に生育した時点(播種後約70日)で、そのコムギに赤さび病菌(Puccinia recondita)の胞子懸濁液を噴霧接種した。接種7日後に、試験1の基準に従って、展開葉の発病指数及び防除価(%)を算出した。結果を第5表及び第6表に示す。 Test Example 2 Wheat red rust control effect test by mixed seed treatment (greenhouse test)
According to the method described in Test Example 1, wheat (variety: chihoku wheat) seeds (dried state) were treated and cultivated. At the time when the wheat grew at the 6-leaf stage / parting stage (about 70 days after sowing), the wheat was spray-inoculated with a spore suspension of Puccinia recondita. Seven days after the inoculation, the disease index and the control value (%) of the developed leaves were calculated according to the criteria of Test 1. The results are shown in Tables 5 and 6.
試験例3.種子処理剤混用によるコムギうどんこ病防除効果試験(圃場試験)
化合物1-93と対照化合物を、表中記載の処理薬量となるよう混用し、コムギ(品種:チホクコムギ)乾燥種子に均一に付着するように処理した。播種量を120kg/ha相当で、上記の種子を2m2(1m×2m)の区画内に条播した。翌年のコムギが出穂する時期(BBCH51-59頃、播種から190~200日後)に、次葉および止葉について、試験例1の基準に従って、自然発生したうどんこ病菌(Blumeria graminis)の発病指数を調査し、防除価(%)を算出した。下記コルビーの計算式に従って、混用による防除効果の期待値を算出し、その値に基づいて化合物1-93と対照化合物の混用処理区における防除効果について相乗性の有無を検定した。結果を第7表に示す。 Test Example 3 Wheat powdery mildew control effect test by mixing seed treatment agent (field test)
Compound 1-93 and the control compound were mixed so as to have the treatment doses shown in the table, and treated so as to uniformly adhere to the dried seeds of wheat (variety: Chihoku wheat). The seeding amount was equivalent to 120 kg / ha, and the above seeds were sown in a 2 m 2 (1 m × 2 m) section. In the next year when wheat emerges (around BBCH 51-59, 190 to 200 days after sowing), the incidence index of the naturally occurring powdery mildew (Blumeria graminis) on the following leaves and leaves according to the criteria of Test Example 1 was calculated. Investigation was made and the control value (%) was calculated. According to the following Colby formula, the expected value of the control effect by the mixed use was calculated, and based on the calculated value, the presence or absence of synergy was tested for the control effect of the compound 1-93 and the control compound in the mixed treatment section. The results are shown in Table 7.
化合物1-93と対照化合物を、表中記載の処理薬量となるよう混用し、コムギ(品種:チホクコムギ)乾燥種子に均一に付着するように処理した。播種量を120kg/ha相当で、上記の種子を2m2(1m×2m)の区画内に条播した。翌年のコムギが出穂する時期(BBCH51-59頃、播種から190~200日後)に、次葉および止葉について、試験例1の基準に従って、自然発生したうどんこ病菌(Blumeria graminis)の発病指数を調査し、防除価(%)を算出した。下記コルビーの計算式に従って、混用による防除効果の期待値を算出し、その値に基づいて化合物1-93と対照化合物の混用処理区における防除効果について相乗性の有無を検定した。結果を第7表に示す。 Test Example 3 Wheat powdery mildew control effect test by mixing seed treatment agent (field test)
Compound 1-93 and the control compound were mixed so as to have the treatment doses shown in the table, and treated so as to uniformly adhere to the dried seeds of wheat (variety: Chihoku wheat). The seeding amount was equivalent to 120 kg / ha, and the above seeds were sown in a 2 m 2 (1 m × 2 m) section. In the next year when wheat emerges (around BBCH 51-59, 190 to 200 days after sowing), the incidence index of the naturally occurring powdery mildew (Blumeria graminis) on the following leaves and leaves according to the criteria of Test Example 1 was calculated. Investigation was made and the control value (%) was calculated. According to the following Colby formula, the expected value of the control effect by the mixed use was calculated, and based on the calculated value, the presence or absence of synergy was tested for the control effect of the compound 1-93 and the control compound in the mixed treatment section. The results are shown in Table 7.
コルビーの計算式
[数式-2]
期待値E=(X+Y)-(X×Y)/100
X:化合物1-93の防除価(%)、Y:混用した対照化合物の防除価(%)
実際の防除価が上記期待値Eよりも大きい場合、その有効性分の組み合わせについて効果が相乗的であると判定される。 Colby's formula
[Formula-2]
Expected value E = (X + Y) − (X × Y) / 100
X: Control value of compound 1-93 (%), Y: Control value of mixed control compound (%)
When the actual control value is larger than the expected value E, it is determined that the effect is synergistic with respect to the combination of the effectiveness.
[数式-2]
期待値E=(X+Y)-(X×Y)/100
X:化合物1-93の防除価(%)、Y:混用した対照化合物の防除価(%)
実際の防除価が上記期待値Eよりも大きい場合、その有効性分の組み合わせについて効果が相乗的であると判定される。 Colby's formula
[Formula-2]
Expected value E = (X + Y) − (X × Y) / 100
X: Control value of compound 1-93 (%), Y: Control value of mixed control compound (%)
When the actual control value is larger than the expected value E, it is determined that the effect is synergistic with respect to the combination of the effectiveness.
殺菌活性を有する対照化合物としては、以下の物質を用いた。
化合物B:ビテルタノール(bitertanol)
化合物C:フベリダゾール(fuberidazole)
化合物D:トリアジメノール(triadimenol)
化合物E:トリチコナゾール(triticonazole)
化合物G:フルキンコナゾール(fluquinconazole)
化合物H:プロクロラズ(prochloraz)
化合物K:テブコナゾール(tebuconazole)
化合物L:プロチオコナゾール(prothioconazole)
化合物M:ピラクロストロビン(pyraclostrobin) The following substances were used as control compounds having bactericidal activity.
Compound B: bittertanol
Compound C: fuberidazole
Compound D: triadimenol
Compound E: triticonazole
Compound G: fluquinconazole
Compound H: prochloraz
Compound K: tebuconazole
Compound L: prothioconazole
Compound M: pyraclostrobin
化合物B:ビテルタノール(bitertanol)
化合物C:フベリダゾール(fuberidazole)
化合物D:トリアジメノール(triadimenol)
化合物E:トリチコナゾール(triticonazole)
化合物G:フルキンコナゾール(fluquinconazole)
化合物H:プロクロラズ(prochloraz)
化合物K:テブコナゾール(tebuconazole)
化合物L:プロチオコナゾール(prothioconazole)
化合物M:ピラクロストロビン(pyraclostrobin) The following substances were used as control compounds having bactericidal activity.
Compound B: bittertanol
Compound C: fuberidazole
Compound D: triadimenol
Compound E: triticonazole
Compound G: fluquinconazole
Compound H: prochloraz
Compound K: tebuconazole
Compound L: prothioconazole
Compound M: pyraclostrobin
試験例4.種子処理剤混用によるコムギ赤さび病防除効果試験(圃場試験)
化合物1-93と対照化合物を、表中記載の処理薬量となるよう混用し、コムギ(品種:ホクシン)乾燥種子に均一に付着するように処理した。播種量を120kg/ha相当で、上記の種子を2m2(1m×2m)の区画内に条播した。翌年のコムギが出穂する時期(BBCH51-59頃、播種から約190~200日後)に、次葉および止葉について、試験例1の基準に従って、自然発生した赤さび病菌(Puccinia recondita)の発病指数を調査し、防除価(%)を算出した。試験3と同様にコルビーの計算式に従って、混用による防除効果の期待値を算出し、その値に基づいて化合物1-93と対照化合物の混用処理区における防除効果について相乗性の有無を検定した。結果を第8表に示す。 Test Example 4 Wheat red rust control effect test by mixing seed treatment agent (field test)
Compound 1-93 and the control compound were mixed so as to have the treatment doses shown in the table, and treated so as to uniformly adhere to the dried seeds of wheat (variety: Hokushin). The seeding amount was equivalent to 120 kg / ha, and the above seeds were sown in a 2 m 2 (1 m × 2 m) section. In the next year when wheat emerges (around BBCH 51-59, approximately 190 to 200 days after sowing), the incidence index of naturally occurring red rust fungus (Puccinia recondita) is determined for the following leaves and leaves in accordance with the criteria of Test Example 1. Investigation was made and the control value (%) was calculated. In the same manner as in Test 3, the expected value of the control effect due to the mixed use was calculated according to Colby's formula, and based on this value, the presence or absence of synergy was tested for the control effect in the mixed treatment area of Compound 1-93 and the control compound. The results are shown in Table 8.
化合物1-93と対照化合物を、表中記載の処理薬量となるよう混用し、コムギ(品種:ホクシン)乾燥種子に均一に付着するように処理した。播種量を120kg/ha相当で、上記の種子を2m2(1m×2m)の区画内に条播した。翌年のコムギが出穂する時期(BBCH51-59頃、播種から約190~200日後)に、次葉および止葉について、試験例1の基準に従って、自然発生した赤さび病菌(Puccinia recondita)の発病指数を調査し、防除価(%)を算出した。試験3と同様にコルビーの計算式に従って、混用による防除効果の期待値を算出し、その値に基づいて化合物1-93と対照化合物の混用処理区における防除効果について相乗性の有無を検定した。結果を第8表に示す。 Test Example 4 Wheat red rust control effect test by mixing seed treatment agent (field test)
Compound 1-93 and the control compound were mixed so as to have the treatment doses shown in the table, and treated so as to uniformly adhere to the dried seeds of wheat (variety: Hokushin). The seeding amount was equivalent to 120 kg / ha, and the above seeds were sown in a 2 m 2 (1 m × 2 m) section. In the next year when wheat emerges (around BBCH 51-59, approximately 190 to 200 days after sowing), the incidence index of naturally occurring red rust fungus (Puccinia recondita) is determined for the following leaves and leaves in accordance with the criteria of Test Example 1. Investigation was made and the control value (%) was calculated. In the same manner as in Test 3, the expected value of the control effect due to the mixed use was calculated according to Colby's formula, and based on this value, the presence or absence of synergy was tested for the control effect in the mixed treatment area of Compound 1-93 and the control compound. The results are shown in Table 8.
殺菌活性を有する対照化合物としては、以下の物質を用いた。
化合物A:フルジオキソニル(fludioxonil)
化合物B:ビテルタノール(bitertanol)
化合物C:フベリダゾール(fuberidazole)
化合物D:トリアジメノール(triadimenol)
化合物E:トリチコナゾール(triticonazole)
化合物G:フルキンコナゾール(fluquinconazole)
化合物H:プロクロラズ(prochloraz)
化合物K:テブコナゾール(tebuconazole)
化合物L:プロチオコナゾール(prothioconazole)
化合物M:ピラクロストロビン(pyraclostrobin) The following substances were used as control compounds having bactericidal activity.
Compound A: fludioxonil
Compound B: bittertanol
Compound C: fuberidazole
Compound D: triadimenol
Compound E: triticonazole
Compound G: fluquinconazole
Compound H: prochloraz
Compound K: tebuconazole
Compound L: prothioconazole
Compound M: pyraclostrobin
化合物A:フルジオキソニル(fludioxonil)
化合物B:ビテルタノール(bitertanol)
化合物C:フベリダゾール(fuberidazole)
化合物D:トリアジメノール(triadimenol)
化合物E:トリチコナゾール(triticonazole)
化合物G:フルキンコナゾール(fluquinconazole)
化合物H:プロクロラズ(prochloraz)
化合物K:テブコナゾール(tebuconazole)
化合物L:プロチオコナゾール(prothioconazole)
化合物M:ピラクロストロビン(pyraclostrobin) The following substances were used as control compounds having bactericidal activity.
Compound A: fludioxonil
Compound B: bittertanol
Compound C: fuberidazole
Compound D: triadimenol
Compound E: triticonazole
Compound G: fluquinconazole
Compound H: prochloraz
Compound K: tebuconazole
Compound L: prothioconazole
Compound M: pyraclostrobin
第7表及び第8表の結果から、すべての対照化合物との混用において、相乗的な効果が認められた。
From the results in Tables 7 and 8, a synergistic effect was observed in the mixed use with all the control compounds.
本発明化合物は従来技術とは異なり、対象植物の種子又は対象植物を播種する担体へ施用するだけで植物の生育盛期から後期に至るまで極めて長期間に渡り病害を防除することを目的としている。その為には優れた防除価に加え長期間の残効性、更には対象植物に対する安全性が要求される。本発明化合物はそれらの要素をすべて兼ね備えたものである。
Unlike the prior art, the compound of the present invention is intended to control a disease for a very long period from the growing season to the late stage of the plant only by applying it to the seed of the target plant or a carrier for seeding the target plant. . For that purpose, in addition to excellent control value, long-term residual effect and further safety for the target plant are required. The compound of the present invention combines all of these elements.
Claims (5)
- 一般式(I):
R6は水素原子;(C1-C8)アルキル基;(C3-C6)シクロアルキル基;フェニル(C1-C6)アルキル基;ハロゲン原子、シアノ基、(C1-C6)アルキル基、ハロ(C1-C6)アルキル基、(C3-C6)シクロアルキル基、ハロ(C3-C6)シクロアルキル基、(C1-C6)アルコキシ基、ハロ(C1-C6)アルコキシ基、カルボキシル基及び(C1-C6)アルコキシカルボニル基からなる群より選択される1または同一もしくは異なっても良い2以上の置換基を環状に有する置換フェニル(C1-C6)アルキル基;フェニル基又はハロゲン原子、シアノ基、(C1-C6)アルキル基、ハロ(C1-C6)アルキル基、(C3-C6)シクロアルキル基、ハロ(C3-C6)シクロアルキル基、(C1-C6)アルコキシ基、ハロ(C1-C6)アルコキシ基、カルボキシル基及び(C1-C6)アルコキシカルボニル基からなる群より選択される1または同一もしくは異なっても良い2以上の置換基を有する置換フェニル基を示す。
Yは酸素原子又は-N(R7)-(式中、R7は水素原子、(C1-C6)アルキル基又は(C3-C6)シクロアルキル基を示す。)
Wは酸素原子又は硫黄原子を示す。}で表される4-シクロプロピル-1,2,3-チアジアゾール誘導体若しくはその塩類と、殺菌活性及び/又は殺虫活性を有する化合物の1種又は2種以上とを有効成分として含有することを特徴とする農園芸用病害虫防除剤組成物。 Formula (I):
R 6 is a hydrogen atom; (C 1 -C 8 ) alkyl group; (C 3 -C 6 ) cycloalkyl group; phenyl (C 1 -C 6 ) alkyl group; halogen atom, cyano group, (C 1 -C 6 ) Alkyl group, halo (C 1 -C 6 ) alkyl group, (C 3 -C 6 ) cycloalkyl group, halo (C 3 -C 6 ) cycloalkyl group, (C 1 -C 6 ) alkoxy group, halo ( C 1 -C 6) alkoxy group, carboxyl group and (C 1 -C 6) alkoxy substituted phenyl having one or the same or different and may be 2 or more substituents selected from the group consisting of a carbonyl group in a ring (C 1- C 6 ) alkyl group; phenyl group or halogen atom, cyano group, (C 1 -C 6 ) alkyl group, halo (C 1 -C 6 ) alkyl group, (C 3 -C 6 ) cycloalkyl group, halo (C Selected from the group consisting of 3- C 6 ) cycloalkyl groups, (C 1 -C 6 ) alkoxy groups, halo (C 1 -C 6 ) alkoxy groups, carboxyl groups and (C 1 -C 6 ) alkoxycarbonyl groups. 1 represents a substituted phenyl group having two or more substituents which may be the same or different.
Y represents an oxygen atom or —N (R 7 ) — (wherein R 7 represents a hydrogen atom, a (C 1 -C 6 ) alkyl group or a (C 3 -C 6 ) cycloalkyl group).
W represents an oxygen atom or a sulfur atom. And a salt thereof and one or more compounds having bactericidal activity and / or insecticidal activity as active ingredients A pest control composition for agricultural and horticultural use. - 殺菌活性を有する化合物がビテルタノール、ブロムコナゾール、シプロコナゾール、ジフェノコナゾール、ジニコナゾール、エニルコナゾール、エポキシコナゾール、フルキンコナゾール、フェンブコナゾール、フルシラゾール、フルトリアホール、ヘキサコナゾール、イミベンコナゾール、イプコナゾール、メトコナゾール、ミクロブタニル、ペンコナゾール、プロピコナゾール、プロチオコナゾール、シメコナゾール、トリアジメホン、トリアジメノール、テブコナゾール、テトラコナゾール、トリチコナゾール、プロクロラズ、ペフラゾエート、イマザリル、トリフルミゾール、シアゾファミド、ベノミル、カルベンダジム、チアベンダゾール、フベリダゾール、エタボキサム、エトリジアゾール、オキスポコナゾールフマル酸、ヒメキサゾール、アゾキシストロビン、ジモキシストロビン、エネストロブリン、フルオキサストロビン、クレソキシムメチル、メトミノストロビン、オリザストロビン、ピコキシストロビン、ピラクロストロビン、トリフロキシストロビン、カルボキシン、ベナラキシル、ボスカリド、ビキサフェン、フェンヘキサミド、フルトラニル、フラメトピル、メプロニル、メタラキシル、メフェノキサム、オフラセ、オキサジキシル、オキシカルボキシン、ペンチオピラド、チフルザミド、チアジニル、ジメトモルフ、フルモルフ、フルメトベル、フルオピコリド、カルプロパミド、ジクロシメット、マンジプロパミド、フルアジナム、ピリフェノックス、ブピリメート、シプロジニル、フェナリモル、フェリムゾン、メパニピリム、ヌアリモール、ピリメタニル、トリホリン、フェンピクロニル、フルジオキソニル、アルジモルフ、ドデモルフ、フェンプロピモルフ、トリデモルフ、フェンプロピジン、イプロジオン、プロシミドン、ビンクロゾリン、ファモキサドン、フェナミドン、オクチリノン、プロベナゾール、アニラジン、ジクロメジン、ピロキロン、プロキナジド、トリシクラゾール、カプタホル、キャプタン、ダゾメット、ホルペット、フェノキサニル、キノキシフェン、アミスルブロム、マンゼブ、マンネブ、メタム、メチラム、ファーバム、プロピネブ、チウラム、ジネブ、ジラム、ジエトフェンカルブ、イプロバリカルブ、ベンチアバリカルブイソプロピル、プロパモカルブ塩酸塩、チオファネートメチル、ピリベンカルブ、ボルドー液、塩基性塩化銅、塩基性硫酸銅、水酸化第二銅、8-ヒドロキシキノリン銅、ドジン、イミノクタジンアルベシル酸塩、イミノクタジン酢酸塩、グアザチン、カスガマイシン、ストレプトマイシン、ポリオキシン、オキシテトラサイクリン、バリダマイシンA、ビナパクリル、ジノカップ、ジノブトン、ジチアノン、イソプロチオラン、エジフェンホス、イプロベンホス、ホセチル、ホセチルアルミニウム、ピラゾホス、トルクロホスメチル、クロロタロニル、ジクロフルアニド、フルスルファミド、ヘキサクロロベンゼン、フサライド、ペンシクロン、キントゼン、シフルフェナミド、シモキサニル、ジメチリモール、エチリモール、フララキシル、メトラフェノン、スピロキサミン、アンバム、硫黄、石灰硫黄合剤、エクロメゾール、炭酸水素カリウム、炭酸水素カルシウム、チアジアジン、テクロフタラム、トリアジン、ノニルフェノールスルホン酸銅、ヒドロキシイソキサゾール、フルオルイミド、ポリカーバメート、メタスルホカルブ、EDDP、IBP、トルフェンピラド、フルオピラム、イソチアニル又はイソピラザムより選択される1種又は2種以上である請求項1に記載の農園芸用殺菌防除剤組成物。 Compounds having bactericidal activity are vitertanol, bromconazole, cyproconazole, difenoconazole, diniconazole, enilconazole, epoxiconazole, fluquinconazole, fenbuconazole, flusilazole, flutriazole, hexaconazole, imibenconazole, Ipconazole, metconazole, microbutanyl, penconazole, propiconazole, prothioconazole, cimeconazole, triazimehon, triazimenol, tebuconazole, tetraconazole, triticonazole, prochloraz, pefazoate, imazalyl, triflumizole, ciazofamide, benomyl, dinomyl , Thiabendazole, fuberidazole, ethaboxam, etridiazole, oxpoconazole fumarate, Xazole, azoxystrobin, dimoxystrobin, enestrobrin, floxastrobin, cresoxime methyl, metminostrobin, orizastrobin, picoxystrobin, pyraclostrobin, trifloxystrobin, carboxin, benalaxyl, Boscalid, bixafen, fenhexamide, flutolanil, furametopyr, mepronil, metalaxyl, mefenoxam, ofrase, oxadixyl, oxycarboxyl, pentiopyrad, tifluzamide, thiazinyl, dimethomorph, flumorph, flumetober, flupicoride, carpropamide, diclopimeflumman Knox, bupirimate, cyprodinil, phenalimol, ferrimzone, mepanipyrim, nuarimol Pyrimethanyl, trifolin, fenpicuronyl, fludioxonil, aldimorph, dodemorph, fenpropimorph, tridemorph, fenpropidin, iprodione, procymidone, vinculozoline, famoxadone, fenamidone, octyrinone, probenazole, anilazine, diclomedin, pyroxanthone, proxidol Dazomet, Holpet, Phenoxanyl, Quinoxifene, Amisulbrom, Manzeb, Manneb, Metam, Methylam, Farbum, Propineb, Thiuram, Dinebu, Diram, Dietofencarb, Iprovalib, Benchavalycarb isopropyl, Propamocarb hydrochloride, Thiophaneto methyl, Pyribencarb Copper chloride, basic copper sulfate , Cupric hydroxide, 8-hydroxyquinoline copper, dodine, iminotadine albecylate, iminotazine acetate, guazatine, kasugamycin, streptomycin, polyoxin, oxytetracycline, validamycin A, vinapacryl, dinocup, dinobutone, dithianone, isoprothiolane, edifenphos , Iprobenfos, fosetyl, fosetylaluminum, pyrazophos, tolcrofosmethyl, chlorothalonil, diclofluuride, fursulfamide, hexachlorobenzene, fusaride, pencyclon, quintozen, cyflufenamide, simoxanyl, dimethylmethylol, ethylimole, flaxyl, metolaphenone, spiroxamine, sulfur, lime, sulfur Mixture, echromesole, potassium hydrogen carbonate, hydrogen carbonate cal One or more selected from um, thiadiazine, teclophthalam, triazine, copper nonylphenol sulfonate, hydroxyisoxazole, fluorimide, polycarbamate, metasulfocarb, EDDP, IBP, tolfenpyrad, fluopyram, isothianyl or isopyrazam The agricultural and horticultural bactericidal control composition according to claim 1.
- 殺虫活性を有する化合物が、アセタミプリド、ピメトロジン、フェニトロチオン、アセフェート、カルバリル、メソミル、カルタップ、シハロトリン、エトフェンプロックス、テフルベンズロン、フルベンジアミド、フルフェノクスロン、テブフェノジド、フェンピロキシメート、ピリダベン、イミダクロプリド、ブプロフェジン、BPMC、MIPC、マラチオン、メチダチオン、フェンチオン、ダイアジノン、オキシデプロホス、バミドチオン、エチオフェンカルブ、ピリミカーブ、ペルメトリン、シペルメトリン、ビフェントリン、ハルフェンプロックス、シラフルオフェン、ニテンピラム、クロルフルアズロン、メトキシフェノジド、テブフェンピラド、ピリミジフェン、ケルセン、プロパルギット、ヘキシチアゾクス、クロフェンテジン、スピノサド、ミルベメクチン、BT(Bacillus thuringiensis)、インドキサカルブ、メタフルミゾン、クロルフェナピル、フィプロニル、エトキサゾール、アセキノシル、ピリミホスメチル、アクリナトリン、キノメチオネート、クロルピリホス、アバメクチン、エマメクチン安息香酸塩、酸化フェンブタスズ、テルブホス、エトプロホス、カズサホス、フェナミフォス、フェンスルフォチオン、DSP、ジクロフェンチオン、ホスチアゼート、オキサミル、イサミドホス、ホスチエタン、イサゾホス、チオナジン、ベンフラカルブ、スピロジクロフェン、エチオフェンカルブ、アジンホス・メチル、ジスルホトン、メチオカルブ、オキシジメトン・メチル、パラチオン、シフルトリン、ベータ・シフルトリン、テブピリムホス、スピロメシフェン、エンドスルファン、アミトラズ、トラロメトリン、アセトプロール、エチプロール、エチオン、トリクロルホン、メタミドホス、ジクロルボス、メビンホス、モノクロトホス、ジメトエート、フォルメタネート、ホルモチオン、メカルバム、チオメトン、ジスルホトン、ナレッド、メチルパラチオン、シアノホス、ジアミダホス、アルベンダゾール、オキシベンダゾール、フェンベンダゾール、オクスフェンダゾール、プロパホス、スルプロホス、プロチオホス、プロフェノホス、イソフェンホス、テメホス、フェントエート、ジメチルビンホス、クロルフェビンホス、テトラクロルビンホス、ホキシム、イソキサチオン、ピラクロホス、クロルピリホス、ピリダフェンチオン、ホサロン、ホスメット、ジオキサベンゾホス、キナルホス、ピレトリン、アレスリン、プラレトリン、レスメトリン、ペルメトリン、テフルトリン、フェンプロパトリン、アルファシペルメトリン、ラムダ・シハルトリン、デルタメトリン、フェンバレレート、エスフェンバレレート、フルシトリネート、フルバリネート、シクロプロトリン、チオジカルブ、アルジカルブ、アラニカルブ、メトルカルブ、キシリカルブ、プロポキスル、フェノキシカルブ、フェノチオカルブ、ビフェナゼート、カルボフラン、カルボスルファン、硫黄、ピリフルキナゾン、フラチオカルブ、ジアフェンチウロン、ジフルベンズロン、ヘキサフルムロン、ノバルロン、ルフェヌロン、クロルフルアズロン、水酸化トリシクロヘキシルスズ、オレイン酸ナトリウム、オレイン酸カリウム、メトプレン、ハイドロプレン、ビナパクリル、アミトラズ、クロルベンジレート、フェニソブロモレート、テトラジホン、ベンスルタップ、ベンゾメート、クロマフェノジド、ハロフェノジド、エンドスルファン、ジオフェノラン、トルフェンピラド、トリアザメート、硫酸ニコチン、チアクロプリド、チアメトキサム、クロチアニジン、ジノテフラン、フルアジナム、ピリプロキシフェン、フルアクリピリム、ヒドラメチルノン、シロマジン、TPIC、チオシクラム、フェナザキン、ポリナクチン複合体、アザディラクチン、ロテノン、ヒドロキシプロピルデンプン、メスルフェンホス、ホスホカルブ、イソアミドホス、アルドキシカルブ、メタム・ナトリウム、酒石酸モランテル、ダゾメット、塩酸レバミゾール、トリクラミド、トルフェンピラド、ピリダリル、クロラントラニリプロール、シエノピラフェン又はシフルメトフェンより選択される1種又は2種以上である請求項1に記載の農園芸用病害虫防除剤組成物。 Compounds having insecticidal activity include acetamiprid, pymetrozine, fenitrothion, acephate, carbaryl, mesomil, cartap, cyhalothrin, etofenprox, teflubenzuron, fulvendiamide, flufenoxuron, tebufenozide, fenpyroximate, pyridaben, imidacloprid, buprofezin, P Malathion, methidathion, fenthione, diazinone, oxydeprophos, bamidione, ethiophene carb, pirimicurve, permethrin, cypermethrin, bifenthrin, halfenprox, silafluophene, nitenpyram, chlorfluazuron, methoxyphenozide, tebufenpyrx, pyrimidifenx, prodexthix Clofe Tezine, spinosad, milbemectin, BT (Bacillus thuringiensis), indoxacarb, metaflumizone, chlorfenapyr, fipronil, etoxazole, acequinosyl, pirimiphosmethyl, acrinathrin, quinomethionate, chlorpyrifos, abamectin, phosphatamine benzoate Fenamifos, Fencerfothione, DSP, Diclofenthion, Phostiazete, Oxamyl, Isamidophos, Phoschietane, Isazofos, Thionazine, Benfuracarb, Spirodroclofen, Ethiophenecarb, Azinphos methyl, Disulfotone, Methiocarb, Oxydimetone methyl, Parathion, Cyfluthrin, Beta Phosphorus, Tebupyrimphos, Spiromesifene, Endosulfan, Amitraz, Tralomethrin, Acetoprole, Ethiprole, Ethion, Trichlorphone, Metamidophos, Dichlorvos, Mevinphos, Monocrotophos, Dimethoate, Formethanate, Formothione, Mecarbam, Thiometone, Disulfotone, Nared, Methylparathion Cyanophos, diamidazos, albendazole, oxybendazole, fenbendazole, oxfendazole, propaphos, sulprophos, prothiophos, profenofos, isofenphos, temefos, phentoate, dimethylvinphos, chlorfevinphos, tetrachlorvinphos, foxime, isoxathione , Pyracrofos, chlorpyrifos, pyridafenthione, hosalon, phosme , Dioxabenzophos, quinalphos, pyrethrin, allethrin, praretrin, resmethrin, permethrin, tefluthrin, fenpropatoline, alpha cypermethrin, lambda shiharthrin, deltamethrin, fenvalerate, esfenvalerate, flucitrinate, fulvalinate, cyclo Protoline, Thiodicarb, Aldicarb, Alanicarb, Matorcarb, Xylcarb, Propoxur, Phenoxycarb, Fenothiocarb, Bifenazate, Carbofuran, Carbosulfan, Sulfur, Pyrifluquinazone, Frathiocarb, Diafentiuron, Diflubenzuron, Hexaflumulone, Roncrolone Fluazuron, tricyclohexyltin hydroxide, sodium oleate, potassium oleate Um, metoprene, hydroprene, binapacryl, amitraz, chlorbenzilate, phenisobromolate, tetradiphone, bensultap, benzomate, chromafenozide, halophenozide, endosulfan, diophenolan, tolfenpyrad, triazamate, nicotine sulfate, thiacloprid, thiamethoxam, crothianidane , Pyriproxyfen, fluacrylpyrim, hydramethylnon, cyromazine, TPIC, thiocyclam, phenazaquin, polynactin complex, azadirachtin, rotenone, hydroxypropyl starch, mesulfenphos, phosphocarb, isoamidophos, aldoxycarb, metam sodium, morantel tartrate, Dazomet, levamisole hydrochloride, triclamide The pest control composition for agricultural and horticultural use according to claim 1, wherein the composition is one or more selected from the group consisting of, tolfenpyrad, pyridalyl, chlorantraniliprole, sienopyrafen, and siflumethofene.
- 請求項1~3に記載の農園芸用病害虫防除剤組成物の有効量で当該病害及び/または害虫の発生が予測される対象植物、対象植物の種子、種子を播種するための栽培担体又は土壌を処理することを特徴とする農園芸用病害虫防除剤組成物の使用方法。 The target plant, the seed of the target plant, the seed of the target plant, the cultivation carrier for sowing the seed, and the soil, in which the occurrence of the disease and / or the pest is predicted with the effective amount of the agricultural and horticultural pest control composition according to claims 1 to 3 A method for using a pest control composition for agricultural and horticultural use, characterized by treating the above.
- 処理が、農園芸用病害虫防除剤組成物溶液への対象植物の種子の浸漬、又は農園芸用病害虫防除剤組成物による種子の粉衣、又は植物体に近接する土壌もしくは栽培担体の処理である請求項4に記載の農園芸用病害虫防除剤組成物の使用方法。 The treatment is immersion of the seed of the target plant in the agricultural / horticultural pest control composition solution, or seed dressing with the agricultural / horticultural pest control composition, or treatment of the soil or the cultivation carrier adjacent to the plant body. The use method of the agricultural and horticultural pest control composition according to claim 4.
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