WO2012124795A1 - Pest control composition and pest control method - Google Patents

Pest control composition and pest control method Download PDF

Info

Publication number
WO2012124795A1
WO2012124795A1 PCT/JP2012/056796 JP2012056796W WO2012124795A1 WO 2012124795 A1 WO2012124795 A1 WO 2012124795A1 JP 2012056796 W JP2012056796 W JP 2012056796W WO 2012124795 A1 WO2012124795 A1 WO 2012124795A1
Authority
WO
WIPO (PCT)
Prior art keywords
pest control
methyl
parts
formulation
control composition
Prior art date
Application number
PCT/JP2012/056796
Other languages
French (fr)
Inventor
Yoshito Tanaka
Original Assignee
Sumitomo Chemical Company, Limited
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Sumitomo Chemical Company, Limited filed Critical Sumitomo Chemical Company, Limited
Publication of WO2012124795A1 publication Critical patent/WO2012124795A1/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N51/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds having the sequences of atoms O—N—S, X—O—S, N—N—S, O—N—N or O-halogen, regardless of the number of bonds each atom has and with no atom of these sequences forming part of a heterocyclic ring

Definitions

  • the present invention relates to a pest control composition and a control method of pests.
  • Patent Literature 1 US 5,034,404
  • Patent Literature 2 US 4,176,189
  • An object of the present invention is to provide a pest control composition and control method of pests having an excellent control effect on pests.
  • the present inventors studied intensively to find a pest control composition having an excellent control effect on pests, and as a result, found that a composition
  • the present invention includes:
  • a pest control composition containing a combination of the Guanidine Compound and the Ester Compound as active ingredients .
  • a control method of pests which comprises applying effective amount of the Guanidine Compound and the Ester Compound .
  • Pest can be controlled by using the pest control composition of the present invention.
  • the pest control composition of the present invention is characterized by containing the combination of the Guanidine Compound and the Ester Compound.
  • the Guanidine Compound can be produced, for example, by process discribed in US 5,034,404.
  • a compound selling on the market in the name of clothianidin (common name) can be used for the Guanidine Compound.
  • the Ester Compound can be produced, for example, by process discribed in, for example, US 4,176,189 and US 4, 827, 020.
  • a compound selling on the market in the name of imiprothrin (common name) [2, 5-dioxo-3- (2-propynyl) -1- imidazolidinyl]methyl (1R) -cis/trans-3- (2-methyl-l- propenyl ) -2 , 2-dimethylcyclopropanecarboxylate) can be used for the Ester Compound.
  • Examples of pests on which the pest control can be used for the Ester Compound.
  • composition of the present invention has a control effect include harmful arthropod pest such as harmful insects and harmful acarines, and more specifically, the following pests:
  • Pyralidae such as Chilo suppressalis, Cnaphalocrosis medinalis, Plodia interpunctella , and Ephestia kuehniella;
  • Noctuidae such as Spodoptera litura, Pseudaletia separata, and Mamestra brassicae
  • Pieridae such as Pieris rapae crucivora
  • Tortricidae such as Adoxopheyes spp.
  • Agrotis spp. such as Agrotis segetum and Agrotis ipsilon
  • Helicoverpa spp. Heliothis spp.; Plutella xylostella; Parnara guttata; Tinea pellionella; Tineola bisselliella , etc .
  • Culex spp. such as Culex pipiens pallens and Culex tritaeniorhynchus; Aedes spp. such as Aedes aegypti and Aedes albopictus; Anopheles spp.
  • Anopheles sinensis such as Anopheles sinensis; Chironomidae; Muscidae such as Musca domestica , Muscina stabulans and Fannia canicularis; Calliphoridae; Sarcophagidae; Anthomyiidae such as Delia phatura and Delia antiqua; Tephritidae; Agromyzidae; Drosophilidae; Psychodidae; Phoridae; Simuliidae; Tabanidae; Stomoxyidae; Ceratopogpnnidae, etc.
  • Hymenoptera insect pests are:
  • Formicidae such as Camponotus japonicus, Tetramorium tsushimae, Lasius niger, Pachycondyla chinensis, Monomorium intrudens, Lasius fuji, Monomorium pharaonis, Formica fusca japonica, Ochetellus glaber, Pristomyrmex punctatus, Pheidole noda, and Linepith ema humile; Vespidae such as Polistes ( Polistes chinensis, Polistes riparius, Polistes jadwigae, Polistes rothneyi, Polistes nipponensis, Polistes snelleni, and Polistes japonicus) , Vespa mandarinia, Vespa simillima xanthoptera, Vespa analis, Vespa crabro, Vespa ducalis, Vespula flaviceps lewisi, Vespula
  • Ctenocephalides canis, Ctenocephalides felis, Pulex irritans, etc.
  • Pediculus humanus Phthirus pubis, Pediculus humanus captis, Pediculus humanus corporis etc.
  • Psocoptera insect pests psocid
  • Subterranean termites such as Reticulitermes speratus, Coptoterm.es formosanus, Reticulitermes flavipes,
  • Reticulitermes hesperus Reticulitermes virginicus, Reticulitermes tibialis, Heterotermes aureus; drywood termites such as Incisitermes minor; and rottenwood termites such as Zootermopsis nevadensis .
  • Delphacidae such as Laodelphax striatellus, Nilaparvara lugens and Sogatella furcifera
  • Deltocephalidae such as Nephotettix cincticeps and Nephotettix virescens
  • Aphididae Pentatomidae such as Nezara antennata, Riptortus clavatus, Eysarcoris lewisi, Eysarcoris parvus, Plautia stali, Halyomorpha mista, Stenotus rubrovittatus, and Trigonotylus caelestialium
  • Aleyrodidae Coccidae
  • Cimicidae such as Cinex lectularius
  • Tingidae Psyllidae, etc .
  • Curculionidae such as Sitophilus zeamais, Lissorhoptrus oryzophilus, Anthonomus grandis grandis and Callosobruchus cheninsis; Tenebrionidae such as Tenebrio molitor and Tribolium castaneum; Chrysomelidae such as Oulema oryzae, Phyllotreta striolata and Aulacophora femoralis; Anobiidae; Epilachna spp.
  • Thysanoptera insect pests are Thysanoptera insect pests:
  • Thrips palmi Frankliniella occidentalis
  • Thrips hawaiiensis etc.
  • Pyroglyphidae such as Dermatophagoides farinae and Dermatophagoides pteronyssinus
  • Arcaridae such as Tyrophagus putrescentiae and Aleuroglyphus oyatus
  • Glycyphagidae such as Glycyphagus privatus, Glycyphagus domesticus and Glycyphagus destructor
  • Cheyletidae such as Cheyletus malaccensis and Cheyletus malaccesis
  • Tetranychidae such as Tetranychus urticae, Tetranychus kanzawai, Panonychus citri and Panonychus ulmi
  • Erythraeidae Ixodidae such as Haemaphysalis longicornis
  • Dermanyssidae such as Ornithonyss
  • Chilopoda such as Scolopendra subsipnipes mutilans
  • Diplopoda such as Oxidus gracilis and Nedyopus tambanus
  • Armadilldiiidae and Porcellionidae such as Armadillidium vulgare
  • Gastropoda such as Limax marginatus and Limax flavus
  • Araneae such as Nephila clavata, Cheiracanthium japonicum and Latrodectus hasselti; etc .
  • the weight ratio of the Guanidine Compound to the Ester Compound is usually within the range of from 50 : 1 to 1 : 50, preferably from 20 : 1 to 1 : 20, more preferably from 20 : 1 to 1 : 10, especially more preferably from 20 : 1 to 1 : 1, most preferably from 20 : 1 to 5 : 1.
  • the pest control composition of the present invention can be a simple mixture of the Guanidine Compound and the Ester Compound. However, it is usually used in the form of various formulations.
  • the formulations include oil solution, emulsifiable concentrate, wettable powder, wettable dispersible granule, suspension concentrate (e.g. suspension in water, and emulsion in water) , microcapsule formulation, gel formulation, dust, granule, tablet, coating formulation, aerosol, carbon dioxide formulation, heating vaporization formulation (e.g. mosquito coil, electric mosquito mat, and fluid absorption wicking-type pesticide) , piezo-type spray insecticide, heating fumigant (e.g.
  • non-heating fumigant e.g. resin fumigant, paper fumigant, unwoven fabric fumigant, woven fabric fumigant, and sublimation tablet
  • smoking formulation e.g. fogging
  • direct contact formulation e.g. sheet type contact formulation, tape type contact formulation, and net type contact formulation
  • ULV formulation e.g. ULV formulation, and poison bait.
  • the formulation can be prepared, for example, by the following methods.
  • the Guanidine Compound and the Ester Compound are mixed with a solid carrier, a liquid carrier, a gaseous carrier or feed and, if necessary, other auxiliary agents for formulations such as a surfactant.
  • a base material is impregnated with the Guanidine Compound and the Ester Compound.
  • the Guanidine Compound is mixed with a solid carrier, a liquid carrier, a gaseous carrier or feed and, if necessary, other auxiliary agents for formulations such as a surfactant to obtain suspension in water containing the Guanidine Compound and the Ester Compound is mixed with a solid carrier, a liquid carrier, a gaseous carrier or feed and, if necessary, other auxiliary agents for formulations such as a surfactant to obtain emulsion in water containing the Ester Compound. Then said suspension in water containing the Guanidine Compound and said emulsion in water containing the Ester Compound are mixed.
  • the Guanidine Compound and the Ester Compound are mixed with a solid carrier, a liquid carrier, a gaseous carrier or feed and, if necessary, other auxiliary agents for formulations such as a surfactant. Then said mixture is ground.
  • These formulations usually contain as a total amount 0.001 to 90% by weight of the Guanidine Compound and the Ester Compound.
  • solid carrier used for the formulation examples include fine powders and granules such as clays (e.g.
  • kaolin clay diatomaceous earth, bentonite, Fubasami clay, and acidic white clay
  • synthetic hydrated silicon oxide talc
  • ceramics other inorganic minerals (e.g. sericite, quarts, sulfur, active carbon, calcium carbonate, and hydrated silica)
  • chemical fertilizers e.g. ammonium sulfate, ammonium phosphate, ammonium nitrate, ammonium chloride, and urea
  • solid materials at ordinary temperature e.g.
  • polyethylene resins such as low-density polyethylene, linear low-density polyethylene, and high- density polyethylene; ethylene-vinyl ester copolymers such as ethylene-vinyl acetate copolymer; ethylene-methacrylate copolymers such as ethylene-methyl methacrylate copolymer, and ethylene-ethyl methacrylate copolymer; ethylene- acrylate copolymers such as ethylene-methyl acrylate copolymer, and ethylene-ethyl acrylate copolymer; ethylene- vinyl carboxyic acid copolymers such as ethylene-acrylic acid copolymer; ethylene-tetracyclododecene copolymer;
  • polypropylene resins such as propylene homopolymer, and propylene-ethylene copolymer; poly-4-methylpentene-l ;
  • polybutene-1 polybutadiene; polystyrene; acrylonitrile- styrene resin; styrene elastomers such as acrylonitrile- butadiene-styrene resin, styrene-conj ugated diene block copolymer, and hydrogenated styrene-conj ugated diene block copolymer; fluorine plastics; acrylic resins such as polymethyl methacrylate; polyamide resins such as nylon 6, and nylon 66; polyester resins such as polyethylene
  • dimethyleneterephthalate polycarbonate; polyacetal;
  • polyacrylsulfone polyarylate; polyhydroxybenzoate ; polyetherimide; polyestercarbonate; polyphenylene ether resin; polyvinyl chloride; polyvinylidene chloride;
  • polyurethane polyurethane
  • porous resins such as foamed polyurethane, foamed polypropylene, and foamed polyethylene) , glass, metals, and ceramics.
  • liquid carrier examples include aromatic or aliphatic hydrocarbons (e.g. xylene, toluene, alkyl
  • naphthalene phenylxylylethane, kerosene, light oil, hexane, and cyclohexane
  • halogenated hydrocarbons e.g.
  • alcohols e.g. methanol, ethanol,
  • ethers e.g. diethylether , ethylene glycol dimethyl ether, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, propylene glycol
  • esters e.g. ethyl acetate, and butyl acetate
  • ketones e.g.
  • nitriles e.g. acetonitrile
  • sulfoxides e.g. dimethyl sulfoxide
  • acid amides e.g. N, N-dimethylformamide, N,N- dimethylacetoamide, and N-methyl-pyrrolidone
  • alkylidene carbonates e.g. propylene carbonate
  • vegetable oils e.g. soybean oil, and cotton oil
  • vegetable essential oil e.g. orange oil, hyssop oil, and lemon oil
  • gaseous carrier examples include butane gas, chlorofluorocarbon gas, liquefied petroleum gas (LPG) , dimethyl ether, and carbon dioxide.
  • LPG liquefied petroleum gas
  • surfactant examples include alkyl sulfate ester salts, alkyl sulfonates, alkylaryl sulfonates, alkylaryl ethers, polyoxyethylenated alkylaryl ethers, polyethylene glycol ethers, polyhydric alcohol esters, sugar alcohol derivatives, lignosulfonates (e.g. sodium lignosulfonate) , and polycarboxylates .
  • the weight ratio of the Guanidine Compound to lignosulfonates is usually within the range of from 50 : 1 to 1 : 1, preferably from 20 : 1 to 1 : 1, more preferably from 20 : 1 to 5 : 1.
  • the weight ratio of the Guanidine Compound to polycarboxylates is usually within the range of from 50 : 1 to 1 : 1, preferably from 20 : 1 to 1 : 1, more preferably from 20 : 1 to 2 : 1.
  • auxiliary agents for formulations include binders, dispersants, and stabilizers. Specific examples thereof include casein, gelatin, polysaccharides (e.g. starch, gum arabic, cellulose derivatives, and
  • arginic acid arginic acid
  • lignin derivatives lignin derivatives
  • bentonite saccharides
  • synthetic water-soluble polymers e.g. polyvinyl alcohol, and polyvinyl pyrrolidone
  • polyacrylic acid e.g. polyacrylic acid, BHT (2,6-di- t-butyl-4-methylphenol)
  • BHA mixture of 2-t-butyl-4- methoxyphenol and 3-t-butyl-4-methoxyphenol
  • Examples of the base material of a mosquito coil include a mixture of plant powder (e.g. wood powder, and pyrethrum) and a binder (e.g. powder of Machilus thunbergii, starch, and gluten) .
  • plant powder e.g. wood powder, and pyrethrum
  • binder e.g. powder of Machilus thunbergii, starch, and gluten
  • Examples of the base material of an electric mosquito mat include cotton linter matted, condensed and pressed in a plate shape, and mixed fibrils of cotton linter and pulp matted, condensed and pressed in a plate shape.
  • fumigant include combustion heat-developing agents such as nitrates, nitrites, guanidine salts, potassium chlorate, nitrocellulose, ethyl cellulose, and wood powder; heat decomposition stimulating agents such as alkali metal salts, alkaline earth metal salts, bichromates, and chromates;
  • oxygen suppliers such as potassium nitrate
  • combustion supporting agents such as melamine, and wheat starch
  • fillers such as diatomaceous earth
  • binders such as synthetic adhesives.
  • Examples of the base material of a chemical reaction type fumigant include heat-developing agents such as
  • sulfide sulfide, polysulfide, and hydrosulfide of alkali metals, and calcium oxide
  • catalysts such as carbonaceous materials, iron carbide, and activated clay
  • organic foaming agents such as azodicarbonamide, benzenesulfonyl hydrazide,
  • polyurethane polyurethane
  • fillers such as natural fibers and
  • Examples of the resin used for, for example, a resin fumigant include polyethylene resins such as low-density polyethylene, linear low-density polyethylene, and high- density polyethylene; ethylene-vinyl ester copolymers such as ethylene-vinyl acetate copolymer; ethylene-methacrylate copolymers such as ethylene-methyl methacrylate copolymer, and ethylene-ethyl methacrylate copolymer; ethylene- acrylate copolymers such as ethylene-methyl acrylate
  • copolymer and ethylene-ethyl acrylate copolymer; ethylene- vinyl carboxylate copolymers such as ethylene-acrylic acid copolymer; ethylene-tetracyclododecene copolymer;
  • polypropylene resins such as propylene homopolymer, and propylene-ethylene copolymer; poly-4-methylpentene-l ; polybutene-1; polybutadiene; polystyrene; acrylonitrile- styrene resin; styrene elastomers such as acrylonitrile- butadiene-styrene resin, styrene-conjugated diene block copolymer, and hydrogenated styrene-conjugated diene block copolymer; fluorine plastics; acrylic resins such as
  • polymethyl methacrylate polymethyl methacrylate
  • polyamide resins such as nylon 6, and nylon 66
  • polyester resins such as polyethylene
  • dimethyleneterephthalate polycarbonate; polyacetal;
  • polyacrylsulfone polyarylate; polyhydroxybenzoate;
  • polyetherimide polyestercarbonate; polyphenylene ether resin; polyvinyl chloride; polyvinylidene chloride; and polyurethane . They can be used alone or in a combination thereof. Further, if necessary, plasticizer such as
  • phthalates e.g. dimethyl phthalate, and dioctyl phthalate
  • adipates e.g. dioctyl phthalate
  • stearic acid e.g. stearic acid
  • the resin fumigant is prepared by kneading the Guanidine Compound and the Ester Compound into the base material, followed by molding it by injection molding, extrusion molding or press molding.
  • the resultant resin formulation can undergo further processes such as molding and cutting, if necessary, processing into a form of plate, film, tape, net or string.
  • These resin formulations can be processed into, for example, collars for animals, ear tags for animals, sheet formulations, guide strings and
  • Examples of the base material for poison bait include feed ingredients such as grain powder, vegetable oil, sugars, and crystalline cellulose; antioxidants such as dibutylhydroxy toluene, and nordihydroguaiaretic acid;
  • preservatives such as dehydroacetic acid; accidental ingestion prevention agents by children and pets such as chili pepper; and pest attractive flavors such as cheese flavor, onion flavor, and peanut oil.
  • control method of pest of the present invention is carried out by applying the pest control composition of the present invention to pests and/or to areas where pests live And the control method of pest of the present invention is also carried out by applying the Guanidine Compound and the Ester Compound to pests and/or to areas where pests live respectively .
  • the application method of the pest control composition of the present invention the following methods can be exemplified, and these methods can be appropriately selected according to, for example, the form of the pest control composition of the present invention, and the application place.
  • the pest control composition of the present invention is applied as it is to pests and/or areas where pests live.
  • the pest control composition of the present invention is diluted with a solvent such as water, followed by applying to pests and/or areas where pests live.
  • the pest control composition of the present invention in the form of, for example, emulsifiable concentrate, wettable powder, suspension concentrate or microcapsule preparation is diluted so that the total concentration of the Guanidine Compound and the Ester Compound becomes 0.1 to 50000 ppm.
  • the pest control composition of the present invention is heated at areas where pests live to vaporize the effective ingredients.
  • the applied rate and concentration of the Guanidine Compound and the Ester Compound can be appropriately determined according to, for example, the form of the pest control composition of the present
  • the application rate is usually from 0.0001 to 1000 mg/m 3 in terms of the total amount of the Guanidine Compound and the Ester
  • the heating vaporization formulation such as mosquito coil and electric mosquito mat is applied by appropriately heating according to the form of the formulation to vaporize the effective ingredients.
  • the non-heating fumigant such as resin fumigant, paper fumigant, sublimation tablet, unwoven fabric fumigant, woven fabric fumigant, and sheet fumigant can be used, for example, by leaving the formulation as it is at the place to be applied, or by making a wind toward the formulation.
  • composition of the present invention is applied for
  • the pest control composition of the present invention can also be applied to outside open space.
  • pest control composition of the present invention is used to livestock such as cows, horses, pigs, sheep, goats and chickens, and small animals such as dogs, cats, rats and mice, for the purpose of controlling
  • veterinary known methods are applied to the animals.
  • the formulation is administered by way of a tablet, mixing in feed, a suppository and injection (including intramuscular, subcutaneous,
  • the formulation is used by way of spraying an oil solution or aqueous solution, pour-on or spot-on treatment, washing an animal with a shampoo formulation, or putting a collar or ear tag made of a resin formulation to an animal, when non-systemic control is intended.
  • the total dosage of the Guanidine Compound and the Ester Compound is usually in the range from 0.01 to 1000 mg per 1 kg of an animal body.
  • composition of the present invention will be described.
  • all the "parts" are by weight unless otherwise stated.
  • a mixture of 8 parts of the Guanidine Compound, 3 parts of the Ester Compound, 35 parts of white carbon containing a half amount of polyoxyethylene alkyl ether sulfate ammonium salt, and 54 parts of water are finely ground by a wet grinding method to obtain a formulation.
  • a mixture of 0.5 part of the Guanidine Compound, 0.05 part of the Ester Compound, 0.01 part of BHT, 5 parts of xylene, 3.44 parts of deodorized kerosine. and 1 part of an emulsifier (Atomos 300, registered trademark of Atomos Chemical Co., Ltd.), and 50 parts of distilled water are filled into an aerosol container, and a valve part is attached. Then, 40 parts of a propellant (LPG) is filled thereinto through the valve under pressure to obtain an aqueous aerosol.
  • LPG propellant
  • KELZAN S tradename of CP Kelco, xanthan gum
  • VEEGUM Granules registered trademark of R.T. Vanderbilt Company, Inc, magnesium aluminum silicate
  • Proxel GXL registered trademark of Avecia Inc.
  • ion-exchanged water for 1 hour, 60 parts by weight of ion-exchanged water and a mixture of 1.5 parts by weight of Reax 910 (tradename of MeadWestvaco Corporation, sodium lignosulfonate) , 11.45 parts by weight of ion-exchanged water, 2 parts by weight of Soprophor FLK (tradename of Rhodia Japan Co; Ltd, potassium polyoxyethylene tristyrylphenylether phosphate), 0.05 part by weight of ANTIFOAM C EMULSION (tradename of Dow Corning Corporation, silicone based defoamer) , and 10 parts by weight of the Guaniidine Compound were added and mixed to give a dilution containing 10 % by weight of the Guanidine Compound (hereinafter refered to as the Dilution A) .
  • Reax 910 tradename of MeadWestvaco Corporation, sodium lignosulfonate
  • Soprophor FLK tradename of Rhodia Japan Co; Ltd, potassium polyoxyethylene
  • KELZAN S tradename of CP Kelco, xanthan gum
  • VEEGUM Granules registered trademark of R.T. Vanderbilt Company, Inc, magnesium aluminum silicate
  • Proxel GXL registered trademark of Avecia Inc.
  • test liquid composition containing the Guanidine Compound and/or the Ester Compound at specified concentration was prepared by mixing the Dilution A, Dilution B and/or pure water.
  • Acetone-diluted solutions were prepared so that predetermined dosage of the Guanidine Compound and the Ester Compound on glass plates indicated in Table 2 would be applied.
  • the acetone-diluted solutions (0.5 ml) were treated on the underside of glass petri dishes with a diameter of 7 cm uniformly and air-dried.
  • Ten female adults of common mosquito (Culex pipiens pallens) were collected by means of a pocket aspirator and placed into the petri dish, then contacted compulsorily with the treated underside of glass petri dishes by covering with a lucid plate made of polyvinyl chloride.

Abstract

The present invention provides a pest control composition containing a combination of (E) - 1 - (2 - chloro - 1, 3 - thiazol - 5 -ylmethyl) - 3 -methyl - 2 - nitroguanidine (clothianidin) and [2, 5-dioxo-3- (2-propynyl) - 1 - imidazolidinyl] methyl 2, 2 - dimethyl - 3 - (2 -methyl - 1 -propenyl) cyclopropanecarboxylate (imiprothrin).

Description

DESCRIPTION
PEST CONTROL COMPOSITION AND PEST CONTROL METHOD
Technical Field
The present invention relates to a pest control composition and a control method of pests.
Background Art
Hitherto, various compounds are known as active ingredient of harmaful arthropod control composition (See e.g., Patent Literature 1 and 2).
Citation List
Patent Literature
Patent Literature 1: US 5,034,404
Patent Literature 2: US 4,176,189
Summary of the Invention
Problems to be Solved by the Invention
An object of the present invention is to provide a pest control composition and control method of pests having an excellent control effect on pests.
Means for Solving the Problems
The present inventors studied intensively to find a pest control composition having an excellent control effect on pests, and as a result, found that a composition
containing a combination of (E) -1- (2-chloro-l, 3-thiazol-5- ylmethyl) -3-methyl-2-nitroguanidine (hereinafter refered to as the Guanidine Compound) and [2, 5-dioxo-3- (2-propynyl) -1- imidazolidinyljmethyl 2, 2-dimethyl-3- (2-methyl-l- propenyl ) cyclopropanecarboxylate (hereinafter refered to as the Ester Compound) has an excellent pest control effect, and led to the invention.
The present invention includes:
[1] A pest control composition containing a combination of the Guanidine Compound and the Ester Compound as active ingredients .
[2] The pest control composition according to [1], wherein the weight ratio of the Guanidine Compound to the Ester Compound is within the range of from 50 : 1 to 1 : 50.
[3] A control method of pests which comprises applying effective amount of the Guanidine Compound and the Ester Compound .
[4] The control method of pest according to [3], wherein the weight ratio of the Guanidine Compound to the Ester Compound is within the range of from 50 : 1 to 1 : 50.
Effect of the Invention
Pest can be controlled by using the pest control composition of the present invention.
Mode for Carrying Out the Invention The pest control composition of the present invention is characterized by containing the combination of the Guanidine Compound and the Ester Compound.
The Guanidine Compound can be produced, for example, by process discribed in US 5,034,404.
A compound selling on the market in the name of clothianidin (common name) can be used for the Guanidine Compound.
The Ester Compound can be produced, for example, by process discribed in, for example, US 4,176,189 and US 4, 827, 020.
In the Ester Compound, there are isomers derived from two asymmetric carbon atoms at the 1-position and the 3- position on the cyclopropane ring. Each isomer having pest control activity or a mixture of those isomers in an arbitrary ratio which has pest control activity is included in the present invention.
A compound selling on the market in the name of imiprothrin (common name) ( [2, 5-dioxo-3- (2-propynyl) -1- imidazolidinyl]methyl (1R) -cis/trans-3- (2-methyl-l- propenyl ) -2 , 2-dimethylcyclopropanecarboxylate) can be used for the Ester Compound. Examples of pests on which the pest control
composition of the present invention has a control effect include harmful arthropod pest such as harmful insects and harmful acarines, and more specifically, the following pests:
Lepidoptera insect pests:
Pyralidae such as Chilo suppressalis, Cnaphalocrosis medinalis, Plodia interpunctella , and Ephestia kuehniella;
Noctuidae such as Spodoptera litura, Pseudaletia separata, and Mamestra brassicae; Pieridae such as Pieris rapae crucivora; Tortricidae such as Adoxopheyes spp.;
Carposinidae; Lyonetiidae; Lymantriidae; Antographa;
Agrotis spp., such as Agrotis segetum and Agrotis ipsilon;
Helicoverpa spp.; Heliothis spp.; Plutella xylostella; Parnara guttata; Tinea pellionella; Tineola bisselliella , etc .
Diptera insect pests:
Culex spp. such as Culex pipiens pallens and Culex tritaeniorhynchus; Aedes spp. such as Aedes aegypti and Aedes albopictus; Anopheles spp. such as Anopheles sinensis; Chironomidae; Muscidae such as Musca domestica , Muscina stabulans and Fannia canicularis; Calliphoridae; Sarcophagidae; Anthomyiidae such as Delia phatura and Delia antiqua; Tephritidae; Agromyzidae; Drosophilidae; Psychodidae; Phoridae; Simuliidae; Tabanidae; Stomoxyidae; Ceratopogpnnidae, etc.
Blattaria insect pests:
Blattella germanica, Periplaneta fuliginosa,
Periplaneta americana, Periplaneta brunnea, Blatta orientalis, etc.
Hymenoptera insect pests:
Formicidae such as Camponotus japonicus, Tetramorium tsushimae, Lasius niger, Pachycondyla chinensis, Monomorium intrudens, Lasius fuji, Monomorium pharaonis, Formica fusca japonica, Ochetellus glaber, Pristomyrmex punctatus, Pheidole noda, and Linepith ema humile; Vespidae such as Polistes ( Polistes chinensis, Polistes riparius, Polistes jadwigae, Polistes rothneyi, Polistes nipponensis, Polistes snelleni, and Polistes japonicus) , Vespa mandarinia, Vespa simillima xanthoptera, Vespa analis, Vespa crabro, Vespa ducalis, Vespula flaviceps lewisi, Vespula shidai, and Dolichovespula media; Bethylidae; Tenthredinidae such as Athalia rosae ruficornis, etc.
Siphonaptera insect pests:
Ctenocephalides canis, Ctenocephalides felis, Pulex irritans, etc.
Anoplura insect pests:
Pediculus humanus, Phthirus pubis, Pediculus humanus captis, Pediculus humanus corporis etc.
Psocoptera insect pests: psocid
Isoptera insect pests:
Subterranean termites such as Reticulitermes speratus, Coptoterm.es formosanus, Reticulitermes flavipes,
Reticulitermes hesperus, Reticulitermes virginicus, Reticulitermes tibialis, Heterotermes aureus; drywood termites such as Incisitermes minor; and rottenwood termites such as Zootermopsis nevadensis .
Hemiptera insect pests:
Delphacidae such as Laodelphax striatellus, Nilaparvara lugens and Sogatella furcifera; Deltocephalidae such as Nephotettix cincticeps and Nephotettix virescens; Aphididae; Pentatomidae such as Nezara antennata, Riptortus clavatus, Eysarcoris lewisi, Eysarcoris parvus, Plautia stali, Halyomorpha mista, Stenotus rubrovittatus, and Trigonotylus caelestialium; Aleyrodidae; Coccidae; Cimicidae such as Cinex lectularius; Tingidae; Psyllidae, etc .
Coleoptera insect pests:
Attagenus unicolor; Anthrenus verbasci; corn rootworms such as Diabrotica virgi era virgifera and Dabrotica undecimpunctaca howardi; scarabaeidae such as Anomala cuprea and Anomala rufocuprea; . Curculionidae such as Sitophilus zeamais, Lissorhoptrus oryzophilus, Anthonomus grandis grandis and Callosobruchus cheninsis; Tenebrionidae such as Tenebrio molitor and Tribolium castaneum; Chrysomelidae such as Oulema oryzae, Phyllotreta striolata and Aulacophora femoralis; Anobiidae; Epilachna spp. such as Henosepilachna vigintioctopunctata ; Lyctidae; Bostrychidae; Ptinidae; Cerambycidae ; Paederus fuscipes; etc .
Thysanoptera insect pests:
Thrips palmi, Frankliniella occidentalis, Thrips hawaiiensis, etc.
Orthoptera insect pests:
Gryllotalpidae, Acrididae, Gryllidae, etc.
Acarina :
Pyroglyphidae such as Dermatophagoides farinae and Dermatophagoides pteronyssinus; Arcaridae such as Tyrophagus putrescentiae and Aleuroglyphus oyatus; Glycyphagidae such as Glycyphagus privatus, Glycyphagus domesticus and Glycyphagus destructor; Cheyletidae such as Cheyletus malaccensis and Cheyletus malaccesis; Tarsonemidae; Chortoglyohidae ; Oribatei; Tetranychidae such as Tetranychus urticae, Tetranychus kanzawai, Panonychus citri and Panonychus ulmi; Erythraeidae; Ixodidae such as Haemaphysalis longicornis; Dermanyssidae such as Ornithonyssus sylvairum and Dermanussus galinae; etc.
Scutigeromorpha, Chilopoda such as Scolopendra subsipnipes mutilans; Diplopoda such as Oxidus gracilis and Nedyopus tambanus; Armadilldiiidae and Porcellionidae such as Armadillidium vulgare; Gastropoda such as Limax marginatus and Limax flavus; and Araneae such as Nephila clavata, Cheiracanthium japonicum and Latrodectus hasselti; etc .
In the pest control composition of the present invention, the weight ratio of the Guanidine Compound to the Ester Compound is usually within the range of from 50 : 1 to 1 : 50, preferably from 20 : 1 to 1 : 20, more preferably from 20 : 1 to 1 : 10, especially more preferably from 20 : 1 to 1 : 1, most preferably from 20 : 1 to 5 : 1.
The pest control composition of the present invention can be a simple mixture of the Guanidine Compound and the Ester Compound. However, it is usually used in the form of various formulations. Examples of the formulations include oil solution, emulsifiable concentrate, wettable powder, wettable dispersible granule, suspension concentrate (e.g. suspension in water, and emulsion in water) , microcapsule formulation, gel formulation, dust, granule, tablet, coating formulation, aerosol, carbon dioxide formulation, heating vaporization formulation (e.g. mosquito coil, electric mosquito mat, and fluid absorption wicking-type pesticide) , piezo-type spray insecticide, heating fumigant (e.g. self-burning fumigant, chemical reaction type fumigant, and porous ceramic plate fumigant) , non-heating fumigant (e.g. resin fumigant, paper fumigant, unwoven fabric fumigant, woven fabric fumigant, and sublimation tablet), smoking formulation (e.g. fogging), direct contact formulation (e.g. sheet type contact formulation, tape type contact formulation, and net type contact formulation) , ULV formulation, and poison bait.
The formulation can be prepared, for example, by the following methods.
(1) The Guanidine Compound and the Ester Compound are mixed with a solid carrier, a liquid carrier, a gaseous carrier or feed and, if necessary, other auxiliary agents for formulations such as a surfactant.
(2) A base material is impregnated with the Guanidine Compound and the Ester Compound.
(3) The Guanidine Compound, the Ester Compound and a base material are mixed, followed by molding.
(4) The Guanidine Compound is mixed with a solid carrier, a liquid carrier, a gaseous carrier or feed and, if necessary, other auxiliary agents for formulations such as a surfactant to obtain suspension in water containing the Guanidine Compound and the Ester Compound is mixed with a solid carrier, a liquid carrier, a gaseous carrier or feed and, if necessary, other auxiliary agents for formulations such as a surfactant to obtain emulsion in water containing the Ester Compound. Then said suspension in water containing the Guanidine Compound and said emulsion in water containing the Ester Compound are mixed.
(5) The Guanidine Compound and the Ester Compound are mixed with a solid carrier, a liquid carrier, a gaseous carrier or feed and, if necessary, other auxiliary agents for formulations such as a surfactant. Then said mixture is ground.
These formulations usually contain as a total amount 0.001 to 90% by weight of the Guanidine Compound and the Ester Compound.
Examples of the solid carrier used for the formulation include fine powders and granules such as clays (e.g.
kaolin clay, diatomaceous earth, bentonite, Fubasami clay, and acidic white clay) , synthetic hydrated silicon oxide, talc, ceramics, other inorganic minerals (e.g. sericite, quarts, sulfur, active carbon, calcium carbonate, and hydrated silica), and chemical fertilizers (e.g. ammonium sulfate, ammonium phosphate, ammonium nitrate, ammonium chloride, and urea) ; and solid materials at ordinary temperature (e.g. 2 , , 6-triisopropyl-l , 3 , 5-trioxane, naphthalene, p-dichlorobenzene, camphor, and adamantane) as well as felt, fibers, cloth, woven fabrics, sheets, paper, threads, foam, porous materials and multifilaments composed of one or more of wool, silk, cotton, hemp, pulp, synthetic resins (e.g. polyethylene resins such as low-density polyethylene, linear low-density polyethylene, and high- density polyethylene; ethylene-vinyl ester copolymers such as ethylene-vinyl acetate copolymer; ethylene-methacrylate copolymers such as ethylene-methyl methacrylate copolymer, and ethylene-ethyl methacrylate copolymer; ethylene- acrylate copolymers such as ethylene-methyl acrylate copolymer, and ethylene-ethyl acrylate copolymer; ethylene- vinyl carboxyic acid copolymers such as ethylene-acrylic acid copolymer; ethylene-tetracyclododecene copolymer;
polypropylene resins such as propylene homopolymer, and propylene-ethylene copolymer; poly-4-methylpentene-l ;
polybutene-1 ; polybutadiene; polystyrene; acrylonitrile- styrene resin; styrene elastomers such as acrylonitrile- butadiene-styrene resin, styrene-conj ugated diene block copolymer, and hydrogenated styrene-conj ugated diene block copolymer; fluorine plastics; acrylic resins such as polymethyl methacrylate; polyamide resins such as nylon 6, and nylon 66; polyester resins such as polyethylene
terephthalate, polyethylene naphthalate, polybutylene terephthalate, and polycyclohexylene
dimethyleneterephthalate; polycarbonate; polyacetal;
polyacrylsulfone; polyarylate; polyhydroxybenzoate ; polyetherimide; polyestercarbonate; polyphenylene ether resin; polyvinyl chloride; polyvinylidene chloride;
polyurethane ; and porous resins such as foamed polyurethane, foamed polypropylene, and foamed polyethylene) , glass, metals, and ceramics.
Examples of the liquid carrier include aromatic or aliphatic hydrocarbons (e.g. xylene, toluene, alkyl
naphthalene, phenylxylylethane, kerosene, light oil, hexane, and cyclohexane) , halogenated hydrocarbons (e.g.
chlorobenzene, dichloromethane, dichloroethane, and
trichloroethane) , alcohols (e.g.. methanol, ethanol,
isopropyl alcohol, butanol, hexanol, benzyl alcohol, and ethylene glycol), ethers (e.g. diethylether , ethylene glycol dimethyl ether, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, propylene glycol
monomethyl ether, tetrahydrofuran, and dioxane) , esters (e.g. ethyl acetate, and butyl acetate), ketones (e.g.
acetone, methyl ethyl ketone, methyl isobutyl ketone, and cyclohexanone ) , nitriles (e.g. acetonitrile, and
isobutyronitrile) , sulfoxides (e.g. dimethyl sulfoxide), acid amides (e.g. N, N-dimethylformamide, N,N- dimethylacetoamide, and N-methyl-pyrrolidone) , alkylidene carbonates (e.g. propylene carbonate), vegetable oils (e.g. soybean oil, and cotton oil), vegetable essential oil (e.g. orange oil, hyssop oil, and lemon oil) and water.
Examples of the gaseous carrier include butane gas, chlorofluorocarbon gas, liquefied petroleum gas (LPG) , dimethyl ether, and carbon dioxide.
Examples of the surfactant include alkyl sulfate ester salts, alkyl sulfonates, alkylaryl sulfonates, alkylaryl ethers, polyoxyethylenated alkylaryl ethers, polyethylene glycol ethers, polyhydric alcohol esters, sugar alcohol derivatives, lignosulfonates (e.g. sodium lignosulfonate) , and polycarboxylates .
In the pest control composition of the present invention, the weight ratio of the Guanidine Compound to lignosulfonates is usually within the range of from 50 : 1 to 1 : 1, preferably from 20 : 1 to 1 : 1, more preferably from 20 : 1 to 5 : 1.
In the pest control composition of the present invention, the weight ratio of the Guanidine Compound to polycarboxylates is usually within the range of from 50 : 1 to 1 : 1, preferably from 20 : 1 to 1 : 1, more preferably from 20 : 1 to 2 : 1.
Examples of other auxiliary agents for formulations include binders, dispersants, and stabilizers. Specific examples thereof include casein, gelatin, polysaccharides (e.g. starch, gum arabic, cellulose derivatives, and
arginic acid) , lignin derivatives, bentonite, saccharides, synthetic water-soluble polymers (e.g. polyvinyl alcohol, and polyvinyl pyrrolidone) , polyacrylic acid, BHT (2,6-di- t-butyl-4-methylphenol) , and BHA (mixture of 2-t-butyl-4- methoxyphenol and 3-t-butyl-4-methoxyphenol ) .
Examples of the base material of a mosquito coil include a mixture of plant powder (e.g. wood powder, and pyrethrum) and a binder (e.g. powder of Machilus thunbergii, starch, and gluten) .
Examples of the base material of an electric mosquito mat include cotton linter matted, condensed and pressed in a plate shape, and mixed fibrils of cotton linter and pulp matted, condensed and pressed in a plate shape.
Examples of the base material of a self-burning
fumigant include combustion heat-developing agents such as nitrates, nitrites, guanidine salts, potassium chlorate, nitrocellulose, ethyl cellulose, and wood powder; heat decomposition stimulating agents such as alkali metal salts, alkaline earth metal salts, bichromates, and chromates;
oxygen suppliers such as potassium nitrate; combustion supporting agents such as melamine, and wheat starch;
fillers such as diatomaceous earth; and binders such as synthetic adhesives.
Examples of the base material of a chemical reaction type fumigant include heat-developing agents such as
sulfide, polysulfide, and hydrosulfide of alkali metals, and calcium oxide; catalysts such as carbonaceous materials, iron carbide, and activated clay; organic foaming agents such as azodicarbonamide, benzenesulfonyl hydrazide,
dinitro pentamethylene tetramine, polystyrene and
polyurethane; and fillers such as natural fibers and
synthetic fibers.
Examples of the resin used for, for example, a resin fumigant include polyethylene resins such as low-density polyethylene, linear low-density polyethylene, and high- density polyethylene; ethylene-vinyl ester copolymers such as ethylene-vinyl acetate copolymer; ethylene-methacrylate copolymers such as ethylene-methyl methacrylate copolymer, and ethylene-ethyl methacrylate copolymer; ethylene- acrylate copolymers such as ethylene-methyl acrylate
copolymer, and ethylene-ethyl acrylate copolymer; ethylene- vinyl carboxylate copolymers such as ethylene-acrylic acid copolymer; ethylene-tetracyclododecene copolymer;
polypropylene resins such as propylene homopolymer, and propylene-ethylene copolymer; poly-4-methylpentene-l ; polybutene-1; polybutadiene; polystyrene; acrylonitrile- styrene resin; styrene elastomers such as acrylonitrile- butadiene-styrene resin, styrene-conjugated diene block copolymer, and hydrogenated styrene-conjugated diene block copolymer; fluorine plastics; acrylic resins such as
polymethyl methacrylate; polyamide resins such as nylon 6, and nylon 66; polyester resins such as polyethylene
terephthalate, polyethylene naphthalate, polybutylene terephthalate, and polycyclohexylene
dimethyleneterephthalate ; polycarbonate; polyacetal;
polyacrylsulfone; polyarylate; polyhydroxybenzoate;
polyetherimide; polyestercarbonate; polyphenylene ether resin; polyvinyl chloride; polyvinylidene chloride; and polyurethane . They can be used alone or in a combination thereof. Further, if necessary, plasticizer such as
phthalates (e.g. dimethyl phthalate, and dioctyl phthalate), adipates, and stearic acid can be added to these base materials. The resin fumigant is prepared by kneading the Guanidine Compound and the Ester Compound into the base material, followed by molding it by injection molding, extrusion molding or press molding. The resultant resin formulation can undergo further processes such as molding and cutting, if necessary, processing into a form of plate, film, tape, net or string. These resin formulations can be processed into, for example, collars for animals, ear tags for animals, sheet formulations, guide strings and
horticultural supports.
Examples of the base material for poison bait include feed ingredients such as grain powder, vegetable oil, sugars, and crystalline cellulose; antioxidants such as dibutylhydroxy toluene, and nordihydroguaiaretic acid;
preservatives such as dehydroacetic acid; accidental ingestion prevention agents by children and pets such as chili pepper; and pest attractive flavors such as cheese flavor, onion flavor, and peanut oil.
The control method of pest of the present invention is carried out by applying the pest control composition of the present invention to pests and/or to areas where pests live And the control method of pest of the present invention is also carried out by applying the Guanidine Compound and the Ester Compound to pests and/or to areas where pests live respectively .
Specifically, as the application method of the pest control composition of the present invention, the following methods can be exemplified, and these methods can be appropriately selected according to, for example, the form of the pest control composition of the present invention, and the application place. (1) The pest control composition of the present invention is applied as it is to pests and/or areas where pests live.
(2) The pest control composition of the present invention is diluted with a solvent such as water, followed by applying to pests and/or areas where pests live.
In this case, usually, the pest control composition of the present invention in the form of, for example, emulsifiable concentrate, wettable powder, suspension concentrate or microcapsule preparation is diluted so that the total concentration of the Guanidine Compound and the Ester Compound becomes 0.1 to 50000 ppm.
(3) The pest control composition of the present invention is heated at areas where pests live to vaporize the effective ingredients.
In this case, the applied rate and concentration of the Guanidine Compound and the Ester Compound can be appropriately determined according to, for example, the form of the pest control composition of the present
invention, the application period, the application place, the application method, and the conditions of damage.
In utilizing the pest control composition of the present invention for preventative purpose, the application rate is usually from 0.0001 to 1000 mg/m3 in terms of the total amount of the Guanidine Compound and the Ester
Compound when applied to space, while it is from 0.0001 to 1000 mg/m2 when applied to plane. The heating vaporization formulation such as mosquito coil and electric mosquito mat is applied by appropriately heating according to the form of the formulation to vaporize the effective ingredients. The non-heating fumigant such as resin fumigant, paper fumigant, sublimation tablet, unwoven fabric fumigant, woven fabric fumigant, and sheet fumigant can be used, for example, by leaving the formulation as it is at the place to be applied, or by making a wind toward the formulation.
Examples of the place wherein the pest control
composition of the present invention is applied for
preventative purpose include closet, dresser, chest, wardrobe, cupboard, toilet, bathroom, storeroom, living room, dining room, warehouse, and inside a car. Further, the pest control composition of the present invention can also be applied to outside open space.
When the pest control composition of the present invention is used to livestock such as cows, horses, pigs, sheep, goats and chickens, and small animals such as dogs, cats, rats and mice, for the purpose of controlling
external parasites, veterinary known methods are applied to the animals. Specifically, the formulation is administered by way of a tablet, mixing in feed, a suppository and injection (including intramuscular, subcutaneous,
intravenous and intraperitoneal injections), when systemic control is intended. On the other hand, the formulation is used by way of spraying an oil solution or aqueous solution, pour-on or spot-on treatment, washing an animal with a shampoo formulation, or putting a collar or ear tag made of a resin formulation to an animal, when non-systemic control is intended. The total dosage of the Guanidine Compound and the Ester Compound is usually in the range from 0.01 to 1000 mg per 1 kg of an animal body.
Examples
Hereinafter, the present invention will be described in more detail by way of Formulation Examples and Test
Examples, but the present invention is not limited to only these Examples .
First, Formulation Examples of the pest control
composition of the present invention will be described. In the Formulation Examples, all the "parts" are by weight unless otherwise stated.
Formulation Example 1
In 37.5 parts of xylene and 37.5 parts of N,N- dimethylformamide, 0.9 part of the Guanidine Compound and 9 parts of the Ester Compound are dissolved. To the resultant solution, 9.1 parts of polyoxyethylene styryl phenyl ether and 6 parts of dodecylbenzenesulfonic acid calcium salt are added, followed by thoroughly mixing to obtain an emulsifiable concentrate.
Formulation Example 2
To 20 parts of the Guanidine Compound and 20 parts of the Ester Compound, 5 parts of SORPOL 5060 (registered trademark of TOHO Chemical Industry Co., Ltd.) is added, followed by thoroughly mixing. To the resultant mixture, 32 parts of CARPLEX #80 (registered trademark of Shionogi & Co., Ltd., dust of synthetic hydrated silicon oxide) and 23 parts of 300 mesh diatomaceous earth are added, followed by mixing with a juice mixer to obtain a wettable powder.
Formulation Example 3
To 3 parts of the Guanidine Compound and 0.3 part of the Ester Compound, 5 parts of dust of synthetic hydrated silicon oxide, 5 parts of dodecylbenzenesulfonic acid sodium salt, 30 parts of bentonite and 56.7 parts of clay are added, followed by thoroughly stirring and mixing. Then, an appropriate amount of water is added to the resultant mixture. The mixture is further stirred, granulated with a- granulator, and air-dried to obtain a granular formulation.
Formulation Example 4
In a mortar, 4.5 parts of the Guanidine Compound, 0.5 part of the Ester Compound, 1 parts of dust of synthetic hydrated silicon oxide, 1 part of DORILES B (trade name, manufacture by Daiichi Sankyo Co., Ltd.) as a flocculating agent and 7 parts of clay are thoroughly mixed, followed by stirring and mixing with a juice mixer. To the resultant mixture, 85.5 parts of cut clay is added, followed by thoroughly stirring and mixing to obtain a dust formulation.
Formulation Example 5
A mixture of 8 parts of the Guanidine Compound, 3 parts of the Ester Compound, 35 parts of white carbon containing a half amount of polyoxyethylene alkyl ether sulfate ammonium salt, and 54 parts of water are finely ground by a wet grinding method to obtain a formulation.
Formulation Example 6
In 10 parts of dichloromethane , 0.05 part of the Guanidine Compound and 0.1 part of the Ester Compound are dissolved, and the resultant solution is mixed with 89.85 parts of an isoparaffin solvent (ISOPAR , registered trademark of Exxon Chemical Co., Ltd.) to obtain an oil solution .
Formulation Example 7
Into an aerosol can, 0.1 part of the Guanidine
Compound, 0.05 part of the Ester Compound, and 49.85 parts of Neothiozole (Chuo Kasei Co., Ltd.) are placed. After mounting an aerosol valve, 25 parts of dimethylether and 25 parts of LPG are filled, followed by shaking and further mounting an actuator to obtain an oily aerosol.
Formulation Example 8
A mixture of 0.5 part of the Guanidine Compound, 0.05 part of the Ester Compound, 0.01 part of BHT, 5 parts of xylene, 3.44 parts of deodorized kerosine. and 1 part of an emulsifier (Atomos 300, registered trademark of Atomos Chemical Co., Ltd.), and 50 parts of distilled water are filled into an aerosol container, and a valve part is attached. Then, 40 parts of a propellant (LPG) is filled thereinto through the valve under pressure to obtain an aqueous aerosol.
Formulation Example 9
A solution prepared by dissolving 60 mg of the
Guanidine Compound and 40 mg of the Ester Compound in an appropriate amount of acetone is impregnated with a porous ceramic plate ( .0cm* .0cm, 1.2cm in thickness) to give a heating fumigant. The following Test Examples show that the pest control composition of the present invention has excellent controlling effect on pests.
Test Example 1
To a solution prepared by stirring a mixture of 0.1 part by weight of KELZAN S (tradename of CP Kelco, xanthan gum), 0.2 part by weight of VEEGUM Granules (registered trademark of R.T. Vanderbilt Company, Inc, magnesium aluminum silicate), 0.2 part by weight of Proxel GXL (registered trademark of Avecia Inc. preservative) and 14.5 parts by weight of ion-exchanged water for 1 hour, 60 parts by weight of ion-exchanged water and a mixture of 1.5 parts by weight of Reax 910 (tradename of MeadWestvaco Corporation, sodium lignosulfonate) , 11.45 parts by weight of ion-exchanged water, 2 parts by weight of Soprophor FLK (tradename of Rhodia Japan Co; Ltd, potassium polyoxyethylene tristyrylphenylether phosphate), 0.05 part by weight of ANTIFOAM C EMULSION (tradename of Dow Corning Corporation, silicone based defoamer) , and 10 parts by weight of the Guaniidine Compound were added and mixed to give a dilution containing 10 % by weight of the Guanidine Compound (hereinafter refered to as the Dilution A) .
To a solution prepared by stirring a mixture of 0.1 part by weight of KELZAN S (tradename of CP Kelco, xanthan gum), 0.2 part by weight of VEEGUM Granules (registered trademark of R.T. Vanderbilt Company, Inc, magnesium aluminum silicate), 0.2 part by weight of Proxel GXL (registered trademark of Avecia Inc. preservative) and 14.5 parts by weight of ion-exchanged water for 1 hour, 25 parts by weight of ion-exchanged water and a mixture of 4 parts by weight of Gohsenol GL-05 (registered trademark of The Nippon Synthetic Chemical Industry Co., Ltd., polyvinyl alcohol), 40.98 parts by weight of ion-exchanged water, 5 parts by weight of propylene glycohol, 0.02 part by weight of ANTIFOAM C EMULSION (tradename of Dow Corning Corporation, silicone based defoamer) , 5 parts by weight of the Ester Compound and 5 parts by weight of isopropyl myristate were added and mixed to give a dilution containing 5 % by weight of the Ester Compound (hereinafter refered to as the Dilution B) .
Each of test liquid composition containing the Guanidine Compound and/or the Ester Compound at specified concentration (refer to Table 1) was prepared by mixing the Dilution A, Dilution B and/or pure water.
Ten adults of German cockroach (Blattella germanica) (5 male and 5 female adults) were released in a test container (diameter: 8.75 cm, height: 7.5 cm, bottom: 16 mesh wire netted) of which inner wall was smeared with butter. The container was placed on the bottom of a test chamber (bottom: 46 cm x 46 cm, height: 70 cm). The liquid composition (0.7 ml) was sprayed from a' height of 60 cm above the upper side of the container using a spray gun (spraying pressure: 0.4 kg/cm2) . Thirty seconds after spraying, the container was taken out from the test chamber At a given period of time after spraying, the number of knocked down insects was counted and a knock down rate was calculated.
As a result, each of knock down rates two minutes after spraying of Example 1 to 4 indicated in Table 1 was shown no less than 80 %, and knock down rates two minutes after spraying of reference 1 and reference 2 indicated in Table 1 were shown 3.3 % and 37 % respectively.
Table 1
Figure imgf000028_0001
Test Example 2
Acetone-diluted solutions were prepared so that predetermined dosage of the Guanidine Compound and the Ester Compound on glass plates indicated in Table 2 would be applied. The acetone-diluted solutions (0.5 ml) were treated on the underside of glass petri dishes with a diameter of 7 cm uniformly and air-dried. Ten female adults of common mosquito (Culex pipiens pallens) were collected by means of a pocket aspirator and placed into the petri dish, then contacted compulsorily with the treated underside of glass petri dishes by covering with a lucid plate made of polyvinyl chloride.
Three minutes after covering, said common mosquitoes were released in nyron cage (size: 16.5 cm x 15.5 cm x 22 cm) . At a given period of time after releasing, the number of knocked down insects was counted and a knock down rate was calculated.
Knock down rates after 45 minutes are shown in Table 2.
Table 2
Figure imgf000029_0001
Industrial Applicability
Because the pest control composition of the present
' invention has an excellent pest control effect, this
invention is useful.

Claims

1. A pest control composition containing a combination of (E) -1- (2-chloro-l, 3-thiazol-5-ylmethyl ) -3-methyl-2- nitroguanidine and [2, 5-dioxo-3- (2-propynyl) -1- imidazolidinyl] methyl 2, 2-dimethyl-3- (2-methyl-l- propenyl ) cyclopropanecarboxylate .
2. The pest control composition according to claim 1, wherein the weight ratio of (E) -1- (2-chloro-l, 3-thiazol-5- ylmethyl ) -3-methyl-2-nitroguanidine to [2, 5-dioxo-3- (2- propynyl) -1-imidazolidinyl ] methyl 2, 2-dimethyl-3- (2-methyl- 1-propenyl) cyclopropanecarboxylate is within the range of from 50 : 1 to 1 : 50.
3. A control method of pests which comprises applying .. effective amount of (E) -1- (2-chloro-l, 3-thiazol-5- ylmethyl) -3-methyl-2-nitroguanidine and [2, 5-dioxo-3- (2- propynyl ) -1-imidazolidinyl ] methyl 2 , 2-dimethyl-3- ( 2-methyl- 1-propenyl ) cyclopropanecarboxylate to the pest or area where the pest live.
4. The control method of pest according to claim 3, wherein the weight ratio of (E) -1- (2-chloro-l, 3-thiazol-5- ylmethyl) -3-methyl-2-nitroguanidine to [ 2 , 5-dioxo-3- (2- propynyl ) -1-imidazolidinyl ] methyl 2 , 2-dimethyl-3- ( 2-methyl- 1-propenyl) cyclopropanecarboxylate is within the range of from 50 : 1 to 1 : 50.
PCT/JP2012/056796 2011-03-17 2012-03-12 Pest control composition and pest control method WO2012124795A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2011-058876 2011-03-17
JP2011058876 2011-03-17

Publications (1)

Publication Number Publication Date
WO2012124795A1 true WO2012124795A1 (en) 2012-09-20

Family

ID=46045043

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2012/056796 WO2012124795A1 (en) 2011-03-17 2012-03-12 Pest control composition and pest control method

Country Status (4)

Country Link
JP (1) JP2012207017A (en)
AR (1) AR085809A1 (en)
TW (1) TW201244632A (en)
WO (1) WO2012124795A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2021086807A1 (en) * 2019-10-28 2021-05-06 Valent U.S.A. Llc Novel clothianidin compositions and methods of use thereof

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4176189A (en) 1977-06-20 1979-11-27 Sumitomo Chemical Company, Limited Insecticidal and acaricidal hydantoin N-methylol esters
US4827020A (en) 1987-03-24 1989-05-02 Sumitomo Chemical Company, Limited Propargyl amide precursor to 1-propargyl-2,4-dioxoimidazolidine
US5034404A (en) 1988-12-27 1991-07-23 Takeda Chemical Industries, Ltd. Guanidine derivatives, their production and insecticides
US6218416B1 (en) * 1999-04-22 2001-04-17 Sumitomo Chemical Company, Limited Pesticidal compositions
WO2002030201A2 (en) * 2000-10-06 2002-04-18 Monsanto Technology, Llc Seed treatment with combinations of pyrethrins/pyrethroids and thiamethoxam
WO2002030202A2 (en) * 2000-10-06 2002-04-18 Monsanto Technology, Llc Seed treatment with combinations of pyrethrins/pyrethroids and clothianidin
WO2006008614A2 (en) * 2004-07-13 2006-01-26 United Phosphorus, Ltd. A synergistic insecticidal composition containing chloronicotynyle and pyrethroids compounds
US20060211655A1 (en) * 2003-01-17 2006-09-21 Bayer Health Care Ag Repellent
EP2272367A1 (en) * 2002-01-31 2011-01-12 Bayer CropScience AG Synergistic insecticidal mixtures

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4176189A (en) 1977-06-20 1979-11-27 Sumitomo Chemical Company, Limited Insecticidal and acaricidal hydantoin N-methylol esters
US4827020A (en) 1987-03-24 1989-05-02 Sumitomo Chemical Company, Limited Propargyl amide precursor to 1-propargyl-2,4-dioxoimidazolidine
US5034404A (en) 1988-12-27 1991-07-23 Takeda Chemical Industries, Ltd. Guanidine derivatives, their production and insecticides
US6218416B1 (en) * 1999-04-22 2001-04-17 Sumitomo Chemical Company, Limited Pesticidal compositions
WO2002030201A2 (en) * 2000-10-06 2002-04-18 Monsanto Technology, Llc Seed treatment with combinations of pyrethrins/pyrethroids and thiamethoxam
WO2002030202A2 (en) * 2000-10-06 2002-04-18 Monsanto Technology, Llc Seed treatment with combinations of pyrethrins/pyrethroids and clothianidin
EP2272367A1 (en) * 2002-01-31 2011-01-12 Bayer CropScience AG Synergistic insecticidal mixtures
US20060211655A1 (en) * 2003-01-17 2006-09-21 Bayer Health Care Ag Repellent
WO2006008614A2 (en) * 2004-07-13 2006-01-26 United Phosphorus, Ltd. A synergistic insecticidal composition containing chloronicotynyle and pyrethroids compounds

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2021086807A1 (en) * 2019-10-28 2021-05-06 Valent U.S.A. Llc Novel clothianidin compositions and methods of use thereof
US11871747B2 (en) 2019-10-28 2024-01-16 Valent U.S.A., Llc Clothianidin compositions and methods of use thereof

Also Published As

Publication number Publication date
TW201244632A (en) 2012-11-16
AR085809A1 (en) 2013-10-30
JP2012207017A (en) 2012-10-25

Similar Documents

Publication Publication Date Title
EP2197281B1 (en) Pesticidal composition and method for controlling pests
WO2009031692A2 (en) Pesticidal composition and method for controlling pests
KR20060127218A (en) Pyrethroid pesticide
KR20090126268A (en) Pesticidal composition and method for controlling harmful insects
KR20090126269A (en) Pesticidal composition and method for controlling harmful insects
KR20090115731A (en) Pesticidal composition and method for controlling a pest
KR20100014578A (en) Cyclopropane carboxylic compounds and their use in pest control
KR101361464B1 (en) A cyclopropane carboxylic acid ester compound and its use in pest control
EP2685830B1 (en) Pest control composition and pest control method
JP2011225542A (en) Ester compound and its pest control application
WO2012124795A1 (en) Pest control composition and pest control method
MX2010011911A (en) Harmful organism-controlling composition and control method of harmful organisms.
MX2010011912A (en) Harmful organisim-controlling composition and control method of harmful organisms.
JP2011225539A (en) Ester compound and its application
JP2011195576A (en) Ester compound and use thereof
KR20100110333A (en) Cyclopropanecarboxylate and pest controlling composition containing the same
MX2010011913A (en) Harmful organisim-controlling composition and control method of harmful organisms.
KR20090018948A (en) Ester compound and its use in pest control
JP5760577B2 (en) Ester compounds and their uses
AU2011250709A1 (en) Pesticidal composition and method for controlling pests
MX2010011914A (en) Harmful organisim-controlling composition and control method of harmful organisms.
MX2010011915A (en) Harmful organism-controlling composition and control method of harmful organisms.
AU2011250704A1 (en) Pesticidal composition and method for controlling pests
AU2011250706A1 (en) Pesticidal composition and method for controlling pests
AU2011250708A1 (en) Pesticidal composition and method for controlling pests

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 12719458

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 12719458

Country of ref document: EP

Kind code of ref document: A1