Patent Application
20230157288
The present invention relates to a pest controlling method, and a pest control agent composition and a pest control agent set. The present invention relates more specifically to a method which does not have a problem with safety and enables controlling various pests even at a low dosage, and a pest control agent composition and a pest control agent set which are suitable to be used for the method. The present application claims priority to Japan Patent Application No. 2020-067049, filed on Apr. 2, 2020, the contents of which are incorporated herein.
Patent document 1 discloses that a pyridyl imidazole compound is useful as an insecticide or an acaricide.
Patent document 2 discloses that an azole compound having a haloalkyl group is useful as an insecticide or an acaricide.
Patent document 3 discloses that a pyridyl imidazole compound having a cyclopropyl group is useful as an insecticide or an acaricide.
An object of the present invention is to provide a method which does not have a problem with safety and enables controlling various pests even at a low dosage, and a pest control agent composition and a pest control agent set which are suitable to be used for the method.
The present inventors have investigated earnestly to achieve the above-mentioned object and consequently completed the present invention, which includes the following aspects.
That is, the present invention includes the following aspects.
[1]
A pest controlling method, comprising applying at least one compound selected from a compound of formula (I):
(wherein, in formula (I),
R1 represents a substituted or unsubstituted C1-6 alkylthio group, a substituted or unsubstituted C1-6 alkylsulfinyl group, or a substituted or unsubstituted C1-6 alkylsulfonyl group,
R2 represents a hydrogen atom or a substituted or unsubstituted C1-6 alkyl group,
R represents a C1-6 haloalkyl group or a C2-6 haloalkenyl group,
X represents a substituted or unsubstituted C1-6 alkyl group, a substituted or unsubstituted C2-6 alkenyl group, a substituted or unsubstituted C2-6 alkynyl group, a hydroxyl group, a substituted or unsubstituted C1-6 alkoxy group, a formyl group, a substituted or unsubstituted C1-6 alkylcarbonyl group, a substituted or unsubstituted C1-6 alkoxycarbonyl group, a mercapto group, a substituted or unsubstituted C1-6 alkylthio group, a substituted or unsubstituted C1-6 alkylsulfinyl group, a substituted or unsubstituted C1-6 alkylsulfonyl group, a substituted or unsubstituted C3-8 cycloalkyl group, a substituted or unsubstituted C6-10 aryl group, a substituted or unsubstituted 5- to 6-membered heteroaryl group, a substituted or unsubstituted amino group, a halogeno group, a cyano group, or a nitro group,
n represents a chemically acceptable number of X, and represents any integer of 0 to 4, and Xs are the same or different when n is 2 or more) and a salt thereof, with an insecticidal or acaricidal active component to an object.
[2]
The pest controlling method according to [1], wherein the insecticidal or acaricidal active component is an active ingredient of an insecticide or an acaricide having a mechanism of action classified according to the IRAC code.
[3]
The pest controlling method according to [1], wherein the insecticidal or acaricidal active component is at least one selected from the group consisting of
alanycarb, aldicarb, bendiocarb, benfuracarb, butocarboxim, butoxycarboxim, carbaryl, carbofuran, carbosulfan, ethiofencarb, fenobucarb, formetanate, furathiocarb, isoprocarb, methiocarb, methomyl, metolcarb, oxamyl, pirimicarb, propoxur, thiodicarb, thiofanox, triazamate, trimethacarb, XMC, xylylcarb, acephate, azamethiphos, azinphos-ethyl, azinphos-methyl, cadusafos, chlorethoxyfos, chlorfenvinphos, chlormephos, chlorpyrifos, chlorpyrifos-methyl, coumaphos, cyanophos, demeton-S-methyl, diazinon, dichlorvos/DDVP, dicrotophos, dimethoate, dimethylvinphos, disulfoton, EPN, ethion, ethoprophos, famphur, fenamiphos, fenitrothion, fenthion, fosthiazate, heptenophos, imicyafos, isofenphos, isopropyl O-(methoxyaminothio-phosphoryl)salicylate, isoxathion, malathion, mecarbam, methamidophos, methidathion, mevinphos, monocrotophos, naled, omethoate, oxydemeton-methyl, parathion, parathion-methyl, phenthoate, phorate, phosalone, phosmet, phosphamidon, phoxim, pirimiphos-methyl, profenofos, propetamphos, prothiofos, pyraclofos, pyridaphenthion, quinalphos, sulfotep, tebupirimfos, temephos, terbufos, tetrachlorvinphos, thiometon, triazophos, trichlorfon, vamidothion, chlordane, endosulfan, ethiprole, fipronil, flufiprole, acrinathrin, allethrin, d-cis-trans allethrin, d-trans-allethrin, bifenthrin, bioallethrin, bioallethrin S-cyclopentenyl-isomer, bioresmethrin, cycloprothrin, cyfluthrin, β-cyfluthrin (beta-cyfluthrin), cyhalothrin, λ-cyhalothrin (lambda-cyhalothrin), γ-cyhalothrin (gamma-cyhalothrin), cypermethrin, α-cypermethrin (alpha-cypermethrin), β-cypermethrin (beta-cypermethrin), θ-cypermethrin (theta-cypermethrin), ζ-cypermethrin (zeta-cypermethrin), cyphenothrin[(1R)-trans-isomers], deltamethrin, empenthrin[(EZ)-(1R)-isomers], esfenvalerate, etofenprox, fenpropathrin, fenvalerate, flucythrinate, flumethrin, z-fluvalinate (tau-fluvalinate), halfenprox, imiprothrin, kadethrin, permethrin, phenothrin[(1R)-trans-isomer], prallethrin, pyrethrins, resmethrin, silafluofen, tefluthrin, tetramethrin, tetramethrin[(1R)-isomers], tralomethrin, transfluthrin, K-bifenthrin (kappa-bifenthrin), chloroprallethrin, heptafluthrin, meperfluthrin, ε-metofluthrin (epsilon-metofluthrin), momfluorothrin, ε-momfluorothrin (epsilon-momfluorothrin), κ-tefluthrin (kappa-tefluthrin), tetramethylfluthrin, bioethanomethrin, DDT, methoxychlor, acetamiprid, clothianidin, dinotefuran, imidacloprid, nitenpyram, thiacloprid, thiamethoxam, nicotine, sulfoxaflor, flupyradifurone, triflumezopyrim, dicloromezotiaz, flupyrimin, spinetoram, spinosad, abamectin, emamectin-benzoate, lepimectin, milbemectin, doramectin, eprinomectin, ivermectin, moxidectin, selamectin, hydroprene, kinoprene, methoprene, fenoxycarb, pyriproxifen, methyl bromide, alkyl halides, chloropicrin, sodium aluminum fluoride, sulfuryl fluoride, borax, boric acid, disodium octaborate, sodium borate, sodium metaborate, tartar emetic, dazomet, metam, pymetrozine, pyrifluquinazon, afidopyropen, clofentezine, diflovidazin, hexythiazox, etoxazole, B. t. subsp. israelensis, B. t. subsp. aizawai, B. t. subsp. kurstaki, B. t. subsp. tenebrionis, proteins contained in B. t. crops (B. t. crop proteins): Cry1Ab, Cry1Ac, Cry1Fa, Cry1A.105, Cry2Ab, Vip3A, mCry3A, Cry3Ab, Cry3Bb, and Cry34Ab1/Cry35Ab1, Bacillus sphaericus, diafenthiuron, azocyclotin, cyhexatin, fenbutatin-oxide, propargite, tetradifon, chlorfenapyr, DNOC (4,6-dinitro-o-cresol), sulfluramid, bensultap, cartap hydrochloride, thiocyclam, thiosultap-sodium, bistrifluron, chlorfluazuron, diflubenzuron, flucycloxuron, flufenoxuron, hexaflumuron, lufenuron, novaluron, noviflumuron, teflubenzuron, triflumuron, buprofezin, cyromazine, chromafenozide, halofenozid, methoxyfenozide, tebufenozide, amitraz, hydramethylnon, acequinocyl, fluacrypyrim, bifenazate, fenazaquin, fenpyroximate, pyridaben, pyrimidifen, tebufenpyrad, tolfenpyrad, rotenone, indoxacarb, metaflumizone, spirodiclofen, spiromesifen, spirotetramat, spiropidion, aluminum phosphide (Al-phosphide), calcium phosphide (Ca-phosphide), phosphine, zinc phosphide (Zn-phosphide), calcium cyanide (Ca-cyanide), sodium cyanide (Na-cyanide), potassium cyanide (K-cyanide), cyenopyrafen, cyflumetofen, pyflubumide, chlorantraniliprole, cyantraniliprole, cyclaniliprole, flubendiamide, cyhalodiamide, tetrachlorantraniliprole, tetraniliprole, flonicamid, broflanilide, fluxametamide, isocycloseram, afoxolaner, fluralaner, lotilaner, sarolaner, azadirachtin, benzoximate, bromopropylate, chinomethionat, dicofol, lime sulfur, mancozeb, pyridalyl, sulfur, acynonapyr, benzpyrimoxan, flometoquin, fluhexafon, oxazosulfyl, and tyclopyrazoflor.
[4]
The pest controlling method according to [1], wherein the insecticidal or acaricidal active component is at least one selected from the group consisting of acephate, carbofuran, fipronil, acetamiprid, spinetoram, abamectin, pymetrozine, flonicamid, cartap hydrochloride, chlorfenapyr, teflubenzuron, tebufenozide, tolfenpyrad, metaflumizone, cyantraniliprole, and fluxametamide.
[5]
The pest controlling method according to [1], wherein the compound of formula (I) is a compound of formula (II), formula (III), or formula (IV):
(wherein the carbon-carbon double stereo bond in formula (II) represents an E-isomer, a Z-isomer, or a mixture thereof)
[6]
The pest controlling method according to any one of [1] to [5], wherein the pests are insects or mites.
[7]
A pest control agent composition, comprising:
at least one compound selected from a compound of formula (I):
(wherein, in formula (I),
R1 represents a substituted or unsubstituted C1-6 alkylthio group, a substituted or unsubstituted C1-6 alkylsulfinyl group, or a substituted or unsubstituted C1-6 alkylsulfonyl group,
R2 represents a hydrogen atom or a substituted or unsubstituted C1-6 alkyl group,
R represents a C1-6 haloalkyl group or a C2-6 haloalkenyl group,
X represents a substituted or unsubstituted C1-6 alkyl group, a substituted or unsubstituted C2-6 alkenyl group, a substituted or unsubstituted C2-6 alkynyl group, a hydroxyl group, a substituted or unsubstituted C1-6 alkoxy group, a formyl group, a substituted or unsubstituted C1-6 alkylcarbonyl group, a substituted or unsubstituted C1-6 alkoxycarbonyl group, a mercapto group, a substituted or unsubstituted C1-6 alkylthio group, a substituted or unsubstituted C1-6 alkylsulfinyl group, a substituted or unsubstituted C1-6 alkylsulfonyl group, a substituted or unsubstituted C3-8 cycloalkyl group, a substituted or unsubstituted C6-10 aryl group, a substituted or unsubstituted 5- to 6-membered heteroaryl group, a substituted or unsubstituted amino group, a halogeno group, a cyano group, or a nitro group,
n represents a chemically acceptable number of X, and represents any integer of 0 to 4, and Xs are the same or different when n is 2 or more) and a salt thereof; and
an insecticidal or acaricidal active component.
[8]
The pest control agent composition according to [7], wherein the insecticidal or acaricidal active component is an active ingredient of an insecticide or an acaricide having a mechanism of action classified according to the IRAC code.
[9]
The pest control composition according to [7], wherein the insecticidal or acaricidal active component is at least one selected from the group consisting of
alanycarb, aldicarb, bendiocarb, benfuracarb, butocarboxim, butoxycarboxim, carbaryl, carbofuran, carbosulfan, ethiofencarb, fenobucarb, formetanate, furathiocarb, isoprocarb, methiocarb, methomyl, metolcarb, oxamyl, pirimicarb, propoxur, thiodicarb, thiofanox, triazamate, trimethacarb, XMC, xylylcarb, acephate, azamethiphos, azinphos-ethyl, azinphos-methyl, cadusafos, chlorethoxyfos, chlorfenvinphos, chlormephos, chlorpyrifos, chlorpyrifos-methyl, coumaphos, cyanophos, demeton-S-methyl, diazinon, dichlorvos/DDVP, dicrotophos, dimethoate, dimethylvinphos, disulfoton, EPN, ethion, ethoprophos, famphur, fenamiphos, fenitrothion, fenthion, fosthiazate, heptenophos, imicyafos, isofenphos, isopropyl O-(methoxyaminothio-phosphoryl)salicylate, isoxathion, malathion, mecarbam, methamidophos, methidathion, mevinphos, monocrotophos, naled, omethoate, oxydemeton-methyl, parathion, parathion-methyl, phenthoate, phorate, phosalone, phosmet, phosphamidon, phoxim, pirimiphos-methyl, profenofos, propetamphos, prothiofos, pyraclofos, pyridaphenthion, quinalphos, sulfotep, tebupirimfos, temephos, terbufos, tetrachlorvinphos, thiometon, triazophos, trichlorfon, vamidothion, chlordane, endosulfan, ethiprole, fipronil, flufiprole, acrinathrin, allethrin, d-cis-trans allethrin, d-trans allethrin, bifenthrin, bioallethrin, bioallethrin S-cyclopentenyl-isomer, bioresmethrin, cycloprothrin, cyfluthrin, β-cyfluthrin (beta-cyfluthrin), cyhalothrin, λ-cyhalothrin (lambda-cyhalothrin), γ-cyhalothrin (gamma-cyhalothrin), cypermethrin, α-cypermethrin (alpha-cypermethrin), β-cypermethrin (beta-cypermethrin), θ-cypermethrin (theta-cypermethrin), ζ-cypermethrin (zeta-cypermethrin), cyphenothrin[(1R)-trans-isomers], deltamethrin, empenthrin[(EZ)-(1R)-isomers], esfenvalerate, etofenprox, fenpropathrin, fenvalerate, flucythrinate, flumethrin, z-fluvalinate (tau-fluvalinate), halfenprox, imiprothrin, kadethrin, permethrin, phenothrin[(1R)-trans-isomer], prallethrin, pyrethrins, resmethrin, silafluofen, tefluthrin, tetramethrin, tetramethrin[(1R)-isomers], tralomethrin, transfluthrin, K-bifenthrin (kappa-bifenthrin), chloroprallethrin, heptafluthrin, meperfluthrin, ε-metofluthrin (epsilon-metofluthrin), momfluorothrin, ε-momfluorothrin (epsilon-momfluorothrin), κ-tefluthrin (kappa-tefluthrin), tetramethylfluthrin, bioethanomethrin, DDT, methoxychlor, acetamiprid, clothianidin, dinotefuran, imidacloprid, nitenpyram, thiacloprid, thiamethoxam, nicotine, sulfoxaflor, flupyradifurone, triflumezopyrim, dicloromezotiaz, flupyrimin, spinetoram, spinosad, abamectin, emamectin-benzoate, lepimectin, milbemectin, doramectin, eprinomectin, ivermectin, moxidectin, selamectin, hydroprene, kinoprene, methoprene, fenoxycarb, pyriproxifen, methyl bromide, alkyl halides, chloropicrin, sodium aluminum fluoride, sulfuryl fluoride, borax, boric acid, disodium octaborate, sodium borate, sodium metaborate, tartar emetic, dazomet, metam, pymetrozine, pyrifluquinazon, afidopyropen, clofentezine, diflovidazin, hexythiazox, etoxazole, B. t. subsp. israelensis, B. t. subsp. aizawai, B. t. subsp. kurstaki, B. t. subsp. tenebrionis, proteins contained in B. t. crops (B. t. crop proteins): Cry1Ab, Cry1Ac, Cry1Fa, Cry1A.105, Cry2Ab, Vip3A, mCry3A, Cry3Ab, Cry3Bb, and Cry34Ab1/Cry35Ab1, Bacillus sphaericus, diafenthiuron, azocyclotin, cyhexatin, fenbutatin-oxide, propargite, tetradifon, chlorfenapyr, DNOC (4,6-dinitro-o-cresol), sulfluramid, bensultap, cartap hydrochloride, thiocyclam, thiosultap-sodium, bistrifluron, chlorfluazuron, diflubenzuron, flucycloxuron, flufenoxuron, hexaflumuron, lufenuron, novaluron, noviflumuron, teflubenzuron, triflumuron, buprofezin, cyromazine, chromafenozide, halofenozid, methoxyfenozide, tebufenozide, amitraz, hydramethylnon, acequinocyl, fluacrypyrim, bifenazate, fenazaquin, fenpyroximate, pyridaben, pyrimidifen, tebufenpyrad, tolfenpyrad, rotenone, indoxacarb, metaflumizone, spirodiclofen, spiromesifen, spirotetramat, spiropidion, aluminum phosphide (Al-phosphide), calcium phosphide (Ca-phosphide), phosphine, zinc phosphide (Zn-phosphide), calcium cyanide (Ca-cyanide), sodium cyanide (Na-cyanide), potassium cyanide (K-cyanide), cyenopyrafen, cyflumetofen, pyflubumide, chlorantraniliprole, cyantraniliprole, cyclaniliprole, flubendiamide, cyhalodiamide, tetrachlorantraniliprole, tetraniliprole, flonicamid, broflanilide, fluxametamide, isocycloseram, afoxolaner, fluralaner, lotilaner, sarolaner, azadirachtin, benzoximate, bromopropylate, chinomethionat, dicofol, lime sulfur, mancozeb, pyridalyl, sulfur, acynonapyr, benzpyrimoxan, flometoquin, fluhexafon, oxazosulfyl, and tyclopyrazoflor.
[10]
The pest control agent composition according to [7], wherein the insecticidal or acaricidal active component is at least one selected from the group consisting of acephate, carbofuran, fipronil, acetamiprid, spinetoram, abamectin, pymetrozine, flonicamid, cartap hydrochloride, chlorfenapyr, teflubenzuron, tebufenozide, tolfenpyrad, metaflumizone, cyantraniliprole, and fluxametamide.
[11]
The pest control agent composition according to [7], wherein the compound of formula (I) is a compound of formula (II), formula (III), or formula (IV):
(wherein the carbon-carbon double stereo bond in formula (II) represents an E-isomer, a Z-isomer, or a mixture thereof)
The pest control agent composition according to any one of [7] to [11], wherein the pest is an insect or a mite.
[13]
A pest control agent set, wherein the pest control agent set is comprised of at least one compound selected from a compound of formula (I):
(wherein, in formula (I),
R1 represents a substituted or unsubstituted C1-6 alkylthio group, a substituted or unsubstituted C1-6 alkylsulfinyl group, or a substituted or unsubstituted C1-6 alkylsulfonyl group,
R2 represents a hydrogen atom or a substituted or unsubstituted C1-6 alkyl group,
R represents a C1-6 haloalkyl group or a C2-6 haloalkenyl group,
X represents a substituted or unsubstituted C1-6 alkyl group, a substituted or unsubstituted C2-6 alkenyl group, a substituted or unsubstituted C2-6 alkynyl group, a hydroxyl group, a substituted or unsubstituted C1-6 alkoxy group, a formyl group, a substituted or unsubstituted C1-6 alkylcarbonyl group, a substituted or unsubstituted C1-6 alkoxycarbonyl group, a mercapto group, a substituted or unsubstituted C1-6 alkylthio group, a substituted or unsubstituted C1-6 alkylsulfinyl group, a substituted or unsubstituted C1-6 alkylsulfonyl group, a substituted or unsubstituted C3-8 cycloalkyl group, a substituted or unsubstituted C6-10 aryl group, a substituted or unsubstituted 5- to 6-membered heteroaryl group, a substituted or unsubstituted amino group, a halogeno group, a cyano group, or a nitro group,
n represents a chemically acceptable number of X, and represents any integer of 0 to 4, and Xs are the same or different when n is 2 or more) and a salt thereof;
and a composition comprising an insecticidal or acaricidal active component,
wherein the compound and the composition are not mixed.
[14]
The pest control agent set according to [13], wherein the insecticidal or acaricidal active component is an active ingredient of an insecticide or an acaricide having a mechanism of action classified according to the IRAC code.
[15]
The pest control agent set according to [13], wherein the insecticidal or acaricidal active component is at least one selected from the group consisting of
alanycarb, aldicarb, bendiocarb, benfuracarb, butocarboxim, butoxycarboxim, carbaryl, carbofuran, carbosulfan, ethiofencarb, fenobucarb, formetanate, furathiocarb, isoprocarb, methiocarb, methomyl, metolcarb, oxamyl, pirimicarb, propoxur, thiodicarb, thiofanox, triazamate, trimethacarb, XMC, xylylcarb, acephate, azamethiphos, azinphos-ethyl, azinphos-methyl, cadusafos, chlorethoxyfos, chlorfenvinphos, chlormephos, chlorpyrifos, chlorpyrifos-methyl, coumaphos, cyanophos, demeton-S-methyl, diazinon, dichlorvos/DDVP, dicrotophos, dimethoate, dimethylvinphos, disulfoton, EPN, ethion, ethoprophos, famphur, fenamiphos, fenitrothion, fenthion, fosthiazate, heptenophos, imicyafos, isofenphos, isopropyl O-(methoxyaminothio-phosphoryl)salicylate, isoxathion, malathion, mecarbam, methamidophos, methidathion, mevinphos, monocrotophos, naled, omethoate, oxydemeton-methyl, parathion, parathion-methyl, phenthoate, phorate, phosalone, phosmet, phosphamidon, phoxim, pirimiphos-methyl, profenofos, propetamphos, prothiofos, pyraclofos, pyridaphenthion, quinalphos, sulfotep, tebupirimfos, temephos, terbufos, tetrachlorvinphos, thiometon, triazophos, trichlorfon, vamidothion, chlordane, endosulfan, ethiprole, fipronil, flufiprole, acrinathrin, allethrin, d-cis-trans allethrin, d-trans allethrin, bifenthrin, bioallethrin, bioallethrin S-cyclopentenyl-isomer, bioresmethrin, cycloprothrin, cyfluthrin, β-cyfluthrin (beta-cyfluthrin), cyhalothrin, λ-cyhalothrin (lambda-cyhalothrin), γ-cyhalothrin (gamma-cyhalothrin), cypermethrin, α-cypermethrin (alpha-cypermethrin), β-cypermethrin (beta-cypermethrin), θ-cypermethrin (theta-cypermethrin), ζ-cypermethrin (zeta-cypermethrin), cyphenothrin[(1R)-trans-isomers], deltamethrin, empenthrin[(EZ)-(1R)-isomers], esfenvalerate, etofenprox, fenpropathrin, fenvalerate, flucythrinate, flumethrin, z-fluvalinate (tau-fluvalinate), halfenprox, imiprothrin, kadethrin, permethrin, phenothrin[(1R)-trans-isomer], prallethrin, pyrethrins, resmethrin, silafluofen, tefluthrin, tetramethrin, tetramethrin[(1R)-isomers], tralomethrin, transfluthrin, K-bifenthrin (kappa-bifenthrin), chloroprallethrin, heptafluthrin, meperfluthrin, ε-metofluthrin (epsilon-metofluthrin), momfluorothrin, ε-momfluorothrin (epsilon-momfluorothrin), κ-tefluthrin (kappa-tefluthrin), tetramethylfluthrin, bioethanomethrin, DDT, methoxychlor, acetamiprid, clothianidin, dinotefuran, imidacloprid, nitenpyram, thiacloprid, thiamethoxam, nicotine, sulfoxaflor, flupyradifurone, triflumezopyrim, dicloromezotiaz, flupyrimin, spinetoram, spinosad, abamectin, emamectin-benzoate, lepimectin, milbemectin, doramectin, eprinomectin, ivermectin, moxidectin, selamectin, hydroprene, kinoprene, methoprene, fenoxycarb, pyriproxifen, methyl bromide, alkyl halides, chloropicrin, sodium aluminum fluoride, sulfuryl fluoride, borax, boric acid, disodium octaborate, sodium borate, sodium metaborate, tartar emetic, dazomet, metam, pymetrozine, pyrifluquinazon, afidopyropen, clofentezine, diflovidazin, hexythiazox, etoxazole, B. t. subsp. israelensis, B. t. subsp. aizawai, B. t. subsp. kurstaki, B. t. subsp. tenebrionis, proteins contained in B. t. crops (B. t. crop proteins): Cry1Ab, Cry1Ac, Cry1Fa, Cry1A.105, Cry2Ab, Vip3A, mCry3A, Cry3Ab, Cry3Bb, and Cry34Ab1/Cry35Ab1, Bacillus sphaericus, diafenthiuron, azocyclotin, cyhexatin, fenbutatin-oxide, propargite, tetradifon, chlorfenapyr, DNOC (4,6-dinitro-o-cresol), sulfluramid, bensultap, cartap hydrochloride, thiocyclam, thiosultap-sodium, bistrifluron, chlorfluazuron, diflubenzuron, flucycloxuron, flufenoxuron, hexaflumuron, lufenuron, novaluron, noviflumuron, teflubenzuron, triflumuron, buprofezin, cyromazine, chromafenozide, halofenozid, methoxyfenozide, tebufenozide, amitraz, hydramethylnon, acequinocyl, fluacrypyrim, bifenazate, fenazaquin, fenpyroximate, pyridaben, pyrimidifen, tebufenpyrad, tolfenpyrad, rotenone, indoxacarb, metaflumizone, spirodiclofen, spiromesifen, spirotetramat, spiropidion, aluminum phosphide (Al-phosphide), calcium phosphide (Ca-phosphide), phosphine, zinc phosphide (Zn-phosphide), calcium cyanide (Ca-cyanide), sodium cyanide (Na-cyanide), potassium cyanide (K-cyanide), cyenopyrafen, cyflumetofen, pyflubumide, chlorantraniliprole, cyantraniliprole, cyclaniliprole, flubendiamide, cyhalodiamide, tetrachlorantraniliprole, tetraniliprole, flonicamid, broflanilide, fluxametamide, isocycloseram, afoxolaner, fluralaner, lotilaner, sarolaner, azadirachtin, benzoximate, bromopropylate, chinomethionat, dicofol, lime sulfur, mancozeb, pyridalyl, sulfur, acynonapyr, benzpyrimoxan, flometoquin, fluhexafon, oxazosulfyl, and tyclopyrazoflor.
[16]
The pest control agent set according to [13], wherein the insecticidal or acaricidal active component is at least one selected from the group consisting of acephate, carbofuran, fipronil, acetamiprid, spinetoram, abamectin, pymetrozine, flonicamid, cartap hydrochloride, chlorfenapyr, teflubenzuron, tebufenozide, tolfenpyrad, metaflumizone, cyantraniliprole, and fluxametamide.
[17]
The pest control agent set according to [13], wherein the compound of formula (I) is a compound of formula (II), formula (III), or formula (IV):
(wherein the carbon-carbon double stereo bond in formula (II) represents an E-isomer, a Z-isomer, or a mixture thereof)
The pest control agent set according to any one of [13] to [17], wherein the pest control agent set is further comprised of at least one selected from the group consisting of a measuring cup, a measuring dropper, a mixing tank, gloves, a mask, and protective goggles.
[19]
A pest control agent set, wherein the pest control agent set is comprised of the pest control agent composition according to any one of [7] to [12] and at least one selected from the group consisting of a measuring cup, a measuring dropper, a mixing tank, gloves, a mask, and protective goggles.
[20]
The pest control agent set according to any one of [13] to [19], wherein the pests is an insect or a mite.
[21]
The pest controlling method according to [1], comprising further applying an active ingredient of a fungicide to the object.
[22]
The pest controlling method according to [21], wherein the active ingredient of a fungicide is an active ingredient of a fungicide having a mechanism of action classified according to the FRAC code.
[23]
The pest controlling method according to [21], wherein the active ingredient of a fungicide is at least one selected from the group consisting of
benalaxyl, benalaxyl-M, furalaxyl, metalaxyl, metalaxyl-M, oxadixyl, clozylacon, ofurace, bupirimate, dimethirimol, ethirimol, hymexazol, octhilinone, oxolinic acid, benomyl, carbendazim, chlorfenazole, fuberidazole, thiabendazole, thiophanate, thiophanate-methyl, diethofencarb, zoxamide, ethaboxam, pencycuron, fluopicolide, diflumetorim, tolfenpyrad, benodanil, flutolanil, mepronil, isofetamid, fluopyram, fenfuram, furmecyclox, carboxin, oxycarboxin, thifluzamide, benzovindiflupyr, bixafen, fluxapyroxad, furametpyr, isopyrazam, penflufen, penthiopyrad, sedaxane, boscalid, pyraziflumid, pydiflumetofen, isoflucypram, inpyrfluxam, azoxystrobin, coumoxystrobin, coumethoxystrobin, enoxastrobin, flufenoxystrobin, picoxystrobin, pyraoxystrobin, pyraclostrobin, pyrametostrobin, triclopyricarb, kresoxim-methyl, trifloxystrobin, dimoxystrobin, fenaminstrobin, metominostrobin, orysastrobin, famoxadone, fluoxastrobin, fenamidone, pyribencarb, mandestrobin, metyltetraprole, cyazofamid, amisulbrom, fenpicoxamid, binapacryl, meptyldinocap, dinocap, fluazinam, ferimzone, fentin acetate, fentin chloride, fentin hydroxide, silthiofam, ametoctradin, andoprim, cyprodinil, mepanipyrim, pyrimethanil, blasticidin-S, kasugamycin, kasugamycin hydrochloride, streptomycin, oxytetracycline, quinoxyfen, proquinazid, fenpiclonil, fludioxonil, chlozolinate, iprodione, procymidone, vinclozolin, edifenphos, iprobenfos, pyrazophos, isoprothiolane, biphenyl, chloroneb, dichloran, quintozene, tecnazene, tolclofos-methyl, etridiazole, iodocarb, propamocarb, propamocarb-hydrochloride, propamocarb-fosetylate, prothiocarb, Bacillus subtilis, Bacillus subtilis strain QST713, Bacillus subtilis strain FZB24, Bacillus subtilis strain MBI600, Bacillus subtilis strain D747, Bacillus amyloliquefaciens, Melaleuca alternifolia (tea tree) extract, triforine, pyrifenox, pyrisoxazole, fenarimol, flurprimidol, nuarimol, imazalil, imazalil-sulfate, oxpoconazole fumarate, pefurazoate, prochloraz, triflumizole, viniconazole, azaconazole, bitertanol, bromuconazole, cyproconazole, diclobutrazol, difenoconazole, diniconazole, diniconazole-M, epoxiconazole, etaconazole, fenbuconazole, fluquinconazole, flusilazole, flutriafol, furconazole, furconazole-cis, hexaconazole, imibenconazole, ipconazole, metconazole, myclobutanil, penconazole, propiconazole, fluquinconazole, simeconazole, tebuconazole, tetraconazole, triadimefon, triadimenol, triticonazole, prothioconazole, voriconazole, mefentrifluconazole, aldimorph, dodemorph, dodemorph acetate, fenpropimorph, tridemorph, fenpropidin, piperalin, spiroxamine, fenhexamid, fenpyrazamine, pyributicarb, naftifine, terbinafine, validamycin, polyoxins, polyoxorim, dimethomorph, flumorph, pyrimorph, benthiavalicarb-isopropyl, iprovalicarb, valifenalate, mandipropamid, fthalide, pyroquilon, tricyclazole, carpropamid, diclocymet, fenoxanil, tolprocarb, acibenzolar-S-methyl, probenazole, tiadinil, isotianil, dichlobentiazox, laminarin, Reynoutria sachalinensis extract, cymoxanil, fosetyl-aluminum, phosphoric acid (phosphate), tecloftalam, triazoxide, flusulfamide, diclomezine, methasulfocarb, cyflufenamid, metrafenone, pyriofenone, dodine, dodine free base, flutianil, copper (copper salt), bordeaux mixture, copper hydroxide, copper naphthalate, copper oxide, copper oxychloride, copper sulfate, sulfur, sulfur product, calcium polysulfide, ferbam, mancozeb, maneb, mancopper, metiram, polycarbamate, propineb, thiram, zineb, ziram, captan, captafol, folpet, chlorothalonil, dichlofluanid, tolylfluanid, guazatine, iminoctadine triacetate, iminoctadine trialbesilate, anilazine, dithianon, quinomethionate, fluoroimide, fluorofolpet, guazatine acetate, bis(8-quinolinolato) copper(II), propamidine, chloropicrin, cyprofuram, Agrobacterium, bethoxazin, diphenylamine, methyl isothiocyanate (MITC), mildiomycin, capsaicin, cufraneb, cyprosulfamide, dazomet, debacarb, dichlorophen, flumetover, fosetyl-calcium, fosetyl-sodium, irumamycin, natamycin, nitrothal isopropyl, oxamocarb, pyrrolnitrin, tebufloquin, tolnifanide, zarilamide, algophase, amicarthiazol, oxathiapiprolin, metiram zinc, benthiazole, trichlamide, uniconazole, oxyfenthiin, picarbutrazox, dichlobentiazox, quinofumelin, thiuram, ambam, Agrobacterium radiobacter, Coniothyrium minitans, Pseudomonas fluorescens, Pseudomonas rhodesiae, Talaromyces flavus, Trichoderma atroviride, avirulent Erwinia carotovora (Erwinia carotovora subsp. Carotovora), Bacillus simplex, Variovorax paradoxus, Lactobacillus plantarum, florylpicoxamid, pyrapropoyne, fluindapyr, aminopyrifen, pyridachlometyl, and ipflufenoquin.
According to a controlling method of the present invention, pests such as insects and mites may be more safely controlled at a lower dosage. In a pest controlling method, especially in the controlling method of the present invention, a pest control agent composition and a pest control agent set of the present invention may be suitably used. The pest control agent composition of the present invention may be suitably used especially for insecticide and acaricide for agriculture and horticulture.
Since the pest control agent composition of the present invention contains a compound of formula (I) or a salt thereof (hereinafter referred to as a “compound A”) and an insecticidal or acaricidal active component (hereinafter referred to as a “compound B”) at a ratio suitable for application objects, trouble in measuring and mixing the compound A and the compound B may be saved. The pest control agent composition of the present invention is packaged, bottled, boxed, and canned depending on the dosage form, and may be stored or transported.
Since chemical compositions required for application operation is gathered into one, the pest control agent set of the present invention save trouble in obtaining chemicals individually, and is excellent in convenience in storage and transport.
A pest controlling method of the present invention comprises applying a compound A with a compound B to an object.
The compound A is a compound of formula (I) (hereinafter described as a compound (I) in some cases) or a salt thereof.
In formula (I),
R1 represents a substituted or unsubstituted C1-6 alkylthio group, a substituted or unsubstituted C1-6 alkylsulfinyl group, or a substituted or unsubstituted C1-6 alkylsulfonyl group,
R2 represents a hydrogen atom or a substituted or unsubstituted C1-6 alkyl group,
R represents a C1-6 haloalkyl group or a C2-6 haloalkenyl group,
X represents a substituted or unsubstituted C1-6 alkyl group, a substituted or unsubstituted C2-6 alkenyl group, a substituted or unsubstituted C2-6 alkynyl group, a hydroxyl group, a substituted or unsubstituted C1-6 alkoxy group, a formyl group, a substituted or unsubstituted C1-6 alkylcarbonyl group, a substituted or unsubstituted C1-6 alkoxycarbonyl group, a mercapto group, a substituted or unsubstituted C1-6 alkylthio group, a substituted or unsubstituted C1-6 alkylsulfinyl group, a substituted or unsubstituted C1-6 alkylsulfonyl group, a substituted or unsubstituted C3-8 cycloalkyl group, a substituted or unsubstituted C6-10 aryl group, a substituted or unsubstituted 5- to 6-membered heteroaryl group, a substituted or unsubstituted amino group, a halogeno group, a cyano group, or a nitro group,
n represents a chemically acceptable number of X, and represents any integer of 0 to 4, and Xs are the same or different when n is 2 or more.
In the present invention, the term “unsubstituted” means a group consisting only of a core. Only the name of a group consisting of a core without the term “substituted” means an “unsubstituted” group unless otherwise specified.
By contrast, the term “substituted” means that any hydrogen atom of a group consisting of a core is replaced by a group (substituent) having a structure that is the same as or different from that of the core. Thus, the “substituent” means another group bound to the group consisting of a core. The number of the substituent may be one or more. Two or more substituents are the same or different.
Terms such as “C1-6” mean that the number of carbon atoms in the group consisting of a core is 1 to 6, and the like. This number of carbon atoms does not include the number of carbon atoms present in the substituent. For example, a butyl group having an ethoxy group as a substituent is classified into a C2 alkoxy C4 alkyl group.
The “substituent” is not particularly limited as long as the substituent is chemically acceptable and produces the effect of the present invention. Hereinafter, a group capable of serving as the “substituent” is exemplified:
a C1-6 alkyl group such as a methyl group, an ethyl group, a n-propyl group, an i-propyl group, a n-butyl group, a s-butyl group, an i-butyl group, a t-butyl group, a n-pentyl group, and a n-hexyl group;
a C2-6 alkenyl group such as a vinyl group, a 1-propenyl group, a 2-propenyl group (allyl group), a 1-butenyl group, a 2-butenyl group, a 3-butenyl group, a 1-methyl-2-propenyl group, and a 2-methyl-2-propenyl group;
a C2-6 alkynyl group such as an ethynyl group, a 1-propynyl group, a 2-propynyl group, a 1-butynyl group, a 2-butynyl group, a 3-butynyl group, and a 1-methyl-2-propynyl group;
a C3-8 cycloalkyl group such as a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, a cyclohexyl group, and a cubanyl group;
a C6-10 aryl group such as a phenyl group and a naphthyl group;
a C6-10 aryl C1-6 alkyl group such as a benzyl group and a phenethyl group;
a 3- to 6-membered heterocyclyl group;
a 3- to 6-membered heterocyclyl C1-6 alkyl group;
a hydroxy group;
a C1-6 alkoxy group such as a methoxy group, an ethoxy group, a n-propoxy group, an i-propoxy group, a n-butoxy group, a s-butoxy group, an i-butoxy group, and a t-butoxy group;
a C2-6 alkenyloxy group such as a vinyloxy group, an allyloxy group, a propenyloxy group, and a butenyloxy group;
a C2-6 alkynyloxy group such as an ethynyloxy group and a propargyloxy group;
a C6-10 aryloxy group such as a phenoxy group and a naphthoxy group;
a C6-10 aryl C1-6 alkoxy group such as a benzyloxy group and a phenethyloxy group;
a 5- or 6-membered heteroaryloxy group such as a thiazolyloxy group and a pyridyloxy group;
a 5- or 6-membered heteroaryl C1-6 alkyloxy group such as a thiazolylmethyloxy group and a pyridylmethyloxy group;
a formyl group;
a C1-6 alkylcarbonyl group such as an acetyl group and a propionyl group;
a formyloxy group;
a C1-6 alkylcarbonyloxy group such as an acetyloxy group and a propionyloxy group;
a C6-10 arylcarbonyl group such as a benzoyl group;
a C1-6 alkoxycarbonyl group such as a methoxycarbonyl group, an ethoxycarbonyl group, a n-propoxycarbonyl group, an i-propoxycarbonyl group, a n-butoxycarbonyl group, and a t-butoxycarbonyl group;
a C1-6 alkoxycarbonyloxy group such as a methoxycarbonyloxy group, an ethoxycarbonyloxy group, a n-propoxycarbonyloxy group, an i-propoxycarbonyloxy group, a n-butoxycarbonyloxy group, and a t-butoxycarbonyloxy group; a carboxy group;
a halogeno group such as a fluoro group, a chloro group, a bromo group, and an iodo group;
a C1-6 haloalkyl group such as a chloromethyl group, a chloroethyl group, a trifluoromethyl group, a 1,2-dichloro-n-propyl group, a 1-fluoro-n-butyl group, and a perfluoro-n-pentyl group;
a C2-6 haloalkenyl group such as a 2-chloro-1-propenyl group and a 2-fluoro-1-butenyl group;
a C2-6 haloalkynyl group such as a 4,4-dichloro-1-butynyl group, a 4-fluoro-1-pentynyl group, and a 5-bromo-2-pentynyl group;
a C1-6 haloalkoxy group such as a trifluoromethoxy group, a 2-chloro-n-propoxy group, and a 2,3-dichlorobutoxy group;
a C2-6 haloalkenyloxy group such as a 2-chloropropenyloxy group and a 3-bromobutenyloxy group;
a C1-6 haloalkylcarbonyl group such as a chloroacetyl group, a trifluoroacetyl group, and a trichloroacetyl group;
an amino group;
a C1-6 alkyl-substituted amino group such as a methylamino group, a dimethylamino group, and a diethylamino group;
a C6-10 arylamino group such as an anilino group and a naphthylamino group;
a C6-10 aryl C1-6 alkylamino group such as a benzylamino group and a phenethylamino group;
a formylamino group;
a C1-6 alkylcarbonylamino group such as an acetylamino group, a propanoylamino group, a butyrylamino group, and an i-propylcarbonylamino group;
a C1-6 alkoxycarbonylamino group such as a methoxycarbonylamino group, an ethoxycarbonylamino group, a n-propoxycarbonylamino group, and an i-propoxycarbonylamino group;
an unsubstituted or substituted aminocarbonyl group such as an aminocarbonyl group, a dimethylaminocarbonyl group, a phenylaminocarbonyl group, a N-phenyl-N-methylaminocarbonyl group, and a 2,2,2-trifluoroethylaminocarbonyl group;
an imino C1-6 alkyl group such as an iminomethyl group, a (1-imino)ethyl group, and a (1-imino)-n-propyl group;
a substituted or unsubstituted N-hydroxyimino C1-6 alkyl group such as a N-hydroxy-iminomethyl group, a (1-(N-hydroxy)-imino) ethyl group, a (1-(N-hydroxy)-imino)propyl group, a N-methoxy-iminomethyl group, and a (1-(N-methoxy)-imino)ethyl group;
an aminocarbonyloxy group;
a C1-6 alkyl-substituted aminocarbonyloxy group such as an ethylaminocarbonyloxy group and a dimethylaminocarbonyloxy group;
a mercapto group;
a C1-6 alkylthio group such as a methylthio group, an ethylthio group, a n-propylthio group, an i-propylthio group, a n-butylthio group, an i-butylthio group, a s-butylthio group, and a t-butylthio group;
a C1-6 haloalkylthio group such as a trifluoromethylthio group and a 2,2,2-trifluoroethylthio group;
a C6-10 arylthio group such as a phenylthio group and a naphthylthio group;
a 5- or 6-membered heteroarylthio group such as a thiazolylthio group and a pyridylthio group;
a C1-6 alkylsulfinyl group such as a methylsulfinyl group, an ethylsulfinyl group, and a t-butylsulfinyl group;
a C1-6 haloalkylsulfinyl group such as a trifluoromethylsulfinyl group and a 2,2,2-trifluoroethylsulfinyl group;
a C6-10 arylsulfinyl group such as a phenylsulfinyl group;
a 5- or 6-membered heteroarylsulfinyl group such as a thiazolylsulfinyl group and a pyridylsulfinyl group;
a C1-6 alkylsulfonyl group such as a methylsulfonyl group, an ethylsulfonyl group, and a t-butylsulfonyl group;
a C1-6 haloalkylsulfonyl group such as a trifluoromethylsulfonyl group and a 2,2,2-trifluoroethylsulfonyl group;
a C6-10 arylsulfonyl group such as a phenylsulfonyl group;
a 5- or 6-membered heteroarylsulfonyl group such as a thiazolylsulfonyl group and a pyridylsulfonyl group;
a C1-6 alkylsulfonyloxy group such as a methylsulfonyloxy group, an ethylsulfonyloxy group, and a t-butylsulfonyloxy group;
a C1-6 haloalkylsulfonyloxy group such as a trifluoromethylsulfonyloxy group and a 2,2,2-trifluoroethylsulfonyloxy group;
a tri-C1-6 alkyl-substituted silyl group such as a trimethylsilyl group, a triethylsilyl group, and a t-butyldimethylsilyl group;
a tri-C6-10 aryl-substituted silyl group such as a triphenylsilyl group;
a cyano group; and
a nitro group.
For these “substituents”, any hydrogen atom in each substituent may be replaced by a group having a distinct structure. In this case, as the “substituent”, a C1-6 alkyl group, a C1-6 haloalkyl group, a C1-6 alkoxy group, a C1-6 haloalkoxy group, a halogeno group, a cyano group, a nitro group, or the like may be exemplified.
The “3- to 6-membered heterocyclyl group” described above contains 1 to 4 heteroatoms selected from the group consisting of a nitrogen atom, an oxygen atom, and a sulfur atom as ring-constituting atoms. The heterocyclyl group may be either monocyclic or polycyclic. The polycyclic heterocyclyl group has at least one hetero ring, and the remaining ring(s) may be any of a saturated alicyclic ring, an unsaturated alicyclic ring and an aromatic ring. As the “3- to 6-membered heterocyclyl group”, a 3- to 6-membered saturated heterocyclyl group, a 5- or 6-membered heteroaryl group, a 5- or 6-membered partially unsaturated heterocyclyl group or the like may be exemplified.
As the 3- to 6-membered saturated heterocyclyl group, an aziridinyl group, an epoxy group, a pyrrolidinyl group, a tetrahydrofuranyl group, a thiazolidinyl group, a piperidyl group, a piperazinyl group, a morpholinyl group, a dioxolanyl group, a dioxanyl group or the like may be exemplified.
As the 5-membered heteroaryl group, a pyrrolyl group, a furyl group, a thienyl group, an imidazolyl group, a pyrazolyl group, an oxazolyl group, an isoxazolyl group, a thiazolyl group, an isothiazolyl group, a triazolyl group, an oxadiazolyl group, a thiadiazolyl group, a tetrazolyl group, or the like may be exemplified.
As the 6-membered heteroaryl group, a pyridyl group, a pyrazinyl group, a pyrimidinyl group, a pyridazinyl group, a triazinyl group, or the like may be exemplified.
As the “C1-6 alkylthio group” of R1, a methylthio group, an ethylthio group, a n-propylthio group, an i-propylthio group, a n-butylthio group, an i-butylthio group, a s-butylthio group, a t-butylthio group, or the like may be exemplified.
As the “C1-6 alkylsulfinyl group” of R1, a methylsulfinyl group, an ethylsulfinyl group, a t-butylsulfinyl group, or the like may be exemplified.
As the “C1-6 alkylsulfonyl group” of R1, a methylsulfonyl group, an ethylsulfonyl group, a t-butylsulfonyl group, or the like may be exemplified.
As a substituent on the “C1-6 alkylthio group”, the “C1-6 alkyl sulfinyl group”, and the “C1-6 alkylsulfonyl group” of R1, a halogeno group such as a fluoro group, a chloro group, a bromo group, or an iodo group may be preferably exemplified.
The “C1-6 alkyl group” of R2 may be linear or branched. As the “C1-6 alkyl group”, a methyl group, an ethyl group, a n-propyl group, a n-butyl group, a n-pentyl group, a n-hexyl group, an i-propyl group, an i-butyl group, a s-butyl group, a t-butyl group, an i-pentyl group, a neopentyl group, a 2-methylbutyl group, an i-hexyl group, or the like may be exemplified.
As a substituent on the “C1-6 alkyl group” of R2, a halogeno group such as a fluoro group, a chloro group, a bromo group, or an iodo group may be preferably exemplified.
As specific examples of the “substituted C1-6 alkyl group”, the following may be exemplified:
a C1-6 haloalkyl group such as a fluoromethyl group, a chloromethyl group, a bromomethyl group, a difluoromethyl group, a dichloromethyl group, a dibromomethyl group, a trifluoromethyl group, a trichloromethyl group, a tribromomethyl group, a 1-chloroethyl group, a 2,2-difluoroethyl group, a 2,2,2-trifluoroethyl group, a 2-chloro-2,2-difluoroethyl group, a 2,2,2-trichloroethyl group, a pentafluoroethyl group, a 3,3,3-trifluoropropyl group, a 2,2,3,3,3-pentafluoropropyl group, a 4-fluorobutyl group, a 2,2,3,3,4,4,4-heptafluorobutyl group, a 4-chlorobutyl group, a 2,2,2-trifluoro-1-trifluoromethylethyl group, a 1,1,1,3,3,3-hexafluoropropan-2-yl group, a perfluoropropan-2-yl group, a perfluorohexyl group, a perchlorohexyl group, a 2,4,6-trichlorohexyl group, or the like.
The “C1-6 haloalkyl group” of R is a C1-6 alkyl group substituted with a halogeno group such as a fluoro group, a chloro group, a bromo group, or an iodo group, and, for example, a fluoromethyl group, a difluoromethyl group, a trifluoromethyl group, a 2,2,2-trifluoroethyl group, a pentafluoroethyl group, a 3,3,3-trifluoropropyl group, a 2,2,3,3,3-pentafluoropropyl group, a 1-chloro-2,2,3,3,3-pentafluoropropyl group, a 1,2,2,3,3,3-hexafluoropropyl group, a perfluoropropyl group, a 2,2,2-trifluoro-1-trifluoromethylethyl group, a perfluoroisopropyl group, a 4-fluorobutyl group, a 1,4,4,4-tetrafluorobutyl group, a 2,2,3,3,4,4,4-heptafluorobutyl group, a 1,2,2,3,3,4,4,4-octafluorobutyl group, a perfluorobutyl group, a 3,3,3-trifluoro-2-trifluoromethylpropyl group, a 1-chloro-2,3,3,3-tetrafluoro-2-trifluoromethylpropyl group, a 1,2,3,3,3-pentafluoro-2-trifluoromethylpropyl group, a 2,2,3,3,4,4,5,5,5-nonafluoropentyl group, a 1-chloro-2,2,3,3,4,4,5,5,5-nonafluoropentyl group, a 1,2,2,3,3,4,4,5,5,5-decafluoropentyl group, a perfluoropentyl group, a perfluorohexyl group, a chloromethyl group, a bromomethyl group, a dichloromethyl group, a dibromomethyl group, a trichloromethyl group, a tribromomethyl group, a 1-chloroethyl group, a 2,2,2-trichloroethyl group, a 4-chlorobutyl group, a perchlorohexyl group, a 2,4,6-trichlorohexyl group, or the like may be exemplified.
The “C2-6 haloalkenyl group” of R is a C2-6 alkenyl group substituted with a halogeno group such as a fluoro group, a chloro group, a bromo group, or an iodo group, and, for example, a C2-6 haloalkenyl group such as a 2-fluoro-2-bromovinyl group, a 2,2-dichlorovinyl group, a 2-chloro-2-iodovinyl group, a 2-chloro-1-propenyl group, a 2,3,3,3-tetrafluoro-1-propenyl group, a 3,3,3-trifluoro-1-propenyl group, a 2-chloro-3,3,3-trifluoro-1-propenyl group, a 2-bromo-3,3,3-trifluoro-1-propenyl group, a 3,3,3-trifluoro-2-trifluoromethyl-1-propenyl group, a 2-fluoro-1-butenyl group, a 3,3,4,4,4-pentafluoro-1-butenyl group, a 2,3,3,4,4,4-hexafluoro-1-butenyl group, a 2-chloro-3,3,4,4,4-pentafluoro-1-butenyl group, a 3,3,4,4,5,5,5-heptafluoro-1-pentenyl group, a 2-chloro-3,3,4,4,5,5,5-heptafluoro-1-pentenyl group, a 2,3,3,4,4,5,5,5-octafluoro-1-pentenyl group, or a 3,3,4,4,5,5,6,6,6-nonafluoro-1-hexenyl group; or the like may be exemplified.
As the “substituted or unsubstituted C1-6 alkyl group” of X, the same as specifically illustrated in R2 may be exemplified.
As the “substituted or unsubstituted C1-6 alkylthio group”, the “substituted or unsubstituted C1-6 alkylsulfinyl group”, and the “substituted or unsubstituted C1-6 alkylsulfonyl group” of X, the same as specifically illustrated in R1 may be exemplified.
As the “C2-6 alkenyl group” of X, a vinyl group, a 1-propenyl group, a 2-propenyl group, a 1-butenyl group, a 2-butenyl group, a 3-butenyl group, a 1-methyl-2-propenyl group, a 2-methyl-2-propenyl group, a 1-pentenyl group, a 2-pentenyl group, a 3-pentenyl group, a 4-pentenyl group, a 1-methyl-2-butenyl group, a 2-methyl-2-butenyl group, a 1-hexenyl group, a 2-hexenyl group, a 3-hexenyl group, a 4-hexenyl group, a 5-hexenyl group, or the like may be exemplified.
As the “C2-6 alkynyl group” of X, an ethynyl group, a 1-propynyl group, a 2-propynyl group, a 1-butynyl group, a 2-butynyl group, a 3-butynyl group, a 1-methyl-2-propynyl group, a 2-methyl-3-butynyl group, a 1-pentynyl group, a 2-pentynyl group, a 3-pentynyl group, a 4-pentynyl group, a 1-methyl-2-butynyl group, a 2-methyl-3-pentynyl group, a 1-hexynyl group, a 1,1-dimethyl-2-butynyl group, or the like may be exemplified.
As the “C1-6 alkoxy group” of X, a methoxy group, an ethoxy group, a n-propoxy group, an i-propoxy group, a n-butoxy group, a s-butoxy group, an i-butoxy group, a t-butoxy group, or the like may be exemplified.
As the “C1-6 alkylcarbonyl group” of X, an acetyl group, a propionyl group, or the like may be exemplified.
As the “C1-6 alkoxycarbonyl group” of X, a methoxycarbonyl group, an ethoxycarbonyl group, a n-propoxycarbonyl group, an i-propoxycarbonyl group, a t-butoxycarbonyl group, or the like may be exemplified.
As a substituent on the “C2-6 alkenyl group”, the “C2-6 alkynyl group”, “C1-6 alkoxy group”, the “C1-6 alkylcarbonyl group”, and the “C1-6 alkoxycarbonyl group” of X, a halogeno group such as a fluoro group a chloro group, a bromo group, or an iodo group; or a cyano group may be preferably exemplified.
As the “C3-8 cycloalkyl group” of X, a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, a cyclohexyl group, or the like may be exemplified.
The “C6-10 aryl group” of X is a group formed by removing one hydrogen on a ring of a monocyclic or polycyclic aromatic hydrocarbon. As the “C6-10 aryl group”, a phenyl group, a naphthyl group, or the like may be exemplified.
The “5- to 6-membered heteroaryl group” of X is a 5- to 6-membered aryl group having an oxygen atom, a nitrogen atom, or a sulfur atom as a heteroatom, and, for example, a 5-membered heteroaryl group such as a pyrrolyl group, a furyl group, a thienyl group, an imidazolyl group, a pyrazolyl group, an oxazolyl group, an isoxazolyl group, a thiazolyl group, an isothiazolyl group, a triazolyl group, an oxadiazolyl group, a thiadiazolyl group, or a tetrazolyl group; or a 6-membered heteroaryl group such as a pyridyl group, a pyrazinyl group, a pyrimidinyl group, a pyridazinyl group, or a triazinyl group may be exemplified.
As a substituent on the “C3-8 cycloalkyl group”, the “C6-10 aryl group”, and the “5- to 6-membered heteroaryl group” of X, a halogeno group such as a fluoro group, a chloro group, a bromo group, or an iodo group; a C1-6 haloalkyl group such as a trifluoromethyl group, a 2,2,2-trifluoroethyl group, or a perfluoroethyl group; or a cyano group may be preferably exemplified.
The “substituted or unsubstituted amino group” of X is a group or the like of “—NRaRb”. In the formula, Ra and Rb each independently represent a hydrogen atom, a C1-6 alkyl group, a C3-8 cycloalkyl group, a formyl group, a C1-6 alkylcarbonyl group, or a C3-8 cycloalkylcarbonyl group.
As the “C1-6 alkyl group” of Ra and Rb, the same as specifically illustrated in R2 may be exemplified.
As the “C1-6 alkylcarbonyl group” and the “C3-8 cycloalkyl group” of Ra and Rb, the same as specifically illustrated in X may be exemplified.
As the “C3-8 cycloalkyl carbonyl group” of Ra and Rb, a cyclopropylcarbonyl group, a cyclobutylcarbonyl group, a cyclopentylcarbonyl group, or the like may be exemplified.
As the “halogeno group” of X, a fluoro group, a chloro group, a bromo group, an iodo group, or the like may be exemplified.
The compound A is preferably a compound of formula (II), formula (III), or formula (IV).
(wherein carbon-carbon double stereo bond in formula (II) represents an E-isomer, a Z-isomer, or a mixture thereof).
A salt of the compound (I) is not particularly limited as long as the salt is agriculturally or horticulturally acceptable. For example, a salt of an inorganic acid such as hydrochloric acid and sulfuric acid; a salt of an organic acid such as acetic acid and lactic acid; a salt of an alkali metal such as lithium, sodium and potassium; a salt of an alkaline earth metal such as calcium and magnesium; a salt of a transition metal such as iron and copper; a salt of an organic base such as triethylamine, tributylamine, pyridine, and hydrazine; an ammonium salt; or the like may be exemplified.
The compound A may be produced based on a well-known production method, for example, a method described in International Publication No. WO2017/104741. In addition, the compound A may be produced based on methods described in International Publication Nos. WO2020/071304 and WO2020/090585. The salt of the compound A may be obtained from the compound A by a well-known technique.
The compound B is an insecticidal or acaricidal active component, and is preferably an active ingredient of an insecticide or an acaricide having a mechanism of action classified according to the IRAC code.
As the insecticide or the acaricide having a mechanism of action classified according to the IRAC code, (1A) an acetylcholine esterase (AChE) inhibitor (carbamate-based), (1B) an acetylcholine esterase (AChE) inhibitor (organophosphorus-based), (2) a GABAergic chloride ion (chlorine ion) channel blocker, (3A) a sodium channel modulator (pyrethroid-based), (3B) a sodium channel modulator (DDTs), (4) a nicotinic acetylcholine receptor (nAChR) competitive modulator, (5) a nicotinic acetylcholine receptor (nAChR) allosteric modulator, (6) a glutamatergic chloride ion (chlorine ion) channel (GluCl) allosteric modulator, (7) a juvenile hormone mimetic agent, (8) other nonspecific (multisite) inhibitors, (9) a chordotonal organ TRPV channel modulator, (10) a mite growth inhibitor, (11) a microorganism-derived insect midgut lining membrane destructive agent, (12) a mitochondrial ATP synthetase inhibitor, (13) an oxidative phosphorylation uncoupler which disrupts proton gradients, (14) a nicotinic acetylcholine receptor (nAChR) channel blocker, (15) a chitin biosynthesis inhibitor, type 0, (16) a chitin biosynthesis inhibitor, type 1, (17) an ecdysis inhibitor, (18) an ecdysis hormone (ecdysone) receptor agonist, (19) an octopamine receptor agonist, (20) a mitochondrial electron transport system complex III inhibitor, (21) a mitochondrial electron transport system complex I inhibitor (METI), (22) a potential-dependent sodium channel blocker, (23) an acetyl-CoA carboxylase inhibitor, (24) a mitochondrial electron transport system complex IV inhibitor, (25) a mitochondrial electron transport system complex III inhibitor, (28) a ryanodine receptor modulator, (29) a chordotonal organ modulator the target site of which is unidentified, (30) a GABAergic chloride ion (chlorine ion) channel allosteric modulator, and (UN) having an unknown or indistinct mechanism of action may be exemplified.
Specific examples of the above-mentioned compound B will be shown hereinafter.
alanycarb, aldicarb, bendiocarb, benfuracarb, butocarboxim, butoxycarboxim, carbaryl, carbofuran, carbosulfan, ethiofencarb, fenobucarb, formetanate, furathiocarb, isoprocarb, methiocarb, methomyl, metolcarb, oxamyl, pirimicarb, propoxur, thiodicarb, thiofanox, triazamate, trimethacarb, XMC, xylylcarb.
acephate, azamethiphos, azinphos-ethyl, azinphos-methyl, cadusafos, chlorethoxyfos, chlorfenvinphos, chlormephos, chlorpyrifos, chlorpyrifos-methyl, coumaphos, cyanophos, demeton-S-methyl, diazinon, dichlorvos/DDVP, dicrotophos, dimethoate, dimethylvinphos, disulfoton, EPN, ethion, ethoprophos, famphur, fenamiphos, fenitrothion, fenthion, fosthiazate, heptenophos, imicyafos, isofenphos, isopropyl O-(methoxyaminothio-phosphoryl)salicylate, isoxathion, malathion, mecarbam, methamidophos, methidathion, mevinphos, monocrotophos, naled, omethoate, oxydemeton-methyl, parathion, parathion-methyl, phenthoate, phorate, phosalone, phosmet, phosphamidon, phoxim, pirimiphos-methyl, profenofos, propetamphos, prothiofos, pyraclofos, pyridaphenthion, quinalphos, sulfotep, tebupirimfos, temephos, terbufos, tetrachlorvinphos, thiometon, triazophos, trichlorfon, and vamidothion.
acrinathrin, allethrin, d-cis-trans-allethrin, d-trans-allethrin, bifenthrin, bioallethrin, bioallethrin S-cyclopentenyl-isomer, bioresmethrin, cycloprothrin, cyfluthrin, β-cyfluthrin (beta-cyfluthrin), cyhalothrin, A-cyhalothrin (lambda-cyhalothrin), γ-cyhalothrin (gamma-cyhalothrin), cypermethrin, α-cypermethrin (alpha-cypermethrin), β-cypermethrin (beta-cypermethrin), θ-cypermethrin (theta-cypermethrin), ζ-cypermethrin (zeta-cypermethrin), cyphenothrin[(1R)-trans-isomers], deltamethrin, empenthrin[(EZ)-(1R)-isomers], esfenvalerate, etofenprox, fenpropathrin, fenvalerate, flucythrinate, flumethrin, z-fluvalinate (tau-fluvalinate), halfenprox, imiprothrin, kadethrin, permethrin, phenothrin[(1R)-trans-isomer], prallethrin, pyrethrins, resmethrin, silafluofen, tefluthrin, tetramethrin, tetramethrin[(1R)-isomers], tralomethrin, transfluthrin, K-bifenthrin (kappa-bifenthrin), chloroprallethrin, heptafluthrin, meperfluthrin, ε-metofluthrin (epsilon-metofluthrin), momfluorothrin, ε-momfluorothrin (epsilon-momfluorothrin), κ-tefluthrin (kappa-tefluthrin), tetramethylfluthrin, and bioethanomethrin.
DDT and methoxychlor.
(4) Nicotinic Acetylcholine Receptor (nAChR) Competitive Modulator
acetamiprid, clothianidin, dinotefuran, imidacloprid, nitenpyram, thiacloprid, thiamethoxam, nicotine, sulfoxaflor, flupyradifurone, triflumezopyrim, dicloromezotiaz, and flupyrimin.
(5) Nicotinic Acetylcholine Receptor (nAChR) Allosteric Modulator
spinetoram and spinosad.
abamectin, emamectin-benzoate, lepimectin, milbemectin, doramectin, eprinomectin, ivermectin, moxidectin, and selamectin.
hydroprene, kinoprene, methoprene, fenoxycarb, and pyriproxifen.
methyl bromide, alkyl halides, chloropicrin, sodium aluminum fluoride, sulfuryl fluoride, borax, boric acid, disodium octaborate, sodium borate, sodium metaborate, tartar emetic, dazomet, and metam.
pymetrozine, pyrifluquinazon, and afidopyropen.
clofentezine, diflovidazin, hexythiazox, and etoxazole.
B. t. subsp. israelensis, B. t. subsp. aizawai, B. t. subsp. kurstaki, B. t. subsp. tenebrionis, proteins contained in B. t. crops (B. t. crop proteins): Cry1Ab, Cry1Ac, Cry1Fa, Cry1A.105, Cry2Ab, Vip3A, mCry3A, Cry3Ab, Cry3Bb, and Cry34Ab1/Cry35Ab1, and Bacillus sphaericus.
diafenthiuron, azocyclotin, cyhexatin, fenbutatin-oxide, propargite, and tetradifon.
(13) Oxidative Phosphorylation Uncoupler which Disrupts Proton Gradients
chlorfenapyr, DNOC (4,6-dinitro-o-cresol), and sulfluramid.
(14) Nicotinic Acetylcholine Receptor (nAChR) Channel Blocker
bensultap, cartap hydrochloride, thiocyclam, and thiosultap-sodium.
bistrifluron, chlorfluazuron, diflubenzuron, flucycloxuron, flufenoxuron, hexaflumuron, lufenuron, novaluron, noviflumuron, teflubenzuron, and triflumuron.
buprofezin.
cyromazine.
chromafenozide, halofenozid, methoxyfenozide, and tebufenozide.
amitraz.
hydramethylnon, acequinocyl, fluacrypyrim, and bifenazate.
fenazaquin, fenpyroximate, pyridaben, pyrimidifen, tebufenpyrad, tolfenpyrad, and rotenone.
indoxacarb and metaflumizone.
spirodiclofen, spiromesifen, spirotetramat, and spiropidion.
aluminum phosphide (Al-phosphide), calcium phosphide (Ca-phosphide), phosphine, zinc phosphide (Zn-phosphide), calcium cyanide (Ca-cyanide) sodium cyanide (Na-cyanide), and potassium cyanide (K-cyanide).
cyenopyrafen, cyflumetofen, and pyflubumide.
chlorantraniliprole, cyantraniliprole, cyclaniliprole, flubendiamide, cyhalodiamide, tetrachlorantraniliprole, and tetraniliprole.
(29) Chordotonal Organ Modulator the Target Site of which is Unidentified
flonicamid.
broflanilide, fluxametamide, isocycloseram, afoxolaner, fluralaner, lotilaner, sarolaner, (UN) azadirachtin, benzoximate, bromopropylate, chinomethionat, dicofol, lime sulfur, mancozeb, pyridalyl, sulfur, acynonapyr, benzpyrimoxan, flometoquin, fluhexafon, oxazosulfyl, and tyclopyrazoflor.
The compound B is preferably acephate, carbofuran, fipronil, acetamiprid, spinetoram, abamectin, pymetrozine, flonicamid, cartap hydrochloride, chlorfenapyr, teflubenzuron, tebufenozide, tolfenpyrad, metaflumizone, cyantraniliprole, or fluxametamide.
The mass ratio of the compound A to the compound B used for the method of the present invention (compound A/compound B) is not particularly limited, but is preferably 200/1 to 1/200, more preferably 100/1 to 1/100, further preferably 50/1 to 1/50, and particularly preferably 10/1 to 1/10.
It is preferable to apply the compound A and the compound B especially at a mass ratio at which a synergistic effect is exhibited. The synergistic effect may be confirmed by the Colby method, which is mentioned below.
Table 1 shows specific examples of the combination of the compound A and the compound B and examples of a preferable mass ratio.
In Table 1, the compound (I) is any of three compounds of formulae (II) to (IV) included in following formula (I).
(wherein carbon-carbon double stereo bond in formula (II) represents an E-isomer, a Z-isomer, or a mixture thereof).
Bacillus
sphaericus
In the method of the present invention, the compound A may be first applied, and the compound B may be subsequently applied. The compound B may be first applied, and the compound A may be subsequently applied. The compound A and the compound B may be applied simultaneously. The compound A and the compound B may be mixed and applied.
In the method of the present invention, the below-mentioned active ingredient contained in other chemicals such as a fungicide, a plant growth regulator, a synergist, a fertilizer, a soil conditioner, and feed for animals (hereinafter referred to as a “compound C”) may be applied with the compound A and the compound B. The order of application is not particularly limited, and the compound A, the compound B, and the compound C may be applied, for example, in the order of the compound A, compound B, and compound C; the compound A, the compound C, and the compound B; the compound C, the compound A, and the compound B; the compound C, the compound B, and the compound A; the compound B, the compound C, and the compound A; or the compound B, the compound A, and the compound C, or the compound A, the compound B, and the compound C may be simultaneously applied.
Although the compound A may be applied as a technical product, it is preferable to apply a composition containing the compound A (chemical composition A). Although the compound B may be applied as a technical product, it is preferable to apply a composition containing the compound B (chemical composition B). The compound C may be applied as a technical product, or a composition containing the compound C (chemical composition C) may be applied.
The chemical composition A, the chemical composition B, and the chemical composition C may be formulated into well-known forms. The chemical composition A, the chemical composition B, and the chemical composition C may be formulated into a form which a common agricultural chemical or an animal drug can take, such as a wettable powder, a granule, a dusting powder, a tablet, an emulsion, a water-soluble powder, a suspension, a granular wettable powder, a flowable, a microcapsule, aerosol, a propellant, a spray, a smoke mist agent, a heat transpiratory preparation, a fumigant, and a bait agent. The chemical composition A, the chemical composition B, and/or the chemical composition C may be a composition in which the compound A, the compound B, and/or the compound C, respectively, is impregnated into a base material such as a porous ceramic plate, a nonwoven fabric, and paper.
The amount of the compound A contained in the chemical composition A, the amount of the compound B contained in the chemical composition B, and the amount of the compound C contained in the chemical composition C are not particularly limited, but are usually 0.1 to 80% by mass with respect to the chemical composition A, the chemical composition B, and the chemical composition C, respectively. The content of the compound A, the content of the compound B, and the content of the compound C in the chemical composition A, the chemical composition B, and the chemical composition C having a dosage form such as an emulsion, a liquid chemical, a wettable powder (for example, a granular wettable powder), an aqueous suspension preparation, or a microemulsion are preferably 1 to 80% by mass and more preferably 10 to 50% by mass with respect to the chemical composition A, the chemical composition B, and the chemical composition C, respectively. The content of the compound A, the content of the compound B, and the content of compound C in the chemical composition A, the chemical composition B, and the chemical composition C having a dosage form such as an oily chemical and a dusting powder are preferably 0.1 to 50% by mass and more preferably 0.1 to 20% by mass with respect to the chemical composition A, the chemical composition B, and the chemical composition C, respectively. The content of the compound A, the content of the compound B, and the content of compound C in the chemical composition A, the chemical composition B, and the chemical composition C having a dosage form such as a granule, a tablet, and a jumbo agent are preferably 0.5 to 50% by mass and more preferably 0.5 to 10% by mass with respect to the chemical composition A, the chemical composition B, and the chemical composition C, respectively.
The chemical composition A, the chemical composition B, and the chemical composition C may contain a liquid medium, a base material, additives, and/or a carrier which are mentioned below besides the compound A, the compound B, and the compound C, respectively.
When the compound A and the compound B (and the compound C if necessary) are simultaneously applied, it is preferable to prepare a composition containing the compound A and the compound B (and the compound C if necessary) (a pest control agent composition of the present invention) and apply the composition.
The total amount of the compound A and the compound B (and the compound C if necessary) contained in the pest control agent composition of the present invention varies a little depending on the dosage form, but is usually 0.1 to 80% by mass with respect to the pest control agent composition. The total content of the compound A and the compound B (and the compound C if necessary) in the pest control agent composition having a dosage form such as an emulsion, a liquid chemical, a wettable powder (for example, a granular wettable powder), an aqueous suspension preparation, and a microemulsion is preferably 1 to 80% by mass and more preferably 10 to 50% by mass with respect to the pest control agent composition. The total content of the compound A and the compound B (and the compound C if necessary) in the pest control agent composition having a dosage form such as an oily chemical and a dusting powder is preferably 0.1 to 50% by mass and more preferably about 0.1 to 20% by mass with respect to the pest control agent composition. The total content of the compound A and the compound B (and the compound C if necessary) in the pest control agent composition having a dosage form such as a granule, a tablet, and a jumbo agent is preferably 0.5 to 50% by mass and more preferably 0.5 to 10% by mass with respect to the pest control agent composition.
In the pest control agent composition of the present invention, the mass ratio of the compound A to the compound B (compound A/compound B) is not particularly limited, but is preferably 200/1 to 1/200, more preferably 100/1 to 1/100, further preferably 50/1 to 1/50, and particularly preferably 10/1 to 1/10. It is preferable to incorporate the compound A and the compound B especially at a mass ratio at which a synergistic effect is exhibited. The synergistic effect may be confirmed by the Colby method, which is mentioned below.
The pest control agent composition of the present invention may contain a liquid medium, a base material, additives, and/or a carrier besides the compound A, the compound B, and the compound C. A liquid medium, a base material, additives, and/or a carrier which can be used for the present invention may be suitably selected from substances known until now depending on the dosage form.
As the additives and the carrier which can be used in a solid preparation, vegetable powder such as soybean flour and flour; mineral fine powder such as diatomite, apatite, gypsum, talc, bentonite, pyrophyllite, and clay; organic and inorganic compounds such as soda benzoate, urea, and mirabilite may be exemplified.
As the liquid medium which can be used in a liquid preparation, a petroleum aromatic hydrocarbon such as kerosene and xylene; cyclohexane; cyclohexanone; dimethylformamide; dimethyl sulfoxide; alcohol; acetone; trichloroethylene; methyl isobutyl ketone; mineral oil; vegetable oil; water; or the like may be exemplified.
As a carrier which can be used at the time of formulation into the propellant, butane gas, LPG, dimethyl ether, carbonic acid gas, or the like may be exemplified.
As the base material which can be used for poison bait, a feed component such as grain powder, vegetable oil, sugar, and crystalline cellulose; an antioxidant such as dibutylhydroxytoluene and nordihydroguaiaretic acid; a preservative such as dehydroacetic acid; an agent for preventing children or pets from eating the poison bait accidentally such as red pepper powder; an insect pest attractant perfume such as cheese perfume and onion perfume; or the like may be exemplified.
A surfactant may be used as an additive. As the surfactant, for example, a nonionic surfactant such as an alkyl phenyl ether to which polyoxyethylene is added, an alkyl ether to which polyoxyethylene is added, a higher fatty acid ester to which polyoxyethylene is added, a sorbitan higher fatty acid ester to which polyoxyethylene is added, and tristyryl phenyl ether to which polyoxyethylene is added; a sulfuric ester salt of an alkyl phenyl ether to which polyoxyethylene is added; an alkylbenzenesulfonic acid salt; a sulfuric ester salt of a higher alcohol; an alkylnaphthalenesulfonic acid salt; a polycarboxylic acid salt; a lignin sulfonic acid salt; a formaldehyde condensate of an alkylnaphthalenesulfonic acid salt; an isobutylene-maleic anhydride copolymer; or the like may be exemplified.
For example, active ingredients of fungicides illustrated by the action mechanism classification of fungicides based on FRAC may be exemplified. The following active ingredients may be specifically exemplified.
(a) RNA polymerase I inhibitors: benalaxyl, benalaxyl-M, furalaxyl, metalaxyl, metalaxyl-M, oxadixyl, clozylacon, and ofurace;
(b) adenosine deaminase inhibitors: bupirimate, dimethirimol, and ethirimol;
(c) DNA/RNA synthesis inhibitors: hymexazol and octhilinone;
(d) DNA topoisomerase II inhibitors: oxolinic acid.
(a) β-tubulin polymerization inhibitors: benomyl, carbendazim, chlorfenazole, fuberidazole, thiabendazole, thiophanate, thiophanate-methyl, diethofencarb, zoxamide, and ethaboxam;
(b) cell division inhibitors: pencycuron;
(c) spectrin-like protein delocalization inhibitors: fluopicolide.
(a) complex I NADH oxidation-reduction enzyme inhibitors: diflumetorim and tolfenpyrad;
(b) complex II succinate dehydrogenase inhibitors: benodanil, flutolanil, mepronil, isofetamid, fluopyram, fenfuram, furmecyclox, carboxin, oxycarboxin, thifluzamide, benzovindiflupyr, bixafen, fluxapyroxad, furametpyr, isopyrazam, penflufen, penthiopyrad, sedaxane, boscalid, pyraziflumid, pydiflumetofen, isoflucypram, and inpyrfluxam;
(c) complex III ubiquinol oxidase Qo inhibitors: azoxystrobin, coumoxystrobin, coumethoxystrobin, enoxastrobin, flufenoxystrobin, picoxystrobin, pyraoxystrobin, pyraclostrobin, pyrametostrobin, triclopyricarb, kresoxim-methyl, trifloxystrobin, dimoxystrobin, fenaminstrobin, metominostrobin, orysastrobin, famoxadone, fluoxastrobin, fenamidone, pyribencarb, mandestrobin, and metyltetraprole;
(d) complex III ubiquinol reductase Qi inhibitors: cyazofamid, amisulbrom, and fenpicoxamid;
(e) oxidative phosphorylation uncoupling agents: binapacryl, meptyldinocap, dinocap, fluazinam, and ferimzone;
(f) oxidative phosphorylation inhibitors (ATP synthetase inhibitors): fentin acetate, fentin chloride, and fentin hydroxide;
(g) ATP production inhibitors: silthiofam;
(h) complex III: Qx (unknown) inhibitor of cytochrome bcl (ubiquinone reductase): ametoctradin.
(a) methionine biosynthesis inhibitors: andoprim, cyprodinil, mepanipyrim, and pyrimethanil;
(b) protein synthesis inhibitors: blasticidin-S, kasugamycin, kasugamycin hydrochloride, streptomycin, and oxytetracycline.
(a) signal transduction inhibitors: quinoxyfen and proquinazid;
(b) MAP/histidine kinase inhibitors in osmotic signal transduction: fenpiclonil, fludioxonil, chlozolinate, iprodione, procymidone, and vinclozolin.
(a) phospholipid biosynthesis, methyltransferase inhibitors: edifenphos, iprobenfos, pyrazophos, and isoprothiolane;
(b) lipid peroxidation agents: biphenyl, chloroneb, dichloran, quintozene, tecnazene, tolclofos-methyl, and etridiazole;
(c) agents that act on cell membranes: iodocarb, propamocarb, propamocarb-hydrochloride, propamocarb-fosetylate, and prothiocarb;
(d) microorganisms that disrupt cell membranes of pathogens: Bacillus subtilis, Bacillus subtilis strain QST713, Bacillus subtilis strain FZB24, Bacillus subtilis strain MBI600, Bacillus subtilis strain D747, and Bacillus amyloliquefaciens;
(e) agents that disrupt cell membranes: Melaleuca alternifolia (tea tree) extract.
(a) C14-demethylation inhibitors in sterol biosynthesis: triforine, pyrifenox, pyrisoxazole, fenarimol, flurprimidol, nuarimol, imazalil, imazalil-sulfate, oxpoconazole fumarate, pefurazoate, prochloraz, triflumizole, viniconazole, azaconazole, bitertanol, bromuconazole, cyproconazole, diclobutrazol, difenoconazole, diniconazole, diniconazole-M, epoxiconazole, etaconazole, fenbuconazole, fluquinconazole, flusilazole, flutriafol, furconazole, furconazole-cis, hexaconazole, imibenconazole, ipconazole, metconazole, myclobutanil, penconazole, propiconazole, fluquinconazole, simeconazole, tebuconazole, tetraconazole, triadimefon, triadimenol, triticonazole, prothioconazole, voriconazole, and mefentrifluconazole;
(b) Δ14 reductase and sterol Δ8→Δ7-isomerase inhibitors in sterol biosynthesis: aldimorph, dodemorph, dodemorph acetate, fenpropimorph, tridemorph, fenpropidin, piperalin, and spiroxamine;
(c) 3-keto reductase inhibitors in C4-demethylation in sterol biosynthesis system: fenhexamid and fenpyrazamine;
(d) squalene epoxidase inhibitors in sterol biosynthesis system: pyributicarb, naftifine, and terbinafine.
(a) trehalase inhibitors: validamycin;
(b) chitin synthetase inhibitors: polyoxins and polyoxorim;
(c) cellulose synthetase inhibitors: dimethomorph, flumorph, pyrimorph, benthiavalicarb-isopropyl, iprovalicarb, valifenalate, and mandipropamid.
(a) melanin biosynthesis reductase inhibitors: fthalide, pyroquilon, and tricyclazole;
(b) melanin biosynthesis anhydrase inhibitors: carpropamid, diclocymet, and fenoxanil;
(c) melanin biosynthesis polyketide synthesis inhibitors: tolprocarb.
(a) agents that act on salicylic acid synthesis pathway: acibenzolar-S-methyl;
(b) others: probenazole, tiadinil, isotianil, dichlobentiazox, laminarin, and Reynoutria sachalinensis extract.
(11) Agents with unknown mode of action: cymoxanil, fosetyl-aluminum, phosphoric acid (phosphate), tecloftalam, triazoxide, flusulfamide, diclomezine, methasulfocarb, cyflufenamid, metrafenone, pyriofenone, dodine, dodine free base, and flutianil.
(12) Agents having multiple active sites: copper (copper salt), bordeaux mixture, copper hydroxide, copper naphthalate, copper oxide, copper oxychloride, copper sulfate, sulfur, sulfur products, calcium polysulfide, ferbam, mancozeb, maneb, mancopper, metiram, polycarbamate, propineb, thiram, zineb, ziram, captan, captafol, folpet, chlorothalonil, dichlofluanid, tolylfluanid, guazatine, iminoctadine triacetate, iminoctadine trialbesilate, anilazine, dithianon, quinomethionate, and fluoroimide.
(13) Other agents: DBEDC, fluorofolpet, guazatine acetate, bis(8-quinolinolato)copper (II), propamidine, chloropicrin, cyprofuram, agrobacterium, bethoxazin, diphenylamine, methyl isothiocyanate (MITC), mildiomycin, capsaicin, cufraneb, cyprosulfamide, dazomet, debacarb, dichlorophen, flumetover, fosetyl-calcium, fosetyl-sodium, irumamycin, natamycin, nitrothal isopropyl, oxamocarb, pyrrolnitrin, tebufloquin, tolnifanide, zarilamide, algophase, amicarthiazol, oxathiapiprolin, metiram zinc, benthiazole, trichlamide, uniconazole, oxyfenthiin, picarbutrazox, dichlobentiazox, quinofumelin, thiuram, ambam, Agrobacterium radiobacter, Coniothyrium minitans, Pseudomonas fluorescens, Pseudomonas rhodesiae, Talaromyces flavus, Trichoderma atroviride, avirulent Erwinia carotovora (Erwinia carotovora subsp. carotovora), Bacillus simplex, Variovorax paradoxus, Lactobacillus plantarum, florylpicoxamid, pyrapropoyne, fluindapyr, aminopyrifen, pyridachlometyl, and ipflufenoquin.
As an active ingredient of a plant growth regulator, for example, the following and the like may be exemplified.
Abscisic acid, kinetin, benzylaminopurine, 1,3-diphenylurea, forchlorfenuron, thidiazuron, chlorfenuron, dihydrozeatin, gibberellin A, gibberellin A4, gibberellin A7, gibberellin A3, 1-methylcyclopropane, N-acetyl aminoethoxyvinyl glycine (also called aviglycine), aminooxyacetate, silver nitrate, cobalt chloride, IAA, 4-CPA, cloprop, 2,4-D, MCPB, indole-3-butyrate, dichlorprop, phenothiol, 1-naphthyl acetamide, ethychlozate, cloxyfonac, maleic acid hydrazide, 2,3,5-triiodobenzoic acid, salicylic acid, methyl salicylate, (−)-jasmonic acid, methyl jasmonate, (+)-strigol, (+)-deoxystrigol, (+)-orobanchol, (+)-sorgolactone, 4-oxo-4-(2-phenylethyl)aminobutyric acid, ethephon, chlormequat, mepiquat chloride, benzyladenine, 5-aminolevulinic acid, and daminozide.
The method for applying the chemical composition A, the chemical composition B, and the chemical composition C is not particularly limited. For example, chemical compositions having dosage forms of a wettable powder, an emulsion, a flowable agent, a water-soluble powder, and a granular wettable powder may be applied by diluting the chemical compositions with water to predetermined concentrations, preparing solutions, suspensions, or emulsions, and sprinkling the dilutions on plants or soil. Chemical compositions having dosage forms of a dusting powder and granules may be applied by scattering the chemical compositions on plants or soil. Chemical compositions having dosage forms such as poison bait and an antimite sheet may be applied by placing the chemical compositions at desired places or hanging the compositions from desired places. In chemical compositions having dosage forms such as aerosol and a smoke mist agent, the chemical compositions may be applied using devices such as a sprayer.
The chemical composition A, the chemical composition B, and the chemical composition C may be applied by a well-known veterinary technique (local, oral, parenteral, or subcutaneous administration). As the veterinary technique, a method for orally administering the compositions to animals with tablets or capsules, or the like or as a mixture with feed; a method for administering the compositions to animals with immersion liquids, suppositories, injections (intramuscular injections, subcutaneous injections, intravenous injections, intraabdominal injections, or the like), or the like; a method for locally administering the compositions by spraying an oily or aqueous liquid chemical, pouring on, spotting on, or the like; a method for locally administering the compositions by kneading an ectoparasite control agent into a resin, molding the kneaded material into suitable shapes such as a collar and an ear tag, equipping animals therewith; or the like is exemplified.
The pest control agent set of the present invention is produced by gathering the chemical composition A and the chemical composition B into one without mixing the chemical composition A and the chemical composition B. The pest control agent set of the present invention may be produced by gathering the composition A, the chemical composition B, and a chemical composition D containing a compound D which is suitable depending on the type of the pest which is an object to be controlled into one without mixing the chemical composition A, the chemical composition B, and the chemical composition D. As the compound D, for example, active ingredients contained in other chemicals such as a fungicide, an insecticide or an acaricide, a nematocide, a plant growth regulator, a synergist, a fertilizer, a soil conditioner, and feed for animals may be exemplified.
The chemical composition D may be formulated into a well-known form. The chemical composition D may be formulated into a form which a common agricultural chemical or an animal drug can take, such as a wettable powder, a granule, a dusting powder, a tablet, an emulsion, a water-soluble powder, a suspension, a granular wettable powder, a flowable, a microcapsule, aerosol, a propellant, a spray, a smoke mist agent, a heat transpiratory preparation, a fumigant, and a bait agent. The chemical composition D may be a composition in which the compound D is impregnated into a base material such as a porous ceramic plate, a nonwoven fabric, and paper.
The amount of the compound D contained in the chemical composition D is not particularly limited, but is usually 0.1 to 80% by mass with respect to the chemical composition D. The content of the compound D in the chemical composition D having a dosage form such as an emulsion, a liquid chemical, a wettable powder (for example, granular wettable powder), an aqueous suspension preparation, and a microemulsion is preferably 1 to 80% by mass and more preferably 10 to 50% by mass with respect to the chemical composition D. The content of the compound D in the chemical composition D having a dosage form such as an oily chemical and a dusting powder is preferably 0.1 to 50% by mass and more preferably 0.1 to 20% by mass with respect to the chemical composition D. The content of the compound D in the chemical composition D having a dosage form such as a granule, a tablet, and a jumbo agent is preferably 0.5 to 50% by mass and more preferably 0.5 to 10% by mass with respect to the chemical composition D. The chemical composition D may contain the above-mentioned liquid medium, base material, additives, and/or carrier besides the compound D.
The pest control agent set of the present invention may be produced by gathering a measuring cup or a measuring dropper, a mixing tank, gloves, a mask, protective goggles, and the like besides the chemical composition A, the chemical composition B, and the chemical composition D, if necessary, into one. The pest control agent set of the present invention may be produced by gathering the pest control agent composition of the present invention and at least one selected from the group consisting of a measuring cup, a measuring dropper, a mixing tank, gloves, a mask, and protective goggles into one.
The form in which the items are gathered is not particularly limited. For example, a set obtained by storing the compositions in bags, boxes, bottles, cans, or the like individually and storing the compositions in one container such as a bag or a box together may be exemplified.
The amount applied to an object is not particularly limited, and may be suitably set depending on the type of the object to be controlled, control time, and the like. For example, the total amount of the compound A and the compound B per 1 are of a field, a paddy field, or the like only has to be suitably selected from the range of 0.1 to 1000 g for application, and is preferably in the range of 1 to 500 g.
As the object of application, a plant such as grain; a vegetable; a root vegetable; a potato; a tree such as a fruit tree, tea, coffee, or cacao; pasture; lawn; a flowering plant; a foliage plant; or a cotton plant may be exemplified. The plant as the application object is not limited depending on whether the plant is a foundation seed, a variety, an improved variety, an agrotype, a mutant, a hybrid body, a genetically modified organism (GMO), or the like. In the method of the present invention, the compositions may be applied to the whole plant or a part of a plant such as a leaf, a stem, a stalk, a flower, a bud, a fruit, a seed, a sprout, a root, a tuber, a tuberous root, a shoot, and a cutting. Seed treatment, foliage spraying, soil application, water surface application, or the like may be performed to control various agricultural insect pests and mites.
As the object of application, a warm-blooded animal such as a pet animal such as a dog and a cat; a pet bird; a domestic animal such as a cow, a horse, a pig, and a sheep; and a fowl or an insect such as a honeybee, a stag beetle, and a beetle which can be a host animal of an ectoparasite may be exemplified.
The pests which may be controlled by the pest controlling method of the present invention are not particularly limited. For example, a sanitary insect pest, a stored grain insect pest, a clothing insect pest, a house insect pest, a parasite, a crop insect pest, or the like may be exemplified. Mites are included in these.
The pest controlling method of the present invention may be performed in all the growth stages of pests which are objects to be controlled. The method of the present invention may be performed, for example, on an egg, a nymph, a larva, a pupa, and an imago.
Examples of the insect pest which is an object to be controlled will be shown below.
(1-a) moths of the family Arctiidae, for example, Hyphantria cunea and Lemyra imparilis;
(1-b) moths of the family Bucculatricidae, for example, Bucculatrix pyrivorella;
(1-c) moths of the family Carposinidae, for example, Carposina sasakii;
(1-d) moths of the family Crambidae, for example, Diaphania indica and Diaphania nitidalis of Diaphania spp.; for example, Ostrinia furnacalis, Ostrinia nubilalis, and Ostrinia scapulalis of Ostrinia spp.; and Chilo suppressalis, Cnaphalocrocis medinalis, Conogethes punctiferalis, Diatraea grandiosella, Glyphodes pyloalis, Hellula undalis, and Parapediasia teterrella of other spp.;
(1-e) moths of the family Gelechiidae, for example, Helcystogramma triannulella, Pectinophora gossypiella, Phthorimaea operculella, and Sitotroga cerealella;
(1-f) moths of the family Geometridae, for example, Ascotis selenaria;
(1-g) moths of the family Gracillariidae, for example, Caloptilia theivora, Phyllocnistis citrella, and Phyllonorycter ringoniella;
(1-h) butterflies of the family Hesperiidae, for example, Parnara guttata;
(1-i) moths of the family Lasiocampidae, for example, Malacosoma neustria;
(1-j) moths of the family Lymantriidae, for example, Lymantria dispar and Lymantria monacha of Lymantria spp.; and Euproctis pseudoconspersa and Orgyia thyellina of other spp.;
(1-k) moths of the family Lyonetiidae, for example, Lyonetia clerkella and Lyonetia prunifoliella malinella of Lyonetia spp.;
(1-l) moths of the family Noctuidae, for example, Spodoptera depravata, Spodoptera eridania, Spodoptera exigua, Spodoptera frugiperda, Spodoptera littoralis, and Spodoptera litura of Spodoptera spp.;
for example, Autographa gamma and Autographa nigrisigna of Autographa spp.;
for example, Agrotis ipsilon and Agrotis segetum of Agrotis spp.;
for example, Helicoverpa armigera, Helicoverpa assulta, and Helicoverpa zea of Helicoverpa spp.;
for example, Heliothis armigera and Heliothis virescens of Heliothis spp.; and
Aedia leucomelas, Ctenoplusia agnata, Eudocima tyrannus, Mamestra brassicae, Mythimna separata, Naranga aenescens, Panolis japonica, Peridroma saucia, Pseudoplusia includens, and Trichoplusia ni of other spp.;
(1-m) moths of the family Nolidae, for example, Earias insulana;
(1-n) butterflies of the family Pieridae, for example, Pieris brassicae and Pieris rapae crucivora of Pieris spp.;
(1-o) moths of the family Plutellidae, for example, Acrolepiopsis sapporensis and Acrolepiopsis suzukiella of Acrolepiopsis spp.; and
Plutella xylostella of other spp.;
(1-p) moths of the family Pyralidae, for example, Cadra cautella, Elasmopalpus lignosellus, Etiella zinckenella, and Galleria mellonella;
(1-q) moths of the family Sphingidae, for example, Manduca quinquemaculata and Manduca sexta of Manduca spp.;
(1-r) moths of the family Stathmopodidae, for example, Stathmopoda masinissa;
(1-s) moths of the family Tineidae, for example, Tinea translucens;
(1-t) moths of the family Tortricidae, for example, Adoxophyes honmai and Adoxophyes orana of Adoxophyes spp.; for example, Archips breviplicanus and Archips fuscocupreanus of Archips spp.; and
Choristoneura fumiferana, Cydia pomonella, Eupoecilia ambiguella, Grapholitha molesta, Homona magnanima, Leguminivora glycinivorella, Lobesia botrana, Matsumuraeses phaseoli, Pandemis heparana, and Sparganothis pilleriana of other spp.;
(1-u) moths of the family Yponomeutidae, for example, Argyresthia conjugella.
(2-a) insect pests of the family Phlaeothripidae, for example, Ponticulothrips diospyrosi;
(2-b) insect pests of the family Thripidae, for example, Frankliniella intonsa and Frankliniella occidentalis of Frankliniella spp.;
for example, Thrips palmi and Thrips tabaci of Thrips spp.; and
Heliothrips haemorrhoidalis and Scirtothrips dorsalis of other spp.
(3-A) the suborder Archaeorrhyncha
(3-A-a) insect pests of the family Delphacidae, for example, Laodelphax striatella, Nilaparvata lugens, Perkinsiella saccharicida, and Sogatella furcifera.
(3-B) the suborder Clypeorrhyncha
(3-B-a) insect pests of the family Cicadellidae, for example, Empoasca fabae, Empoasca nipponica, Empoasca onukii, and Empoasca sakaii of Empoasca spp.; and
Arboridia apicalis, Balclutha saltuella, Epiacanthus stramineus, Macrosteles striifrons, and Nephotettix cinctinceps of other spp.
(3-C) the suborder Heteroptera
(3-C-a) insect pests of the family Alydidae, for example, Riptortus clavatus;
(3-C-b) insect pests of the family Coreidae, for example, Cletus punctiger and Leptocorisa chinensis;
(3-C-c) insect pests of the family Lygaeidae, for example, Blissus leucopterus, Cavelerius saccharivorus, and Togo hemipterus;
(3-C-d) insect pests of the family Miridae, for example, Halticus insularis, Lygus lineolaris, Psuedatomoscelis seriatus, Stenodema sibiricum, Stenotus rubrovittatus, and Trigonotylus caelestialium;
(3-C-e) insect pests of the family Pentatomidae, for example, Nezara antennata and Nezara viridula of Nezara spp.; for example, Eysarcoris aeneus, Eysarcoris lewisi, and
Eysarcoris ventralis of Eysarcoris spp.; and Dolycoris baccarum, Eurydema rugosum, Glaucias subpunctatus, Halyomorpha halys, Piezodorus hybneri, Plautia crossota, and Scotinophora lurida of other spp.;
(3-C-f) insect pests of the family Pyrrhocoridae, for example, Dysdercus cingulatus;
(3-C-g) insect pests of the family Rhopalidae, for example, Rhopalus msculatus;
(3-C-h) insect pests of the family Scutelleridae, for example, Eurygaster integriceps;
(3-C-i) insect pests of the family Tingidae, for example, Stephanitis nashi.
(3-D) the suborder Sternorrhyncha
(3-D-a) insect pests of the family Adelgidae, for example, Adelges laricis;
(3-D-b) insect pests of the family Aleyrodidae, for example, Bemisia argentifolii and Bemisia tabaci of Bemisia spp.; and
Aleurocanthus spiniferus, Dialeurodes citri, and Trialeurodes vaporariorum of other spp.;
(3-D-c) insect pests of the family Aphididae, for example, Aphis craccivora, Aphis fabae, Aphis forbesi, Aphis gossypii, Aphis pomi, Aphis sambuci, and Aphis spiraecola of Aphis spp.;
for example, Rhopalosiphum maidis and Rhopalosiphum padi of Rhopalosiphum spp.;
for example, Dysaphis plantaginea and Dysaphis radicola of Dysaphis spp.;
for example, Macrosiphum avenae and Macrosiphum euphorbiae of Macrosiphum spp.;
for example, Myzus cerasi, Myzus persicae, and Myzus varians of Myzus spp.; and
Acyrthosiphon pisum, Aulacorthum solani, Brachycaudus helichrysi, Brevicoryne brassicae, Chaetosiphon fragaefolii, Hyalopterus pruni, Hyperomyzus lactucae, Lipaphis erysimi, Megoura viciae, Metopolophium dirhodum, Nasonovia ribis-nigri, Phorodon humuli, Schizaphis graminum, Sitobion avenae, and Toxoptera aurantii of other spp.;
(3-D-d) insect pests of the family Coccidae, for example, Ceroplastes ceriferus and Ceroplastes rubens of Ceroplastes spp.;
(3-D-e) insect pests of the family Diaspididae, Pseudaulacaspis pentagona and Pseudaulacaspis prunicola of Pseudaulacaspis spp.;
for example, Unaspis euonymi and Unaspis yanonensis of Unaspis spp.; and
Aonidiella aurantii, Comstockaspis perniciosa, Fiorinia theae, and Pseudaonidia paeoniae of other spp.;
(3-D-f) insect pests of the family Margarodidae, for example, Drosicha corpulenta and Icerya purchasi;
(3-D-g) insect pests of the family Phylloxeridae, for example, Viteus vitifolii;
(3-D-h) insect pests of the family Pseudococcidae, for example, Planococcus citri and Planococcus kuraunhiae of Planococcus spp.; and
Phenacoccus solani and Pseudococcus comstocki of other spp.;
(3-D-i) insect pests of the family Psyllidae, for example, Psylla mali and Psylla pyrisuga of Psylla spp.; and Diaphorina citri of other spp.
(4-a) insect pests of the family Anobiidae, for example, Lasioderma serricorne;
(4-b) insect pests of the family Attelabidae, for example, Byctiscus betulae and Rhynchites heros;
(4-c) insect pests of the family Bostrichidae, for example, Lyctus brunneus;
(4-d) insect pests of the family Brentidae, for example, Cylas formicarius;
(4-e) insect pests of the family Buprestidae, for example, Agrilus sinuatus;
(4-f) insect pests of the family Cerambycidae, for example, Anoplophora malasiaca, Monochamus alternatus, Psacothea hilaris, and Xylotrechus pyrrhoderus;
(4-g) insect pests of the family Chrysomelidae, for example, Bruchus pisorum and Bruchus rufimanus of Bruchus spp.; for example, Diabrotica barberi, Diabrotica undecimpunctata, and Diabrotica virgifera of Diabrotica spp.;
for example, Phyllotreta nemorum and Phyllotreta striolata of Phyllotreta spp.; and
Aulacophora femoralis, Callosobruchus chinensis, Cassida nebulosa, Chaetocnema concinna, Leptinotarsa decemlineata, Oulema oryzae, and Psylliodes angusticollis of other spp.;
(4-h) insect pests of the family Coccinellidae, for example, Epilachna varivestis and Epilachna vigintioctopunctata of Epilachna spp.;
(4-i) insect pests of the family Curculionidae, for example, Anthonomus grandis and Anthonomus pomorum of Anthonomus spp.; for example, Sitophilus granarius and Sitophilus zeamais of Sitophilus spp.; and Echinocnemus squameus, Euscepes postfasciatus, Hylobius abietis, Hypera postica, Lissohoptrus oryzophilus, Otiorhynchus sulcatus, Sitona lineatus, and Sphenophorus venatus of other spp.;
(4-j) insect pests of the family Elateridae, for example, Melanotus fortnumi and Melanotus tamsuyensis of Melanotus spp.;
(4-k) insect pests of the family Nitidulidae, for example, Epuraea domina;
(4-l) insect pests of the family Scarabaeidae, for example, Anomala cuprea and Anomala rufocuprea of Anomala spp.; and Cetonia aurata, Gametis jucunda, Heptophylla picea, Melolontha melolontha, and Popillia japonica of other spp.;
(4-m) insect pests of the family Scolytidae, for example, Ips typographus;
(4-n) insect pests of the family Staphylinidae, for example, Paederus fuscipes;
(4-o) insect pests of the family Tenebrionidae, for example, Tenebrio molitor and Tribolium castaneum;
(4-p) insect pests of the family Trogossitidae, for example, Tenebroides mauritanicus.
(5-A) the suborder Brachycera
(5-A-a) insect pests of the family Agromyzidae, for example, Liriomyza bryoniae, Liriomyza chinensis, Liriomyza sativae, and Liriomyza trifolii of Liriomyza spp.; and
Chromatomyia horticola and Agromyza oryzae of other spp.;
(5-A-b) insect pests of the family Anthomyiidae, for example, Delia platura and Delia radicum of Delia spp.; and Pegomya cunicularia of other spp.;
(5-A-c) insect pests of the family Drosophilidae, for example, Drosophila melanogaster and Drosophila suzukii of Drosophila spp.;
(5-A-d) insect pests of the family Ephydridae, for example, Hydrellia griseola;
(5-A-e) insect pests of the family Psilidae, for example, Psila rosae;
(5-A-f) insect pests of the family Tephritidae, for example, Bactrocera cucurbitae and Bactrocera dorsalis of Bactrocera spp.;
for example, Rhagoletis cerasi and Rhagoletis pomonella of Rhagoletis spp.; and
Ceratitis capitata and Dacus oleae of other spp.
(5-B) the suborder Nematocera
(5-B-a) insect pests of the family Cecidomyiidae, for example, Asphondylia yushimai, Contarinia sorghicola, Mayetiola destructor, and Sitodiplosis mosellana.
(6-a) insect pests of the family Acrididae, for example, Schistocerca americana and Schistocerca gregaria of Schistocerca spp.; and
Chortoicetes terminifera, Dociostaurus maroccanus, Locusta migratoria, Locustana pardalina, Nomadacris septemfasciata, and Oxyayezoensis of other spp.;
(6-b) insect pests of the family Gryllidae, for example, Acheta domestica and Teleogryllus emma;
(6-c) insect pests of the family Gryllotalpidae, for example, Gryllotalpa orientalis;
(6-d) insect pests of the family Tettigoniidae, for example, Tachycines asynamorus.
(7-A) Acaridida of the order Astigmata
(7-A-a) mites of the family Acaridae, for example, Rhizoglyphus echinopus and Rhizoglyphus robini of Rhizoglyphus spp.;
for example, Tyrophagus neiswanderi, Tyrophagus perniciosus, Tyrophagus putrescentiae, and Tyrophagus similis of Tyrophagus spp.; and
Acarus siro, Aleuroglyphus ovatus, and Mycetoglyphus fungivorus of other spp.;
(7-B) Actinedida of the order Prostigmata
(7-B-a) mites of the family Tetranychidae, for example, Bryobia praetiosa and Bryobia rubrioculus of Bryobia spp.;
for example, Eotetranychus asiaticus, Eotetranychus boreus, Eotetranychus celtis, Eotetranychus geniculatus, Eotetranychus kankitus, Eotetranychus pruni, Eotetranychus shii, Eotetranychus smithi, Eotetranychus suginamensis, and Eotetranychus uncatus of Eotetranychus spp.;
for example, Oligonychus hondoensis, Oligonychus ilicis, Oligonychus karamatus, Oligonychus mangiferus, Oligonychus orthius, Oligonychus perseae, Oligonychus pustulosus, Oligonychus shinkajii, and Oligonychus ununguis of Oligonychus spp.;
for example, Panonychus citri, Panonychus mori, and Panonychus ulmi of Panonychus spp.;
for example, Tetranychus cinnabarinus, Tetranychus evansi, Tetranychus kanzawai, Tetranychus ludeni, Tetranychus quercivorus, Tetranychus phaselus, Tetranychus urticae, and Tetranychus viennensis of Tetranychus spp.;
for example, Aponychus corpuzae and Aponychus firmianae of Aponychus spp.;
for example, Sasanychus akitanus and Sasanychus pusillus of Sasanychus spp.;
for example, Schizotetranychus celarius, Schizotetranychus longus, Schizotetranychus miscanthi, Schizotetranychus recki, and Schizotetranychus schizopus of Schizotetranychus spp.; and
Tetranychina harti, Tuckerella pavoniformis, and Yezonychus sapporensis of other spp.;
(7-B-b) mites of the family Tenuipalpidae, for example, Brevipalpus lewisi, Brevipalpus obovatus, Brevipalpus phoenicis, Brevipalpus russulus, and Brevipalpus californicus of Brevipalpus spp.;
for example, Tenuipalpus pacificus and Tenuipalpus zhizhilashviliae of Tenuipalpus spp.; and
Dolichotetranychus floridanus of other spp.;
(7-B-c) mites of the family Eriophyidae, for example, Aceria diospyri, Aceria ficus, Aceria japonica, Aceria kuko, Aceria paradianthi, Aceria tiyingi, Aceria tulipae, and Aceria zoysiea of Aceria spp.;
for example, Eriophyes chibaensis and Eriophyes emarginatae of Eriophyes spp.;
for example, Aculops lycopersici and Aculops pelekassi of Aculops spp.;
for example, Aculus fockeui and Aculus schlechtendali of Aculus spp.; and
Acaphylla theavagrans, Calacarus carinatus, Colomerus vitis, Calepitrimerus vitis, Epitrimerus pyri, Paraphytoptus kikus, Paracalacarus podocarpi, and Phyllocotruta citri of other spp.;
(7-B-d) mites of the family Trasonemidae, for example, Tarsonemus bilobatus and Tarsonemus waitei of Tarsonemus spp.; and
Phytonemus pallidus and Polyphagotarsonemus latus of other spp.;
(7-B-e) mites of the family Penthaleidae, for example, Penthaleus erythrocephalus and Penthaleus major of Penthaleus spp.
Ectoparasites which are objects to be controlled include ectoparasites which parasitize the backs, armpits, lower abdomens, inner thighs, or the like of host animals and live by obtaining nutrients such as blood or dandruff from the animals and ectoparasites which come flying to the backs, rumps, or the like of host animals and live by obtaining nutrients such as blood or dandruff from the animals. As the ectoparasite, for example, mites, lice, fleas, a mosquito, a stable fly, a flesh fly, or the like may be exemplified. Specific examples of the ectoparasite will be shown below.
mites of the family Dermanyssidae, mites of the family Macronyssidae, mites of the family Laelapidae, mites of the family Varroidae, mites of the family Argasidae, mites of the family Ixodidae, mites of the family Psoroptidae, mites of the family Sarcoptidae, mites of the family Knemidokoptidae, mites of the family Demodixidae, and mites of the family Trombiculidae.
lice of the family Haematopinidae, lice of the family Linognathidae, bird lice of the family Menoponidae, bird lice of the family Philopteridae, and bird lice of the family Trichodectidae.
fleas of the family Pulicidae, for example, Ctenocephalides canis and Ctenocephalides felis of Ctenocephalides spp.; fleas of the family Tungidae, fleas of the family Ceratophyllidae, and fleas of the family Leptopsyllidae.
insects of the family Cimicidae, insects of the family Reduviidae, and insects of the family Triatominae.
mosquitos of the family Culicidae, black flies of the family Simuliidae, biting midges of the family Ceratopogonidae, horseflies of the family Tabanidae, flies of the family Muscidae, tsetse flies of the family Glossinidae, flesh flies of the family Sarcophagidae, flies of the family Hippoboscidae, flies of the family Calliphoridae, and flies of the family Oestridae.
The present invention is additionally excellent in control effect on insect pests that have a stinger or venom and harm humans and animals, insect pests that mediate various pathogens or disease-causing microorganisms, or insect pests that cause discomfort to humans (toxic pests, sanitary insect pests, obnoxious pests, and the like).
Specific examples thereof will be shown below.
bees of the family Argidae, bees of the family Cynipidae, bees of the family Diprionidae, ants of the family Formicidae, bees of the family Mutillidae, and bees of the family Vespidae.
Blattodea, termites, Araneae, centipedes, millipedes, crustacea, and Cimex lectularius.
Although some Formulation Examples of the chemical composition will be shown, additives and the added ratio should not be limited to these Examples, and may be varied widely. “Part” in the Formulation Examples represents “part by mass”. The compound A is used as an active ingredient in the chemical composition A. The compound B is used as an active ingredient in the chemical composition B. The compound C is used as an active ingredient in the chemical composition C. The compound D is used as an active ingredient in the chemical composition D. The compound A and the compound B, and the compound C if needed are used as an active ingredient in the pest control agent composition of the present invention.
Formulation Examples for agriculture and horticulture will be shown.
The above were uniformly mixed and fine pulverized to obtain a wettable powder containing 40% of the active ingredient.
The above were mixed and dissolved to obtain an emulsion containing 30% of the active ingredient.
The above were mixed to obtain a flowable agent containing 30% of the active ingredient.
The above were mixed to obtain a flowable agent containing 20% of the active ingredient.
Formulation Examples for the prevention of epidemics and for animals will be shown.
The active ingredient is dissolved in an organic solvent and the solution is sprayed on the carrier, the solvent is then evaporated at reduced pressure. This type of granules may be mixed with feed for animals.
After preparation, the mixture is sterile filtered with a sterilization filter.
The compound of formula (I) may be applied with the above-mentioned fungicide. Tables 2 shows specific examples of the combination of the compound of formula (I) and the fungicide and examples of the preferable mass ratio.
In Table 2, the compound (I) is any of the compounds of formulae (II) to (IV) included in the compound of the following formula (I) in the same way as in Table 1.
Bacillus subtilis strain QST713
Bacillus subtilis strain FZB24
Bacillus subtilis strain MBI600
Bacillus subtilis strain D747
Bacillus mycoides isolate J
Then, an effect when the pest controlling method of the present invention was implemented will be shown by the following Test Examples. The compound B used in the Test Examples may be obtained by a well-known production method or by extraction using liquid separation operation from a commercially available product.
Test for Confirming Effect on Plutella xylostella
A flowable agent containing the compound A was diluted with water containing RABIDEN® 3S diluted 5000 times to prepare chemical solutions A containing the compound A at twice concentrations described in Table 3.
A preparation containing the compound B or a flowable agent containing the compound B was diluted with water containing RABIDEN 3S diluted 5000 times to prepare chemical solutions B containing the compound B at twice concentrations described in Table 3, respectively.
Cabbage leaves were immersed in a mixed solution obtained by mixing the chemical solution A and the chemical solution B in an equivalent amount for 30 seconds, and these cabbage leaves were placed in a petri dish, and five second-instar Plutella xylostella larvae were released (AB mixture application plot).
The chemical solution A and the chemical solution B were twice diluted with the water containing RABIDEN 3S diluted 5000 times to obtain a chemical solution A′ and a chemical solution B′.
Cabbage leaves were immersed in the chemical solution A′ for 30 seconds, and these cabbage leaves were placed in another petri dish, and five second-instar Plutella xylostella larvae were released (A single application plot). Cabbage leaves were immersed in the chemical solution B′ for 30 seconds, and these cabbage leaves were placed in another petri dish, and five second-instar Plutella xylostella larvae were released (B single application plot).
Then, these petri dishes were placed in a thermostatic chamber at a temperature of 25° C. and a humidity of 60%. Three days after the larva release, viability determination was performed, and the insecticidal rate was calculated by the following equation. The test was repeated twice.
Insecticidal rate (%)=(the number of dead insects/the number of tested insects)×100
To show the degree of a synergistic effect, the “effectiveness expectation” was calculated based on the Colby method. When the effectiveness is higher than the “effectiveness expectation”, it is determined that there is a synergistic effect.
Expectation of insecticidal rate (%) (E)=X+Y−XY/100
X: measurement of insecticidal rate in B single application plot (%)
Y: measurement of insecticidal rate in A single application plot (%)
Table 3 shows the test results.
In Table 3, a compound (II) is the compound of the following formula (II).
(wherein carbon-carbon double stereo bond in formula (II) represents an E-isomer, a Z-isomer, or a mixture thereof).
In Table 3, a compound (III) is the compound of the following formula (III).
In Table 3, a compound (IV) is the compound of the following formula (IV).
Test for confirming effect on Aphis gossypii A flowable agent containing the compound A was diluted with water containing RABIDEN 3S diluted 5000 times to prepare chemical solutions A containing the compound A at twice concentrations described in Table 4.
A preparation containing the compound B or a flowable agent containing the compound B was diluted with water containing RABIDEN 3S diluted 5000 times to prepare chemical solutions B containing the compound B at twice concentrations described in Table 4.
First, 9-cm pots were sown with cucumbers. Aphis gossypii female imagoes were released on the cucumbers 10 days after the sprouting. The borne first-instar larvae were left, and the female imagoes were removed on the next day. A mixed solution obtained by mixing the chemical solution A and the chemical solution B in an equivalent amount was sprinkled on the cucumbers (AB mixture application plot).
The chemical solution A and the chemical solution B were twice diluted with the water containing RABIDEN 3S diluted 5000 times to obtain a chemical solution A′ and a chemical solution B′.
The chemical solution A′ was sprinkled on the cucumbers sown with the first-instar larvae by the same method as in the AB mixture application plot (A single application plot). The chemical solution B′ was sprinkled on the cucumbers sown with the first-instar larvae by the same method as in the AB mixture application plot (B single application plot).
Then, the cucumbers sprinkled with the chemical solutions were placed in a thermostatic chamber at a temperature of 25° C. and a humidity of 60%, the viability of the Aphis gossypii was inspected after 6 days, and the insecticidal rate was calculated by the following equation. The test was repeated twice.
Insecticidal rate (%)=(the number of dead insects/the number of tested insects)×100
To show the degree of a synergistic effect, the “effectiveness expectation” was calculated based on the Colby method. When the effectiveness is higher than the “effectiveness expectation”, it is determined that there is a synergistic effect.
Expectation of insecticidal rate (%) (E)=X+Y−XY/100
X: measurement of insecticidal rate in B single application plot (%)
Y: measurement of insecticidal rate in A single application plot (%)
Table 4 shows the test results.
In Table 4, compounds (II) to (IV) are the same as the compounds (II) to (IV) in Table 3.
Test for Confirming Effect on Phyllotreta striolata
A flowable agent containing the compound A was diluted with water containing RABIDEN 3S diluted 5000 times to prepare chemical solutions A containing the compound A at twice concentrations described in Table 5.
A preparation containing the compound B or a flowable agent containing the compound B was diluted with water containing RABIDEN 3S diluted 5000 times to prepare chemical solutions B containing the compound B at twice concentrations described in Table 5.
A mixed solution obtained by mixing the chemical solution A and the chemical solution B in an equivalent amount was sprinkled on bok choy seedlings (at the seventh true leaf stage) planted in 9-cm pots. After air dry, these bok choy seedlings were placed in plastic cups, and ten Phyllotreta striolata imagoes were released (AB mixture application plot).
The chemical solution A and the chemical solution B were twice diluted with the water containing RABIDEN 3S diluted 5000 times to obtain a chemical solution A′ and a chemical solution B′.
The chemical solution A′ was sprinkled on bok choy seedlings (at the seventh true leaf stage) planted in 9-cm pots. After air dry, these bok choy seedlings were placed in plastic cups, and ten Phyllotreta striolata imagoes were released (A single application plot). The chemical solution B′ was sprinkled on bok choy seedlings (at the seventh true leaf stage) planted in 9-cm pots. After air dry, these bok choy seedlings were placed in plastic cups, and ten Phyllotreta striolata imagoes were released (B single application plot).
Then, the bok choy seedlings sprinkled with the chemical solutions were placed in a thermostatic chamber at a temperature of 25° C. and a humidity of 60%, viability determination was performed 6 days after the insect release, and the insecticidal rate was calculated by the following equation. The test was repeated twice.
Insecticidal rate (%)=(the number of the dead insects/the number of tested insects)×100
To show the degree of a synergistic effect, the “effectiveness expectation” was calculated based on the Colby method. When the effectiveness is higher than the “effectiveness expectation”, it is determined that there is a synergistic effect.
Expectation of insecticidal rate (%) (E)=X+Y−XY/100
X: measurement of insecticidal rate in B single application plot (%)
Y: measurement of insecticidal rate in A single application plot (%)
Table 5 shows the test results.
In Table 5, compounds (II) to (IV) are the same as the compounds (II) to (IV) in Table 3.
As shown in the Test Example, a synergistic effect is exhibited by applying the compound A with the compound B to an object. The pest controlling method of the present invention and the pest control agent composition of the present invention enable controlling pests such as insects and mites more safely at a lower dosage.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2020-067049 | Apr 2020 | JP | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP2021/012299 | 3/24/2021 | WO |
