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US20010056111A1 - Synergistic pesticidal composition of pyrethroid and N-phenyl-pyrazole - Google Patents

Synergistic pesticidal composition of pyrethroid and N-phenyl-pyrazole Download PDF

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Publication number
US20010056111A1
US20010056111A1 US09/826,817 US82681701A US2001056111A1 US 20010056111 A1 US20010056111 A1 US 20010056111A1 US 82681701 A US82681701 A US 82681701A US 2001056111 A1 US2001056111 A1 US 2001056111A1
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composition
weight
cyano
amino
dichloro
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US6432998B2 (en
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Hiroshi Kodama
Yasuhiro Wada
Rikio Yamaguchi
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BASF Agro BV Arnhem NL Zweigniederlassung Freienbach
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    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
    • A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom

Definitions

  • the present invention relates to a termite control composition for soil treatment containing a 3-cyano-1-(substituted phenyl)-pyrazole derivative and a pyrethroid compound as effective ingredients.
  • the pyrazole derivatives as effective ingredients of the termite control composition of the present invention are known compounds described in European patent publication 0295117 as well as in the international patent publications WO 93/06089 and 94/21606, which disclose that the compounds have a pesticidal effect on arthropods, vegetable nematodes, protozoan pests, and other pests. Many other pesticidal compounds can be used in combination with N-phenyl pyrazole derivatives. Pyrethroid compounds such as cyfluthrin, cypermethrin, deltamethrin, fenpropathrin, fenvalerate, and permethrin are recited among many possibilities without any reference to any specific effect in any conditions.
  • a first object of the instant invention is to provide synergistic compositions of 3-cyano-1-(substituted phenyl)-pyrazole derivatives.
  • Another object of the instant invention is to provide specific compositions which have an improved activity against pests, especially against insects.
  • Another object of the instant invention is to provide specific compositions which have an improved activity against termites.
  • a further object of the instant invention is to provide a novel termite control composition (preferably for soil treatment) which has a strong termite control effect as well as the ability to prevent termites from passing through the pesticidally treated layer.
  • compositions of the present invention comprise, as effective ingredients, a pyrethroid compound and a compound of formula (I)
  • R 1 is halogen, lower haloalkyl, lower haloalkoxy or SF 5 (lower being an integer from 1 to 4, preferably one),
  • R 2 is halogen, the various R 2 being identical or different,
  • R 4 is halogen, lower alkyl or haloalkyl
  • R 5 is halogen, lower alkyl or amino
  • Halo before the name of a radical means that this radical may be substituted by one or more halogen atoms.
  • a preferred compound of formula (I) is 5-amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-trifluoromethylsulphinylpyrazole (Compound A).
  • compositions of the invention comprise a synergistic amount of active ingredients.
  • Pyrethroid compounds which can be used in the present invention include all kinds of pyrethroids, especially pyrethroids other than cyfluthrin, cypermethrin, deltamethrin, fenpropathrin, fenvalerate, and permethrin.
  • pyrethroids which can be used in the invention are compounds selected from a group consisting of the following pyrethroid compounds, even though not limited to these pyrethroid compounds:
  • compositions of the invention are compositions wherein the ratio by weight of the pyrethroid compound to the compound of formula (I) is between 0.1 and 10, preferably between 0.5 and 5.
  • compositions of the invention are compositions, which are most useful for termite control, preferably with soil treatment.
  • the invention is also directed to a method of control of pests, especially of termites, which comprises applying an effective amount of the compositions according to the invention, as herein described.
  • the liquid compositions of the invention generally comprises 0.001 to 50% (all percentages are by weight in the instant specification, unless specifically indicated otherwise) of compound of formula (I), preferably from 0.005 to 10%.
  • the concentrated compositions which are those used for storage and commercial purposes comprise generally from 1 to 20% of this compound of formula (I).
  • the quantity of the effective ingredient may be within a range between 0.01 g and 7 g, preferably between 0.1 g and 5 g per square meter.
  • the method of control of pests, especially of termites, according to the invention is impregnating the wood by means of a composition as hereinbefore defined.
  • compositions of the invention to animals is generally made at 0.1 to 100 mg, preferably at 2 to 20 mg per kilogram of body weight of the animal.
  • the termite control composition of the present invention has a high significant termite control effect on house damaging termites, for example Coptotermes formosanusus (Shiraki), Reticulitermes speratus (Kolbe), Odontotermes formosanus (Shiraki), and Cryptotermes domesticus (Haviland), as well as the ability to prevent termites from passing through pesticidally treated materials.
  • the composition may be applied to or adsorbed in building materials, furniture, leather, fabrics, vinyl coated articles, electric wires, or cables.
  • the composition may be dissolved, suspended, mixed, adsorbed, or adhered on an appropriate solid and/or liquid vehicle (this word is used as a synonym of “carrier”) according to the formulation generally used, together with auxiliary agents if required.
  • This composition may be formulated into forms suited to the object of use, for example, an oil solution, emulsion, water solution, powder, granules, wettable powder, aerosol, smoking agent, or flowable agent.
  • Solid vehicles used in the present invention include, for example, clays such as kaolin, bentonite, and acid clay; talc materials such as talc and pyrophylite; siliceous materials such as diatomaceous earth, silica sand, mica, synthetic silicates, and high dispersion synthetic silicates; and inorganic mineral powders such as pumice and sand.
  • clays such as kaolin, bentonite, and acid clay
  • talc materials such as talc and pyrophylite
  • siliceous materials such as diatomaceous earth, silica sand, mica, synthetic silicates, and high dispersion synthetic silicates
  • inorganic mineral powders such as pumice and sand.
  • Liquid vehicles include, for example, alcohols such as methanol, ethanol, and ethylene glycol; ketones such as acetone, methyl ethyl ketone, and cyclohexanone; ethers such as ethyl ether, dioxane, tetrahydrofuran, and cellosolve; aliphatic hydrocarbons such as kerosene; aromatic hydrocarbons such as benzene, toluene, xylene, solvent naphtha, cyclohexane, and methyl naphthalene; and halogenated hydrocarbons such as chloroform, carbon tetrachloride, and chlorobenzene. These solid or liquid vehicles may be used alone or in combination.
  • Auxiliary agents used in the present invention include propellants, surface-active agents, fixing agents, dispersing agents, thickening agents, and bonding agents.
  • Propellants include, for example, liquefied petroleum gas, dimethyl ether, and fluorocarbons.
  • Surface-active agents include, for example, polyoxyethylene alkylaryl ether, polyoxyethylene sorbitane monolaurate, alkylallyl sorbitane monolaurate, alkylbenzene sulfonate, alkylnaphthalene sulfonate, lignin sulfonate, and sulfuric acid ester salts of higher alcohols. These surface-active agents may be used alone or in combination.
  • Fixing agents, dispersing agents, thickening agents, and bonding agents include, for example, casein, gelatine, starch, carboxymethyl cellulose, alginic acid, agar, polyvinyl alcohol, polyethylene glycol, polysodium acrylate, gum arabic, and xanthane gum, which may be used if required.
  • the termite control composition for soil treatment of the present invention may contain co-operating agents such as sinepyrin 500, piperonyl butoxide, and S-421.
  • the termite control composition of the present invention may be used not only for treating the surface or the interior of surrounding soil or under-floor soil for protecting wood such as trees, fences, and railroad ties, or buildings such as houses, warehouses, and industrial plants, but also in timber products such as plywood and furniture, wood products such as particle boards and half boards, and vinyl products such as coated wires and sheets.
  • the present invention also includes the aspects for preventive uses in places where the breeding of termites is expected as well as the above aspects.
  • Emulsifying agents which may be used are one or more of those selected from non-ionic or anionic emulsifying agents.
  • non-ionic emulsifying agents which may be mentioned include polyoxyethylenealkylphenyl ether, polyoxyethylenealkyl ether, polyethyleneglycol fatty ester, sorbitan fatty ester, polyoxyethylene sorbitan fatty ester, polyoxyethylenesorbitol fatty ester, polyoxyethylenepolyoxypropylenealkyl ether.
  • anionic emulsifying agents examples include alkyl sulfates, polyxyethylenealkyl ether, sulfates, sulfosuccinates, taurine derivatives, sarcosine derivatives, phosphoric esters, alkylbenezenesulfonates and the like.
  • a mixture consisting of polyoxyethylenestyrylphenyl ether and calcium alkylbenzenesulfonate is preferred.
  • These emulsifying agents may be used in an amount of 5 to 20 weight parts per 100 weight parts of the composition of the present invention.
  • compositions of the present invention may be prepared by any of conventional procedures suitable for emulsifiable concentrates.
  • part(s) means part(s) by weight.
  • the test method of embodiments was in accordance with Japan Wood Preservation Association Standards No. 13, 1987, “Standards for Testing Methods of Termite Controlling Effects and Performance of Termite Controlling Agents for Soil Treatment (I)”.
  • Embodiment 1 consists of: Compound A 8.00 parts Bifenthrin 2.00 parts Propylene glycol 5.00 parts Anionic surface-active agent 1.00 part Non-ionic surface-active agent 5.00 parts Xanthane gum .25 part Silicone defoaming agent .50 part Water 78.25 parts
  • Embodiment 2 consists of: Compound A 1.00 part Bifenthrin .40 part Propylene glycol 5.00 parts Anionic surface-active agent 1.00 part Non-ionic surface-active agent 5.00 parts Xanthane gum 0.40 part Silicone defoaming agent 0.50 part Water 86.70 parts
  • Embodiment 3 consists of: Compound A 4.00 parts Permethrin 20.00 parts Anionic surface-active agent 10.00 parts N-methyl-2-pyrrolidone 10.00 parts Aromatic solvent 56.00 parts
  • a testing apparatus was used in which two glass cylinders (each about 5 cm in diameter and about 12 cm in height) are connected at about 2 cm from the bottom with a glass tube about 1.5 cm in diameter and about 10 cm in length (graduated at 5-mm intervals for 5 cm at the center).
  • the one glass cylinder was filled with about 60 g of non-treated soil adjusted to a moisture content of about 25%, and the other glass cylinder was filled with about 0.29 g of filter paper (5.5 mm in diameter).
  • the glass tube was filled, at a thickness of 1 cm, with test soil prepared by mixing 2.4 g of non-treated sandy soil which had passed through a 20-mesh screen and had been dried at 60° C. until a constant weight had been achieved, with 0.45 g of the solution of the test composition of a predetermined concentration, and the mixture was allowed to stand for 3 weeks in a room without weather resistance treatment.
  • the glass tube was connected to the glass cylinders.
  • Results are shown in Table 1: Termite Bored Damage control depth by effect Embodi- Test (mm) eating 14 days ments composition Concentration (%) 14 DAT 14 DAT later Compound A + 0.01 + 0.01 3 None A bifenthrin 0.01 + 0.005 2 None A 0.005 + 0.01 3 None A 0.005 + 0.005 7 None A 0.0025 + 0.01 5 None A 0.0025 + 0.005 9 None A 0.00125 + 0.01 7 None A 0.00125 + 0.005 9 None A Compound A + 0.02 + 0.05 2 None A fenvalerate 0.005 + 0.05 6 None A 0.02 + 0.01 1 None A 0.005 + 0.01 3 None A Compound A 0.02 + 0.025 0 None A + 0.005 + 0.025 0 None A cypermethrin 0.02 + 0.005 2 None A 0.005 + 0.005 3 None A Compound A + 0.02 + 0.1 0 None A permethrin 0.005 + 0.1 6 None A 0.
  • Bored Damage Termite depth by control (mm) eating effect Test Concentration 14 days 14 days 14 days 14 days composition (%) later later later later Com- Compound A 0.02 >10 + A para- 0.01 >10 + A tive 0.005 >10 ++ A Examples Bifenthrin 0.01 >10 +++ D 0.005 >10 +++ D Fenvalerate 0.05 >10 + A 0.01 >10 +++ D Cyperme- 0.025 >10 None D thrin 0.005 >10 +++ D Permethrin 0.1 >10 None D 0.02 >10 +++ D Tralomethrin 0.01 >10 +++ D 0.002 >10 +++ D Fluvalinate 0.05 >10 +++ D Cyfluthrin 0.025 >10 None D 0.005 >10 +++ D Ethofenprox 0.1 >10 None D 0.02 >10 +++ D Silafluofen 0.05 >10 + A 0.01 >10 +++ D Non- >10 +++ D treatment

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  • Life Sciences & Earth Sciences (AREA)
  • Agronomy & Crop Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Catching Or Destruction (AREA)

Abstract

The present invention provides an insecticidal composition comprising, as active ingredients, (a) at least one pyrethroid compound and (b) an N-arylpyrazole compound such as 5-amino-3-cyano-1-(2,6-dichloro)-4-trifluoromethylphenyl)-4-trifluoromethylsulfinylpyrazole, and an insecticidal method which comprises applying the composition.

Description

    CROSS-REFERENCE TO RELATED APPLICATIONS
  • This application is a division of copending application Ser. No. 09/457,861, filed Dec. 10, 1999, now allowed, which is a division of application Ser. No. 09/268,686, filed Mar. 16, 1999, now U.S. Pat. No. 6,060,497, which is a division of application Ser. No. 08/855,606, filed May 13, 1997, now U.S. Pat. No. 5,916,909, which is a division of application Ser. No. 08/700,520, filed Dec. 11, 1996, now U.S. Pat. No. 5,747,519, which is the U.S. national phase of International Pat. Application No. PCT/EP95/00601, filed Feb. 20, 1995 and designating the United States, which was published by the International Bureau in English as WO 95/22902 on Aug. 31, 1995. applications Ser. Nos. 09/457,861, 09/268,686 and 08/855,606 are incorporated by reference herein in their entireties and relied upon.[0001]
  • The present invention relates to a termite control composition for soil treatment containing a 3-cyano-1-(substituted phenyl)-pyrazole derivative and a pyrethroid compound as effective ingredients. [0002]
  • The pyrazole derivatives as effective ingredients of the termite control composition of the present invention are known compounds described in European patent publication 0295117 as well as in the international patent publications WO 93/06089 and 94/21606, which disclose that the compounds have a pesticidal effect on arthropods, vegetable nematodes, protozoan pests, and other pests. Many other pesticidal compounds can be used in combination with N-phenyl pyrazole derivatives. Pyrethroid compounds such as cyfluthrin, cypermethrin, deltamethrin, fenpropathrin, fenvalerate, and permethrin are recited among many possibilities without any reference to any specific effect in any conditions. [0003]
  • A first object of the instant invention is to provide synergistic compositions of 3-cyano-1-(substituted phenyl)-pyrazole derivatives. [0004]
  • Another object of the instant invention is to provide specific compositions which have an improved activity against pests, especially against insects. [0005]
  • Another object of the instant invention is to provide specific compositions which have an improved activity against termites. [0006]
  • There are mainly two types of termite control methods: namely, wood application by applying a control agent to wood, and soil treatment by spraying a control agent on the soil and/or under the floor. For existing houses, since the application of the agent to wood is rather difficult, soil treatment is generally used. In many cases, however, termites pass through the treated layer and eat the wood, and therefore, it is desired to develop a termite control agent which has both the termite control effect and the ability to prevent termites from passing through the pesticidally treated layer. [0007]
  • A further object of the instant invention is to provide a novel termite control composition (preferably for soil treatment) which has a strong termite control effect as well as the ability to prevent termites from passing through the pesticidally treated layer. [0008]
  • It has been found that these goals may be reached by means of the compositions of the instant invention. [0009]
  • The compositions of the present invention comprise, as effective ingredients, a pyrethroid compound and a compound of formula (I)[0010]
  • 1-[4-R12,6-(R2)pphenyl]3-cyano-4-[R4-S(O)n]5-R5pyrazole  (I)
  • wherein: [0011]
  • R[0012] 1 is halogen, lower haloalkyl, lower haloalkoxy or SF5 (lower being an integer from 1 to 4, preferably one),
  • R[0013] 2 is halogen, the various R2 being identical or different,
  • R[0014] 4 is halogen, lower alkyl or haloalkyl,
  • R[0015] 5 is halogen, lower alkyl or amino,
  • n is 0 or 1 or 2; p is 1 or 2 or 3 or 4, preferably 2. [0016]
  • Halo before the name of a radical means that this radical may be substituted by one or more halogen atoms. [0017]
  • A preferred compound of formula (I) is 5-amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-trifluoromethylsulphinylpyrazole (Compound A). [0018]
  • The compositions of the invention comprise a synergistic amount of active ingredients. [0019]
  • Pyrethroid compounds which can be used in the present invention include all kinds of pyrethroids, especially pyrethroids other than cyfluthrin, cypermethrin, deltamethrin, fenpropathrin, fenvalerate, and permethrin. Advantageously, pyrethroids which can be used in the invention are compounds selected from a group consisting of the following pyrethroid compounds, even though not limited to these pyrethroid compounds: [0020]
  • 1. Allethrin [dl-3-allyl-2-methyl-4-oxo-2-cyclopentenyl-dl-cis, trans-chrysanthemate][0021]
  • 2. Ethofenprox [2-(4-ethoxyphenyl)-2-methylpropyl-3-phenoxybenzyl ether][0022]
  • 3. Cycloprothrin [(RS)-a-cyano-3-phenoxybenzyl (RS)-2,2-dichloro-1-(4-ethoxyphenyl)cyclopropane carboxylate][0023]
  • 4. Cyhalothrin [(RS)-a-cyano-3-phenoxybenzyl (Z)-(1RS,3RS) 3-(2-chloro-3,3, 3-trifluoro-1-propenyl)-2,2-dimethylcyclopropane carboxylate][0024]
  • 5. Cyfluthrin [(RS)-a-cyano-4-fluoro-3-phenoxybenzyl (IRS,3RS)-(1RS,3RS)-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropane carboxylate][0025]
  • 6. Cypermethrin [(RS)-a-cyano-3-phenoxybenzyl (1RS,3RS)-(1RS,3SR)-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropane carboxylate][0026]
  • 7. Pyrethrin [0027]
  • 8. Tralomethrin [(S)-a-cyano-3-phenoxybenzyl (1R, 3S)-2,2-dimethyl-3-(1,2,2,2-tetrabromoethyl)cyclopropane carboxylate][0028]
  • 9. Fenvalerate [(RS)-a-cyano-3-phenoxybenzyl (RS)-2-(4-chlorophenyl)-3-methylbutanoate][0029]
  • 10. Fenpropathrin [(RS)-a-cyano-3-phenoxybenzyl-2,2,3,3-tetramethylcyclopropane carboxylate][0030]
  • 11. Flucythrinate [(RS)-a-cyano-3-phenoxybenzyl-(S)-2-(4-difluoromethoxyphenyl)-3-methyl butylate][0031]
  • 12. Permethrin [3-phenoxybenzyl (1RS,3RS)-(1RS,3RS)-(2,2-dichlorovinyl)-2,2-dimethylcyclopropane carboxylate][0032]
  • 13. Bifenthrin [2-methylbiphenyl-3-yl-methyl (Z)- 1RS,3RS)-3-(2-chloro-3,3,3-trifluoroprop-1-enyl)-2-2-dimethylcyclopropane carboxylate][0033]
  • 14. Silafluofen [4-ethoxyphenyl-[3-(3-phenoxy-4-fluorophenyl)propyl] (dimethyl)silane][0034]
  • 15. Lesmethrin [5-benzyl-3-furylmethyl dl-cis, trans-chrysanthemate][0035]
  • 16. Tefluthrin [2,3,5,6-tetrafluoro-4-methylbenzyl-(1RS)-cis-3-(Z-2-chloro-3,3, 3-trifluoroprop-1-enyl)-2,2-dimethylcyclopropane carboxylate][0036]
  • 17. Acrinathrin [(S)-a-cyano-3-phenoxybenzyl (Z)-(1R,3S)-2,2-dimethyl-3-[2-(2,2,2-trifluoro-1-trifluoromethylethoxycarbonyl)vinyl]cyclopropane carboxylate][0037]
  • 18. Prarethrin [(RS)-2-methyl-4-oxo-3-prop-2-enylcyclopent-2-enyl (1RS)-cis,trans-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane carboxylate][0038]
  • 19. Cismethrin [5-benzyl-3-furylmethyl (1R)-trans-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane carboxylate][0039]
  • 20. d-Phenothrin [3-phenoxybenzyl (1RS)-cis, trans-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane carboxylate][0040]
  • 21. Deltamethrin [(S)-cyano-3-phenoxybenzyl (1R)cis-3-(2,2-dibromovinyl)-2,2-dimethylcyclopropane carboxylate][0041]
  • 22. Tetramethrin [cyclohex-1-ene-1,2-dicarboximide methyl (1RS,3RS, 1RS ,3SR)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane carboxylate]. [0042]
  • The synergistic compositions of the invention are compositions wherein the ratio by weight of the pyrethroid compound to the compound of formula (I) is between 0.1 and 10, preferably between 0.5 and 5. [0043]
  • The synergistic compositions of the invention are compositions, which are most useful for termite control, preferably with soil treatment. Thus, the invention is also directed to a method of control of pests, especially of termites, which comprises applying an effective amount of the compositions according to the invention, as herein described. [0044]
  • The liquid compositions of the invention generally comprises 0.001 to 50% (all percentages are by weight in the instant specification, unless specifically indicated otherwise) of compound of formula (I), preferably from 0.005 to 10%. The concentrated compositions which are those used for storage and commercial purposes comprise generally from 1 to 20% of this compound of formula (I). [0045]
  • When the compositions for soil treatment of the present invention are used for termite control, especially for soil treatment and/or for treating under-floor soil, the quantity of the effective ingredient may be within a range between 0.01 g and 7 g, preferably between 0.1 g and 5 g per square meter. For wood treatment, such as timber or all kind of wood, the method of control of pests, especially of termites, according to the invention is impregnating the wood by means of a composition as hereinbefore defined. [0046]
  • The application of the compositions of the invention to animals is generally made at 0.1 to 100 mg, preferably at 2 to 20 mg per kilogram of body weight of the animal. [0047]
  • The termite control composition of the present invention has a high significant termite control effect on house damaging termites, for example [0048] Coptotermes formosanusus (Shiraki), Reticulitermes speratus (Kolbe), Odontotermes formosanus (Shiraki), and Cryptotermes domesticus (Haviland), as well as the ability to prevent termites from passing through pesticidally treated materials. The composition may be applied to or adsorbed in building materials, furniture, leather, fabrics, vinyl coated articles, electric wires, or cables.
  • For the efficient use of the termite control composition for material or soil treatment of the present invention, the composition may be dissolved, suspended, mixed, adsorbed, or adhered on an appropriate solid and/or liquid vehicle (this word is used as a synonym of “carrier”) according to the formulation generally used, together with auxiliary agents if required. This composition may be formulated into forms suited to the object of use, for example, an oil solution, emulsion, water solution, powder, granules, wettable powder, aerosol, smoking agent, or flowable agent. [0049]
  • Solid vehicles used in the present invention include, for example, clays such as kaolin, bentonite, and acid clay; talc materials such as talc and pyrophylite; siliceous materials such as diatomaceous earth, silica sand, mica, synthetic silicates, and high dispersion synthetic silicates; and inorganic mineral powders such as pumice and sand. Liquid vehicles include, for example, alcohols such as methanol, ethanol, and ethylene glycol; ketones such as acetone, methyl ethyl ketone, and cyclohexanone; ethers such as ethyl ether, dioxane, tetrahydrofuran, and cellosolve; aliphatic hydrocarbons such as kerosene; aromatic hydrocarbons such as benzene, toluene, xylene, solvent naphtha, cyclohexane, and methyl naphthalene; and halogenated hydrocarbons such as chloroform, carbon tetrachloride, and chlorobenzene. These solid or liquid vehicles may be used alone or in combination. [0050]
  • Auxiliary agents used in the present invention include propellants, surface-active agents, fixing agents, dispersing agents, thickening agents, and bonding agents. Propellants include, for example, liquefied petroleum gas, dimethyl ether, and fluorocarbons. Surface-active agents include, for example, polyoxyethylene alkylaryl ether, polyoxyethylene sorbitane monolaurate, alkylallyl sorbitane monolaurate, alkylbenzene sulfonate, alkylnaphthalene sulfonate, lignin sulfonate, and sulfuric acid ester salts of higher alcohols. These surface-active agents may be used alone or in combination. [0051]
  • Fixing agents, dispersing agents, thickening agents, and bonding agents include, for example, casein, gelatine, starch, carboxymethyl cellulose, alginic acid, agar, polyvinyl alcohol, polyethylene glycol, polysodium acrylate, gum arabic, and xanthane gum, which may be used if required. [0052]
  • The termite control composition for soil treatment of the present invention may contain co-operating agents such as sinepyrin 500, piperonyl butoxide, and S-421. [0053]
  • The termite control composition of the present invention may be used not only for treating the surface or the interior of surrounding soil or under-floor soil for protecting wood such as trees, fences, and railroad ties, or buildings such as houses, warehouses, and industrial plants, but also in timber products such as plywood and furniture, wood products such as particle boards and half boards, and vinyl products such as coated wires and sheets. [0054]
  • The present invention also includes the aspects for preventive uses in places where the breeding of termites is expected as well as the above aspects. [0055]
  • Emulsifying agents which may be used are one or more of those selected from non-ionic or anionic emulsifying agents. Examples of non-ionic emulsifying agents which may be mentioned include polyoxyethylenealkylphenyl ether, polyoxyethylenealkyl ether, polyethyleneglycol fatty ester, sorbitan fatty ester, polyoxyethylene sorbitan fatty ester, polyoxyethylenesorbitol fatty ester, polyoxyethylenepolyoxypropylenealkyl ether. Examples of anionic emulsifying agents which may be mentioned include alkyl sulfates, polyxyethylenealkyl ether, sulfates, sulfosuccinates, taurine derivatives, sarcosine derivatives, phosphoric esters, alkylbenezenesulfonates and the like. A mixture consisting of polyoxyethylenestyrylphenyl ether and calcium alkylbenzenesulfonate is preferred. These emulsifying agents may be used in an amount of 5 to 20 weight parts per 100 weight parts of the composition of the present invention. [0056]
  • Compositions of the present invention may be prepared by any of conventional procedures suitable for emulsifiable concentrates. [0057]
  • The present invention is illustrated by the following examples, comparative examples and experimental examples, but is not limited to the details thereof.[0058]
    • EXAMPLES
  • Typical embodiments and test examples of the present invention will be shown below, but the present invention is not limited to these embodiments. [0059]
  • In the description of these embodiments, the term “part(s)” means part(s) by weight. The test method of embodiments was in accordance with Japan Wood Preservation Association Standards No. 13, 1987, “Standards for Testing Methods of Termite Controlling Effects and Performance of Termite Controlling Agents for Soil Treatment (I)”. [0060]
  • Embodiment 1 consists of: [0061]
    Compound A 8.00 parts
    Bifenthrin 2.00 parts
    Propylene glycol 5.00 parts
    Anionic surface-active agent 1.00 part 
    Non-ionic surface-active agent 5.00 parts
    Xanthane gum  .25 part 
    Silicone defoaming agent  .50 part 
    Water 78.25 parts 
  • The above materials are uniformly mixed and suspended to form a flowable agent. [0062]
  • Embodiment 2 consists of: [0063]
    Compound A 1.00 part 
    Bifenthrin  .40 part 
    Propylene glycol 5.00 parts
    Anionic surface-active agent 1.00 part 
    Non-ionic surface-active agent 5.00 parts
    Xanthane gum 0.40 part 
    Silicone defoaming agent 0.50 part 
    Water 86.70 parts 
  • The above materials are uniformly mixed and suspended to form a flowable agent. [0064]
  • Embodiment 3 consists of: [0065]
    Compound A  4.00 parts
    Permethrin 20.00 parts
    Anionic surface-active agent 10.00 parts
    N-methyl-2-pyrrolidone 10.00 parts
    Aromatic solvent 56.00 parts
  • The above materials are uniformly dissolved to form an emulsion. [0066]
    • Test Example 1
  • A testing apparatus was used in which two glass cylinders (each about 5 cm in diameter and about 12 cm in height) are connected at about 2 cm from the bottom with a glass tube about 1.5 cm in diameter and about 10 cm in length (graduated at 5-mm intervals for 5 cm at the center). The one glass cylinder was filled with about 60 g of non-treated soil adjusted to a moisture content of about 25%, and the other glass cylinder was filled with about 0.29 g of filter paper (5.5 mm in diameter). The glass tube was filled, at a thickness of 1 cm, with test soil prepared by mixing 2.4 g of non-treated sandy soil which had passed through a 20-mesh screen and had been dried at 60° C. until a constant weight had been achieved, with 0.45 g of the solution of the test composition of a predetermined concentration, and the mixture was allowed to stand for 3 weeks in a room without weather resistance treatment. The glass tube was connected to the glass cylinders. [0067]
  • In the glass cylinder filled with non-treated soil, 200 workers and 20 soldiers of [0068] Coptotermes formosanus Shiraki were placed, and the testing apparatus was kept at a constant temperature chamber controlled at a temperature of 28° C., and a relative humidity of 70% or higher.
  • The bored depth (millimeters=mm), damage by eating, and the termite control effect were determined 14 days after insects were put in place, and the effect was evaluated in accordance with the following criteria: [0069]
  • Damage by eating: [0070]
    + 10% or less compared with non-treatment
    ++ 11-50 % or less compared with non-treatment
    +++ 51% or more compared with non-treatment
  • Termite Control Effect: [0071]
    A 100% lethal
    B 80-99% lethal
    C 50-79% lethal
    D 49% lethal or less
  • Results are shown in Table 1: [0072]
    Termite
    Bored Damage control
    depth by effect
    Embodi- Test (mm) eating 14 days
    ments composition Concentration (%) 14 DAT 14 DAT later
    Compound A + 0.01 + 0.01 3 None A
    bifenthrin  0.01 + 0.005 2 None A
    0.005 + 0.01  3 None A
    0.005 + 0.005 7 None A
    0.0025 + 0.01  5 None A
    0.0025 + 0.005  9 None A
    0.00125 + 0.01   7 None A
    0.00125 + 0.005  9 None A
    Compound A + 0.02 + 0.05 2 None A
    fenvalerate 0.005 + 0.05  6 None A
    0.02 + 0.01 1 None A
    0.005 + 0.01  3 None A
    Compound A  0.02 + 0.025 0 None A
    + 0.005 + 0.025 0 None A
    cypermethrin  0.02 + 0.005 2 None A
    0.005 + 0.005 3 None A
    Compound A + 0.02 + 0.1  0 None A
    permethrin 0.005 + 0.1  6 None A
    0.02 + 0.02 8 None A
    Compound A + 0.02 + 0.01 6 None A
    tralomethrin 0.005 + 0.01  4 None A
     0.02 + 0.002 2 None A
    0.005 + 0.002 8 None A
    Compound A + 0.02 + 0.05 8 None A
    fluvalinate
    Compound A +  0.02 + 0.025 6 None A
    cyfluthrin 0.005 + 0.025 6 None A
     0.02 + 0.005 6 None A
    Compound A + 0.02 + 0.1  2 None A
    ethofenprox 0.005 + 0.1  8 None A
    0.02 + 0.02 4 None A
    0.005 + 0.02  7 None A
    Compound A + 0.02 + 0.05 6 None A
    silafluofen 0.005 + 0.05  5 None A
    0.02 + 0.01 7 None A
  • [0073]
    Bored Damage Termite
    depth by control
    (mm) eating effect
    Test Concentration 14 days 14 days 14 days
    composition (%) later later later
    Com- Compound A 0.02 >10 + A
    para- 0.01 >10 + A
    tive 0.005 >10 ++ A
    Examples Bifenthrin 0.01 >10 +++ D
    0.005 >10 +++ D
    Fenvalerate 0.05 >10 + A
    0.01 >10 +++ D
    Cyperme- 0.025 >10 None D
    thrin 0.005 >10 +++ D
    Permethrin 0.1 >10 None D
    0.02 >10 +++ D
    Tralomethrin 0.01 >10 +++ D
    0.002 >10 +++ D
    Fluvalinate 0.05 >10 +++ D
    Cyfluthrin 0.025 >10 None D
    0.005 >10 +++ D
    Ethofenprox 0.1 >10 None D
    0.02 >10 +++ D
    Silafluofen 0.05 >10 + A
    0.01 >10 +++ D
    Non- >10 +++ D
    treatment

Claims (32)

What is claimed is:
1. A pesticidal composition which comprises, as effective ingredients, a pyrethroid and a compound of formula (I)
1-[4-R12,6-(R2)pphenyl]3-cyano 4-[R4-S(O)n]5-R5pyrazole  (I)
wherein R1 is halogen, lower haloalkyl, lower haloalkoxy or SF5; R2 is halogen, the various R2 being identical or different; R4 is halogen, lower alkyl or haloalkyl; R5 is halogen, lower alkyl or amino; n is 0 or 1 or 2; and p is 1 or 2 or 3 or 4.
2. A composition according to
claim 1
, wherein the effective ingredients are present in the composition in a synergistically effective amount.
3. A composition according to
claim 1
, wherein the ratio by weight of pyrethroid compound to compound of formula (I) is between 0.1 and 10.
4. A composition according to
claim 1
, which comprises between 0.001% and 50% of compound of formula (I).
5. A composition according to
claim 1
, which comprises between 1 and 20% of compound of formula (I).
6. A composition according to
claim 1
, when used against termites.
7. A composition according to
claim 1
, wherein the compound of formula (I) is 5-amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-trifluoromethylsulphinylpyrazole.
8. A composition according to
claim 1
, wherein the pyrethroid compound is other than cyfluthrin, cypermethrin, deltamethrin, fenpropathrin, fenvalerate or permethrin.
9. A composition according to
claim 1
, wherein the pyrethroid compound is selected from a group consisting of allethrin, ethofenprox, cycloprothrin, cyhalothrin, cyfluthrin, cypermethrin, pyrethrin, tralomethrin, fenvalerate, fenpropathrin, flucythrinate, permethrin, bifenthrin, silafluofen, lesmethrin, tefluthrin, acrinathrin, prarethrin, cismethrin, d-phenothrin, deltamethrin and tetramethrin.
10. A method for controlling and preventing termites from passing through a pesticidally treated layer of soil or material comprising treating said layer with an effective amount of a composition according to
claim 1
.
11. A method for controlling termites comprising treating soil with 0.1 g/m2 to 5 g/m2 of a termite control composition according to
claim 1
.
12. A method for controlling pests of animals comprising treating an animal with a composition according to
claim 1
, the rate of application being between 0.1 and 100 mg per kilo of body weight of the animal.
13. A termiticidal combination comprising (a) fenvalerate and (b) 5-amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-trifluoromethylsulphinylpyrazole, in a combined synergistic termiticidally effective amount, the ratio by weight of (a) to (b) being between 0.1 and 10.
14. A combination as claimed in
claim 13
, wherein the ratio by weight of (a) to (b) is between 0.5 and 5.
15. A termiticidal composition comprising:
(a) fenvalerate and (b) 5-amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-trifluoromethylsulphinylpyrazole, in a combined synergistic termiticidally effective amount, the ratio by weight of (a) to (b) being between 0.1 and 10; and (c) an acceptable carrier therefor.
16. A composition as claimed in
claim 15
, wherein the ratio by weight of (a) to (b) is between 0.5 and 5.
17. A composition as claimed in
claim 15
, being in liquid form and comprising from 0.001% to 50% by weight of 5-amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-trifluoromethylsulphinylpyrazole.
18. A composition as claimed in
claim 16
, being in liquid form and comprising from 0.001% to 50% by weight of 5-amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-trifluoromethylsulphinylpyrazole.
19. A composition as claimed in
claim 17
, comprising from 0.005% to 10% by weight of 5-amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-trifluoromethylsulphinylpyrazole.
20. A composition as claimed in
claim 18
, comprising from 0.005% to 10% by weight of 5-amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-trifluoromethylsulphinylpyrazole.
21. A composition as claimed in
claim 15
, being in the form of a concentrate and comprising from 1% to 20% by weight of 5-amino-3-cyano-1-(2, 6-dichloro-4-trifluoromethylphenyl)-4-trifluoromethylsulphinylpyrazole.
22. A composition as claimed in
claim 16
, being in the form of a concentrate and comprising from 1% to 20% by weight of 5-amino-3-cyano-1-(2, 6-dichloro-4-trifluoromethylphenyl)-4-trifluoromethylsulphinylpyrazole.
23. A method for controlling termites and for preventing them from passing through a layer of soil or other material, said method comprising treating said layer with a termiticidally effective amount of a termiticidal composition comprising (a) fenvalerate and (b) 5-amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-trifluoromethylsulphinylpyrazole, in a combined synergistic termiticidally effective amount, the ratio by weight of (a) to (b) being between 0.1 and 10; and (c) an acceptable carrier therefor.
24. A method as claimed in
claim 23
, wherein the ratio by weight of (a) to (b) is between 0.5 and 5.
25. A method as claimed in
claim 23
, wherein said composition is in liquid form and comprises from 0.001% to 50% by weight of 5-amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-trifluoromethylsulphinylpyrazole.
26. A method as claimed in
claim 24
, wherein said composition is in liquid form and comprises from 0.001% to 50% by weight of 5-amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylsulphinylpyrazole.
27. A method as claimed in
claim 25
, wherein said composition comprises from 0.005% to 10% by weight of 5-amino-3-cyano-l-(2,6-dichloro-4-trifluoromethylphenyl)-4-trifluoromethylsulphinylpyrazole.
28. A method as claimed in
claim 26
, wherein said composition comprises from 0.005% to 10% by weight of 5-amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-trifluoromethylsulphinylpyrazole.
29. A method as claimed in
claim 23
, wherein a layer of soil is treated and wherein an amount between 0.01 g/m2 and 7 g/m2 of active ingredients (a) and (b) is applied.
30. A method as claimed in
claim 24
, wherein a layer of soil is treated and wherein an amount between 0.01 g/m2 and 7 g/m2 of active ingredients (a) and (b) is applied.
31. A method as claimed in
claim 29
, wherein the amount of active ingredients (a) and (b) applied is between 0.1 g/m2 and 5 g/m2.
32. A method as claimed in
claim 30
, wherein the amount of active ingredients (a) and (b) applied is between 0.1 g/m2 and 5 g/m2.
US09/826,817 1994-02-27 2001-04-06 Synergistic pesticidal composition of pyrethroid and N-phenyl-pyrazole Expired - Lifetime US6432998B2 (en)

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US08/855,606 US5916909A (en) 1994-02-27 1997-05-13 Synergistic pesticidal composition of pyrazole and N-phenyl-pyrazole
US09/268,686 US6060497A (en) 1994-02-27 1999-03-16 Synergistic pesticidal composition of pyrethroid and N-phenyl-pyrazole
US09/457,861 US6258835B1 (en) 1994-02-27 1999-12-10 Synergistic pesticidal composition of pyrethroid and N-phenyl-pyrazole
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US09/268,686 Expired - Lifetime US6060497A (en) 1994-02-27 1999-03-16 Synergistic pesticidal composition of pyrethroid and N-phenyl-pyrazole
US09/457,861 Expired - Lifetime US6258835B1 (en) 1994-02-27 1999-12-10 Synergistic pesticidal composition of pyrethroid and N-phenyl-pyrazole
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ATE181206T1 (en) 1999-07-15
CA2183341A1 (en) 1995-08-31
US6432998B2 (en) 2002-08-13
DK0746205T3 (en) 1999-11-22
GR3030451T3 (en) 1999-09-30
ZA951611B (en) 1995-12-07
AU679622B2 (en) 1997-07-03
US6258835B1 (en) 2001-07-10
US6060497A (en) 2000-05-09
ES2135704T3 (en) 1999-11-01
CA2183341C (en) 2006-11-07
WO1995022902A1 (en) 1995-08-31
AU1810495A (en) 1995-09-11
CN1141580A (en) 1997-01-29
US5916909A (en) 1999-06-29
CN1071089C (en) 2001-09-19
US5747519A (en) 1998-05-05
EP0746205B1 (en) 1999-06-16
DE69510333T2 (en) 1999-10-14
TR28559A (en) 1996-09-30
EG20441A (en) 1999-04-29
BR9507118A (en) 1997-08-12
DE69510333D1 (en) 1999-07-22
US6472417B1 (en) 2002-10-29

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