Composition for thermal evaporation and method for exterminating harmful arthropods using the same

A composition for thermal evaporation with natural pyrethrins and pyrethroid compounds in a specific ratio addresses the inadequacy of existing methods, achieving enhanced extermination of harmful arthropods by leveraging synergistic effects.

JP7814376B2Active Publication Date: 2026-02-16SUMITOMO CHEM CO LTD
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Patent Information

Application Number
JP2023513008
Authority / Receiving Office
JP · JP
Patent Type
Patents
Current Assignee / Owner
Priority Date
2021-04-05
Filing Date
2022-04-01
Publication Date
2026-02-16
Estimated Expiration
2042-04-01

AI Technical Summary

Technical Problem

Existing compositions for thermal evaporation may not have sufficient efficacy in exterminating harmful arthropods.

Method used

A composition for thermal evaporation containing natural pyrethrins and pyrethroid compounds in a specific ratio, with a weight ratio of natural pyrethrin to pyrethroid compound ranging from 20:1 to 200:1, and pyrethroid compounds having a vapor pressure of 0.00001 Pa to 0.1 Pa at 25°C, is used to enhance extermination effectiveness.

Benefits of technology

The composition exhibits excellent efficacy in exterminating harmful arthropods, demonstrating higher knockdown rates than expected from the individual components when used together.

✦ Generated by Eureka AI based on patent content.

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Abstract

The present invention provides a heat transpiration composition characterized by having excellent ability in exterminating harmful arthropods and by comprising a natural pyrethrin and a pyrethroid compound, and characterized in that the weight ratio of an active ingredient of the natural pyrethrin and the pyrethroid compound is within a range of 20:1 to 200:1.
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Description

[Technical Field]

[0001] This patent application claims priority under the Paris Convention and the benefit of Japanese Patent Application No. 2021-063990 (filed April 5, 2021), the entire contents of which are incorporated herein by reference. The present invention relates to a composition for thermal evaporation containing natural pyrethrins and pyrethroids, and a method for exterminating harmful arthropods using the same. [Background technology]

[0002] Various methods have been investigated to date for the purpose of exterminating harmful arthropods. For example, Patent Document 1 describes that a certain type of composition for thermal evaporation has an effect of exterminating mosquitoes. [Prior art documents] [Patent documents]

[0003] [Patent Document 1] Japanese Patent Application Publication No. 9-268104 Summary of the Invention [Problem to be solved by the invention]

[0004] However, the composition for heating and evaporation may not always have sufficient efficacy in exterminating harmful arthropods. [Means for solving the problem]

[0005] The present inventors have conducted research to provide a composition for thermal evaporation that is effective in exterminating harmful arthropods, and as a result, have found that a composition for thermal evaporation containing natural pyrethrins and pyrethroid compounds in a specific ratio exhibits excellent effectiveness in exterminating harmful arthropods, thereby completing the present invention.

[0006] The present invention includes, but is not limited to, the following aspects. 1. A composition for thermal evaporation containing natural pyrethrin and a pyrethroid compound, wherein the weight ratio of the active ingredient of the natural pyrethrin to the pyrethroid compound is in the range of 20:1 to 200:1. 2. The composition for thermal evaporation according to the preceding paragraph 1, wherein the pyrethroid compound has a vapor pressure of 0.00001 Pa to 0.1 Pa at 25°C. 3. A composition for heating and evaporation according to the preceding item 1 or 2, wherein the pyrethroid compound is at least one pyrethroid compound selected from the group consisting of metofluthrin, dimefluthrin, transfluthrin, profluthrin, mepafluthrin, heptafluthrin, tetramethylfluthrin, and lenofluthrin. 4. Incense sticks containing the composition according to any one of the preceding items 1 to 3. 5. A method for exterminating mosquitoes, which uses the composition or incense described in any one of items 1 to 4 above. 6. A matte formulation comprising the composition according to any one of items 1 to 3 above. 7. A method for exterminating mosquitoes, which uses the composition or mat preparation described in any one of items 1 to 3 and 6 above. 8. A pest control formulation for thermal evaporation, comprising the composition according to any one of items 1 to 3 above. 9. A method for exterminating mosquitoes, which uses the composition or the pest control formulation for thermal evaporation described in any one of items 1 to 3 and 8 above. [Effects of the Invention]

[0007] The composition for thermal evaporation of the present invention exhibits excellent efficacy. DETAILED DESCRIPTION OF THE INVENTION

[0008] The natural pyrethrins used in the present invention contain six types of compounds as active ingredients: pyrethrin I, pyrethrin II, cinerin I, cinerin II, jasmoline I, and jasmoline II. Natural pyrethrins are typically available as pyrethrum dried powder or as an extract obtained by extracting only the flower buds of pyrethrum (scientific names: Tanacetum cinerariifolium or Chrysanthemum cinerariaefolium) from powder that has been collected, dried, and crushed using an appropriate solvent that dissolves the active ingredients, such as an organic solvent such as methanol. In addition to the six types of compounds mentioned above, natural pyrethrins may also contain plant-derived impurities (such as fatty acids and flavonoids). In addition to the white daisy, other plants known to produce natural pyrethrins include Calendula officinalis, Chrysanthemum coccinum, Tagetes erecta, Tagetes minuta, Zinnia elegans, and Zinnia linnearis (Reference 1: Adnane, H. Alain, C. & Chantal, B. 2000. The Production of Pyrethrins by Plant Cell and Tissue Cultures of Chrysanthemum cinerariaefolium and Tagetes Species. Critical Reviews in Plant Sciences, 19(1):69-89; Reference 2: Kudakasseril, GJ and Staba, EJ 1988. Insecticidal phytochemicals. In: Cell Culture and Somatic Cell Genetics of Plants. pp. 537-552. Constabel, F. and Vasil, IK, Eds., Academic Press, New York, Reference 3: John E. Casida, Gary B. Quistad. 1995. PYRETHRUM FLOWERS, Production, Chemistry, Toxicology, and Uses. pp. 123-125, Oxford University Press.).

[0009] The plant species and varieties that serve as the source of the natural pyrethrins used in the present invention are not limited to those mentioned above. The cultivation method, cultivation conditions (weather, place of origin, soil type, etc.), harvest time, harvest part, harvesting method, washing method, extraction method, and purification method of the plant are not particularly limited. The natural pyrethrins used in the present invention also include, for example, natural pyrethrins obtained using a vector into which a gene encoding a pyrethrin biosynthetic enzyme has been inserted.

[0010] The weight ratios of the six compounds in natural pyrethrins, pyrethrin I, pyrethrin II, cinerin I, cinerin II, jasmolin I, and jasmolin II, are not particularly limited and can be set at any weight ratio within the range of 0.001 to 99%, respectively. However, natural pyrethrins are typically contained in weight ratios of 10 to 70% pyrethrin I, 10 to 70% pyrethrin II, 1 to 20% cinerin I, 1 to 20% cinerin II, 1 to 20% jasmolin I, and 1 to 20% jasmolin II.

[0011] Examples of natural pyrethrins include those containing pyrethrin I (total amount of pyrethrin I, cinerin I, and jasmolin I) and pyrethrin II (total amount of pyrethrin II, cinerin II, and jasmolin II) in an amount of 20 to 40% pyrethrin I and 12 to 31% pyrethrin II. The total amount of pyrethrin I and pyrethrin II in the natural pyrethrin is usually 10 to 99%, preferably 15 to 90%, and more preferably 20 to 85%.

[0012] Natural pyrethrins are usually plant extracts, and therefore may contain, in addition to the six compounds mentioned above, plant-derived impurities as well as auxiliary ingredients such as solvents and stabilizers. As the solvent, a petroleum-based solvent, a vegetable oil-based solvent, etc. can be used, and as the stabilizer, a synthetic stabilizer, a natural stabilizer, etc. can be used.

[0013] In the present invention, the active ingredients of natural pyrethrins refer to pyrethrin I and pyrethrin II, and the weight ratio of the active ingredients of natural pyrethrins to pyrethroid compounds in the range of 20:1 to 200:1 is defined as the ratio of the total weight of pyrethrin I and pyrethrin II to the weight of pyrethroid compounds in the range of 20:1 to 200:1.

[0014] Examples of pyrethroid compounds used in the present invention include those described in the reference (The Pesticide Manual, Eighteenth Edition, J.A. Turner, British Crop Production Council, ISBN 978-1-9998966-1-4). From the viewpoint of volatility, pyrethroid compounds having a vapor pressure of 0.00001 Pa to 0.1 Pa at 25°C are preferred. More specifically, from the viewpoints of volatility and efficacy, examples include at least one compound selected from the group consisting of metofluthrin, dimefluthrin, transfluthrin, profluthrin, mepafluthrin, heptafluthrin, tetramethylfluthrin, and lenofluthrin. The vapor pressure is measured using the method described in Example 1 of JP-A-2006-284560.

[0015] The composition for thermal evaporation of the present invention can also be described as an insecticidal composition for thermal evaporation.

[0016] The following describes a formulation using the composition for thermal evaporation of the present invention. Examples of formulations using the composition for thermal evaporation include incense sticks, mosquito repellent mats, and pest control formulations for thermal evaporation. However, it is not intended that the formulations be limited to the configurations described in the embodiments described below.

[0017] <Incense>

[0018] The incense stick of the present invention typically comprises the above-mentioned composition for thermal evaporation, a carbonized base material, a combustion assisting agent, a bulking agent, a binder, and the like.

[0019] Specific examples of the carbonized substrate include plant-derived carbonized substrates such as charcoal, bamboo charcoal, plant-based activated carbon, coconut shell charcoal, and coffee grounds charcoal, as well as non-plant-derived carbonized substrates such as carbon black, graphite, acetylene black, coal-based activated carbon, and petroleum-based activated carbon, with plant-based carbonized substrates being particularly preferred. These are typically used alone or in combination of two or more.

[0020] Examples of combustion-supporting agents include dried plant powders such as wood flour, tabu (tabu tree bark powder), lees powder (pyrethrum extract powder), citrus peel powder, tea powder, palm oil powder, coconut shell powder, and walnut shell powder, as well as carbon powders such as charcoal powder, activated carbon powder, and coal powder, and these can be used alone or in combination of two or more.

[0021] Examples of the extender include diatomaceous earth, talc, clay, kaolin, etc. These extenders are usually used alone or in combination of two or more.

[0022] Examples of binders include polymeric compounds such as tabu flour, starch (gelatinized starch, tapioca starch, corn starch, wheat starch, etc.), casein, siamese flour, methyl cellulose, carboxymethyl cellulose, and polyvinyl alcohol, and these are usually used alone or in combination of two or more.

[0023] The amounts of the carbonized base material, combustion enhancer, bulking agent, binder, etc. can be freely adjusted depending on the desired quality, but the total amount of these ingredients should be 85% by weight or more, more preferably 90% by weight or more, of the total weight of the mosquito coil.

[0024] The incense of the present invention can be obtained, for example, by adding an appropriate amount of water to a mixture containing the heat-transferable composition and the incense base material, kneading the mixture, molding the mixture using an extruder, a punching machine, or the like, and then drying the mixture naturally or by heating. The composition for thermal evaporation may not be directly mixed with a mixture containing an incense base material, but the liquid containing the composition for thermal evaporation may be applied or sprayed onto the incense base material after molding the incense base material alone.

[0025] The shape of the incense coil of the present invention is not particularly limited, and the shape of the long-lasting mosquito coil can be selected appropriately depending on the purpose of use, such as stick, spiral, cone, or plate, with stick, spiral, or plate shapes being preferred. The size is also not particularly limited, and for example, if the incense coil is stick-shaped, it is preferably set to a total length of 100 mm or less, a thickness of 7 mm or less, and a weight of 5 g or less, and more preferably a total length of 20 to 90 mm, a thickness of 2 to 5 mm, and a weight of 0.2 to 3 g. If the incense coil is spiral-shaped, it is preferably set to a total length of 150 cm or less, a thickness of 7 mm or less, and a weight of 50 g or less, and more preferably a total length of 30 to 90 cm, a thickness of 2 to 5 mm, and a weight of 5 to 20 g. In the case of spiral type, the size is usually a set of two, with a diameter of 12 cm and a thickness of about 3 to 5 mm.

[0026] In actual use, incense is usually given a scent appropriate for the incense, and recently, various volatile fragrance ingredients have been added to achieve aromatic and relaxing effects. Various fragrance ingredients can also be added to the incense of the present invention to achieve aromatic and relaxing effects. Examples of fragrance ingredients include galaxolide, musk ketone, hexyl cinnamic aldehyde, isoe super, methyl dihydrojasmonate, ethylene brassylate, geraniol, methyl atralate, hexyl salicylate, tricyclodecenyl acetate, orange crystal, ambroxan, tonalide (6-acetyl-1,1,2,4,4,7-hexamethyltetralin), γ-undecalactone, cashmeran, calone, heliotropin, dihydroindenyl-2,4-dioxane, α-methyl-2,4-dioxane, α-methyl-1,1,2,4,4,7-hexamethyltetralin ... Examples of fragrance components include α-isomethyl ionone, indole, methyl cedryl ketone, methyl β-naphthyl ketone, rosephenone, coumarin, vanillin, styrax resinoid, benzyl benzoate, undecanal, benzyl salicylate, ionone, α-ionone, β-ionone, lily aldehyde, 3,5-dinitro-2,6-dimethyl-4-t-butylacetophenone, acetyl cedrene, 2-cyclohexylidene-2-phenylacetaldehyde, isolongifolanon, and cis-3-hexenol. These fragrance components can be used alone or in combination. The content of the fragrance component is preferably 0.001 to 5 wt %, and more preferably 0.01 to 1 wt %, based on the weight of the entire incense stick. If the content of the fragrance component is less than 0.001 wt %, the fragrance may not be able to fully exude a fragrance. If the content of fragrance ingredients exceeds 5% by weight, the odor or irritation may become too strong.

[0027] The incense of the present invention may contain other ingredients such as antifungal agents, preservatives, stabilizers, efficacy enhancers, deodorizers, etc. Examples of antifungal agents or preservatives include dehydroacetates, sorbates, p-hydroxybenzoates, etc. Examples of stabilizers include 2,6-di-tert-butyl-4-methylphenol (BHT), 2,2'-methylenebis(4-methyl-6-tert-butylphenol), 2,2'-methylenebis(4-ethyl-6-tert-butylphenol), 4,4'-butylidenebis(3-methyl-6-tert-butylphenol), 4,4'-thiobis(3-methyl-6-tert-butylphenol), 2-tert-butyl-6-(3-tert-butyl-2-hydroxy-5-methylbenzyl)-4-methylphenyl acrylate, 2,4-di-tert-butylphenyl 3,5-di-tert-butyl-4-hydroxybenzoate, etc. The addition of such stabilizers not only improves the stability of the composition for thermal evaporation over time during storage, but also significantly enhances its stability during smoking, and can also contribute to improving the sustained efficacy of the composition for thermal evaporation after evaporation. The stabilizer is preferably added in an amount of 0.01 to 0.5 times the amount of the composition for thermal evaporation. Examples of potency enhancers include piperonyl butoxide and N-(2-ethylhexyl)-bicyclo[2,2,1]hept-5-ene-2,3-dicarboximide. The incense of the present invention can also contain coloring agents such as malachite green and food additives (e.g., Food Blue No. 1, Food Yellow No. 4, and Food Red No. 106).

[0028] <Matte formulation> The mat preparation of the present invention can be produced, for example, by impregnating a fibrous carrier or a porous carrier with a solution obtained by mixing the heat-transferable composition with a solvent, a dye, an antioxidant, a synergist, a stabilizer, a fragrance, etc. The mat preparation can be used, for example, as an electric mosquito repellent mat.

[0029] Examples of fibrous carriers include natural fibers such as pulp, cellulose, and cotton; synthetic fibers such as polyester and acrylic; and inorganic fibers such as glass fiber and asbestos. Examples of porous carriers include porous inorganic materials such as diatomaceous earth; porous magnetic materials such as unglazed clay; and porous resins such as urethane foam and polypropylene foam.

[0030] Electric mosquito repellent mats typically measure approximately 2.2 cm × 3.5 cm × 0.28 cm, but are not limited to this shape, and the amounts and ratios of the heat-transmittable composition and other ingredients can be adjusted appropriately to suit changes in the shape, size, thickness, etc. of the mat. In the present invention, the content of the heat-transmittable composition per 2.2 cm × 3.5 cm × 0.28 cm mat varies depending on the type and content of the heat-transmittable composition, the duration of use of the electric mosquito repellent mat, etc., but is usually about 1 to 2000 mg, preferably about 1 to 100 mg.

[0031] <Pest control formulation for thermal evaporation> The pest control formulation for thermal evaporation of the present invention is a formulation that can be used in a thermal evaporation type insecticidal device, for example, as shown in FIG. 1. A solution 1 containing a composition for thermal evaporation is filled in a liquid solution bottle 4. An absorbent wick 3 is partially immersed in the solution 1, allowing the absorbent wick to absorb the solution containing the composition for thermal evaporation, and the upper part of the absorbent wick can be heated by a heating element 2. By indirectly heating the upper part of the absorbent wick to a temperature of about 60°C to about 135°C by the heating element 2, the composition for thermal evaporation absorbed into the absorbent wick is evaporated into the atmosphere, thereby controlling pests. The pest control formulation for thermal evaporation of the present invention is not limited to the device shown in FIG. 1, and can be applied to any of the conventionally known thermal evaporation type insecticidal devices, and excellent effects can be obtained. Heat-transportation type insecticide devices to which the heat-transportation pest control formulation of the present invention can be applied are also described in, for example, JP-B No. 52-12106, JP-A No. 58-45670, and JP-A No. 2012-176947.

[0032] In the pest control formulation for thermal evaporation of the present invention, the composition for thermal evaporation is prepared in the form of a solution (solution 1) containing the composition for thermal evaporation. As the solvent for preparing the pest control formulation for thermal evaporation, an oil-based solvent or an aqueous solvent is used. When an oily solvent is used, it is usually an oily solvent with a boiling point of 350°C or less. As such an oily solvent, various organic solvents, typically hydrocarbon solvents, can be used, but aliphatic hydrocarbons (paraffinic hydrocarbons and unsaturated aliphatic hydrocarbons) with a boiling point range of 150 to 350°C are particularly preferred. Examples of such solvents include deodorized kerosene, n-paraffin, isoparaffin (e.g., IP Solvent (manufactured by Idemitsu Kosan Co., Ltd.)), and Sowing Glue (manufactured by ENEOS). Examples of organic solvents other than the above hydrocarbons include glycerin, propylene glycol, methanol, acetone, xylene, chlorthene, isopropanol, and chloroform. When an aqueous solvent is used, glycol ether and water are usually used. Examples of such glycol ethers include ethylene glycol ethers, propylene glycol ethers, and dialkyl glycol ethers, with ethylene glycol ethers being preferred. Among the ethylene glycol ethers, ethylene glycol monobutyl ether, diethylene glycol monobutyl ether, propylene glycol monomethyl ether, propylene glycol monoethyl ether, and propylene glycol monopropyl ether are preferred. One or a mixture of two or more glycol ethers can be used. The weight ratio of glycol ether to water is usually in the range of 1:0.4 to 1:8.5, preferably 1:1 to 1:8.5, and more preferably 1:1.4 to 1:3.6. The concentration of the composition for thermal evaporation in the pest control formulation for thermal evaporation is usually adjusted to about 6 to 80% by weight, preferably about 10 to 75% by weight, and more preferably about 15 to 50% by weight. The pest control formulation for thermal vaporization of the present invention may also contain other ingredients such as a thickener, a surfactant, a stabilizer, a preservative, and a synergist.

[0033] Furthermore, the heating element (heating element 2) used in the thermal evaporation type insecticide device is usually a heating element that generates heat when electricity is passed through it, but it is not limited to this, and any known heating element can be used, such as an air oxidation heating element, a heating element that uses a platinum catalyst, etc.

[0034] The liquid-absorbent wick 3 is generally made of a porous material. Examples of such porous materials include inorganic powders such as clay, talc, kaolin, diatomaceous earth, gypsum, perlite, bentonite, acid clay, glass fiber, and asbestos, which are bound and molded with a sizing agent such as carboxymethyl cellulose, starch, gum arabic, gelatin, and polyvinyl alcohol. The liquid-absorbent wick may also contain dyes, preservatives, antioxidants, and the like, as appropriate. These can be incorporated, for example, by mixing the inorganic powder with the sizing agent during the sizing process.

[0035] TIFF0007814376000001.tif4871

[0036] Target pests for control by the heat-transferable composition of the present invention and formulations using the heat-transferable composition include various harmful insects, arthropods such as mites, and particularly harmful flying pests, such as Culex pipiens pallens, Culex tritaeniorhynchus, Culex quinquefasciatus, and Culex molestus, Aedes mosquitoes such as Aedes aegypti and Aedes albopictus, Anopheles mosquitoes such as Anopheles sinensis, midges, house flies such as Musca domestica, Musca domestica, and Musca canina, blow flies, flesh flies, Drosophila, moth flies, phorid flies, horseflies, black flies, stable flies, and midges. Among these, mosquitoes such as Culex pipiens, Aedes mosquitoes, and Anopheles mosquitoes are particularly suitable as target pests for control. [Example]

[0037] The present invention will be explained in more detail below by giving production examples and test examples, but the present invention is not limited to these examples.

[0038] Manufacturing example 1 (Kneaded incense sticks 1) A mixture of 1 part by weight of natural pyrethrin, 0.05 part by weight of dimefluthrin, and 39 parts by weight of tabu powder, 30 parts by weight of dregs powder, and 30 parts by weight of wood flour as combustion supporters was added, and 0.3 parts by weight of green pigment was added. After stirring and mixing uniformly, 120 parts by weight of water was added and thoroughly kneaded. The kneaded mixture was formed into a sheet, punched into spiral shapes, and dried until the moisture content was approximately 7 to 10% by weight, producing the incense formulation of the present invention.

[0039] Manufacturing example 2 (Kneaded incense sticks 2) A mixture of 1 part by weight of natural pyrethrin, 0.05 parts by weight of dimefluthrin, 50 parts by weight of charcoal as a carbonized substrate, 0.8 parts by weight of a mixed fragrance containing galaxolide and musk ketone as a fragrance component, 17 parts by weight of oak groats and 10.7 parts by weight of wood flour as combustion supporters, 3 parts by weight of diatomaceous earth as a bulking agent, and 14 parts by weight of pregelatinized starch and 3 parts by weight of carboxymethyl cellulose as binders was thoroughly kneaded with 90 parts by weight of water. The kneaded mixture was extruded into a rod shape and then dried to a moisture content of approximately 7-10% by weight to produce the incense formulation of the present invention.

[0040] Manufacturing Example 3 (Matte Formulation 1) An electric mosquito repellent mat formulation of the present invention is prepared by uniformly impregnating 120 mg of a solution obtained by mixing 10.5 parts by weight of natural pyrethrins, 0.5 parts by weight of transfluthrin, 39.5 parts by weight of acetyltributyl citrate, 39.5 parts by weight of isononyl adipate, 5 parts by weight of blue pigment, and 5 parts by weight of fragrance into an electric mat substrate (a fibrous carrier made of pulp and cotton linters) measuring 2.1 cm x 3.4 cm and 0.22 cm thick.

[0041] Manufacturing Example 4 (Matte Formulation 2) An electric mosquito repellent mat formulation of the present invention was prepared by dissolving 8 mg of 1,4-dibutylaminoanthraquinone and 40 mg of 1,8-bis(phenylthio)dodecahydroanthraquinone in 5 g of a solution consisting of 20.0 wt % natural pyrethrins, 1.0 wt % metofluthrin, 10 wt % dibutylhydroxytoluene, 25 wt % diisononyl adipate, 30 wt % tributyl acetate citrate, and 14.0 wt % isoparaffin solvent (manufactured by Showa Shell Sekiyu K.K., trade name: Merveille 40), and uniformly impregnating 120 mg of the solution into an electric mat substrate (a fibrous carrier made of pulp and cotton linters) measuring 2.2 cm x 3.5 cm and 0.28 cm thick.

[0042] Manufacturing Example 5 (Matte Formulation 3) An electric mosquito repellent mat formulation of the present invention is prepared by dissolving 8 mg of 1,4-dibutylaminoanthraquinone and 40 mg of 1,8-bis(phenylthio)dodecahydroanthraquinone in 5 g of a solution consisting of 50.0 wt % natural pyrethrins, 0.25 wt % metofluthrin, 15 wt % dibutylhydroxytoluene, 4.75 wt % diisononyl adipate, 20 wt % tributyl acetate citrate, and 10 wt % isoparaffin solvent (manufactured by Showa Shell Sekiyu K.K., trade name: Merveille 40), and uniformly impregnating 500 mg of the solution into an electric mat substrate (a fibrous carrier made of pulp and cotton linters) measuring 2.2 cm x 3.5 cm and 0.28 cm thick.

[0043] Manufacturing Example 6 (Matte Formulation 4) An electric mosquito repellent mat formulation of the present invention is prepared by dissolving 8 mg of 1,4-dibutylaminoanthraquinone and 40 mg of 1,8-bis(phenylthio)dodecahydroanthraquinone in 5 g of a solution consisting of 50.0 wt % natural pyrethrins, 0.25 wt % metofluthrin, 15 wt % dibutylhydroxytoluene, 4.75 wt % diisononyl adipate, 20 wt % tributyl acetate citrate, and 10 wt % isoparaffin solvent (manufactured by Showa Shell Sekiyu K.K., trade name: Merveille 40). 2,000 mg of the solution is uniformly impregnated into an electric mat substrate (a fibrous carrier made of pulp and cotton linters) measuring 2.2 cm x 3.5 cm and 0.28 cm thick.

[0044] Production Example 7 (Pest Control Formulation 1 for Heat Vaporization) 2.0 parts by weight of natural pyrethrin, 0.1 parts by weight of metofluthrin, 9.965 parts by weight of IP Solvent 2028 (Idemitsu Kosan Co., Ltd., 50% distillation temperature approximately 233°C) and Soinglub N-15 (ENEOS Corporation, 50% distillation temperature approximately 265°C) were mixed to make 100 parts by weight, and the resulting solution was filled into a 45 mL plastic container. A porous liquid-absorbing wick whose top could be heated with a heater was inserted via the inner stopper, thereby preparing the pest control formulation for thermal evaporation of the present invention.

[0045] Production Example 8 (Pest Control Formulation 2 for Heat Vaporization) 10.5 parts by weight of natural pyrethrin and 0.5 parts by weight of metofluthrin are mixed and dissolved in 89 parts by weight of deodorized kerosene, and the resulting solution is filled into a 45 mL polyvinyl chloride container. A porous liquid-absorbing wick (made by solidifying inorganic powder with a binder and sintering it) whose top can be heated with a heater is inserted through the inner stopper to prepare the thermal evaporation pest control formulation of the present invention.

[0046] Production Example 9 (thermal vaporization pest control formulation 3) 10.5 parts by weight of natural pyrethrin and 0.5 parts by weight of metofluthrin are mixed and dissolved in 50 parts of diethylene glycol monobutyl ether, 1.8 parts of dibutylhydroxytoluene, and 46.7 parts of water, and the resulting solution is filled into a 45 mL plastic container. A porous liquid-absorbing wick whose top can be heated with a heater is inserted via an inner stopper to prepare the pest control formulation for thermal evaporation of the present invention.

[0047] The effects of the present invention will be demonstrated below by test examples.

[0048] Preparation of test preparations (incense sticks) 75 parts by weight of wood flour, 5 parts by weight of tabu flour, 5 parts by weight of lees flour, 10 parts by weight of Siamese flour, and 5 parts by weight of tapioca starch were mixed, and an appropriate amount of water was added and thoroughly kneaded. The kneaded mixture was formed into a sheet, punched into a spiral shape, and then dried until the moisture content was about 7 to 10% by weight to produce blank incense sticks. A test formulation was prepared by dropping an acetone solution of the test compound diluted to a predetermined concentration onto the blank incense sticks obtained and air-drying the mixture.

[0049] Test Example 1 Twenty adult female Culex pipiens pallens were placed in a 4.5cm diameter, 12cm tall glass tube, and the top and bottom openings of the tube were secured with 16-mesh nylon netting using rubber bands to confine the tube. A 22cm diameter, 83cm tall metal tube was placed upright, and two of the glass tubes containing the Culex pipiens pallens were placed upright and secured to the top openings. The formulation prepared using the above method was ignited and placed in the bottom opening of the metal tube. The number of Culex pipiens knocked down was recorded after 6 minutes. The experiment was repeated three times to determine the knockdown rate (hereafter abbreviated as KD rate). In addition, the expected KD rates when natural pyrethrins and each pyrethroid compound are mixed are calculated from the KD rates when they are used alone using Colby's formula, and are shown as expected values ​​in Table 1. The concentration of natural pyrethrins indicates the concentration of the active ingredient in natural pyrethrins. Theoretical expectation based on Colby's formula (%) = A+(100-A)×B / 100 In the above formula, A and B represent the following numbers: A: KD rate (%) when only A is treated B: KD rate (%) when only B is treated

[0050] [Table 1]

[0051] Test Example 2 Twenty adult female Culex pipiens pallens were placed in a 4.5cm diameter, 12cm tall glass tube, and the top and bottom openings of the tube were secured with 16-mesh nylon netting using rubber bands to confine the tube. A 22cm diameter, 83cm tall metal tube was placed upright, and two of the glass tubes containing the Culex pipiens pallens were placed upright and secured to the top opening. The formulation prepared using the above method was ignited and placed in the bottom opening of the metal tube. The number of Culex pipiens knocked down (KD) was recorded after 7 minutes. The experiment was repeated three times to determine the KD rate. In addition, the KD rates expected from the KD rates when natural pyrethrins and each pyrethroid compound are used alone are calculated using Colby's formula and are also shown as expected values ​​in Table 2 below.

[0052] [Table 2]

[0053] Test Example 3 Twenty adult female Culex pipiens pallens (Culex pipiens pallens) were placed in a 4.5 cm diameter, 12 cm tall glass tube, and the top and bottom openings of the tube were sealed with 16-mesh nylon netting secured with rubber bands. A 22 cm diameter, 83 cm tall metal tube was placed upright, and two of the glass tubes containing the mosquitoes were placed upright and secured to the top openings. The formulation prepared by the above method was ignited and placed in the bottom opening of the metal tube. The number of knocked-down (KD) mosquitoes was recorded after 10 minutes. The experiment was repeated three times to determine the KD rate. The expected KD rates based on the KD rates for natural pyrethrins and each pyrethroid compound used alone were calculated using Colby's formula and are shown in Table 3 below.

[0054] [Table 3]

[0055] As shown in Test Examples 1 to 3, the incense sticks of the present invention, which contain natural pyrethrins and each pyrethroid compound in a predetermined mixing ratio, were shown to exhibit effects greater than those expected from the effects of natural pyrethrins or each pyrethroid compound alone.

[0056] Test Example 4 Twenty adult female Culex pipiens pallens mosquitoes were placed in a 4.5 cm diameter, 12 cm tall glass tube, and the top and bottom openings of the tube were sealed with 16-mesh nylon netting secured with rubber bands. A 22 cm diameter, 83 cm tall metal tube was placed upright, and two glass tubes containing the Culex pipiens mosquitoes were placed upright and secured to the upper openings. The mat formulation of the present invention was prepared according to Formulation Example 3 or 4. The mat formulation was placed in a commercially available insecticidal mat heater, placed at the lower opening of the metal tube, and heated. After 10 minutes, the number of Culex pipiens mosquitoes knocked down (KD) was recorded and the KD rate was calculated. It was confirmed that the mat formulation of the present invention, which contains natural pyrethrins and various pyrethroid compounds in a specified mixture ratio, exhibits greater efficacy than would be expected from the effects of natural pyrethrins or various pyrethroid compounds alone. Examples of compositions for thermal evaporation used in matte formulations that have been confirmed to be highly effective in this test example include the compositions for thermal evaporation shown in Table 4 below.

[0057] [Table 4]

[0058] Test Example 4 confirms that the mat preparation of the present invention, which contains natural pyrethrins and each pyrethroid compound in a predetermined mixing ratio, exhibits an effect greater than that expected from the effect of natural pyrethrins or each pyrethroid compound alone.

[0059] Test Example 5 Twenty adult female Culex pipiens pallens mosquitoes were placed in a 4.5 cm diameter, 12 cm tall glass tube, and the top and bottom openings of the tube were sealed with 16-mesh nylon netting secured with rubber bands. A 22 cm diameter, 83 cm tall metal tube was placed upright, and two of the glass tubes containing the Culex pipiens mosquitoes were placed upright and secured to the upper openings. A thermal vaporization insecticide formulation of the present invention was prepared according to Formulation Example 7, 8, or 9. The thermal vaporization insecticide formulation was placed in the thermal vaporization insecticide device shown in Figure 1, placed at the lower opening of the metal tube, and heated. After 10 minutes, the number of knocked-down (KD) Culex pipiens mosquitoes was recorded to determine the KD rate. It has been confirmed that the pest control formulation for thermal evaporation of the present invention, which contains natural pyrethrins and each pyrethroid compound in a predetermined mixing ratio, exhibits an effect greater than that expected from the effect exhibited by either natural pyrethrins or each pyrethroid compound alone. Examples of compositions for thermal evaporation used in pest control formulations for thermal evaporation that have been confirmed to be highly effective in this test example include the compositions for thermal evaporation shown in Table 5 below.

[0060] [Table 5]

[0061] Test Example 5 confirms that the pest control formulation for thermal evaporation of the present invention, which contains natural pyrethrins and each pyrethroid compound in a predetermined mixing ratio, exhibits a higher effect than would be expected from the effect of natural pyrethrins or each pyrethroid compound alone. [Industrial Applicability]

[0062] By using the composition for heating and evaporation of the present invention, harmful arthropods can be controlled.

Claims

1. It contains natural pyrethrins and pyrethroid compounds, and the weight ratio of the active ingredient of the natural pyrethrins to the pyrethroid compounds is in the range of 20:1 to 200:1, A composition for thermal evaporation, characterized in that the pyrethroid compound is a pyrethroid compound having a vapor pressure of 0.00001 Pa to 0.1 Pa at 25°C.

2. 2. The composition for heating and evaporation according to claim 1, wherein the pyrethroid compound is at least one pyrethroid compound selected from the group consisting of metofluthrin, dimefluthrin, transfluthrin, profluthrin, mepafluthrin, heptafluthrin, tetramethylfluthrin, and lenofluthrin.

3. An incense stick comprising the composition of claim 1.

4. A method for controlling mosquitoes, which uses the composition or incense according to any one of claims 1 to 3.

5. A matting formulation comprising the composition of claim 1.

6. A method for controlling mosquitoes, which uses the composition or mat preparation according to any one of claims 1 to 2 and claim 5.

7. A pest control formulation for thermal vaporization, comprising the composition according to claim 1.

8. A method for exterminating mosquitoes, which uses the composition or the pest control formulation for thermal evaporation according to any one of claims 1 to 2 and claim 7.

Citation Information

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