JPH08208413A - Aerosolagent for controlling interior mite - Google Patents
Aerosolagent for controlling interior miteInfo
- Publication number
- JPH08208413A JPH08208413A JP7272306A JP27230695A JPH08208413A JP H08208413 A JPH08208413 A JP H08208413A JP 7272306 A JP7272306 A JP 7272306A JP 27230695 A JP27230695 A JP 27230695A JP H08208413 A JPH08208413 A JP H08208413A
- Authority
- JP
- Japan
- Prior art keywords
- mites
- permethrin
- ene
- ethylhexyl
- mite
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 150000001875 compounds Chemical class 0.000 claims abstract description 22
- SESFRYSPDFLNCH-UHFFFAOYSA-N benzyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OCC1=CC=CC=C1 SESFRYSPDFLNCH-UHFFFAOYSA-N 0.000 claims abstract description 14
- RLLPVAHGXHCWKJ-UHFFFAOYSA-N permethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 RLLPVAHGXHCWKJ-UHFFFAOYSA-N 0.000 claims abstract description 14
- 229960000490 permethrin Drugs 0.000 claims abstract description 14
- 239000000443 aerosol Substances 0.000 claims abstract description 11
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims abstract description 8
- 229960002903 benzyl benzoate Drugs 0.000 claims abstract description 7
- 239000004480 active ingredient Substances 0.000 claims abstract description 6
- LNJXZKBHJZAIKQ-UHFFFAOYSA-N 1,1,1,2-tetrachloro-3-(2,3,3,3-tetrachloropropoxy)propane Chemical compound ClC(Cl)(Cl)C(Cl)COCC(Cl)C(Cl)(Cl)Cl LNJXZKBHJZAIKQ-UHFFFAOYSA-N 0.000 claims abstract description 4
- GNEPLYVYORHREW-UHFFFAOYSA-N 1,1,3,3,6-pentamethyl-7-nitro-2h-inden-5-amine Chemical compound CC1=C(N)C=C2C(C)(C)CC(C)(C)C2=C1[N+]([O-])=O GNEPLYVYORHREW-UHFFFAOYSA-N 0.000 claims abstract description 4
- FIPWRIJSWJWJAI-UHFFFAOYSA-N Butyl carbitol 6-propylpiperonyl ether Chemical compound C1=C(CCC)C(COCCOCCOCCCC)=CC2=C1OCO2 FIPWRIJSWJWJAI-UHFFFAOYSA-N 0.000 claims abstract description 4
- 229960005235 piperonyl butoxide Drugs 0.000 claims abstract description 4
- MMOXZBCLCQITDF-UHFFFAOYSA-N N,N-diethyl-m-toluamide Chemical compound CCN(CC)C(=O)C1=CC=CC(C)=C1 MMOXZBCLCQITDF-UHFFFAOYSA-N 0.000 claims abstract description 3
- -1 2-ethylhexyl Chemical group 0.000 claims description 4
- MVKYQJHRHHQPDM-UHFFFAOYSA-N synepirin 500 Chemical compound C1CC2(C)C3C(=O)N(CC(CC)CCCC)C(=O)C3C1(C(C)C)C=C2 MVKYQJHRHHQPDM-UHFFFAOYSA-N 0.000 claims 1
- 241000238876 Acari Species 0.000 abstract description 36
- 239000003795 chemical substances by application Substances 0.000 abstract description 13
- 239000000203 mixture Substances 0.000 description 17
- 230000000895 acaricidal effect Effects 0.000 description 13
- 239000002728 pyrethroid Substances 0.000 description 12
- VEMKTZHHVJILDY-UXHICEINSA-N bioresmethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-UXHICEINSA-N 0.000 description 11
- 241000607479 Yersinia pestis Species 0.000 description 9
- 241000238713 Dermatophagoides farinae Species 0.000 description 8
- 230000000694 effects Effects 0.000 description 8
- 239000005871 repellent Substances 0.000 description 8
- 230000002940 repellent Effects 0.000 description 8
- 229960003536 phenothrin Drugs 0.000 description 7
- SBNFWQZLDJGRLK-RTWAWAEBSA-N (1R)-trans-phenothrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 SBNFWQZLDJGRLK-RTWAWAEBSA-N 0.000 description 6
- 239000000428 dust Substances 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- 239000000642 acaricide Substances 0.000 description 5
- 239000002253 acid Substances 0.000 description 5
- 230000000749 insecticidal effect Effects 0.000 description 5
- 229940108410 resmethrin Drugs 0.000 description 5
- VEMKTZHHVJILDY-FIWHBWSRSA-N resmethrin Chemical compound CC1(C)[C@H](C=C(C)C)C1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-FIWHBWSRSA-N 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 229940126062 Compound A Drugs 0.000 description 4
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 4
- 239000003350 kerosene Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- 241000255925 Diptera Species 0.000 description 3
- 241000196324 Embryophyta Species 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 235000019441 ethanol Nutrition 0.000 description 3
- 239000002917 insecticide Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000004563 wettable powder Substances 0.000 description 3
- QPUYECUOLPXSFR-UHFFFAOYSA-N 1-methylnaphthalene Chemical compound C1=CC=C2C(C)=CC=CC2=C1 QPUYECUOLPXSFR-UHFFFAOYSA-N 0.000 description 2
- 241000238631 Hexapoda Species 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- 241000488581 Panonychus citri Species 0.000 description 2
- 241001454295 Tetranychidae Species 0.000 description 2
- ZVQOOHYFBIDMTQ-UHFFFAOYSA-N [methyl(oxido){1-[6-(trifluoromethyl)pyridin-3-yl]ethyl}-lambda(6)-sulfanylidene]cyanamide Chemical compound N#CN=S(C)(=O)C(C)C1=CC=C(C(F)(F)F)N=C1 ZVQOOHYFBIDMTQ-UHFFFAOYSA-N 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 238000013329 compounding Methods 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- FHIVAFMUCKRCQO-UHFFFAOYSA-N diazinon Chemical compound CCOP(=S)(OCC)OC1=CC(C)=NC(C(C)C)=N1 FHIVAFMUCKRCQO-UHFFFAOYSA-N 0.000 description 2
- 235000005911 diet Nutrition 0.000 description 2
- 230000037213 diet Effects 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- ZNOLGFHPUIJIMJ-UHFFFAOYSA-N fenitrothion Chemical compound COP(=S)(OC)OC1=CC=C([N+]([O-])=O)C(C)=C1 ZNOLGFHPUIJIMJ-UHFFFAOYSA-N 0.000 description 2
- 230000005764 inhibitory process Effects 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 230000001850 reproductive effect Effects 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- RELMFMZEBKVZJC-UHFFFAOYSA-N 1,2,3-trichlorobenzene Chemical compound ClC1=CC=CC(Cl)=C1Cl RELMFMZEBKVZJC-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- LDMOEFOXLIZJOW-UHFFFAOYSA-N 1-dodecanesulfonic acid Chemical compound CCCCCCCCCCCCS(O)(=O)=O LDMOEFOXLIZJOW-UHFFFAOYSA-N 0.000 description 1
- SFHVXKNMCGSLAR-UHFFFAOYSA-N 2,2,3,3-tetramethylcyclopropanecarboxylic acid Chemical compound CC1(C)C(C(O)=O)C1(C)C SFHVXKNMCGSLAR-UHFFFAOYSA-N 0.000 description 1
- JVGPVVUTUMQJKL-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethyl thiocyanate Chemical compound CCCCOCCOCCSC#N JVGPVVUTUMQJKL-UHFFFAOYSA-N 0.000 description 1
- XXUNIGZDNWWYED-UHFFFAOYSA-N 2-methylbenzamide Chemical compound CC1=CC=CC=C1C(N)=O XXUNIGZDNWWYED-UHFFFAOYSA-N 0.000 description 1
- MDDVEUPIZIKAJU-UHFFFAOYSA-N 3-methyl-4-pent-2-enylpyrrolidine-2,5-dione Chemical compound CCC=CCC1C(C)C(=O)NC1=O MDDVEUPIZIKAJU-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 241000239290 Araneae Species 0.000 description 1
- AUBVWVOTOYCWPE-UHFFFAOYSA-N CCCCCC(CC)C(C1)(C2C(N3)=O)C=CC1C2C3=O Chemical compound CCCCCC(CC)C(C1)(C2C(N3)=O)C=CC1C2C3=O AUBVWVOTOYCWPE-UHFFFAOYSA-N 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 241000254173 Coleoptera Species 0.000 description 1
- 241000238710 Dermatophagoides Species 0.000 description 1
- 241000851181 Eutetranychus orientalis Species 0.000 description 1
- 208000010201 Exanthema Diseases 0.000 description 1
- 206010061217 Infestation Diseases 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- WLLGXSLBOPFWQV-UHFFFAOYSA-N MGK 264 Chemical compound C1=CC2CC1C1C2C(=O)N(CC(CC)CCCC)C1=O WLLGXSLBOPFWQV-UHFFFAOYSA-N 0.000 description 1
- VCUFZILGIRCDQQ-KRWDZBQOSA-N N-[[(5S)-2-oxo-3-(2-oxo-3H-1,3-benzoxazol-6-yl)-1,3-oxazolidin-5-yl]methyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C1O[C@H](CN1C1=CC2=C(NC(O2)=O)C=C1)CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F VCUFZILGIRCDQQ-KRWDZBQOSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 241000238711 Pyroglyphidae Species 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical class [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- 241000256856 Vespidae Species 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 125000003158 alcohol group Chemical group 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 201000009961 allergic asthma Diseases 0.000 description 1
- 208000026935 allergic disease Diseases 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 208000006673 asthma Diseases 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 201000005884 exanthem Diseases 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 230000009969 flowable effect Effects 0.000 description 1
- 235000013355 food flavoring agent Nutrition 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 239000003502 gasoline Substances 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 229940046533 house dust mites Drugs 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000012669 liquid formulation Substances 0.000 description 1
- 206010025482 malaise Diseases 0.000 description 1
- 230000010534 mechanism of action Effects 0.000 description 1
- 230000002503 metabolic effect Effects 0.000 description 1
- 230000003129 miticidal effect Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000000877 morphologic effect Effects 0.000 description 1
- 150000002826 nitrites Chemical class 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 230000003071 parasitic effect Effects 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000000644 propagated effect Effects 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 239000008213 purified water Substances 0.000 description 1
- 206010037844 rash Diseases 0.000 description 1
- 231100000046 skin rash Toxicity 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、パーメスリン、又
はパーメスリンとピレスロイド用共力剤及び害虫忌避剤
の1種又は2種とよりなるカーペット処理用の屋内ダニ
防除用エアゾール剤に関する。TECHNICAL FIELD The present invention relates to an aerosol agent for controlling indoor mites for carpet treatment, which comprises permethrin, or permethrin and one or two synergists for pyrethroids and pest repellents.
【0002】[0002]
【従来の技術】地球上には極めて多種のダニ類が生息
し、例えば植物に寄生するミカンハダニ、ナミハダニ類
等は、農作物に多大な被害を与えている。これら農業用
途を目的とした殺ダニ剤は古くから開発が進められ、最
近新しい有望な化合物が次々と発見されている。2. Description of the Related Art A great variety of mites live on the earth, and, for example, citrus red mite and spider mites parasitic on plants cause great damage to agricultural products. These acaricides for agricultural use have been developed for a long time, and recently new promising compounds have been discovered one after another.
【0003】[0003]
【発明が解決しようとする課題】一方、近年居住環境の
変化から家庭内に、コナダニ、チリダニ、ホコリダニ等
が発生し、不快感を与えるばかりでなく、アレルギー性
喘息や皮疹を惹起する等の問題を生じている。スミチオ
ンやダイアジノンのような有機リン剤がこれら屋内の発
生するダニ類に効果があることは知られていたが、人畜
に対する安全性や抵抗性問題のため実用化には障害があ
り、的確な駆除方法の確立が切望されるようになった。On the other hand, in recent years, due to changes in the living environment, house dust mites, dust mites, dust mites, etc. occur in the home, which not only causes discomfort, but also causes allergic asthma and skin rash. Is occurring. It was known that organophosphorus agents such as Sumithion and diazinon are effective against mites generated in these indoors, but there are obstacles to their practical use due to safety and resistance problems for humans and animals, and proper disinfection. The establishment of a method has been earnestly desired.
【0004】[0004]
【課題を解決するための手段】本発明者らは上記現状に
鑑み、屋内で安全に使用できる殺ダニ剤の開発を目的と
して鋭意研究を続けた結果、フェノトリン、パーメスリ
ン、レスメトリン及び3'−フエノキシベンジル 2,
2,3,3−テトラエチルシクロプロパンカルボキシレー
トの1種又は2種の化合物、又はこれにチオシアノ酢酸
イソボルニル(以降IBTAと称す)、オクタクロロジ
プロピルエーテル(以降S−421と称す)、ピペロニ
ルブトキサイド、N−2(−エチルヘキシル)−ビシクロ
[2,2,1]ヘプタ−5−エン−2,3−ジカルボキシイ
ミド(以降サイネピリン222と称す)、N−(2−エ
チルヘキシル)−1−イソプロピル−4−メチルビシク
ロ[2,2,2]オクト−5−エン−2,3−ジカルボキシ
イミド(以降サイネピリン500と称す)、2−ブトキ
シ−2'−チオシアノジエチルエーテル(以降リーセン
384と称す)のようなピレスロイド用共力剤、及び
N,N−ジエチル−m−トルアミド(以降ディートと称
す)、ベンジルベンゾエートのような害虫忌避剤の1種
又は2種を加えた組成物が、コナダニ、チリダニ、ホコ
リダニ等に極めて高し殺ダニ効果を示すことを見い出し
本発明を完成した。[Means for Solving the Problems] In view of the above situation, the inventors of the present invention have conducted extensive studies for the purpose of developing an acaricide that can be safely used indoors, and as a result, phenothrin, permethrin, resmethrin and 3'-fu Enoxybenzyl 2,
One or two compounds of 2,3,3-tetraethylcyclopropanecarboxylate, or isobornyl thiocyanoacetate (hereinafter referred to as IBTA), octachlorodipropyl ether (hereinafter referred to as S-421), piperonylbutane Toxide, N-2 (-ethylhexyl) -bicyclo
[2,2,1] hepta-5-ene-2,3-dicarboximide (hereinafter referred to as cinepyrine 222), N- (2-ethylhexyl) -1-isopropyl-4-methylbicyclo [2,2,2 ] A synergist for pyrethroids such as oct-5-ene-2,3-dicarboximide (hereinafter referred to as cinepyrine 500), 2-butoxy-2′-thiocyanodiethyl ether (hereinafter referred to as Resen 384), and A composition containing one or two pest repellents such as N, N-diethyl-m-toluamide (hereinafter referred to as diet) and benzylbenzoate is extremely effective against mites, dust mites, dust mites, etc. The present invention has been completed by finding that
【0005】本発明は、有効成分としてのパーメスリン
よりなる、あるいはパーメスリンとオクタクロロジプロ
ピルエーテル、N−(2−エチルヘキシル)−1−イソ
プロピル−4−メチルビシクロ[2,2,2]オクト−5
−エン−2,3−ジカルボキシイミド、N−(2−エチ
ルヘキシル)−ビシクロ[2,2,1]ヘプタ−5−エン
−2,3−ジカルボキシイミド、ピペロニルブトキサイ
ド、チオシアノ酢酸イソボルニル、2−ブトキシ−2’
−チオシアノエチルエーテル、N,N−ジエチル−m−
トルアミドおよびベンジルベンゾエートよりなる群から
選択される1種または2種の化合物とよりなるカーペッ
ト処理用の屋内ダニ防除用エアゾール剤を提供するもの
である。The present invention comprises permethrin as an active ingredient, or permethrin and octachlorodipropyl ether, N- (2-ethylhexyl) -1-isopropyl-4-methylbicyclo [2,2,2] oct-5.
-Ene-2,3-dicarboximide, N- (2-ethylhexyl) -bicyclo [2,2,1] hept-5-ene-2,3-dicarboximide, piperonyl butoxide, isobornyl thiocyanoacetate , 2-butoxy-2 '
-Thiocyanoethyl ether, N, N-diethyl-m-
The present invention provides an aerosol agent for controlling indoor mites for carpet treatment, which comprises one or two compounds selected from the group consisting of toluamide and benzylbenzoate.
【0006】[0006]
【発明の実施の態様】ところで、フェノトリン、パーメ
スリン、レスメトリン及び3'−フエノキシベンジル
2,2,3,3−テトラメチルシクロプロパンカルボキシ
レート(以後化合物Aと称す)のピレスロイドは高い殺
虫力と広い殺虫スペクトラムを有し、安全性の高い殺虫
剤として家庭用、農業用に広く使用されているものであ
るが、ミカンハダニ、ナミハダニ類に対する殺ダニ力は
極めて弱く、従来、ダニ類全般にその適用は困難とされ
ていた。しかるに本発明者らは、ミカンハダニ、ナミハ
ダニ等植物につくダニ類と、コナダニ、チリダニ等屋内
に発生するダニ類に生態的に何らかの差があるものと考
え、種々の化合物について、後者のダニ類に対する効果
を検討した結果、前記4種のピレスロイド(フェノトリ
ン、パーメスリン、レスメトリン及び化合物A)が屋内
に生育するダニ類に特異的に高い殺ダニ効力を有するこ
と、特にチリダニ類に対してはスミチオン、ダイアジノ
ンをしのぐ活性を有すること、そして最近殺ハダニ活性
が優れていると発表されたいくつかの新ピレスロイドが
必ずしも屋内に生育するダニ類に有効でないことを発見
した。更に、フェノトリン、パーメスリン及び化合物A
とアルコール部のベンジル位にシアノ基を導入した化合
物は、もとの化合物に較べ一般に殺虫力、殺ハダニ活性
は優れているのであるが、屋内に生育するダニ類に対し
ては逆に活性の低下を示すことが明らかとなった。これ
らの発見は従来の知見からは全く予期しえないものであ
り、又本発明の前記ピレスロイドが人畜に対して安全な
殺虫剤として広く実用に供されていることを考慮すれ
ば、屋内用殺ダニ剤の開発をめざすうえで極めて有用性
が高い。DETAILED DESCRIPTION OF THE INVENTION By the way, phenothrin, permethrin, resmethrin and 3'-phenoxybenzyl.
Pyrethroid of 2,2,3,3-tetramethylcyclopropanecarboxylate (hereinafter referred to as compound A) has high insecticidal activity and broad insecticidal spectrum, and is widely used as a highly safe insecticide for household and agricultural purposes. However, the acaricidal activity against citrus red mite and spider mites is extremely weak, and it has been conventionally difficult to apply it to mites in general. However, the present inventors believe that there are some ecological differences between mites attached to plants such as citrus mites, mitid mites, and mites that occur indoors such as mites, dust mites, and for various compounds, for the latter mites As a result of examining the effect, it was found that the above-mentioned four types of pyrethroids (phenothrin, permethrin, resmethrin and compound A) have a particularly high acaricidal effect on mites growing indoors, and especially for mites, sumithione and diazinon. It has been discovered that some of the new pyrethroids, which have recently been shown to be superior in spidericidal activity, are not always effective against mites growing indoors. Furthermore, phenothrin, permethrin and compound A
Compounds with a cyano group introduced at the benzyl position of the alcohol part are generally superior to the original compounds in insecticidal activity and acaricidal activity, but on the contrary, they are more active against mites growing indoors. It became clear that it showed a decrease. These findings are completely unexpected from conventional knowledge, and considering that the pyrethroid of the present invention is widely used as a safe insecticide for humans and animals, it can be killed indoors. It is extremely useful for the development of tick agents.
【0007】特に、カーペツト類に発生するコナヒョウ
ヒダニはアレルギー性疾患や人体内ダニ症の原因と目さ
れており、これらにピレスロイド化合物が有効であると
いう知見は、保健衛生上、医学上意義深い。なお、フェ
ノトリン、パーメスリン及びレスメトリンの酸部には2
つの不斉炭素が存在し、4つの光学異性体が可能である
が、それらの各々あるいは任意の混合物ももちろん本発
明に含まれる。[0007] In particular, it is thought that Dermatophagoides farinae which occurs in carpets is a cause of allergic diseases and sickness in the human body, and the finding that pyrethroid compounds are effective for these is significant in health and medical terms. It should be noted that 2 in the acid part of phenothrin, permethrin and resmethrin.
There are four asymmetric carbons and four optical isomers are possible, but each or any mixture thereof is of course included in the present invention.
【0008】又、IBTA、S−421、ピペロニルブ
トキサイド、サイネピリン222、サイネピリン50
0、リーセン384のようなピレスロイド用共力剤およ
びディート、ベンジルベンゾエートのような害虫忌避剤
にも程度の差はあれ、殺ダニ効果が認められ、更に本発
明と前記4種のピレスロイドの1種又は2種に、上記共
力剤および害虫忌忌避剤の1種又は2種を加えた組成物
が相加的以上の極めて高い殺ダニ効果を示すことが確認
された。IBTA, S-421, piperonyl butoxide, cinepyrine 222, cinepyrine 50
0, a synergist for pyrethroids such as Reisen 384 and pest repellents such as diet and benzyl benzoate, to some extent, a miticidal effect was observed, and further, the present invention and one of the four pyrethroids described above. Alternatively, it was confirmed that a composition obtained by adding one or two of the above synergists and pest repellents to the two kinds exhibits an extremely high acaricidal effect which is additive or higher.
【0009】前記4種のピレスロイドが屋内に発生する
コナダニ、チリダニ類に特異的に駆除効果が高い理由に
ついてはなお不明な点が多いが、この種のダニが無気門
類に属し、一方植物につくハダニ類が前気門類であると
いう形態上の違いが一部関連しているものと考えられ
る。ピレスロイド用共力剤は、それ自体殺虫力はなく、
ピレスロイドと共に用いられた時、昆虫体内におけるピ
レスロイドの代謝分解を抑えてその殺虫力を向上させる
ことが知られているが、屋内に発生するダニ類に対して
はそれ自体若干もしくはかなりの殺ダニ力を示し、昆虫
とダニ類における作用機作の違いを示唆している。又、
ピレスロイドとピレスロイド用共力剤の混合物が高い相
乗効果を示すことは、後者が非常に安価であることから
実用上の価値が高い。デイート、ベンジルベンゾエート
は蚊、ハエ等の忌避剤として広く実用に供されている化
合物であるが、殺ダニ効果を示したことは興味深く、こ
れを含む本発明組成物は、不快害虫の忌避、ダニ類の駆
除を含めた多目的組成物として使用できる。There are many unclear points as to why the above-mentioned four kinds of pyrethroids have a high specific exterminating effect on the mites and dust mites that occur indoors. It is considered that the morphological difference that the phytoseiid mites are pre-Amphitates are related in part. Pyrethroid synergists have no insecticidal power themselves,
When used together with pyrethroids, it is known to suppress the metabolic decomposition of pyrethroids in insects and improve their insecticidal activity, but it itself has some or considerable acaricidal activity against mites that occur indoors. , Suggesting a difference in mechanism of action between insects and mites. or,
The high synergistic effect of the mixture of pyrethroid and synergist for pyrethroid has high practical value because the latter is very cheap. Although date and benzyl benzoate are compounds that have been widely put to practical use as repellents for mosquitoes, flies, etc., it is interesting that they showed an acaricidal effect, and the composition of the present invention containing them is repellent of unpleasant pests and mites. It can be used as a multipurpose composition including the extermination of genus.
【0010】本発明の殺ダニ剤は上記有効成分をそのま
ま適用することも可能であるが、通常好ましくは適当な
担体その他の配合剤を用いて、使用目的に応じ、各種の
液剤(ここで液剤とは、水溶状、乳化状、もしくは懸濁
状を呈する液状の製剤を意味し、乳剤、水和剤、油剤、
フロアブル剤、水溶剤等を含む)やエアゾール剤として
使用される。液状の担体としては例えば、水、アルコー
ル類(メチルアルコール、エチルアルコール、エチレン
グライコール等)、ケトン類(アセトン、メチルエチル
ケトン、シクロヘキサノン等)、エーテル類(エチルエ
ーテル、ジオキサン、セロソルブ類等)、脂肪族炭化水
素類(ガソリン、ケロシン、灯油類等)、芳香族炭化水
素類(ベンゼン、トルエン、キシレン、メチルナフタレ
ン等)、ハロゲン化炭化水素類(ジクロルメタン、トリ
クロルベンゼン等)、エステル類、酸アミド類、ニトリ
ル類などの溶媒が適当であり、そしてこれらの1種また
は2種以上の混合物が使用される。また、固体の担体と
しては、例えば粘土類(カオリン、ベントナイト等)、
タルク類、シリカ類、アルミナ粉末、活性炭類、植物性
粉末等が適当であり、そしてこれらの1種または2種以
上の混合物が使用される。また、配合剤としては乳化
剤、分散剤、展着剤、浸透剤、界面活性剤、安定剤等が
適当であり、これらの1種又は2種以上の混合物が使用
される。Although the above-mentioned active ingredients can be applied as they are to the acaricide of the present invention, it is usually preferable to use various carriers (wherein the liquid formulation is used here) according to the purpose of use by using a suitable carrier and other compounding agents. The term, means a liquid preparation having a water-soluble form, an emulsified form, or a suspension form, an emulsion, a wettable powder, an oil formulation,
It is used as a flowable agent, water solvent, etc.) and an aerosol agent. Examples of the liquid carrier include water, alcohols (methyl alcohol, ethyl alcohol, ethylene glycol etc.), ketones (acetone, methyl ethyl ketone, cyclohexanone etc.), ethers (ethyl ether, dioxane, cellosolves etc.), aliphatic Hydrocarbons (gasoline, kerosene, kerosene, etc.), aromatic hydrocarbons (benzene, toluene, xylene, methylnaphthalene, etc.), halogenated hydrocarbons (dichloromethane, trichlorobenzene, etc.), esters, acid amides, Solvents such as nitrites are suitable, and one or a mixture of two or more thereof is used. Examples of solid carriers include clays (kaolin, bentonite, etc.),
Talcs, silicas, alumina powders, activated carbons, vegetable powders and the like are suitable, and one or a mixture of two or more thereof is used. Suitable compounding agents include emulsifiers, dispersants, spreading agents, penetrants, surfactants, stabilizers, etc., and one or a mixture of two or more of these is used.
【0011】あるいはまた、本発明有効成分の活性を阻
害する惧れのない他の殺ダニ剤、酸化防止剤、殺虫剤、
殺菌剤、防黴剤、着香料、着色料を配合してもよい。Alternatively, other acaricides, antioxidants, insecticides, which are not likely to inhibit the activity of the active ingredient of the present invention,
You may mix | blend a bactericide, a fungicide, a flavoring agent, and a coloring agent.
【0012】本発明殺ダニ剤中の有効成分量及びその使
用量はその剤型や適用対象、適用方法、適用場所等に応
じて適宜決定される。例えばコナダニ等畳に生息するダ
ニの駆除には1畳あたり、0.1mg以上好ましくは1mg
〜2gの前記ピレスロイド化合物が使用される。なお畳
にはシバンムシ類やアリガタバチ類等の害虫が生息して
いるが、本発明組成物はこれらの害虫をも同時に駆除で
きうるものである。また、カーペツト類に生息するコナ
ヒョウヒダニ類等の駆除には1m2あたり0.5mg〜2g
のピレスロイド化合物が適用されるのが好ましい。The amount of the active ingredient in the acaricide of the present invention and the amount thereof used are appropriately determined depending on the dosage form, application target, application method, application site and the like. For example, to control mites that live in tatami mats such as mites, 0.1 mg or more per 1 tatami, preferably 1 mg
~ 2g of the pyrethroid compound is used. The tatami mats are infested with pests such as beetles and wasps, and the composition of the present invention can also control these pests at the same time. In addition, 0.5 mg to 2 g per 1 m 2 is used for extermination of Dermatophagoides farinae which inhabit the carpets.
It is preferred that the pyrethroid compound of is applied.
【0013】[0013]
【実施例】以下、実施例により本発明を更に詳細に説明
するが、本発明はその要旨を越えない限り以下の例に限
定されるものではない。The present invention will be described in more detail with reference to the following examples, but the present invention is not limited to the following examples as long as the gist thereof is not exceeded.
【0014】試験例 1 供試化合物で処理した粉末飼料10gと約2500匹の
ケナガコナダニを含む粉末飼料10gを混和し、所定濃
度の供試粉末飼料を得た。この粉末飼料を5gずつ直径
6cmのシャーレに入れ、温度25℃、湿度75%の条件
下に置いた。1週間後及び2週間後に飽和食塩水浮遊法
により飼料0.2g中の生存ダニ数を調べ、下式に従っ
て繁殖抑制率を計算した。試験は各濃度につき3回繰返
し行った。Test Example 1 10 g of the powdered feed treated with the test compound and 10 g of the powdered feed containing about 2500 mosquito mites were mixed to obtain a test powdered feed having a predetermined concentration. 5 g of each of the powdered feeds was placed in a petri dish having a diameter of 6 cm and placed under the conditions of a temperature of 25 ° C. and a humidity of 75%. After 1 week and 2 weeks, the number of living mites in 0.2 g of the feed was examined by the saturated saline floating method, and the reproductive inhibition rate was calculated according to the following formula. The test was repeated 3 times for each concentration.
【0015】[0015]
【数1】 [Equation 1]
【0016】なお、供試化合物、ピレスロイド中の符号
(a)、(b)、(c)、(d)はそれぞれ下記の意味を表す。 (a) ;酸部dl−cis/trans体 (b) ;酸部d−cis/trans体 (c) ;酸部dl−cis体 (d) ;酸部d−trans体The symbols in the test compounds and pyrethroids
(a), (b), (c) and (d) have the following meanings. (a); Acid part dl-cis / trans form (b); Acid part d-cis / trans form (c); Acid part dl-cis form (d); Acid part d-trans form
【0017】[0017]
【表1】 [Table 1]
【0018】[0018]
【化1】 Embedded image
【0019】上記結果より、本発明組成物すなわち、フ
ェノトリン、パーメスリン、レスメトリン及び化合物A
の1種又は2種の化合物、又はこれにピレスロイド用共
力剤及び害虫忌避剤の1種又は2種を加えた組成物(供
試化合物例1〜7)はすぐれた殺ダニ効果を示した。一
方他のピレスロイド系化合物(対照化合物(A)、(B)、
(C))及び、ピレスロイド用共力剤又は害虫忌避剤単独
の活性は非常に低く、本発明組成物の有用性が確認され
た。From the above results, the composition of the present invention, namely phenothrin, permethrin, resmethrin and compound A
The composition (test compound examples 1 to 7) containing one or two compounds of the above, or one or two synergists for pyrethroids and pest repellents showed excellent acaricidal effect. . On the other hand, other pyrethroid compounds (control compounds (A), (B),
The activity of (C)) and the synergist for pyrethroid or the pest repellent alone is very low, confirming the usefulness of the composition of the present invention.
【0020】試験例 2 供試化合物で処理した粉末飼料10gと、約1500匹
のコナヒョウヒダニを含む粉末飼料10gを混和し、所
定濃度の供試粉末飼料を得た。この粉末飼料5gを用い
て試験例1と同様に試験し、1週間後及び2週間後の繁
殖抑制率を求めた。Test Example 2 10 g of the powdered feed treated with the test compound and 10 g of the powdered feed containing about 1500 Dermatophagoides farinae were mixed to obtain a test powdered feed having a predetermined concentration. The same test as in Test Example 1 was carried out using 5 g of this powdered feed, and the rate of reproductive inhibition after 1 week and 2 weeks was determined.
【0021】なお、供試ピレスロイド中の符号(a)、
(b)、(c)、(d)は試験例1と同様の意味を表し、対照化
合物(D)は次の化合物を示す。The symbols (a) in the sample pyrethroid,
(b), (c) and (d) have the same meanings as in Test Example 1, and the control compound (D) is the following compound.
【0022】[0022]
【化2】 Embedded image
【0023】[0023]
【表2】 [Table 2]
【0024】上記結果より、本発明組成物は、コナヒョ
ウヒダニに対し、従来有効であるとされた有機リン剤の
スミチオンより高い殺ダニ効果を示した。又、対照化合
物(D)は殺ハダニ活性の高い新規ピレスロイドとして紹
介されているものであるが、コナヒョウヒダニに対する
活性は低く、植物につくダニ類と屋内に発生するダニ類
の生態的な差が示唆された。From the above results, the composition of the present invention showed a higher acaricidal effect on the mites of Dermatophagoides farinae than the organic phosphorus agent Sumithion, which has been considered to be conventionally effective. The control compound (D) was introduced as a new pyrethroid with high spider mitericidal activity, but its activity against Dermatophagoides farinae was low, suggesting an ecological difference between mites attached to plants and mites occurring indoors. Was done.
【0025】実施例 1 d−フェノトリン2.0g、IBTA5.0gを精製灯油
に溶解し、エアゾール容器に充填しバルブ部分を取り付
けた後、該バルブ部分を通じて噴射剤を加圧充填してエ
アゾールを得た。ケナガコナダニが繁殖した6畳の部屋
で、上記調製エアゾールを約1/4量畳に内部注入し、
1週間後のコナダニの生息密度を調べたところ5%以上
に減少していた。また、精製灯油の代わりにエタノール
を用いて調製したエアゾールをコナヒョウヒダニの繁殖
が認められたカーペットに処理した場合も同様に高い駆
除効果が得られた。Example 1 d-phenothrin (2.0 g) and IBTA (5.0 g) were dissolved in refined kerosene, filled into an aerosol container and fitted with a valve portion, and then a propellant was filled under pressure through the valve portion to obtain an aerosol. It was In a room of 6 tatami mats, in which the mite mite was propagated, the above-mentioned prepared aerosol was infused internally into about 1/4 tatami mat,
When the population density of mites was examined one week later, it was reduced to 5% or more. Similarly, when the aerosol prepared by using ethanol instead of refined kerosene was treated on the carpet in which the reproduction of Dermatophagoides farinae was observed, the same high exterminating effect was obtained.
【0026】実施例 2 パーメスリン5部、ベンジルベンゾエート5部に、ソル
ポールSM−100(東邦化学登録商標名)15部、精
製水75部を加え、水性乳剤を得た。この乳剤を水で5
00倍に希釈し、基布m2あたり100gを処理した
後、乾燥して得られたカーペツトに、コナヒョウヒダニ
約300匹を放ち、2日後に生存コナヒョウヒダニ数を
調査したところ5匹以下であった。Example 2 To 5 parts of permethrin and 5 parts of benzyl benzoate, 15 parts of Solpol SM-100 (registered trademark of Toho Kagaku) and 75 parts of purified water were added to obtain an aqueous emulsion. 5 times this emulsion with water
After diluting to 00 times and treating 100 g per m 2 of the base fabric, about 300 pieces of Dermatophagoides farinae were released on the carpet obtained by drying, and the number of surviving Dermatophagoides faridae was examined 2 days later and it was 5 or less.
【0027】実施例 3 dl−シス−フェノトリン10部、IBTA20部、硅藻
土35部、クレー30部、ラウリルスルホン酸塩3部、
カルボキシメチルセルロース2部を粉砕混合して水和剤
を得た。この水和剤を水で1000倍に希釈し、カーペ
ツトの表面に100g/m2あたり処理した。乾燥後、
このカーペツトを使用したが、ヒョウヒダニ類の生息を
認めず、また異臭等の問題もなかった。Example 3 10 parts of dl-cis-phenothrin, 20 parts of IBTA, 35 parts of diatomaceous earth, 30 parts of clay, 3 parts of lauryl sulfonate,
A wettable powder was obtained by pulverizing and mixing 2 parts of carboxymethyl cellulose. This wettable powder was diluted 1000 times with water and treated on the surface of a carpet at 100 g / m 2 . After drying
This carpet was used, but no infestation of Dermatophagoides farinae was observed, and there was no problem such as an offensive odor.
【0028】[0028]
【発明の効果】本発明により、屋内ダニ防除に優れたエ
アゾール剤が提供される。INDUSTRIAL APPLICABILITY The present invention provides an aerosol agent excellent in controlling indoor mites.
Claims (1)
る、あるいはパーメスリンとオクタクロロジプロピルエ
ーテル、N−(2−エチルヘキシル)−1−イソプロピ
ル−4−メチルビシクロ[2,2,2]オクト−5−エン
−2,3−ジカルボキシイミド、N−(2−エチルヘキ
シル)−ビシクロ[2,2,1]ヘプタ−5−エン−2,
3−ジカルボキシイミド、ピペロニルブトキサイド、チ
オシアノ酢酸イソボルニル、2−ブトキシ−2’−チオ
シアノエチルエーテル、N,N−ジエチル−m−トルア
ミドおよびベンジルベンゾエートよりなる群から選択さ
れる1種または2種の化合物とよりなるカーペット処理
用の屋内ダニ防除用エアゾール剤。1. Permethrin as an active ingredient, or permethrin and octachlorodipropyl ether, N- (2-ethylhexyl) -1-isopropyl-4-methylbicyclo [2,2,2] oct-5-ene -2,3-dicarboximide, N- (2-ethylhexyl) -bicyclo [2,2,1] hept-5-ene-2,
1 or 2 selected from the group consisting of 3-dicarboximide, piperonyl butoxide, isobornyl thiocyanoacetate, 2-butoxy-2′-thiocyanoethyl ether, N, N-diethyl-m-toluamide and benzylbenzoate. An indoor mite control aerosol for carpet treatment, consisting of several compounds.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7272306A JPH08208413A (en) | 1995-10-20 | 1995-10-20 | Aerosolagent for controlling interior mite |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7272306A JPH08208413A (en) | 1995-10-20 | 1995-10-20 | Aerosolagent for controlling interior mite |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP59019060A Division JPS60163805A (en) | 1984-02-04 | 1984-02-04 | Acaricide for indoor use |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH08208413A true JPH08208413A (en) | 1996-08-13 |
Family
ID=17512047
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP7272306A Pending JPH08208413A (en) | 1995-10-20 | 1995-10-20 | Aerosolagent for controlling interior mite |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH08208413A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2011063605A (en) * | 2003-11-26 | 2011-03-31 | Syngenta Participations Ag | Method to control fungi and mites in fiber base |
| JP2014136682A (en) * | 2013-01-15 | 2014-07-28 | Fumakilla Ltd | Aerosol composition for pest control |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS57122737A (en) * | 1981-01-19 | 1982-07-30 | Earth Chemical Co | Treating tool of "tatami" |
| JPS57175101A (en) * | 1981-03-26 | 1982-10-28 | Robins Co Inc A H | Killing agent composition for furniture treatment |
-
1995
- 1995-10-20 JP JP7272306A patent/JPH08208413A/en active Pending
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS57122737A (en) * | 1981-01-19 | 1982-07-30 | Earth Chemical Co | Treating tool of "tatami" |
| JPS57175101A (en) * | 1981-03-26 | 1982-10-28 | Robins Co Inc A H | Killing agent composition for furniture treatment |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2011063605A (en) * | 2003-11-26 | 2011-03-31 | Syngenta Participations Ag | Method to control fungi and mites in fiber base |
| JP2014136682A (en) * | 2013-01-15 | 2014-07-28 | Fumakilla Ltd | Aerosol composition for pest control |
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