JPS60142906A - Acaricide for indoor use - Google Patents
Acaricide for indoor useInfo
- Publication number
- JPS60142906A JPS60142906A JP58245990A JP24599083A JPS60142906A JP S60142906 A JPS60142906 A JP S60142906A JP 58245990 A JP58245990 A JP 58245990A JP 24599083 A JP24599083 A JP 24599083A JP S60142906 A JPS60142906 A JP S60142906A
- Authority
- JP
- Japan
- Prior art keywords
- mites
- acaricide
- pyrethroid
- indoor use
- compound
- 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.)
- Granted
Links
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は一般式
(式中、Xはメチル基又はクロル原子を示す。)で示さ
れる化合物又はこれにピレスロイド用共力剤および害虫
忌避剤の1種又は2種を加える仁とを特徴とする屋内用
殺ダニ剤に関する。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#It′i、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。DETAILED DESCRIPTION OF THE INVENTION The present invention provides a compound represented by the general formula (wherein X represents a methyl group or a chloro atom) or one or two of a pyrethroid synergist and an insect repellent. This invention relates to an indoor acaricide characterized by adding kernels. An extremely wide variety of mites inhabit the earth, such as the citrus spider mite and the two-spot spider mite #It'i, which parasitize plants and cause great damage to agricultural crops. These acaricides for agricultural use have been under development for a long time, and new and promising compounds have recently been discovered one after another.
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、アレルギー性祷息や皮疹を惹起する等の問題を
生じている。On the other hand, due to changes in the living environment in recent years, dust mites, dust mites, etc. have appeared in homes, causing not only discomfort but also problems such as allergic breathing and skin rashes.
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
屋内に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
障害があシ、的確な駆除方法の確立が切望されるように
なった。It was known that organic phosphorus agents such as Sumithion and Diazinon were effective against these indoor mites, but there were obstacles to practical application due to safety and resistance issues for humans and livestock. There is a strong desire to establish a method for extermination.
本発明者らは上記現状に鑑み、屋内で安全に使用てきる
殺ダニ剤の開発を目的として鋭意研究を続けた結果、一
般式(I)で表わされるピレスロイド系化合物(X =
CH3i フェノトリン、X=CA’;バーメスリン
)単独、又はこれにIBTA、S−421,ビペロニル
プトキサイド、サイネピリン222.サイネビリン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。In view of the above-mentioned current situation, the present inventors continued intensive research with the aim of developing a miticide that can be safely used indoors, and as a result, a pyrethroid compound represented by the general formula (I) (X =
CH3i phenothrin, X=CA'; vermethrin) alone, or in combination with IBTA, S-421, biperonyl ptoxide, cinepirin 222. Cynevirin 50
0. Synergists for pyrethroids such as Riessen 384 and DEET.
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
等に極めて高い殺ダニ効果を示すことを見い出し本発明
を完成した。One or two pest repellents such as benzyl benzoate
The present invention has been completed by discovering that a composition containing seeds exhibits an extremely high acaricidal effect on white mites, house dust mites, dust mites, and the like.
ところで、一般式(I)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、鵞<べきことに一般式CI)のピレスロイドが
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、そして最近膜かグ二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、一般式(
I)の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、殺ハグニ活
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。Incidentally, the pyrethroid of general formula (I) has high insecticidal power and a wide insecticidal spectrum, and is widely used for household and agricultural purposes as a highly safe insecticide.
Its miticidal power against orange spider mites and two-spotted spider mites is extremely weak, and it has been difficult to apply it to mites in general. However, the present inventors believe that there are some ecological differences between mites that live on plants, such as citrus spider mites and red-spotted spider mites, and mites that occur indoors, such as white mites and house dust mites, and have investigated the effects of various compounds on the latter mites. As a result of the study, it was announced that the pyrethroid with the general formula CI has a high acaricidal effect specifically against mites growing indoors, and it has recently been announced that the pyrethroid has excellent acaricidal activity. We discovered that some new pyrethroids are not necessarily effective against mites that grow indoors. Furthermore, the general formula (
Compounds with a cyano group introduced into the benzyl position of the alcohol moiety in I) generally have superior insecticidal and agnicidal activity compared to the original compound, but they have less activity against mites growing indoors. It became clear that the results showed a decrease in
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
であシ、又、一般式(I)の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。なお、一般式(I)の化合物の酸部には
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。These findings were completely unexpected based on conventional knowledge, and considering that the pyrethroids of general formula (I) are widely used as insecticides that are safe for humans and livestock. , which is extremely useful for developing indoor acaricides. There are two asymmetric carbon atoms in the acid moiety of the compound of general formula (I), and four optical isomers are possible, and each of these or any mixture thereof is of course included in the present invention.
又、よりTA、S−421,ビベロニルズトキサイド、
サイネピリン222.サイネビリン500゜リーセン3
84のようなピレスロイド用共力剤オヨヒティート、ベ
ンジルベンゾエートのような害虫忌避剤にも若干の殺ダ
ニ効果があることが明らかとなり、更に一般式(I)の
ピレスロイドに上記共力剤および害虫忌避剤の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。Also, more TA, S-421, biveronyl toxide,
Cinepirin 222. Cynevirin 500° Risen 3
It has become clear that insect repellents such as oyohytito, a synergist for pyrethroids such as No. 84, and benzyl benzoate have some acaricidal effect. It has been confirmed that a composition containing one or two of these exhibits an extremely high acaricidal effect that is more than additive.
一般式(I)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
上の虚いが一部関連しているものと考えられる。There are still many unknowns as to why the pyrethroids of the general formula (I) have a high extermination effect specifically against white mites and dust mites that occur indoors. This is thought to be partially related to the morphological vacancy of spider mites, which are prospirochlear.
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。Synergists for pyrethroid do not have insecticidal power by themselves, but when used together with pyrethroids, they are known to suppress the metabolic decomposition of pyrethroids in insect bodies and improve their insecticidal power. It itself shows some acaricidal activity against insects, suggesting a difference in the mechanism of action between insects and mites.
又、一般式(I)のピレスロイドとピレスロイド用共力
剤の混合組成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。Furthermore, the fact that a mixed composition of the pyrethroid of general formula (I) and a pyrethroid synergist exhibits a high synergistic effect has high practical value because the latter is very inexpensive.
ディート、ペンジルベンゾエートハ蚊、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。DEET, pendyl benzoate, is a compound that is widely used as a repellent for mosquitoes, flies, etc., and it is interesting that it shows acaricidal effects. It can be used as a multipurpose composition including extermination of mites.
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形態例えば乳
剤、水和剤、粉剤、油剤、エアゾール剤等として使用さ
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1.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、グロシン、灯油等)、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種まだは2種
以上の混合物が使用される。Although it is possible to apply the above-mentioned active ingredients as they are to the acaricide of the present invention, it is usually preferably prepared in various forms such as emulsions, wettable powders, etc., depending on the purpose of use, using suitable carriers and other compounding agents. Used as powder, oil, aerosol, etc. Examples of liquid carriers include water, alcohols (
Methyl alcohol, ethyl alcohol 1. ethylene glycol, etc.), ketones (acetone, methyl ethyl ketone, cyclohexanone, etc.), ethers (ethyl ether, dioxane, cellosolves, etc.), aliphatic hydrocarbons (gasoline, glocine, kerosene, etc.), aromatic hydrocarbons (
benzene, toluene, xylene, methylnaphthalene, etc.)
, halogenated hydrocarbons (dichloromethane, trichlorobenzene, etc.), esters, acid amides, nitriles and the like are suitable, and one type or a mixture of two or more of these may be used.
また固体の担体としては、例えば粘土類(六方リン、ベ
ントナイト#l)、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。Suitable solid carriers include, for example, clays (hexagonal phosphorus, bentonite #l), talcs, silicas, alumina powder, activated carbons, vegetable powders, and one or more of these. A mixture is used. Further, as compounding agents, emulsifiers, dispersants, spreading agents, penetrants, surfactants, stabilizers, etc. are suitable, and one type or a mixture of two or more of these can be used.
あるいはまた、本発明有効成分の活性を阻害する慣れの
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 unfamiliar acaricides, antioxidants, insecticides, fungicides, fungicides, flavorings, and coloring agents that inhibit the activity of the active ingredient of the present invention may be added.
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t
ri1畳あたり、0.11ng以上好ましくは1rne
〜2gの一般式(I)のピレスロイド系化合物が使用さ
れる。The amount of the active ingredient in the acaricide of the present invention and its usage amount are appropriately determined depending on the dosage form, application target, application method, application location, etc. For example, it can be used to exterminate mites that live on tatami mats, such as Kona mites.
0.11 ng or more preferably 1 rne per ri 1 tatami
~2 g of pyrethroid compound of general formula (I) are used.
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O
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。Note that tatami mats are inhabited by insect pests such as grass beetles and wasps, and the composition of the present invention can also exterminate these pests at the same time. However, the present invention is not limited to the following examples unless it exceeds the gist thereof.
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
6aのシャーレに入れ、温度25°csR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
返し行なった。Test Example 1 10 g of powdered feed treated with the test compound and 10 g of powdered feed containing approximately 2,500 woolly mites were mixed to obtain a test powdered feed of a predetermined concentration. Each 5 g of this powdered feed was placed in a petri dish with a diameter of 6a and placed at a temperature of 25° CsR degree of 75%. One week and two weeks later, the number of surviving mites in 0.2 g of feed was determined by the saturated saline suspension method, and the reproduction suppression rate was calculated according to the formula below. The test was repeated three times for each concentration.
なお、供試化合物一般式(I)中の符号a) 、b)
。Note that the symbols a) and b) in the general formula (I) of the test compound
.
Q)、d) はそれぞれ下記の意味を表わす。Q) and d) each represent the following meanings.
a);酸部 di −cis/1rans体b);酸部
d −cis/1rans体c);酸部 di−ai
s体
d);酸部 d −trans体
しN
上記結果より、本発明組成物すなわち一般式(I)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1〜5)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(Al l (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。a); Acid part di-cis/1rans form b); Acid part d-cis/1rans form c); Acid part di-ai
s form d); acid moiety d -trans form N Based on the above results, the composition of the present invention, that is, the compound of general formula (I), or one or two of a pyrethroid synergist and an insect repellent were added to it. The compositions (test compound examples 1 to 5) showed excellent acaricidal effects. On the other hand, the activity of other pyrethroid compounds (control compounds (Al (B), (C)) and pyrethroid synergists or pest repellents alone was very low, confirming the usefulness of the composition of the present invention. .
実施例1゜
d−7エノトリン2.0g、よりTA5.Ogを精製灯
油に溶解し、エアゾール容器に充填しパルプ部分を取り
付けた後該パルプ部分を通じて噴射剤?IJ!臣充填し
てエアゾールを得た。Example 1 TA5. After dissolving Og in refined kerosene, filling it into an aerosol container and attaching a pulp part, a propellant is passed through the pulp part. IJ! I filled it up and got an aerosol.
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%以下に減少していた。In a 6-tatami room where woolly mites were breeding, approximately 1/4 of the above-prepared aerosol was injected into the tatami area, and when the population density of mites was examined one week later, it was found to have decreased to less than 5%.
実施例2゜
パーメスリンo、sg、ベンジルベンゾエート1.0部
とクレー98.5部をよく粉砕混合して粉剤を得た。Example 2 Permethrin O, SG, 1.0 part of benzyl benzoate, and 98.5 parts of clay were thoroughly ground and mixed to obtain a powder.
コナヒせクヒダニ約300頭を接種した10σ平方のカ
ーペットに上記調製粉剤を1ばあたり20gの割合で散
布し、2日後に生存コナヒョクヒダニ数を調査したとこ
ろ5頭以下であった。The above powder preparation was sprayed on a 10σ square carpet inoculated with approximately 300 P. elegans mites at a rate of 20 g per carpet, and two days later, the number of surviving P. elegans was found to be less than 5.
手続補正書(自発) 昭和59年10月3L日 1、事件の表示 唱和88年特許願第245990号 8、補正をする者 4、代理人 7、補正の内容Procedural amendment (voluntary) October 3L, 1981 1. Display of incident Chowa 1988 Patent Application No. 245990 8. Person who makes corrections 4. Agent 7. Contents of correction
Claims (1)
れる化合物又はこれにピレスロイド用共力剤および害虫
忌避剤の1種又は2種を加えることを特徴とする屋内用
殺ダニ剤。(1) For indoor use, characterized by adding one or two of a pyrethroid synergist and an insect repellent to a compound represented by the general formula (in the formula, or a methyl group or a chloro atom); Acaricide.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58245990A JPS60142906A (en) | 1983-12-28 | 1983-12-28 | Acaricide for indoor use |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58245990A JPS60142906A (en) | 1983-12-28 | 1983-12-28 | Acaricide for indoor use |
Related Child Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3301378A Division JPH0578216A (en) | 1991-09-02 | 1991-09-02 | Miticide for indoor use |
JP7272308A Division JPH08225417A (en) | 1995-10-20 | 1995-10-20 | Aerosol agent for controlling house tick |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS60142906A true JPS60142906A (en) | 1985-07-29 |
JPH0461842B2 JPH0461842B2 (en) | 1992-10-02 |
Family
ID=17141823
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP58245990A Granted JPS60142906A (en) | 1983-12-28 | 1983-12-28 | Acaricide for indoor use |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS60142906A (en) |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6191103A (en) * | 1984-10-11 | 1986-05-09 | Earth Chem Corp Ltd | Acaricide |
US4800196A (en) * | 1985-08-06 | 1989-01-24 | Earth Chemical Co., Ltd. | Phenyl salicylate and benzyl salicylate as acaricidal agents |
JPS6461403A (en) * | 1987-08-31 | 1989-03-08 | Osaka Seiyaku Kk | Miticide |
JPH02282308A (en) * | 1989-04-07 | 1990-11-19 | Earth Chem Corp Ltd | Insect pest control agent composition |
JPH08225417A (en) * | 1995-10-20 | 1996-09-03 | Katsuta Yoshio | Aerosol agent for controlling house tick |
WO1998036640A1 (en) * | 1997-02-20 | 1998-08-27 | Reckitt & Colman Inc. | Dust mite control compositions containing benzyl benzoate and alcohol |
US6228384B1 (en) * | 1996-04-23 | 2001-05-08 | Chugai Seiyaku Kabushiki Kaisha | Capturing and detecting mites using 3-phenoxybenzyl chrysanthemate |
EP1169920A1 (en) * | 2000-07-06 | 2002-01-09 | Produits Berger | Process to control parasites and arthropodes |
US6428801B1 (en) * | 1997-08-06 | 2002-08-06 | Reckitt Benckiser Inc. | Methods for controlling dust mites and the allergens produced by dust mites |
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JPS5132728A (en) * | 1974-09-09 | 1976-03-19 | Sumitomo Chemical Co | Sotsukoseisatsuchu satsudanisoseibutsu |
JPS55122702A (en) * | 1979-02-07 | 1980-09-20 | Morgan Ward Critchley Co Ltd | Miticidal composition |
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 |
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---|---|---|---|---|
JPS5025727A (en) * | 1973-07-10 | 1975-03-18 | ||
JPS5132728A (en) * | 1974-09-09 | 1976-03-19 | Sumitomo Chemical Co | Sotsukoseisatsuchu satsudanisoseibutsu |
JPS55122702A (en) * | 1979-02-07 | 1980-09-20 | Morgan Ward Critchley Co Ltd | Miticidal composition |
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 |
JPS632909A (en) * | 1987-06-24 | 1988-01-07 | Earth Chem Corp Ltd | Mite controlling agent for indoor use |
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6191103A (en) * | 1984-10-11 | 1986-05-09 | Earth Chem Corp Ltd | Acaricide |
US4800196A (en) * | 1985-08-06 | 1989-01-24 | Earth Chemical Co., Ltd. | Phenyl salicylate and benzyl salicylate as acaricidal agents |
JPS6461403A (en) * | 1987-08-31 | 1989-03-08 | Osaka Seiyaku Kk | Miticide |
JPH02282308A (en) * | 1989-04-07 | 1990-11-19 | Earth Chem Corp Ltd | Insect pest control agent composition |
JPH0453842B2 (en) * | 1989-04-07 | 1992-08-27 | Earth Chemical Co | |
JPH08225417A (en) * | 1995-10-20 | 1996-09-03 | Katsuta Yoshio | Aerosol agent for controlling house tick |
US6228384B1 (en) * | 1996-04-23 | 2001-05-08 | Chugai Seiyaku Kabushiki Kaisha | Capturing and detecting mites using 3-phenoxybenzyl chrysanthemate |
WO1998036640A1 (en) * | 1997-02-20 | 1998-08-27 | Reckitt & Colman Inc. | Dust mite control compositions containing benzyl benzoate and alcohol |
US5916917A (en) * | 1997-02-20 | 1999-06-29 | Reckitt & Colman Inc. | Dust mite control compositions containing benzyl benzoate and alcohol |
US6428801B1 (en) * | 1997-08-06 | 2002-08-06 | Reckitt Benckiser Inc. | Methods for controlling dust mites and the allergens produced by dust mites |
EP1169920A1 (en) * | 2000-07-06 | 2002-01-09 | Produits Berger | Process to control parasites and arthropodes |
FR2811202A1 (en) * | 2000-07-06 | 2002-01-11 | Prod Berger | METHOD OF DIFFUSION OF A ACARICIDE COMPOSITION CONSISTING OF PERMETHRIN AND TETRAMETHRIN AND USE OF A CATALYTIC COMBUSTION FLASK FOR IMPLEMENTATION OF SUCH A PROCESS |
US6451841B2 (en) | 2000-07-06 | 2002-09-17 | Produits Berger | Method of diffusing an acaricidal composition comprising permethrin and tetramethrin, and the use of a catalytic combustion flask for implementing such a method |
Also Published As
Publication number | Publication date |
---|---|
JPH0461842B2 (en) | 1992-10-02 |
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