JPH08225417A - Aerosol agent for controlling house tick - Google Patents

Aerosol agent for controlling house tick

Info

Publication number
JPH08225417A
JPH08225417A JP7272308A JP27230895A JPH08225417A JP H08225417 A JPH08225417 A JP H08225417A JP 7272308 A JP7272308 A JP 7272308A JP 27230895 A JP27230895 A JP 27230895A JP H08225417 A JPH08225417 A JP H08225417A
Authority
JP
Japan
Prior art keywords
mites
formula
pyrethroid
phenothrin
ene
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
Application number
JP7272308A
Other languages
Japanese (ja)
Inventor
Yoshihiro Namite
良裕 南手
Tsutomu Kanzaki
務 神崎
Kyoko Chisaka
京子 千坂
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to JP7272308A priority Critical patent/JPH08225417A/en
Publication of JPH08225417A publication Critical patent/JPH08225417A/en
Pending legal-status Critical Current

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Abstract

PURPOSE: To provide an aerosol agent having excel lent house tick controllability, safely usable in the interior of house, suitable for controlling acarids in a carpet, comprising phenothrin or phenothrin and a synergist for pyrethroid or a propellant for insect pests. CONSTITUTION: This aerosol agent comprises (A) a pyrethroid-based compound phenothrin of the formula or (B) the component A and octachlorodipropyl ether, N-(2-ethylhexyl)-1-isopropyl-4-methylbicyclo[2,2,2]oct-5-ene-2,3-dicar boximide, 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- toluamide or benzyl benzoate.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【発明の属する技術分野】本発明は、式(I):TECHNICAL FIELD The present invention relates to formula (I):

【化2】 で示される化合物(フェノトリン)、又は式(I)で示
される化合物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。
Embedded image (Phenothrin) or a compound represented by formula (I) and one or two synergists for pyrethroids and pest repellents, and an aerosol agent for indoor mite control for carpet treatment.

【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
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. Organophosphorus agents such as Sumithion and Diazinon were known to be effective against mites that occur indoors, but there are obstacles to their practical use due to safety and resistance problems to 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、式(I)で表されるピレス
ロイド系化合物フェノトリン単独よりなる、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。
SUMMARY OF THE INVENTION In view of the above situation, the inventors of the present invention have conducted diligent research for the purpose of developing an acaricide that can be safely used indoors, and as a result, the pyrethroid system represented by the formula (I). Compound phenothrin alone, or isobornyl thiocyanoacetate (hereinafter referred to as IBTA),
Octachlorodipropyl ether (hereinafter referred to as S-421), piperonyl butoxide, N-2 (-ethylhexyl) -bicyclo [2,2,1] hept-5-ene-2,3-
Dicarboximide (hereinafter referred to as cinepyrine 222), N- (2-ethylhexyl) -1-isopropyl-
4-methylbicyclo [2,2,2] oct-5-ene-2,
A synergist for pyrethroid such as 3-dicarboximide (hereinafter referred to as cinepyrine 500), 2-butoxy-2′-thiocyanodiethyl ether (hereinafter referred to as Resen 384), and N, N-diethyl-m-toluamide. (Hereinafter referred to as diet), a composition containing one or two pest repellents such as benzylbenzoate,
The present invention has been completed by finding that it shows a very high acaricidal effect against dust mites and dust mites.

【0005】本発明は、有効成分としての式(I):The present invention provides the formula (I) as an active ingredient:

【化3】 で示される化合物よりなる、あるいは式(I)で示され
る化合物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。
Embedded image Or a compound of formula (I) 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] hepta From the group consisting of -5-ene-2,3-dicarboximide, piperonyl butoxide, isobornyl thiocyanoacetate, 2-butoxy-2'-thiocyanoethyl ether, N, N-diethyl-m-toluamide and benzylbenzoate. 1 or 2 selected
PROBLEM TO BE SOLVED: To provide an aerosol agent for controlling indoor mites for carpet treatment, which comprises various compounds.

【0006】[0006]

【発明の実施の態様】ところで、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、驚くべきことに式(I)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、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、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、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。
BEST MODE FOR CARRYING OUT THE INVENTION By the way, the pyrethroid of the formula (I) has a high insecticidal activity and a broad insecticidal spectrum and is widely used as a highly safe insecticide for household and agricultural purposes. The acaricidal activity against citrus red mite and spider mites is extremely weak, and it has been conventionally difficult to apply them to mites in general. However, the present inventors consider 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, surprisingly, the pyrethroid of the formula (I) has a particularly high acaricidal effect specifically on mites growing indoors, and in particular, has an activity surpassing Sumithion and diazinon against dust mites. It has been discovered that some new pyrethroids, which have recently been shown to have excellent spidericidal activity, are not always effective against mites growing indoors. Further, the compound of the formula (I) in which a cyano group is introduced at the benzyl position of the alcohol part is generally superior in insecticidal activity and acaricidal activity as compared with the original compound. On the contrary, it was revealed that the activity was decreased. These findings are completely unexpected from conventional findings, and considering that the pyrethroid of formula (I) is widely used as a safe insecticide for humans and animals, it can be used indoors. It is extremely useful for the development of acaricide. In addition, although two asymmetric carbons are present in the acid part of the compound of the formula (I) and four optical isomers are possible, each of them or any mixture thereof is of course included in the present invention.

【0007】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
にも若干の殺ダニ効果があることが明らかとなり、更に
式(I)のピレスロイド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 pyrethroid synergist such as Reisen 384, and pest repellents such as diet and benzyl benzoate were also found to have some acaricidal effect. Furthermore, the pyrethroid of the formula (I) was supplemented with the above synergist and It was confirmed that the composition containing one or two pest repellents exhibits extremely high acaricidal effect which is additive or higher.

【0008】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
いう形態上の違いが一部関連しているものと考えられ
る。
Although there are many unclear points as to why the pyrethroid of the formula (I) has a high specific control effect against the mites and dust mites that occur indoors, this type of mite belongs to the astigmatid species, while the plant It is considered that the morphological difference that the spider mites that attach to the mosquito are pre-Amphitates are related in part.

【0009】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 pyrethroids have no insecticidal activity themselves, and when used together with pyrethroids, they are known to suppress the metabolic decomposition of pyrethroids in insect bodies and improve their insecticidal activity. It shows some acaricidal activity against the mites that develop, suggesting a difference in mechanism of action between insects and mites.

【0010】又、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。
Further, the fact that the mixed composition of the pyrethroid of the formula (I) and the synergist for the pyrethroid shows a high synergistic effect,
The latter is very cheap and has high practical value.

【0011】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。
[0011] 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 have an acaricidal effect, and the composition of the present invention containing them is suitable for the treatment of unpleasant pests. It can be used as a multipurpose composition including repellent and control of mites.

【0012】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。
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 (including liquids) depending on the purpose of use, by using an appropriate carrier or other compounding agent. 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.

【0013】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。
Examples of solid carriers include clays (kaolin, bentonite, etc.), talcs, silicas,
Alumina powder, activated carbon, vegetable powder, etc. are suitable,
And these 1 type or a mixture of 2 or more types is used. Suitable compounding agents include emulsifiers, dispersants, spreading agents, penetrants, surfactants, stabilizers, etc.
One kind or a mixture of two or more kinds is used.

【0014】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.

【0015】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の式(I)のピレスロイド系化合物が使用され
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。
The amount of the active ingredient in the acaricide of the present invention and the amount thereof used are appropriately determined according to 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 of formula (I) 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.

【0016】[0016]

【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.

【0017】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 helminth 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.

【0018】[0018]

【数1】 [Equation 1]

【0019】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

【0020】[0020]

【表1】 [Table 1]

【0021】[0021]

【化4】 [Chemical 4]

【0022】上記結果より、本発明組成物すなわち、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(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, that is, the compound of formula (I) or a composition obtained by adding one or two of a synergist for pyrethroid and a pest repellent (test compound examples 1 to 5) ) Showed an excellent acaricidal effect. On the other hand, the activity of the other pyrethroid compounds (control compounds (A), (B), (C)) and the synergist for pyrethroid or the pest repellent alone is very low, and the usefulness of the composition of the present invention was confirmed. It was

【0023】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 2.0 g of d-phenothrin and 5.0 g of IBTA were dissolved in refined kerosene, filled into an aerosol container and attached 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.

【0024】実施例 2 d−フェノトリン5部ベンジルベンゾエート5部に、ソ
ルボール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
500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ットに、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 5 parts of d-phenothrin 5 parts of benzyl benzoate, 15 parts of Solbol SM-100 (trade name of Toho Kagaku),
75 parts of purified water was added to obtain an aqueous emulsion. This emulsion was diluted 500 times with water, treated with 100 g per m 2 of base cloth, and dried to release about 300 Knotweed mites on the carpet. Two days later, the number of surviving Dermatophagoides farinae was examined and found to be 5 It was below.

【0025】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.

【0026】[0026]

【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.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 A01N 43:38) (A01N 53/08 43:30) (A01N 53/08 47:48) (A01N 53/08 37:18) (A01N 53/08 37:10) ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 6 Identification code Internal reference number FI Technical display area A01N 43:38) (A01N 53/08 43:30) (A01N 53/08 47:48) (A01N 53/08 37:18) (A01N 53/08 37:10)

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 有効成分としての式(I): 【化1】 で示される化合物よりなる、あるいは式(I)で示され
る化合物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. Formula (I) as an active ingredient: Or a compound of formula (I) 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] hepta From the group consisting of -5-ene-2,3-dicarboximide, piperonyl butoxide, isobornyl thiocyanoacetate, 2-butoxy-2'-thiocyanoethyl ether, N, N-diethyl-m-toluamide and benzylbenzoate. 1 or 2 selected
An indoor mite control aerosol for carpet treatment, consisting of several compounds.
JP7272308A 1995-10-20 1995-10-20 Aerosol agent for controlling house tick Pending JPH08225417A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP7272308A JPH08225417A (en) 1995-10-20 1995-10-20 Aerosol agent for controlling house tick

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7272308A JPH08225417A (en) 1995-10-20 1995-10-20 Aerosol agent for controlling house tick

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
JP58245990A Division JPS60142906A (en) 1983-12-28 1983-12-28 Acaricide for indoor use

Publications (1)

Publication Number Publication Date
JPH08225417A true JPH08225417A (en) 1996-09-03

Family

ID=17512075

Family Applications (1)

Application Number Title Priority Date Filing Date
JP7272308A Pending JPH08225417A (en) 1995-10-20 1995-10-20 Aerosol agent for controlling house tick

Country Status (1)

Country Link
JP (1) JPH08225417A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20030035755A (en) * 2001-10-30 2003-05-09 다이니혼 죠츄기쿠 가부시키가이샤 Miticide for controlling house dust mite
JP2014136682A (en) * 2013-01-15 2014-07-28 Fumakilla Ltd Aerosol composition for pest control

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5025727A (en) * 1973-07-10 1975-03-18
JPS57122737A (en) * 1981-01-19 1982-07-30 Earth Chemical Co Treating tool of "tatami"
JPS60142906A (en) * 1983-12-28 1985-07-29 Katsuta Yoshio Acaricide for indoor use
JPH0734699A (en) * 1993-07-21 1995-02-03 Ishikawajima Harima Heavy Ind Co Ltd Elevator type parking device

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5025727A (en) * 1973-07-10 1975-03-18
JPS57122737A (en) * 1981-01-19 1982-07-30 Earth Chemical Co Treating tool of "tatami"
JPS60142906A (en) * 1983-12-28 1985-07-29 Katsuta Yoshio Acaricide for indoor use
JPH0734699A (en) * 1993-07-21 1995-02-03 Ishikawajima Harima Heavy Ind Co Ltd Elevator type parking device

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20030035755A (en) * 2001-10-30 2003-05-09 다이니혼 죠츄기쿠 가부시키가이샤 Miticide for controlling house dust mite
JP2014136682A (en) * 2013-01-15 2014-07-28 Fumakilla Ltd Aerosol composition for pest control

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