JPH07138112A - Indoor dusty acaricide - Google Patents

Indoor dusty acaricide

Info

Publication number
JPH07138112A
JPH07138112A JP31264593A JP31264593A JPH07138112A JP H07138112 A JPH07138112 A JP H07138112A JP 31264593 A JP31264593 A JP 31264593A JP 31264593 A JP31264593 A JP 31264593A JP H07138112 A JPH07138112 A JP H07138112A
Authority
JP
Japan
Prior art keywords
mites
mite
compound
agent
indoor
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
JP31264593A
Other languages
Japanese (ja)
Inventor
Yoshio Katsuta
純郎 勝田
Schubert Hans
シューベルト ハンス
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.)
Bayer CropScience AG
Dainihon Jochugiku Co Ltd
Original Assignee
Hoechst Schering Agrevo GmbH
Dainihon Jochugiku Co Ltd
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 Hoechst Schering Agrevo GmbH, Dainihon Jochugiku Co Ltd filed Critical Hoechst Schering Agrevo GmbH
Priority to JP31264593A priority Critical patent/JPH07138112A/en
Priority to CA002176596A priority patent/CA2176596A1/en
Priority to EP95900706A priority patent/EP0729301A1/en
Priority to JP51420395A priority patent/JP3170286B2/en
Priority to US08/646,259 priority patent/US5854288A/en
Priority to PCT/EP1994/003728 priority patent/WO1995013703A1/en
Priority to MX9408958A priority patent/MX9408958A/en
Publication of JPH07138112A publication Critical patent/JPH07138112A/en
Pending legal-status Critical Current

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Abstract

PURPOSE: To obtain a miticide exhibiting high miticidal action on house dust mites such as acarid mite, Dermatophagoides farinae and Cheyletidae mite, harmless to man and beast and effective as a preventing agent as well as an eliminating agent for house dust mites. CONSTITUTION: This miticide for house dust mites contains N-(2-chlorobenzoyl)-N '-[4-(2-chloro-4-trifluoromethyl-1-phenylmercapto)phenyl]urea.

Description

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

【0001】[0001]

【産業上の利用分野】本発明はN−(2−クロロベンゾ
イル)−N’−〔4−(2−クロロ−4−トリフルオロ
メチル−1−フェニルメルカプト)フェニル〕ウレアを
含有する殺屋内塵性ダニ剤に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an indoor dust containing N- (2-chlorobenzoyl) -N '-[4- (2-chloro-4-trifluoromethyl-1-phenylmercapto) phenyl] urea. It concerns a sex tick agent.

【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。これらのダニ類
に対する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。一方、近年居住環境の変化から家庭内に、コ
ナダニ、ヒョウヒダニ、ツメダニ等の屋内塵性ダニが発
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やフェノトリン、ペル
メトリンのようなピレスロイド剤が、これらの屋内に発
生する屋内塵性ダニ類に効果を示すことは知られている
が、これら殺ダニ効果を有する殺虫成分はいずれも接触
毒であるから、薬剤とダニとの接触が必須である。すな
わち、薬剤をダニの生息する例えばカーペット基部に全
面均一に処理するためには、多量散布することが必要と
なり、処理方法が非常に困難であると同時に、人間、特
に小児に対する安全性の懸念から実用的でないのが現状
である。また、屋内塵性ダニ類は総じて熱に弱く、70
℃、数分でほぼ完全に死滅し、更に乾燥状態での生育も
不可能なことから、畳やカーペットの高周波熱処理や布
団乾燥などの物理的ダニ防除法も効果的であるが、簡便
性の点で障害が大きく、的確な駆除方法の確立が切望さ
れている。
2. Description of the Related Art A great variety of mites live on the earth, and for example, citrus spider mites and worm spiders parasitic on plants cause great damage to agricultural products. Acaricides for the purpose of agricultural use against these mites have been developed for a long time, and recently new promising compounds have been discovered one after another. On the other hand, in recent years, due to changes in the living environment, indoor dust mites such as mites, leopard mites, and tick mites occur, which not only causes discomfort, but also causes problems such as causing allergic asthma and skin rashes. . It is known that organophosphorus agents such as Sumithion and diazinon, and pyrethroid agents such as phenothrin and permethrin show effects on indoor dust mites that occur indoors, but insecticides with these acaricidal effects. Since all of the components are contact poisons, contact between the drug and ticks is essential. That is, in order to uniformly treat the drug on the entire surface of the carpet where mites inhabit, for example, it is necessary to spray a large amount, and the treatment method is very difficult, and at the same time, from the concern of safety for humans, especially for children. The current situation is that it is not practical. In addition, indoor dust mites are generally vulnerable to heat,
Physical mite control methods such as high-frequency heat treatment of tatami mats and carpets and futon drying are also effective, although they die almost completely in a few minutes at ℃ and cannot grow in a dry state. In that respect, there are major obstacles, and it is earnestly desired to establish an accurate method of extermination.

【0003】[0003]

【発明が解決しようとする課題】本発明は、上記現状に
鑑み、屋内で安全に使用できる殺屋内塵性ダニ剤の開発
を目的としてなされたものである。
SUMMARY OF THE INVENTION In view of the above situation, the present invention has been made with the object of developing an indoor slaughterhouse dust mite agent that can be safely used indoors.

【0004】[0004]

【課題を解決するための手段】上記目的を達成するた
め、本発明者等は、鋭意研究を続けた結果、N−(2−
クロロベンゾイル)−N’−〔4−(2−クロロ−4−
トリフルオロメチル−1−フェニルメルカプト)フェニ
ル〕ウレアを含有する組成物が、コナダニ、ヒョウヒダ
ニ、ツメダニ等の屋内塵性ダニ類に対して高い殺ダニ効
果を示すことを見出し、さらに研究を進め、本発明を完
成させた。すなわち、本発明は、N−(2−クロロベン
ゾイル)−N’−〔4−(2−クロロ−4−トリフルオ
ロメチル−1−フェニルメルカプト)フェニル〕ウレア
(以下、化合物Aと記載する)を含有することを特徴と
する殺屋内塵性ダニ剤に関する。
[Means for Solving the Problems] To achieve the above object, the inventors of the present invention conducted extensive studies and found that N- (2-
Chlorobenzoyl) -N '-[4- (2-chloro-4-
A composition containing trifluoromethyl-1-phenylmercapto) phenyl] urea was found to show a high acaricidal effect against indoor dust mites such as mites, deer mites, and tick mites, and further research has been conducted. Completed the invention. That is, the present invention provides N- (2-chlorobenzoyl) -N '-[4- (2-chloro-4-trifluoromethyl-1-phenylmercapto) phenyl] urea (hereinafter referred to as compound A). The present invention relates to an indoor bactericidal dust mite agent characterized by containing.

【0005】ところで、化合物Aは、昆虫やダニ類のキ
チン生合成の阻害剤として知られるベンゾイルウレア系
化合物に該当し、特開平2−270号公報において、
蚊、ハエ、ゴキブリをはじめとする各種害虫や、植物に
つくダニ類に対して高い殺虫、殺ダニ効果を示すことが
開示されている。しかし、屋内塵性ダニ類に対する効果
は不明のままであった。
Incidentally, the compound A corresponds to a benzoylurea compound known as an inhibitor of chitin biosynthesis in insects and mites, and is disclosed in JP-A-2-270.
It is disclosed that various insect pests such as mosquitoes, flies, and cockroaches and mites attached to plants exhibit high insecticidal and acaricidal effects. However, its effect on indoor dust mites remained unclear.

【0006】これまでに開発されたジフルベンズロンや
テフルベンズロンのようなベンゾイルウレア系化合物
は、蚊、ハエ、ゴキブリ等の衛生害虫や、植物につくハ
ダニ類に対して高い殺虫、殺ダニ活性を示すものの、屋
内塵性ダニ類にはほとんど効果を示さない。これは、植
物につくハダニ類が有気門類に属するのに対し、屋内塵
性ダニ類が無気門類に属するという形態上の違いが大き
く影響しているものと考えられる。従って、当初、化合
物Aについても、屋内塵性ダニ類に対する活性は全く予
見できなかったものである。
Although the benzoylurea compounds such as diflubenzuron and teflubenzuron which have been developed so far show high insecticidal and acaricidal activity against hygienic pests such as mosquitoes, flies and cockroaches and spider mites attached to plants, Shows little effect on indoor dust mites. This is thought to be due to the morphological difference that the house dust mites belonging to plants belong to the aerial phylum, whereas the indoor dust mites belong to the aerial phylum. Therefore, initially, the activity of the compound A against indoor dust mites could not be predicted at all.

【0007】しかるに本発明者等は、従来の有機リン剤
やピレスロイド剤が神経毒として作用するのに対し、キ
チン生合成の阻害剤作用点が、昆虫やダニ類に特有なキ
チン質で、人畜にほとんど無害であることから、ベンゾ
イルウレア系化合物が殺屋内塵性ダニ剤の有効成分とし
て最適と考え、この系統の種々の化合物についてスクリ
ーニングを行った。その結果、化合物Aのみが、他のベ
ンゾイルウレア系化合物と異なり、特異的に屋内塵性ダ
ニ類に高い殺ダニ効果を示すことを見出し、本発明に至
ったものである。
However, while the conventional organophosphorus agents and pyrethroid agents act as neurotoxins, the present inventors have found that the site of action of inhibitors of chitin biosynthesis is chitin, which is peculiar to insects and mites. Since it is almost harmless to benzoylurea compounds, we considered that benzoylurea compounds were the most suitable active ingredients for indoor dust mites, and screened various compounds of this system. As a result, they have found that, unlike other benzoylurea-based compounds, only compound A specifically shows a high acaricidal effect on indoor dust mites, which led to the present invention.

【0008】本発明で用いられる化合物Aは、特開平2
−270号公報に記載されている合成方法に準じて容易
に製造され、常温で固体である。化合物Aを、本発明の
殺屋内塵性ダニ剤の有効成分として用いる場合は、他に
何らの成分を加えずに、そのまま使用してもよいが、固
体担体、液体担体、ガス状担体、界面活性剤、その他の
製剤用補助剤、飼料等と混合し、粉剤、粒剤、エアゾー
ル剤、乳剤、水溶剤、燻煙剤、毒餌剤、シート等に製剤
化して用いるのが一般的である。
Compound A used in the present invention is disclosed in
-270 is easily manufactured according to the synthetic method described in the gazette, and is a solid at room temperature. When the compound A is used as an active ingredient of the indoor miticidal mite agent of the present invention, it may be used as it is without adding any other component, but it may be used as a solid carrier, a liquid carrier, a gaseous carrier, an interface. It is generally used by mixing with an active agent, other auxiliary agents for formulation, feed, etc., and formulated into powders, granules, aerosols, emulsions, water solutions, smoke agents, poison baits, sheets and the like.

【0009】固体担体としては、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、植物粉末等が挙げられ、液体担体とし
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、エチレングリコール等)、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(ジクロロメタン、トリクロロベンゼン等)、エ
ステル類、酸アミド類、ニトリル類等の溶媒が適当であ
り、そしてこれらの1種または2種以上の混合物が使用
され得る。また、ガス状担体としてLPG(液化石油ガ
ス)、ジメチルエーテル、フロンガス等があり、界面活
性剤としては、アルキル硫酸エステル塩、アルキルスル
ホン酸塩、ポリオキシエチレンアルキルエーテル、ソル
ビタン脂肪酸エステル、ポリオキシエチレンポリオキシ
プロピレンブロックポリマー等、通常入手できる物質を
任意に使用できる。更に、製剤用補助剤としては、分散
剤、固着剤、安定剤等が適宜用いられる。
Examples of solid carriers include clays (kaolin, bentonite, etc.), talcs, silicas, alumina powder, activated carbons, plant powders, and the like, and liquid carriers include, for example, water and 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.), aromatics Suitable solvents include hydrocarbons (benzene, toluene, xylene, methylnaphthalene, etc.), halogenated hydrocarbons (dichloromethane, trichlorobenzene, etc.), esters, acid amides, nitriles, etc., and one of these. Alternatively, a mixture of two or more can be used. In addition, there are LPG (liquefied petroleum gas), dimethyl ether, flon gas, etc. as the gaseous carrier, and as the surfactant, alkyl sulfate ester salt, alkyl sulfonate, polyoxyethylene alkyl ether, sorbitan fatty acid ester, polyoxyethylene poly Any commonly available substance such as oxypropylene block polymer may be used. Furthermore, as the formulation auxiliary agent, a dispersant, a sticking agent, a stabilizer, etc. are appropriately used.

【0010】本発明の殺屋内塵性ダニ剤には、化合物A
の活性を阻害しない限り、他の殺ダニ剤、殺虫剤、殺菌
剤、忌避剤、共力剤、防黴剤、成長調整剤、着香料、着
色料等を配合して多目的組成物を得ることもできる。例
えば、殺虫剤としてはフェニトロチオン、ダイアジノ
ン、プロペタンホス等の有機リン剤、フェノトリン、ペ
ルメトリン、レスメトリン、エトフェンプロックス、エ
ムペントリン等のピレスロイド剤、シラフルオフェン、
ジフルベンズロン、テフルベンズロン、クロルフルアズ
ロン、フルフェノクスロン、ピリプロキシフェン等の化
合物が挙げられる。また、忌避剤として、N,N−ジエ
チル−m−トルアミド、ベンジルベンゾエート等を、共
力剤として、ピペロニルブトキサイド、オクタクロロジ
プロピルエーテル、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、チオシアノ酢酸イソボルニル等を例示で
きる。
The indoor dust-eliminating mites of the present invention include compound A
Other acaricides, insecticides, bactericides, repellents, synergists, mildew-proofing agents, growth regulators, flavoring agents, coloring agents, etc. to obtain a multipurpose composition unless it inhibits the activity of You can also For example, as insecticides fenitrothion, diazinon, organophosphorus agents such as propetanphos, phenothrin, permethrin, resmethrin, etofenprox, pyrethroid agents such as empentrin, silafluofen,
Examples thereof include compounds such as diflubenzuron, teflubenzuron, chlorfluazuron, flufenoxuron and pyriproxyfen. Further, N, N-diethyl-m-toluamide, benzylbenzoate and the like are used as repellents, and piperonyl butoxide, octachlorodipropyl ether, N- (2-ethylhexyl) -bicyclo [2. 2.1] Hepta-5-ene-2,3-dicarboximide, isobornyl thiocyanoacetate and the like can be exemplified.

【0011】本発明の殺屋内塵性ダニ剤中の有効成分量
およびその使用量は、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、カーペッ
ト類に生息するヒョウヒダニ類等の駆除には1m2 あた
り、0.1mg以上の化合物Aが適用されるのが好まし
い。また、化合物Aは接触毒のみならず、食毒としても
作用するので、飼料等に混入する毒餌剤は有用な使用形
態であり、この場合、0.1ppm〜1.0%の範囲で
十分な効果が得られる。更に、化合物Aは接触毒と食毒
の両作用性により、全面均一処理でなく、部分処理でも
高い殺ダニ効果を奏し得るという特徴を有する。一方、
従来の有機リン剤やピレスロイド剤は接触毒としてのみ
作用し、屋内塵性ダニ類に対して少なからず忌避性を示
すので、部分処理では殺ダニ効果が得られない。
The amount of the active ingredient and the amount of the active ingredient used in the indoor dust-removing mite agent of the present invention are as follows:
It is appropriately determined according to the application place and the like. For example, it is preferable that 0.1 mg or more of the compound A is applied per 1 m 2 for the control of deer spider mites and the like that inhabit carpets. Further, since compound A acts not only as a contact poison but also as a food poison, a poison bait agent mixed in feed or the like is a useful use form. In this case, 0.1 ppm to 1.0% is sufficient. The effect is obtained. Further, Compound A has a feature that it can exhibit a high acaricidal effect not only by the uniform treatment on the entire surface but also by the partial treatment because of the dual action of contact poison and food poison. on the other hand,
Conventional organophosphorus agents and pyrethroids act only as contact poisons and repel a lot of indoor dust mites, so partial treatment does not provide an acaricidal effect.

【0012】[0012]

【作用】このように、本発明の殺屋内塵性ダニ剤は、コ
ナダニ、ヒョウヒダニ、ツメダニ等の屋内塵性ダニ類に
対して高い殺ダニ効果を示し、しかも人畜に対して極め
て安全であるので、本発明は従来の有機リン剤やピレス
ロイド剤による方法に替わる的確な薬剤処理方法を提供
するものである。また、化合物Aは化学的に安定で残効
性にすぐれるので、本剤は屋内塵性ダニ発生後の駆除処
理のみならず、カーペットや布団等を予め処理する、い
わゆる予防処理剤としても極めて有用である。
As described above, the indoor miticidal mite agent of the present invention exhibits a high miticidal effect against indoor mite dust mites such as mites, deer mites and claw mites, and is extremely safe for humans and animals. The present invention provides an accurate method for treating a drug, which is an alternative to the conventional method using an organic phosphorus agent or a pyrethroid agent. In addition, since Compound A is chemically stable and has a good residual effect, this agent is extremely useful not only as a disinfection treatment after the occurrence of indoor dust mites, but also as a so-called preventive treatment agent that pre-treats carpets, duvets, etc. It is useful.

【0013】[0013]

【実施例】以下、試験例および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。 試験例1 実験動物用粉末飼料に供試薬剤を混和して、所定の2倍
濃度の培地を調製した。この培地にダニを含む飼育培地
を1:1の割合で十分に混和し、所定濃度の処理培地と
した。なお、処理培地のダニ密度はヤケヒョウヒダニが
1g中約450匹、ケナガコナダニが1g中約100匹
とした。同様に無処理培地を調製し、これらの試験培地
をそれぞれ直径4.5cm、高さ1.5cmのペトリ皿
に5gずつ入れ、相対湿度をヤケヒョウヒダニの場合、
約65%、ケナガコナダニの場合、約85%に調整した
容器に入れ、温度25±1℃の恒温室で飼育した。観察
は処理後2および3週間目に、培地を軽く攪拌し、試験
培地のダニを均一に分散させて、それぞれの試験培地か
ら0.1g秤量し、実体顕微鏡下で生ダニ数を数えた。
試験は各試験区から3回繰り返し秤量し、その平均値か
ら次式によって処理2週間後および3週間後の増殖抑制
率を算出した。結果を表1に示す。 増殖抑制率(%)=〔{(無処理区の生ダニ数)−(処
理区の生ダニ数)}/(無処理区の生ダニ数)〕×10
EXAMPLES The present invention will be described in more detail with reference to test examples and examples, but the present invention is not limited to the following examples as long as the gist thereof is not exceeded. Test Example 1 A reagent medium was mixed with powder feed for experimental animals to prepare a medium having a predetermined double concentration. A breeding medium containing mites was thoroughly mixed with this medium at a ratio of 1: 1 to obtain a treated medium having a predetermined concentration. In addition, the mite density of the treatment medium was set at about 450 mosquitoes of Pleurotus cornucopiae and about 100 of Mite mosquitoes. Similarly, a non-treated medium was prepared, and 5 g of each of these test mediums was placed in a Petri dish having a diameter of 4.5 cm and a height of 1.5 cm.
Approximately 65%, and in the case of Physcomitrella patens, it was placed in a container adjusted to approximately 85% and reared in a thermostatic chamber at a temperature of 25 ± 1 ° C. The observation was carried out two and three weeks after the treatment by lightly stirring the medium to uniformly disperse the mites in the test medium, weighing 0.1 g from each test medium, and counting the number of live mites under a stereomicroscope.
The test was weighed three times from each test section, and the growth inhibition rate after 2 weeks and 3 weeks after the treatment was calculated from the average value by the following formula. The results are shown in Table 1. Growth inhibition rate (%) = [{(number of live mites in untreated plot)-(number of live mites in treated plot)} / (number of live mites in untreated plot)] × 10
0

【0014】[0014]

【表1】 [Table 1]

【0015】試験の結果、化合物Aは培地に混入後供餌
させる方法において、ヤケヒョウヒダニおよびケナガコ
ナダニに対し、低濃度で極めて高い増殖抑制率を示し
た。これに対し、対照として用いたジフルベンズロンや
テフルベンズロンのような他のベンゾイルウレア系化合
物、メトプレン、ピリプロキシフェンのような幼若ホル
モン剤はほとんど増殖抑制効果がなく、屋内塵性ダニ類
に対する殺ダニ活性は、ベンゾイルウレア系化合物の中
でも、化合物Aに特異的な特性であることが明らかとな
った。一方、従来の屋内塵性ダニ剤の有効成分として主
に使用されているピレスロイド剤のフェノトリンは、殺
ダニ活性を示すのに高濃度を要した。従って、作用機作
上、人畜にほとんど無害で、しかも低濃度で極めて高い
殺ダニ活性を示す化合物Aは、フェノトリン等の従来の
有効成分に替わり、極めて有用な殺屋内塵性ダニ剤を提
供するものである。
As a result of the test, the compound A showed a very high growth inhibitory rate at a low concentration in the method of feeding after being mixed in the medium, against the house dust mite and the mite. In contrast, other benzoylurea compounds such as diflubenzuron and teflubenzuron used as controls, juvenile hormone agents such as methoprene and pyriproxyfen had almost no growth inhibitory effect, and had acaricidal activity against indoor dust mites. It was revealed that is a characteristic specific to Compound A among the benzoylurea compounds. On the other hand, the pyrethroid agent phenothrin, which is mainly used as an active ingredient of conventional indoor dust mite agents, required a high concentration to exhibit acaricidal activity. Therefore, compound A, which is almost harmless to humans and animals in terms of mechanism of action, and has extremely high acaricidal activity at low concentration, replaces conventional active ingredients such as phenothrin and provides a very useful indoor dust-carrying acaricide. It is a thing.

【0016】試験例2 供試カーペットとして、市販のカーペット(ウール10
0%,ウールマークなし,カットタイプ,パイル長7m
m)を5cm×5cmの大きさに切断して用いた。この
カーペットに、小型ガラス噴霧器を用いて供試薬剤のア
セトン溶液を1m2 あたり20mgまたは100mg
と、コントロールとしてアセトンのみを噴霧し3時間風
乾した。各カーペット上にヤケヒョウヒダニ約450匹
を含む培地0.5gを植付け、相対湿度約65%に調整
した容器に入れ、温度25±1℃の恒温室に置いた。観
察はホットプレートを用いた加熱追い出し法により生ダ
ニ数を数えた。試験はそれぞれ3連制で行い、薬剤処理
区、コントロール区の生ダニ数より次式により増殖抑制
率を算出した。また、薬剤処理後1ヵ月間40℃に保存
したカーペットについても同様に供試した。結果を表2
に示す。 増殖抑制率(%)=〔{(コントロール区の生ダニ数)
−(薬剤処理区の生ダニ数)}/(コントロール区の生
ダニ数)〕×100
Test Example 2 As a test carpet, a commercially available carpet (wool 10
0%, no wool mark, cut type, pile length 7m
m) was used after being cut into a size of 5 cm × 5 cm. To this carpet, using a small glass sprayer, an acetone solution of the reagent agent is added at 20 mg or 100 mg per 1 m 2.
As a control, only acetone was sprayed and air dried for 3 hours. On each carpet, 0.5 g of a medium containing about 450 mosquitoes was planted, placed in a container adjusted to a relative humidity of about 65%, and placed in a temperature-controlled room at a temperature of 25 ± 1 ° C. For observation, the number of live mites was counted by the heat-discharging method using a hot plate. Each test was carried out in triplicate, and the growth inhibition rate was calculated from the number of live mites in the drug-treated group and the control group by the following formula. Further, the same test was carried out on a carpet stored at 40 ° C. for one month after the chemical treatment. The results are shown in Table 2.
Shown in. Growth inhibition rate (%) = [{(number of live mites in control area)
-(Number of live mites in chemical treatment area)} / (Number of live mites in control area)] x 100

【0017】[0017]

【表2】 [Table 2]

【0018】試験の結果、予めカーペットに薬剤処理す
る、いわゆる予防処理においても、化合物Aは低濃度で
極めて高い増殖抑制率を示し、また、耐候性にもすぐれ
るので、カーペットや布団等の屋内塵性ダニ予防処理剤
として極めて有用であることが確認された。なお、ジフ
ルベンズロンやテフルベンズロンのような他のベンゾイ
ルウレア系化合物には同様な効果は認められなかった。
As a result of the test, even in a so-called preventive treatment in which the carpet is preliminarily treated with a chemical, the compound A shows a very high growth inhibitory rate at a low concentration and has excellent weather resistance, so that it can be used indoors such as carpets and futons. It was confirmed to be extremely useful as a dust mite preventive treatment agent. Similar effects were not observed with other benzoylurea compounds such as diflubenzuron and teflubenzuron.

【0019】試験例3 試験例2に用いた5cm×5cmのカーペット中央部を
薬剤無処理区とし、外側周囲1cm幅を、試験例2に準
じて薬剤処理した。ただし、供試薬剤の処理量は、5c
m×5cmのカーペットの全面に対する量とした。この
カーペット中央部の薬剤無処理区上に、ヤケヒョウヒダ
ニ約200匹を含む培地0.2gを植付け、相対湿度約
65%に調整した容器に入れ、温度25±1℃の恒温室
に置いた。試験例2と同様に増殖抑制率を算出した結果
を表3に示す。
Test Example 3 The central portion of the 5 cm × 5 cm carpet used in Test Example 2 was set as a chemical untreated section, and the outer peripheral 1 cm width was treated with the chemical according to Test Example 2. However, the processing amount of the reagent is 5c
It is the amount for the entire surface of the m × 5 cm carpet. 0.2 g of a medium containing about 200 mosquito deer mosquitoes was planted on the chemical-untreated section in the center of the carpet, placed in a container adjusted to a relative humidity of about 65%, and placed in a temperature-controlled room at a temperature of 25 ± 1 ° C. Table 3 shows the results of calculating the growth inhibition rate in the same manner as in Test Example 2.

【0020】[0020]

【表3】 [Table 3]

【0021】試験の結果、薬剤を部分処理し、かつヤケ
ヒョウヒダニを薬剤無処理区に植付けたカーペットにお
いても、化合物Aは高い殺ダニ効果を示した。これは化
合物Aが忌避性を示さず、また、接触毒のみならず、食
毒としても作用するという化合物Aの特性に基づくもの
と考えられる。一方、ピレスロイド剤のフェノトリン
は、この濃度で全面均一処理方法においてある程度の殺
ダニ効果を示したものの、本試験の部分処理方法では、
ほとんど殺ダニ効果が認められなかった。すなわち、フ
ェノトリンの忌避性によりダニとの接触が妨げられ、接
触毒として作用し得なかったためと推定される。実際の
処理場面で必ずしも全面均一に処理できないことを考慮
すると、化合物Aが部分処理でも有効なことは、極めて
実用的な長所といえる。
As a result of the test, the compound A showed a high acaricidal effect even on the carpet partially treated with the drug and planted with the house dust mite mite-treated area. It is considered that this is based on the property of compound A that compound A does not exhibit repellent properties and acts not only as a contact poison but also as a food poison. On the other hand, the pyrethroid agent phenothrin showed a certain degree of acaricidal effect in the entire uniform treatment method at this concentration, but in the partial treatment method of this test,
Almost no acaricidal effect was observed. That is, it is presumed that the repellent property of phenothrin hindered contact with mites and could not act as a contact poison. Considering that it is not always possible to treat the entire surface uniformly in an actual treatment scene, it can be said that Compound A is effective even in the partial treatment, which is a very practical advantage.

【0022】実施例1 化合物A0.7gをエタノールに溶解し、エアゾール容
器に充填後、バルブ部分を取付け、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(300ml)を得
た。上記エアゾールを広さ2畳のカーペットに30ml
(有効成分として20mg/m2 )噴霧し、1ヵ月後に
コナヒョウヒダニ約500頭を接種したところ、ダニの
増殖を抑え、やがて生息密度は初期の5%以下に減少
し、高い予防効果が認められた。
Example 1 0.7 g of Compound A was dissolved in ethanol and filled in an aerosol container, and then a valve portion was attached, and a propellant was pressure-filled through the valve portion to obtain an aerosol (300 ml). 30ml of the above aerosol on a carpet of 2 tatami mats
After spraying (20 mg / m 2 as an active ingredient) and inoculating about 500 Kata leopard mite one month later, the growth of mites was suppressed, and the habitat density was reduced to 5% or less of the initial time, and a high preventive effect was observed. .

【0023】実施例2 化合物A0.1g、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0.2gと粉末飼料99.7gを十分に粉
砕混合して毒飼剤を得た。ヤケヒョウヒダニ約300頭
とツメダニ約200頭を接種した10cm平方のカーペ
ットに上記調整毒餌剤を1m2 あたり20g(有効成分
として20mg/m2 )の割合で散布し、2週間後に生
存ダニ数を調査したところ、いずれも10頭以下に減少
していた。
Example 2 0.1 g of compound A, 0.2 g of N- (2-ethylhexyl) -bicyclo [2.2.1] hept-5-ene-2,3-dicarboximide and 99.7 g of powdered feed. The mixture was thoroughly pulverized and mixed to obtain a poison veterinary preparation. About 20 g of the adjusted poison bait was sprayed at a rate of 20 g per 1 m 2 (20 mg / m 2 as an active ingredient) on a 10 cm square carpet inoculated with about 300 blemishes and about 200 mites, and the number of living mites was examined 2 weeks later. However, in all cases, the number was reduced to 10 or less.

【0024】[0024]

【発明の効果】以上詳細に説明したように、本発明の殺
屋内塵性ダニ剤は、コナダニ、ヒョウヒダニ、ツメダニ
などの屋内塵性ダニ類に対して高い殺ダニ活性を示し、
しかも従来の薬剤に比べて安全性が格段にすぐれるた
め、その実用性は極めて高い。
INDUSTRIAL APPLICABILITY As described in detail above, the indoor miticidal mite agent of the present invention exhibits a high acaricidal activity against indoor mite mites such as mites, leopard mites, and tick mites,
Moreover, its safety is far superior to that of conventional drugs, and therefore its practicality is extremely high.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 ハンス シューベルト 東京都品川区大井7−4−35 ─────────────────────────────────────────────────── ─── Continued Front Page (72) Inventor Hans Schubert 7-4-35 Oi, Shinagawa-ku, Tokyo

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 N−(2−クロロベンゾイル)−N’−
〔4−(2−クロロ−4−トリフルオロメチル−1−フ
ェニルメルカプト)フェニル〕ウレアを含有することを
特徴とする殺屋内塵性ダニ剤。
1. N- (2-chlorobenzoyl) -N'-
[4- (2-chloro-4-trifluoromethyl-1-phenylmercapto) phenyl] urea is contained, which is an indoor dust-killing agent.
JP31264593A 1993-11-18 1993-11-18 Indoor dusty acaricide Pending JPH07138112A (en)

Priority Applications (7)

Application Number Priority Date Filing Date Title
JP31264593A JPH07138112A (en) 1993-11-18 1993-11-18 Indoor dusty acaricide
CA002176596A CA2176596A1 (en) 1993-11-18 1994-11-11 Use of benzoylureas for controlling house dust mites
EP95900706A EP0729301A1 (en) 1993-11-18 1994-11-11 Use of benzoylureas for controlling house dust mites
JP51420395A JP3170286B2 (en) 1993-11-18 1994-11-11 Use of Benzoylureas for Control of House Dust Mites
US08/646,259 US5854288A (en) 1993-11-18 1994-11-11 Use of benzoylureas for controlling house dust mites
PCT/EP1994/003728 WO1995013703A1 (en) 1993-11-18 1994-11-11 Use of benzoylureas for controlling house dust mites
MX9408958A MX9408958A (en) 1993-11-18 1994-11-17 Miticide for house dust mites.

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP31264593A JPH07138112A (en) 1993-11-18 1993-11-18 Indoor dusty acaricide

Publications (1)

Publication Number Publication Date
JPH07138112A true JPH07138112A (en) 1995-05-30

Family

ID=18031708

Family Applications (1)

Application Number Title Priority Date Filing Date
JP31264593A Pending JPH07138112A (en) 1993-11-18 1993-11-18 Indoor dusty acaricide

Country Status (1)

Country Link
JP (1) JPH07138112A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2011049065A1 (en) * 2009-10-21 2011-04-28 日本曹達株式会社 Tick control bait

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2011049065A1 (en) * 2009-10-21 2011-04-28 日本曹達株式会社 Tick control bait
JP5449387B2 (en) * 2009-10-21 2014-03-19 日本曹達株式会社 Mite control bait

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