JPH0475201B2 - - Google Patents

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Publication number
JPH0475201B2
JPH0475201B2 JP59021219A JP2121984A JPH0475201B2 JP H0475201 B2 JPH0475201 B2 JP H0475201B2 JP 59021219 A JP59021219 A JP 59021219A JP 2121984 A JP2121984 A JP 2121984A JP H0475201 B2 JPH0475201 B2 JP H0475201B2
Authority
JP
Japan
Prior art keywords
mites
rhodan
present
butoxy
diethyl ether
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.)
Expired - Lifetime
Application number
JP59021219A
Other languages
Japanese (ja)
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JPS60163804A (en
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
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Priority to JP2121984A priority Critical patent/JPS60163804A/en
Publication of JPS60163804A publication Critical patent/JPS60163804A/en
Publication of JPH0475201B2 publication Critical patent/JPH0475201B2/ja
Granted legal-status Critical Current

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Description

【発明の詳細な説明】[Detailed description of the invention]

本発明はβ−ブトキシ−β′−ロダンジエチルエ
ーテル又はラウリン酸β−ロダンエチルエステル
を含有するこ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、ナミハダニ類等
は農作物に多大な被害を与えている。これらの農
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、チリダニ、ホモリダニ、イエダニ、ヒゼン
ダニ、ツメダニ、ニクダニ、サトウダニ等が発生
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つた。 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、β−ブトキシ−β′−ロダンジエチル
エーテル又はラウリン酸β−ロダンエチルエステ
ルを含有する組成物が、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。 本発明に使用するβ−ブトキシ−β′−ロダンジ
エチルエーテル又はラウリン酸β−ロダンエチル
エステルはピレスロイド用共力剤として知られて
いる化合物である。すなわち、β−ブトキシ−
β′−ロダンジエチルエーテル又はラウリン酸β−
ロダンエチルエステルは、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
おけるポ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驚くべきことにそれ自体
極めて高い殺ダニ力を示し、昆虫とダニ類におけ
る作用機作の違いを示唆した。これらのピレスロ
イド用共力剤は人畜に対する毒性が非常に低く又
極めて安価であることから、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。特に、カ
ーペツト類に発生するコナヒヨウヒダニはアレル
ギー性疾患や人体内ダ症の原因と目されており、
これらにピレスロイド用共力剤が有効であるとい
う知見は、保健衛生上、医学上意義深い。 又、本発明には、フエノトリン、パーメスリ
ン、レスメトリン、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
ルボキシレートのようなピレスロイド系化合物、
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500のような他の
ピレスロイド用共力剤、あるいは、デイート、ベ
ンジルベンゾエートのような害虫忌避剤、又、毒
性等が問題とならない程度のスミチオン、ダイア
ジノン等の有機リン剤系殺虫剤あるいはツマサイ
ド、メオパールのようなカーバメート系殺虫剤、
その他の殺虫剤、殺菌剤、防黴剤等との併用もも
ちろん可能であり、その組成物は、多目的組成物
として使用できる。 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、ケトン類、エ
ーテル類、脂肪族炭化水素類、ハロゲン化炭化水
素類、エステル類、酸アミド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
粉末等が適しており、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種また
は2種以上の混合物が使用される。 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〜5gの前記β−ブトキシ−β′−ロ
ダンジエチルエーテル又はラウリン酸β−ロダン
エチルエステルが使用される。なお、家庭内で畳
に処理する場合にはエアゾール剤が使いやすく、
畳表の下、畳と畳の間に処理すれば効果的であ
り、一方畳を製造する際本発明組成物を適用する
ことももちろん可能である。また、カーペツト類
に生息するコナヒヨウヒダニ類等の駆除には1m2
あたり、0.5mg〜5gの本発明ピレスロイド用共力
剤の適用が好ましく、エアゾール剤、粉剤等の形
態で簡便に使用でき、効果、安全性の面でも優れ
ている。又、カーペツト製造時に処理する場合に
は、カーペツトのバツキング材に乳剤を混合して
使用することも可能である。更に、部屋全体を一
時に処理するには燻煙剤が便利である。 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。 試験例 1 供試化合物で処理した粉末飼料10gと約2000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のシヤーレに入れ、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、下式に従つて繁殖抑制率を計算し
た。試験は各濃度につき3回繰返し行なつた。 繁殖抑制率=無処理区のダニ数−
処理区のダニ数/無処理区のダニ数×100 なお、供試ピレスロイド共力剤中の符号A,B
はそれぞれ下記の意味を表わす。 A;β−ブトキシ−β′−ロダンジエチルエー
テル B;ラウリン酸β−ロダンエチルエステル
The present invention relates to an indoor acaricide characterized by containing β-butoxy-β'-rhodan diethyl ether or β-rhodan ethyl lauric acid ester. An extremely wide variety of mites inhabit the earth, and for example, citrus spider mites, two-spotted spider mites, etc. that parasitize plants cause great damage to agricultural crops. Acaricides aimed at these agricultural applications have been under development for a long time, and new promising compounds have recently been discovered one after another. On the other hand, due to changes in the living environment in recent years, dust mites, dust mites, brown dust mites, dust mites, dust mites, claw mites, sugar mites, etc. have appeared in homes, and they not only cause discomfort, but also cause allergic asthma and skin rashes. It's causing problems. It has been known that organic phosphorus agents such as Sumithion and Diazinon are effective against these indoor mites, but there are obstacles to practical application due to safety and resistance issues for humans and livestock, and accurate extermination is difficult. There was an urgent need to establish a method. 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, we found that β-butoxy-β'-rhodan diethyl ether or β-rhodan ethyl lauric acid ester. The present invention has been completed by discovering that the composition containing the present invention exhibits an extremely high acaricidal effect on powder mites, house dust mites, dust mites, and the like. β-Butoxy-β'-rhodan diethyl ether or β-rhodan ethyl laurate used in the present invention is a compound known as a synergist for pyrethroids. That is, β-butoxy-
β'-Rhodan diethyl ether or β-lauric acid
Rodan ethyl ester itself does not have insecticidal power, but when used together with pyrethroids, it is known to suppress the metabolic decomposition of pyrethroid in the insect body and improve its insecticidal power. Surprisingly, it itself showed extremely high acaricidal activity, suggesting a difference in the mechanism of action between insects and mites. These pyrethroid synergists have very low toxicity to humans and livestock and are extremely inexpensive, so they are extremely useful in the development of indoor acaricides. In particular, Dermatophagoides mites, which occur on carpets, are thought to be the cause of allergic diseases and human infections.
The knowledge that pyrethroid synergists are effective against these is of great health and medical significance. The present invention also includes phenothrin, permethrin, resmethrin, 3'-phenoxybenzyl,
pyrethroid compounds such as 2,2,3,3-tetramethylcyclopropanecarboxylate,
Other pyrethroid synergists such as IBTA, S-421, piperonyl butoxide, cinepirin-222, cinepirin 500, or pest repellents such as DEET, benzyl benzoate, and toxicity are not a problem. Organic phosphorus insecticides such as Sumithion and Diazinon, or carbamate insecticides such as Tsumaside and Meopal,
Of course, it is also possible to use it in combination with other insecticides, fungicides, fungicides, etc., and the composition can be used as a multipurpose composition. 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. powder, oil,
Used as an aerosol agent, etc. Suitable liquid carriers include solvents such as water, alcohols, ketones, ethers, aliphatic hydrocarbons, halogenated hydrocarbons, esters, and acid amides; Mixtures of two or more are used. In addition, suitable solid carriers include, for example, clays (kaolin, bentonite, etc.), talcs, silicas, alumina powder, activated carbons, vegetable powders, etc., and one or a mixture of two or more of these is suitable. 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. 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, to exterminate mites living on tatami mats such as mites, 0.1 mg or more, preferably 1 mg to 5 g of the β-butoxy-β'-rhodan diethyl ether or β-rhodan ethyl lauric acid ester is used per 1 tatami mat. In addition, when treating tatami mats at home, an aerosol agent is easy to use.
It is effective to treat the composition under the tatami surface and between the tatami mats, and it is of course also possible to apply the composition of the present invention when manufacturing tatami mats. In addition, 1 m 2 can be used to exterminate mites, etc. that live in carpets.
It is preferable to apply 0.5 mg to 5 g of the synergist for pyrethroid of the present invention per dose, and it can be easily used in the form of an aerosol, powder, etc., and is excellent in terms of effectiveness and safety. In addition, when the emulsion is treated during carpet production, it is also possible to use the emulsion mixed with the backing material of the carpet. Additionally, fumigants are useful for treating an entire room at once. EXAMPLES Hereinafter, the present invention will be explained in more detail with reference to examples, but the present invention is not limited to the following examples unless the gist thereof is exceeded. Test Example 1 10g of powdered feed treated with the test compound and 10g of powdered feed containing approximately 2000 woolly mites were mixed,
A test powder feed of a predetermined concentration was obtained. This powdered feed
Place 5g each in a 6cm diameter chalet and heat at 25℃.
It was placed under conditions of 75% humidity. 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. Reproduction suppression rate = number of mites in untreated area -
Number of mites in treated area/number of mites in untreated area x 100 Note that the codes A and B in the sample pyrethroid synergist
represent the following meanings. A: β-butoxy-β'-rhodan diethyl ether B: lauric acid β-rhodan ethyl ester

【表】 上記結果より、本発明組成物すなわち、β−ブ
トキシ−β′−ロダンジエチルエーテル又はラウリ
ン酸β−ロダンエチルエステルを含有する殺ダニ
剤、又はこれに他の薬剤を併用した組成物(共試
化合物1〜5)は優れた殺ダニ効果を示した。一
方、他のピレスロイド用共力剤単独(対照化合
物;供試化合物例6〜7)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。 試験例 2 供試化合物で処理した粉末飼料10gと、約1200
匹のコナヒヨウ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。
[Table] From the above results, it was found that the composition of the present invention, that is, the acaricide containing β-butoxy-β'-rhodan diethyl ether or β-rhodan ethyl lauric acid, or the composition using this in combination with other drugs ( Co-test compounds 1 to 5) showed excellent acaricidal effects. On the other hand, the activity of other pyrethroid synergists alone (control compounds; test compound examples 6 to 7) was very low;
The usefulness of the composition of the present invention was confirmed. Test Example 2 10g of powdered feed treated with the test compound and approx.
10 g of a powdered feed containing 100.000 mites was mixed to obtain a test powdered feed with a predetermined concentration. A test was conducted in the same manner as in Test Example 1 using 5 g of this powdered feed, and the reproduction suppression rate was determined after 1 week and 2 weeks.

【表】【table】

【表】 上記結果より、本発明組成物は、コナヒヨウヒ
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、一方、
他のピレスロイド用共力剤であるサイネピリン
222の活性は非常に低く、本発明のβ−ブトキシ
−β′−ロダンジエチルエーテル又はラウリン酸β
−ロダンエチルエステルが特異的に屋内に発生す
るダニ類に効果が高いことが確認された。 実施例 1 β−ブトキシ−β′−ロダンジエチルエーテル
2.0g、レスメトリン1.0g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
下に減少していた。 実施例 2 ラウリン酸β−ロダンエチルエステル1.0部、
パーメスリン0.5部、S−421 1.0部とクレー97.5
部をよく粉砕混合して粉剤を得た。 コナヒヨウヒダニ約400頭を接種した10cm平方
のカーペツトに上記調製粉剤を1m2あたり20gの
割合で散布し、2日後に生存コナヒヨウヒダニ数
を調査したところ5頭以下であつた。
[Table] From the above results, the composition of the present invention exhibits a higher acaricidal effect against Dermatophagoides nigricans than Sumithion, an organic phosphorus agent that has been considered to be effective in the past;
Cinepirin, a synergist for other pyrethroids
The activity of 222 is very low, and the activity of β-butoxy-β'-rhodan diethyl ether or lauric acid β-
- It was confirmed that rhodan ethyl ester is highly effective against specifically indoor mites. Example 1 β-Butoxy-β'-rhodan diethyl ether
Dissolve 2.0g and 1.0g of resmethrin in refined kerosene,
After filling the aerosol container and attaching the valve part, the propellant was filled under pressure through the valve part to obtain an aerosol. 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 the density of mites was examined one week later and found to have decreased to less than 5%. Example 2 1.0 part of lauric acid β-rodane ethyl ester,
0.5 parts permethrin, 1.0 part S-421 and 97.5 parts clay
The mixture was thoroughly ground and mixed to obtain a powder. The above-mentioned powder preparation was applied to a 10 cm square carpet inoculated with about 400 Dermatophagoides nigricans at a rate of 20 g per 1 m 2 . Two days later, the number of surviving Dermatophagoides nigra was less than 5.

Claims (1)

【特許請求の範囲】[Claims] 1 β−ブトキシ−β′−ロダンジエチルエーテル
又はラウリン酸β−ロダンエチルエステルを含有
することを特徴とする屋内用殺ダニ剤。
1. An indoor acaricide characterized by containing β-butoxy-β'-rhodan diethyl ether or β-rhodan ethyl lauric acid ester.
JP2121984A 1984-02-06 1984-02-06 Acaricide for indoor use Granted JPS60163804A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2121984A JPS60163804A (en) 1984-02-06 1984-02-06 Acaricide for indoor use

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2121984A JPS60163804A (en) 1984-02-06 1984-02-06 Acaricide for indoor use

Publications (2)

Publication Number Publication Date
JPS60163804A JPS60163804A (en) 1985-08-26
JPH0475201B2 true JPH0475201B2 (en) 1992-11-30

Family

ID=12048897

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2121984A Granted JPS60163804A (en) 1984-02-06 1984-02-06 Acaricide for indoor use

Country Status (1)

Country Link
JP (1) JPS60163804A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2645315B2 (en) * 1988-04-30 1997-08-25 アース製薬株式会社 Powder for controlling mites and method for controlling mites

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59167501A (en) * 1983-03-14 1984-09-21 Dainippon Jiyochiyuugiku Kk Aerosol injection agent

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59167501A (en) * 1983-03-14 1984-09-21 Dainippon Jiyochiyuugiku Kk Aerosol injection agent

Also Published As

Publication number Publication date
JPS60163804A (en) 1985-08-26

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