JP2796588B2 - Indoor acaricide - Google Patents

Indoor acaricide

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Publication number
JP2796588B2
JP2796588B2 JP1218381A JP21838189A JP2796588B2 JP 2796588 B2 JP2796588 B2 JP 2796588B2 JP 1218381 A JP1218381 A JP 1218381A JP 21838189 A JP21838189 A JP 21838189A JP 2796588 B2 JP2796588 B2 JP 2796588B2
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JP
Japan
Prior art keywords
acaricide
mites
present
indoor
group
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 - Fee Related
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JP1218381A
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Japanese (ja)
Other versions
JPH0381202A (en
Inventor
和志 菅本
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.)
Dainihon Jochugiku Co Ltd
Original Assignee
Dainihon Jochugiku Co Ltd
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Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、桂皮酸誘導体を有効成分として含有するこ
とを特徴とする屋内用殺ダニ剤に関する。
The present invention relates to an indoor acaricide characterized by containing a cinnamic acid derivative as an active ingredient.

〔従来の技術〕[Conventional technology]

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。
An extremely large variety of mites inhabit the earth, and for example, citrus spider mites and spider mites, which are parasitic on plants, cause great damage to agricultural crops. These acaricides for agricultural use have been developed for a long time, and new 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
リン剤がこれらの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
のため実用下には障害があり、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, due to changes in the living environment in recent years, household mites,
Dust mites, dust mites, and the like are generated, causing not only discomfort but also problems such as causing allergic asthma and rash. It has been known that organophosphorus agents such as sumithion and diazinon are effective against these indoor mites, but there are obstacles in practical use due to safety and resistance to humans and animals, The establishment of an extermination method has been eagerly awaited.

最近、安全性の高いピレスロイド剤の適用や、テルペ
ン系化合物を用いる殺ダニ剤が、特開昭63−104905号公
報や、特開平1−163104号公報に開示されているがその
駆除効果は必ずしも満足できるものでなく、また、殺ダ
ニ剤のかわりにダニ忌避剤を使用する試みについても生
息場所を移動させるのみで根本的な駆除方法とはいえ
ず、的確な殺ダニ剤の開発が切望されているのが現状で
ある。
Recently, the application of highly safe pyrethroids and acaricides using terpene compounds have been disclosed in JP-A-63-104905 and JP-A-1-163104, but the control effect is not necessarily. Unsatisfactory, and attempts to use acaricides instead of acaricides are not a fundamental extermination method because they only move the habitat, and the development of an accurate acaricide is desired. That is the current situation.

〔発明が解決しようとする問題点〕[Problems to be solved by the invention]

本発明は、従来の屋内用殺ダニ剤が有している人畜へ
の毒性上の問題、不十分な駆除効力等の欠点を解消し、
安全性、有効性にすぐれ、しかも安価で使いやすい屋内
用殺ダニ剤を提供するものである。
The present invention solves the problem of toxicity to humans and animals having the conventional indoor acaricide, disadvantages such as insufficient control effect,
An object of the present invention is to provide an indoor acaricide that is excellent in safety and effectiveness, and is inexpensive and easy to use.

〔問題点を解決するための手段〕[Means for solving the problem]

上記目的を達成するため本発明者らは鋭意研究を重ね
た結果、 一般式(I) (式中、 R1は水素原子又はメチル基を表し、 R2は水素原子又は炭素原子数1ないし8のアルキル基
を表し、そして Rはアルデヒド基、ヒドロキシメチル基、炭素原子数
1ないし4のアルコキシカルボニル基又は炭素原子数1
ないし4のアルキルカルボキシメチル基を表すが、ただ
し R1およびR2が共に水素原子を表す場合、Rはアルデヒ
ド基を表さない)で表される桂皮酸誘導体を有効成分と
して含有する屋内用殺ダニ剤が、ヒョウヒダニ、コナダ
ニ、ホコリダニ等住居内に生息するダニ類に対して高い
殺ダニ効果を示し、しかも低毒性であることを見い出し
本発明を完成した。
The present inventors have conducted intensive studies to achieve the above object, and as a result, the general formula (I) (Wherein, R 1 represents a hydrogen atom or a methyl group, R 2 represents a hydrogen atom or an alkyl group having 1 to 8 carbon atoms, and R represents an aldehyde group, a hydroxymethyl group, a C 1-4 alkyl group. Alkoxycarbonyl group or carbon atom number 1
Wherein R 1 and R 2 both represent a hydrogen atom, R does not represent an aldehyde group), and the cinnamic acid derivative represented by the formula (1) is used as an active ingredient. It has been found that the acaricide exhibits a high acaricidal effect on mites, such as Dermatophagoides, Acarina, and Dust mites, which live in the house and has low toxicity, and thus completed the present invention.

本発明で用いられる桂皮酸誘導体は、香料として汎用
されているが、殺虫性を示さないことが知られており、
殺ダニ効果を奏するという本発明は全く予想外のことで
あった。
The cinnamic acid derivative used in the present invention is widely used as a fragrance, but is known not to exhibit insecticidal properties,
The present invention having an acaricidal effect was completely unexpected.

一般式(I)で示される具体例をあげれば以下の如く
であるがもちろんこれらのみに限定されるものではな
い。
Specific examples represented by the general formula (I) are as follows, but are not limited thereto.

なお、一般式(I)にはR2がアルキル基の場合炭素間
2重結合に基づく2種類の幾何異性体が存在するが、そ
れらの各々あるいは混合物いずれも本発明に含まれる。
In the general formula (I), when R 2 is an alkyl group, there are two kinds of geometric isomers based on a carbon-carbon double bond, and each of them or a mixture thereof is included in the present invention.

本発明屋内用殺ダニ剤の有効成分は、通常液体、又は
固体であり、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、塗布剤、錠剤等として
使用される。
The active ingredient of the acaricide for indoor use of the present invention is usually a liquid or a solid, and it is possible to apply the active ingredient as it is. However, it is usually preferable to use an appropriate carrier or other compounding agent according to the purpose of use. And various forms such as emulsions, wettable powders, powders, oils, aerosols, coatings, tablets and the like.

また、上記有効成分は従来殺ダニ剤と比べると揮散性
が高く、常温徐放性製剤やあるいは例えばパルプ板状の
適当な保持体に含浸させたのち適当な加熱蒸散器により
加熱蒸散させるいわゆる加熱蒸散剤や燻蒸剤として適用
することも可能である。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、フロン113、フロン114B
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、ペントナイト等)、タルク類、シリ
カ類、炭酸カルシウム、アルミナ粉末、活性炭類、木
粉、でん粉、小麦粉などの植物性粉末、シクロデキスト
リン等が適当であり、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、噴射剤、浸透剤、界面活性剤、安
定剤、塗膜形成剤、揮散調整剤等が適当であり、これら
の1種又は2種以上の混合物が使用される。
In addition, the above-mentioned active ingredient has a higher volatility than the conventional acaricide, so-called heating which is impregnated in a room temperature sustained-release preparation or a suitable holding material such as a pulp plate and then heated and evaporated by a suitable heating evaporator. It can also be applied as a transpirant or fumigant. As a liquid carrier, for example,
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, Freon 113, Freon 114B
Etc.), esters, acid amides, nitriles and the like are suitable, and one or a mixture of two or more thereof is used. Examples of the solid carrier include clays (kaolin, pentonite, etc.), talc, silicas, calcium carbonate, alumina powder, activated carbons, wood flour, starch, vegetable powders such as flour, cyclodextrin and the like. Suitable and mixtures of one or more of these are used. Further, as the compounding agent, an emulsifier, a dispersant, a spreading agent, a propellant, a penetrant, a surfactant, a stabilizer, a film forming agent, a volatilization modifier, and the like are appropriate, and one or more of these may be used. Is used.

なお、塗膜形成剤としては、セルロース誘導体、ビニ
ール系樹脂、アルキッド系樹脂、ユリア系樹脂、シリコ
ン系樹脂、ウレタン系樹脂、エポキシ系樹脂などをあげ
るこができ、揮散調整剤としては、トリシクロデカン、
シクロドデカン、2,4,6−トリイソプロピル−1,3,5−ト
リオキサン、トリメチレンノルボルネンなどの昇華性担
体や、保留剤としての例えばステアリン酸ブチル、ミリ
スチン酸イソプロピルなどの高級脂肪酸エステルや、ピ
ペロニルブトキサイド、サイネピリン500などを例示で
きる。
Examples of the coating film forming agent include cellulose derivatives, vinyl resins, alkyd resins, urea resins, silicon resins, urethane resins, epoxy resins, and the like. Decane,
Sublimable carriers such as cyclododecane, 2,4,6-triisopropyl-1,3,5-trioxane, trimethylene norbornene, higher fatty acid esters such as butyl stearate, isopropyl myristate, etc. Ronyl butoxide, Sinepirin 500 and the like can be exemplified.

更に、本発明の屋内用殺ダニ剤は、各種の殺虫剤、協
力剤、酸化防止剤、殺菌剤、防黴剤、忌避剤、香料、着
色料等を配合してもよい。配合可能な殺虫剤としては、
アレスリン、d−T80−アレスリン、プラレトリン、d
−T80−フラメトリン、d−T80−フタルスリン、d−T8
0−レスメトリン、フェノトリン、ペルメトリン、サイ
フェノトリン、サイペルメトリン、フェンバレレート、
エトフェンプロックスなどのピレストロイド系化合物、
フェニトロチオン、ダイアジノン、ピリダフェンチオン
などの有機リン系化合物や、NAC、MTMC、PHCなどのカー
バメート系化合物などをあげることができる。
Further, the indoor acaricide of the present invention may contain various insecticides, synergists, antioxidants, fungicides, fungicides, repellents, fragrances, coloring agents, and the like. As pesticides that can be blended,
Aresulin, d-T80-aresulin, praletrin, d
-T80-Flamethrin, d-T80-phthalsulin, d-T8
0-resmethrin, phenothrin, permethrin, cyphenothrin, cypermethrin, fenvalerate,
Pyrethroid compounds such as etofenprox,
Examples include organic phosphorus compounds such as fenitrothion, diazinon, and pyridafenthion, and carbamate compounds such as NAC, MTMC, and PHC.

また、本発明に屋内用殺ダニ剤にエムペントリンやDD
VP、あるいはパラジクロロベンゼン、ナフタリン、樟脳
などの揮散性防虫剤を組み合わせたり、ディート、N−
ブチルアセトアニリド、N,N−ジエチルサクシナメート
などの忌避剤を適宜混合し効果のすぐれた多目的殺ダニ
剤を得ることもできる。
In addition, empentrin and DD are used as indoor acaricides in the present invention.
VP, or a combination of volatile insect repellents such as paradichlorobenzene, naphthalene, and camphor;
A repellent such as butylacetanilide and N, N-diethylsuccinamate may be appropriately mixed to obtain a multipurpose acaricide having an excellent effect.

本発明屋内用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
記有効成分を、また、カーペット類に生息するヒョウダ
ニ類の駆除には1m2あたり0.5mg〜2gの有効成分を処理す
るのが望ましい。
The amount of the active ingredient and the amount used in the indoor acaricide of the present invention are appropriately determined according to the dosage form, the application target, the application method, the application place, and the like. For example, for the control of mites that live in mats such as mites, per tatami, 0.1 mg or more, preferably 1 mg to 2 g of the active ingredient, and for the control of house dust mites that live in carpets, 0.5 mg to 2 g per square meter. Of the active ingredient.

本発明は、また、上記殺ダニ剤を基材に保持させてな
るダニ防除材をも提供するものである。該ダニ防除材
は、その基材の特性を利用してダニ防除性を有するフィ
ルム、シート、クッション、寝具類用充填材、建築、構
築材料として用いられる。ここで基剤としては例えば、
ポリエチレン、ポリプロピレン、ポリエステル、エチレ
ン−酢酸ビニール等の合成樹脂シート、動植物質又は無
機質繊維体シートなどや、クッション、寝具類用充填材
としての天然綿、合成繊維綿、羽毛、ソバ殻、発泡プラ
スチックなどがあげられる。
The present invention also provides a miticide obtained by holding the above-mentioned acaricide on a substrate. The mite control material is used as a film, a sheet, a cushion, a filler for bedding, a building material, and a construction material having mite control properties by utilizing the properties of the base material. Here, as the base, for example,
Synthetic resin sheets such as polyethylene, polypropylene, polyester, ethylene-vinyl acetate, animal and plant or inorganic fibrous sheets, and natural cotton, synthetic fiber cotton, feathers, buckwheat hulls, foam plastic, etc. as cushioning and bedding fillers Is raised.

本発明が提供するダニ防除材の好ましい一実施形態と
しては、ダニ防除カーペットの例示できる。該ダニ防除
カーペットは、例えばパイル、第一基布、パッキング剤
及び第二基布より成る通常のカーペットを作成後、必要
に応じて塗膜形成剤を配合した液剤形態を有する本発明
の屋内用殺ダニ剤を噴霧塗布するか、上記カーペットの
作成に先立ち、パリル、第一基布及び第二基布のいずれ
か少なくとも1種に本発明の屋内用殺ダニ剤を処理しこ
れらを用いてカーペットを作成することにより得られ
る。上記の如く作成されるダニ防除カーペットは、カー
ペット面積1m2当りに有効成分を約0.1〜10g保持させる
ことが好ましい。
One preferred embodiment of the tick control material provided by the present invention is a tick control carpet. The mite control carpet is an indoor carpet of the present invention having a liquid form in which, for example, a normal carpet including a pile, a first base cloth, a packing agent, and a second base cloth is prepared, and then a film forming agent is added as necessary. Spray-applying the acaricide or prior to the preparation of the carpet, at least one of paryl, the first base fabric and the second base fabric is treated with the indoor acaricide of the present invention, and the carpet is used using these. Is obtained. The mite control carpet prepared as described above preferably holds about 0.1 to 10 g of the active ingredient per 1 m 2 of carpet area.

こうして得られた本発明の屋内用殺ダニ剤あるいはこ
れを保持させてなるダニ防除材は、種々のダニに対して
高い駆除効果を示し、特に、気管示喘息、アトピー性皮
膚炎、鼻アレルギーなどを惹起するといわれているコナ
ヒョウヒダニやヤケヒョウヒダニなどのヒョウヒダニ
類、アレルギー疾患や人体内ダニ症の病原と目されてい
るケナガコナダニやムギコナダニなどのコナダニ類、ニ
クダニ類、ツメダニ類、ホコリダニ類、イエダニ類など
の駆除に極めて有用なものである。
The acaricide for indoor use of the present invention thus obtained or a mite control material obtained by retaining the same exhibits a high extermination effect on various mites, particularly, tracheal asthma, atopic dermatitis, nasal allergy and the like. Eradication of house dust mites such as Dermatophagoides farinae and Dermatophagoides pteronyssinus, which are said to cause terrestrial mite, Dermatophagoides farinae and Dermatophagoides farinae, which are considered to be pathogenic for allergic diseases and mite mites in the human body. Is extremely useful.

以下、試験例ならびに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。
Hereinafter, 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 is not exceeded.

試験例1 5cm×10cmの長方形のろ紙に供試化合物の10mMアセト
ン溶液を0.5ml滴下し、風乾後、2つ折りし間にコナヒ
ョウヒダニを50〜150匹放飼した。この2つ折ろ紙を2
ヶのアクリル円筒(内径4.1cm、高さ2cm)で挟み、輪ゴ
ムで固定後、容積が1の蓋付き容器内(27〜28℃、65
%RH)に設置し、24時間放置後生ダニ数及び死ダニ数を
数え、各供試化合物の殺ダニ効力を調べた。
Test Example 1 0.5 ml of a 10 mM acetone solution of a test compound was dropped on a 5 cm × 10 cm rectangular filter paper, air-dried, and 50 to 150 Dermatophagoides farinae were released between two folds. Put these two fold papers in 2
Acrylic cylinders (inner diameter 4.1cm, height 2cm) sandwiched and fixed with rubber bands.
% RH), and after standing for 24 hours, the number of live mites and the number of dead mites were counted, and the acaricidal efficacy of each test compound was examined.

なお、対照化合物としては、ピレスロイド化合物のd
−T80−レスメトリンならびに特開平1−163104号公報
開示のシトラール、カルボンを用いた。
As a control compound, d of the pyrethroid compound was used.
-T80-resmethrin and citral and carvone disclosed in JP-A-1-163104 were used.

試験の結果、本発明で用いる桂皮酸誘導体はコナヒョ
ウヒダニに対して高い接触殺ダニ効力を示し、対照化合
物のd−T80−レスメトリンや特開平1−163104号公報
開示のシトラール、カルボンより非常にすぐれていた。
As a result of the test, the cinnamic acid derivative used in the present invention shows high contact acaricidal activity against Dermatophagoides farinae, and is very superior to the control compounds d-T80-resmethrin and citral and carvone disclosed in JP-A-1-163104. Was.

試験例2 供試化合物の揮散分子の殺ダニ効力を調べるため、試
験例1と同様な装置を用いて試験を行った。約1cm四方
の布地に供試化合物の100mMアセトン溶液100μl(ケナ
ガコナダニの場合200μl)を滴下し、風乾後下方のア
クリル円筒の底に置き、更にコナヒョウヒダニ又はケナ
ガコナダニ100〜200匹を無処理の2つ折ろ紙の間に挟ん
で1の容器内に設置した。24時間放置後、生ダニ数及
び死ダニ数を数え、揮散した各供試化合物の致死効力を
求めたところ下表の如くであった。なお、対照化合物と
しては、常温揮散性ピレスロイドであるエムペントリン
ならびにシトラール、シトロネラール、トランスーシン
ナミックアシッドを用いた。
Test Example 2 A test was conducted using the same apparatus as in Test Example 1 in order to examine the acaricide efficacy of the test compound on volatile compounds. 100 μl of a 100 mM acetone solution of the test compound (200 μl in the case of P. aeruginosa) was dropped onto about 1 cm square cloth, air-dried, and placed on the bottom of the lower acrylic cylinder. And placed in one container. After standing for 24 hours, the number of live mites and the number of dead mites were counted, and the lethal efficacy of each test compound volatilized was determined, as shown in the table below. As control compounds, empentrin, which is a volatile volatile pyrethroid, and citral, citronellal, and trans-cinnamic acid were used.

試験の結果、本発明で用いる桂皮酸誘導体は揮散分子
の殺ダニ効力も極めて高く、徐放性製剤や加熱蒸散製剤
への適用も有用であることが確認された。
As a result of the test, it was confirmed that the cinnamic acid derivative used in the present invention has an extremely high acaricidal effect on volatile molecules and is useful for application to sustained-release preparations and heat-evaporation preparations.

一方、防虫剤として広く使用されているエムペントリ
ンや、特開平1−163104号公報開示のシトラールやシト
ロネラール、あるいは桂皮酸自体の殺ダニ効力は非常に
弱いことも明らかとなった。
On the other hand, it was also revealed that empentrin, which is widely used as an insect repellent, citral and citronellal disclosed in JP-A-1-163104, and cinnamic acid itself have very weak acaricidal efficacy.

実施例1 前記化合物No.(2),(6),(8),(10)およ
び(13)各々10gに、香料を微量、ケロシンを加えて全
体を120mlとし、これと液化石油ガス及びジメチルエー
テル混合物(1:1容積比)の180mlとをエアゾール用耐圧
缶に充填後噴射装置を取付けてエアゾール剤の形態とし
ての本発明屋内用殺ダニ剤を得た。
Example 1 To 10 g of each of the above compound Nos. (2), (6), (8), (10) and (13), a very small amount of fragrance and kerosene were added to make a total of 120 ml, which was combined with liquefied petroleum gas and dimethyl ether. After filling 180 ml of the mixture (1: 1 volume ratio) into a pressure-resistant can for aerosol, an injection device was attached to obtain an acaricide for indoor use of the present invention in the form of an aerosol.

ヒョウヒダニが発生したカーペットに1m2あたり20ml
噴射し1日後にカーペット中のダニ数を観察したところ
回収ダニ数に対する死ダニ数の比率はいずれも90%以上
であった。
20ml per 1m 2 in the carpet house dust mite has occurred
One day after the injection, the number of mites in the carpet was observed. The ratio of the number of dead mites to the number of collected mites was 90% or more.

実施例2 下表の仕様にて本発明屋内用殺ダニ剤を処理したカー
ペットを作製した。
Example 2 A carpet treated with the indoor acaricide of the present invention according to the specifications shown in the following table was produced.

なお、化合物番号は前記化合物例のものと同一であ
る。
The compound numbers are the same as those of the above compound examples.

本発明殺ダニ剤を処理したカーペットを20×20cmの大
きさに切り取り、中央部にコナヒョウヒダニ約5,000頭
を含むダニ培地を置き、25℃、60%RH条件下で2日間保
存後掃除機でカーペット表面又は裏面のダニを吸い取
り、所定の方法に従って生存ダニ数を数え、次式 X;薬剤無処理カーペット区の生存ダニ数 Y;殺ダニ済処理カーペット区の生存ダニ数により死虫
率を求めたところいずれも90%以上であった。
The carpet treated with the acaricide of the present invention is cut into a size of 20 × 20 cm, a tick culture medium containing about 5,000 Dermatophagoides farinae is placed in the center, stored at 25 ° C. and 60% RH for 2 days, and then carpeted with a vacuum cleaner. Suck the mites on the front or back, count the number of live mites according to the prescribed method, X: Number of surviving mites in the carpet untreated carpet Y; The mortality was determined by the number of surviving mites in the carpet treated with the acaridide.

また、これらのカーペットは匂いや刺激性の点でも問
題なく本発明屋内用殺ダニ剤の有用性が確認された。
In addition, these carpets confirmed the usefulness of the indoor acaricide of the present invention without any problem in terms of odor and irritation.

実施例3 前記化合物No.(2),(4),(7)および(11)
各々2gにゲル化剤8gを配合し常法により錠剤形態の本発
明屋内用殺ダニ剤を調整した。
Example 3 Compound Nos. (2), (4), (7) and (11)
8 g of a gelling agent was added to 2 g of each, and the acaricide for indoor use of the present invention in the form of a tablet was prepared by a conventional method.

布団を収納した布製袋内に上記錠剤(和紙で包装した
もの)2ヶ入れて保存したところ、布団にはダニ類の生
息は全くみられなかった。
When two of the above tablets (packed with Japanese paper) were stored in a cloth bag containing the futon and stored, no ticks were found on the futon.

〔発明の効果〕〔The invention's effect〕

本発明屋内用殺ダニ剤は、有効成分として一般式
(I)の桂皮酸誘導体を含有することに基づいて、安全
性、使用性にすぐれ、高い殺ダニ効力を奏するものであ
る。
INDUSTRIAL APPLICABILITY The indoor acaricide of the present invention is excellent in safety and usability and exhibits high acaricidal efficacy based on containing a cinnamic acid derivative of the general formula (I) as an active ingredient.

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】一般式(I) (式中、 R1は水素原子又はメチル基を表し、 R2は水素原子又は炭素原子数1ないし8のアルキル基を
表し、そしてRはアルデヒド基、ヒドロキシメチル基、
炭素原子数1ないし4のアルコキシカルボニル基又は炭
素原子数1ないし4のアルキルカルボキシメチル基を表
すが、ただし R1およびR2が共に水素原子を表す場合、Rはアルデヒド
基を表さない)で表される桂皮酸誘導体を有効成分とし
て含有することを特徴とする屋内用殺ダニ剤。
1. The compound of the general formula (I) Wherein R 1 represents a hydrogen atom or a methyl group, R 2 represents a hydrogen atom or an alkyl group having 1 to 8 carbon atoms, and R represents an aldehyde group, a hydroxymethyl group,
Represents an alkoxycarbonyl group having 1 to 4 carbon atoms or an alkylcarboxymethyl group having 1 to 4 carbon atoms, provided that when R 1 and R 2 both represent a hydrogen atom, R does not represent an aldehyde group) An indoor acaricide comprising the cinnamic acid derivative represented as an active ingredient.
JP1218381A 1989-08-24 1989-08-24 Indoor acaricide Expired - Fee Related JP2796588B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1218381A JP2796588B2 (en) 1989-08-24 1989-08-24 Indoor acaricide

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1218381A JP2796588B2 (en) 1989-08-24 1989-08-24 Indoor acaricide

Publications (2)

Publication Number Publication Date
JPH0381202A JPH0381202A (en) 1991-04-05
JP2796588B2 true JP2796588B2 (en) 1998-09-10

Family

ID=16719010

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1218381A Expired - Fee Related JP2796588B2 (en) 1989-08-24 1989-08-24 Indoor acaricide

Country Status (1)

Country Link
JP (1) JP2796588B2 (en)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07103001B2 (en) * 1989-10-19 1995-11-08 高砂香料工業株式会社 Acaricide
EP0597660A2 (en) * 1992-11-10 1994-05-18 Sumitomo Chemical Company, Limited Propargyl ester compounds, acaricides containing the same as an active ingredient and an acaricidal method
US5439690A (en) * 1993-05-21 1995-08-08 Ecosmart, Inc. Non-hazardous pest control
US6750256B1 (en) 1994-12-30 2004-06-15 Proguard, Inc. Use of aromatic aldehydes as insecticides
US5839224A (en) * 1994-12-30 1998-11-24 Proguard, Inc. Aromatic aldehydes as insecticides and for killing arachnids
US5536501A (en) 1994-12-30 1996-07-16 Proguard, Inc. Use of flavenoid aldehydes as insecticides and for killing arachnids
WO1996040831A1 (en) * 1995-06-07 1996-12-19 Proguard, Inc. Flavonoid aldehydes and use in paint
DE19611825A1 (en) * 1996-03-26 1997-10-02 Desowag Materialschutz Gmbh Wood preservative
KR100350391B1 (en) * 2000-12-23 2002-08-28 주식회사 내츄로바이오텍 Composition contained acaricidal activity derived from plant
JP4641773B2 (en) * 2004-09-27 2011-03-02 大日本除蟲菊株式会社 Indoor dust mite repellent
JP4716826B2 (en) * 2005-09-08 2011-07-06 大日本除蟲菊株式会社 Chemical volatilizer
WO2011051834A1 (en) * 2009-11-02 2011-05-05 Firmenich Sa Odorants with anisic notes

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0366602A (en) * 1989-08-07 1991-03-22 Osaka Seiyaku:Kk Miticide

Also Published As

Publication number Publication date
JPH0381202A (en) 1991-04-05

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