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JP2775482B2 - Indoor acaricide - Google Patents

Indoor acaricide

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Publication number
JP2775482B2
JP2775482B2 JP22630089A JP22630089A JP2775482B2 JP 2775482 B2 JP2775482 B2 JP 2775482B2 JP 22630089 A JP22630089 A JP 22630089A JP 22630089 A JP22630089 A JP 22630089A JP 2775482 B2 JP2775482 B2 JP 2775482B2
Authority
JP
Japan
Prior art keywords
mites
acaricide
present
indoor
carpet
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
JP22630089A
Other languages
Japanese (ja)
Other versions
JPH0390004A (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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Application filed by Dainihon Jochugiku Co Ltd filed Critical Dainihon Jochugiku Co Ltd
Priority to JP22630089A priority Critical patent/JP2775482B2/en
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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、選ばれた芳香族アルデヒドあるいは芳香族
カルボン酸エステル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。
Description: TECHNICAL FIELD The present invention relates to an acaricide for indoor use, comprising a selected aromatic aldehyde or aromatic carboxylic acid ester 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. 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る。
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 for these indoor mites, but there is an obstacle to practical use due to safety and resistance to humans and livestock.

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、p−アニスアルデヒド、m−アニスアルデヒ
ド、ヘリオトロピン、p−アニス酸メチル、m−アニス
酸メチル、o−アニス酸メチルおよびフェニル酢酸エチ
ルからなる群から選ばれた1種または2種以上を有効成
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。
To achieve the above object, the present inventors have made intensive studies and found that p-anisaldehyde, m-anisaldehyde, heliotropin, methyl p-anisate, methyl m-anisate, methyl o-anisate and phenyl An indoor acaricide containing one or more selected from the group consisting of ethyl acetate as an active ingredient exhibits a high acaricidal effect on mites, such as house dust mites, mites, dust mites, which live in houses. In addition, they have found that they have low toxicity and completed the present invention.

本発明で用いられる前記化合物群は、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見は全く予想外のことで
あった。
The compound group used in the present invention is widely used as a fragrance, but is known to exhibit no insecticidal properties,
This discovery of acaricidal effect was completely unexpected.

化合物群の構造式を示せば次のとおりである。 The structural formula of the compound group is as follows.

(1) p−アニスアルデヒド (2) m−アニスアルデヒド (5) ヘリオトロピン (6) p−アニス酸メチル (7) m−アニス酸メチル (8) O−アニス酸メチル (9) フェニル酢酸エチル 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。
(1) p-anisaldehyde (2) m-anisaldehyde (5) Heliotropin (6) Methyl p-anisate (7) methyl m-anisate (8) O-Methyl anisate (9) Ethyl phenylacetate The active ingredient of the indoor acaricide of the present invention is usually a liquid or a solid, and the active ingredient can be applied as it is. However, it is usually preferable to use an appropriate carrier or other compounding agents. Depending on the purpose, it is used in various forms, for example, emulsions, wettable powders, powders, oils, aerosols, coatings, tablets and the like.

また、上記有効成分は従来の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煙剤として適
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、ベントナイト等)、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 a conventional acaricide, and is so-called heat-evaporated by a suitable heat-evaporator after being impregnated in a room-temperature sustained-release preparation or an appropriate support such as a pulp plate. It is also possible to apply as a heating transpiration agent or a smoke agent. 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. Suitable solid carriers include, for example, clays (kaolin, bentonite, etc.), talc, silicas, calcium carbonate, alumina powder, activated carbons, wood flour, starch, plant powders such as flour, cyclodextrin and the like. 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
ることができ、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, silicone resins, urethane resins, epoxy resins, and the like. Decane, cyclododecane, 2,4,6-triisopropyl-1,3,5
-Trioxane, sublimable carriers such as trimethylene norbornene, and as a retention agent, for example, butyl stearate,
Examples include higher fatty acid esters such as isopropyl myristate, piperonyl butoxide, and sinepirin 500.

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。また、本発
明の屋内用殺ダニ剤にエムペントリンやDDVP、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−ジエチルサクシネ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。
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,
Examples include pyrethroid compounds such as etofenprox, organic phosphorus compounds such as fenitrothion, diazinon and pyridafenthion, and carbamate compounds such as NAC, MTMC, and PHC. Further, the indoor acaricide of the present invention may be combined with a volatile insecticide such as empentrin, DDVP, or paradichlorobenzene, naphthalene, or camphor, or a repellent such as diet, N-butylacetanilide, or N, N-diethylsuccinate. Can be mixed as appropriate 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ヒダ
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 inhabit the mites such as mites, 0.1 mg or more, preferably 1 mg to 2 g of the above-mentioned active ingredient per tatami, and for the control of Dermatophagoides mite that inhabits carpets, 0.5 mg to 2 g per 1 m2 are used. It is desirable to process the active ingredients.

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。ここで基材としては例えば、
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 substrate, 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を例示できる。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、パイル、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。上記の如くして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。
As a preferred embodiment of the tick control material provided by the present invention, a tick control carpet can be exemplified. 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 a pile, a first base fabric and a 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 created as described above,
It is preferable to about 0.1~10g hold the active ingredient per carpet area 1 m 2.

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、気管支喘息、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, and particularly exhibits bronchial asthma, atopic dermatitis, nasal allergy and the like. For the control of Dermatophagoides, Dermatophagoides and Dermatophagoides pteronyssinus, which are said to cause, Dermatophagoides farinae and Dermatophagoides, such as Dermatophagoides farinae and Dermatophagoides farinae, which are regarded as pathogens of allergic diseases and mite mites in humans. It 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。
Test Example 1 0.5 ml of a 10 mM acetone solution of the 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.

この2つ折ろ紙を2ケのアクリル円筒(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。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1−163
104号公報開示のシトラール、カルボンを用いた。
This two-fold filter paper is put into two acrylic cylinders (inner diameter 4.1cm,
After fixing it with a rubber band, place it in a container with a cap of 1 (27-28 ° C, 65% RH), leave it for 24 hours, count the number of live mites and dead mites, and test each sample The acaricidal efficacy of the compounds was investigated. In addition, as a control compound, pyrethroid compound d-T80-resmethrin and JP-A-1-163
Citral and carvone disclosed in Japanese Patent Publication No. 104 were used.

試験の結果、本発明で用いる選ばれた芳香族アルデヒ
ドあるいは芳香族カルボン酸エステル誘導体はコナヒョ
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 selected aromatic aldehyde or aromatic carboxylic acid ester derivative used in the present invention shows high contact acaricidal activity against Dermatophagoides farinae, and the control compound d-T80-resmethrin and JP-A-1-163104 are disclosed. The disclosed citral and carvone were much better.

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。
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.

約1cm四方の布地に供試化合物の100mMアセトン溶液10
0μl(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。
A 100 mM acetone solution 10 of the test compound was applied to about 1 cm square fabric.
After dropping 0 μl (200 μl in the case of Acarina mites), air-drying and placing it on the bottom of the lower acrylic cylinder, 100-200 Dermatophagoides farinae or Acarina mites were placed between two untreated folded papers and placed in one container. After leaving 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. The results are as shown in the table below.

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
ールを用いた。
In addition, empentrin which is a volatile volatile pyrethroid, citral, and citronellal were used as control compounds.

試験の結果、本発明で用いる選ばれた芳香族アルデヒ
ドあるいは芳香族カルボン酸エステル誘導体は揮散分子
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 selected aromatic aldehyde or aromatic carboxylate derivative used in the present invention has extremely high acaricidal effect on volatile molecules, and is useful for application to sustained-release preparations and heat evaporation preparations. Was done.

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, and citral and citronellal disclosed in JP-A-1-163104 have very weak acaricidal efficacy.

実施例1 前記化合物No.(1),(2),(5),(6)およ
び(9)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. (1), (2), (5), (6) and (9), a very small amount of a fragrance and kerosene were added to make a total of 120 ml, which was mixed 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 次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;殺ダニ剤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: The number of surviving mites in the carpet untreated Y drug; The mortality was determined by the number of surviving mites in the carpet treated with the acaricide.

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),(5)及び(8)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
ダニ剤を調製した。
Example 3 8 g of a gelling agent was added to 2 g of each of the above compound Nos. (2), (5) and (8) to prepare a tablet-form acaricide for indoor use of the present invention in a conventional manner.

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ケ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 tablets (packaged with Japanese paper) were stored in a cloth bag storing the futon, no mites 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、有効成分として選ばれた芳
香族アルデヒドあるいは芳香族カルボン酸エステル誘導
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 an aromatic aldehyde or an aromatic carboxylic acid ester derivative selected as an active ingredient. .

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】p−アニスアルデヒド、m−アニスアルデ
ヒド、ヘリオトロピン、p−アニス酸メチル、m−アニ
ス酸メチル、o−アニス酸メチルおよびフェニル酢酸エ
チルからなる群から選ばれた1種または2種以上を有効
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. One or two members selected from the group consisting of p-anisaldehyde, m-anisaldehyde, heliotropin, methyl p-anisate, methyl m-anisate, methyl o-anisate and ethyl phenylacetate. An acaricide for indoor use, comprising at least one species as an active ingredient.
JP22630089A 1989-08-30 1989-08-30 Indoor acaricide Expired - Lifetime JP2775482B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP22630089A JP2775482B2 (en) 1989-08-30 1989-08-30 Indoor acaricide

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP22630089A JP2775482B2 (en) 1989-08-30 1989-08-30 Indoor acaricide

Publications (2)

Publication Number Publication Date
JPH0390004A JPH0390004A (en) 1991-04-16
JP2775482B2 true JP2775482B2 (en) 1998-07-16

Family

ID=16843051

Family Applications (1)

Application Number Title Priority Date Filing Date
JP22630089A Expired - Lifetime JP2775482B2 (en) 1989-08-30 1989-08-30 Indoor acaricide

Country Status (1)

Country Link
JP (1) JP2775482B2 (en)

Families Citing this family (3)

* 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
KR20030000680A (en) * 2001-06-26 2003-01-06 주식회사 내츄로바이오텍 Composition of acaricidal components
JP4641773B2 (en) * 2004-09-27 2011-03-02 大日本除蟲菊株式会社 Indoor dust mite repellent

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
「生薬学雑誌」 43(2) 平成元年6月20日発行 P.163〜168

Also Published As

Publication number Publication date
JPH0390004A (en) 1991-04-16

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