JPH01224302A - Controller against indoor acarids - Google Patents

Controller against indoor acarids

Info

Publication number
JPH01224302A
JPH01224302A JP5047288A JP5047288A JPH01224302A JP H01224302 A JPH01224302 A JP H01224302A JP 5047288 A JP5047288 A JP 5047288A JP 5047288 A JP5047288 A JP 5047288A JP H01224302 A JPH01224302 A JP H01224302A
Authority
JP
Japan
Prior art keywords
active ingredient
mites
acarids
controller against
parts
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
JP5047288A
Other languages
Japanese (ja)
Inventor
Hitoshi Kawada
均 川田
Ryoko Otani
大谷 良子
Goro Shinjo
新庄 五朗
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.)
Sumitomo Chemical Co Ltd
Original Assignee
Sumitomo Chemical 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 Sumitomo Chemical Co Ltd filed Critical Sumitomo Chemical Co Ltd
Priority to JP5047288A priority Critical patent/JPH01224302A/en
Publication of JPH01224302A publication Critical patent/JPH01224302A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To obtain a controller against indoor acarids, showing excellently controlling effects on various acarids such as American house dust mite or Throphagus dimidiatus living in dust inside of a house, comprising a specific compound as an active ingredient. CONSTITUTION:A controller against indoor acarids comprising a compound shown by the formula (R is CCl3, lower alkoxycarbonyl, CH3 or cyclopropyl) such as kelthane (R=CCl3) or chlorobenzilate (R=COC2H5) well-known as a controller against agricultural insect pests such as spider mites as an active ingredient. The active ingredient is blended with a carrier and an auxiliary, prepared into emulsion, wettable powder, dust, granule, oil, aerosol, etc. and used for treating TATAMI (straw matting), carpet, mattress, sofa, bedding such as FUTON (thick bedquilt or pillow, closest, storehouse, etc. by a method such as scattering, spraying, coating, misting, vaporization under heating, setting, etc. The amount of the active ingredient in preparation is 0.001-95wt.% and application amount is >=10mg/m<2> active component.

Description

【発明の詳細な説明】 〈産業上の利用分野〉 本発明は、一般式CI) 〔式中、Rはトリクロロメチル基、低級アルコキシカル
ボニル基、メチル基またはシクロプロピル基を表わす。
DETAILED DESCRIPTION OF THE INVENTION <Industrial Application Field> The present invention relates to a compound of the general formula CI) [wherein R represents a trichloromethyl group, a lower alkoxycarbonyl group, a methyl group or a cyclopropyl group].

〕 で示される化合物を有効成分とする屋内塵性ダニ類防除
剤1こ関するものである。
] This relates to an indoor dust mite control agent containing the compound shown below as an active ingredient.

〈従来の技術〉 近年、一般家屋の室内塵中に生息するダニ類が、生活様
式の変化、住宅構造の変化などにより、時として多発生
し、住民に不快感をもたらすのみならず小児喘息やダニ
アレルギー、ダニ刺咬症の原因にもなり社会問題化しつ
つある。
<Prior art> In recent years, due to changes in lifestyles and housing structures, mites that live in the indoor dust of ordinary houses have sometimes appeared in large numbers, causing not only discomfort to residents but also childhood asthma and other problems. It is becoming a social problem as it causes tick allergies and tick bites.

従来より、このようなダニ類昏こ対する防除剤としては
、例えばフェニトロチオン、フェンチオン、ジクロルボ
ス、ダイアジノン等の有機リン化合物、プロボクサール
、カルバリル等のカーバメート化合物、レスメトリン、
フエノトリン、ペルメトリン等のピレスロイド化合物な
どが知られており、畳、カーペットなどにエアゾール、
乳剤、油剤等の形態で直接噴霧処理したり、防虫紙、カ
ーペット等への含浸、燻煙等の方法で用いられることが
知られている。
Conventionally, as a control agent for such mites, for example, organic phosphorus compounds such as fenitrothion, fenthion, dichlorvos, and diazinon, carbamate compounds such as proboxal and carbaryl, resmethrin,
Pyrethroid compounds such as phenothrin and permethrin are known, and they can be used as aerosols on tatami mats, carpets, etc.
It is known to be used by direct spraying in the form of emulsions, oils, etc., by impregnating insect repellent paper, carpets, etc., and by smoking.

〈発明が解決しようとする課題〉 しかしながら、有機リン化合物は一般に毒性の高いもの
が多く、また、特有の悪臭を有するものが多い。さらに
、コナダニ類に対する効力は高(′ものの、ヒーウヒダ
ニ預等に対する効力の点で必ずしも充分とは言えない。
<Problems to be Solved by the Invention> However, many organic phosphorus compounds are generally highly toxic, and many have a unique bad odor. Furthermore, although it is highly effective against mites, it cannot necessarily be said to be sufficiently effective against mites.

また、カーバメート化合物も一般に毒性の高いものが多
(、ヒ冒つヒダニ類等に対する効力の点で必ずしも充分
とは言えない。
In addition, many carbamate compounds are generally highly toxic (and their efficacy against insects that infect humans, such as spider mites, is not necessarily sufficient).

ざらに、ピレスロイド化合物は一般に低毒性ではあるも
のの、コナダニ類等普こ対する効力の点で必ずしも充分
とは甘えない。
Generally speaking, although pyrethroid compounds generally have low toxicity, they are not necessarily sufficiently effective against common insects such as the mites.

く課題を解決するための手段〉 そこで、本発明者らは上記のような欠点の少ない、多種
のダニ類に対して有効なダニ防除剤を開発すべく稽々検
討した結果、前記一般式(I)で示される化合物が、屋
内塵性ダニ類の防除に極めて有効であることを見出し本
発明昏こ至 っ すこ 。
Means for Solving the Problems> Therefore, the present inventors have diligently studied to develop a mite control agent that is effective against various types of mites and has fewer of the above-mentioned drawbacks. The present invention has been made based on the discovery that the compound represented by I) is extremely effective in controlling indoor dust mites.

尚、前記一般式CI)で示される化合物はハダニ類等の
農業害虫の防除剤として知られており、例えば、下記の
第1表Gζ示される化合物が挙げられる。
The compound represented by the general formula CI) is known as a control agent for agricultural pests such as spider mites, and includes, for example, the compounds shown in Table 1 Gζ below.

第   1   表 本発明において、対象となる屋内塵性ダニ類としては、
例えばコナヒ冒つヒダニ、ヤケヒ嘗つヒダニ等のヒ曹つ
ヒダニ類、ケナガコナダニ、ムギコナダニ等のコナダニ
類、チリニクダニ、イエニクダニ等のニクダニ類、クワ
ガタツメダニ、フトツメダニ等のツメダニ類、マルニク
ダ二類、イエササラダニ類などが挙げられる。
Table 1 In the present invention, the indoor dust mites targeted are:
For example, spider mites such as the spider mites that infect the skin and the yellow spider mites, the mites such as the woolly spider mites and the wheat mites, the mites such as the dust mites and the dust mites, the stag mites such as the stag beetle mites and the foot mites, the two types of common spider mites, and the common mites. Examples include.

一般式(I)で示される化合物を屋内塵性ダニ類防除剤
の有効成分として用いる場合は、他の何らの成分を加え
ずそのままで用いてもよいが、通常は、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
、餌等と混合し、乳剤、水和剤、粉剤、粒剤、油剤、エ
アゾール、フォッギング等の煙霧剤、毒餌等に製剤して
用いる。
When the compound represented by the general formula (I) is used as an active ingredient of an indoor dust mite control agent, it may be used as it is without adding any other ingredients, but it is usually used in the form of a solid carrier, liquid carrier, It is mixed with gaseous carriers, surfactants, other formulation auxiliaries, baits, etc., and used in formulations such as emulsions, wettable powders, powders, granules, oils, aerosols, fogging agents such as fogging, and poison baits.

これらの製剤中には一般式CI)で示される化合物が有
効成分としてo、oot〜95重量%含有される。
These preparations contain o, oot to 95% by weight of the compound represented by the general formula CI) as an active ingredient.

製剤に際して用いられる固体担体としては、例えばカオ
リンクレー、アッタパルジャイトクレー、ベントナイト
、酸性白土、ピロフィライト、タルク、珪藻土、方解石
、トウモロコシ穂軸粉、クル電殻粉、尿素、硫酸アンモ
ニウム、合成含水酸化珪素等の微粉末あるいは粒状物が
挙げられ、液体担体としては、例えばケロシン、灯油等
の脂肪族炭化水素類、ベンゼン、トルエン、キシレン、
メチルナフタレン等の芳香族炭化水紫類、ジクロロエタ
ン、トリクロロエチレン、四塩化炭素等のハロゲン化炭
化水素類、メタノール、エタノール、イソプロパツール
、エチレングリコール、セロソルブ等のアルコール類、
アセトン、メチルエチルケトン、シクロヘキサノン、イ
ソホロン等のケトン類、ジエチルエーテル、ジオキサン
、テトラヒドロフラン等のエーテル類、酢酸エチル等の
エステル類、アセトニトリル、インブチロニトリル等の
ニドリール類、ジメチルホルムアミド、ジメチルアセト
アミド等の酸アミド類、ジメチルスルホキシド、大豆油
、綿実油等の植物油等が挙げられ、ガス状担体としては
、例えばフロンガス、LPG。
Examples of solid carriers used in formulations include kaolin clay, attapulgite clay, bentonite, acid clay, pyrophyllite, talc, diatomaceous earth, calcite, corn cob powder, electric shell powder, urea, ammonium sulfate, synthetic hydrous silicon oxide, etc. Examples of liquid carriers include aliphatic hydrocarbons such as kerosene and kerosene, benzene, toluene, xylene,
Aromatic hydrocarbons such as methylnaphthalene, halogenated hydrocarbons such as dichloroethane, trichloroethylene, and carbon tetrachloride, alcohols such as methanol, ethanol, isopropanol, ethylene glycol, and cellosolve,
Ketones such as acetone, methyl ethyl ketone, cyclohexanone, and isophorone; ethers such as diethyl ether, dioxane, and tetrahydrofuran; esters such as ethyl acetate; nidolyls such as acetonitrile and imbutyronitrile; acid amides such as dimethylformamide and dimethylacetamide. Examples of gaseous carriers include chlorofluorocarbon gas and LPG.

ジメチルエーテル等が挙げられる。界面活性剤としては
、例えば乳化、分散、湿層等のために用いられるアルキ
ル硫酸エステル塩、アルキル(アリール)スルホン酸塩
、ジアルキルスルホこはく酸塩、ポリオキシエチレンア
ルキルアリールエーテルリン酸エステル塩、ナフタレン
スルホン酸ホルマリン縮合物等の陰イオン界面活性剤、
ポリオキシエチレンアルキルエーテル、ポリオキシエチ
レンポリオキシプロピレンブロックコボリマー、ソルビ
タン脂肪酸エステル、ポリオキシエチレンソルビタン脂
肪酸エステル等の非イオン界面活性剤が挙げられる。そ
の他の製剤用補助剤としては、例えば固着剤や分散剤と
して、リグニンスルホン酸塩、アルギル酸塩、ポリビニ
ルアルコール、アラビアガム、糖蜜、カゼイン、ゼラチ
ン、CMC(カルボキシメチルセルロース)、松根油、
寒天等が挙げられ、安定剤としては、例えばPAP (
酸性リン酸イソプロピル)、TCP(リン酸トリクレジ
ル)等のリン酸アルキル、植物油、エポキシ上池、前記
の界面活性剤、BHT、BHA等の酸化防止剤、オレイ
ン酸ナトリウム、ステアリン酸カルシウム等の脂肪酸塩
、オレイン酸メチル、ステアリン酸メチル等の脂肪酸エ
ステルなどが挙げられる。
Examples include dimethyl ether. Examples of surfactants include alkyl sulfate salts, alkyl (aryl) sulfonates, dialkyl sulfosuccinates, polyoxyethylene alkylaryl ether phosphate salts, naphthalene used for emulsification, dispersion, wet layer, etc. Anionic surfactants such as sulfonic acid formalin condensates,
Examples include nonionic surfactants such as polyoxyethylene alkyl ether, polyoxyethylene polyoxypropylene block copolymer, sorbitan fatty acid ester, and polyoxyethylene sorbitan fatty acid ester. Other formulation auxiliaries include, for example, lignin sulfonates, algylates, polyvinyl alcohol, gum arabic, molasses, casein, gelatin, CMC (carboxymethylcellulose), pine oil, as fixing agents and dispersants.
Examples of stabilizers include agar, and examples of stabilizers include PAP (
acidic isopropyl phosphate), alkyl phosphates such as TCP (tricresyl phosphate), vegetable oils, epoxy Kamiike, the above-mentioned surfactants, antioxidants such as BHT and BHA, fatty acid salts such as sodium oleate and calcium stearate, Examples include fatty acid esters such as methyl oleate and methyl stearate.

本願のダニ類防除剤は、畳、カーペット、マツトレス、
ラフ1−1布団、枕等の寝具、押入れ、倉庫などに散布
、噴霧、塗布、煙霧、加熱蒸散、設置などの方法により
処理することにより用いられる。
The mite control agent of this application is suitable for use on tatami mats, carpets, pine trees,
Rough 1-1 It is used by treating bedding such as futons and pillows, closets, warehouses, etc. by methods such as scattering, spraying, coating, fogging, heating evaporation, and installation.

さらに、本願のダニ類防除剤は各種の殺虫剤、殺ダニ剤
、共力剤、害虫忌避剤、ネズミ忌避剤、殺菌剤、防黴剤
、香料、着色料等を混合して使用することもできる。混
合使用できる代表的な薬剤の例を第2表に示す。
Furthermore, the mite control agent of the present application may be used in combination with various insecticides, acaricides, synergists, pest repellents, rat repellents, fungicides, fungicides, fragrances, colorants, etc. can. Examples of typical drugs that can be used in combination are shown in Table 2.

尚、−数式(I)で示される化合物を有効成分とするダ
ニ類防除剤を用いる場合、その施用量は通常、処理すべ
き面積IF7/当たり、有効成分を1019以上、また
は適用空間11rI当たり1ダ以上が望ましい。
In addition, when using a mite control agent containing the compound represented by formula (I) as an active ingredient, the application rate is usually 1019 or more of the active ingredient per area to be treated IF7/, or 1 per 11 rI of applied space. It is desirable to have at least 100 yen.

第    2    表 〈実施例〉 以下、製剤例および試験例にて本発明をより詳しく説明
するが、本発明はこれらの例のみに限定されるものでは
ない。
Table 2 (Examples) The present invention will be explained in more detail below using formulation examples and test examples, but the present invention is not limited to these examples.

尚、供試化合物は第1表の化合物番号および第2表の化
合物記号で表わした。また、部は重量部を意味する。
The test compounds are represented by the compound numbers in Table 1 and the compound symbols in Table 2. Moreover, parts mean parts by weight.

製剤例1 化合物(1)または(2) 0.2部、キシレン2部お
よび白灯油97.8部を混合して油剤を得る。
Formulation Example 1 An oil solution is obtained by mixing 0.2 parts of compound (1) or (2), 2 parts of xylene, and 97.8 parts of white kerosene.

製剤例2 化合物(1)〜(5)の各々10部、ポリオキシエチレ
ンスチリルフェニルエーテル14部、ドデシルベンゼン
スルホン酸カルシウム6部およびキシレン70部をよ(
混合して各々の乳剤を得る。
Formulation Example 2 10 parts each of compounds (1) to (5), 14 parts of polyoxyethylene styrylphenyl ether, 6 parts of calcium dodecylbenzenesulfonate and 70 parts of xylene (
Mix to obtain each emulsion.

製剤例8 化合物(1)または(2) 20部、化合物(財)10
部、リグニンスルホン酸カルシウム8部、ラウリル硫酸
ナトリウム2部および合成含水酸化珪素65部をよく粉
砕混合して水和剤を得る。
Formulation Example 8 Compound (1) or (2) 20 parts, compound (goods) 10
1 part, 8 parts of calcium ligninsulfonate, 2 parts of sodium lauryl sulfate, and 65 parts of synthetic hydrous silicon oxide are thoroughly ground and mixed to obtain a wettable powder.

製剤例4 化合物(1)または(2)1部、化合物02部、カオリ
ンクレー87部およびタルク10部をよく粉砕混合して
粉剤を得る。
Formulation Example 4 1 part of Compound (1) or (2), 2 parts of Compound 0, 87 parts of kaolin clay, and 10 parts of talc are thoroughly ground and mixed to obtain a powder.

製剤例6 化合物(1)または(2)5部、合成含水酸化珪素1部
、リグニンスルホン酸カルシウム2部、ベントナイト8
0部およびカオリンクレー62部をよく粉砕混合し、水
を加えてよく練り合せた後、造粒乾燥して粒剤を得る。
Formulation Example 6 5 parts of compound (1) or (2), 1 part of synthetic hydrous silicon oxide, 2 parts of calcium ligninsulfonate, 8 parts of bentonite
0 parts and 62 parts of kaolin clay are thoroughly ground and mixed, water is added and the mixture is thoroughly kneaded, and then granulated and dried to obtain granules.

製剤例6 化合物(1)または(2) 0.05部、化合物00.
2部、化合物(F)0.05部、キシレン7部および脱
臭灯油82.7部を混合溶解し、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(液化石油ガス)60部を加圧充填してエアゾー
ルを得る。
Formulation Example 6 Compound (1) or (2) 0.05 part, Compound 00.
2 parts of compound (F), 0.05 parts of xylene, and 82.7 parts of deodorized kerosene are mixed and dissolved, filled into an aerosol container, and a valve part is attached. ) to obtain an aerosol.

試験例! 容N 20 ccのガラス製スクリュー管の内壁に、供
試化合物の所定濃度アセトン溶液0.2CCを均一に塗
布し、風乾した。これに供試ダニ(コナヒ冒つヒダ二ま
たはケナガコナダニ)の成ダニ各20頭を放ち蓋をした
。24時間後にダニの生死を判定し、致死率を求めた(
8反復)。
Test example! 0.2 cc of an acetone solution of a test compound at a predetermined concentration was uniformly applied to the inner wall of a glass screw tube having a volume of N 20 cc and air-dried. 20 adult mites each of the test mites (Konahi-infecting mites or woolly mites) were placed in the container and the lid was placed on the container. After 24 hours, the ticks were determined to be alive or dead, and the mortality rate was calculated (
8 repetitions).

コナヒ四つヒダニの致死率を第8表に、ケナガコナダニ
の致死率を第4表に示す。
Table 8 shows the mortality rate of the four-spotted mite, and Table 4 shows the mortality rate of the woolly mite.

第     8     表 コナヒ、ウヒダニEζ対する試験結果 第     4     表 ケナガコナダニに対する試験結果 試験例2 供試化合物10yとキシレン14+w/lこ脱臭灯油を
加えて全体を150 mlとしたものをエアゾール容器
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(液化石油ガス)150g?を加圧充填し
てエアゾールを得た。
Table 8 Test results against Kanahi mite Eζ Table 4 Test results against Kanahi mite E After installing the part, 150g of propellant (liquefied petroleum gas) is passed through the valve part. was filled under pressure to obtain an aerosol.

r紙(80emX80傭)(こ上記エアゾールを8秒間
均一にスプレーし、24時間風乾後、これを5αXIO
αの大きさのシートに切り取った。該シートの長辺を半
分に折り、両端を金属製クリップにて封じた後、開口部
より供試ダニ(コナヒ、ウヒダ二またはケナガコナダニ
)の成ダニ各20頭を各々放ち、開口後をさらにクリッ
プにて封じた。24時間後にダニの生成を判定し、致死
率を求めた。
R paper (80em x 80mm) (Spray the above aerosol evenly for 8 seconds, air dry for 24 hours, then apply 5α
Cut it into a sheet of size α. After folding the long side of the sheet in half and sealing both ends with metal clips, 20 adult mites each of the test mites (Konahi, Uhidani, or Woolly mites) are released from the opening, and the opening is further clipped. It was sealed. After 24 hours, the production of mites was determined and the mortality rate was calculated.

コナヒヨウヒダニの致死率を第5表に、ケナガコナダニ
の致死率を第6表に示す。
Table 5 shows the mortality rate of Dermatophagoides mites, and Table 6 shows the mortality rate of Dermatophagus mites.

第   5   表 コナヒ曽つヒダニ醗ζ対する試験結果 筒   6   表 〈発明の効果〉 本発明のダニ類防除剤は、屋内の塵中に生息する各種の
ダニ類の防除において、優れた防除効果を示すものであ
る。
Table 5 Test results for Konahi Sotsu Dermatode mites ζ Table 6 <Effects of the invention> The mite control agent of the present invention exhibits excellent control effects in controlling various types of mites living in indoor dust. It is something.

/ / // / /

Claims (1)

【特許請求の範囲】[Claims] (1)一般式 ▲数式、化学式、表等があります▼ 〔式中、Rはトリクロロメチル基、低級アルコキシカル
ボニル基、メチル基またはシクロプロピル基を表わす。 〕 で示される化合物を有効成分として含有することを特徴
とする屋内塵性ダニ類防除剤。
(1) General formula▲ Numerical formula, chemical formula, table, etc.▼ [In the formula, R represents a trichloromethyl group, a lower alkoxycarbonyl group, a methyl group, or a cyclopropyl group. ] An indoor dust mite control agent characterized by containing a compound represented by the following as an active ingredient.
JP5047288A 1988-03-02 1988-03-02 Controller against indoor acarids Pending JPH01224302A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5047288A JPH01224302A (en) 1988-03-02 1988-03-02 Controller against indoor acarids

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5047288A JPH01224302A (en) 1988-03-02 1988-03-02 Controller against indoor acarids

Publications (1)

Publication Number Publication Date
JPH01224302A true JPH01224302A (en) 1989-09-07

Family

ID=12859837

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5047288A Pending JPH01224302A (en) 1988-03-02 1988-03-02 Controller against indoor acarids

Country Status (1)

Country Link
JP (1) JPH01224302A (en)

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