JPH04103502A - Mite-controlling agent for indoor use - Google Patents

Mite-controlling agent for indoor use

Info

Publication number
JPH04103502A
JPH04103502A JP2222184A JP22218490A JPH04103502A JP H04103502 A JPH04103502 A JP H04103502A JP 2222184 A JP2222184 A JP 2222184A JP 22218490 A JP22218490 A JP 22218490A JP H04103502 A JPH04103502 A JP H04103502A
Authority
JP
Japan
Prior art keywords
mite
controlling agent
mites
indoor use
isopropyl
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.)
Granted
Application number
JP2222184A
Other languages
Japanese (ja)
Other versions
JP3049564B2 (en
Inventor
Michihiro Yasui
安井 通宏
Takahiro Wada
和田 恭弘
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.)
Nihon Nohyaku Co Ltd
Original Assignee
Nihon Nohyaku 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 Nihon Nohyaku Co Ltd filed Critical Nihon Nohyaku Co Ltd
Priority to JP2222184A priority Critical patent/JP3049564B2/en
Publication of JPH04103502A publication Critical patent/JPH04103502A/en
Application granted granted Critical
Publication of JP3049564B2 publication Critical patent/JP3049564B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Abstract

PURPOSE:To provide a mite-controlling agent for indoor use, containing buprofezin and/or isoprothiolane as active components and effective against dust mites in room such as Dermatophagoidae, Acaridiae and Cheyletoidae. CONSTITUTION:The objective mite-controlling agent for indoor use contains buprofezin (2-tert. butylimino-3-isopropyl-5-phenyl-3,4,5,6-tetrahydro-2H-1,3,5- thiadiazin-5-one) and/or isoprothiolane (isopropyl-1,3-dithiolan-2-ylidene malonate) as active components. Although the above compound can be applied as it is as a miticide, it is preferable to use the compound in the form of powder, wettable powder, granule, emulsifiable concentrate, etc., using proper carrier or other additives according to the purpose.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は屋内用ダニ防除剤に関する。[Detailed description of the invention] [Industrial application field] The present invention relates to an indoor mite control agent.

〔従来の技術〕[Conventional technology]

近年、生活様式、住宅構造の変化などにより、家庭内に
チリダニ、コナダニ、ホコリダニ等のダニ類が発生し、
居住者に不快感をもたらすのみならず、アレルギー性喘
息、アトピー性皮膚炎などの原因となり社会問題となり
つつある。
In recent years, due to changes in lifestyles and housing structures, dust mites, dust mites, dust mites, and other mites have appeared in homes.
Not only does it cause discomfort to residents, it also causes allergic asthma, atopic dermatitis, etc., and is becoming a social problem.

従来より、このようなダニ類に対する防除剤としては、
たとえばフェニトロチオン、ダイアジノン等の有機リン
化合物、レスメスリン、パーメスリン等のピレスロイド
化合物などが知られていて、乳剤、油剤等の形で直接噴
霧処理したり、防虫紙、カーペット等への含浸、燻煙等
の方法で用いられている。
Conventionally, as a control agent for such mites,
For example, organic phosphorus compounds such as fenitrothion and diazinon, and pyrethroid compounds such as resmethrin and permethrin are known. used in the method.

[発明が解決しようとする課題1 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。
[Problem to be Solved by the Invention 1] However, many organic phosphorus compounds are generally highly toxic, and many have a unique bad odor.

また、ピレスロイド化合物は一般に低毒性であるものの
、コナダニ、ツメダニに対する効果の点で必ずしも充分
とは言えない。
Furthermore, although pyrethroid compounds generally have low toxicity, they are not necessarily sufficiently effective against white mites and black mites.

[課題を解決するための手段] 本発明者らは上記問題点を解決するために鋭意検討した
結果、2−タシャリ−ブチルイミノ−3−イソプロピル
−5−フェニル、3,4゜5.6−テトラヒドロ−2H
−1,3,5−チアジアジン−5−オン(以下ブプロフ
ェジンという)およびジイソプロピル−1,3−ジチオ
ラン−2−イリデン−マロネート(以下イソブロチオラ
ンという)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を完成したものである。
[Means for Solving the Problems] As a result of intensive studies to solve the above problems, the present inventors found that 2-tashary-butylimino-3-isopropyl-5-phenyl, 3,4°5.6-tetrahydro -2H
-1,3,5-thiadiazin-5-one (hereinafter referred to as buprofezin) and diisopropyl-1,3-dithiolane-2-ylidene-malonate (hereinafter referred to as isobrothiolane) are extremely effective in controlling indoor dust mites. This discovery led to the completion of the present invention.

したがって、本発明の屋内用ダニ防除剤はブプロフェジ
ンまたは/およびイソブロチオランを有効成分として含
有することを特徴とする。
Therefore, the indoor mite control agent of the present invention is characterized by containing buprofezin and/or isobrothiolane as an active ingredient.

本発明で使用するブプロフェジンは特開昭54−308
3号公報で農園芸用殺虫殺ダニ剤として、またイソブロ
チオランは特開昭50−100229号公報で農園芸用
殺虫殺ダニ剤として公知の化合物であるが、これらが室
内塵性ダニ類に有効であることは従来の知見からは全く
予想できなかったことである。
The buprofezin used in the present invention is disclosed in Japanese Patent Application Laid-open No. 54-308.
3 as an insecticide and acaricide for agriculture and horticulture, and isobrothiolane is a compound known as an insecticide and acaricide for agriculture and horticulture in Japanese Patent Application Laid-Open No. 100229/1983, but these compounds are known to be effective against indoor dust mites. The fact that it is effective is something that could not have been expected from conventional knowledge.

本発明において対象となる屋内塵性ダニ類としては、例
えばコナヒヨウヒダニ、ヤケヒヨウヒダニ等のヒヨウヒ
ダニ類、ケナガコナダニ、ムギコナグニ等のコナダニ類
、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、フトツメグニ等のツメダニ類、イエササラ
グ二類などが挙げられる。
Indoor dust mites that are targeted in the present invention include, for example, Dermatophagoides mites such as Dermatophagoides nigricans and Dermatophagoides nigricans, Dermatophagoides mites such as Dermatophagoides nigricans, Dermatophagoides erectus mites, Mugi mites, etc.; Examples include the following.

本発明の殺ダニ剤は前記化合物をそのまま適用すること
もできるが、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粉剤、水和剤
、粒剤、乳剤、液剤、懸濁剤、エアゾール剤等として使
用される。液状の担体としては、水、四塩化炭素、塩化
メチレン、二塩化エチレン、エチルアルコール、イソプ
ロピルアルコール、エチレングリコール、プロピレング
リコール、ジエチルエーテル、ジオキサン、テトラヒド
ロフラン、アセトン、シクロヘキサノン、酢酸エチル、
ジブチルフタレート、トルエン、キシレン、ケロシン、
及びメチルナフタレンなどの棺媒が適当であり、そして
これらの一種または二種以上の混合物が用いられる。
The acaricide of the present invention can be applied as the above-mentioned compound as it is, but it is usually preferable to use suitable carriers and other compounding agents to form various forms depending on the purpose of use, such as powders, wettable powders, granules, emulsions, etc. Used as liquids, suspensions, aerosols, etc. Liquid carriers include water, carbon tetrachloride, methylene chloride, ethylene dichloride, ethyl alcohol, isopropyl alcohol, ethylene glycol, propylene glycol, diethyl ether, dioxane, tetrahydrofuran, acetone, cyclohexanone, ethyl acetate,
dibutyl phthalate, toluene, xylene, kerosene,
and methylnaphthalene are suitable, and one or a mixture of two or more of these may be used.

また固体の担体としてはカオリン、ベントナイト、タル
ク、軽石、シリカ、炭酸カルシウム、活性炭、ケイソウ
土、植物性粉末等が適当であり、そしてこれらの一種ま
たは二種以上の混合物が用いられる。
Suitable solid carriers include kaolin, bentonite, talc, pumice, silica, calcium carbonate, activated carbon, diatomaceous earth, and vegetable powder, and one or a mixture of two or more of these may be used.

また配合剤としては湿潤剤、展着剤、分散助剤、乳化剤
、安定剤または懸濁剤が用いられ、そしてこれらの一種
または二種以上の混合物が用いられる。これらは通常こ
の分野で用いられるものが使用できる。
Further, as compounding agents, wetting agents, spreading agents, dispersing aids, emulsifiers, stabilizers, or suspending agents are used, and one or a mixture of two or more of these is used. Those commonly used in this field can be used.

本発明のダニ防除剤中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選択されるが、通常
、有効成分がブプロフェジンの場合には、使用濃度が1
ゴ当たり 0.001〜Ig、イソブロチオランの場合
には、 0.015〜2gの範囲で使用される。
The amount used in the mite control agent of the present invention depends on its dosage form and application target.
It is selected as appropriate depending on the application method, application location, etc., but usually when the active ingredient is buprofezin, the concentration used is 1.
In the case of isobrothiolane, it is used in a range of 0.001 to 2 g per gram.

〔処方例1 次に本発明の殺ダニ剤の処方例を示すが、本発明はこれ
らのみに限定されるものではない。
[Formulation Example 1 Next, prescription examples of the acaricide of the present invention will be shown, but the present invention is not limited to these.

処方例1 本発明化合物            50部ケイソウ
土・クレーの混合物     45部ポリオキシエチレ
ンノニルフェニル エーテル               5部以上を均
一に混合粉砕して水和剤とする。
Formulation Example 1 Compound of the present invention 50 parts Diatomaceous earth/clay mixture 45 parts Polyoxyethylene nonylphenyl ether 5 parts or more are uniformly mixed and pulverized to prepare a wettable powder.

処方例2 本発明化合物            20部テトラヒ
ドロフラン         20部キシレン    
          45部ポリオキシエチレンノニル
フェニル エーテルとアルキルベンゼンスルホ ン酸の混合物            15部を均一に
混合溶解して乳剤とする。
Formulation Example 2 Compound of the present invention 20 parts Tetrahydrofuran 20 parts Xylene
45 parts of a mixture of polyoxyethylene nonylphenyl ether and 15 parts of alkylbenzene sulfonic acid are uniformly mixed and dissolved to obtain an emulsion.

処方例3 本発明化合物            4部ケイソウ土
・クレー・タルクの混合物 95部ステアリン酸カルシ
ウム       1部以上を均一に混合溶解して粉剤
とする。
Formulation Example 3 Compound of the present invention 4 parts Mixture of diatomaceous earth, clay and talc 95 parts Calcium stearate 1 part or more are uniformly mixed and dissolved to form a powder.

処方例4 本発明化合物            2部ブロビレン
グリコールモノメチル エーテル              75部を溶解し
たものに噴射剤として 液化石油ガス23部を加えて全量を100容量部として
加圧充填してエアゾールとする。
Formulation Example 4 Compound of the present invention 2 parts 75 parts of brobylene glycol monomethyl ether are dissolved and 23 parts of liquefied petroleum gas is added as a propellant to make the total amount 100 parts by volume, and the mixture is filled under pressure to obtain an aerosol.

〔発明の効果〕〔Effect of the invention〕

次に本発明殺ダニ剤の効果について試験例を挙げて説明
するが、これらのみに限定されるものではない。
Next, the effects of the acaricide of the present invention will be explained using test examples, but the effects are not limited to these.

試験例1 ダニの培地(マウス飼料:エビオス=l:1)に所定濃
度の2倍のアセトン希釈薬液を等量処理し、風乾してア
セトンを揮散後、その50mgにケナガコナダニを含む
培地(56,7頭/100mg) 50mgを混合して
10m℃の管ビンに入れ、管ビンの下部を、飽和硝酸カ
リウム水溶液に浸し、28℃、湿度75〜85%の恒温
、恒温室に保管した。調査は所定日数後に培地100m
g中の生存ダニ数を計数した61区3連制、結果を表1
に示す。
Test Example 1 A mite culture medium (mouse feed: Ebios = 1:1) was treated with an equal amount of acetone diluted drug solution twice the predetermined concentration, air-dried to volatilize the acetone, and 50 mg of the medium containing woolly mites (56, 7 cows/100 mg) were mixed and placed in a 10 m°C tube bottle, the lower part of the tube bottle was immersed in a saturated potassium nitrate aqueous solution, and stored in a thermostatic chamber at 28°C and humidity of 75-85%. The survey will be carried out on 100 m of culture medium after a specified number of days.
The number of living mites in 61 wards was counted in triplicate, and the results are shown in Table 1.
Shown below.

表1 試験例2 ダニの培地(マウス飼料:エビオス=1=1)に所定濃
度の2倍のアセトン希釈薬液を等量処理し、風乾してア
セトンを揮散後、その50mgにコナヒヨウヒダニを含
む培地(61,3頭/100mg) 50ragを混合
して10 rnAの管ビンに入れ、管ビンの下部を、飽
和硝酸カリウム水溶液に浸し、28℃、湿度75〜85
%の恒温、恒温室に保管した。調査は所定日数後に培地
100mg中の生存ダニ数を計数した。1区3連制、結
果を表2に示す。
Table 1 Test Example 2 A mite culture medium (mouse feed: Ebios = 1 = 1) was treated with an equal amount of acetone diluted chemical solution twice the predetermined concentration, air-dried to volatilize the acetone, and 50 mg of the medium was treated with a medium containing Dermatophagoides diluted ( 61.3 head/100mg) 50rag was mixed and placed in a 10 rnA tube bottle, the lower part of the tube bottle was immersed in a saturated potassium nitrate aqueous solution, and the temperature was kept at 28℃ and humidity 75-85℃.
% and stored in a constant temperature room. In the investigation, the number of surviving mites in 100 mg of the medium was counted after a predetermined number of days. Table 2 shows the results of three consecutive races in one ward.

表2 100mgをひろげて置き、ふたをして28℃、湿度7
5〜85%の恒温、恒湿室に保管した。調査は所定日数
後に培地100mg中の生存ダニ数を計数した。1区3
連制、結果を表3に示す。
Table 2 Spread out 100mg, cover with a lid, and keep at 28℃ and humidity 7.
It was stored in a constant temperature and humidity room of 5 to 85%. In the investigation, the number of surviving mites in 100 mg of the medium was counted after a predetermined number of days. Ward 1 3
The results are shown in Table 3.

表3 試験例3 直径9cmのシャーレ中の直径8.5cmの濾紙に所定
濃度のアセトン希釈薬液を1.5mI2処理し、風乾し
てアセトンを揮散後、処理濾紙中央にケナガコナダニを
含む培地(56,7頭7100mg)C)無処理区の固
体数(3運平均偵ン 試験例4 ダニの培地(マウス飼料:エビオス=11)に所定濃度
の2倍のアセトン希釈薬液を等量処理し、風乾してアセ
トンを揮散後、その500mgにコナヒヨウヒダニを含
む培地(593頭/ 100mg) 500mgを混合
して10 nlの管ビンに入れ、管ビンの下部を、飽和
塩化ナトリウム水溶液に浸し、28°C,湿度75〜8
5%の恒温、恒温室に保管した。調査は所定日数後に培
地100mg中の生存ダニ数を計数した。1区3連制、
結果を表4に示す。
Table 3 Test Example 3 A filter paper with a diameter of 8.5 cm in a Petri dish with a diameter of 9 cm was treated with 1.5 ml of acetone diluted chemical solution of a predetermined concentration, air-dried to volatilize the acetone, and a medium (56, 7 animals 7100 mg) C) Number of individuals in untreated area (3 luck average reconnaissance test example 4) Treat the tick culture medium (mouse feed: Ebios = 11) with an equal amount of acetone diluted chemical solution with twice the prescribed concentration and air dry. After volatilizing the acetone, mix the 500 mg with 500 mg of a culture medium containing Dermatophagoids nigricans (593 heads/100 mg), place the mixture in a 10 nl tube, immerse the lower part of the tube in a saturated aqueous sodium chloride solution, and store at 28°C and humidity. 75-8
It was stored in a thermostatic room with a constant temperature of 5%. In the investigation, the number of surviving mites in 100 mg of the medium was counted after a predetermined number of days. 1st ward triple system,
The results are shown in Table 4.

表4Table 4

Claims (1)

【特許請求の範囲】[Claims] 2−タシャリ−ブチルイミノ−3−イソプロピル−5−
フェニル、3,4,5,6−テトラヒドロ−2H−1,
3,5−チアジアジン−5−オンまたは/およびジイソ
プロピル−1,3−ジチオラン−2−イリデン−マロネ
ートを有効成分として含有することを特徴とする屋内用
ダニ防除剤。
2-Tashary-butylimino-3-isopropyl-5-
Phenyl, 3,4,5,6-tetrahydro-2H-1,
An indoor mite control agent characterized by containing 3,5-thiadiazin-5-one or/and diisopropyl-1,3-dithiolan-2-ylidene-malonate as an active ingredient.
JP2222184A 1990-08-23 1990-08-23 Indoor dust mite control agent Expired - Lifetime JP3049564B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2222184A JP3049564B2 (en) 1990-08-23 1990-08-23 Indoor dust mite control agent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2222184A JP3049564B2 (en) 1990-08-23 1990-08-23 Indoor dust mite control agent

Publications (2)

Publication Number Publication Date
JPH04103502A true JPH04103502A (en) 1992-04-06
JP3049564B2 JP3049564B2 (en) 2000-06-05

Family

ID=16778476

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2222184A Expired - Lifetime JP3049564B2 (en) 1990-08-23 1990-08-23 Indoor dust mite control agent

Country Status (1)

Country Link
JP (1) JP3049564B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103651342A (en) * 2012-08-31 2014-03-26 江苏长青农化股份有限公司 Wettable powder with buprofezin content being 25 percent

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103651342A (en) * 2012-08-31 2014-03-26 江苏长青农化股份有限公司 Wettable powder with buprofezin content being 25 percent

Also Published As

Publication number Publication date
JP3049564B2 (en) 2000-06-05

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