JPH09227310A - Acaricide for indoor dust mites - Google Patents

Acaricide for indoor dust mites

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Publication number
JPH09227310A
JPH09227310A JP8311705A JP31170596A JPH09227310A JP H09227310 A JPH09227310 A JP H09227310A JP 8311705 A JP8311705 A JP 8311705A JP 31170596 A JP31170596 A JP 31170596A JP H09227310 A JPH09227310 A JP H09227310A
Authority
JP
Japan
Prior art keywords
acaricide
mites
dust mites
agent
indoor dust
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
JP8311705A
Other languages
Japanese (ja)
Inventor
Mitsunobu Shibata
光信 柴田
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.)
Mitsubishi Chemical Corp
Original Assignee
Mitsubishi Chemical Corp
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 Mitsubishi Chemical Corp filed Critical Mitsubishi Chemical Corp
Priority to JP8311705A priority Critical patent/JPH09227310A/en
Publication of JPH09227310A publication Critical patent/JPH09227310A/en
Pending legal-status Critical Current

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Abstract

PROBLEM TO BE SOLVED: To obtain the above acaricide having a sufficient exterminating effect at a low dose by using a specific compound having a wide and a potent acaricidal effect to an in house dust acarid singly or simultaneously with another insecticide. SOLUTION: This acaricide for an in house dust acarid contains chlorophenapyle*, i.e., 4-bromo-2-(4- chlorophenyl)-1-(ethoxymethyl)-5-(trifluoromethyl)pyrrol-3-carbonitrile as an active ingredient, and also is used by blending the chlorophenapyle* with at least one or more kinds selected from a pyrethroide-based insecticide, an organophosphorus-based insecticide, an organic bactericide or an inorganic bactericide. The acaricidal composition is preferably further blended with a cooperating agent. In this preparation, 0.1-95% active ingredient is contained, and especially 0.5-20% in an oil preparation, 10-50% in art emulsion, 30-80% in a hydrated preparation, 5-40% in a powder, 10-50% in a granular preparation, 1-20% in a fumigating agent, 0.1-20% in an aerosol agent and 0.05-10g/m<2> in a sheet agent. Chlorophenapyle*: probably a gerneric name of the subject compound, spelling thereof is not clear.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【発明の属する技術分野】本発明は、屋内塵性ダニ用殺
ダニ剤に関するものであり、本発明の殺ダニ剤は各種の
屋内塵性ダニ類の駆除に極めて有効である。
TECHNICAL FIELD The present invention relates to an acaricide for indoor dust mites, and the acaricide of the present invention is extremely effective for exterminating various indoor dust mites.

【0002】[0002]

【従来の技術】衛生害虫である屋内塵性ダニ類は、アレ
ルギー性喘息、小児喘息、アトピー性皮膚炎等の原因と
云われており、また刺咬、吸血による各種皮膚炎、さら
には疥癬症の原因となっている。また、これらのダニ類
は異常発生による不快感や食品類の品質の劣化等の被害
ももたらす。これらのダニ類の蔓延は、人類の衛生的、
健康的な生活維持を脅かし、著しく阻害するものであ
り、早急かつ確実に殺滅させる必要がある。従来、屋内
塵性ダニであるケナガコナダニ、コナヒョウヒダニ、ツ
メダニ、ササラダニ、シラミダニ、ホコリダニなどのダ
ニ類に対しては、レスメトリン、ペルメトリン、フェノ
トリン等のピレスロイド系殺虫剤(特開昭63−290
9号、特開昭60−142906号公報)、ダイアジノ
ン、ジクロルボス、フェニトロチオン、トリクロルホ
ン、マラチオン、フェンチオン等の有機燐系殺虫剤(白
坂昭子ら,衛生動物,22,210〜212,(197
1))、カーバメート系殺虫剤のプロポクスルの(椎山
松記,美しい環境,7,65〜7,(1982))など
の各種殺虫剤が使用されている。
2. Description of the Related Art Indoor dust mites, which are hygiene pests, are said to be a cause of allergic asthma, childhood asthma, atopic dermatitis, etc. Also, various dermatitis due to bites, blood feeding, and scabies. Is the cause. In addition, these mites also cause damage such as discomfort due to abnormal occurrence and deterioration of the quality of foods. The spread of these mites is due to human hygiene,
It threatens and significantly impedes the maintenance of a healthy life, and there is a need for immediate and reliable killing. Conventionally, pyrethroid insecticides such as resmethrin, permethrin, and phenothrin against mites such as house dust mites, Dermatophagoides farinae, Dermatophagoides farinae, horn ticks, Saladani, lice mites and dust mites (JP-A-63-290).
9, JP-A-60-142906), diazinon, dichlorvos, fenitrothion, trichlorfon, malathion, fenthion and other organophosphorus insecticides (Shirasaka et al., Sanitary animals, 22, 210-212, (197).
1)), various insecticides such as carbamate insecticide propoxur (Mr. Shiiyama, beautiful environment, 7, 65-7, (1982)).

【0003】また、クロルフェナピル(特開平1−10
4042号公報)は、殺ダニ剤として知られているが、
対象となるダニは屋外性のハダニに関してであり、屋内
塵性のダニについては開示されていない。ハダニと屋内
塵性ダニは、分類学的、生態学的、生理学的に異なって
おり、薬剤に対する感受性も一致しない。したがって、
防除を考える上ではまったく異なった生物である。
In addition, chlorfenapyr (Japanese Patent Laid-Open No. 1-10
No. 4042) is known as an acaricide,
The target mites are outdoor spider mites, and indoor dust mites are not disclosed. Tick mites and house dust mites are taxonomically, ecologically, and physiologically different, and their sensitivities to drugs are also inconsistent. Therefore,
It is a completely different organism in terms of control.

【0004】[0004]

【発明が解決しようとする課題】屋内塵中には無気門
類、前気門類、中気門類、隠気門類などの形態的にも生
理的にも異なる各種のダニ類が同時に生息している。し
かしながら従来これらのダニ類の駆除に使用されている
ピレスロイド系、有機燐系、カーバメート系の各種殺虫
剤はイエダニ等の中気門類に属するダニ類に対しては高
い殺ダニ効果を有しているものの、その他のダニ類に対
してはあまり効果がなく、色々な種類の屋内塵性ダニ類
を同時に駆除することは困難であった。また、従来屋内
塵性ダニ類の駆除に使用されてきたピレスロイド系、有
機燐系、カーバメート系の各種殺虫剤を屋内に処理した
場合、たとえ駆除ができたとしてもハエ、ゴキブリなど
の害虫の駆除に必要な薬量に比べて比較にならないほど
の多量の薬剤を必要とするために、人が生活する室内で
のこれらの殺虫剤の散布は安全性の面で問題があった。
[Problems to be Solved by the Invention] Various indoor and indoor mites of various morphologically and physiologically different mites such as ascidians, prestigmatics, middle ascidians, and respirators are simultaneously present. . However, various pyrethroid-based, organophosphorus-, and carbamate-type insecticides conventionally used for controlling these mites have a high acaricidal effect on mites belonging to the midgastricial group such as house dust mites. However, it was not very effective against other mites, and it was difficult to simultaneously exterminate various kinds of indoor dust mites. In addition, when various pyrethroid-based, organophosphorus-based and carbamate-based insecticides that have been conventionally used to control indoor dust mites are treated indoors, even if they can be controlled, pests such as flies and cockroaches can be controlled. The application of these pesticides in a room where a person lives is problematic in terms of safety, because they require an incomparably large amount of drug compared to the amount required for the drug.

【0005】[0005]

【課題を解決するための手段】本発明者らは上記課題を
解決すべく鋭意検討をした結果、クロルフェナピルが、
ケナガコナダニ、コナヒョウヒダニ、ヤケヒョウヒダ
ニ、クワガタツメダニ、フトツメダニ、ホソツメダニ、
ミナミツメダニ、ホコリダニ、ササラダニ等の屋内塵性
ダニ類に対して、従来になく巾広く、強力な殺ダニ効力
を示すことを見いだし、さらには低薬量で十分な駆除効
果を有することを見いだし本発明を完成するに至った。
[Means for Solving the Problems] As a result of intensive studies to solve the above problems, the present inventors found that chlorfenapyr was
Dermatophagoides farinae, Dermatophagoides farinae, Dermatophagoides farinae, Stag beetle mite, Dromedary spider mite, Dick mite,
It has been found that it has a broader and more powerful acaricidal effect than ever before against indoor dust mites such as Southern mites, dust mites, and Saladani, and found that it has a sufficient disinfecting effect even at low doses. The invention was completed.

【0006】すなわち、本発明の要旨は、クロルフェナ
ピルを有効成分として含有することを特徴とする屋内塵
性ダニ用殺ダニ組成物。クロルフェナピル並びにピレス
ロイド系殺虫剤、有機リン系殺虫剤、有機殺菌剤もしく
は無機殺菌剤より選ばられる少なくとも一種以上の有害
生物防除剤を含有する屋内塵性ダニ用殺ダニ組成物。さ
らにこれらの屋内塵性ダニ用殺ダニ組成物に共力剤を配
合する屋内塵性ダニ用殺ダニ剤に存する。
That is, the gist of the present invention is an acaricidal composition for indoor dust mites, characterized by containing chlorfenapyr as an active ingredient. An acaricidal composition for indoor dust mites, which contains chlorfenapyr and at least one or more pest control agents selected from pyrethroid insecticides, organic phosphorus insecticides, organic fungicides or inorganic fungicides. Furthermore, there exists an acaricide for indoor dust mites, in which a synergist is added to these acaricidal compositions for indoor dust mites.

【0007】[0007]

【発明の実施の形態】以下、本発明を詳細に説明する。
本発明で使用されるクロルフェナピル(4−ブロモ−2
−(4−クロロフェニル)−1−(エトキシメチル)−
5−(トリフルオロメチル)ピロール−3−カルボニト
リルの一般名)は、有効成分として単独でも十分に屋内
塵性ダニ用殺ダニ効果を有する屋内塵性ダニ用殺ダニ組
成物となるが、さらに有害生物防除剤を混合することに
よってより強力な屋内塵性ダニ用殺ダニ効果を有する屋
内塵性ダニ用殺ダニ組成物となる。
BEST MODE FOR CARRYING OUT THE INVENTION The present invention will be described in detail below.
Chlorfenapyr (4-bromo-2) used in the present invention
-(4-chlorophenyl) -1- (ethoxymethyl)-
5- (trifluoromethyl) pyrrole-3-carbonitrile (generic name), even if used alone as an active ingredient, it becomes an acaricidal composition for indoor dust mites having a sufficient acaricidal effect for indoor dust mites. By mixing with a pesticide, an acaricidal composition for indoor dust mites having a stronger acaricidal effect for indoor dust mites can be obtained.

【0008】この有害生物防除剤としては、レスメトリ
ン、ペルメトリン、フェノトリン等のピレスロイド系殺
虫剤;ダイアジノン、ジクロルボス、フェニトロチオン
等の有機燐系殺虫剤;デヒドロ酢酸ナトリウム等の酸化
亜鉛等の無機殺菌剤が挙げられる。さらに屋内塵性ダニ
用殺ダニ組成物に、オクタクロロジプロピルエーテル
(略称S−421)、イソボルニルチオシアノアセテー
ト(略称IBTA)、ピペロニルブトキサイド、N−
(2−エチルヘキシル)−ビシクロ−〔2,2,1〕−
ヘプタ−5−エン−2,3−ジカルボキシイミド(略称
MGK−264)、N−(2−エチルヘキシル)−1−
イソプロピル−4−メチルビシクロ−〔2,2,2〕−
オクト−5−エン−2,3−ジカルボキシイミド(略称
サイネピリン500)等の共力剤を混合して使用するこ
とにより、一層の効力増強が認められる屋内塵性ダニ用
殺ダニ剤が得られる。
Examples of the pest control agent include pyrethroid insecticides such as resmethrin, permethrin and phenothrin; organic phosphorus insecticides such as diazinon, dichlorvos and fenitrothion; and inorganic fungicides such as zinc oxide such as sodium dehydroacetate. To be Furthermore, for the acaricidal composition for indoor dust mites, octachlorodipropyl ether (abbreviation S-421), isobornyl thiocyanoacetate (abbreviation IBTA), piperonyl butoxide, N-
(2-Ethylhexyl) -bicyclo- [2,2,1]-
Hepta-5-ene-2,3-dicarboximide (abbreviation MGK-264), N- (2-ethylhexyl) -1-
Isopropyl-4-methylbicyclo- [2,2,2]-
By mixing and using a synergist such as octo-5-ene-2,3-dicarboximide (abbreviated as sinepyrine 500), an acaricide for indoor dust mites, which is further enhanced in efficacy, can be obtained. .

【0009】また、クロルフェナピルおよび有害生物防
除剤を、本発明の殺ダニ剤または殺ダニ組成物の有効成
分として用いる場合、通常、固体担体、液体担体、ガス
状担体、餌等と混入するかまたはマット、紙、布、皮
革、樹脂等に含浸させ、必要があれば界面活性剤または
その他の製剤補助剤を添加し、油剤、乳剤、水和剤、粉
剤、粒剤、燻蒸剤、アエゾール剤、シート剤、フロアブ
ル剤等に製剤化して使用する。
When chlorfenapyr and the pest control agent are used as the active ingredients of the acaricide or the acaricidal composition of the present invention, they are usually mixed with a solid carrier, a liquid carrier, a gaseous carrier, a bait or the like, or It is impregnated with mat, paper, cloth, leather, resin, etc., and if necessary, surfactants or other formulation auxiliary agents are added, and oils, emulsions, wettable powders, powders, granules, fumigants, azole agents, It is used after being formulated into a sheet or flowable agent.

【0010】これらの製剤化で使用する固体担体として
は、ケイ酸、カオリン、タルク、クレー、炭酸カルシウ
ム、ベントナイト、珪藻土等の鉱物質粉末または木粉、
大豆粉、澱粉粉等の植物質粉末等が利用できる。液体担
体としては、エチルアルコール、イソプロピルアルコー
ル等のアルコール類;アセトン、メチルエチルケトン等
のケトン類;テトラヒドロフラン、ジオキサン、ジエチ
ルエーテル等のエーテル類;ヘキサンケロシン、パラフ
ィン、石油ベンジン等の炭化水素類;オレイン酸等の脂
肪酸類;酢酸エチル、オレイン酸メチル、ミリスチン酸
イソプロピル等のエステル類;ベンゼン、トルエン等の
芳香族炭化水素類;クロロホルム、ジクロロエタン等の
ハロゲン化炭化水素類等が挙げられる。
As solid carriers used in these formulations, mineral powder or wood powder such as silicic acid, kaolin, talc, clay, calcium carbonate, bentonite, diatomaceous earth, etc.,
Vegetable powder such as soybean powder and starch powder can be used. Liquid carriers include alcohols such as ethyl alcohol and isopropyl alcohol; ketones such as acetone and methyl ethyl ketone; ethers such as tetrahydrofuran, dioxane and diethyl ether; hydrocarbons such as hexane kerosene, paraffin and petroleum benzine; oleic acid and the like. Fatty acids; esters such as ethyl acetate, methyl oleate, isopropyl myristate; aromatic hydrocarbons such as benzene and toluene; halogenated hydrocarbons such as chloroform and dichloroethane.

【0011】ガス状担体としては、プロパン、ブタン等
の炭化水素類;ジメチルエーテル等のエーテル類;ヘリ
ウム、ネオン、アルゴン等の不活性ガス;酸素;窒素;
炭酸ガス;圧縮空気;水素等が挙げられる。界面活性剤
としては、例えば石鹸類、ポリオキシエチレンオレイル
エーテル、ポリオキシエチレンノニルフェニルエーテル
等のポリオキシエチレンアルキルエーテル;ポリオキシ
エチレン脂肪酸エステル;脂肪酸グリセリド;ソルビタ
ン脂肪酸エステル;高級アルコールの硫酸エステル;ド
デシルベンゼンスルホン酸ソーダ等のアルキルスルホン
酸塩等が挙げられる。
As the gaseous carrier, hydrocarbons such as propane and butane; ethers such as dimethyl ether; inert gas such as helium, neon and argon; oxygen; nitrogen;
Carbon dioxide gas; compressed air; hydrogen and the like. Examples of the surfactant include polyoxyethylene alkyl ethers such as soaps, polyoxyethylene oleyl ether, and polyoxyethylene nonylphenyl ether; polyoxyethylene fatty acid esters; fatty acid glycerides; sorbitan fatty acid esters; sulfuric acid esters of higher alcohols; dodecyl. Examples thereof include alkyl sulfonates such as sodium benzene sulfonate.

【0012】これらの製剤には本発明の殺ダニ組成物、
または有害生物防除剤を含む殺ダニ組成物が、有効成分
として0.1%〜95%含有される。とくに、油剤とし
ては0.5%〜20%、乳剤としては10%〜50%、
水和剤としては30%〜80%、粉剤としては5%〜4
0%、粒剤としては10%〜50%、燻蒸剤としては1
%〜20%、エアゾール剤としては0.1%〜20%、
シート剤としては0.05g/m2 〜10g/m2 、フ
ロアブル剤としては1%〜50%になるように製剤化さ
れるのが一般的である。
These formulations include the acaricidal composition of the present invention,
Alternatively, an acaricidal composition containing a pesticide is contained as an active ingredient in an amount of 0.1% to 95%. In particular, 0.5% to 20% as an oil agent, 10% to 50% as an emulsion,
30% -80% as a wettable powder, 5% -4 as a powder
0%, 10% -50% for granules, 1 for fumigants
% To 20%, as an aerosol agent 0.1% to 20%,
The sheet material 0.05g / m 2 ~10g / m 2 , as a flowable formulation being formulated to be 1% to 50% are common.

【0013】[0013]

【実施例】次に、実施例及び試験例を示して、本発明の
効果について具体的に説明するが、本発明はその要旨を
超えない限り、以下の実施例に限定されるものではな
い。 〈実施例1〜5〉クロルフェナピル、またはクロルフェ
ナピルと表1に示す各種薬剤との合剤を、キシロールお
よび白灯油の混合液に溶解させ、原体として0.5%を
含有する油剤形態の殺ダニ剤をそれぞれ調製した。 〈比較例1〜3〉従来屋内塵性ダニ用殺ダニ剤として知
られている害虫忌避剤N,N−ジメチル−m−トルアミ
ド(略称DEET)、共力剤MGK−264またはS−
421を、キシロールおよび白灯油の混合液に溶解さ
せ、原体として0.5%を含有する油剤形態の殺ダニ剤
をそれぞれ調製した。 〈試験例1〉(ろ紙接触試験) 実施例1〜5および比較例1〜3で得られた各油剤の一
部をとってアセトンで希釈し、直径9cmのろ紙(東洋
ろ紙5A)に所定の薬量が均一に付着するように塗布し
た。乾燥した後、ろ紙を二つに折り、約50匹のケナガ
コナダニないしはコナヒョウヒダニを中に入れて三辺を
クリップで止め、強制的に接触させ、24時間後の供試
虫の死亡率を調査し、50%致死濃度(LC50)を算出
した。その結果を表1に示す。
EXAMPLES Next, the effects of the present invention will be specifically described by showing Examples and Test Examples, but the present invention is not limited to the following Examples unless it exceeds the gist. <Examples 1 to 5> Chlorfenapyr or a mixture of chlorfenapyr and various drugs shown in Table 1 was dissolved in a mixed solution of xylol and white kerosene to contain 0.5% as a drug substance, acaricide in the form of an oil agent. Each agent was prepared. <Comparative Examples 1 to 3> Pest repellent N, N-dimethyl-m-toluamide (abbreviated to DEET), a synergist MGK-264 or S-, which is conventionally known as an acaricide for indoor dust mites.
421 was dissolved in a mixed solution of xylol and white kerosene to prepare an acaricide in the form of an oil containing 0.5% as a drug substance. <Test Example 1> (filter paper contact test) A part of each of the oil solutions obtained in Examples 1 to 5 and Comparative Examples 1 to 3 was taken and diluted with acetone, and a predetermined size was applied to a filter paper (Toyo Filter Paper 5A) having a diameter of 9 cm. It was applied so that the dose would be evenly adhered. After drying, fold the filter paper in half, put about 50 Plutella xylostella mites or Dermatophagoides farinae in it, clip on three sides, forcibly contact it, and investigate the mortality of the test insects after 24 hours, The 50% lethal concentration (LC 50 ) was calculated. Table 1 shows the results.

【0014】クロルフェナピルは、公知の殺ダニ剤に比
べて、高い殺ダニ効力を有しており、実用上は原体濃度
として0.5g/m2 程含有せしめればよいと考えられ
る。また、クロルフェナピルおよびS−421の合剤、
クロルフェナピルおよび3−フェノキシベンジル DL
−シス/トランス−3−(2,2−ジクロロビニル)−
2,2−ジメチル−1−シクロプロパンカルボキシラー
ト(略称ペルメトリン)の合剤、クロルフェナピルおよ
びO,O−ジメチル O−(3−メチル−4−ニトロフ
ェニル)ホスホロチオエイト(略称フェニトロチオン)
の合剤はそれぞれ単剤で用いた場合より高い殺ダニ効果
を示した。
Chlorfenapyr has a higher acaricidal effect than known acaricides, and it is considered that chlorfenapyr should be contained in an actual concentration of about 0.5 g / m 2 in practical use. In addition, a combination drug of chlorfenapyr and S-421,
Chlorfenapyr and 3-phenoxybenzyl DL
-Cis / trans-3- (2,2-dichlorovinyl)-
2,2-Dimethyl-1-cyclopropanecarboxylate (abbreviation permethrin) mixture, chlorfenapyr and O, O-dimethyl O- (3-methyl-4-nitrophenyl) phosphorothioate (abbreviation fenitrothion)
Each of these combinations showed a higher acaricidal effect than when used alone.

【0015】[0015]

【表1】 [Table 1]

【0016】〈実施例6〜8〉クロルフェナピル、また
はクロルフェナピルと表2に示す各種薬剤との合剤をエ
タノールに溶解させ、噴射ガスとともにエアゾール缶に
充填し、総薬量として1.0%を含有するエアゾール形
態の殺ダニ剤をそれぞれ調製した。 〈比較例4〜7〉比較例として2,2,−ジクロロビニ
ル ジメチル フォスフェート(略称ジクロルボス)、
DEET、MGK−264またはS−421をそれぞれ
エタノールに溶解させ、噴射ガスとともにエアゾール缶
に充填し、総薬量として1.0%を含有するエアゾール
形態の殺ダニ剤をそれぞれ調製した。 〈試験例2〉(エアゾール準実地試験) 20cm×20cm×6cmHのミニ畳を、温度26±
2℃にて、飽和塩化カリウム水溶液(湿度84%RH)
で湿度を調整した容器内に保存し、ケナガコナダニを培
地ごと2.0g(約20,000匹)植え付け、再び上
記の条件下に保存した。約2週間後、ミニ畳上に10c
m×10cmの黒紙2枚を10分間置き、黒紙の表裏を
活動するダニ数を調査し、これを処理前の生ダニ数とし
た。このミニ畳を1辺1m(1m3 )のガラスチャンバ
ーの底面に置き、約30cmの高さから実施例6〜8お
よび比較例4〜7の各エアゾールを10秒間噴霧塗布し
た。5分後に畳を取り出し、これらを再び前述の条件下
に保存した。処理後の生ダニ数の調査は、所定日数経過
後、処理前と同様に行った。試験は3回繰り返して行
い、数式(1)より各試験毎の増殖比を算出し、その平
均値から数式(2)より減少指数を求めた。結果を表2
に示す。
<Examples 6 to 8> Chlorfenapyr or a mixture of chlorfenapyr and various drugs shown in Table 2 was dissolved in ethanol and filled in an aerosol can together with a propellant gas, and the total dose was 1.0%. The respective acaricides in the form of aerosols were prepared. <Comparative Examples 4 to 7> As a comparative example, 2,2, -dichlorovinyl dimethyl phosphate (abbreviation dichlorvos),
DEET, MGK-264 or S-421 was dissolved in ethanol and filled in an aerosol can together with a propellant gas to prepare an acaricide in the form of an aerosol containing 1.0% as a total dose. <Test Example 2> (Aerosol Quasi-Field Test) A 20 cm × 20 cm × 6 cmH mini tatami mat was used at a temperature of 26 ±
Saturated potassium chloride aqueous solution (humidity 84% RH) at 2 ° C
The sample was stored in a container whose humidity was adjusted in 2., 2.0 g (approximately 20,000) of the mite, Plutella xylostella, were planted together with the medium, and stored again under the above conditions. About 2 weeks later, 10c on a mini tatami mat
Two pieces of black paper of m × 10 cm were placed for 10 minutes, and the number of mites that were active on the front and back of the black paper was examined. This mini tatami mat was placed on the bottom of a glass chamber having a side length of 1 m (1 m 3 ) and the aerosols of Examples 6 to 8 and Comparative Examples 4 to 7 were spray-applied for 10 seconds from a height of about 30 cm. After 5 minutes, the tatami mats were taken out and stored again under the above-mentioned conditions. The investigation of the number of live mites after the treatment was conducted after a predetermined number of days had passed, in the same manner as before the treatment. The test was repeated 3 times, the growth ratio for each test was calculated from the formula (1), and the decrease index was calculated from the average value from the formula (2). Table 2 shows the results
Shown in

【0017】[0017]

【数1】 (但し、減少指数がマイナス(−)の場合は効果なし
(0)とする)
[Equation 1] (However, if the decrease index is negative (-), there is no effect (0))

【0018】[0018]

【表2】 [Table 2]

【0019】〈試験例3〉(エアゾール準実地試験) 20cm×20cmに切断した純毛製カーペットを温度
26±2℃にて飽和塩化ナトリウム溶液(湿度75%R
H)で湿度を調整した容器内に置き、コナヒョウヒダニ
を培地ごと2.0g(約1,000匹)植え付け、保存
した。約2週間後、純毛製カーペット上に10cm×1
0cmの黒紙2枚を30分間置き、黒紙の表裏を活動す
るダニ数を調査し、これを処理前の生ダニ数とした。こ
のカーペットを1辺1m(1m3 )のガラスチャンバー
の底面に置き、約30cmの高さから実施例6〜8およ
び比較例4〜7のエアゾールを5秒間噴霧塗布した。5
分後にカーペットを取り出し、これらを再び前述の条件
下に保存した。処理後の生ダニ数の調査は、所定日数経
過後、処理前と同様に行った。試験は3回繰り返して行
い、数式(1)より各試験毎の増殖比を算出し、その平
均値から数式(2)より減少指数を求めた。結果を表3
に示す。
<Test Example 3> (Aerosol Quasi-Practical Test) A pure-hair carpet cut to 20 cm × 20 cm was saturated sodium chloride solution (humidity 75% R at a temperature of 26 ± 2 ° C.).
It was placed in a container whose humidity was adjusted by H), 2.0 g (approximately 1,000) of the medium was planted with the Dermatophagoides farinae and stored. About 2 weeks later, 10 cm x 1 on a pure wool carpet
Two 0 cm pieces of black paper were placed for 30 minutes, and the number of ticks on the front and back of the black paper was examined, and this was taken as the number of live mites before treatment. This carpet was placed on the bottom of a glass chamber having a side length of 1 m (1 m 3 ) and the aerosols of Examples 6 to 8 and Comparative Examples 4 to 7 were spray-applied for 5 seconds from a height of about 30 cm. 5
After a minute, the carpets were removed and stored again under the above conditions. The investigation of the number of live mites after the treatment was conducted after a predetermined number of days had passed, in the same manner as before the treatment. The test was repeated 3 times, the growth ratio for each test was calculated from the formula (1), and the decrease index was calculated from the average value from the formula (2). Table 3 shows the results
Shown in

【0020】[0020]

【表3】 [Table 3]

【0021】〈実施例9〜11〉クロルフェナピル、ま
たはクロルフェナピルと表4に示す各種薬剤との合剤を
トルエンに溶解させ、これをトータル1.0g/m2
割合になるようにクラフト紙に均一に塗布、乾燥し、シ
ート形態の殺ダニ剤をそれぞれ調製した。 〈比較例8〜11〉比較例としてジクロルボス、DEE
T、MGK−264またはS−421をそれぞれトルエ
ンに溶解させ、これをトータル1.0g/m2 の割合に
なるようにクラフト紙に均一に塗布、乾燥し、シート形
態の殺ダニ剤をそれぞれ調製した。 〈試験例4〉(シート剤準実地試験) 20cm×20cm×6cmHのミニ畳を、温度26±
2℃にて飽和塩化カリウム水溶液(湿度84%RH)で
湿度を調整した容器内に保存し、ケナガコナダニを培地
ごと2g(約20,000匹)植え付け、再び上記の条
件下に保存した。約2週間後、ミニ畳上に10cm×1
0cmの黒紙2枚を10分間置き、黒紙の表裏を活動す
るダニ数を調査し、これを処理前の生ダニ数とした。次
に、実施例9〜11および比較例8〜10のシートを2
0cm×20cmに切り、このシートで畳の表面を覆
い、これらを再び前述の条件下に保存した。処理後の生
ダニ数の調査は、所定日数経過後、処理前と同様に行っ
た。試験は3回繰り返して行い、数式(1)より各試験
毎の増殖比を算出し、その平均値から数式(2)より減
少指数を求めた。結果を表4に示す。
<Examples 9 to 11> Chlorfenapyr or a mixture of chlorfenapyr and various drugs shown in Table 4 was dissolved in toluene, and this was uniformly applied to kraft paper so that the total ratio was 1.0 g / m 2. And then dried to prepare sheet-like acaricides. <Comparative Examples 8 to 11> As comparative examples, dichlorvos, DEE
Dissolve each of T, MGK-264 or S-421 in toluene, apply the solution evenly on kraft paper so that the total ratio is 1.0 g / m 2 , and dry to prepare a sheet-like acaricide. did. <Test Example 4> (Semi-on-site test for sheet material) A 20 cm x 20 cm x 6 cmH mini tatami mat was placed at a temperature of 26 ±
It was stored in a container whose humidity was adjusted with a saturated potassium chloride aqueous solution (humidity 84% RH) at 2 ° C., and 2 g (approximately 20,000) of Plutella xylostella mites were planted together with the medium and stored again under the above conditions. About 2 weeks later, 10 cm x 1 on a mini tatami mat
Two 0 cm pieces of black paper were placed for 10 minutes, and the number of ticks that were active on the front and back of the black paper was examined. Next, 2 sheets of Examples 9 to 11 and Comparative Examples 8 to 10 were prepared.
It was cut into 0 cm x 20 cm, the surface of the tatami mat was covered with this sheet, and these were again stored under the above-mentioned conditions. The investigation of the number of live mites after the treatment was conducted after a predetermined number of days had passed, in the same manner as before the treatment. The test was repeated 3 times, the growth ratio for each test was calculated from the formula (1), and the decrease index was calculated from the average value from the formula (2). The results are shown in Table 4.

【0022】[0022]

【表4】 [Table 4]

【0023】〈実施例12〜14〉クロルフェナピル、
またはクロルフェナピルと表5に示す各種薬剤との合剤
をエタノールに溶解させ、噴射ガスとともにエアゾール
缶に充填し、全量噴射型のボタンをとりつけ、総薬量と
して1.0%を含有するエアゾール型燻蒸剤をそれぞれ
調製した。 〈比較例12〜16〉比較例としてジクロルボス、DE
ET、MGK−264、S−421、2−イソプロポキ
シフェニール メチルカーバメイト(略称プロポクサ
ー)をそれぞれエタノールに溶解させ、噴射ガスととも
にエアゾール缶に充填し、全量噴射型のボタンをとりつ
け、総薬量として1.0%を含有するエアゾール型燻蒸
剤をそれぞれ調製した。
<Examples 12 to 14> Chlorfenapyr,
Alternatively, a mixture of chlorfenapyr and various chemicals shown in Table 5 is dissolved in ethanol, and an aerosol can is filled with a propellant gas, and a full amount injection type button is attached, and an aerosol type fumigation containing 1.0% as a total dose. Each agent was prepared. <Comparative Examples 12 to 16> As comparative examples, dichlorvos, DE
ET, MGK-264, S-421, 2-isopropoxyphenyl methyl carbamate (abbreviated as propoxer) are each dissolved in ethanol and filled in an aerosol can together with a propellant gas, and a total amount injection type button is attached, giving a total dose of 1 Aerosol fumigants containing 0.0% were prepared respectively.

【0024】試験例5(エアゾール型燻蒸剤準実地試
験) 20cm×20cm×6cmHのミニ畳を、温度26±
2℃にて飽和塩化カリウム水溶液(湿度84%RH)で
湿度を調整した容器内に保存し、ケナガコナダニを培地
ごと2g(約20,000匹)植え付け、再び上記の条
件下に保存した。約2週間後、ミニ畳上に10cm×1
0cmの黒紙2枚を10分間置き、黒紙の表裏を活動す
るダニ数を調査し、これを処理前の生ダニ数とした。こ
のミニ畳を6畳の部屋の四隅に置き、実施例12〜14
および比較例12〜16の燻蒸剤100mlを部屋の中
央で燻煙した。2時間後に畳を部屋から取り出し、これ
らを再び前述の条件下に保存した。処理後の生ダニ数の
調査は、所定日数経過後に処理前と同様に行った。試験
は3回繰り返して行い、数式(1)より各試験毎の増殖
比を算出し、その平均値から数式(2)より減少指数を
求めた。結果を表5に示す。
Test Example 5 (Aerosol type fumigant quasi-field test) A 20 cm × 20 cm × 6 cmH mini tatami mat was placed at a temperature of 26 ±
It was stored in a container whose humidity was adjusted with a saturated potassium chloride aqueous solution (humidity 84% RH) at 2 ° C., 2 g (approximately 20,000) of Plutella xylostella was inoculated together with the medium, and stored again under the above conditions. About 2 weeks later, 10 cm x 1 on a mini tatami mat
Two 0 cm pieces of black paper were placed for 10 minutes, and the number of ticks on the front and back of the black paper was examined, and this was taken as the number of live mites before treatment. This mini tatami mat is placed in the four corners of a 6 tatami mat room, and examples 12 to 14 are used.
And 100 ml of the fumigant of Comparative Examples 12 to 16 was smoked in the center of the room. After 2 hours, the tatami mats were taken out of the room and stored again under the above-mentioned conditions. The number of live mites after the treatment was investigated in the same manner as before the treatment after the lapse of a predetermined number of days. The test was repeated 3 times, the growth ratio for each test was calculated from the formula (1), and the decrease index was calculated from the average value from the formula (2). Table 5 shows the results.

【0025】[0025]

【表5】 [Table 5]

【0026】[0026]

【発明の効果】クロルフェナピルを屋内塵性ダニ類に対
して殺ダニ剤として使用することにより、低薬量で、従
来になく巾広い屋内塵性ダニ類に十分な駆除効果を示
す。
EFFECTS OF THE INVENTION By using chlorfenapyr as an acaricide against indoor dust mites, it exhibits a sufficient control effect against a wide range of indoor dust mites with a low dose and unprecedented.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 (A01N 43/36 57:12) (A01N 43/36 57:14) (A01N 43/36 59:16) (A01N 43/36 31:14 37:32 43:36 37:10 43:50) ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 6 Identification code Internal reference number FI Technical indication (A01N 43/36 57:12) (A01N 43/36 57:14) (A01N 43/36 59: 16) (A01N 43/36 31:14 37:32 43:36 37:10 43:50)

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】 クロルフェナピル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用殺ダニ組成物。
1. An acaricidal composition for indoor dust mites, which contains chlorfenapyr as an active ingredient.
【請求項2】 クロルフェナピル並びにピレスロイド系
殺虫剤、有機リン系殺虫剤、有機殺菌剤もしくは無機殺
菌剤より選ばれる少なくとも一種以上の有害生物防除剤
を含有することを特徴とする屋内塵性ダニ用殺ダニ組成
物。
2. An insecticidal agent for indoor dust mites, characterized by containing chlorphenapyr and at least one or more pesticides selected from pyrethroid insecticides, organophosphorus insecticides, organic fungicides or inorganic fungicides. Tick composition.
【請求項3】 屋内塵性ダニ用殺ダニ組成物に共力剤を
配合することを特徴とする請求項1または2記載の屋内
塵性ダニ用殺ダニ剤。
3. The acaricide for indoor dust mites according to claim 1 or 2, wherein a synergist is added to the acaricidal composition for indoor dust mites.
JP8311705A 1995-12-21 1996-11-22 Acaricide for indoor dust mites Pending JPH09227310A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP8311705A JPH09227310A (en) 1995-12-21 1996-11-22 Acaricide for indoor dust mites

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP33349595 1995-12-21
JP7-333495 1995-12-21
JP8311705A JPH09227310A (en) 1995-12-21 1996-11-22 Acaricide for indoor dust mites

Publications (1)

Publication Number Publication Date
JPH09227310A true JPH09227310A (en) 1997-09-02

Family

ID=26566859

Family Applications (1)

Application Number Title Priority Date Filing Date
JP8311705A Pending JPH09227310A (en) 1995-12-21 1996-11-22 Acaricide for indoor dust mites

Country Status (1)

Country Link
JP (1) JPH09227310A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998025461A1 (en) * 1996-12-11 1998-06-18 American Cyanamid Company Insecticidal and miticidal compositions

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998025461A1 (en) * 1996-12-11 1998-06-18 American Cyanamid Company Insecticidal and miticidal compositions
US6649646B2 (en) * 1996-12-11 2003-11-18 Basf Aktiengesellschaft Insecticidal and miticidal compositions

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