JPH02152911A - Control agent against indoor acaridae - Google Patents
Control agent against indoor acaridaeInfo
- Publication number
- JPH02152911A JPH02152911A JP30642188A JP30642188A JPH02152911A JP H02152911 A JPH02152911 A JP H02152911A JP 30642188 A JP30642188 A JP 30642188A JP 30642188 A JP30642188 A JP 30642188A JP H02152911 A JPH02152911 A JP H02152911A
- Authority
- JP
- Japan
- Prior art keywords
- agent
- control agent
- bcp
- mites
- acaridae
- 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
Links
- 241000132121 Acaridae Species 0.000 title abstract 2
- 239000000642 acaricide Substances 0.000 claims description 8
- WYVVKGNFXHOCQV-UHFFFAOYSA-N 3-iodoprop-2-yn-1-yl butylcarbamate Chemical compound CCCCNC(=O)OCC#CI WYVVKGNFXHOCQV-UHFFFAOYSA-N 0.000 claims description 3
- 239000004480 active ingredient Substances 0.000 claims description 3
- 239000003795 chemical substances by application Substances 0.000 abstract description 21
- 239000000839 emulsion Substances 0.000 abstract description 7
- 239000000443 aerosol Substances 0.000 abstract description 4
- 238000002156 mixing Methods 0.000 abstract description 4
- 230000000887 hydrating effect Effects 0.000 abstract description 3
- 239000011248 coating agent Substances 0.000 abstract description 2
- 239000003405 delayed action preparation Substances 0.000 abstract description 2
- 230000000391 smoking effect Effects 0.000 abstract description 2
- ZZHGIUCYKGFIPV-UHFFFAOYSA-N butylcarbamic acid Chemical compound CCCCNC(O)=O ZZHGIUCYKGFIPV-UHFFFAOYSA-N 0.000 abstract 2
- 238000005507 spraying Methods 0.000 abstract 1
- 241000238876 Acari Species 0.000 description 16
- 239000003814 drug Substances 0.000 description 10
- 229940079593 drug Drugs 0.000 description 10
- 239000003921 oil Substances 0.000 description 6
- 230000000694 effects Effects 0.000 description 5
- 241000238631 Hexapoda Species 0.000 description 4
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 4
- 239000003350 kerosene Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 235000019645 odor Nutrition 0.000 description 4
- 239000008096 xylene Substances 0.000 description 4
- 229920000742 Cotton Polymers 0.000 description 3
- 241000282373 Panthera pardus Species 0.000 description 3
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 239000003995 emulsifying agent Substances 0.000 description 3
- 239000000835 fiber Substances 0.000 description 3
- 239000002917 insecticide Substances 0.000 description 3
- 238000004898 kneading Methods 0.000 description 3
- 239000004745 nonwoven fabric Substances 0.000 description 3
- 150000002903 organophosphorus compounds Chemical class 0.000 description 3
- 239000002728 pyrethroid Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 241000238710 Dermatophagoides Species 0.000 description 2
- PNVJTZOFSHSLTO-UHFFFAOYSA-N Fenthion Chemical compound COP(=S)(OC)OC1=CC=C(SC)C(C)=C1 PNVJTZOFSHSLTO-UHFFFAOYSA-N 0.000 description 2
- 240000001857 Phyllostachys elegans Species 0.000 description 2
- 241000700159 Rattus Species 0.000 description 2
- 206010040880 Skin irritation Diseases 0.000 description 2
- 208000006673 asthma Diseases 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- ZNOLGFHPUIJIMJ-UHFFFAOYSA-N fenitrothion Chemical compound COP(=S)(OC)OC1=CC=C([N+]([O-])=O)C(C)=C1 ZNOLGFHPUIJIMJ-UHFFFAOYSA-N 0.000 description 2
- 239000000417 fungicide Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- VEMKTZHHVJILDY-FIWHBWSRSA-N resmethrin Chemical compound CC1(C)[C@H](C=C(C)C)C1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-FIWHBWSRSA-N 0.000 description 2
- 229940108410 resmethrin Drugs 0.000 description 2
- 230000036556 skin irritation Effects 0.000 description 2
- 231100000475 skin irritation Toxicity 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 241000931705 Cicada Species 0.000 description 1
- 241000283973 Oryctolagus cuniculus Species 0.000 description 1
- 208000003251 Pruritus Diseases 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- 230000000895 acaricidal effect Effects 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 230000007059 acute toxicity Effects 0.000 description 1
- 231100000403 acute toxicity Toxicity 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 201000009961 allergic asthma Diseases 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- OOCMUZJPDXYRFD-UHFFFAOYSA-L calcium;2-dodecylbenzenesulfonate Chemical compound [Ca+2].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O.CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O OOCMUZJPDXYRFD-UHFFFAOYSA-L 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 239000013256 coordination polymer Substances 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- FHIVAFMUCKRCQO-UHFFFAOYSA-N diazinon Chemical compound CCOP(=S)(OCC)OC1=CC(C)=NC(C(C)C)=N1 FHIVAFMUCKRCQO-UHFFFAOYSA-N 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000002085 irritant Substances 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- 230000007803 itching Effects 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 231100001231 less toxic Toxicity 0.000 description 1
- 229940040145 liniment Drugs 0.000 description 1
- 239000000865 liniment Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000003094 microcapsule Substances 0.000 description 1
- RLLPVAHGXHCWKJ-UHFFFAOYSA-N permethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 RLLPVAHGXHCWKJ-UHFFFAOYSA-N 0.000 description 1
- 229960000490 permethrin Drugs 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- -1 polyoxyethylene nonylphenyl ether Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 230000002940 repellent Effects 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000013268 sustained release Methods 0.000 description 1
- 239000012730 sustained-release form Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
【発明の詳細な説明】
[a業上の利用分野]
本発明は、屋内性ダニの防除に有用な薬剤に関するもの
である。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Use] The present invention relates to a drug useful for controlling indoor mites.
[従来の技術]
住宅構造や生活様式の変化に伴なフて、ヒヨウヒダニ類
、コナダニ類、ツメダニ類等の屋内性ダニの発生が頻繁
になり、それによる被害も大きくなっている。これらの
屋内性ダニは、人体に痒みや不快感を与えるばかりでな
く、アレルギー性喘息や支給を惹起する原因にもなって
いる。[Prior Art] With changes in housing structures and lifestyles, the occurrence of indoor mites such as Dermatophagoides mites, Dermatophagoides mites, and Cicada mites has become more frequent, and the damage caused by them has also increased. These indoor mites not only cause itching and discomfort to the human body, but also cause allergic asthma and asthma.
従来の屋内性ダニ防除用薬剤としては、有害な昆虫の防
除に実績のある殺虫剤を転用することが行なわれてきた
。この様な薬剤としては例えばフェニトロチオン、フェ
ンチオン、ダイアジノン等の有機燐系化合物;ブロポク
スルやNAC等のカルバメート系化合物;或はレスメト
リン、ペルメトリン、フエノトリン等のピレスロイド系
化合物等が知られている。As conventional indoor mite control agents, insecticides that have a proven track record for controlling harmful insects have been repurposed. Known examples of such drugs include organic phosphorus compounds such as fenitrothion, fenthion, and diazinon; carbamate compounds such as bropoxur and NAC; and pyrethroid compounds such as resmethrin, permethrin, and phenotrin.
これらの薬剤は、
■適当な溶剤で希釈して噴霧剤、塗布剤、注入剤として
用いる、
■適当な担体で希釈して散布剤として用いる、■適当な
樹脂膜中に練り込んだり、マイクロカプセル化して徐放
性製剤として用いる等の手法によって使用されている。These drugs are: - diluted with an appropriate solvent and used as a spray, liniment, or injection; - diluted with an appropriate carrier and used as a dispersant; - kneaded into an appropriate resin film or made into microcapsules. It is used in various ways, such as by converting it into a sustained-release preparation.
[発明が解決しようとする課題]
しかしながらダニ類は形態学的および生理学的に見て昆
虫類とは異なる生物であるので、昆虫類の駆除に有効な
殺虫剤がダニ類の防除用薬剤として全く同じ様な有効性
を示すとは限らないと考えるべきである。これ迄の経験
では、上記殺虫剤の中にはある程度のダニ防除効果を発
揮し得るものも存在することが知られているが、その効
果を発揮させるには昆虫類の防除に必要な量に比べて遥
かに多量の薬剤を必要とするというのが実体である。こ
の様に多量の薬剤を使用することは、例えば比較的毒性
の強い有機燐系化合物やカルバメート系化合物では人体
に対する安全面の点で、また高価なピレスロイド系化合
物では価格面で夫々問題がある。[Problem to be solved by the invention] However, since mites are morphologically and physiologically different organisms from insects, insecticides that are effective for exterminating insects are not effective at all as agents for controlling mites. It should be considered that they do not necessarily show the same effectiveness. Based on our experience, it is known that some of the insecticides mentioned above can exhibit some degree of mite control effect, but in order to achieve this effect, it is necessary to increase the amount required to control insects. The reality is that much larger amounts of drugs are required. The use of such large amounts of drugs has problems, for example, in terms of safety for the human body when using relatively toxic organic phosphorus compounds and carbamate compounds, and in terms of cost when using expensive pyrethroid compounds.
また、同じ薬剤を使用した場合であっても、ダニの種類
によってはその効果に顕著な違いがある。例えばピレス
ロイド系化合物ではコナダニ類に対して効果が低く、カ
ルバメート系化合物や有機燐系化合物の中にはヒョウダ
ニ類に対する効果の低いものがあることが知られている
。Furthermore, even when the same drug is used, there are significant differences in its effectiveness depending on the type of tick. For example, it is known that pyrethroid compounds are less effective against mites, and some carbamate compounds and organic phosphorus compounds are less effective against leopard mites.
更に薬剤の多くは安定性を示すpH範囲が5〜7と狭く
、この範囲を外れた使用条件では長期間の効力が期待で
きないという欠点がある。また上記薬剤を繊維製品に付
着加工処理する場合には、薬剤の耐熱性が不十分である
ことから処理工程での損耗が大きく、実用的でないとい
う欠点が。Furthermore, most of the drugs have a narrow pH range of 5 to 7 in which they exhibit stability, and there is a drawback that long-term efficacy cannot be expected under usage conditions outside this range. Furthermore, when applying the above-mentioned chemicals to textile products, there is a drawback that the heat resistance of the chemicals is insufficient, resulting in large amounts of wear and tear during the treatment process, making it impractical.
ある。そればかりか上記薬剤は不快臭を発生したり、皮
膚を刺激するものが多く、日常生活に密着した屋内で使
用する薬剤としては好ましくない。be. Moreover, many of the above-mentioned drugs emit unpleasant odors and irritate the skin, making them undesirable for use indoors, where they are closely connected to daily life.
本発明はこうした技術的課題を解決する為になされたも
のであって、その目的は、不快臭や皮膚刺激性がなく、
安全性や安定性を大幅に改善し、各種のダニに対して普
遍的に強力な効力を示すダニ防除剤を提供することにあ
る。The present invention was made to solve these technical problems, and its purpose is to have no unpleasant odor or skin irritation,
The object of the present invention is to provide a mite control agent that has greatly improved safety and stability and exhibits universally strong efficacy against various mites.
[課題を解決する為の手段]
上記目的を達成し得た本発明とは、N−ノルマル−ブチ
ルカルバミン酸3−ヨード−2−プロピニルエステルを
活性成分として含有する点に要旨を有する屋内性ダニ防
除剤である。[Means for Solving the Problems] The present invention, which has achieved the above object, is a method for producing indoor mites containing N-normal-butylcarbamic acid 3-iodo-2-propynyl ester as an active ingredient. It is a pest control agent.
[作用]
本発明者らは、各種のダニに対して普遍的な効力を発揮
し、人体に対する毒性も低く、実用上の物性も優れたダ
ニ防除剤を開発する目的で様々な角度から検討を重ねた
。その結果、N−ノルマル−ブチルカルバミン酸3−ヨ
ード−2−プロピニルエステル(以下BCPと略称する
)を活性成分とすれば上記要求を満足するダニ防除剤が
実現できることを見出し、本発明を完成した。[Effect] The present inventors conducted studies from various angles with the aim of developing a mite control agent that is universally effective against various types of mites, has low toxicity to the human body, and has excellent practical physical properties. Layered. As a result, the inventors discovered that a tick control agent that satisfies the above requirements can be realized by using N-normal-butylcarbamic acid 3-iodo-2-propynyl ester (hereinafter abbreviated as BCP) as an active ingredient, and completed the present invention. .
BCPは白色乃至黄色の結晶性粉末または粒状固体であ
り、臭いはわずかである。また毒性は少なく、急性毒性
LDsoは経口で1470 mg/kg(ラット)、経
皮で2000mg以上/kg(ラットおよびラビット)
であり、皮膚刺激性もない。BCP is a white to yellow crystalline powder or granular solid with a slight odor. It is also less toxic, with acute toxicity of LDso being 1470 mg/kg (rats) orally and over 2000 mg/kg (rats and rabbits) dermally.
and has no skin irritation.
従って後述する実用使用量の範囲では、従来技術で述べ
た様な不都合は生じない。そればかりか効力は非常に強
く、各種のダニに対して普遍的に殺ダニ効果を発揮する
。Therefore, within the range of the amount of practical use described later, the disadvantages mentioned in the prior art do not occur. Not only that, but it is extremely effective and exhibits a universal acaricidal effect against various types of mites.
BCPは弱酸性から弱アルカリ性の広いpH範囲で安定
であり、また180℃の短時間加熱ではほとんど損耗す
ることがなく、製剤化、加工処理、効力維持等の点でも
好ましい特性を備えている。BCP is stable in a wide pH range from weak acidity to weak alkalinity, and is hardly damaged by short-term heating at 180° C., and has favorable properties in terms of formulation, processing, maintenance of efficacy, etc.
本発明のダニ防除剤は、上記BCPを適当な担体に担持
させ、或は適当な配合剤を加え、その使用目的に応じて
各種の形態で使用できる。例えばアルコール類、ケトン
類、エーテル類1石油類。The mite control agent of the present invention can be used in various forms depending on the purpose of use, by supporting the above-mentioned BCP on a suitable carrier or adding suitable compounding agents. For example, alcohols, ketones, ethers, 1 petroleum.
ハロゲン化炭化水素類等の溶剤の1種または2種以上を
適宜選んでこれにBCPを溶解して油剤とし、また乳化
剤を加えて乳剤とし、噴露若しくは塗布剤として使用で
きる。またタルクやクレー等を混合して散布剤とし、あ
るいは適当な助剤を加えて水和剤、エアゾール剤、燻煙
剤としても使用できる。その他■合成樹脂シート中に練
り込む、■ラテックスに配合してカーペット等のバッキ
ング材に練り込んで徐放効果を発揮させる、■ta維に
含浸させる、■接着剤とともに付着させる等の様々な形
態で使用できる。BCP is dissolved in one or more appropriately selected solvents such as halogenated hydrocarbons to form an oil agent, and an emulsifier is added to form an emulsion, which can be used as a spray or coating agent. It can also be used as a dispersing agent by mixing with talc, clay, etc., or as a hydrating agent, aerosol agent, or smoking agent by adding an appropriate auxiliary agent. Other various forms include ■Kneading into synthetic resin sheets, ■Kneading into latex and kneading into backing materials such as carpets to exert a sustained release effect, ■Impregnating Ta fibers, and ■Adhering with adhesives. Can be used in
尚本発明のダニ防除剤の使用に当たっては、他の屋内性
ダニ防除剤や忌避剤或は刺激防止剤、芳香料、殺菌剤、
防かび剤等を適宜併用する様にしてもよい。When using the mite control agent of the present invention, other indoor mite control agents, repellents, anti-irritants, fragrances, fungicides,
A fungicide or the like may be used in combination as appropriate.
BCPの配合割合(実用使用量)は、その剤型、適用方
法および適用場所等に応じて適宜決定すればよいが、油
剤やエアゾール剤の形態では0.05〜10!i量%程
度、乳剤や水和剤の形態では0.1〜50重量%重量上
程るのが好ましく、その通用量は例えば繊維に付着させ
て使用する場合は、原綿にはその0.01〜5重量%程
度を含有させるのが好ましく(より好ましくは0.05
〜1.0 重量%)、布(不織布を含む)や紙では0,
05〜10g/m2程度が好ましい(より好ましくは0
.1〜5g/m2)。更にカーペットのバッキング材に
混入する場合は、0.5〜10重量%程度使用すればよ
い。The blending ratio (practical usage amount) of BCP may be determined as appropriate depending on the dosage form, application method, application location, etc., but in the form of oil or aerosol, it is 0.05 to 10! In the form of an emulsion or a wettable powder, it is preferably about 0.1% to 50% by weight, and the common amount is, for example, when used by adhering to fibers, 0.01% to 50% by weight for raw cotton. It is preferable to contain about 5% by weight (more preferably 0.05% by weight).
~1.0% by weight), 0 for cloth (including non-woven fabrics) and paper,
Approximately 05 to 10 g/m2 is preferable (more preferably 0
.. 1-5 g/m2). Furthermore, when it is mixed into a carpet backing material, it may be used in an amount of about 0.5 to 10% by weight.
以下本発明を実施例によって更に詳細に説明するが、下
記実施例は本発明を限定する性質のものではなく、前・
後記の趣旨に徴して設計変更することはいずれも本発明
の技術的範囲に含まれるものである。Hereinafter, the present invention will be explained in more detail with reference to examples, but the following examples are not intended to limit the present invention.
Any design changes for the purposes described below are included within the technical scope of the present invention.
[実施例]
実施例1
下記第1表に示す各種薬剤をo 、 I W / V%
アセトン溶液とし、ポリエステル長繊維の原綿200m
gに0.1 ml、 0.2 mlまたは0.4 ml
均一に含浸させた後乾燥し、原綿重量に対して各種薬剤
が0.05゜0.1または0.2重量%付着した検体を
作成した。[Example] Example 1 Various drugs shown in Table 1 below were adjusted to o, IW/V%.
Acetone solution and 200m raw polyester long fiber cotton
0.1 ml, 0.2 ml or 0.4 ml in g
After uniformly impregnating and drying, specimens were prepared in which various chemicals were attached in an amount of 0.05°, 0.1 or 0.2% by weight based on the weight of the raw cotton.
この検体を高さ4 cm、直径1.8cm 、容量5m
lのスクリュー管に入れ、一方コナヒョウダニ、ケナガ
コナダニまたはミナミツメダニのいずれかを約30頭含
む50mgの培地を準備してこれを前記スクリュー管に
入れ、48時間後の死亡率を調べた。2回の試験結果の
平均値を第1表に併記する。This specimen has a height of 4 cm, a diameter of 1.8 cm, and a capacity of 5 m.
On the other hand, 50 mg of a medium containing about 30 of either P. leopard mites, P. elegans mites, or P. elegans was prepared and placed in the screw tube, and the mortality rate after 48 hours was examined. The average value of the two test results is also listed in Table 1.
実施例2
BCPSfi量部をキシレン15!重量部に溶解し、こ
れにポリオキシエチレンノニルフェニルエーテルとドデ
シルベンゼンスルホン酸カルシウム塩の混合物6重量部
(乳化剤)を加え、更に灯油74重量部で溶解して本発
明の乳剤を調製した。Example 2 The amount of BCPSfi is 15 parts xylene! 6 parts by weight of a mixture of polyoxyethylene nonylphenyl ether and dodecylbenzenesulfonic acid calcium salt (emulsifier) was added thereto, and further dissolved in 74 parts by weight of kerosene to prepare the emulsion of the present invention.
比較例として、BCPの代わりにフェンチオン(5重量
部)を用いた以外は上記と同様にした乳剤をも調製した
。またブランクとしてキシレン。As a comparative example, an emulsion was also prepared in the same manner as above except that fenthion (5 parts by weight) was used instead of BCP. Also xylene as a blank.
乳化剤および灯油のみの混合物も調製した。A mixture of emulsifier and kerosene only was also prepared.
これらの各乳剤を水で10倍に希釈し、10x10(c
ab)の上質和紙に噴霧処理した後乾燥した。尚このと
きのBCPの付着量は2501g/ m2とした。Each of these emulsions was diluted 10 times with water and 10x10 (c
The high-quality Japanese paper of ab) was sprayed and dried. The amount of BCP deposited at this time was 2501 g/m2.
次ニコレらの和紙1枚当たりに、コナヒョウダニ約30
頭を放ち、48時間後の死亡率を調査したところ、下記
第2表に示す結果が得られた。Approximately 30 Kona leopard mites per sheet of Japanese paper by Nikole et al.
When the heads were released and the mortality rate 48 hours later was investigated, the results shown in Table 2 below were obtained.
第 2 表 したところ、下記第3表に示す結果が得られた。Table 2 As a result, the results shown in Table 3 below were obtained.
第 3 表
実施例3
BCPl、0gをキシレン5gに溶解し、これに灯油を
加えて100m1の油剤を調製した。比較例として、B
CPの代わりにフェニトロチオンまたはレスメトリンの
1.0gを用いた他は上記と全く同様にした油剤を調製
した。またブランクとしてキシレンおよび灯油のみの混
合物も調製した。Table 3 Example 3 0 g of BCPl was dissolved in 5 g of xylene, and kerosene was added thereto to prepare a 100 ml oil solution. As a comparative example, B
An oil solution was prepared in exactly the same manner as above except that 1.0 g of fenitrothion or resmethrin was used instead of CP. A mixture of only xylene and kerosene was also prepared as a blank.
これらの各油剤を、10x 10 (cm)のアクリル
繊維製不織布に50m1/m2の割合で含浸させ、十分
に風乾した後不織布1枚当たりにミナミッメダニ約20
頭を放ち、48時間後の死亡率を調査[発明の効果]
以上述べた如く本発明によれば、従来の薬剤による臭気
、刺激性、安全性、安定性等の欠点を悉く改善し得ると
共に、各種のダニに普遍的に強力な効力を発揮するダニ
防除剤が実現できた。A 10 x 10 (cm) acrylic non-woven fabric was impregnated with each of these oils at a rate of 50 m1/m2, and after being thoroughly air-dried, approximately 20 minamimites per non-woven fabric were impregnated with each of these oils.
The heads were released and the mortality rate was investigated 48 hours later [Effects of the Invention] As described above, according to the present invention, it is possible to improve all the drawbacks of conventional drugs such as odor, irritation, safety, and stability. We were able to create a mite control agent that is universally effective against various types of mites.
Claims (1)
ロピニルエステルを活性成分として含有することを特徴
とする屋内性ダニ防除剤。An indoor mite control agent characterized by containing N-normal-butylcarbamic acid 3-iodo-2-propynyl ester as an active ingredient.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP30642188A JPH02152911A (en) | 1988-12-02 | 1988-12-02 | Control agent against indoor acaridae |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP30642188A JPH02152911A (en) | 1988-12-02 | 1988-12-02 | Control agent against indoor acaridae |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH02152911A true JPH02152911A (en) | 1990-06-12 |
Family
ID=17956818
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP30642188A Pending JPH02152911A (en) | 1988-12-02 | 1988-12-02 | Control agent against indoor acaridae |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH02152911A (en) |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE633594A (en) * | ||||
JPS5031036A (en) * | 1973-07-11 | 1975-03-27 |
-
1988
- 1988-12-02 JP JP30642188A patent/JPH02152911A/en active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE633594A (en) * | ||||
JPS5031036A (en) * | 1973-07-11 | 1975-03-27 |
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