JPH0543412A - Insecticide composition for liquid-sucking wick - Google Patents

Insecticide composition for liquid-sucking wick

Info

Publication number
JPH0543412A
JPH0543412A JP3206947A JP20694791A JPH0543412A JP H0543412 A JPH0543412 A JP H0543412A JP 3206947 A JP3206947 A JP 3206947A JP 20694791 A JP20694791 A JP 20694791A JP H0543412 A JPH0543412 A JP H0543412A
Authority
JP
Japan
Prior art keywords
composition
insecticide
liquid
agent
present
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
JP3206947A
Other languages
Japanese (ja)
Inventor
Takahiro Hasegawa
隆啓 長谷川
Mikihiro Kio
幹広 木尾
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.)
Earth Corp
Original Assignee
Earth 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 Earth Chemical Co Ltd filed Critical Earth Chemical Co Ltd
Priority to JP3206947A priority Critical patent/JPH0543412A/en
Publication of JPH0543412A publication Critical patent/JPH0543412A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To provide an insecticide composition for liquid-sucking wick, capable of stably dissipating an insecticide without adding an agent for preventing the clogging of wick and having high safety. CONSTITUTION:The objective composition contains an ester compound of chrysanthemum-monocarboxylic acid or its derivative and 2,3,5,6- tetrafluorobenzyl alcohol expressed by formula (X and Y are Cl or CH3), especially (+)-1R,3S-trans-2,2-dimethyl-3-(2,2-dichlorovinyl) cyclopropanecarboxylic acid 2,3,5,6tetrafluorobenzyl ester as an active component at a concentration of usually 0.1-5wt.%, preferably 0.5-4wt.%. The insecticide composition for liquid-sucking wick enables the stable dissipation of the insecticide over a long period without using a clogging preventing agent and, furthermore, it is safe to accidental swallowing. The composition is suitable for an insecticide- dissipating agent or device such as fumigant, thermal dissipation agent, electric mosquito repellent and liquid-sucking electric mosquito repellent.

Description

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

【0001】[0001]

【産業上の利用分野】本発明は、新規な吸液芯用殺虫剤
組成物に関するものであり、更に詳しくは、殺虫剤を蒸
散させる場合に好適に使用できる新規な吸液芯用殺虫剤
組成物に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a novel insecticidal composition for absorbent cores, and more specifically, a novel insecticidal composition for absorbent cores that can be suitably used when the insecticide is evaporated. It is about things.

【0002】[0002]

【従来の技術】従来より殺虫の目的で殺虫剤を加熱蒸散
させる方法としては、くん煙剤、加熱蒸散剤、電気蚊取
器及び吸液芯型電気蚊取器等が挙げられる。特に、近年
吸液芯型電気蚊取器は、その操作が簡便で連続的に長時
間(約360時間あるいは1日12時間使用で約30日
間)使用でき、かつ火器を使用しない事より火炎の心配
がない等、従来の製剤に比べて非常に優れていることか
ら、多く利用される様になった。これに伴い各種の検討
が続けられ、数多くの発明がなされている。特に殺虫剤
(殺虫組成物)を安定に揮散させることが吸液芯の目詰
まりを防止することで可能となり、吸液芯型電気蚊取器
が実用化された事より、この目詰まり防止に関しては多
くの知見がある。例えば、特開昭63−63330号公
報には目詰まり防止の為、吸液芯自体に2,2′−メチ
レンビス(4−エチル−6−t−ブチルフェノール)等
の化合物を保持させる方法が開示され、特公平2−25
885号公報には殺虫剤含有組成物中に3,5−ジ−t
−ブチル−4−ヒドロキシトルエン等の化合物を添加し
た吸液芯用殺虫剤組成物が示されている。
2. Description of the Related Art Conventionally, as a method for heating and evaporating an insecticide for the purpose of insecticidal, a smoker, a heating and evaporating agent, an electric mosquito trap, a liquid-wicking electric mosquito trap, and the like can be mentioned. Especially in recent years, the liquid-wicking electric mosquito catcher is easy to operate and can be used continuously for a long time (about 360 hours or 12 hours a day for about 30 days), and since it does not use a firearm Since it is extremely superior to conventional preparations such as no worries, it has come to be widely used. Along with this, various studies have been continued and many inventions have been made. In particular, it is possible to volatilize the insecticide (insecticidal composition) stably by preventing clogging of the absorbent core, and since the absorbent core type electric mosquito catcher has been put into practical use, Has a lot of knowledge. For example, JP-A-63-63330 discloses a method of holding a compound such as 2,2'-methylenebis (4-ethyl-6-t-butylphenol) on the absorbent core itself in order to prevent clogging. 2-25
No. 885 discloses 3,5-di-t in a composition containing an insecticide.
An insecticide composition for absorbent cores containing compounds such as -butyl-4-hydroxytoluene is shown.

【0003】一方、特開昭63−203649号公報に
は(+)1R,3S−トランス−2,2−ジメチル−3
−(2,2−ジクロロビニル)シクロプロパンカルボン
酸2,3,5,6−テトラフルオロベンジルが殺虫剤と
して有効であり、製剤化するときには活性化合物を徐々
に計量された量で放出する、いわゆる緩徐放出配合剤、
重合体物質の微小カプセル、燃焼装置、燻蒸カートリッ
ジ、燻蒸カン蚊取りコイルならびに電気的及び化学的熱
的加熱装置中で用いるための蒸発錠剤に添加することが
提案されている。
On the other hand, JP-A-63-203649 discloses (+) 1R, 3S-trans-2,2-dimethyl-3.
2,3,5,6-Tetrafluorobenzyl- (2,2-dichlorovinyl) cyclopropanecarboxylate is effective as an insecticide, releasing gradually the active compound in a metered amount when formulated, the so-called Slow release formulation,
It has been proposed to add microcapsules of polymeric materials, combustors, fumigation cartridges, fumigation mosquito coils and evaporative tablets for use in electrical and chemical thermal heating devices.

【0004】[0004]

【発明が解決しようとする課題】上述した特開昭63−
203649号公報には、有効成分を加熱して利用する
種々の剤型、装置について開示されてはいるが、吸液芯
用殺虫剤組成物として利用することに関しては記載もな
ければ示唆もなく、ましてや目詰まり防止剤なしに長期
安定に吸液芯用殺虫剤組成物として利用しうることにつ
いては、全く予測もつかないことである。
DISCLOSURE OF THE INVENTION Problems to be Solved by the Invention
No. 203649 discloses various dosage forms and apparatus for heating and using an active ingredient, but there is no description or suggestion as to use as an insecticidal composition for absorbent cores, Furthermore, it is completely unpredictable that it can be stably used as a pesticide composition for absorbent cores for a long period of time without using an anti-clogging agent.

【0005】そこで本発明は吸液芯の目詰まり防止の為
の薬剤を添加せずに安定に蒸散でき、かつその殺虫剤の
安全性の高い組成物を得ることを目的としてなされたも
のである。
Therefore, the present invention has been made for the purpose of obtaining a composition which can be stably evaporated without adding a chemical agent for preventing clogging of the absorbent core and which is highly safe for the insecticide. ..

【0006】[0006]

【課題を解決するための手段】本発明は数多くの殺虫剤
の中から下記化2の一般式(1)の薬剤を吸液芯用殺虫
剤組成物の有効成分とする時に全く予期せぬ上記目的を
達成しうることを見出した。
In the present invention, when a drug represented by the general formula (1) represented by the following chemical formula 2 is used as an active ingredient of a pesticidal composition for absorbent cores, among the numerous pesticides, the above-mentioned unexpected problems occur. We have found that we can achieve the purpose.

【0007】すなわち、本発明は、That is, the present invention is

【0008】[0008]

【化2】 [Chemical 2]

【0009】(但し、X、Yは塩素またはメチル基を表
し、互いに同一でも異なってもよい。)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吸液芯用
殺虫剤組成物に係わる。
(In the formula, X and Y represent chlorine or a methyl group and may be the same or different from each other.) A pesticidal composition for absorbent cores containing as an active ingredient. Involve

【0010】前記一般式(1)で示される化合物(以
下、本発明の化合物と言う)は、第1菊酸またはその誘
導体と2,3,5,6−テトラフルオロベンジルアルコ
ールとのエステル化合物であり、任意の光学異性体、幾
何異性体等の立体異性体を包含する。例えば、本発明の
化合物の菊酸誘導体部において、1R−トランス、1R
−シス,トランス、1R−シス、1RS−シス,トラン
ス等が挙げられる。特に、本発明の化合物としては、
(+)1R,3S−トランス−2,2−ジメチル−3−
(2,2−ジクロロビニル)シクロプロパンカルボン酸
2,3,5,6−テトラフルオロベンジルが好まし
い。
The compound represented by the general formula (1) (hereinafter referred to as the compound of the present invention) is an ester compound of primary chrysanthemic acid or its derivative and 2,3,5,6-tetrafluorobenzyl alcohol. And includes any stereoisomers such as optical isomers and geometric isomers. For example, in the chrysanthemic acid derivative part of the compound of the present invention, 1R-trans, 1R
-Cis, trans, 1R-cis, 1RS-cis, trans and the like. Particularly, as the compound of the present invention,
(+) 1R, 3S-trans-2,2-dimethyl-3-
(2,2-Dichlorovinyl) cyclopropanecarboxylic acid 2,3,5,6-tetrafluorobenzyl is preferred.

【0011】本発明の組成物は、本発明の化合物を単独
で使用してもその他の任意の薬剤と併用してもよく、ま
た、各種公知の添加剤を包含できる。例えば、本発明の
化合物とピレスロイド系の殺虫剤の共力剤であるα−
〔2−(2−ブトキシエトシキ)エトキシ〕−4,5−
メチレンジオキシ−2−プロピルトルエン(ピペロニル
ブトキサイド)、N−(2−エチルヘキシル)ビシクロ
〔2,2,2′〕ヘプタ−5−エン−2,3−ジカルボ
キシイミド(MGK−264)、オクタクロロジイソプ
ロピルエーテル(S−421)、チオシアノ酢酸イソボ
ニル(IBTA)、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(サイネ
ピリン500)など、その他アレスリン、ピレトリンな
どに対して有効な既知の共力剤と混合使用することによ
って効力を増強することができる。
The composition of the present invention may use the compound of the present invention alone or in combination with any other drug, and may include various known additives. For example, α-, which is a synergist of the compound of the present invention and a pyrethroid insecticide.
[2- (2-butoxyethoxy) ethoxy] -4,5-
Methylenedioxy-2-propyltoluene (piperonyl butoxide), N- (2-ethylhexyl) bicyclo [2,2,2 '] hept-5-ene-2,3-dicarboximide (MGK-264) , Octachlorodiisopropyl ether (S-421), isobornyl thiocyanoacetate (IBTA), N- (2-ethylhexyl) -1-
Mixing with isopropyl-4-methylbicyclo [2,2,2 '] oct-5-ene-2,3-dicarboximide (Cinepyrine 500) and other known synergists effective against allethrin and pyrethrin. Potency can be enhanced by use.

【0012】尚、光に対する安定性を高めるために紫外
線吸収剤を本組成物に添加して使用することにより、効
力を安定させることができる。紫外線吸収剤としては、
例えばBTHのようなフェノール誘導体、ビスフェノー
ル誘導体またはフェニル−d−ナフチルアミン、フェニ
ル−β−ナフチルアミン、フェネチジンとアセトンとの
縮合物等のアリールアミン類、ベンゾフェノン系化合物
が挙げられる。
The effect can be stabilized by adding an ultraviolet absorber to the composition in order to increase the stability against light. As an ultraviolet absorber,
Examples thereof include phenol derivatives such as BTH, bisphenol derivatives, phenyl-d-naphthylamine, phenyl-β-naphthylamine, arylamines such as condensates of phenetidine and acetone, and benzophenone compounds.

【0013】本発明の吸液芯用殺虫剤組成物(以下、本
組成物という)を調製するための溶剤としては、各種の
有機溶剤、代表的には炭化水素系溶剤をいずれも使用で
きる。特に沸点範囲が約150〜350℃の脂肪族系炭
化水素(パラフィン系炭化水素及び不飽和脂肪族炭化水
素)は好ましく、上記沸点範囲のn−パラフィン中には
炭素数10〜18のものが包含される Dictionary of O
rganic Compounds,5th ed, 1982参照 。これらの内で
特にn−パラフィン、イソパラフィン、流動パラフィン
等は実用上毒性がなく、臭いがなくしかも火炎の危険も
極めて少ない点において好適である。上記炭化水素以外
の有機溶剤としては、例えばグリセリン、プロピレング
リコール、イソプロパノール、1−オクタノール、1−
ドデカノール等のアルコール類、アセトフェノン等のケ
トン類、ジエチレングリコールジチルエーテル等のエー
テル類、アジピン酸ジオクチル、マロン酸ジエチル、フ
タル酸ジエチル等のエステル類、キシレン、クロルセ
ン、クロロホルム、シリコーンオイル等を例示できる。
場合に応じては水も使用することができる。また、溶剤
が混合物である場合の「沸点」は、JIS 2254−
1990に記載のある初留点及び終点を示す。例えば、
「沸点が150〜180℃/760mmHgの脂肪族炭
化水素」の記載は、約150℃の初留点および約180
℃の終点の蒸留性状を示す脂肪族炭化水素を示す。一般
にn−パラフィン、イソパラフィン、流動パラフィン等
の石油製品の性状は蒸留性状および/またはその溶剤中
に含まれている炭化水素化合物の構成炭素数の範囲、例
えば炭素数10〜15等で規定される。
As a solvent for preparing the insecticidal composition for absorbent cores of the present invention (hereinafter referred to as the present composition), various organic solvents, typically hydrocarbon solvents, can be used. Aliphatic hydrocarbons (paraffinic hydrocarbons and unsaturated aliphatic hydrocarbons) having a boiling point range of about 150 to 350 ° C. are particularly preferable, and n-paraffins having the above boiling point range include those having 10 to 18 carbon atoms. Dictionary of O
See rganic Compounds, 5th ed, 1982. Of these, n-paraffin, isoparaffin, liquid paraffin, etc. are particularly preferable in that they are practically nontoxic, have no odor, and have a very low risk of flame. Examples of the organic solvent other than the hydrocarbon include glycerin, propylene glycol, isopropanol, 1-octanol, 1-
Examples thereof include alcohols such as dodecanol, ketones such as acetophenone, ethers such as diethylene glycol dityl ether, esters such as dioctyl adipate, diethyl malonate, diethyl phthalate, xylene, chlorsene, chloroform and silicone oil.
Water can also be used if desired. The "boiling point" when the solvent is a mixture is JIS 2254-
The initial boiling point and end point described in 1990 are shown. For example,
The description of “aliphatic hydrocarbon having a boiling point of 150 to 180 ° C./760 mmHg” refers to an initial boiling point of about 150 ° C. and about 180 ° C.
The aliphatic hydrocarbon showing the distillation property at the end point of ° C is shown. Generally, the properties of petroleum products such as n-paraffin, isoparaffin, liquid paraffin, etc. are defined by the distillation property and / or the range of the number of constituent carbon atoms of the hydrocarbon compound contained in the solvent, for example, the number of carbon atoms is 10-15. ..

【0014】前記溶剤中の本発明の化合物の濃度は、そ
の該化合物の殺虫力や殺虫液の安全性に応じて適宜決定
される。特に限定されるものではないが、通常その濃度
が0.1〜5重量%、好ましくは0.5〜4重量%、よ
り好ましくは1.0〜3.5重量%であるように殺虫剤
液を調製するのがよい。
The concentration of the compound of the present invention in the solvent is appropriately determined depending on the insecticidal activity of the compound and the safety of the insecticidal solution. Although not particularly limited, the insecticide liquid is usually adjusted so that its concentration is 0.1 to 5% by weight, preferably 0.5 to 4% by weight, more preferably 1.0 to 3.5% by weight. Should be prepared.

【0015】そして殺虫剤の単位時間当たりの揮散量の
調節は適宜、溶剤自体の沸点あるいは異なる沸点の溶剤
の混合により調製しうる。例えば、アセトフェノンのよ
うな202℃と沸点が高い溶剤を用いたものと、イソプ
ロパノールのような82.4℃と沸点が低い溶剤を用い
たものでは、自ずと本組成物の単位時間当たりの揮散量
は異なり、低沸点の溶剤を用いることで殺虫効果を増強
しえる。
The volatilization amount of the insecticide per unit time can be adjusted by appropriately adjusting the boiling point of the solvent itself or mixing the solvents having different boiling points. For example, when using a solvent having a high boiling point such as 202 ° C. such as acetophenone and using a solvent having a low boiling point such as 82.4 ° C. such as isopropanol, the volatilization amount of this composition per unit time is naturally Differently, the insecticidal effect can be enhanced by using a low boiling point solvent.

【0016】本組成物は、従来公知の各種吸液芯を利用
した吸上式加熱蒸散型殺虫装置に適用して、いずれも前
記した所期の優れた効果を奏し得る。本組成物の適用で
きる上記装置は、例えば特公昭52−12108号公
報、実開昭58−45670号公報等に記載されてい
る。その一具体例を添付図面に示す。
The composition of the present invention can be applied to a wicking type heat evaporation type insecticidal device utilizing various conventionally known liquid absorbent wicks, and any of them can exhibit the above-mentioned desired excellent effects. The above apparatus to which the present composition can be applied is described, for example, in Japanese Examined Patent Publication No. 52-12108 and Japanese Utility Model Laid-Open No. 58-45670. One specific example is shown in the accompanying drawings.

【0017】図1は、本組成物を適用するに適した吸上
式加熱蒸散型殺虫装置の概略図であり、該装置は吸液芯
1を支持するための芯支持体2を有する本組成物収容容
器3と、上記容器内にその上部を突出して挿入された吸
液芯1と、その上側面部を間接的に加熱するための中空
円板発熱体4、該発熱体4を支持するための支持部5及
び支持脚6を有する発熱体支持台7とから成っており、
上記発熱体4は、これに通電して発熱させるためのコー
ド(図示せず)を有している。
FIG. 1 is a schematic view of a wicking type heat evaporation type insecticidal device suitable for applying the present composition, which has the wick support 2 for supporting a liquid wick 1. An object storage container 3, a liquid absorbent core 1 inserted into the container by projecting an upper part thereof, a hollow disc heating element 4 for indirectly heating an upper side surface thereof, and supporting the heating element 4. A heating element support base 7 having a support portion 5 and support legs 6 for
The heating element 4 has a cord (not shown) for energizing the heating element 4 to generate heat.

【0018】上記装置に利用される吸液芯1としては、
通常用いられている各種素材、例えば、フェルト、木
綿、パルプ、不織布、石綿、無機質成型物等のいずれで
もよく、フェルト芯(樹脂焼結芯を含む)、素焼芯、パ
ルプ芯及び無機質成型芯が好ましい。上記無機質成型芯
の具体例としては、多孔質セラミックスやグラスファイ
バー、石綿等の無機繊維を石膏やベントナイト等の結合
剤で固めたものや、カオリン、活性白土、タルク、ケイ
ソウ土、クレー、パーライト、石膏、ベントナイト、ア
ルミナ、シリカ、アルミナシリカ、チタニウム、ガラス
質火山岩焼成粉末、ガラス質火山灰焼成粉末等の鉱物質
粉末を単独で又は木粉、炭粉、活性炭等と共に糊剤、例
えばデキストリン、デンプン、アラビアゴム、合成糊、
CMC等で固めたものを例示できる。特に好ましい吸液
芯は、上記鉱物質粉末100重量部と木粉又は該木粉に
等重量までの炭粉および/または活性炭を混合した混合
物10〜300重量部とに糊剤を全吸液芯重量の5〜2
5重量%となるまで配合し、さらにこれらに水を加えて
混合後、押出成型し乾燥することにより製造される。
As the liquid absorbent core 1 used in the above apparatus,
Various commonly used materials such as felt, cotton, pulp, non-woven fabric, asbestos, inorganic moldings, etc. may be used. preferable. Specific examples of the inorganic molding core, porous ceramics and glass fiber, those obtained by fixing inorganic fibers such as asbestos with a binder such as gypsum and bentonite, kaolin, activated clay, talc, diatomaceous earth, clay, perlite, Gypsum, bentonite, alumina, silica, alumina silica, titanium, vitreous volcanic rock firing powder, mineral powder such as vitreous volcanic ash firing powder alone or with wood powder, charcoal powder, activated carbon, etc., sizing agent, for example dextrin, starch, Gum arabic, synthetic glue,
An example is one that is hardened with CMC or the like. A particularly preferred liquid absorbent core is 100 parts by weight of the above mineral powder and 10 to 300 parts by weight of wood powder or a mixture of the wood powder up to an equal weight of carbon powder and / or activated carbon. 5 to 2 of weight
It is manufactured by blending to 5% by weight, further adding water to these, mixing, extruding and drying.

【0019】該吸液芯は、吸収液速度が1〜40時間、
好ましくは8〜21時間であるのが望ましい。この吸液
速度とは、液温25℃のn−パラフィン液中に直径7m
m×長さ70mmの吸液芯をその下部より15mmまで
浸漬し、芯頂にn−パラフィンが達するまでの時間を測
定することにより求められた値を意味する。また上記吸
液芯中には、上記鉱物質粉末、木粉及び糊剤の他、更に
必要に応じてマラカイトグリーン等の色素、ソルビン酸
及びその塩類、デヒドロ酢酸等のカビ止め剤等を配合す
ることもできる。
The absorbent core has an absorbent speed of 1 to 40 hours,
It is preferably 8 to 21 hours. The liquid absorption rate is 7 m in diameter in n-paraffin liquid at a liquid temperature of 25 ° C.
It means a value obtained by immersing a liquid-absorbent core having a length of m × 70 mm up to 15 mm from its lower part, and measuring the time until n-paraffin reaches the core top. Further, in the liquid absorbent core, in addition to the mineral powder, the wood powder and the sizing agent, if necessary, a pigment such as malachite green, sorbic acid and its salts, a fungicide such as dehydroacetic acid, etc. are blended. You can also

【0020】また、吸液芯1の別の実施可能な形態とし
て、吸液芯の中心に多孔質の吸液蒸散層を有し、周囲に
保持材層を有する構造の吸液芯が例示できる。多孔質の
吸液蒸散層としては、前記吸液芯として例示したフェル
ト、木綿、パルプ、不織布、石綿、無機質成型物に加え
ポリエステルなどの合成繊維、吸水性の高い材木が好適
である。そして周囲の保持材層としてはチューブ状の力
学的に十分な強度を有し、本組成物に対して及び熱に対
して十分な耐性を有するものから選択される材料、例え
ば、ポリエステル、ナイロン等の合成繊維、無機繊維、
ポリエチレン、ポリプロピレン、ポリ塩化ビニルなどの
プラスチック、銅、真鍮、鉄、ステンレス鋼、アルミニ
ウムなどの金属、陶磁器、ガラス等から構成される。そ
して、フェルト、木綿、パルプ、不織布、石綿、無機質
成型物などにリン酸バリウムを付着させることで、その
殺虫剤吸上げ性能が長時間安定に維持することができ
る。
Another possible embodiment of the liquid absorbent core 1 is a liquid absorbent core having a structure having a porous liquid absorbent evaporation layer at the center of the liquid absorbent core and a holding material layer around the liquid absorbent core. .. As the porous liquid-absorption / evaporation layer, felt, cotton, pulp, non-woven fabric, asbestos, inorganic moldings as well as synthetic fibers such as polyester, and lumber having high water absorption are suitable as the liquid-absorption / evaporation layer. And as the surrounding holding material layer, a material selected from those having a tube-like mechanically sufficient strength and having sufficient resistance to the present composition and to heat, for example, polyester, nylon, etc. Synthetic fiber, inorganic fiber,
It is composed of plastics such as polyethylene, polypropylene and polyvinyl chloride, metals such as copper, brass, iron, stainless steel and aluminum, ceramics and glass. By attaching barium phosphate to felt, cotton, pulp, non-woven fabric, asbestos, inorganic molding, etc., the insecticide wicking performance can be stably maintained for a long time.

【0021】また上記装置に利用される発熱体として
は、通常通電により発熱する発熱体が汎用されている
が、これに限定されることなく、例えば、石油ベンジン
式カイロ、空気酸化発熱材、白金触媒等を利用した発熱
材等の公知のいかなる発熱体であってもかまわない。
As the heating element used in the above-mentioned apparatus, a heating element which normally generates heat by energization is generally used, but the heating element is not limited to this, and examples thereof include petroleum benzine type body warmers, air oxidation heating materials and platinum. Any known heat generating element such as a heat generating material using a catalyst may be used.

【0022】本組成物を上記装置に適用して殺虫を行う
方法は、従来のこの種装置の利用法と全く同様でよく、
本組成物が吸液芯より蒸散し得る適当な温度に吸液芯を
加熱処理操作すればよい、該加熱温度は、殺虫剤の種類
等に応じて適宜に決定され、特に限定されないが、通常
約70〜150℃、好ましくは105〜145℃の範囲
の発熱体表面温度とされ、これは、吸液芯表面温度約6
0〜145℃、好ましくは約100〜143℃に相当す
る。
The method of applying the present composition to the above-mentioned device to kill insects may be exactly the same as the conventional method of using this kind of device,
The composition may be heat-treated to an appropriate temperature at which the composition can evaporate from the absorbent core. The heating temperature is appropriately determined depending on the kind of insecticide and the like, but is not particularly limited. The heating element surface temperature is in the range of about 70 to 150 ° C, preferably 105 to 145 ° C.
Corresponding to 0-145 ° C, preferably about 100-143 ° C.

【0023】このような発熱体を利用した前記の加熱発
熱装置を室内、貯蔵庫、引き出し、衣服タンス、押入
れ、倉庫、車両内、船舶内、飛行機内、店舗内、排水溝
内、汚水溝内、鶏畜舎内等の比較的閉鎖された場所に設
置した場合に、とりわけ優れた殺虫効果を発揮する。
The above-mentioned heating and heating device using such a heating element is used in a room, a storage, a drawer, a clothes closet, a closet, a warehouse, a vehicle, a ship, an airplane, a store, a drain, a waste ditch, When installed in a relatively closed place such as in a chicken barn, it exhibits a particularly excellent insecticidal effect.

【0024】[0024]

【作用】本発明は、従来殺虫活性を示すことが知られて
いた一般式(I)で示される本発明の化合物を吸液芯用
殺虫剤組成物として適用したところ、従来必要であった
目詰まり防止剤を用いることなく、本組成物を極めて効
率よく加熱蒸散しうるのは、その詳細な機構は明らかで
はないが、本発明の化合物の構造および該化合物、溶剤
と吸液芯との相互作用に起因するものと考えられる。
In the present invention, the compound of the present invention represented by the general formula (I), which has been known to exhibit insecticidal activity, was applied as an insecticidal composition for absorbent cores. It is not possible to elucidate the detailed mechanism of heating and evaporating the composition extremely efficiently without using a clogging preventive agent, but the structure of the compound of the present invention and the mutual interaction between the compound, the solvent and the absorbent core It is thought to be due to the action.

【0025】[0025]

【実施例】以下本発明をさらに詳しく説明するが、本発
明はこれに限定されるものではない。また、実施例中の
溶剤Aとしては炭素数13〜19、沸点が240〜35
0℃/760mmHg、溶剤Bとしては炭素数13〜1
6、沸点が240〜275℃/760mmHgの性状の
溶剤を用いた。
The present invention will be described in more detail below, but the present invention is not limited thereto. The solvent A in the examples has 13 to 19 carbon atoms and a boiling point of 240 to 35.
0 ° C./760 mmHg, Solvent B has 13 to 1 carbon atoms
6. A solvent having a boiling point of 240 to 275 ° C./760 mmHg was used.

【0026】殺虫剤A(本発明の化合物)〔(+)1
R,3S−トランス−2,2−ジメチル−3−(2,2
−ジクロロビニル)シクロプロパンカルボン酸 2,
3,5,6−テトラフルオロベンジル〕を1.44(w
/w)%となるように溶剤Aに混合し、本組成物A 4
5mlを得た。また、比較として殺虫剤Aを1.44
(w/w)%、3,5−ジ−t−ブチル−4−ヒドロキ
シトルエン(目詰まり防止剤)を0.3(w/w)%に
なるように溶剤Aに混合した本組成物B 45mlを得
た。更に殺虫剤dl−3−アリル−2−メチルシクロペ
ンタ−2−エン−4−オン−1−イル d−シス/トラ
ンス−クリサンテマート(商品名ピナミンフォンテ:住
友化学工業株式会社)を3.6(w/w)%となるよう
に溶剤Bに混合して参考組成物C 45mlを、そして
前記組成物Cと同様の処方に更に目詰まり防止剤を0.
3(w/w)%となるように添加混合した参考組成物D
45mlを各々調製した。
Insecticide A (compound of the invention) [(+) 1
R, 3S-trans-2,2-dimethyl-3- (2,2
-Dichlorovinyl) cyclopropanecarboxylic acid 2,
3,5,6-tetrafluorobenzyl] to 1.44 (w
/ W)% so that the composition A 4 is mixed with the solvent A.
5 ml was obtained. As a comparison, the insecticide A was 1.44
The present composition B in which (w / w)% and 3,5-di-t-butyl-4-hydroxytoluene (anti-clogging agent) are mixed in the solvent A so as to be 0.3 (w / w)% Obtained 45 ml. Further, 3 insecticides dl-3-allyl-2-methylcyclopent-2-en-4-one-1-yl d-cis / trans-chrysanthemate (trade name Pinaminefonte: Sumitomo Chemical Co., Ltd.) are used. The composition B was mixed with Solvent B at a concentration of 0.6 (w / w) to prepare 45 ml of the reference composition C, and the same formulation as the composition C was further supplemented with an anti-clogging agent.
Reference composition D added and mixed at 3 (w / w)%
45 ml each was prepared.

【0027】各々の組成物をポリ塩化ビニル製容器に入
れ、吸液芯(φ7×72.5mm、吸液速度8〜15時
間)を挿入して、各殺虫液ボトルを得て、各ボトルの吸
液芯端を約142℃となるよう図1に記載の装置にて間
接加熱した。加熱は約300時間連続して行い、その揮
散量を測定した。この試験を3回行い、その1時間当た
りの各組成物の平均揮散量(mg/時間)を結果として
表1に示した。尚、揮散時間298〜322においても
組成物A〜Dの液は残存しているが、組成物、C、Dに
おいては、既にこの前の時間で揮散量の違いが明瞭に示
されたので測定を省略した。
Each composition was placed in a polyvinyl chloride container, and a liquid absorbent core (φ7 × 72.5 mm, liquid absorption speed 8 to 15 hours) was inserted to obtain each insecticidal liquid bottle. The liquid absorption core end was indirectly heated by the apparatus shown in FIG. The heating was continuously performed for about 300 hours, and the amount of volatilization was measured. This test was performed 3 times, and the average volatilization amount (mg / hour) of each composition per hour is shown in Table 1 as a result. Incidentally, the liquids of the compositions A to D remained even after the volatilization time of 298 to 322, but in the compositions, C, and D, the difference in the volatilization amount was already clearly shown at the time before this, so the measurement was performed. Was omitted.

【0028】[0028]

【表1】 [Table 1]

【0029】表1の結果から明らかな通り、本発明の化
合物を含み、目詰まり防止剤を含有しない本組成物A
は、本発明の化合物を使用しかつ目詰まり防止剤を使用
した本組成物Bとほぼ同じ揮散量を維持できることを示
していることから、本組成物においては、目詰まり防止
剤は不要であることがわかる。一方、参考組成物Cは、
目詰まり防止剤を含まないためにそれを含む参考組成物
Dより揮散量が経時に低減することがわかる。即ち、本
発明の化合物は、参考組成物C、Dの殺虫剤とは異なる
優れた特性を有していることが実証された。
As is clear from the results shown in Table 1, the present composition A containing the compound of the present invention and containing no anti-clogging agent
Shows that the same amount of volatilization can be maintained as in the present composition B using the compound of the present invention and using the anti-clogging agent, and thus the anti-clogging agent is not necessary in the present composition. I understand. On the other hand, the reference composition C is
It can be seen that the volatilization amount is reduced with time as compared with the reference composition D containing the clogging inhibitor because it does not contain the clogging inhibitor. That is, it was demonstrated that the compound of the present invention has excellent properties different from those of the insecticides of Reference Compositions C and D.

【0030】[0030]

【発明の効果】本発明は、従来公知の殺虫剤から選択し
た一般式(I)で表される本発明の化合物を殺虫剤とし
て吸液芯用殺虫剤組成物を構成することにより、目詰ま
り防止剤を含むことなく、長時間安定して殺虫剤を揮散
することができるだけでなく、該本組成物の誤飲に対し
ても安全な組成物を提供しうる。
INDUSTRIAL APPLICABILITY According to the present invention, the compound of the present invention represented by the general formula (I) selected from the conventionally known insecticides is used as an insecticide to form an insecticide composition for absorbent cores, which causes clogging. It is possible to provide a composition which can stably volatilize an insecticide for a long time without containing an inhibitor and is safe against accidental ingestion of the present composition.

【図面の簡単な説明】[Brief description of drawings]

【図1】本組成物を適用するに適した吸上式加熱蒸散型
殺虫装置の断面概略図である。
FIG. 1 is a schematic cross-sectional view of a wicking type heat-transpiration type insecticide suitable for applying the present composition.

【符号の説明】[Explanation of symbols]

1 吸液芯 2 芯支持体 3 本組成物収容容器 4 中空円板発熱体 5 支持部 6 支持脚 7 発熱体支持台 DESCRIPTION OF SYMBOLS 1 Liquid absorption core 2 Core support 3 This composition storage container 4 Hollow disk heating element 5 Support part 6 Support leg 7 Heating element support stand

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 下記化1の一般式(I) 【化1】 (但し、X、Yは塩素またはメチル基を表し、互いに同
一でも異なってもよい。)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吸液芯用殺虫剤組成
物。
1. A general formula (I) of the following chemical formula 1 (However, X and Y represent chlorine or a methyl group, and they may be the same or different from each other.) An insecticide composition for absorbent cores, which comprises as an active ingredient.
JP3206947A 1991-08-19 1991-08-19 Insecticide composition for liquid-sucking wick Pending JPH0543412A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3206947A JPH0543412A (en) 1991-08-19 1991-08-19 Insecticide composition for liquid-sucking wick

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3206947A JPH0543412A (en) 1991-08-19 1991-08-19 Insecticide composition for liquid-sucking wick

Publications (1)

Publication Number Publication Date
JPH0543412A true JPH0543412A (en) 1993-02-23

Family

ID=16531666

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3206947A Pending JPH0543412A (en) 1991-08-19 1991-08-19 Insecticide composition for liquid-sucking wick

Country Status (1)

Country Link
JP (1) JPH0543412A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0596317A1 (en) * 1992-11-05 1994-05-11 Sumitomo Chemical Company, Limited Insecticidal composition
CN102204533A (en) * 2011-04-02 2011-10-05 中山榄菊日化实业有限公司 Electrothermal mosquito-repellent liquid and preparation method thereof
WO2012043437A1 (en) * 2010-09-30 2012-04-05 小林製薬株式会社 Chemical volatilization method and chemical volatilizer

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6348201A (en) * 1986-08-14 1988-02-29 Fumakiraa Kk Insecticidal process by thermal evaporation
JPS63203649A (en) * 1987-02-19 1988-08-23 バイエル・アクチエンゲゼルシヤフト (+)1r-trans-2,2-dimethyl-3-(2,2-dichlorovinyl)- cyclopropanecarboxylic acid 2,3,5,6- tetrafluorobenzyl
JPH037207A (en) * 1989-03-02 1991-01-14 Dainippon Jochugiku Co Ltd Aqueous insecticide for heat evaporation and method for killing insect
JPH04270205A (en) * 1990-09-25 1992-09-25 Bayer Ag Combination of pyrethroid activated compounds containing benfurtolin and prartolin
JPH0543411A (en) * 1991-08-12 1993-02-23 Sumitomo Chem Co Ltd Thermally dissipating insecticidal process

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6348201A (en) * 1986-08-14 1988-02-29 Fumakiraa Kk Insecticidal process by thermal evaporation
JPS63203649A (en) * 1987-02-19 1988-08-23 バイエル・アクチエンゲゼルシヤフト (+)1r-trans-2,2-dimethyl-3-(2,2-dichlorovinyl)- cyclopropanecarboxylic acid 2,3,5,6- tetrafluorobenzyl
JPH037207A (en) * 1989-03-02 1991-01-14 Dainippon Jochugiku Co Ltd Aqueous insecticide for heat evaporation and method for killing insect
JPH04270205A (en) * 1990-09-25 1992-09-25 Bayer Ag Combination of pyrethroid activated compounds containing benfurtolin and prartolin
JPH0543411A (en) * 1991-08-12 1993-02-23 Sumitomo Chem Co Ltd Thermally dissipating insecticidal process

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0596317A1 (en) * 1992-11-05 1994-05-11 Sumitomo Chemical Company, Limited Insecticidal composition
TR27910A (en) * 1992-11-05 1995-10-11 Sumitomo Chemical Co An insecticidal composition relates to an insecticidal composition, particularly suitable for heating fumigation.
WO2012043437A1 (en) * 2010-09-30 2012-04-05 小林製薬株式会社 Chemical volatilization method and chemical volatilizer
JP2012075665A (en) * 2010-09-30 2012-04-19 Kobayashi Pharmaceutical Co Ltd Chemical volatilization method and chemical volatilizer
CN102204533A (en) * 2011-04-02 2011-10-05 中山榄菊日化实业有限公司 Electrothermal mosquito-repellent liquid and preparation method thereof

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