JPH10182304A - Insect repellent - Google Patents
Insect repellentInfo
- Publication number
- JPH10182304A JPH10182304A JP8356346A JP35634696A JPH10182304A JP H10182304 A JPH10182304 A JP H10182304A JP 8356346 A JP8356346 A JP 8356346A JP 35634696 A JP35634696 A JP 35634696A JP H10182304 A JPH10182304 A JP H10182304A
- Authority
- JP
- Japan
- Prior art keywords
- water
- insect repellent
- weight
- surfactant
- organic solvent
- 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
Links
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- 239000002917 insecticide Substances 0.000 claims abstract description 36
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- 239000003960 organic solvent Substances 0.000 claims abstract description 26
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- 239000000203 mixture Substances 0.000 abstract description 44
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- ZTHYODDOHIVTJV-UHFFFAOYSA-N Propyl gallate Chemical compound CCCOC(=O)C1=CC(O)=C(O)C(O)=C1 ZTHYODDOHIVTJV-UHFFFAOYSA-N 0.000 description 2
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- 238000002845 discoloration Methods 0.000 description 2
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- 238000009826 distribution Methods 0.000 description 2
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- 229920000573 polyethylene Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 229920002503 polyoxyethylene-polyoxypropylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 235000010388 propyl gallate Nutrition 0.000 description 1
- 235000019423 pullulan Nutrition 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 229910021647 smectite Inorganic materials 0.000 description 1
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
- 235000010234 sodium benzoate Nutrition 0.000 description 1
- 239000004299 sodium benzoate Substances 0.000 description 1
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- 235000019721 spearmint oil Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 235000010384 tocopherol Nutrition 0.000 description 1
- 229960001295 tocopherol Drugs 0.000 description 1
- 229930003799 tocopherol Natural products 0.000 description 1
- 239000011732 tocopherol Substances 0.000 description 1
- 231100000167 toxic agent Toxicity 0.000 description 1
- 239000003440 toxic substance Substances 0.000 description 1
- 239000012498 ultrapure water Substances 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000000341 volatile oil Substances 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
- GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 0.000 description 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
(57)【要約】
【課題】 有効成分の残存量及び終点が容易かつ明瞭に
確認でき、防虫効力も高く、しかも水系組成物であるに
も拘らず充分な薬剤安定性を有する安全性の高い衣料用
防虫剤を提供する。
【解決手段】 防虫剤は、蒸気圧が10-4〜10-1mm
Hg(20℃)の常温蒸散性ピレスロイド系殺虫剤、吸
水性高分子、水、及び安定剤を含有する。好適には、常
温蒸散性ピレスロイド系殺虫剤がエムペントリン及び/
又はテラレスリンであり、安定剤が界面活性剤及び/又
は有機溶剤からなり、吸水性高分子が、自重の10〜
1,000倍の吸水能力を有する高吸水性合成高分子か
らなる。PROBLEM TO BE SOLVED: To easily and clearly confirm the remaining amount and the end point of an active ingredient, to have high insect repellent effect, and to have sufficient drug stability despite being an aqueous composition and high safety. Provide an insect repellent for clothing. SOLUTION: The insect repellent has a vapor pressure of 10 -4 to 10 -1 mm.
Contains Hg (20 ° C.) room temperature transpirable pyrethroid insecticide, water-absorbing polymer, water, and stabilizer. Preferably, the cold-vaporizable pyrethroid insecticide is empentrin and / or
Or terarethrine, wherein the stabilizer comprises a surfactant and / or an organic solvent, and the water-absorbing polymer has a weight of 10 to 10%.
It is composed of a highly water-absorbing synthetic polymer having a water absorption capacity of 1,000 times.
Description
【0001】[0001]
【発明の属する技術分野】本発明は、常温蒸散性ピレス
ロイド系殺虫剤を有効成分として含有し、薬剤残存量及
び終点が容易かつ明瞭に確認できるインジケーター機能
を備えた水系の防虫剤に関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a water-based insect repellent which contains a normal-temperature transpirable pyrethroid insecticide as an active ingredient and has an indicator function for easily and clearly confirming the residual amount and end point of the drug. .
【0002】[0002]
【従来の技術】薬剤の残存状態や終点を認知できるよう
にした衣料用防虫剤としては、種々の形態のものが提案
されており、例えば、薬剤の残存状態をその色の変化に
よって認知できるようにした発色タイプ、昇華剤の残存
量で薬剤の残存量を認知できるようにした昇華剤タイ
プ、液状の薬剤の残存量を透明フィルムを通して見える
ようにした液状タイプ、ゲル化剤を用い、経時的に小さ
くなるゲル状タイプのものなどがある。有効成分として
ピレスロイド系殺虫剤を用いた防虫剤としては、上記発
色タイプ、液状タイプ、ゲル状タイプのものが提案され
ており、発色タイプのものとして、例えば、特開平7−
324003号公報には、揮散性減感性薬剤、電子供与
性呈色性色素、及び無機顕色性化合物から成るインジケ
ーター機能を有する防虫剤が開示されており、上記揮散
性減感性薬剤として殺虫及び防虫効果を有する常温揮散
性ピレスロイド系殺虫剤を用いることで、有効成分のピ
レスロイド系殺虫剤が揮散し、減少するに従い呈色し、
その揮散経過及び終点が認知できると記載されている。2. Description of the Related Art Various types of insect repellents for clothing have been proposed as being capable of recognizing the residual state and end point of a drug. For example, the repellent state of a drug can be recognized by its color change. Using a color-developing type, a sublimation type that allows the remaining amount of the drug to be recognized by the remaining amount of the sublimation agent, a liquid type that allows the remaining amount of the liquid drug to be seen through the transparent film, and a gelling agent, There is a gel type that becomes smaller. As the insect repellent using a pyrethroid-based insecticide as an active ingredient, the above-mentioned coloring type, liquid type, and gel type have been proposed.
JP-A-324003 discloses an insect repellent having an indicator function consisting of a volatile desensitizing agent, an electron-donating color-developing dye, and an inorganic color-developing compound. As the volatile desensitizing agent, insecticide and insect repellent are disclosed. By using a normal-temperature volatile pyrethroid insecticide having an effect, the pyrethroid insecticide of the active ingredient is volatilized, and as it decreases in color,
It states that the volatilization process and the end point can be recognized.
【0003】また、液状タイプのものとして、例えば特
開平1−175911号公報には、ピレスロイド系殺虫
剤の一種であるエムペントリンを液浸出透過性の透明樹
脂フィルムから成る扁平な袋容器中に充填し、これをさ
らに通気性のある外装ケース内に保持させて構成される
防虫剤が開示されている。さらに、ゲル状タイプのもの
が特開昭63−222104号公報に開示されており、
当該公報によれば、エムペントリン等の常温揮散性の防
殺虫剤を特定のゲル化剤及び炭化水素系溶剤を用いるこ
とによってゲル化させることで、長期間防殺虫効果を発
揮でき、上記防殺虫剤揮散後は残渣が殆ど残らないた
め、終点を判別できるとされている。As a liquid type, for example, Japanese Patent Application Laid-Open No. 1-175911 discloses that a flat bag container made of a transparent resin film permeable by liquid is filled with empentrin, which is a kind of pyrethroid insecticide. There is disclosed an insect repellent which is constituted by holding this in an outer case having further air permeability. Further, a gel type is disclosed in JP-A-63-222104,
According to this publication, a pesticidal agent which is volatile at normal temperature such as empentrin is gelated by using a specific gelling agent and a hydrocarbon-based solvent, so that a long-term pesticidal effect can be exhibited. It is said that the end point can be determined because little residue remains after volatilization.
【0004】[0004]
【発明が解決しようとする課題】しかしながら、前記発
色タイプのものは、呈色するか否かは揮散性減感性薬剤
の減感作用と顕色性化合物の顕色作用の強弱によって決
まるため、終点が不明瞭であることに加えて、有効成分
の残存量を判別し難いという欠点がある。一方、前記液
状タイプのものは、透明フィルムを通して薬剤残存量を
認知できるが、液漏れする恐れがある。さらに、前記ゲ
ル状のものは、N−アシルアミノ酸誘導体系ゲル化剤と
共に灯油等の炭化水素系溶剤を用いているため引火性が
あり、また、特異臭があるという問題がある。さらにオ
イルゲル組成物であるため一般に製造時に加熱工程が必
要となり、また製造工程での有効成分の損失も大きいと
いう難点がある。However, in the case of the above-mentioned color-forming type, whether or not to develop a color is determined by the intensity of the desensitizing action of the volatile desensitizing agent and the developing action of the developing compound. Is unclear, and it is difficult to determine the remaining amount of the active ingredient. On the other hand, in the case of the liquid type, the remaining amount of the drug can be recognized through the transparent film, but there is a possibility that the liquid leaks. Furthermore, since the gel-like thing uses a hydrocarbon-based solvent such as kerosene together with the N-acylamino acid derivative-based gelling agent, there is a problem that it is flammable and has a peculiar odor. Further, since it is an oil gel composition, a heating step is generally required at the time of production, and there is a disadvantage that the loss of the active ingredient in the production step is large.
【0005】また、従来、常温蒸散性ピレスロイド系殺
虫剤は水中での分解性が迅速であると認識されているた
め、本発明組成物に類似の水系組成物は従来全く知られ
ていなかった。従って、本発明の目的は、有効成分の残
存量及び終点が容易かつ明瞭に確認でき、防虫効力も高
く、しかも水系組成物であるにも拘らず充分な薬剤安定
性を有する安全性の高い防虫剤、特に衣料用防虫剤を提
供することにある。[0005] Further, since it has been conventionally recognized that a normal-temperature transpirable pyrethroid insecticide is rapidly decomposable in water, an aqueous composition similar to the composition of the present invention has not been known at all. Accordingly, an object of the present invention is to provide a highly safe insect repellent which has a high insect repellent effect, and has sufficient drug stability despite being an aqueous composition. An object of the present invention is to provide an insect repellent for clothing.
【0006】[0006]
【課題を解決するための手段】前記目的を達成するた
め、本発明によれば、蒸気圧が10-4〜10-1mmHg
(20℃)の範囲内にある常温蒸散性ピレスロイド系殺
虫剤、吸水性高分子、水及び安定剤を含有することを特
徴とする防虫剤が提供される。好適には、上記常温蒸散
性ピレスロイド系殺虫剤として、(R,S)−1−エチ
ニル−2−メチルペント−2−エニル(1R)−シス、
トランスクリサンテマート(以下、エムペントリンとい
う)及び/又は3−アリル−2−メチルシクロペント−
2−エン−4−オン−1−イル−2,2,3,3−テト
ラメチルシクロプロパンカルボキシレート(以下、テラ
レスリンという)が用いられ、上記安定剤が界面活性剤
及び/又は有機溶剤から成る。さらに好適な態様におい
ては、上記有機溶剤として、その蒸気圧が10-2〜10
2 mmHg(20℃)の範囲内にあり、且つ水に対する
溶解度が10重量%(20℃)以上のアルコール類、グ
リコール類、エーテル類、エステル類及びケトン類から
なる群より選ばれた1種又は2種以上の有機溶剤が用い
られ、また、上記界面活性剤として、HLB値9〜18
の非イオン系界面活性剤又は該非イオン系界面活性剤を
含む混合界面活性剤が用いられ、さらに上記吸水性高分
子として、室温(20℃)において自重の10〜1,0
00倍の吸水能力を有する吸水性高分子が用いられる。According to the present invention, a vapor pressure of 10 -4 to 10 -1 mmHg is attained.
(20 ° C.) An insect repellent comprising a normal temperature transpirable pyrethroid insecticide, a water-absorbing polymer, water and a stabilizer in the range of (20 ° C.) is provided. Preferably, (R, S) -1-ethynyl-2-methylpent-2-enyl (1R) -cis or (R, S) -1-ethynyl-2-methylpent-2-enyl (1R) is used as the cold-vaporizable pyrethroid insecticide.
Transchrysanthemate (hereinafter referred to as empentrin) and / or 3-allyl-2-methylcyclopent-
2-en-4-one-1-yl-2,2,3,3-tetramethylcyclopropanecarboxylate (hereinafter referred to as teraresulin) is used, and the stabilizer comprises a surfactant and / or an organic solvent. . In a further preferred embodiment, the organic solvent has a vapor pressure of 10 -2 to 10.
One selected from the group consisting of alcohols, glycols, ethers, esters and ketones having a solubility in water of 2 mmHg (20 ° C.) and 10% by weight (20 ° C.) or more, or Two or more organic solvents are used, and the surfactant has an HLB value of 9 to 18.
Nonionic surfactants or mixed surfactants containing the nonionic surfactants are used, and the water-absorbing polymer has a weight of 10 to 1,0 at room temperature (20 ° C.).
A water-absorbing polymer having a water absorption capacity of 00 times is used.
【0007】[0007]
【発明の実施の形態】本発明の防虫剤は、吸水性高分子
に水を吸収させた半固形状物中に安定剤(界面活性剤及
び/又は水混和性の有機溶剤、例えば極性溶剤)の存在
下に常温蒸散性ピレスロイド系殺虫剤を安定的に含有せ
しめたものである。すなわち、水中に直接上記ピレスロ
イド系殺虫剤を溶解分散させたものではなく、吸水性高
分子に水を吸収させた半固形状物中に上記安定剤を介し
て溶解分散させたものであるため、ピレスロイド系殺虫
剤の分解が抑制され、水系組成物であるにも拘らず上記
ピレスロイド系殺虫剤を安定して保有しており、しか
も、常温蒸散性ピレスロイド系殺虫剤の特徴である蒸散
性は失われず、防虫効力も高く、有効成分の残存量及び
終点を容易にかつ明瞭に確認できる。すなわち、本発明
の防虫剤を微小通気孔もしくは通気性を有する容器、袋
体等に充填して使用に供すると、常温蒸散性ピレスロイ
ド系殺虫剤が水及びその他の揮発成分と共に経時的に空
気中に蒸散することにより、衣料害虫を殺虫及び忌避す
ると共にそれらによる食害を阻止し、長期間に亘り一定
の防虫効果を発揮することができる。そして、それに伴
い組成物自体の重量並びに体積が減少するのでインジケ
ーター機能を発揮し、使用過程において一見しただけで
残存量を把握することができ、最終的には微量の不揮発
性成分のみが残渣となり、防虫剤としての有効期限が終
了したことが誰の目にも明らかとなる。BEST MODE FOR CARRYING OUT THE INVENTION The insect repellent of the present invention contains a stabilizer (a surfactant and / or a water-miscible organic solvent, for example, a polar solvent) in a semi-solid product in which water is absorbed by a water-absorbing polymer. In which a normal-temperature transpirable pyrethroid-based insecticide is stably contained in the presence of. That is, the pyrethroid-based insecticide is not directly dissolved and dispersed in water, but is dissolved and dispersed via a stabilizer in a semi-solid substance in which water is absorbed by a water-absorbing polymer. Decomposition of the pyrethroid insecticide is suppressed, and the pyrethroid insecticide is stably possessed in spite of being an aqueous composition, and the transpiration characteristic of a normal temperature transpirable pyrethroid insecticide is lost. In addition, the insect repellent effect is high, and the remaining amount and end point of the active ingredient can be easily and clearly confirmed. That is, when the insect repellent of the present invention is filled into a microporous or air-permeable container, bag or the like for use, the room-temperature transpirable pyrethroid-based insecticide is dissolved in the air over time together with water and other volatile components. By transpiration, the insect pests can be killed and repelled, and the food damage caused by the insects can be prevented, and a constant insect repellent effect can be exhibited over a long period of time. And, as the weight and volume of the composition itself decrease along with it, it exerts an indicator function, and the residual amount can be grasped at a glance in the use process, and finally, only a small amount of the non-volatile component becomes a residue. It is clear to everyone that the expiration date of the insect repellent has expired.
【0008】単に薬剤残存量及び終点が容易かつ明瞭に
確認できるという発想では過去にオイルゲル組成物が各
種提案されているが、このオイルゲル組成物は油系であ
って水系でないという点において本発明の組成物とは根
本的に異なることに加え、以下の点で大きく異なる。ま
ず、本発明の組成物では引火の可能性が極めて低い点で
ある。オイルゲル組成物の場合、製造時、一般に高温加
熱工程が必要であり、製造工程におけるオイルの引火に
よる火災、爆発等に対して充分配慮した設備設計及び設
備投資が必要である。さらに流通途上においては、消防
法上、危険物取扱いに関する法の規制も受ける。加えて
異なる点は、本発明の組成物がほぼ無臭に近く、水を主
成分としているため、衣料用に適しているという点であ
る。オイルゲル組成物のほぼ90%以上を占める有機溶
剤は、一般に不快な臭気が強く、かつ樹脂等に対する攻
撃性が強く、繊維、特に合成繊維やボタン、各種装飾
物、ハンガー、タンス、塗装面等への影響を考慮する
と、衣料用防虫剤としては決して満足いくものではなか
った。また、本発明の組成物の場合、蒸散する水分に調
湿作用もあり、乾燥時の加湿効果もあるという別の利点
も得られる。Various oil gel compositions have been proposed in the past simply based on the idea that the residual amount of the drug and the end point can be easily and clearly confirmed. However, the oil gel composition of the present invention is oil-based and not water-based. In addition to being fundamentally different from compositions, they differ greatly in the following respects. First, the composition of the present invention has a very low possibility of ignition. In the case of an oil gel composition, a high-temperature heating step is generally required at the time of production, and equipment design and investment must be made with due consideration given to fire, explosion, and the like due to oil ignition in the production step. Furthermore, in the course of distribution, the Fire Services Act is also subject to the regulations of the handling of dangerous goods. In addition, the difference is that the composition of the present invention is almost odorless and contains water as a main component, so that it is suitable for clothing. Organic solvents, which account for about 90% or more of the oil gel composition, generally have a strong unpleasant odor and a strong aggressiveness against resins and the like, and are used for fibers, especially synthetic fibers and buttons, various decorative articles, hangers, closets, painted surfaces, and the like. In view of the effects of the above, it was never satisfactory as an insect repellent for clothing. Further, in the case of the composition of the present invention, there is obtained another advantage that the evaporated water also has a humidity control effect and also has a humidifying effect upon drying.
【0009】前記常温蒸散性ピレスロイド系殺虫剤とし
ては、常温で蒸散して長期に亘って優れた防虫効果を発
揮するように、その蒸気圧が10-4〜10-1mmHg
(20℃)の範囲内にあるピレスロイド系殺虫剤であれ
ば全て使用可能であるが、好ましくは安全性の高い常温
蒸散性ピレスロイド系殺虫剤であるエムペントリン及び
テラレスリンを挙げることができる。上記常温蒸散性ピ
レスロイド系殺虫剤の配合量は、使用される種類にもよ
るが、一般的に組成物全量の約0.05〜5重量%が適
当であり、より好ましくは0.1〜1重量%である。該
殺虫剤の量が0.05重量%未満では充分な防殺虫効果
が得られず、一方、5重量%より多いと安定剤としての
界面活性剤及び/又は有機溶剤が多量に必要となり、使
用終了時の残渣が多くて終点が不明瞭となり易く、また
該殺虫剤の残余分が多くなり不経済である。尚、二種類
以上のピレスロイド系殺虫剤を混合して用いることも可
能である。[0009] The normal temperature transpirable pyrethroid insecticide has a vapor pressure of 10 -4 to 10 -1 mmHg so as to evaporate at normal temperature and exhibit an excellent insect repellent effect over a long period of time.
Any pyrethroid insecticide within the range of (20 ° C.) can be used, and preferably, empentrin and terarethrin, which are highly safe room temperature transpirable pyrethroid insecticides, can be used. The amount of the normal-temperature transpirable pyrethroid-based insecticide depends on the kind used, but is generally about 0.05 to 5% by weight of the total amount of the composition, and more preferably 0.1 to 1% by weight. % By weight. When the amount of the insecticide is less than 0.05% by weight, a sufficient insecticidal effect cannot be obtained. On the other hand, when the amount is more than 5% by weight, a large amount of a surfactant and / or an organic solvent as a stabilizer is required. The end point tends to be unclear due to a large amount of residue at the end, and the residue of the insecticide increases, which is uneconomical. It is also possible to use a mixture of two or more pyrethroid insecticides.
【0010】前記吸水性高分子としては、水を吸収でき
るものであれば特に限定されず、種々の物質が使用可能
である。例えば、ジュランガム、キサンタンガム、ロー
カストビーンガム、カラギーナン、プルラン、ゼラチン
等の天然由来高分子、或いはポリビニルアルコール、カ
ルボキシメチルセルロース、ポリアクリル酸ソーダ、ポ
リアクリルアミド等の合成高分子が使用可能である。但
し、上記物質の多くは、使用するうえで加熱、攪拌等が
必要となる。そのため、製造工程がやや煩雑であるう
え、その工程中に有効成分の蒸発、分解等のロスがあ
り、また防虫剤として使用中に徐々に表面に皮膜を形成
する傾向があるため薬剤蒸散速度が後半やや落ち込むと
いう難点がある。そのため有効成分を予め多めに配合し
ておく等の対策が必要である。The water absorbing polymer is not particularly limited as long as it can absorb water, and various substances can be used. For example, naturally occurring polymers such as juran gum, xanthan gum, locust bean gum, carrageenan, pullulan, and gelatin, or synthetic polymers such as polyvinyl alcohol, carboxymethyl cellulose, sodium polyacrylate, and polyacrylamide can be used. However, many of the above substances require heating, stirring, etc. in use. Therefore, the manufacturing process is rather complicated, and there is a loss such as evaporation and decomposition of the active ingredient during the process. There is a drawback that the second half is slightly depressed. For this reason, it is necessary to take measures such as premixing the active ingredient in a large amount.
【0011】このような不利益がないという点で、常温
で自重の10〜1,000倍程度の吸水性を有する吸水
性高分子を用いることが有利であり、製造工程における
成分の変質、蒸散性物質の蒸散等によるロスを防ぐこと
ができる。このような、吸水性高分子としては、エチレ
ン、プロピレン、ブテン−1、イソブチレン、ジイソブ
チレン等のα−オレフィンと無水マレイン酸もしくはそ
の誘導体との共重合体又はそのアルカリ中和物の架橋体
(例えば(株)クラレ製KIゲル);メチルビニルエー
テル、酢酸ビニル、スチレン等の重合性ビニル化合物と
無水マレイン酸もしくはその誘導体との共重合体又はそ
のアルカリ中和物の架橋体;アクリル酸もしくはメタク
リル酸の重合体、それらを主体とする共重合体又はそれ
ら(共)重合体のアルカリ中和物の架橋体(例えば、和
光純薬工業(株)製ハイビスワコー、中外貿易(株)製
カーボポール等);アクリル酸塩もしくはメタクリル酸
塩から得られる架橋型アクリル酸塩重合体(例えば、荒
川化学工業(株)製アラソーブ等);酢酸ビニルと(メ
タ)アクリル酸エステルとの共重合体のケン化物;デン
プン−ポリ(メタ)アクリロニトリルグラフト共重合体
のアルカリ中和物;デンプンもしくはセルロースと水溶
性単量体(無水マレイン酸、アクリル酸等)とのグラフ
ト重合体の架橋体(例えば、三洋化成工業(株)製サン
フレッシュST−500S)等に代表される高吸水性合
成高分子が挙げられる。From the viewpoint that there is no such disadvantage, it is advantageous to use a water-absorbing polymer having a water absorption of about 10 to 1,000 times its own weight at room temperature, and it is advantageous that the components are degraded and evaporated in the production process. It is possible to prevent loss due to transpiration of the toxic substance. As such a water-absorbing polymer, a copolymer of an α-olefin such as ethylene, propylene, butene-1, isobutylene, diisobutylene and maleic anhydride or a derivative thereof or a crosslinked product of an alkali neutralized product thereof ( For example, KI gel manufactured by Kuraray Co., Ltd.); a copolymer of a polymerizable vinyl compound such as methyl vinyl ether, vinyl acetate, and styrene with maleic anhydride or a derivative thereof or a crosslinked product of an alkali neutralized product thereof; acrylic acid or methacrylic acid Or copolymers containing them as main components or cross-linked products of alkali-neutralized products thereof (for example, Hibiswako manufactured by Wako Pure Chemical Industries, Ltd., Carbopol manufactured by Chugai Trading Co., Ltd., etc.) ); A crosslinked acrylate polymer obtained from acrylate or methacrylate (for example, Arakawa Chemical Industry Co., Ltd. Saponified product of a copolymer of vinyl acetate and (meth) acrylic acid ester; alkali-neutralized product of starch-poly (meth) acrylonitrile graft copolymer; starch or cellulose and a water-soluble monomer (maleic anhydride) Highly water-absorbing synthetic polymers represented by a crosslinked product of a graft polymer with an acid, acrylic acid, and the like (for example, Sunfresh ST-500S manufactured by Sanyo Chemical Industries, Ltd.) and the like.
【0012】前記吸水性高分子の配合量は、組成物全量
の0.1〜10重量%が好ましい。吸水性高分子の量が
0.1重量%未満の場合、吸水が充分に行われず、離
液、漏出等の問題が生じる恐れがあり、一方、10重量
%を超えると、該吸水性高分子は残渣として残るので防
虫剤の終点が不明瞭になり易くなる。The compounding amount of the water-absorbing polymer is preferably 0.1 to 10% by weight of the total amount of the composition. When the amount of the water-absorbing polymer is less than 0.1% by weight, water absorption is not sufficiently performed, and problems such as syneresis and leakage may occur. Remains as a residue, so that the end point of the insect repellent tends to be unclear.
【0013】前記安定剤としては、前記したように界面
活性剤や有機溶剤を好適に使用できる。界面活性剤の種
類としては、陽イオン系界面活性剤、陰イオン系界面活
性剤、両性界面活性剤、非イオン系界面活性剤を任意に
組み合わせて使用することが可能であるが、HLB値7
〜20、特にHLB値9〜18の非イオン系界面活性剤
又は該非イオン系界面活性剤を含む混合界面活性剤が、
製剤安定性、経済性等の点から好ましい。上記非イオン
系界面活性剤の例としては、ポリオキシエチレンアルキ
ルエーテル、ポリオキシエチレンポリオキシプロピレン
アルキルエーテル、ポリオキシエチレンアルキルフェニ
ルエーテル、ポリオキシエチレンヒマシ油、ポリオキシ
エチレン硬化ヒマシ油誘導体等を挙げることが出来る。
また、シリコーン系及びフッ素系の界面活性剤も好適に
用いることが出来る。界面活性剤の配合量は組成物全量
の20重量%以下が好ましく、より好ましくは5重量%
以下である。20重量%より多いと、使用終了時の残渣
が多くなるほか、着(変)色、製造時並びに流通時の発
泡等の問題が生じたり、或いは吸水性高分子の吸水能力
が充分に発揮できなくなったりするなど、防虫剤として
安定性が損なわれる恐れがある。As the stabilizer, a surfactant and an organic solvent can be suitably used as described above. As the type of the surfactant, a cationic surfactant, an anionic surfactant, an amphoteric surfactant, and a nonionic surfactant can be used in any combination.
-20, especially a nonionic surfactant having an HLB value of 9 to 18 or a mixed surfactant containing the nonionic surfactant,
It is preferable in terms of formulation stability, economy, and the like. Examples of the nonionic surfactant include polyoxyethylene alkyl ether, polyoxyethylene polyoxypropylene alkyl ether, polyoxyethylene alkyl phenyl ether, polyoxyethylene castor oil, and polyoxyethylene hydrogenated castor oil derivative. I can do it.
Also, silicone-based and fluorine-based surfactants can be suitably used. The amount of the surfactant is preferably 20% by weight or less of the total amount of the composition, more preferably 5% by weight.
It is as follows. If the content is more than 20% by weight, the residue at the end of use increases, and problems such as color change (discoloration), foaming during production and distribution, or the water absorbing ability of the water-absorbing polymer can be sufficiently exhibited. There is a possibility that stability may be impaired as an insect repellent such as disappearance.
【0014】一方、前記有機溶剤としては、ピレスロイ
ド系殺虫剤の蒸散と共に蒸散して無くなるものが望まし
く、蒸気圧が10-2〜102 mmHgの範囲内にあるも
のが特に好ましい。蒸気圧が10-2mmHgより小さい
場合、有機溶剤のみが必要以上の長期に亘り残存してし
まう可能性があり、それによって使用途中で組成物のバ
ランスが大きく崩れ、ひいてはインジケーター機能が損
なわれてしまう恐れがある。他方、蒸気圧が102 mm
Hgより大きい有機溶剤を用いた場合は、逆に有機溶剤
が他の成分より早期に蒸散してしまう可能性があり、や
はり使用途中で組成物のバランスが大きく崩れ、インジ
ケーター機能を発揮でき無くなる恐れがある。また、こ
のような蒸散性の強い有機溶剤を用いて防虫剤を調製し
た場合、臭気が強過ぎて衣料用防虫剤としては不適当で
あるばかりか、過った取扱いによって引火の可能性もあ
る。[0014] On the other hand, examples of the organic solvent, it is desirable that no by evaporation with transpiration of pyrethroid insecticides, vapor pressure particularly preferably those in the range of 10 -2 ~10 2 mmHg. If the vapor pressure is less than 10 -2 mmHg, only the organic solvent may remain for an unnecessarily long period of time, whereby the balance of the composition may be greatly lost during use, and the indicator function may be impaired. There is a risk that it will. On the other hand, the vapor pressure is 10 2 mm
If an organic solvent larger than Hg is used, on the contrary, the organic solvent may evaporate earlier than the other components, and the balance of the composition may be significantly lost during use, and the indicator function may not be able to be exhibited. There is. In addition, when an insect repellent is prepared using such a highly transpirable organic solvent, not only is the odor too strong to be unsuitable as an insect repellent for clothing, but there is a possibility of ignition due to excessive handling. .
【0015】さらに、有機溶剤は水と混和する必要があ
るため、水に対する溶解度が10重量%(20℃)以上
あるアルコール類、グリコール類、エーテル類、エステ
ル類、ケトン類などが望ましい。例として、ジエチレン
グリコールモノブチルエーテル、ジエチレングリコール
モノエチルエーテル、ジエチレングリコールモノメチル
エーテル、エチレングリコール、プロピレングリコー
ル、エタノール、イソプロパノール、メチルエチルケト
ン等、水と自由な比率で混和できる溶剤を挙げることが
できるが、これらに限定されるものではない。Further, since the organic solvent must be mixed with water, alcohols, glycols, ethers, esters, ketones, and the like having a solubility in water of 10% by weight (20 ° C.) or more are desirable. Examples include, but are not limited to, diethylene glycol monobutyl ether, diethylene glycol monoethyl ether, diethylene glycol monomethyl ether, ethylene glycol, propylene glycol, ethanol, isopropanol, methyl ethyl ketone, and other solvents miscible with water in a free ratio. Not something.
【0016】有機溶剤の配合量は組成物全量の30重量
%以下が好ましい。有機溶剤の量が30重量%を超える
と吸水性高分子による吸水が困難になったり、臭気が強
くなるなど、衣料用防虫剤として不適当である。また、
万一の誤飲、誤食に対する安全性上も問題となる。これ
ら有機溶剤には組成物の融点降下作用もあり、冬期にお
ける商品の凍結破損を防止すると共に組成物の安定性を
向上させる効果も有する。尚、上記界面活性剤と有機溶
剤は目的とする使用期間等に応じて、それらを任意の比
率で組み合わせて使用しても、単独で使用しても構わな
い。The amount of the organic solvent is preferably not more than 30% by weight of the total amount of the composition. If the amount of the organic solvent exceeds 30% by weight, water absorption by the water-absorbing polymer becomes difficult, and the odor becomes strong. Also,
In the event of accidental ingestion or ingestion, there is also a problem in safety. These organic solvents also have the effect of lowering the melting point of the composition, and also have the effect of preventing freezing damage to commodities in winter and improving the stability of the composition. The surfactant and the organic solvent may be used in combination at any ratio or may be used alone depending on the intended use period and the like.
【0017】水については、一般の水道水で充分である
が、イオン交換水、蒸留水、純水等純度の高いものが組
成物安定性の点からなお望ましい。衣料用防虫剤の場
合、水の使用量は目的とする有効期間、容器形態等によ
り大きく異なるが、本発明では3〜24カ月、好ましく
は6〜12カ月を想定しており、この場合、1製剤当り
3〜500g程度が好ましい。さらに、洋服ダンス、ク
ローゼット等の大空間では20〜300g、より好まし
くは50〜200gである。引き出し、衣装ケース、納
戸等の小空間では5〜100g、より好ましくは10〜
50gである。配合割合としては組成物全量の30重量
%以上において任意であるが、安全性の点からは50重
量%以上がより好適である。As for water, general tap water is sufficient, but high-purity water such as ion-exchanged water, distilled water and pure water is more desirable from the viewpoint of composition stability. In the case of insect repellents for clothing, the amount of water used varies greatly depending on the intended shelf life, container form, etc., but in the present invention, 3 to 24 months, preferably 6 to 12 months is assumed. About 3 to 500 g per preparation is preferable. Furthermore, in a large space such as a clothes dance or a closet, the weight is 20 to 300 g, more preferably 50 to 200 g. 5-100g, more preferably 10-10g in small space such as drawer, costume case, storage room
50 g. The blending ratio is arbitrary at 30% by weight or more of the total amount of the composition, but from the viewpoint of safety, 50% by weight or more is more preferable.
【0018】本発明の防虫剤は、前記必須成分に加え
て、有効成分の安定性をより一層向上させるために酸化
防止剤を配合することができる。酸化防止剤の配合割合
は、常温蒸散性ピレスロイド系殺虫剤の10分の1〜1
0倍量、すなわち組成物全体に対して0.01〜10重
量%、より好ましくは0.1〜1重量%が経済的であ
る。0.01重量%より少ないと充分な酸化防止効果が
得られず、一方、10重量%より多いとこれを可溶化す
るためにさらに界面活性剤や有機溶剤が必要となるほ
か、変色等の原因となる。酸化防止剤の例としては、ジ
ブチルヒドロキシトルエン(略称BHT)、ブチルヒド
ロキシアニソール(略称BHA)、4,4−チオビス−
(6−t−ブチル−3−メチルフェノール)(商品名ヨ
シノックスSR、吉富製薬(株)製)、4,4−ブチリ
デンビス−(6−t−ブチル−3−メチルフェノール)
(商品名ヨシノックスBB、吉富製薬(株)製)、2,
2−メチレンビス−(4−メチル−6−t−ブチルフェ
ノール)(商品名ヨシノックス2246G、吉富製薬
(株)製)、2,2−メチレンビス−(4−エチル−6
−t−ブチルフェノール)(商品名ヨシノックス42
5、吉富製薬(株)製)、n−オクタデシル−3−(4
−ヒドロキシ−3,5−ジ−t−ブチルフェニル)プロ
ピオネート(商品名イルガノックス1076、日本チバ
ガイギー(株)製)、1,6−ヘキサンジオール−ビス
[3−(3,5−ジ−t−ブチル−4−ヒドロキシフェ
ニル)プロピオネート](商品名イルガノックス25
9、日本チバガイギー(株)製)、ペンタエリスリチル
−テトラキス[3−(3,5−ジ−t−ブチル−4−ヒ
ドロキシフェニル)プロピオネート](商品名イルガノ
ックス1010、日本チバガイギー(株)製)、ジラウ
リルチオプロピオネート(略称DLTP)、ジステアリ
ルチオジプロピオネート(略称DSTP)、オクチル化
ジフェニルアミン(商品名イルガノックス5057、日
本チバガイギー(株)製)、トコフェロール、没食子酸
n−プロピル等が挙げられるが、これらに限定されるも
のではない。The insect repellent of the present invention may further contain, in addition to the above essential components, an antioxidant to further improve the stability of the active ingredient. The compounding ratio of the antioxidant is one-tenth to one-tenth that of the normal-temperature transpirable pyrethroid insecticide.
A 0-fold amount, that is, 0.01 to 10% by weight, more preferably 0.1 to 1% by weight based on the whole composition is economical. If the amount is less than 0.01% by weight, a sufficient antioxidant effect cannot be obtained. On the other hand, if the amount is more than 10% by weight, a surfactant or an organic solvent is further required to solubilize the same, and discoloration may be caused. Becomes Examples of the antioxidant include dibutylhydroxytoluene (abbreviated as BHT), butylhydroxyanisole (abbreviated as BHA), 4,4-thiobis-
(6-t-butyl-3-methylphenol) (trade name: Yoshinox SR, manufactured by Yoshitomi Pharmaceutical Co., Ltd.), 4,4-butylidenebis- (6-t-butyl-3-methylphenol)
(Trade name: Yoshinox BB, manufactured by Yoshitomi Pharmaceutical Co., Ltd.), 2,
2-methylenebis- (4-methyl-6-t-butylphenol) (trade name: Yoshinox 2246G, manufactured by Yoshitomi Pharmaceutical Co., Ltd.), 2,2-methylenebis- (4-ethyl-6)
-T-butylphenol) (trade name: Yoshinox 42)
5, Yoshitomi Pharmaceutical Co., Ltd.), n-octadecyl-3- (4
-Hydroxy-3,5-di-t-butylphenyl) propionate (trade name Irganox 1076, manufactured by Nippon Ciba Geigy Co., Ltd.), 1,6-hexanediol-bis [3- (3,5-di-t- Butyl-4-hydroxyphenyl) propionate] (trade name Irganox 25)
9, Nippon Ciba Geigy Co., Ltd.), pentaerythrityl-tetrakis [3- (3,5-di-t-butyl-4-hydroxyphenyl) propionate] (trade name: Irganox 1010, Nippon Ciba Geigy Co., Ltd.) , Dilauryl thiopropionate (abbreviated DLTP), distearyl thiodipropionate (abbreviated as DSTP), octylated diphenylamine (trade name Irganox 5057, manufactured by Nippon Ciba Geigy Co., Ltd.), tocopherol, n-propyl gallate, etc. But are not limited to these.
【0019】また、本発明の防虫剤は、商品中での微生
物増殖による汚染を防止するために、防腐・防カビ剤を
配合することも任意である。例えばパラオキシ安息香酸
及びその誘導体、安息香酸、安息香酸ナトリウム等を挙
げることができる。尚、本発明の防虫剤に安定剤として
用いられる一部の有機溶剤、例えばエチルアルコール、
イソプロピルアルコール等、及び一部の界面活性剤、例
えば第4級アンモニウム塩等が防腐、防カビ効果を有す
ることは一般的に広く知られており、これらを安定剤と
して用いる場合には前記防腐・防カビ剤をあえて配合す
る必要がないことは言うまでもない。Further, the insect repellent of the present invention may optionally contain an antiseptic / antifungal agent in order to prevent contamination due to microbial growth in the product. For example, paraoxybenzoic acid and its derivatives, benzoic acid, sodium benzoate and the like can be mentioned. In addition, some organic solvents used as a stabilizer in the insect repellent of the present invention, for example, ethyl alcohol,
It is generally widely known that isopropyl alcohol and the like, and some surfactants such as quaternary ammonium salts have an antiseptic and antifungal effect. Needless to say, it is not necessary to add a fungicide.
【0020】さらに本発明の防虫剤は、紫外線により蒸
散性ピレスロイド系殺虫剤が分解されるのを防止すると
共に、吸水性高分子の分子量低下、即ち粘度低下を防止
するために紫外線吸収剤を配合することもできる。紫外
線吸収剤としては、2−(5−メチル−2−ヒドロキシ
フェニル)ベンゾトリアゾール(商品名チヌビンP、日
本チバガイギー(株)製)、2−(3,5−ジ−t−ブ
チル−2−ヒドロキシフェニル)ベンゾトリアゾール
(商品名チヌビン320、日本チバガイギー(株)
製)、2−(3−t−ブチル−5−メチル−2−ヒドロ
キシフェニル)−5−クロロベンゾトリアゾール(商品
名チヌビン326、日本チバガイギー(株)製)、2−
(3,5−ジ−t−ブチル−2−ヒドロキシフェニル)
−5−クロロベンゾトリアゾール(商品名チヌビン32
7、日本チバガイギー(株)製)、2−ヒドロキシ−4
−n−オクトキシベンゾフェノン(商品名トミソーブ8
00、吉富製薬(株)製)、2−ヒドロキシ−4−メト
キシベンゾフェノン(商品名バイオソーブ110、共同
薬品(株)製)等が挙げられる。Further, the insect repellent of the present invention contains an ultraviolet absorber to prevent the decomposition of the transpirable pyrethroid-based insecticide by ultraviolet rays and to reduce the molecular weight of the water-absorbing polymer, ie, the viscosity. You can also. Examples of the ultraviolet absorber include 2- (5-methyl-2-hydroxyphenyl) benzotriazole (trade name: Tinuvin P, manufactured by Nippon Ciba Geigy Co., Ltd.), 2- (3,5-di-t-butyl-2-hydroxy) Phenyl) benzotriazole (trade name: Tinuvin 320, Nippon Ciba Geigy Co., Ltd.)
), 2- (3-t-butyl-5-methyl-2-hydroxyphenyl) -5-chlorobenzotriazole (trade name: Tinuvin 326, manufactured by Nippon Ciba Geigy Co., Ltd.), 2-
(3,5-di-t-butyl-2-hydroxyphenyl)
-5-chlorobenzotriazole (trade name Tinuvin 32
7, Nippon Ciba Geigy Co., Ltd.), 2-hydroxy-4
-N-octoxybenzophenone (Tomisorb 8 trade name)
00, manufactured by Yoshitomi Pharmaceutical Co., Ltd.) and 2-hydroxy-4-methoxybenzophenone (trade name: Biosorb 110, manufactured by Kyodo Yakuhin Co., Ltd.).
【0021】その他、本発明の防虫剤は、各種植物精油
等の天然系害虫忌避剤、例えばアーモンド油、シダーウ
ッド油、ジンジャー油、シンナモン油、セロリー油、ス
ペアミント油、ヒノキ油、ヒバ油、ペリーラ油、ライム
油、シトロネラ油、ハッカ油、ユーカリ油、ペパーミン
ト油、レモン油、レモングラス油、ワサビ油等や、さら
に香料、共力剤、色素、蓄光物質、消臭剤、脱臭剤、蒸
散性殺菌剤(イソプロピルメチルフェノール、パラクロ
ルメタキシレノール、オルソフェニルフェノール等)、
蒸散性防錆剤、N,N−ジエチル−m−トルアミド(略
称DEET)等の蒸散性合成害虫忌避剤、蒸散性昆虫成
長制御剤、増粘剤例えばモンモリロナイト等の鉱物質の
シリカ等(日本シリカ工業(株)製ラボナイト、コープ
ケミカル(株)製合成スメクタイト等)、粘性低下防止
剤、PH調整剤等も任意に添加できるほか、装飾を目的
とした樹脂小片、金属箔等を添加しても構わない。In addition, the insect repellents of the present invention include natural pest repellents such as various plant essential oils, such as almond oil, cedarwood oil, ginger oil, cinnamon oil, celery oil, spearmint oil, hinoki oil, hiba oil and perilla oil. , Lime oil, citronella oil, peppermint oil, eucalyptus oil, peppermint oil, lemon oil, lemongrass oil, wasabi oil, etc., as well as fragrances, synergists, pigments, luminous substances, deodorants, deodorants, transpiration sterilization Agents (isopropylmethylphenol, parachlorometaxylenol, orthophenylphenol, etc.),
Evaporative rust inhibitor, Evaporative synthetic pest repellent such as N, N-diethyl-m-toluamide (abbreviated as DEET), Evaporative insect growth regulator, Thickener such as mineral silica such as montmorillonite (Nippon Silica) Rabonite manufactured by Kogyo Co., Ltd., synthetic smectite manufactured by Corp Chemical Co., Ltd.), a viscosity lowering inhibitor, a pH adjuster, and the like can be arbitrarily added. I do not care.
【0022】本発明の防虫剤の使用形態としては、微小
通気孔もしくは通気性を有する容器、通気性を有する不
織布、樹脂シート等の袋体などの包納手段に本発明の防
虫剤を充填して用いることにより、防虫剤の有効成分を
蒸散できると同時に、防虫剤自体が直接衣類に触れて汚
染することを防ぐことができる。上記容器の材質として
はガラス、樹脂、陶器等、流動物を保持できるものであ
れば特に問わないが、透明性及び流動物バリヤー性が高
く、しかも軽量で経済性の高い塩化ビニル樹脂、ポリメ
チルペンテン、ポリエチレンテレフタレート、ポリエチ
レン、ポリプロピレン、ポリアクリロニトリル、ポリカ
ーボネート等が好ましい。容器開口部には蒸散速度を調
整したり、転倒時の成分漏出による衣類の汚染、誤飲、
誤食等の事故を防ぐための各種シート、フィルム、蓋体
等を組合せることができる。また、このような容器、袋
体及びその外装フィルム等は、店頭陳列等における品質
劣化の原因となる紫外線を遮断するため、先に例示した
様な紫外線吸収剤或いは顔料等を混練して製造すること
もできる。The insect repellent of the present invention may be used in a form such as a container having fine air holes or air permeability, a nonwoven fabric having air permeability, or a bag such as a resin sheet. By using it, the active ingredient of the insect repellent can be evaporated, and at the same time, the insect repellent itself can be prevented from directly touching and contaminating clothing. The material of the container is not particularly limited as long as it can hold a fluid such as glass, resin, and pottery. However, the transparency and the barrier property of the fluid are high, and the lightweight and economical vinyl chloride resin and polymethyl resin are used. Pentene, polyethylene terephthalate, polyethylene, polypropylene, polyacrylonitrile, polycarbonate and the like are preferred. Adjust the evaporation rate at the opening of the container.
Various sheets, films, lids, and the like for preventing accidents such as accidental eating can be combined. Further, such a container, a bag and its outer film are manufactured by kneading an ultraviolet absorber or a pigment as exemplified above in order to block ultraviolet rays which cause quality deterioration in store display or the like. You can also.
【0023】また、使用者の都合、使用場所等によって
は、さらに強い殺虫効力、或いはより早い効力発現が望
まれる場合がある。そのような場合、上記包納手段に、
さらに吸液芯、含浸揮散体、揮散補助部材、有効揮散面
積可変装置、加熱装置、送風装置、超音波振動子等を組
み合わせることも有効である。また、設置を容易にする
ための各種吊り下げ具、固定具、粘着剤等を組み合わせ
ることができる。本発明の防虫剤は、衣類が収納されて
いるタンス等に使用して衣料害虫に対して好適に防殺虫
効力を発揮するが、食料庫、床下、流しの下、食器棚、
本棚等に設置することによって、衣料害虫以外のチャタ
テムシ、シバンムシ等の不快害虫、コクヌストモドキ、
コクゾウムシ等の貯穀害虫、ゴキブリ等の衛生害虫、シ
ミ等の書籍害虫等を対象として応用することもできる。Further, depending on the convenience of the user, the place of use, etc., there may be a case where a stronger insecticidal effect or a faster onset of the effect is desired. In such a case,
It is also effective to combine a liquid absorbing core, an impregnated volatilizer, a volatilization auxiliary member, an effective volatilization area variable device, a heating device, a blower, an ultrasonic vibrator, and the like. Further, various hanging tools, fixing tools, adhesives, and the like for facilitating installation can be combined. The insect repellent of the present invention is preferably used in a closet or the like in which clothes are stored and exerts a suitable insecticidal effect on clothing pests, but food storage, under the floor, under the sink, cupboards,
By installing it on a bookshelf, etc., non-clothing pests such as caterpillars, unpleasant pests such as shibanmushi, kokunustomodoki,
The present invention can also be applied to storage pests such as weevil, hygiene pests such as cockroaches, and book pests such as spots.
【0024】[0024]
【実施例】以下、実施例を示して本発明についてさらに
具体的に説明するが、本発明が下記実施例に限定される
ものでないことはもとよりである。EXAMPLES Hereinafter, the present invention will be described more specifically with reference to examples, but it is needless to say that the present invention is not limited to the following examples.
【0025】製剤例1〜11 下記表1に示す組合せで、蒸散性殺虫剤、安定剤(界面
活性剤、有機溶剤)、その他の成分(酸化防止剤、防腐
剤)の順に秤量し、これらを充分に攪拌混合したのち、
水を加えて均一にし、さらに吸水性高分子を混合して澄
明な半固体を得た。但し、製剤例10及び11に関して
は、各成分を加熱しながら攪拌混合した後、放冷を行っ
た。Formulation Examples 1 to 11 In the combinations shown in Table 1 below, transpirable insecticides, stabilizers (surfactants, organic solvents), and other components (antioxidants, preservatives) are weighed in this order, and these are weighed. After mixing thoroughly,
Water was added to make the mixture uniform, and a water-absorbing polymer was mixed to obtain a clear semi-solid. However, with respect to Formulation Examples 10 and 11, each component was stirred and mixed while being heated, and then allowed to cool.
【表1】 [Table 1]
【0026】比較製剤例1〜4 比較として、下記表2に示す組合せで前記製剤例1〜1
1と同様にして比較製剤1〜4を得た。但し、比較製剤
例3及び4に関しては、前記製剤例10及び11と同
様、各成分を加熱しながら攪拌混合した後、放冷した。Comparative Formulation Examples 1 to 4 For comparison, the formulation examples 1 to 1 were used in combinations shown in Table 2 below.
In the same manner as in Example 1, Comparative Preparations 1 to 4 were obtained. However, in Comparative Formulation Examples 3 and 4, similarly to Formulation Examples 10 and 11, each component was stirred and mixed while heating, and then allowed to cool.
【表2】 [Table 2]
【0027】試験方法:前記のように調製した製剤例1
〜11及び比較製剤例1〜4に関して効力、安定性、イ
ンジケーター機能を調べた。尚、評価方法はそれぞれ以
下のように行った。 効力:約500リットル(幅90cm×高さ110cm
×奥行50cm)の空間に防虫剤及び衣料2kgを設置
した。設置直後及び以後1カ月毎に代表的衣料害虫であ
るイガ及びヒメカツオブシムシをシャーレに入れて空間
内に配置した。シャーレを3日後に回収し、衣料害虫の
状態を観察した。 ○:衣料害虫が3〜9カ月に亘り全数ノックダウンして
いた。 △:設置直後のみノックダウンが見られたが、以降は衣
料害虫に変化が見られなかった。 ×:衣料害虫に全く変化が見られなかった。Test method: Formulation example 1 prepared as described above
The efficacy, stability, and indicator function were examined for Nos. ~ 11 and Comparative Formulation Examples 1-4. In addition, each evaluation method was performed as follows. Efficacy: about 500 liters (90 cm wide x 110 cm high)
× 50 cm in depth) was provided with an insect repellent and 2 kg of clothing. Immediately after the installation and every month thereafter, typical clothing pests such as iga and maggot were placed in a petri dish and placed in the space. The petri dish was collected 3 days later, and the state of the clothing pest was observed. :: All the insect pests were knocked down for 3 to 9 months. Δ: Knockdown was observed only immediately after installation, but no change was observed in clothing pests thereafter. ×: No change was observed in the clothing pests.
【0028】安定性:防虫剤を40℃に暗所に密閉保存
し、6カ月後の殺虫剤残存率を分析した。 ○:90%以上残存 △:60〜90%残存 ×:残存率60%未満Stability: The insecticide was stored tightly closed at 40 ° C. in a dark place, and the residual rate of the insecticide after 6 months was analyzed. :: 90% or more remaining △: 60 to 90% remaining ×: Residual rate less than 60%
【0029】インジケーター機能:3〜9カ月に亘り殺
虫剤の揮散に合わせて防虫剤全体が減量したかどうかで
評価した。 ○:殺虫剤と防虫剤全体の減量割合がほぼ一致。 ×:殺虫剤と防虫剤全体の減量割合が全く一致せず。Indicator function: Evaluation was made as to whether or not the whole insect repellent was reduced in weight according to the volatilization of the insecticide over 3 to 9 months. :: The weight loss ratio of the insecticide and the whole insect repellent was almost the same. X: The weight loss ratio of the insecticide and the whole insect repellent does not match at all.
【0030】総合評価:以上3項目にさらに安全性、臭
気性を加味して衣料用防虫剤として適当かどうか評価し
た。 ○:衣料用防虫剤に適している。 ×:衣料用防虫剤として不適。Overall evaluation: In addition to the above three items, safety and odor were further taken into consideration to determine whether or not the composition was suitable as an insect repellent for clothing. :: Suitable for insect repellent for clothing. ×: Not suitable as an insect repellent for clothing.
【0031】以上の評価方法に基づいて行った試験結果
を下記表3に示す。Table 3 below shows the test results based on the above evaluation methods.
【表3】 上記表3に示される結果から明らかなように、本発明に
従って調製された製剤例1〜11は上記全ての評価項目
について良好な結果を示したが、比較製剤例1〜4は、
効力、安定性、インジケーター機能のいずれかに問題が
あり、衣料用防虫剤として満足いくものは得られなかっ
た。[Table 3] As is clear from the results shown in Table 3 above, Formulation Examples 1 to 11 prepared according to the present invention showed good results for all the evaluation items described above, whereas Comparative Formulation Examples 1 to 4
There were problems with any of the efficacy, stability, and indicator function, and no satisfactory insect repellent for clothing was obtained.
【0032】比較試験例1 有機溶剤の配合量の変化による影響を調べるため、下記
表4に示す組合せで前記製剤例1〜11と同様にして防
虫剤を得た。なお、例No.1は前記製剤例6と同じで
ある。Comparative Test Example 1 Insect repellents were obtained in the same manner as in Formulation Examples 1 to 11 by using the combinations shown in Table 4 below in order to examine the influence of changes in the amount of the organic solvent. In addition, Example No. 1 is the same as in Formulation Example 6.
【表4】 [Table 4]
【0033】得られた各防虫剤について、前記試験方法
と同様にして効力、安定性、インジケーター機能を調べ
た。その結果を表5に示す。Each of the obtained insect repellents was examined for efficacy, stability and indicator function in the same manner as in the above test method. Table 5 shows the results.
【表5】 表5に示す結果から、有機溶剤を多量に配合した場合
(例No.2〜4)、インジケーター機能に問題を生ず
ることがわかる。[Table 5] From the results shown in Table 5, it can be seen that a large amount of the organic solvent (Example Nos. 2 to 4) causes a problem in the indicator function.
【0034】[0034]
【発明の効果】以上のように、本発明の防虫剤は、水系
組成物であるにも拘らず有効成分としての常温蒸散性ピ
レスロイド系殺虫剤を安定して含有しており、長期に亘
り徐放的に上記有効成分を蒸散して優れた防殺虫効力を
発揮すると共に、有効成分の減少と共に防虫剤全体の重
量及び体積が減少するため、有効成分の残存量及び終点
を容易かつ明瞭に認知することができる。また、水系組
成物であるため、ほぼ無臭に近く、樹脂や繊維類に対す
る侵蝕性も殆どなく、しかも製造中及び使用中に引火等
の危険性もないので安全性にも優れている。さらに、防
虫剤は半固体状なので従来の液状タイプの防虫剤に起こ
り得る液状薬剤の漏出による衣類の汚染等の心配は無
く、取扱い性にも優れている。As described above, the insect repellent of the present invention stably contains a normal temperature transpirable pyrethroid-based insecticide as an active ingredient despite being an aqueous composition, The above-mentioned active ingredient is evaporatively released to exhibit excellent insecticidal effect, and the weight and volume of the whole insect repellent decrease with the decrease of the active ingredient, so that the remaining amount and end point of the active ingredient can be easily and clearly recognized. can do. Further, since it is a water-based composition, it is almost odorless, has almost no corrosiveness to resins and fibers, and has excellent safety because there is no danger of inflammation during production and use. Further, since the insect repellent is semi-solid, there is no fear of contamination of clothing due to leakage of the liquid medicine which may occur in the conventional liquid type insect repellent, and the handleability is excellent.
Claims (6)
℃)の範囲内にある常温蒸散性ピレスロイド系殺虫剤、
吸水性高分子、水及び安定剤を含有することを特徴とす
る防虫剤。A vapor pressure of 10 -4 to 10 -1 mmHg (20
C) in the range of room temperature transpirable pyrethroid insecticides,
An insect repellent comprising a water-absorbing polymer, water and a stabilizer.
(R,S)−1−エチニル−2−メチルペント−2−エ
ニル(1R)−シス、トランスクリサンテマート及び/
又は3−アリル−2−メチルシクロペント−2−エン−
4−オン−1−イル−2,2,3,3−テトラメチルシ
クロプロパンカルボキシレートであることを特徴とする
請求項1に記載の防虫剤。2. The cold-vaporizable pyrethroid insecticide according to claim 1, wherein the (R, S) -1-ethynyl-2-methylpent-2-enyl (1R) -cis, transchrysanthemate and / or
Or 3-allyl-2-methylcyclopent-2-ene-
The insect repellent according to claim 1, which is 4-one-1-yl-2,2,3,3-tetramethylcyclopropanecarboxylate.
溶剤からなることを特徴とする請求項1又は2に記載の
防虫剤。3. The insect repellent according to claim 1, wherein the stabilizer comprises a surfactant and / or an organic solvent.
2 mmHg(20℃)の範囲内にあり、且つ水に対する
溶解度が10重量%(20℃)以上のアルコール類、グ
リコール類、エーテル類、エステル類及びケトン類から
なる群より選ばれる1種又は2種以上の有機溶剤である
ことを特徴とする請求項3に記載の防虫剤。4. The organic solvent has a vapor pressure of 10 −2 to 10
One or more selected from the group consisting of alcohols, glycols, ethers, esters and ketones having a water solubility within a range of 2 mmHg (20 ° C.) and 10% by weight (20 ° C.) or more in water. The insect repellent according to claim 3, which is at least one kind of organic solvent.
非イオン系界面活性剤又は該非イオン系界面活性剤を含
む混合界面活性剤であることを特徴とする請求項3に記
載の防虫剤。5. The insect repellent according to claim 3, wherein the surfactant is a nonionic surfactant having an HLB value of 9 to 18 or a mixed surfactant containing the nonionic surfactant. Agent.
おいて自重の10〜1,000倍の吸水能力を有するこ
とを特徴とする請求項1乃至5のいずれか一項に記載の
防虫剤。6. The insect repellent according to claim 1, wherein the water-absorbing polymer has a water-absorbing ability at room temperature (20 ° C.) 10 to 1,000 times its own weight. Agent.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP35634696A JP3916716B2 (en) | 1996-12-26 | 1996-12-26 | Insect repellent |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP35634696A JP3916716B2 (en) | 1996-12-26 | 1996-12-26 | Insect repellent |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH10182304A true JPH10182304A (en) | 1998-07-07 |
JP3916716B2 JP3916716B2 (en) | 2007-05-23 |
Family
ID=18448571
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP35634696A Expired - Lifetime JP3916716B2 (en) | 1996-12-26 | 1996-12-26 | Insect repellent |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3916716B2 (en) |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2001078508A1 (en) * | 2000-04-13 | 2001-10-25 | Fumakilla Limited | Method for controlling insect pests by vaporization of pesticides |
JP2003063905A (en) * | 2001-08-29 | 2003-03-05 | Toppan Forms Co Ltd | Insect repellent composition containing microparticle of superabsorbent polymer carrying insect repellent and manufacturing method thereof |
JP2004204111A (en) * | 2002-12-26 | 2004-07-22 | Earth Chem Corp Ltd | Film forming composition |
JP2005097294A (en) * | 2003-09-01 | 2005-04-14 | Earth Chem Corp Ltd | Fiber insect pest repellent, fiber insect pest egg ovicide, fiber insect pest insecticide and antifungal agent |
JP2007082553A (en) * | 2002-10-09 | 2007-04-05 | Earth Chem Corp Ltd | Method for spraying water-soluble insecticide, aerosol spraying device and insecticidal liquid |
JPWO2006013972A1 (en) * | 2004-08-06 | 2008-05-01 | 日本曹達株式会社 | Elution controlled pesticide formulation |
JP2010503638A (en) * | 2006-09-14 | 2010-02-04 | ビーエーエスエフ ソシエタス・ヨーロピア | Insecticide composition |
CN104621101A (en) * | 2013-11-13 | 2015-05-20 | 大日本除虫菊株式会社 | Anti-insect agent for clothes |
JP2016040307A (en) * | 2015-10-30 | 2016-03-24 | スティッチング グロニンゲン セントル フォー ドラッグ リサーチ | Ph-controlled pulsatile delivery system, methods for preparation and use thereof |
-
1996
- 1996-12-26 JP JP35634696A patent/JP3916716B2/en not_active Expired - Lifetime
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2001078508A1 (en) * | 2000-04-13 | 2001-10-25 | Fumakilla Limited | Method for controlling insect pests by vaporization of pesticides |
JP2003063905A (en) * | 2001-08-29 | 2003-03-05 | Toppan Forms Co Ltd | Insect repellent composition containing microparticle of superabsorbent polymer carrying insect repellent and manufacturing method thereof |
JP2007082553A (en) * | 2002-10-09 | 2007-04-05 | Earth Chem Corp Ltd | Method for spraying water-soluble insecticide, aerosol spraying device and insecticidal liquid |
JP2004204111A (en) * | 2002-12-26 | 2004-07-22 | Earth Chem Corp Ltd | Film forming composition |
JP2005097294A (en) * | 2003-09-01 | 2005-04-14 | Earth Chem Corp Ltd | Fiber insect pest repellent, fiber insect pest egg ovicide, fiber insect pest insecticide and antifungal agent |
JPWO2006013972A1 (en) * | 2004-08-06 | 2008-05-01 | 日本曹達株式会社 | Elution controlled pesticide formulation |
JP2011001371A (en) * | 2004-08-06 | 2011-01-06 | Nippon Soda Co Ltd | Agrochemical preparation controlled in elution |
JP4625811B2 (en) * | 2004-08-06 | 2011-02-02 | 日本曹達株式会社 | Elution controlled pesticide formulation |
JP2010503638A (en) * | 2006-09-14 | 2010-02-04 | ビーエーエスエフ ソシエタス・ヨーロピア | Insecticide composition |
CN104621101A (en) * | 2013-11-13 | 2015-05-20 | 大日本除虫菊株式会社 | Anti-insect agent for clothes |
JP2016040307A (en) * | 2015-10-30 | 2016-03-24 | スティッチング グロニンゲン セントル フォー ドラッグ リサーチ | Ph-controlled pulsatile delivery system, methods for preparation and use thereof |
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