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JPS5839603A - Repellent for wool vermin - Google Patents

Repellent for wool vermin

Info

Publication number
JPS5839603A
JPS5839603A JP13937081A JP13937081A JPS5839603A JP S5839603 A JPS5839603 A JP S5839603A JP 13937081 A JP13937081 A JP 13937081A JP 13937081 A JP13937081 A JP 13937081A JP S5839603 A JPS5839603 A JP S5839603A
Authority
JP
Japan
Prior art keywords
repellent
wool
fatty acid
vermin
boiling point
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP13937081A
Other languages
Japanese (ja)
Other versions
JPS6059881B2 (en
Inventor
Teiichi Aikawa
相川 禎一
Yasuko Tsujii
辻井 康子
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.)
National Institute of Advanced Industrial Science and Technology AIST
Original Assignee
Agency of Industrial Science and Technology
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 Agency of Industrial Science and Technology filed Critical Agency of Industrial Science and Technology
Priority to JP13937081A priority Critical patent/JPS6059881B2/en
Publication of JPS5839603A publication Critical patent/JPS5839603A/en
Publication of JPS6059881B2 publication Critical patent/JPS6059881B2/en
Expired legal-status Critical Current

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  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

PURPOSE:To provide a wool vermin repellent having excellent mothproofing effect, long durability of the effect, and high safety, at a low cost, by using a 10-11C fatty acid linear ester having a specific boiling point range such as n-actyl acetate, as an active component. CONSTITUTION:The objective wool vermin repellent can be obtained by using a 10-11C fatty acid linear ester having a boiling point of 200-230 deg.C under normal pressure (e.g. n-amyl valerate, n-decyl formate, n-nonyl acetate, etc.) as an active component. The repellent has ingestion-inhibiting activity, repelling activity and insecticidal activity to wool vermin such as clothes moth, KOIGA (Tineola bisselliela), varied carpet beetle, etc.

Description

【発明の詳細な説明】 本発明は、羊毛害虫用忌避剤に関するものであり、さら
に詳しくいえば、羊毛害虫であるイガ、コイガ、ヒメマ
ルカツオブシムシ、ヒメカツオプシムシなどに対して、
摂食阻害作用、忌避作用、殺虫作用などの活性を有する
脂肪族鎖状エステルを有効成分とする忌避剤に関するも
のである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a repellent for wool pests, and more specifically, it is a repellent for wool pests such as burr, carp moth, Japanese carp beetle, and Japanese carp beetle.
The present invention relates to a repellent containing an aliphatic chain ester as an active ingredient, which has anti-feeding, repellent, and insecticidal activities.

従来、衣類用害虫忌避剤としてはナフタリン、ショウノ
ウ、バラジクロロベンゼンなどが用いられており、なか
でも殺虫効果が強く安価であるという点で、バラジクロ
ロベンゼンが最も広く用いられている。
Conventionally, naphthalene, camphor, baladichlorobenzene, and the like have been used as insect repellents for clothing, and among them, baladichlorobenzene is the most widely used because it has a strong insecticidal effect and is inexpensive.

しかしながら、バラジクロロベンゼンは有機塩素系薬剤
の1種であって、生物体内に蓄積し害を与えるおそれが
あるため、その使用については規制される方向にあり、
すでに、繊維加工の防虫処理剤である有機塩素系薬剤の
アルドリン、デルドリンは、その使用が禁止されている
However, as Balajichlorobenzene is a type of organic chlorine drug and may accumulate in living organisms and cause harm, its use is becoming regulated.
The use of organic chlorine agents aldrin and deldrin, which are used as insect repellents for textile processing, is already prohibited.

したがって、近年バラジクロロベンゼンに代るべき防虫
剤あるいは忌避剤として多くの化合物又 、5゜はその
組合わせが提案されている。例えば、トリイソプロピル
−e−)リオキサン又はトリ第三う゛チルーS −)リ
オキサンとりナロール、アネトール、メントール、ケイ
皮アルデヒド、チモール、オイゲノール又はこれらの誘
導体との組合わせを有効成分とした羊毛用防虫剤(特開
昭50−24436号公報)、エーテル結合を有する炭
素数10個の環式化合物を有効成分とする防虫剤(特開
昭52−110823号公報)、アダマンタン、昇華性
炭化水素、及び昇華性又は揮発性を有する極性化合物を
配合して成る昇華性防虫剤(%開昭5.3−12193
6号公報)、ナフタリンとチモールとの組合わせを有効
成分とする防虫剤(特開昭53−109938号公報)
、ナフタリンと2−イソプロピル−5−メチルフェノー
ルとの組合わせを有効成分とする衣料用防虫剤(特開昭
54−32620号公報)、アセトキシムを主成分とす
る衣料用防虫剤(特開昭54−101425号公報)、
α−位に分枝を有する炭素鎖などの置換基をもった芳香
族化合物を活性成分として含有している防虫剤(特開昭
54−110321号公報)、を−カルボンを有効成分
とする芳香性防虫−(特開昭55−19229号公報)
などが提案されている。
Therefore, in recent years, many compounds or combinations thereof have been proposed as insect repellents or repellents to replace Baladichlorobenzene. For example, an insect repellent for wool containing as an active ingredient a combination of triisopropyl-e-)lioxane or tri-tertiary-s-)lioxane and naol, anethole, menthol, cinnamaldehyde, thymol, eugenol, or a derivative thereof. (Japanese Patent Application Laid-open No. 50-24436), an insect repellent containing a cyclic compound having 10 carbon atoms and an ether bond as an active ingredient (Japanese Patent Application Laid-Open No. 110823/1982), adamantane, sublimable hydrocarbon, and sublimation Sublimation insect repellent (% 1975-12193
6), an insect repellent containing a combination of naphthalene and thymol as active ingredients (Japanese Unexamined Patent Publication No. 109938/1982)
, an insect repellent for clothing containing a combination of naphthalene and 2-isopropyl-5-methylphenol as an active ingredient (JP-A-54-32620), an insect repellent for clothing containing acetoxime as a main ingredient (JP-A-54-1988) -101425 Publication),
An insect repellent containing as an active ingredient an aromatic compound having a substituent such as a carbon chain having a branch at the α-position (Japanese Unexamined Patent Publication No. 110321/1989), an aromatic compound containing -carvone as an active ingredient. Sexual insect repellent (Japanese Unexamined Patent Publication No. 19229/1983)
etc. have been proposed.

しかしながら、これらの防虫剤はいずれもバラジクロロ
ベンゼンに比べると高価であるとか、その防虫効果が著
しく劣るとか、あるいは揮発性が大きいため持続性が乏
しいとか、または経時変化が著しいなどの欠点を有し、
実用上十分満足しうるものとはいえない。
However, all of these insect repellents have disadvantages, such as being more expensive than Balajichlorobenzene, having significantly lower insect repellent effects, being highly volatile and having poor sustainability, and changing significantly over time. death,
This cannot be said to be fully satisfactory in practical terms.

本発明者らは、このような事情に鑑み、安価で、防虫効
果に優れかつその効果の持続性が長く、その上安全性の
高い実用的な防虫剤を開発すべく鋭意研究を重ねた結果
、ある沸点範囲を有する炭素数10又は11の脂肪酸鎖
状エステルを有効成分として用いることによシ、その目
的を達成しうろことを見出し、この知見に基づいて本発
明を完成するに至った。
In view of these circumstances, the present inventors have conducted intensive research to develop a practical insect repellent that is inexpensive, has excellent insect repellent effects, has a long-lasting effect, and is highly safe. The inventors have discovered that the object can be achieved by using a fatty acid chain ester having 10 or 11 carbon atoms having a certain boiling point range as an active ingredient, and based on this knowledge, the present invention has been completed.

すなわち、本発明は、全炭素数が10又は11で、かつ
常圧下における沸点が200〜230℃の範囲にある脂
肪酸鎖状エステルlの中から選ばれた少なくとも1種を
有効成分として含有することを特徴とする羊毛害虫用忌
避剤を提供するものである。
That is, the present invention contains as an active ingredient at least one fatty acid chain ester l having a total carbon number of 10 or 11 and a boiling point in the range of 200 to 230°C under normal pressure. The present invention provides a wool pest repellent characterized by the following.

本発明の忌避剤に用いる脂肪酸鎖状エステルは、全炭素
数が10又は11で、かつ常圧下における沸点が200
〜2−30℃の範囲であることが必要である。沸点が2
00℃未満のエステルでは、その揮発性が大きくて防虫
効果の持続性に乏しく、たえず薬剤を補充せねばならず
実用的でない。また230℃を超えるエステルでは、そ
の蒸気圧が低すぎて期待する防虫効果が得られない。
The fatty acid chain ester used in the repellent of the present invention has a total number of carbon atoms of 10 or 11 and a boiling point of 200 at normal pressure.
It is necessary that the temperature is in the range of ~2-30°C. boiling point is 2
Esters at temperatures below 00° C. are highly volatile and have poor lasting insect repellent effects, requiring constant replenishment of chemicals, which is impractical. Furthermore, if the temperature of the ester exceeds 230°C, its vapor pressure will be too low and the expected insect repellent effect will not be obtained.

この脂肪酸鎖状エステルは、例えば炭素数1〜10の脂
肪族モノカルボン酸と炭素数1〜10の脂肪族1価アル
コールの中からそれぞれカルボン酸とアルコールを選び
、全炭素数が10又は11になるようにカルボン酸とア
ルコールを組合わせ、常法に従いエステル化を行うこと
によって得ることができる。
This fatty acid chain ester is prepared by selecting a carboxylic acid and an alcohol from aliphatic monocarboxylic acids having 1 to 10 carbon atoms and aliphatic monohydric alcohols having 1 to 10 carbon atoms, respectively, and reducing the total number of carbon atoms to 10 or 11. It can be obtained by combining a carboxylic acid and an alcohol and esterifying them according to a conventional method.

炭素数1〜10の脂肪族モノカルボン酸として、直鎖又
は側鎖の飽和脂肪酸や不飽和脂肪酸が用いられるが、好
ましい脂肪酸としては、ギ酸、酢酸、吉草酸、イソ吉草
酸、エナン゛ト酸、カプリル酸、ペラルゴン酸及びカプ
リン酸のような飽和脂肪酸、チグリン酸及びアンゲリカ
酸のような不飽和脂肪酸が挙げられる。
As the aliphatic monocarboxylic acid having 1 to 10 carbon atoms, linear or side chain saturated fatty acids and unsaturated fatty acids are used, and preferred fatty acids include formic acid, acetic acid, valeric acid, isovaleric acid, and enanthoic acid. , saturated fatty acids such as caprylic acid, pelargonic acid and capric acid, and unsaturated fatty acids such as tiglic acid and angelic acid.

また、炭素数1〜10の脂肪族−価アルコールとして、
直鎖又は側鎖の飽和アルコールや不飽和アルコールが用
いられるが、好ましいアルコールトシテハ、メチルアル
コール、エチルアルコール、n−ブチルアルコール、n
−アミルアルコール、イソアミルアルコール、n−ヘキ
シルアルコール、n −オクチルアルコール、n−ノニ
ルアルコール及びn−デシルアルコールのような飽和ア
ルコール、アリルアルコールのような不飽和アルコール
が挙けられる。
In addition, as an aliphatic alcohol having 1 to 10 carbon atoms,
Straight-chain or side-chain saturated alcohols and unsaturated alcohols are used, and preferred alcohols include methyl alcohol, ethyl alcohol, n-butyl alcohol, and n-butyl alcohol.
- Saturated alcohols such as amyl alcohol, isoamyl alcohol, n-hexyl alcohol, n-octyl alcohol, n-nonyl alcohol and n-decyl alcohol, and unsaturated alcohols such as allyl alcohol.

本発明で用いられる脂肪酸鎖状エステルとしては酢酸n
−オクチル、吉草酸n−アミル、チグリン酸イソアミル
、アンゲリカ蚕イソアミル、・エナント酸アリル、カプ
リル酸エチル、ペラルゴン酸メチル、ギ酸n−デシル、
酢酸n−ノニル、イソ吉草酸n−ヘキシル、エナント酸
n−ブチル、カプリル酸アリル、ペラルゴン酸エチル及
びカプリン酸メチルなどである。
The fatty acid chain ester used in the present invention is acetic acid n
-octyl, n-amyl valerate, isoamyl tiglate, isoamyl angelica silkworm, allyl enanthate, ethyl caprylate, methyl pelargonate, n-decyl formate,
These include n-nonyl acetate, n-hexyl isovalerate, n-butyl enanthate, allyl caprylate, ethyl pelargonate, and methyl caprate.

本発明の忌避剤においては、前記エステル類を単独で用
いてもよいし、また2種以上混合して用いてもよい。さ
らに、所望に応じて香料などの添加剤を配合することも
できる。
In the repellent of the present invention, the above esters may be used alone or in combination of two or more. Furthermore, additives such as fragrances can be added as desired.

本発明の忌避剤は、そのまま適当な容器に封入して用い
てもよいし、またシリカゲル、タルク、布、紙などの支
持体に担持させて使用するこζもできる。
The repellent of the present invention may be used as is by being sealed in a suitable container, or may be supported on a support such as silica gel, talc, cloth, or paper.

本発明の忌避剤は安価であシ、防虫効果に優れかつその
効果の持続性もよく、その上安全性の高い実用的な一羊
毛害虫忌避剤であって、イガ、コイガ、ジュウタンガ、
ヒメカツ牙ブシムシ、ヒメマルカツオプシムシなどの羊
毛害虫の駆除に有効である。
The repellent of the present invention is inexpensive, has an excellent insect repellent effect, has a long-lasting effect, and is a highly safe and practical repellent for insects.
It is effective in exterminating woolly pests such as the Japanese bush beetle and the common Japanese bush beetle.

次に実施例によって本発明をさらに詳細に説明するO 実施例 容量500−のびんの底に、沸点200〜230℃、全
炭素数10又は11の脂肪酸鎖状エステル類50■を入
れ、その5cIn上方に30日令、平均体重30〜35
■/1,0頭のイガ幼虫10頭と羊毛標準試験布(2c
ynX2副、40〜45■)を入れたかごを固定した・
次にびんを密閉し、30℃、湿度65チの恒温恒湿室内
に7日間放置したのち、羊毛布を取シ出して食害量を測
定し、虫の死亡数を数えた。生存している虫はさらに自
然状態で1日放置し、再び死亡数を数え死亡率を求めた
Next, the present invention will be explained in more detail with reference to examples.OExample: 50 μm of a fatty acid chain ester having a boiling point of 200 to 230°C and a total number of carbon atoms of 10 or 11 is placed in the bottom of a 500-volume bottle, and the 5 cIn. Upper 30 days old, average weight 30-35
■/10 burr larvae and wool standard test cloth (2c
ynX2 vice, 40~45■) was fixed in the basket
Next, the bottle was sealed and left in a constant temperature and humidity chamber at 30° C. and humidity of 65° C. for 7 days, after which the wool was removed, the amount of feeding damage was measured, and the number of dead insects was counted. The surviving insects were left in their natural state for another day, and the number of dead insects was counted again to determine the mortality rate.

結果をエステルの沸点とともに゛第1表に示す。The results are shown in Table 1 along with the boiling point of the ester.

なお、表中の値は試験を5〜9回行って得られた平均値
である。また、食害率はブランクテストとして薬剤を用
いずに試験した布の食害量に対する百分率で表わす。死
亡率は7日間放置後、・さらに自然状態で1日放置した
のちの値である。
Note that the values in the table are average values obtained by conducting the test 5 to 9 times. Moreover, the feeding damage rate is expressed as a percentage of the amount of feeding damage on the fabric tested as a blank test without using any chemicals. The mortality rate is the value after being left for 7 days and after being left in a natural state for 1 day.

比較例 実施例における沸点200〜230℃で全炭素数10類
(1)、全炭素数11.12のテルペンエステル類(至
)、全炭素数12の脂肪酸鎖状エステル(I[)及び全
炭素数9〜11の芳香族エステル類(財)を用いる以外
は、実施例と全く同様にして試験を行った。その結果を
エステルの沸点とともに第2表に示す〇なお、食害率、
死亡率は実施例と同様の方法によシ求めたものである。
Comparative Examples Examples with a boiling point of 200 to 230°C, total carbon number of 10 classes (1), total carbon number of 11.12 terpene esters (total), total carbon number of 12 fatty acid chain esters (I[) and total carbon number The test was conducted in exactly the same manner as in the example except that aromatic esters numbered 9 to 11 were used. The results are shown in Table 2 along with the boiling point of the ester. In addition, the feeding damage rate,
The mortality rate was determined by the same method as in the examples.

Claims (1)

【特許請求の範囲】 1 全炭素数が10又は11で、かつ常圧下における沸
点が200〜230℃の範囲にちる脂肪酸鎖状エステル
の中から選ばれた少なくとも1種を有効成分として成る
羊毛害虫用忌避剤。 2 脂肪酸鎖状エステルが、酢酸n−オクチル、吉草酸
n−アミル、チグリン酸イソアミル、アンゲリカ酸イソ
アミル、エナント酸アリル、カプリル酸エチル及びペラ
ルゴン酸メチルである特許請求の範囲第1項記載の方法
。 3 脂肪酸鎖状エステルが、ギ酸n−デシル、酢酸n−
ノニル、イソ吉草酸n−ヘキシル、エナント酸n−ブチ
ル、カプリル酸アリル、ペラルゴン酸エチル及びカプリ
ン酸メチルである特許請求の範囲第1項記載の方法。
[Scope of Claims] 1. A wool pest comprising as an active ingredient at least one fatty acid chain ester having a total carbon number of 10 or 11 and a boiling point in the range of 200 to 230°C under normal pressure. repellent. 2. The method according to claim 1, wherein the fatty acid chain ester is n-octyl acetate, n-amyl valerate, isoamyl tiglate, isoamyl angelate, allyl enanthate, ethyl caprylate, and methyl pelargonate. 3 Fatty acid chain ester is n-decyl formate, n-acetate
2. The method according to claim 1, wherein the organic acids are nonyl, n-hexyl isovalerate, n-butyl enanthate, allyl caprylate, ethyl pelargonate and methyl caprate.
JP13937081A 1981-09-03 1981-09-03 Wool pest repellent Expired JPS6059881B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13937081A JPS6059881B2 (en) 1981-09-03 1981-09-03 Wool pest repellent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13937081A JPS6059881B2 (en) 1981-09-03 1981-09-03 Wool pest repellent

Publications (2)

Publication Number Publication Date
JPS5839603A true JPS5839603A (en) 1983-03-08
JPS6059881B2 JPS6059881B2 (en) 1985-12-27

Family

ID=15243740

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13937081A Expired JPS6059881B2 (en) 1981-09-03 1981-09-03 Wool pest repellent

Country Status (1)

Country Link
JP (1) JPS6059881B2 (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4206090A1 (en) * 1992-02-27 1993-09-02 Perycut Chemie Ag INSECT REPELLENT
WO1997041728A1 (en) * 1996-05-06 1997-11-13 Bayer Aktiengesellschaft Arthropod repellant
JPH10287507A (en) * 1997-04-14 1998-10-27 S T Chem Co Ltd Hatching inhibitor of fiber pest egg and insect control
JP2005350411A (en) * 2004-06-11 2005-12-22 Dainippon Jochugiku Co Ltd Flying insect pest repellent
CN100361575C (en) * 2005-12-06 2008-01-16 西北大学 Plant growth regulator and it preparing method
JP2011236136A (en) * 2010-05-07 2011-11-24 Dainippon Jochugiku Co Ltd Agent for preventing vermin damage by clothes moth
JP2011246364A (en) * 2010-05-25 2011-12-08 Dainippon Jochugiku Co Ltd Clothes pest egg hatching inhibitor and pest controlling method using the same
JP2013177342A (en) * 2012-02-28 2013-09-09 Kao Corp Insect-controlling agent

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4206090A1 (en) * 1992-02-27 1993-09-02 Perycut Chemie Ag INSECT REPELLENT
US5589181A (en) * 1992-02-27 1996-12-31 Franz Bencsits Insect repellent
DE4206090C2 (en) * 1992-02-27 1998-02-05 Perycut Chemie Ag Insect repellent
WO1997041728A1 (en) * 1996-05-06 1997-11-13 Bayer Aktiengesellschaft Arthropod repellant
JPH10287507A (en) * 1997-04-14 1998-10-27 S T Chem Co Ltd Hatching inhibitor of fiber pest egg and insect control
JP4311773B2 (en) * 1997-04-14 2009-08-12 エステー株式会社 Fiber insect pest egg hatching inhibitor and insect control method
JP2005350411A (en) * 2004-06-11 2005-12-22 Dainippon Jochugiku Co Ltd Flying insect pest repellent
JP4743825B2 (en) * 2004-06-11 2011-08-10 大日本除蟲菊株式会社 Mosquito, moth, chironomid repellent
CN100361575C (en) * 2005-12-06 2008-01-16 西北大学 Plant growth regulator and it preparing method
JP2011236136A (en) * 2010-05-07 2011-11-24 Dainippon Jochugiku Co Ltd Agent for preventing vermin damage by clothes moth
JP2011246364A (en) * 2010-05-25 2011-12-08 Dainippon Jochugiku Co Ltd Clothes pest egg hatching inhibitor and pest controlling method using the same
JP2013177342A (en) * 2012-02-28 2013-09-09 Kao Corp Insect-controlling agent

Also Published As

Publication number Publication date
JPS6059881B2 (en) 1985-12-27

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