JPS58198403A - Insect repellent composition - Google Patents

Insect repellent composition

Info

Publication number
JPS58198403A
JPS58198403A JP8120682A JP8120682A JPS58198403A JP S58198403 A JPS58198403 A JP S58198403A JP 8120682 A JP8120682 A JP 8120682A JP 8120682 A JP8120682 A JP 8120682A JP S58198403 A JPS58198403 A JP S58198403A
Authority
JP
Japan
Prior art keywords
insect repellent
diethyltoluamide
group
repellent composition
ethanol
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
JP8120682A
Other languages
Japanese (ja)
Other versions
JPH024563B2 (en
Inventor
Shinichi Akimoto
秋本 新一
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.)
NOF Corp
Original Assignee
NOF Corp
Nippon Oil and Fats 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 NOF Corp, Nippon Oil and Fats Co Ltd filed Critical NOF Corp
Priority to JP8120682A priority Critical patent/JPS58198403A/en
Publication of JPS58198403A publication Critical patent/JPS58198403A/en
Publication of JPH024563B2 publication Critical patent/JPH024563B2/ja
Granted legal-status Critical Current

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  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

PURPOSE:An insect repellent composition, prepared by incorporating a specific amount of a specific amine oxide with N,N-diethyltoluamide, and solubilizing the N,N-diethyltoluamide without incorporating ethanol, usable in horses for races, and having a higher lasting effect than the composition containing the ethanol. CONSTITUTION:An insect repellent composition prepared by incorporating (a) 5-25wt% N,N-diethyltoluamide, e.g. N,N-diethyl-m-toluamide, with (b) 4-20wt% compound of the formula (R is 8-22C alkyl or alkenyl; R<1> and R<2> are CH3, C2H5, C2H4OH or C3H6OH; m is 1 or 2; n is 0 or 1) and (c) 50-90wt% water, and preferably further (d) 20wt% or less another surfactant, e.g. a cationic or ampholytic surfactant having the germicidal activity or a nonionic surfactant capable of assisting the solubilization of the component (a). The composition containing no ethanol is usable in horses for races just before the races in which the use of the ethanol is prohibited.

Description

【発明の詳細な説明】 この発明はN、N−ジエチルトルアミドを含む虫よけ剤
組成物に関するものである。
DETAILED DESCRIPTION OF THE INVENTION This invention relates to an insect repellent composition containing N,N-diethyltoluamide.

蚊、あぶ、刺ばえ、ぶよ等の害虫から、人や動物等の□
肌を守る虫よけ剤としてN、N−ジエチルトルアミドが
使用されている。このN、N−ジエチルトルアミドは水
に不溶であるため、20〜50チエタノール水溶液に、
5〜15チの濃度に溶解して使用するのが一般的である
From pests such as mosquitoes, gadflies, biting flies, and gnats, to people and animals, etc.
N,N-diethyltoluamide is used as an insect repellent to protect the skin. Since this N,N-diethyltoluamide is insoluble in water, it is added to a 20-50 diethanol aqueous solution.
It is generally used after being dissolved at a concentration of 5 to 15%.

ところが、このような虫よけ剤組成物は人間に対して使
用する場合はとくに問題はないが、競争馬などのように
、エタノールの使用が禁じられている場合には、レース
直前には使用できないという問題があり、このためレー
ス直前でも使用できる虫よけ剤組成物の開発が渇望され
ていた。
However, although there are no particular problems with such insect repellent compositions when used on humans, in cases where the use of ethanol is prohibited, such as on racehorses, it is recommended that they be used immediately before a race. Therefore, there has been a desire to develop an insect repellent composition that can be used even just before a race.

この発明は、このような要望に応えるためになされたも
ので、特定のアミンオキシドを配合することにより、エ
タノールを使用することなく、N。
This invention was made in response to such a demand, and by blending a specific amine oxide, N can be produced without using ethanol.

N−ジエチルトルアミドを溶解でき、しかも持続効果が
大きい虫よけ剤組成物を提供することを目的としている
The object of the present invention is to provide an insect repellent composition that can dissolve N-diethyltoluamide and has a long-lasting effect.

この発明はN、N−ジエチルトルアミド5〜251 (ただし、Rは炭素数8〜22のアルキル基またはアル
ケニル基 BlおよびWはメチル基、エチル基、ヒドロ
キシエチル基、またはヒドロキシプロピル基、mは1ま
たは2、nは0または1である。) N、N−ジエチルトルアミドとしては、N、 N−ジエ
チル−m−)ルアミドが使用できる。
This invention relates to N,N-diethyltoluamide 5-251 (wherein, R is an alkyl group or alkenyl group having 8 to 22 carbon atoms, Bl and W are methyl group, ethyl group, hydroxyethyl group, or hydroxypropyl group, m is 1 or 2, and n is 0 or 1.) As the N,N-diethyltoluamide, N,N-diethyl-m-)ylamide can be used.

上記一般式(1)において、Rで表わされる炭素数8〜
22のアルキル基またはアルケニル基としてハ、オクチ
ル基、2−エチルヘキシル基、ノニル基、デシル基、ウ
ンデシル基、ラウリル基、トリデシル基、ミリスチル基
、パルミチル基、ステアリル基、イソステアリル基、オ
レイル基、リノール基、ベヘニル基などが例示でき、こ
れらは1種でも数種でもよく、またヤシアルキル基のよ
うに、これらを複数棟含む天然物に起因する基であって
もよい。
In the above general formula (1), the number of carbon atoms represented by R is 8 to
As the alkyl group or alkenyl group of 22, octyl group, 2-ethylhexyl group, nonyl group, decyl group, undecyl group, lauryl group, tridecyl group, myristyl group, palmityl group, stearyl group, isostearyl group, oleyl group, linole Examples thereof include behenyl groups, behenyl groups, etc., and these may be one type or several types, or groups derived from natural products containing a plurality of these groups, such as a coconut alkyl group.

本発明の虫よけ剤は、N、N−ジエチル)/レアミド、
一般式+1)のアミンオキシドおよび水を前記割合で混
合することによって製造される。N、N−ジエチルトル
アミドの配合割合は10〜20重量%が好ましい。上記
の混合の順序は特に限定されず、任意の順序で混合する
ことができるが、N。
The insect repellent of the present invention comprises N,N-diethyl)/reamide,
It is produced by mixing the amine oxide of general formula +1) and water in the above proportions. The blending ratio of N,N-diethyltoluamide is preferably 10 to 20% by weight. The order of the above mixing is not particularly limited and may be mixed in any order.

N−ジエチルトルアミドをアミンオキシド単独で可溶化
する場合は、N、N−ジエチルトルアミド100重を部
をアミンオキシド75〜110重量部で可溶化するのが
望ましい。また混合時の温度も特に限定されないが、N
、N−ジエチルトルアミドが揮発性であるため、60℃
以下で混合するのが望ましい。
When N-diethyltoluamide is solubilized with amine oxide alone, it is desirable to solubilize 100 parts by weight of N,N-diethyltoluamide with 75 to 110 parts by weight of amine oxide. Also, the temperature during mixing is not particularly limited, but N
, 60°C because N-diethyltoluamide is volatile.
It is preferable to mix the following:

本発明において、N、N−ジエチルトルアミドの配合割
合が限定されるのは、5重量%未満であると持続効果が
なく、また25重量%を越えるとアミンオキシドの配合
割合を増加する必要があり、組成物の粘度が著しく上昇
してスプレーすることが不可能になるためである。アミ
ンオキシドの配合割合が限定されるのは、4重量%未満
であると他の界面活性剤を併用しても、#、N−ジエチ
ルトルアミドを溶解することができず、組成物が白濁し
、経時的に分離するためであり、また20重it%を越
えると組成物の粘度が著しく上昇してスプレーすること
が不可能になるためである。
In the present invention, the blending ratio of N,N-diethyltoluamide is limited because if it is less than 5% by weight, there will be no sustained effect, and if it exceeds 25% by weight, it is necessary to increase the blending ratio of amine oxide. This is because the viscosity of the composition increases significantly, making it impossible to spray. The reason why the blending ratio of amine oxide is limited is that if it is less than 4% by weight, #,N-diethyltoluamide cannot be dissolved even if other surfactants are used together, and the composition becomes cloudy. This is because the composition will separate over time, and if it exceeds 20% by weight, the viscosity of the composition will increase significantly, making it impossible to spray.

本発明の虫よけ剤組成物は上記のように配合されたもの
をそのまま使用してもよいが、さらに20重量%以下の
他の界面活性剤を配合してもよい。
The insect repellent composition of the present invention may be used as it is as formulated as described above, but may further contain 20% by weight or less of other surfactants.

この界面活性剤としては、組成物に殺菌性を持たせるだ
めの、アルキルジメチルベンジルアンモニウムクロリド
、アルキルトリメチルアンモニウムクロリド等の陽イオ
ン性界面活性剤およびアルキルベタイン等の両性界面活
性剤、あるいはN、N−ジエチルメタトルアミドの可溶
化を補助するための、ポリオキシエチレンアルキルエー
テル、ポリオキシエチレンアルキルアリールエーテル等
の非イオン性界面活性剤などがあげられる。このほか本
発明の効果を損なわない範囲で他の成分を配合すること
も可能である。
Examples of the surfactant include cationic surfactants such as alkyldimethylbenzylammonium chloride and alkyltrimethylammonium chloride, and amphoteric surfactants such as alkylbetaine, which impart bactericidal properties to the composition; - Nonionic surfactants such as polyoxyethylene alkyl ether and polyoxyethylene alkylaryl ether are used to assist in solubilizing diethyl metatoluamide. In addition, it is also possible to blend other components within a range that does not impair the effects of the present invention.

以上によって得られる虫よけ剤組成物は、大または動物
等の皮膚に直接塗布あるいはスプレー等の手段によシ施
用することにより、蚊、あぶ、刺ばえ、ぶよ等の害虫よ
り肌を守ることができる。
The insect repellent composition obtained in the above manner protects the skin from pests such as mosquitoes, gadflies, bites, and gnats by directly applying it to the skin of animals or animals, or by applying it by means such as spraying. be able to.

以上説明してきたように、本発明によれば、虫よけ剤組
成物に特定のアミンオキシドを配合したので、エタノー
ルを配合することなく、N、N−ジエチルトルアミドを
可溶化できるため、競争馬にも使用可能であり、しかも
エタノールで可溶化したものよりも持続効果が大きいな
どの効果がある。
As explained above, according to the present invention, since a specific amine oxide is blended into the insect repellent composition, N,N-diethyltoluamide can be solubilized without blending ethanol, which makes it possible to compete with It can also be used on horses, and it has a longer lasting effect than those made solubilized with ethanol.

次に本発明の実施例について説明する。Next, examples of the present invention will be described.

実施例1 N、N−ジエチル−m−)ルアミドiog、表1に示し
だ界面活性剤10g、および水80gを混合し、N、N
−ジエチル−m−トルアミドの溶解性を外観−察により
調べた。結果を表1に示す。
Example 1 N,N-diethyl-m-)ylamide iog, 10 g of the surfactant shown in Table 1, and 80 g of water were mixed,
- The solubility of diethyl-m-toluamide was examined by visual observation. The results are shown in Table 1.

“表1において、ポリオキシエチレンに付記した数字は
エチレンオキシドの平均付加モル数を示す。
“In Table 1, the number appended to polyoxyethylene indicates the average number of moles of ethylene oxide added.

表1の結果より、アミンオキシドを前記範囲で配合する
ことにより、N、N−ジエチル−m−トルアミドを可溶
化できることがわかる。
The results in Table 1 show that N,N-diethyl-m-toluamide can be solubilized by blending amine oxide within the above range.

実施例2 N、N−ジエチ/l/ −m−トルアミド120g、ジ
メチル2ウリルアミンオキシドの35重@′チ水溶液2
40,9.およびヤシアルキルジメチルベンジルアンモ
ニウムクロリドの40重量%水溶液10.9を混合し、
次いで水630gを加えて均一透明な虫よけ剤組成物を
得た。
Example 2 120 g of N,N-diethyl/l/-m-toluamide, 35% aqueous solution of dimethyl diurylamine oxide 2
40,9. and 10.9% of a 40% by weight aqueous solution of coconut alkyldimethylbenzyl ammonium chloride,
Next, 630 g of water was added to obtain a uniform and transparent insect repellent composition.

この組成物を0℃および50℃で1ケ月放置したところ
、白濁、分離、着色等の経時変化は認められず、安定で
あった。また10人を対象として、上記組成物を約5 
mlスプレーし、効果の持続時間を測定したところ、1
0〜12時間持続した。比較のために、N、N−ジエチ
ル−m−トルアミド12gをエタノールの35重量係水
溶液8811に溶解した組成物を、約5ml同様にスプ
レーし、効果の持続時間を測定したところ、6〜8時間
であった。
When this composition was left for one month at 0° C. and 50° C., no changes over time such as clouding, separation, or coloring were observed, and it was stable. In addition, for 10 people, about 50% of the above composition was administered.
ml sprayed and measured the duration of the effect, 1
Lasted 0-12 hours. For comparison, approximately 5 ml of a composition prepared by dissolving 12 g of N,N-diethyl-m-toluamide in a 35 weight percent aqueous solution of ethanol 8811 was sprayed in the same manner, and the duration of the effect was measured. Met.

以上の結果より、本発明の虫よけ剤組成物は経時変化を
起こさず、安定しており、エタノールに溶解したものよ
りも持続効果が優れていることがわかる。
From the above results, it can be seen that the insect repellent composition of the present invention does not change over time, is stable, and has a longer lasting effect than one dissolved in ethanol.

代理人 弁理士  柳 原    成Agent Patent Attorney Sei Yanagi Hara

Claims (1)

【特許請求の範囲】 fl+#、#−ンエテルトルアミド5〜25重@qb、
下記−・般式il+で示されるアミンオキシド4〜20
重11%、および水50〜90重量%ヲ含む虫よけ剤組
成物3、I R〔(OCH,CH,)mOCH,CH,)、 −N→
O・−Ill2 (ただし、Rは炭素数8〜22のアルキル基またたはア
ルケニル基、R1およびR2はメチル基、エテル基、ヒ
ドロキシエテル基、またはヒドロキシプロピル基、mは
1または2、nは0または1である1、)12120重
t%以下の他の界面活性剤をさらに含む特許請求の範囲
第1項記載の虫よけ剤組成物。 (3)他の界面活性剤は殺菌性を有する陽イオン性もし
くは両性界面活性剤、またFi# 、N−ジエチルトル
アミドの可溶化を補助する非イオン性界面活性剤である
特許請求の範囲第1項または第2項記載の虫よけ剤組成
物。 (4)#、#−ジエチルトルアミドはN、N−ジxチル
ーm−トルアミドである特許請求の範囲第1項ないし第
3項のいずれかに記載の虫よけ剤組成物。
[Claims] fl+#, #-n ethertoluamide 5 to 25 times @qb,
Amine oxides 4 to 20 represented by the following general formula il+
Insect repellent composition 3, IR[(OCH,CH,)mOCH,CH,), -N→
O・-Ill2 (wherein, R is an alkyl group or alkenyl group having 8 to 22 carbon atoms, R1 and R2 are a methyl group, ether group, hydroxyether group, or hydroxypropyl group, m is 1 or 2, and n is The insect repellent composition according to claim 1, further comprising 12120% by weight or less of another surfactant, which is 0 or 1. (3) The other surfactant is a cationic or amphoteric surfactant having bactericidal properties, or a nonionic surfactant that assists in solubilizing Fi#, N-diethyltoluamide. The insect repellent composition according to item 1 or 2. (4) The insect repellent composition according to any one of claims 1 to 3, wherein #, #-diethyltoluamide is N,N-dixthyl-m-toluamide.
JP8120682A 1982-05-14 1982-05-14 Insect repellent composition Granted JPS58198403A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP8120682A JPS58198403A (en) 1982-05-14 1982-05-14 Insect repellent composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP8120682A JPS58198403A (en) 1982-05-14 1982-05-14 Insect repellent composition

Publications (2)

Publication Number Publication Date
JPS58198403A true JPS58198403A (en) 1983-11-18
JPH024563B2 JPH024563B2 (en) 1990-01-29

Family

ID=13740005

Family Applications (1)

Application Number Title Priority Date Filing Date
JP8120682A Granted JPS58198403A (en) 1982-05-14 1982-05-14 Insect repellent composition

Country Status (1)

Country Link
JP (1) JPS58198403A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6646011B2 (en) 1998-06-03 2003-11-11 Johnson & Johnson Consumer Companies, Inc. Insect repellant compositions
JP2005170914A (en) * 2003-12-15 2005-06-30 Dainippon Jochugiku Co Ltd Repellant composition for flying noxious insect
JP2010083903A (en) * 2002-05-31 2010-04-15 Kao Corp Agricultural chemical composition
CN102920617A (en) * 2012-11-15 2013-02-13 四川大学 Liquid type deet composition and preparation thereof

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6646011B2 (en) 1998-06-03 2003-11-11 Johnson & Johnson Consumer Companies, Inc. Insect repellant compositions
JP2010083903A (en) * 2002-05-31 2010-04-15 Kao Corp Agricultural chemical composition
JP2005170914A (en) * 2003-12-15 2005-06-30 Dainippon Jochugiku Co Ltd Repellant composition for flying noxious insect
JP4526264B2 (en) * 2003-12-15 2010-08-18 大日本除蟲菊株式会社 Flying pest repellent composition
CN102920617A (en) * 2012-11-15 2013-02-13 四川大学 Liquid type deet composition and preparation thereof

Also Published As

Publication number Publication date
JPH024563B2 (en) 1990-01-29

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