JPS5943444B2 - textile pest repellent - Google Patents
textile pest repellentInfo
- Publication number
- JPS5943444B2 JPS5943444B2 JP20519882A JP20519882A JPS5943444B2 JP S5943444 B2 JPS5943444 B2 JP S5943444B2 JP 20519882 A JP20519882 A JP 20519882A JP 20519882 A JP20519882 A JP 20519882A JP S5943444 B2 JPS5943444 B2 JP S5943444B2
- Authority
- JP
- Japan
- Prior art keywords
- fluorene
- naphthalene
- acenaphthene
- repellent
- textile
- 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.)
- Expired
Links
- 239000005871 repellent Substances 0.000 title claims description 14
- 230000002940 repellent Effects 0.000 title claims description 14
- 241000607479 Yersinia pestis Species 0.000 title claims description 11
- 239000004753 textile Substances 0.000 title claims description 11
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims description 34
- NIHNNTQXNPWCJQ-UHFFFAOYSA-N fluorene Chemical compound C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 claims description 33
- CWRYPZZKDGJXCA-UHFFFAOYSA-N acenaphthene Chemical compound C1=CC(CC2)=C3C2=CC=CC3=C1 CWRYPZZKDGJXCA-UHFFFAOYSA-N 0.000 claims description 28
- HXGDTGSAIMULJN-UHFFFAOYSA-N acetnaphthylene Natural products C1=CC(C=C2)=C3C2=CC=CC3=C1 HXGDTGSAIMULJN-UHFFFAOYSA-N 0.000 claims description 13
- 239000004480 active ingredient Substances 0.000 claims description 7
- 239000000077 insect repellent Substances 0.000 description 21
- 230000000694 effects Effects 0.000 description 7
- 241000238631 Hexapoda Species 0.000 description 6
- 230000006378 damage Effects 0.000 description 6
- 239000000126 substance Substances 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 4
- 210000002268 wool Anatomy 0.000 description 4
- DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 description 3
- 241000723346 Cinnamomum camphora Species 0.000 description 3
- 241000252233 Cyprinus carpio Species 0.000 description 3
- 229960000846 camphor Drugs 0.000 description 3
- 229930008380 camphor Natural products 0.000 description 3
- 231100000053 low toxicity Toxicity 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- ORILYTVJVMAKLC-UHFFFAOYSA-N adamantane Chemical compound C1C(C2)CC3CC1CC2C3 ORILYTVJVMAKLC-UHFFFAOYSA-N 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- ULDHMXUKGWMISQ-UHFFFAOYSA-N carvone Chemical compound CC(=C)C1CC=C(C)C(=O)C1 ULDHMXUKGWMISQ-UHFFFAOYSA-N 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 230000034994 death Effects 0.000 description 2
- 231100000517 death Toxicity 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 230000000749 insecticidal effect Effects 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 230000007886 mutagenicity Effects 0.000 description 2
- 231100000299 mutagenicity Toxicity 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- MGSRCZKZVOBKFT-UHFFFAOYSA-N thymol Chemical compound CC(C)C1=CC=C(C)C=C1O MGSRCZKZVOBKFT-UHFFFAOYSA-N 0.000 description 2
- 241000283690 Bos taurus Species 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 206010007269 Carcinogenicity Diseases 0.000 description 1
- 239000005973 Carvone Substances 0.000 description 1
- 241000282412 Homo Species 0.000 description 1
- 241000124008 Mammalia Species 0.000 description 1
- 239000005844 Thymol Substances 0.000 description 1
- PXAJQJMDEXJWFB-UHFFFAOYSA-N acetone oxime Chemical compound CC(C)=NO PXAJQJMDEXJWFB-UHFFFAOYSA-N 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 231100000260 carcinogenicity Toxicity 0.000 description 1
- 230000007670 carcinogenicity Effects 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- 210000000695 crystalline len Anatomy 0.000 description 1
- 150000001923 cyclic compounds Chemical class 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003344 environmental pollutant Substances 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Chemical group CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 150000002220 fluorenes Chemical class 0.000 description 1
- 238000004508 fractional distillation Methods 0.000 description 1
- 244000144972 livestock Species 0.000 description 1
- 230000005923 long-lasting effect Effects 0.000 description 1
- RLSSMJSEOOYNOY-UHFFFAOYSA-N m-cresol Chemical compound CC1=CC=CC(O)=C1 RLSSMJSEOOYNOY-UHFFFAOYSA-N 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000011812 mixed powder Substances 0.000 description 1
- 210000004877 mucosa Anatomy 0.000 description 1
- 231100000572 poisoning Toxicity 0.000 description 1
- 230000000607 poisoning effect Effects 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 238000000859 sublimation Methods 0.000 description 1
- 230000008022 sublimation Effects 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 229960000790 thymol Drugs 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
【発明の詳細な説明】
本発明は、人体に対して毒性が極めて低く、優れた繊維
害虫食害抑制作用を有する繊維害虫忌避剤に関するもの
である。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a textile insect repellent that has extremely low toxicity to the human body and has an excellent effect of suppressing damage caused by textile insects.
従来、羊毛、絹などの繊維の害虫防除剤として、ナフタ
リン、ショウノウ、バラジクロロベンゼンなどが通常用
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, and baladichlorobenzene have been commonly used as pest control agents for fibers such as wool and silk, and among them, baladichlorobenzene is the most widely used because it has a strong insecticidal effect and is inexpensive. ing.
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
あり、また眼粘膜と結合して水晶体の混濁を起こすおそ
れがある(実業中毒便覧)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、アルドリンは、その
使用が禁止されている。However, Balajichlorobenzene is a type of organic chlorine drug that can accumulate in living organisms and cause harm, and can also combine with the ocular mucosa and cause clouding of the crystalline lens (Industrial Poisoning Handbook). The use of organic chlorine aldrin, which is an insect repellent treatment agent 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繊維
害虫防除剤あるいは忌避剤として多くの化合物又はその
組合わせが提案されている。Therefore, in recent years, many compounds or combinations thereof have been proposed as textile pest control agents or repellents to replace Baladichlorobenzene.
例えば、トリイソプロピル−8−トリオキサン又はトリ
第三ブチル−8−ト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(特開
昭53−121936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53−1
09938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54−10
1425号公報)、α一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
成る防虫剤(特開昭54−110321号公報)、l−
カルボンを有効成分とする芳香性防虫剤(特開昭55−
19229号公報)などが提案されている。For example, insect repellents for wool (specially JP-A No. 52-110823), an insect repellent containing as an active ingredient a cyclic compound having 10 carbon atoms and an ether bond (JP-A No. 52-110823);
A sublimable insect repellent containing adamantane, a sublimable hydrocarbon, and a sublimable or volatile polar compound (Japanese Unexamined Patent Publication No. 121936/1983), an insect repellent containing a combination of naphthalene and thymol as active ingredients. Agent (Unexamined Japanese Patent Publication No. 53-1
09938), naphthalene and 2-isopropyl-
Insect repellent for clothing containing a combination of 5-methylphenol as an active ingredient (Japanese Patent Application Laid-Open No. 54-32620), insect repellent for clothing containing acetoxime as the main ingredient (Japanese Patent Application Laid-open No. 54-10)
1425), 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-1 position (Japanese Unexamined Patent Publication No. 110321/1982), l-
Aromatic insect repellent containing carvone as an active ingredient
19229) and the like 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、衣料用防虫剤のこのような実状に鑑み、
人体に対して極めて安全で、防虫効果に優れ、かつその
効果持続性に優れた実用的防虫剤を開発すべく、特には
乳動物に対する毒性の極めて低いが防虫効果に難点のあ
るナフタリンの防虫力を向上させるために、種々研究を
重ねた結果、フルオレン又はアセナフテンを共力剤とし
て用いることによりその目的を達成しうることを見出し
、この知見に基づいて本発明をなすに至った。In view of the current situation regarding insect repellents for clothing, the present inventors have
In order to develop a practical insect repellent that is extremely safe for the human body, has an excellent insect repellent effect, and has an excellent long-lasting effect, we focused on the insect repellent power of naphthalene, which has extremely low toxicity to mammals but has a drawback in its insect repellent effect. As a result of various studies in order to improve this, it was discovered that the objective could be achieved by using fluorene or acenaphthene as a synergist, and based on this knowledge, the present invention was accomplished.
すなわち、本発明は、ナフタリンとフルオレン又はアセ
ナフテンとの組合せを有効成分として含有する繊維害虫
忌避剤を提供するものである。That is, the present invention provides a textile pest repellent containing a combination of naphthalene and fluorene or acenaphthene as active ingredients.
本発明の忌避剤に用いられるナフタリンは、防虫力は比
較的弱いが、人畜に対する毒性が極めて低く、繊維害虫
忌避剤として古くから使用されている物質である。Naphthalene used in the repellent of the present invention has relatively weak insect repellent power, but has extremely low toxicity to humans and livestock, and is a substance that has been used as a textile pest repellent for a long time.
また、本発明の忌避剤において、ナフタリンと組み合わ
せて用いられるフルオレン共力剤やアセナフテン共力剤
はそれぞれコールクールの分留によりたがいに近接留分
として得られる安価な炭化水素で殺虫力は皆無であり、
食害抑制作用も極めて弱い物質である。Furthermore, in the repellent of the present invention, the fluorene synergist and acenaphthene synergist used in combination with naphthalene are inexpensive hydrocarbons obtained as fractions close to each other through coal-coeur fractional distillation, and have no insecticidal power. can be,
It is also an extremely weak substance that suppresses feeding damage.
このように防虫力を実質的に有しないフルオレンやアセ
ナフテンがナフタリンの共力剤として極めて優れた作用
を有し、特に繊維害虫の食害を実質的に完全に抑制しう
ろことは全く予想外のことであった。It is completely unexpected that fluorene and acenaphthene, which have virtually no insect-repellent properties, have extremely excellent synergistic effects as naphthalene synergists, and in particular can virtually completely suppress feeding damage from textile pests. Met.
フルオレンは融点116〜7°C1沸点295°Cの固
体であって、発ガン性及び変異原性を示さない物質で、
アセナフテンは融点95℃、沸点279℃の固体で変異
原性を示さない物質(化学の領域「環境汚染物質と毒性
有機物質部」増刊129号、第128ページ参照)であ
り、人体に極めて安全なものである。Fluorene is a solid with a melting point of 116-7°C and a boiling point of 295°C, and is a substance that does not show carcinogenicity or mutagenicity.
Acenaphthene is a solid substance with a melting point of 95°C and a boiling point of 279°C that does not show mutagenicity (see the Chemistry Area "Environmental Pollutants and Toxic Organic Substances Department" Special Issue No. 129, page 128), and is extremely safe for the human body. It is something.
このフルオレフィンやアセナフテンをナフタリンに配合
するには、通常両成分を粉末にして混合すればよく、そ
の配合割合は特に制限されないが、フルオレン又はアセ
ナフテンが多すぎると実際に使用した場合、ナフタリン
が全部昇華したのちに、単独では忌避効力のないフルオ
レン又はアセナフテンのみが残存するので実用上不適当
である。In order to blend this fluorene or acenaphthene with naphthalene, it is usually enough to mix both components into powder, and the blending ratio is not particularly limited, but if too much fluorene or acenaphthene is actually used, all of the naphthalene will be After sublimation, only fluorene or acenaphthene, which has no repellent effect when used alone, remains and is therefore unsuitable for practical use.
このため、ナフタリンに対し等量以下好ましくはナフタ
リンとフルオレン又はアセナフテンの合計量100重量
部当リフすオレン又はアセナフテン2〜30重量部の範
囲内になるように選択される。Therefore, the amount is selected to be equal to or less than naphthalene, preferably within a range of 2 to 30 parts by weight of fluorene or acenaphthene per 100 parts by weight of the total amount of naphthalene and fluorene or acenaphthene.
また、所望ならばフルオレンとアセナフテンをその合計
量が前記の範囲内になる割合で併用することもできる。Further, if desired, fluorene and acenaphthene can be used together in such a ratio that the total amount falls within the above range.
混合粉末は均一に混合したまま使用してもよいが、圧縮
成形などにより所定量の錠剤にして使用しやすくするこ
とができる。The mixed powder may be used as it is uniformly mixed, but it can be made into tablets of a predetermined amount by compression molding or the like to make it easier to use.
本発明の害虫忌避剤は安価で、しかも人体に対し無害で
ある上に、イガ、コイ力、ジュウクンガ、ヒメマルカツ
オブシムシ、ヒメカツオブシムシ、シラオビカツオブシ
ムシなどの繊維害虫に対して優れた防虫効果を示すので
実用的価値が高いものである。The pest repellent of the present invention is not only inexpensive and harmless to the human body, but also exhibits excellent insect repellent effects against textile pests such as burr, carp, Japanese carp, Japanese burr, Japanese carp, and white-tailed cutlet. It has high practical value.
次に、実施例により本発明をさらに詳細に説明する。Next, the present invention will be explained in more detail with reference to Examples.
実施例 1
フルオレンとナフタリンを粉砕して、それぞれの粉末を
第1表に示す種々の割合で混合し、各混合物をよく混ぜ
て均一化し、忌避剤を調製した。Example 1 A repellent was prepared by pulverizing fluorene and naphthalene, mixing the respective powders in various proportions shown in Table 1, and thoroughly mixing each mixture to homogenize it.
これら各忌避剤の防虫効果を次の方法により試験した。The insect repellent effect of each of these repellents was tested by the following method.
なお、この試験における供試虫としては、イガ゛(Ti
nea pellionella)の30〜36日令の
幼虫を用いた。The test insects used in this test were Ti
The 30- to 36-day-old larvae of P. nea pellionella were used.
試験方法;
2007711容のシャーレに供試虫10頭と羊毛深型
試験布(2CIIL×2CI′rL140〜451ng
)を入れ40メツシユの金網で蓋をした。Test method; 10 test insects and wool deep test cloth (2 CIIL x 2 CI'rL 140-451 ng
) and covered with a 40 mesh wire mesh.
その金網の中央に濾紙をのせ、その上に忌避剤50〜を
置き、別のシャーレをその上にかぶせ、2個のシャーレ
の合わせ目を密閉した。A filter paper was placed in the center of the wire mesh, 50~ of repellent was placed on it, another Petri dish was placed on top of it, and the seam between the two Petri dishes was sealed.
これを温度30℃、湿度65%の恒温恒湿室内に7日間
放置したのち、羊毛布を取り出し食害量を測定し、虫の
死亡数を数えた。After this was left in a constant temperature and humidity room at a temperature of 30° C. and a humidity of 65% for 7 days, the wool cloth was removed and the amount of feeding damage was measured and the number of dead insects was counted.
牛、存している虫を自然状態でさらに1日放置し、再び
死亡数を数えた。The cows and any insects present were left in their natural state for an additional day, and the number of deaths was counted again.
結果を次表に示す。The results are shown in the table below.
表中の値は、試験を3〜5回行って得られた値の平均値
である。The values in the table are the average values obtained by conducting the test 3 to 5 times.
また、比較のためにナフタリン単独、フルオレン単独及
びカンファー単独並びにカンファーと本発明の共力剤フ
ルオレン混合物についても同様に試験し、それらの食害
量及び害虫死亡率をまとめて第1表に示した。For comparison, naphthalene alone, fluorene alone, camphor alone, and a mixture of camphor and the synergist fluorene of the present invention were similarly tested, and the amounts of feeding damage and insect mortality rates are summarized in Table 1.
実施例 2
ナフタリンとアセナフテンを粉砕して、それぞれの粉末
を第2表に示す割合で混合し、実施例1と同様にして繊
維害虫忌避剤を調製した。Example 2 Naphthalene and acenaphthene were ground and the respective powders were mixed in the proportions shown in Table 2 to prepare a fiber pest repellent in the same manner as in Example 1.
このものについて、実施例1と同様にして試験した結果
をまとめて第2表に示した。This product was tested in the same manner as in Example 1, and the results are summarized in Table 2.
Claims (1)
せを有効成分として含有する繊維害虫忌避剤。 2 ナフタリンとフルオレン又はアセナフテンの合計量
100重量部当りフルオレン又はアセナフテン2〜30
重量部とする特許請求の範囲第1項記載の繊維害虫忌避
剤。[Scope of Claims] 1. A textile pest repellent containing a combination of naphthalene and fluorene or acenaphthene as active ingredients. 2 2 to 30 fluorene or acenaphthene per 100 parts by weight of the total amount of naphthalene and fluorene or acenaphthene
The textile pest repellent according to claim 1, expressed in parts by weight.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP20519882A JPS5943444B2 (en) | 1982-11-22 | 1982-11-22 | textile pest repellent |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP20519882A JPS5943444B2 (en) | 1982-11-22 | 1982-11-22 | textile pest repellent |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5995201A JPS5995201A (en) | 1984-06-01 |
| JPS5943444B2 true JPS5943444B2 (en) | 1984-10-22 |
Family
ID=16503023
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP20519882A Expired JPS5943444B2 (en) | 1982-11-22 | 1982-11-22 | textile pest repellent |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5943444B2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01118938U (en) * | 1988-01-30 | 1989-08-11 |
-
1982
- 1982-11-22 JP JP20519882A patent/JPS5943444B2/en not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01118938U (en) * | 1988-01-30 | 1989-08-11 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5995201A (en) | 1984-06-01 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| KR101773442B1 (en) | Repellent Composition against Biting Arthropods | |
| US20050112164A1 (en) | Insect repellent composition containing essential oils | |
| AU2006238677A1 (en) | Aerosol insecticide composition | |
| CN101843268A (en) | Botanical synergistic compound aphicide and preparation method thereof | |
| CN104472520A (en) | Pesticide composition containing pyriproxyfen and hexaflumuron | |
| JPS5943444B2 (en) | textile pest repellent | |
| JPH0461842B2 (en) | ||
| CN109793000A (en) | A kind of 16% emamectin benzoate and indoxacarb mixing missible oil and preparation method thereof | |
| US2639259A (en) | Insecticides | |
| KR102898451B1 (en) | The formulation of eco-friendly winged insect repellent and their preparation method | |
| US2386779A (en) | Insecticidal compositions | |
| JPH01163104A (en) | Extermination agent for household mite | |
| JP2729397B2 (en) | Acaricide composition | |
| CN109820002A (en) | An insecticide composition for controlling the population of stored grain pests | |
| JPS5921841B2 (en) | textile pest repellent | |
| JPS5925761B2 (en) | Insect repellent for clothing pests | |
| JPS5943445B2 (en) | textile pest control agent | |
| KR102162492B1 (en) | Composition of tick repellent agent | |
| JPH04210605A (en) | Sublimable insect-proofing and insecticidal agent composition | |
| JPS609004B2 (en) | insect repellent | |
| JP3286416B2 (en) | Flea control agent | |
| JPS6053011B2 (en) | Repellent against textile pests | |
| KR20060110655A (en) | Compounds showing acaricide | |
| KR100654902B1 (en) | Acaricide | |
| US2089766A (en) | Insecticide |