JPH0244442B2 - - Google Patents
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- Publication number
- JPH0244442B2 JPH0244442B2 JP59275294A JP27529484A JPH0244442B2 JP H0244442 B2 JPH0244442 B2 JP H0244442B2 JP 59275294 A JP59275294 A JP 59275294A JP 27529484 A JP27529484 A JP 27529484A JP H0244442 B2 JPH0244442 B2 JP H0244442B2
- Authority
- JP
- Japan
- Prior art keywords
- cockroaches
- cockroach repellent
- cockroach
- test specimen
- repellent
- 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 - Lifetime
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- Agricultural Chemicals And Associated Chemicals (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
〔産業上の利用分野〕
本発明は、ゴキブリの防除に長期間効力を奏
し、しかも従来の忌避剤と比較して、ゴキブリが
各段に敏感に感応して忌避行動をとるゴキブリ忌
避剤に関するものである。
〔従来技術、および解決すべき問題点〕
ゴキブリは、シロアリと共に網翅目に属する昆
虫で、石炭紀より地球上に出現した最も古い昆虫
であると云われ、人家に侵入して腐つた動植物の
遺骸を食し、夜間処構わず這い回つて伝染病を媒
介するので衛生害虫として人々から特に嫌悪され
ている。そのようなことから、ゴキブリを防除す
るのに有効な薬剤が求められているのであるが、
生命力の頗る旺盛なゴキブリに対して有効で、し
かも人畜には無害なゴキブリ忌避剤というと、そ
の開発は非常に困難であつて、未だ満足な実用例
を聞かないのが現状である。
ちなみに、これまでに提案されたゴキブリ忌避
技術についてみてみると、まず、フエニトロチオ
ン〔0,0―ジメチル―0―(3―メチル―4―
ニトロフエニル)チオホスフエート〕をゴキブリ
忌避剤に利用しようというものがある。だが、フ
エニトロチオンは非常に速効性に富んでゴキブリ
殺傷力が強く、かつ人畜に対する毒性も低いので
速効的殺虫剤としての特性は理想的なのである
が、分解し易く効力持続性が不十分であるところ
から、忌避剤として長期間の効力を期待すること
ができないという難点があつた。
ところが最近、R―NH―CH2―CH2―OH(R
は炭素数1〜4のアルキル基)で示されるアミノ
アルコール類(例えば、N―メチルアミノエタノ
ールや、N―エチルアミノエタノール)に対し
て、ゴキブリ忌避反応を示すこと判明し、これを
ゴキブリ忌避剤として利用しようという提案がな
されるようになつた(特開昭50―40727号公報参
照)。しかし、このアミノアルコール系ゴキブリ
忌避剤もまた、蒸散が活発で長期間効力を持続さ
せることができないという難点があつた。
本発明の契機は、ゴキブリの反応が敏感で死殺
力に富んだフエニトロチオンの特性と、ゴキブリ
を死殺する程の効力はないがゴキブリ独特の忌避
性向を示すアミノアルコール系ゴキブリ忌避剤の
特性とを上手に組合せれば、ゴキブリ衛生を害す
るような箇所(例えば、台所・食堂・座敷など)
で処構わず死ぬことがなく、しかも人の嫌う箇所
にも出没させることのない理想的ゴキブリ忌避剤
が得られるとの見込のものと種々の調合・ゴキブ
リ反応実験を繰り返したことにある。
〔課題解決の手段〕
本発明者が最初に採択した方法は、上記フエニ
トロチオン〔0,0―ジメチル―0―(3―メチ
ル―4―ニトロフエニル)チオホスフエート〕
と、N―メチルアミノエタノール、またはN―エ
チルアミノエタノールとを混合させることであつ
た。
ところが、このようにして得た薬剤は、ゴキブ
リ忌避性においては作用が弱く、また効力の持続
性の面においては安定性が乏しく、ゴキブリ忌避
剤としては全く実用に供しないものであつた。
しかるところ、たまたま偶然に其処へ、更にピ
レスロイド系殺虫剤〔3―フエノキシベンジル―
dl―シス/トランス―3(2,2―ジククロロビ
ニル)―2,2―ジメチル―1―シクロプロパン
カルボキシラート〕を加えると、ゴキブリに対し
て速効に過ぎず、しかも長期に亙つてゴキブリ忌
避作用を発揮するゴキブリ忌避剤となることが判
明した。しかも、かくして得られたゴキブリ忌避
剤は、合成樹脂との相溶性が良好であつて、これ
を合成樹脂液中に混入させると、非常に理態的な
ゴキブリ忌避塗料やゴキブリ忌避接着剤となり、
またこれを合成樹脂中に混入して、例えば床シー
トその他の建材に成形すると、長期間に亙つてゴ
キブリ忌避作用を奏する建築用品が得られること
も分かつたのである。
以下、本発明の作用効果を、実施例に基いて、
詳述する。
〔実施例 〕
(a) 3―フエノキシベンジル―dl―シス/トラン
ス―3(2,2―ジクロロビニル)―2,2―
ジメチル―1―シクロプロパンカルボキシラー
ト
〔住友化学工業(株)商品名:エクスミン〕
(b) 0,0―ジメチル―0―(3―メチル―4―
ニトロフエニル)チオホスフエート;
〔住友化工学業(株)商品名:スミチオン〕
(c) N―メチルアミノエタノール
〔日本乳化剤(株)製〕
上記(a),(b)および(c)の各剤を、重量比1:1:
1の割合にて混合してゴキブリ忌避剤を調製した
が、これら(a),(b)および(c)の各剤は頗る良く解け
合つた。
かくして、得られたゴキブリ忌避剤を、アミノ
アルキド樹脂液中に混入したところ、木材等に対
する接着性の良好な接着剤となつた。
つぎに、上記のようにして得た塩化ビニル樹脂
に充填剤と共に混入して成形したところ床シート
として使用可能な塩化ビニルシートが得られた。
〔実施例 〕
(a) 3―フエノキシベンジル―dl―シス/トラン
ス―3(2,2―ジクロロビニル)―2,2―
ジメチル―1―シクロプロパンカルボキシラー
ト
〔住友化学工業(株)商品名:エクスミン〕
(b) 0,0―ジメチル―0―(3―メチル―4―
ニトロフエニル)チオホスフエート;
〔住友化学工業(株)商品名:スミチオン〕
(d) N―エチルアミノエタノール
〔日本乳化剤(株)製〕
上記(a),(b)および(d)の各剤を、重量比1:1:
0.5の割合にて混合してゴキブリ忌避剤を調製し
たが、これら(a),(b)および(d)の各剤も頗る良く解
け合つた。
かくして、得られたゴキブリ忌避剤を、アミノ
アルキド樹脂液中に混入したところ、木材等に対
する接着性の良好な接着剤となり、また塩化ビニ
ル樹脂に充填剤と共に混入して成形したところ床
シートとして使用可能な塩化ビニルシートが得ら
れ、上記実施例と同様に合成樹脂に対し、非常
に順調な相溶性を示した。
〔実験例〕
本発明ゴキブリ忌避剤の薬効を検証するため、
次の実験を行つた。
(実験薬剤)
実施例により調製した薬剤
実施例により調製した薬剤
エクスミンとスミチオンとの混合薬剤(混合
重量比=1:1)
エクスミンとN―メチルアミノエタノールと
の混合薬剤(混合重量比=1:1)
スミチオンとN―メチルアミノメタノールと
の混合薬剤(混合重量比=1:1)
(試験体の作製)
予じめ重量を測定しておいた濾紙を、トルエン
により所定濃度に調えた薬剤液に浸漬し、素早く
重量を測つてから溶媒を飛ばし、薬剤の有効成分
量を算出した。なお、試験体は各剤について各々
5枚ずつ作製し、有効成分量はその平均値をとつ
た。
その結果、
上記実験薬剤にあつては430mg/m2、実験薬
剤にあつては390mg/m2、
また実験薬剤にあつては600mg/m2、実験薬
剤にあつては600mg/m2、実験薬剤にあつて
は400mg/m2であつた。
(実験方法)
大型シヤーレの中に薬剤を含まない無処理の試
験体(blank)または上記〜の薬剤を含む試
験体2枚を対称的に置いてチヤバネゴキブリ8匹
を放つ一方、その中央にはゴキブリが好む顆粒状
餌を置いてゴキリブリの反応を観察評価した。
なお、この実験においては、24時間に亙つてゴ
キブリの歩行状態、および餌のバラツキ状況を標
準化して、次表のような評価値を与えた。
[Field of Industrial Application] The present invention relates to a cockroach repellent that is effective in controlling cockroaches for a long period of time, and that cockroaches are more sensitive to each stage and take repellent actions compared to conventional repellents. It is. [Prior Art and Problems to be Solved] Cockroaches are insects that belong to the order Apiptera, along with termites, and are said to be the oldest insects that appeared on earth from the Carboniferous period. They are particularly disliked by people as sanitary pests because they feed on corpses and crawl around at night, transmitting infectious diseases. For this reason, there is a need for effective agents to control cockroaches.
It is extremely difficult to develop a cockroach repellent that is effective against vigorous cockroaches and is harmless to humans and animals, and there are currently no satisfactory examples of practical use. By the way, if we look at cockroach repellent technologies that have been proposed so far, the first one is fenitrothion [0,0-dimethyl-0-(3-methyl-4-
There is a proposal to use nitrophenyl thiophosphate] as a cockroach repellent. However, fenitrothion is extremely fast-acting, has strong cockroach-killing power, and has low toxicity to humans and animals, making it ideal as a fast-acting insecticide. Therefore, the problem was that it could not be expected to have long-term efficacy as a repellent. However, recently, R-NH-CH 2 -CH 2 -OH (R
It has been found that amino alcohols (such as N-methylaminoethanol and N-ethylaminoethanol) represented by an alkyl group having 1 to 4 carbon atoms exhibit a cockroach repellent reaction, and this is used as a cockroach repellent. Proposals began to be made to use it as a tool (see Japanese Patent Application Laid-open No. 40727/1983). However, this aminoalcohol-based cockroach repellent also has the disadvantage that transpiration is active and its effectiveness cannot be maintained for a long period of time. The impetus for the present invention was the characteristics of fenitrothion, which has a sensitive reaction to cockroaches and is highly lethal, and the characteristics of an aminoalcohol-based cockroach repellent, which is not effective enough to kill cockroaches but exhibits a unique repellency to cockroaches. If you combine them properly, you can remove cockroaches from areas that harm hygiene (for example, kitchens, dining rooms, parlors, etc.)
It is hoped that an ideal cockroach repellent that will not kill people no matter where they are exposed to, and will not cause them to infest places that people dislike, is the result of repeated experiments with various formulations and reactions to cockroaches. [Means for Solving the Problem] The method first adopted by the present inventor is the above-mentioned fenitrothion [0,0-dimethyl-0-(3-methyl-4-nitrophenyl)thiophosphate]
and N-methylaminoethanol or N-ethylaminoethanol. However, the drug thus obtained had a weak effect in repelling cockroaches, and had poor stability in terms of duration of efficacy, so that it could not be put to practical use as a cockroach repellent at all. However, by chance, I happened to find a pyrethroid insecticide [3-phenoxybenzyl-
dl-cis/trans-3(2,2-dichlorovinyl)-2,2-dimethyl-1-cyclopropanecarboxylate] has only a quick effect on cockroaches, and is effective in repelling cockroaches for a long period of time. It has been found to be an effective cockroach repellent. Moreover, the cockroach repellent thus obtained has good compatibility with synthetic resins, and when mixed into a synthetic resin liquid, it becomes a very logical cockroach repellent paint or cockroach repellent adhesive.
It has also been found that if this is mixed into a synthetic resin and molded into, for example, floor sheets or other building materials, construction products that exhibit a long-term cockroach-repelling effect can be obtained. Hereinafter, the effects of the present invention will be explained based on Examples.
Explain in detail. [Example] (a) 3-phenoxybenzyl-dl-cis/trans-3(2,2-dichlorovinyl)-2,2-
Dimethyl-1-cyclopropanecarboxylate [Sumitomo Chemical Co., Ltd. trade name: Exmin] (b) 0,0-dimethyl-0-(3-methyl-4-
(Nitrophenyl) thiophosphate; [Sumitomo Chemical Co., Ltd., trade name: Sumithion] (c) N-methylaminoethanol [Nippon Nyukazai Co., Ltd.] Each of the above agents (a), (b) and (c) was added by weight. Ratio 1:1:
A cockroach repellent was prepared by mixing these agents at a ratio of 1:1, and these agents (a), (b), and (c) dissolved very well. When the thus obtained cockroach repellent was mixed into an aminoalkyd resin liquid, it became an adhesive with good adhesion to wood and the like. Next, the mixture was mixed with a filler into the vinyl chloride resin obtained as described above and molded, resulting in a vinyl chloride sheet that could be used as a floor sheet. [Example] (a) 3-phenoxybenzyl-dl-cis/trans-3(2,2-dichlorovinyl)-2,2-
Dimethyl-1-cyclopropanecarboxylate [Sumitomo Chemical Co., Ltd. trade name: Exmin] (b) 0,0-dimethyl-0-(3-methyl-4-
(nitrophenyl) thiophosphate; [Sumitomo Chemical Co., Ltd., trade name: Sumithion] (d) N-ethylaminoethanol [manufactured by Nippon Nyukazai Co., Ltd.] Each of the above agents (a), (b) and (d) was added by weight. Ratio 1:1:
A cockroach repellent was prepared by mixing them at a ratio of 0.5, and these agents (a), (b), and (d) also dissolved very well. When the cockroach repellent thus obtained was mixed into an aminoalkyd resin liquid, it became an adhesive with good adhesion to wood, etc., and when mixed with a filler and molded into vinyl chloride resin, it was used as a floor sheet. A suitable vinyl chloride sheet was obtained, which showed very good compatibility with synthetic resins as in the above examples. [Experimental example] In order to verify the efficacy of the cockroach repellent of the present invention,
The following experiment was conducted. (Experimental drugs) Drugs prepared according to Examples Drugs prepared according to Examples Mixed drugs of Exmin and Sumithion (mixed weight ratio = 1:1) Mixed drugs of Exmin and N-methylaminoethanol (mixed weight ratio = 1: 1) Mixed drug of sumithion and N-methylaminomethanol (mixed weight ratio = 1:1) (Preparation of test specimen) A drug solution prepared by adjusting the weight of a filter paper in advance to a predetermined concentration with toluene. After quickly measuring the weight, the solvent was evaporated and the amount of the active ingredient of the drug was calculated. Incidentally, five test specimens were prepared for each agent, and the amount of the active ingredient was taken as the average value. As a result, 430 mg/m 2 for the above experimental drug, 390 mg/m 2 for the experimental drug, and 600 mg/m 2 for the experimental drug; For drugs, it was 400mg/ m2 . (Experimental method) An untreated test specimen (blank) containing no drug or two test specimens containing the above-mentioned drugs were placed symmetrically in a large shear dish, and eight German cockroaches were released into the center. observed and evaluated cockroaches' reactions by placing granular baits that cockroaches prefer. In this experiment, the walking state of the cockroaches and the variation in food were standardized over a 24-hour period, and evaluation values were given as shown in the following table.
【表】【table】
【表】
上記評価基準によつて、試験体〜の評価を
したところ、次のような結果が得られた。なお、
念のため付言しておくならば、ゴキブリ忌避剤と
しては平均評価値「2」以上の評価が出なければ
製品価値があるとは云えないのである。
評価結果
試験体 平均評価値 3.5
試験体 〃 3.6
試験体 〃 1.7
試験体 〃 1.0
試験体 〃 1.2
更に、試験体〜を3ケ月間(昭和59年7月
1日〜同年9月30日まで)気温40℃の室内に放置
して置き、これを用いて上記と同様のゴキブリの
反応を評価したところ、次のような結果になつ
た。
評価結果
試験体 平均評価値 3.0
試験体 〃 3.2
試験体 〃 0.5
試験体 〃 0
試験体 〃 0
以上の実験結果から、本発明に係るゴキブリ忌
避剤はゴキブリ防除力が優れ、しかも効力の持続
性にも富んでいることが判明した。[Table] When the test specimens ~ were evaluated according to the above evaluation criteria, the following results were obtained. In addition,
Just to be sure, a cockroach repellent cannot be said to have product value unless it receives an average rating of "2" or higher. Evaluation results Test specimen Average evaluation value 3.5 Test specimen 〃 3.6 Test specimen 〃 1.7 Test specimen 〃 1.0 Test specimen 〃 1.2 In addition, the temperature of the test specimen ~ was evaluated for 3 months (from July 1, 1980 to September 30 of the same year) When we left it in a room at 40°C and used it to evaluate the reaction of cockroaches in the same way as above, we got the following results. Evaluation results Test specimen Average evaluation value 3.0 Test specimen 〃 3.2 Test specimen 〃 0.5 Test specimen 〃 0 Test specimen 〃 0 From the above experimental results, the cockroach repellent according to the present invention has excellent cockroach control power and has a long-lasting effect. It also turned out to be rich.
Claims (1)
4のアルキル基)で示されるアミノアルコール類
と;0,0―ジメチル―0―(3―メチル―4―
ニトロフエニル)チオホスフエートと; 3―フエノキシベンジル―dl―シス/トランス
―3(2,2―ジクロロビニル)―2,2―ジメ
チル―1―シクロプロパンカルボキシラートとを
含むことを特徴とするゴキブリ忌避剤。[Claims] 1 R—NH—CH 2 —CH 2 —OH (R has 1 to 1 carbon atoms
4 alkyl group); and 0,0-dimethyl-0-(3-methyl-4-
A cockroach repellent comprising: (nitrophenyl) thiophosphate; and 3-phenoxybenzyl-dl-cis/trans-3(2,2-dichlorovinyl)-2,2-dimethyl-1-cyclopropanecarboxylate. agent.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59275294A JPS61158906A (en) | 1984-12-29 | 1984-12-29 | Cockroach repellant |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59275294A JPS61158906A (en) | 1984-12-29 | 1984-12-29 | Cockroach repellant |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS61158906A JPS61158906A (en) | 1986-07-18 |
| JPH0244442B2 true JPH0244442B2 (en) | 1990-10-04 |
Family
ID=17553423
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP59275294A Granted JPS61158906A (en) | 1984-12-29 | 1984-12-29 | Cockroach repellant |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS61158906A (en) |
-
1984
- 1984-12-29 JP JP59275294A patent/JPS61158906A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS61158906A (en) | 1986-07-18 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EXPY | Cancellation because of completion of term |