JPS5926601B2 - Pyrethroid insecticidal composition - Google Patents

Pyrethroid insecticidal composition

Info

Publication number
JPS5926601B2
JPS5926601B2 JP51159568A JP15956876A JPS5926601B2 JP S5926601 B2 JPS5926601 B2 JP S5926601B2 JP 51159568 A JP51159568 A JP 51159568A JP 15956876 A JP15956876 A JP 15956876A JP S5926601 B2 JPS5926601 B2 JP S5926601B2
Authority
JP
Japan
Prior art keywords
insecticidal
tocopherol
mat
hours
pyrethroid
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
Application number
JP51159568A
Other languages
Japanese (ja)
Other versions
JPS5386023A (en
Inventor
孝信 柏原
則明 大下
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.)
AASU SEIYAKU KK
Original Assignee
AASU SEIYAKU KK
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 AASU SEIYAKU KK filed Critical AASU SEIYAKU KK
Priority to JP51159568A priority Critical patent/JPS5926601B2/en
Priority to GR53886A priority patent/GR63567B/en
Priority to GB5336377A priority patent/GB1553805A/en
Priority to IT526777A priority patent/IT1089666B/en
Priority to FR7739617A priority patent/FR2375826A1/en
Publication of JPS5386023A publication Critical patent/JPS5386023A/en
Publication of JPS5926601B2 publication Critical patent/JPS5926601B2/en
Expired legal-status Critical Current

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Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N25/00Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/22Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing ingredients stabilising the active ingredients
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N53/00Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof

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  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • Agronomy & Crop Science (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Toxicology (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Description

【発明の詳細な説明】 本発明はピレスロイド系殺虫組成物、更に詳しくは電気
蚊取器等により殺虫成分を加熱揮散させる方式の殺虫剤
の改良に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a pyrethroid insecticidal composition, and more particularly to an improvement in an insecticide in which the insecticidal component is heated and volatilized using an electric mosquito repellent or the like.

蚊や蝿等の室内害虫を駆除する方法として、油剤、乳剤
、エアゾール剤等を直接害虫に噴霧したり床面に噴霧し
て塗布面に接触した害虫を殺す方法(噴霧法)、蚊取線
香、電気蚊取器用マット等を加熱して殺虫成分を揮散さ
せることによる方法(加熱揮散方法)等が知られている
Methods for exterminating indoor pests such as mosquitoes and flies include methods such as spraying oils, emulsions, aerosols, etc. directly onto the pests or on the floor to kill the pests that come into contact with the applied surface (spraying method), and mosquito coils. , a method of heating an electric mosquito repellent mat or the like to volatilize the insecticidal component (heating volatilization method) is known.

これらの方法の中で加熱揮散方法は、噴霧法に比較して
長時間に亘って殺虫成分を放出ししかもその殺虫効力を
高い状態に維持し得るために現在広く採用されている。
Among these methods, the heating volatilization method is currently widely employed because it releases the insecticidal component over a longer period of time than the spraying method and can maintain its insecticidal efficacy at a high level.

電気蚊取器用マット等による加熱揮散方法に於ては一般
にピレスロイド系殺虫剤が使用されており、之をパルプ
、多孔性合成樹脂等から形成されたマットに吸収させ該
マットを110〜200℃の温度に加熱して殺虫成分を
揮散させる方法が採られている。
Pyrethroid insecticides are generally used in heating volatilization methods using electric mosquito repellent mats, etc., and the insecticides are absorbed into a mat made of pulp, porous synthetic resin, etc., and the mat is heated at 110 to 200°C. The method used is to heat it to a high temperature to volatilize the insecticidal ingredients.

しかしながらこの電気蚊取器用マットによる加熱揮散方
法では殺虫成分を有効に揮散させるということは不可能
であり、加熱開始から9時間の間にマット中に吸収され
た殺虫成分の約40重量%が揮散されるに過ぎない。
However, it is impossible to effectively volatilize insecticidal ingredients using this heating volatilization method using electric mosquito repellent mats, and approximately 40% by weight of the insecticidal ingredients absorbed into the mat volatilize within 9 hours from the start of heating. It's just being done.

さらに該方法では、マットは初期の短時間には強力な殺
虫作用を発揮するが数時間経過後には殺虫効力が極端に
減少したり或いは殺虫効力を殆んど発揮し得なくなる傾
向があり、またピレスロイド系殺虫成分は不安定で分解
を受けやすく該マットの貯蔵安定性に於ても問題がある
Furthermore, in this method, the mat exhibits a strong insecticidal effect in the initial short period of time, but after several hours, the insecticidal effect tends to decrease drastically or become almost impossible to exert. Pyrethroid insecticidal ingredients are unstable and susceptible to decomposition, which also poses a problem in the storage stability of the mat.

このために例えば2・6−ジーtert −ブチル−4
−メチルフェノール等の分解防止剤をピレスロイド系殺
虫剤中に含有せしめる試みもなされているが、これら分
解防止剤を配合しても上記欠点を尚充分には解消できな
い。
For this purpose, for example, 2,6-tert-butyl-4
- Attempts have been made to incorporate decomposition inhibitors such as methylphenol into pyrethroid insecticides, but even if these decomposition inhibitors are incorporated, the above-mentioned drawbacks cannot be sufficiently overcome.

従って電気蚊取器用マットから殺虫成分を有効に揮散さ
せることができしかも貯蔵安定性にも優れた殺虫剤の出
現が望まれているのが現状である。
Therefore, there is currently a desire for an insecticide that can effectively volatilize insecticidal ingredients from electric mosquito repellent mats and has excellent storage stability.

本発明者は斯かる現状に鑑み上記欠点を解消すべく種々
の研究を重ねてきた。
In view of the current situation, the present inventor has conducted various studies in order to eliminate the above-mentioned drawbacks.

その結果ピレスロイド系殺虫成分とトコフェロール及び
/又はトコフェロールの酢酸エステルとを併用した場合
に所期の目的を達成し得ることを発見して本発明を完成
するに至った。
As a result, they discovered that the desired objective could be achieved when a pyrethroid insecticidal component and tocopherol and/or tocopherol acetate were used in combination, leading to the completion of the present invention.

即ち本発明はピレスロイド系殺虫成分にトコフェロール
及ヒ/又ハトコフエロールの酢酸エステルを配合するこ
とを特徴とするピレスロイド系殺虫組成物に係る。
That is, the present invention relates to a pyrethroid insecticidal composition characterized in that the pyrethroid insecticidal component contains tocopherol and acetate ester of hatcopherol.

本発明に依れば、殺虫成分の揮散を効率よ(高めしかも
加熱による殺虫成分の分解を抑制し、8時間以上という
長時間に亘りその殺虫効力を持続し得る。
According to the present invention, the insecticidal component can be volatilized efficiently (increased), and decomposition of the insecticidal component due to heating can be suppressed, and its insecticidal effect can be maintained for a long time of 8 hours or more.

更に本発明に係るピレスロイド系殺虫剤は長期貯蔵によ
っても該殺虫剤中の殺虫成分が分解せず貯蔵時の安定性
に於ても優れている。
Furthermore, the pyrethroid insecticide according to the present invention has excellent stability during storage, as the insecticidal component in the insecticide does not decompose even after long-term storage.

本発明で使用されるピレスロイド系殺虫成分としては公
知のものを広く使用でき、代表的なものとして3−アリ
ル−2−メチルシクロペンタ−2−エンー4−オンー1
−イル−di−シス、トランスークリサンテマート(商
標名;ピナミン、住友化学工業■製、以下この化合物を
「アレスリン」と称スる)、3−アリル−2−メチルシ
クロペンタ−2−エン−4−オン−1−イルーd−シス
、トランスークリサンテマート(商標名;ピナミンフォ
ルテ、住友化学工業■製、以下この化合物を「ピナミン
フォルテ」と称する)、2−メチル−5−(2−7’ロ
ピル)−3−フリルメテルクリサンテマート等を例示で
きる。
As the pyrethroid insecticidal component used in the present invention, a wide range of known ones can be used, and a typical example is 3-allyl-2-methylcyclopent-2-ene-4-one-1.
-yl-di-cis, trans-chrysanthemate (trade name: Pinamine, manufactured by Sumitomo Chemical, hereinafter referred to as "allethrin"), 3-allyl-2-methylcyclopent-2-ene -4-one-1-yl-d-cis, trans-chrysanthemate (trade name: Pinaminforte, manufactured by Sumitomo Chemical, hereinafter this compound will be referred to as "Pinaminforte"), 2-methyl-5- Examples include (2-7'lopyl)-3-furylmethel chrysanthemate.

本発明では上記殺虫成分にトコフェロール及び/又はト
コフェロールの酢酸エステル(酢酸トコフェロール)が
配合される。
In the present invention, tocopherol and/or acetate ester of tocopherol (tocopherol acetate) is blended with the insecticidal component.

トコフェロールとしてはα−トコフェロール、β−トコ
フェロール、γ−トコフェロール、δ−トコフェロール
等等測例示きる。
Examples of tocopherol include α-tocopherol, β-tocopherol, γ-tocopherol, and δ-tocopherol.

之等のトコフェロール及びその酢酸エステルは天然のも
のであっても合成されたものであってもよい。
These tocopherols and their acetate esters may be natural or synthetic.

トコフェロール及び/又はトコフェロールの酢酸エステ
ルの殺虫成分に対する配合割合は特に限定がなく使用さ
れる殺虫成分の種類、加熱温度等に応じ広範囲の中から
適宜選択されるが、通常殺虫成分100重量部に対し1
0〜300重量部、好ましくは20〜100重量部であ
る。
The blending ratio of tocopherol and/or tocopherol acetate to the insecticidal ingredient is not particularly limited and can be appropriately selected from a wide range depending on the type of insecticidal ingredient used, heating temperature, etc., but usually it is based on 100 parts by weight of the insecticidal ingredient. 1
The amount is 0 to 300 parts by weight, preferably 20 to 100 parts by weight.

トコフェロール及ヒ/又ハトコフエロールの酢酸エステ
ルの量が少な(なると所期の効果を発揮し得なくなる傾
向となり、また逆に該量が多くなってもそれ以上の効果
を期待し得ない。
If the amount of tocopherol and/or acetate ester of hatcopherol is small, the desired effect will not be exhibited, and conversely, even if the amount is large, no further effect can be expected.

本発明では例えばピレスロイド系殺虫成分とトコフェロ
ール及び/又ハトコフエロールノ酢酸エステルとの混合
物をパルプ、石綿、多孔性合成樹脂、珪藻土、クレー等
の鉱物質粉末物質、素焼等の多孔性磁性物質等に含浸さ
せることにより電気橋台蚊取器用マットが得られ、該マ
ットを加熱(通常的110〜200℃)することにより
本発明の所期の目的が達成される。
In the present invention, for example, a mixture of a pyrethroid insecticidal component and tocopherol and/or pigeon pherol noacetate is used in pulp, asbestos, porous synthetic resin, mineral powder materials such as diatomaceous earth and clay, and porous magnetic materials such as bisque. A mat for an electric abutment mosquito repellent is obtained by impregnating the mat with the above-described method, and the intended object of the present invention is achieved by heating the mat (usually at 110 to 200° C.).

あるいは上記混合物を慣用手段によりペースト状、クリ
ーム状等の各種形態に製剤し、これを発熱体上で揮散さ
せてもよい。
Alternatively, the above mixture may be formulated into various forms such as paste or cream by conventional means and volatilized on a heating element.

本発明に於ては種々の目的に応じさらに共力剤、分解防
止剤、忌避剤等各種添加剤を配合してもよい。
In the present invention, various additives such as a synergist, a decomposition inhibitor, and a repellent may be added depending on various purposes.

斯かる共力剤としてはピペロニルブトキサイド、オクタ
クロロジプロピルエーテル、MGK264、サイネピリ
ン等を、分解防止剤としては2・6−ジーtert
−ブチル−4−メチルフェノール(BHT)、2・5−
ジーte?t −ブチルハイドロキノン等を、忌避剤と
してはN−N−ジエチルメタトルアミド、ジ−n−ブチ
ルサクシネート等を例示できる。
Such synergists include piperonyl butoxide, octachlorodipropyl ether, MGK264, cinepirin, etc., and the decomposition inhibitors include 2,6-di-tert.
-Butyl-4-methylphenol (BHT), 2,5-
Geete? Examples of repellents include t-butylhydroquinone and the like, and N-N-diethyl metatoluamide, di-n-butyl succinate, and the like.

本発明をより一層間らかにするために実施例を以下に掲
げる。
Examples are given below to further clarify the present invention.

実施例 1 殺虫成分としてアレスリン、ピナミンフォルテを使用し
下記第1表に示す処方についC1大きな2.2CrfL
X 3.5CIIlX 0127cIrLのパルプ板に
均一に吸収させ電気蚊取器用マットを調製する。
Example 1 Using allethrin and pinamin forte as insecticidal ingredients, the formulation shown in Table 1 below had a large C1 of 2.2CrfL.
A mat for an electric mosquito repellent is prepared by uniformly absorbing X 3.5CIIlX 0127cIrL onto a pulp board.

トコフェロール及びその酢酸エステルとしては(a)d
i−α−トコフェロール(和光紬薬製)、(b)酢酸ト
コフェロール(商標名;埋研Eアセテート960、理研
ビタミン油■製) 、(C)天然ミックストコフェロー
ル800(商標名;埋研Eオイル800、理研ビタミン
油■製)及び(d)天然ミックストコフェロール600
(商標名;埋研Eオイル600、理研ビタミン油■製)
〔これらを総称してトコフェロール類という〕を用いた
Tocopherol and its acetate include (a)d
i-α-tocopherol (manufactured by Wako Tsumugi Pharmaceutical Co., Ltd.), (b) tocopherol acetate (trade name; Buken E Acetate 960, manufactured by Riken Vitamin Oil ■), (C) natural mixed tocopherol 800 (trade name; Buken E Oil 800) , manufactured by Riken Vitamin Oil ■) and (d) Natural Mixed Tocopherol 600
(Trade name: Buken E Oil 600, manufactured by Riken Vitamin Oil)
[These are collectively referred to as tocopherols] were used.

斯(して調製された電気蚊取器用マット(マット中の殺
虫成分の量:A)を表面温度164〜168℃の発熱体
上に置き、これを直径20ぼ、高さ20口のガラス円筒
に入れ上方をガラス板で密閉し3.6及び9時間通電加
熱して殺虫成分を揮散させた。
The thus prepared electric mosquito repellent mat (amount of insecticidal ingredient in the mat: A) was placed on a heating element with a surface temperature of 164 to 168°C, and this was placed in a glass cylinder with a diameter of 20 mm and a height of 20 holes. The container was placed in a container, the upper part of which was sealed with a glass plate, and heated with electricity for 3.6 and 9 hours to volatilize the insecticidal components.

3.6及び9時間経過後円筒内に浮遊している殺虫成分
を放冷して壁面に凝縮吸着させた後円筒を石油エーテル
にて洗浄しガスクロマトグラフィーで殺虫成分の揮散i
B)を調べ揮散率(−X100)を求める。
3. After 6 and 9 hours have elapsed, the insecticidal components floating in the cylinder are allowed to cool and are condensed and adsorbed on the wall surface, then the cylinder is washed with petroleum ether and the insecticidal components are volatilized by gas chromatography.
Examine B) and determine the volatilization rate (-X100).

その結果を第2表に示す。The results are shown in Table 2.

尚第2表中括弧で示した0〜6時間の揮散率は0〜3時
間の揮散率と3〜6時間の揮散率とを加えることにより
求めた。
The volatilization rate for 0 to 6 hours shown in parentheses in Table 2 was determined by adding the volatilization rate for 0 to 3 hours and the volatilization rate for 3 to 6 hours.

0〜9時間の揮散率についても同様である。The same applies to the volatilization rate for 0 to 9 hours.

また3、6及び9時間経過後マット中に残存する殺虫成
分の量(C)を測定し残在車(−xloO)を求める。
Further, after 3, 6, and 9 hours have elapsed, the amount (C) of the insecticidal component remaining in the mat is measured to determine the remaining amount (-xloO).

さらに上記で求めた揮散率と残存率から分解率を求める
Furthermore, the decomposition rate is determined from the volatilization rate and residual rate determined above.

A−(B+C) 分解率(%)= X100☆ このよう
にして求めた残存率及び分解率を第3表に示す。
A-(B+C) Decomposition rate (%) = X100☆ The residual rate and decomposition rate thus determined are shown in Table 3.

第2表及び第3表からトコフェロール類を配合すること
により殺虫成分を効率よく多量に揮散させ得ると共に加
熱による殺虫成分の熱分解を抑制し9時間経過後におい
ても揮散率が優れていることがわかる。
Tables 2 and 3 show that by blending tocopherols, it is possible to volatilize a large amount of insecticidal ingredients efficiently, and to suppress the thermal decomposition of insecticidal ingredients due to heating, resulting in an excellent volatilization rate even after 9 hours have passed. Recognize.

特に第2表に於て0〜3時間での揮散率は従来のものの
それに比べて約10%優れており3〜6時間及び6〜9
時間での揮散率は従来のもののそれに比べると約15%
と一段と優れたものとなり、殺虫効果が長時間持続され
ることがわかる。
In particular, Table 2 shows that the volatilization rate for 0 to 3 hours is approximately 10% superior to that of the conventional product, and for 3 to 6 hours and 6 to 9 hours.
The volatilization rate over time is approximately 15% compared to that of conventional products.
It can be seen that the insecticidal effect is even better and the insecticidal effect lasts for a long time.

而して0〜9時間の揮散率も従来のもののそれに比して
約30%以上という極めて高い値となっている。
The volatilization rate from 0 to 9 hours is also extremely high, about 30% or more, compared to that of conventional products.

実施例 2 実施例1で調製された電気蚊取器用マットを室温下に保
存し6ケ月、12ケ月及び24ケ月後ソックスレーにて
石油エーテルで抽出して経時的安定性をガスクロマトグ
ラフィーにより殺虫成分の含量を求めることにより試験
する。
Example 2 The electric mosquito repellent mat prepared in Example 1 was stored at room temperature, and after 6 months, 12 months, and 24 months, it was extracted with petroleum ether using a Soxhlet machine, and its stability over time was determined by gas chromatography. Test by determining the content of

その結果を第4表に示す。The results are shown in Table 4.

第4表から明らかなようにトコフェロール類ヲ配合した
ものは24ケ月経過しても殺虫成分の分解率は100%
以下であり貯蔵安定性に優れている。
As is clear from Table 4, the decomposition rate of insecticidal ingredients is 100% even after 24 months in products containing tocopherols.
It has excellent storage stability.

実施例 3 実施例1で調製された電気蚊取器用マットにつき通気装
置法〔殺虫剤効力試験法に関する研究論文集第2報勝田
純部1968.3月参照〕により殺虫効力を調べた。
Example 3 The insecticidal efficacy of the electric mosquito repellent mat prepared in Example 1 was examined using the aeration device method [see Collection of Research Papers on Insecticide Efficacy Testing Methods, Vol. 2, Junbe Katsuta, March 1968].

即ちアカイエカ雌成虫約20匹を放ち表面温度164〜
168℃の発熱体上にマットを置き、時間と落下抑転虫
数との関係を)25℃前後の温度条件下で観察する。
In other words, about 20 adult Culex Culex mosquitoes are released at a surface temperature of 164~
The mat was placed on a heating element at 168°C, and the relationship between time and the number of insects inhibited from falling was observed at a temperature of around 25°C.

これを3回繰返し相対効力を求める。This is repeated three times to determine the relative potency.

この結果を第1図に示す。The results are shown in FIG.

第1図から明らかな通りピナミンフォルテにトコフェロ
ール類を配合して得たマット(遥6及び; 扁8)は9
時間経過後においても高い落下抑転率を示し殺虫効力が
長時間持続されていることがわかる。
As is clear from Fig. 1, the matte obtained by blending tocopherols with Pinamin Forte (Haruka 6 and ; Bian 8) is 9.
It can be seen that the insecticidal effect is maintained for a long time, showing a high drop inhibition rate even after the passage of time.

一方ピナミンフォルテを吸収させたマット(&4)及び
ピナミンフォルテにBHTを添加しこれを吸収させたマ
ット(A5)は6時間経過後; その殺虫効力が急激に
低下している。
On the other hand, after 6 hours, the insecticidal efficacy of the mat (&4) in which Pinamin Forte was absorbed and the mat (A5) in which BHT was added and absorbed by Pinamin Forte decreased rapidly.

【図面の簡単な説明】[Brief explanation of drawings]

第1図は実施例3の記載の方法により測定した電気蚊取
器用マットの経時的殺虫効力を示すグラフである。
FIG. 1 is a graph showing the insecticidal efficacy of the electric mosquito repellent mat over time measured by the method described in Example 3.

Claims (1)

【特許請求の範囲】[Claims] 1 ピレスロイド系殺虫成分にトコフェロール及び/又
はトコフェロールの酢酸エステルを配合スることを特徴
とするピレスロイド系殺虫組成物。
1. A pyrethroid insecticidal composition comprising tocopherol and/or tocopherol acetate as a pyrethroid insecticidal ingredient.
JP51159568A 1976-12-29 1976-12-29 Pyrethroid insecticidal composition Expired JPS5926601B2 (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
JP51159568A JPS5926601B2 (en) 1976-12-29 1976-12-29 Pyrethroid insecticidal composition
GR53886A GR63567B (en) 1976-12-29 1977-07-05 Pyrethroid-type insecticidal compositions
GB5336377A GB1553805A (en) 1976-12-29 1977-12-21 Insecticidal compositions
IT526777A IT1089666B (en) 1976-12-29 1977-12-23 PYRETHRO INSECTICIDE COMPOUNDS
FR7739617A FR2375826A1 (en) 1976-12-29 1977-12-29 INSECTICIDE COMPOSITIONS BASED ON SUBSTANCES OF THE PYRETHROID TYPE

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP51159568A JPS5926601B2 (en) 1976-12-29 1976-12-29 Pyrethroid insecticidal composition

Publications (2)

Publication Number Publication Date
JPS5386023A JPS5386023A (en) 1978-07-29
JPS5926601B2 true JPS5926601B2 (en) 1984-06-29

Family

ID=15696556

Family Applications (1)

Application Number Title Priority Date Filing Date
JP51159568A Expired JPS5926601B2 (en) 1976-12-29 1976-12-29 Pyrethroid insecticidal composition

Country Status (5)

Country Link
JP (1) JPS5926601B2 (en)
FR (1) FR2375826A1 (en)
GB (1) GB1553805A (en)
GR (1) GR63567B (en)
IT (1) IT1089666B (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5756405A (en) * 1980-09-19 1982-04-05 Sumitomo Chem Co Ltd Stabilizing method
US4451482A (en) * 1982-04-22 1984-05-29 Shell Oil Company Method of preventing or ameliorating pyrethroid skin sensory stimulation
JPS60233001A (en) * 1984-05-07 1985-11-19 Earth Chem Corp Ltd Chemical solution composition for liquid absorbing core
US5591727A (en) * 1990-09-12 1997-01-07 Perycut-Chemie Ag Insecticidal composition
DE9013000U1 (en) * 1990-09-12 1991-10-10 Perycut-Chemie AG, Zürich Insecticidal composition
JP4660885B2 (en) * 2000-05-26 2011-03-30 住友化学株式会社 Electric mosquito mat

Also Published As

Publication number Publication date
JPS5386023A (en) 1978-07-29
FR2375826A1 (en) 1978-07-28
GB1553805A (en) 1979-10-10
IT1089666B (en) 1985-06-18
FR2375826B1 (en) 1980-02-01
GR63567B (en) 1979-11-20

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