JPS58203904A - Insecticidal composition - Google Patents

Insecticidal composition

Info

Publication number
JPS58203904A
JPS58203904A JP8852882A JP8852882A JPS58203904A JP S58203904 A JPS58203904 A JP S58203904A JP 8852882 A JP8852882 A JP 8852882A JP 8852882 A JP8852882 A JP 8852882A JP S58203904 A JPS58203904 A JP S58203904A
Authority
JP
Japan
Prior art keywords
insecticidal
effect
insects
thiodan
effective against
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.)
Pending
Application number
JP8852882A
Other languages
Japanese (ja)
Inventor
Takaaki Ito
伊藤 高明
Kunihiro Kawachi
邦弘 河地
Toshiaki Ozaki
俊明 尾崎
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.)
Sumitomo Chemical Co Ltd
Original Assignee
Sumitomo Chemical 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 Sumitomo Chemical Co Ltd filed Critical Sumitomo Chemical Co Ltd
Priority to JP8852882A priority Critical patent/JPS58203904A/en
Priority to ZA833764A priority patent/ZA833764B/en
Publication of JPS58203904A publication Critical patent/JPS58203904A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:An insecticidal composition for agricultural and gardening control, obtained by blending a specific compound with thiodan, having synergistic action of each insecticidal effect, effective against noxious insects resistant to insecticides, having low toxicity, prolonged effect, immediate insecticidal effect, and improved fatal effect. CONSTITUTION:alpha-Cyano-3 -phenoxybenzyl-2-( 4-chlorophenyl )isovalerate( containing optical isomer of acid side and alcohol side) shown by the formula, capable of being prepared easily and inexpensively, showing high insecticidal activity against various kinds of lepidopeterous larvae, leafhoppers, insects belonging to the genus Deltocephalidae, insects belonging to the genus Aphididae, cockroaches, etc., effective against noxious insects resistant to organophosphorus agent and carbamate-based insecticides, is blended with thiodan ( =6,7,8,9,10,10-hexachloro-1,5,5a,6,9,9a -hexahydro-6, 9-methano-2,4,3-benzodioxathiepin 3-oxide ) to give a mixture, a composition having low toxicity to men and beasts and low environmental pollution.

Description

【発明の詳細な説明】 本発明はa−シアノ−3−フェノキシベンジル −−(
4t−クロロフェニル)イソバレレート(以下化合物(
1)と称する)とチオダン(6゜7、に、?、/θ、/
θ−へキサクロロ−/。
DETAILED DESCRIPTION OF THE INVENTION The present invention provides a-cyano-3-phenoxybenzyl --(
4t-chlorophenyl)isovalerate (hereinafter compound (
1)) and thiodane (6゜7, ni, ?, /θ, /
θ-hexachloro-/.

3、jh、4.り、りIL’−Atキサハイドロ−6゜
?−メタノー、2,4t、J−ベンゾジオキサチェピン
 J−オキサイド(以下化合物(至)と称する))との
混合物を含有する殺虫組成物に関し、その目的は速効性
にして人畜に低毒性な環境汚染の少ない農園芸用防疫用
殺虫剤を安価に提供しようとするものである。
3, jh, 4. Ri, Ri IL'-At Kisahydro-6°? - Concerning an insecticidal composition containing a mixture of methanol, 2,4t, and J-benzodioxachepine J-oxide (hereinafter referred to as compound), its purpose is to be fast-acting and have low toxicity to humans and animals. The aim is to provide an inexpensive agricultural and horticultural epidemic prevention insecticide that causes less environmental pollution.

近年、水稲のツマグロミコバイやウンカ類、各種作物を
加害するハダニ類、家畜に寄生するやカーバメイト系殺
虫剤の実用性が危なくなって亀ている。
In recent years, the practicality of carbamate-based insecticides has become jeopardized as they infect paddy rice planthoppers and planthoppers, spider mites that damage various crops, and livestock.

そこで本発明者は有機リン剤やカーバメイト系殺虫剤に
抵抗性の発達した害虫に有効であり、しかも低毒性で、
速効性および残効性を持つ殺虫剤を開発すべく、鋭意研
究を進めた結果、上記の混合組成物がそれらの条件にあ
てはまる理想的な殺虫剤であることを見出した。
Therefore, the present inventor has developed a method that is effective against pests that have developed resistance to organophosphorus agents and carbamate insecticides, and is low in toxicity.
As a result of intensive research aimed at developing an insecticide with immediate and residual effects, it was discovered that the above-mentioned mixed composition is an ideal insecticide that satisfies these conditions.

しかもこの混合組成物の特徴は前記一種それぞれ単独で
の性質が相加わったものではなく、それぞれの殺虫効力
が相乗的に働くという新しい知見を得た。
Furthermore, we have obtained new knowledge that the characteristic of this mixed composition is not that the properties of each of the above-mentioned species are added to each other, but that the insecticidal effects of each species work synergistically.

本発明の混合組成物に含有されるチオダンは速効性に欠
ける嫌いがあり、残効性も充分とは言えない0また有機
リン剤低抗性の害虫には効果不十分である。
The thiodane contained in the mixed composition of the present invention tends to lack fast-acting properties, has insufficient residual effectiveness, and is insufficiently effective against pests with low resistance to organic phosphorus agents.

一方、本発明の混合組成物に含有される化合物(1)は
下記の構造を有する化合物である。
On the other hand, the compound (1) contained in the mixed composition of the present invention is a compound having the following structure.

(酸側およびアルコール鋼の光学異性体を含む。) この化合物は容易かつ安価に製造することができ、しか
も各種m翅目幼虫、ウンカ、ヨコバイ類、アブラムシ類
、ゴキブリ等の害虫にきわめて速効的に強い殺虫活性を
示し、有機リン剤やカーバメイト系殺虫剤に抵抗性の発
達した害虫にも有効である。しかしながら、浸透性に乏
しくハダニやアブラムシに対する効力は弱い。
(Contains optical isomers of acid side and alcohol steel.) This compound can be easily and inexpensively produced, and is extremely effective against pests such as larvae of various ptera, planthoppers, leafhoppers, aphids, and cockroaches. It exhibits strong insecticidal activity against insects that have developed resistance to organic phosphorus agents and carbamate insecticides. However, it has poor penetration and is less effective against spider mites and aphids.

これらの性質を異にする一種の化合物を混合することに
よって、両者の欠、、坐を改善することができた。その
上、殺虫剤抵抗性は解除され、残効、速効性殺虫効力お
よび欽死効カは相乗的に動くことを見出した。
By mixing a type of compound with different properties, it was possible to improve the deficiencies of both. Furthermore, it was found that insecticide resistance was eliminated, and that residual efficacy, immediate insecticidal efficacy, and killing efficacy worked synergistically.

以下に製剤例および実施例で本発明の詳細な説明するが
、本発明がこれらに限定されるものではない。
The present invention will be explained in detail below using formulation examples and examples, but the present invention is not limited thereto.

尚、下記の製剤例において部とは重量部を表わす。In addition, in the following formulation examples, parts represent parts by weight.

製剤例/ 乳 剤 化合物(1)70部、化合物G2−0部、ツルポール8
M−一〇〇(東邦化学登録商標名)70部およびキシレ
ン60部を加え、攪拌混合溶解すれば均質な乳剤を得る
Formulation example/emulsion Compound (1) 70 parts, Compound G2-0 parts, Tsurpol 8
Add 70 parts of M-100 (registered trademark of Toho Chemical) and 60 parts of xylene, stir, mix and dissolve to obtain a homogeneous emulsion.

製剤例コ 粉 剤 化合物0.2部、化合物一部を7セトン一θ部に溶解し
、タルクr0g部を加え、情潰器中にて充分攪拌混合し
た彼、7セトンを揮散させれは粉剤を得る。
Formulation Example Powder Dissolve 0.2 parts of the compound and a part of the compound in 7 parts of setone and 1 θ part, add 0 g of talc, stir thoroughly in a crusher, mix, and volatilize 7 setsone to form a powder. get.

製剤例3 水和剤 化合物(470部、化合物(I2)3部部、トクシノー
ル■−N(徳山曹達登録商標名)70部、ラジオライト
L(昭和化学商品名)111部およびツルポール39に
−G(東邦化学登録商標名)5部をよく混合すれば水利
剤を得る。
Formulation Example 3 Wettable powder compound (470 parts, Compound (I2) 3 parts, Toxinol ■-N (Tokuyama Soda registered trademark name) 70 parts, Radiolite L (Showa Kagaku brand name) 111 parts and Tsurupol 39-G (Toho Chemical registered trademark name) Mix 5 parts well to obtain an irrigation agent.

実施例/ 有機リン剤抵抗性系統のリンゴコカクモンハ
マキに対する殺虫効力 有機リン剤に抵抗性の発達し九圃場から採集したリン等
寓りモンハマキ2〜3令幼虫を、水さししたリンゴの枝
(長さ−03)に約7θ頭接撞し、製剤例3の水利剤を
水で希釈し、枝尚り/3dターンテーブル上で散布した
。散布後、経時的に落下仰転虫数を観察し1.24を時
間後に生死を調査した0爽験は3反復で行った。結果は
次に示す。
Example / Insecticidal efficacy against organophosphorus agent-resistant strains of apple tree rootworm larvae, which had developed resistance to organic phosphorus agents and were collected from nine fields. The irrigation agent of Formulation Example 3 was diluted with water and sprayed on a 3D turntable. After spraying, the number of fallen and supine insects was observed over time, and the survival and death tests were conducted 1.24 hours later.The zero-surge experiment was repeated three times. The results are shown below.

なお、化合物(1)および−)を、夫々製剤偽3に準じ
て水利剤を作製し、比較した。
In addition, compounds (1) and -) were respectively prepared into aquariums according to Preparation No. 3, and compared.

実施例−白菜害虫に対する圃場での効果率Jk/θ〜7
.2葉期に育った白菜に製剤例/の乳剤を水で希釈し、
以下の要領で散布し、散布/週間後に各区j株ぬき取り
各害虫の密度を調査した。
Example - Effectiveness rate Jk/θ~7 in the field against Chinese cabbage pests
.. Dilute the emulsion in formulation example/with water on Chinese cabbage that has grown to the two-leaf stage,
The seeds were sprayed in the following manner, and after one week of spraying, j plants were removed from each plot and the density of each pest was investigated.

品種ニー号白菜 区劃:7区6−3反復 散布: I301//θaになるようにハンドスブレヤ
ーにて散布 結果を次表に示す。
Cultivar Ni Chinese cabbage plot: 7 plots 6-3 repeated spraying: The results of spraying with a hand blower to achieve I301//θa are shown in the table below.

なお、化合物(1)および−)を夫々製剤例に準じて乳
剤を作製し、比較した。
In addition, emulsions of compounds (1) and -) were prepared according to the formulation example, and compared.

※ アオムシ、ヨトウムシについては3区合計虫数で示
し、ニセダイコンアブラムシについては、[−:全く認
められなかった。
* Regarding green caterpillars and armyworms, the total number of insects in the three areas is shown, and for false radish aphids, [-: Not observed at all.

〜+:かなり認められた。」の判定基準で示した。~+: Fairly recognized. ” criteria.

Claims (1)

【特許請求の範囲】[Claims] α−シアノ−3−フェノキシベンジル −−<tit−
クロロフェニル)イソバレレートとチオダンとの混合物
を含有することを特徴とする殺虫組成物。
α-cyano-3-phenoxybenzyl --<tit-
An insecticidal composition comprising a mixture of (chlorophenyl)isovalerate and thiodane.
JP8852882A 1982-05-24 1982-05-24 Insecticidal composition Pending JPS58203904A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
JP8852882A JPS58203904A (en) 1982-05-24 1982-05-24 Insecticidal composition
ZA833764A ZA833764B (en) 1982-05-24 1983-05-24 Insecticidal composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP8852882A JPS58203904A (en) 1982-05-24 1982-05-24 Insecticidal composition

Publications (1)

Publication Number Publication Date
JPS58203904A true JPS58203904A (en) 1983-11-28

Family

ID=13945334

Family Applications (1)

Application Number Title Priority Date Filing Date
JP8852882A Pending JPS58203904A (en) 1982-05-24 1982-05-24 Insecticidal composition

Country Status (2)

Country Link
JP (1) JPS58203904A (en)
ZA (1) ZA833764B (en)

Also Published As

Publication number Publication date
ZA833764B (en) 1984-04-25

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