JPS5946207A - Insecticide against nephotettix cincticeps uhlera - Google Patents

Insecticide against nephotettix cincticeps uhlera

Info

Publication number
JPS5946207A
JPS5946207A JP14312483A JP14312483A JPS5946207A JP S5946207 A JPS5946207 A JP S5946207A JP 14312483 A JP14312483 A JP 14312483A JP 14312483 A JP14312483 A JP 14312483A JP S5946207 A JPS5946207 A JP S5946207A
Authority
JP
Japan
Prior art keywords
uhlera
dimethyl
insecticide
acephate
pap
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
JP14312483A
Other languages
Japanese (ja)
Other versions
JPS6028806B2 (en
Inventor
Kentaro Nakaomi
中臣 謙太郎
Koichi Ishibe
石部 公一
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.)
Hokko Chemical Industry Co Ltd
Original Assignee
Hokko Chemical Industry 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 Hokko Chemical Industry Co Ltd filed Critical Hokko Chemical Industry Co Ltd
Priority to JP14312483A priority Critical patent/JPS6028806B2/en
Publication of JPS5946207A publication Critical patent/JPS5946207A/en
Publication of JPS6028806B2 publication Critical patent/JPS6028806B2/en
Expired legal-status Critical Current

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  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

PURPOSE:An insecticide against Nephotottix cincticeps Uhlera showing synergistic effect and different kinds of controlling effects obtained by adding only a small amount of ''acephate'' (O,S-dimethyl N-acetyl phosphoroamidothioate) to O,O-dimethyl S-[alpha-(ethoxycarbonyl)benzyl]phosphorothiolothionate. CONSTITUTION:Acephate is blended with O,O-dimethyl S-[alpha-(ethoxycarbonyl) benzyl]phosphorothiolothionate (PAP for short) to give an insecticide composition against Nephotettix cincticeps Uhlera. An insecticidal effect on Nephotettix cincticeps Uhlera can be increased synergistically only by adding a small amount of acephate to PAP. The blending can reduce further the concentration for practical use of each of the single agent, and can be used as an insecticide economically and safely without affecting any phytotoxicity to useful plants.

Description

【発明の詳細な説明】 較元明は01S−ジメチルN−ホスホロアミドチオエー
ト(以ドアセフエートと略称す―)、と、。
DETAILED DESCRIPTION OF THE INVENTION Caligenming is 01S-dimethyl N-phosphoroamidothioate (hereinafter abbreviated as acephate).

02O−ジメチルS−(α−(工トキシ力ルポニ几・)
ベンジル〕ホスホロチオロチオネート(以ドPAPと略
称する)とを有効成分として含・イJすることを特徴と
するツマグロヨコバイ防除剤組成物に関する。
02O-dimethyl S-(α-
The present invention relates to a leafhopper control agent composition containing benzyl phosphorothiorothionate (hereinafter abbreviated as PAP) as an active ingredient.

従来イ1槻燐系殺虫剤は我が国では水IBの主要害虫で
あるウンカ・ヨコバイ類、パニルメ、イ虫等の防除に特
効薬として重要な殺虫剤であり、多量に使用されている
。しかしなから使用される化合物によっては必ずしもそ
の効果が十分でなく、作物の生で1ト好ましくない結果
が現れており、これらの主要害虫に対する防除薬剤の開
発が急務となってきた。
BACKGROUND OF THE INVENTION In Japan, phosphorus-based insecticides are important insecticides as specific drugs for controlling planthoppers, leafhoppers, panirus, caterpillars, etc., which are major pests of water IB, and are used in large quantities. However, depending on the compound used, the effect is not always sufficient, and some unfavorable results have appeared on crops, and there has been an urgent need to develop control agents for these major pests.

木発明者らは、従来の有機燐系殺虫剤では効果のト分で
ないウンカ・ツマプロ類、−ニルメイ虫等λこ対しても
高い防除効果を奏しイする薬剤を開発す条ために種々研
究した。その結果アセフェ−1・とpAPとを含イ」す
る殺虫剤組成物がそれぞれ単独の有効成分化合物では効
果が1−分でないウンカ・ヨコバイ類に対して極めて高
い防除効果を発揮することを見出した。
The inventors conducted a variety of research in order to develop a drug that was highly effective in controlling planthoppers, planthoppers, and other insects that were not as effective with conventional organophosphorus insecticides. . As a result, it was found that an insecticide composition containing Acephe-1 and pAP exhibited an extremely high control effect against planthoppers and leafhoppers, which was not effective for 1 minute with each active ingredient alone. .

本発明に係る殺虫剤の防除効果は各有効成分を?11独
で使用した場合の相加効果からは予想もできない程の大
きな相乗効果を発・揮し、・単独成分を使用した場合に
は見られない異種の防除効果を発揮する・ 木発り1に係るツマグロヨコバイ防除剤組成物はアセフ
ェ−1・とPAPとを混合してなるものであリ、PAP
にアセフェートを少量添加するだけでPAPのツマグロ
ヨコバイに対する殺虫効果を相乗的に“増加させること
ができる。また混合することによって谷々単剤に於ける
実用濃度を一段と下−ぼることができ、有用植物に何ら
の薬害を与えることなく極めてfUれた薬剤であり、経
済的「1一つ安全に殺虫剤として使用することができる
。完全に殺虫の目的を達しうるものである。
What is the control effect of each active ingredient of the insecticide according to the present invention? 11 It exerts a great synergistic effect that cannot be predicted from the additive effect when used alone, and exerts a control effect on different species that cannot be seen when using individual ingredients. The leafhopper control agent composition according to the above is a mixture of Acephe-1 and PAP.
Adding a small amount of acephate to PAP can synergistically increase the insecticidal effect of PAP against leafhoppers.Additionally, by mixing it, the practical concentration of Taniya alone can be lowered even further, and it is possible to increase the effectiveness of PAP against leafhoppers. It is an extremely futuristic drug that does not cause any chemical damage to humans, and can be safely used as an economical insecticide.It can completely achieve the purpose of killing insects.

木゛発明に係るツマグロヨコバイ防除剤組成物は公知の
処方にて粉剤、乳剤、粉剤、水和剤、微粒i’il1等
の適宜の形態に調剤することができる。坦体としては農
園芸用薬剤に常用されるものなら固体または液体のいず
れでも使用でき、4¥定のものに限定されるものではな
い。例えば固体坦体としてはタルり、クレー、カオリン
、シリカ、けいそう(、、ベントナイト キジロール、メチルナフタレン、シクロヘキサノン等の
溶剤が挙げられるが、勿論これらに限定されるものでは
ない。また農園芸用薬剤に使用される補助剤、例えば乳
化剤、湿潤剤、展着剤,分散剤等を添加して効果の確実
向1−も期待できる。
The leafhopper control agent composition according to the present invention can be formulated into an appropriate form such as a powder, emulsion, powder, wettable powder, fine granules, etc. using a known formulation. As the carrier, any solid or liquid carrier commonly used for agricultural and horticultural chemicals can be used, and the carrier is not limited to ¥4. For example, solid carriers include, but are not limited to, solvents such as tar, clay, kaolin, silica, diatomaceous, bentonite, methylnaphthalene, and cyclohexanone. By adding auxiliary agents used in pharmaceuticals, such as emulsifiers, wetting agents, spreading agents, and dispersants, it is also possible to improve the effectiveness.

次に本発明に係るツマグロヨコバイ防除剤の実施例を若
干挙げるが、本発明は以トーの実施例に限定されるもの
ではない(以下実施例中、部は重量部を示す)。
Next, some examples of the leafhopper control agent according to the present invention will be listed, but the present invention is not limited to the following examples (in the following examples, parts indicate parts by weight).

実施例 I PAP40部、アセクレー11 0部、ナフタレンスル
ホン酸ソーダホルマリン3部、]・テシルベンゼンスル
ホン酩ソーダ5部およびクレー42部を均一に4部コ合
粉砕して水和剤を得る。
Example I 40 parts of PAP, 110 parts of aceclay, 3 parts of sodium naphthalene sulfonate formalin, 5 parts of sodium tesilbenzenesulfone and 42 parts of clay are uniformly combined and pulverized in 4 parts to obtain a wettable powder.

実施例 2 PAPZ部、アセフェ−1・1部、ホワイ1カーボン1
部、タルク20部およびクレー76部を均・に4部コ合
粉砕して粉剤を得る。
Example 2 PAPZ part, Acephe-1.1 part, Why 1 Carbon 1 part
1 part, 20 parts of talc, and 76 parts of clay were evenly ground together to obtain a powder.

実施例 3 FA−PL.5部、アセフェ−1・0.5部、PVA1
部およびクレー97部を均一に程合粉砕して、加水しな
がら転動造粒し、乾燥篩別して65〜250メツシユの
微粒剤を得る。
Example 3 FA-PL. 5 parts, Acephe-1.0.5 parts, PVA1
1 part and 97 parts of clay are uniformly pulverized, granulated by rolling while adding water, and dried and sieved to obtain fine granules of 65 to 250 mesh.

実施例 4 P p, P 4 BH、アセフェ−1・1部、ドデシ
ルベンゼンスルホン酪ソーダ1.5部、ヘン)・ナイト
l燥、整粒および篩別して釈1剤をIIる。
Example 4 P p, P 4 BH, 1.1 part of acephene, 1.5 parts of dodecylbenzenesulfone-butyric soda, 1.5 parts of dodecylbenzenesulfone-butyric soda, and night powder, dried, sized, and sieved to obtain a solution.

次に本発明に係るツマグロヨコバイ防除剤組成物の石川
性を試験例を挙げて囲体的に説明する。
Next, the Ishikawa properties of the leafhopper control agent composition according to the present invention will be comprehensively explained using test examples.

試験例1 ツマグロヨコ/<イに対する防除効果試験 鉢植水稲に所定濃度の薬液昂釈液をlOアール゛1′1
す100文の割合でヌブレーガンで均一・にIk hし
、散在2時間後に水稲の草葉部を切り取って試験’i’
i’ (i’i< 2 6 c m.長さ20cm)に
入れ、その試験管にツマグロヨコバイ♀成由(羽化5[
1後)を20匹放ち24時間後の仰転虫率を求めた。1
区5連性で試験し、xF均仰転虫率を算出した。次にそ
の試験結果を示せば第1表のとおりである。
Test Example 1 Test for the control effect on Prunus spp.
Ik h uniformly with a Nubra gun at a rate of 100 strands, and after 2 hours of scattering, cut out the grass part of the paddy rice and test 'I'.
i'(i'i< 2 6 cm. Length 20 cm), and put the black leafhopper ♀ (emergence 5 [
After 24 hours, 20 insects were released and the supine insect rate was determined. 1
The test was conducted in five consecutive plots, and the xF flattened insect rate was calculated. Next, the test results are shown in Table 1.

第1表Table 1

Claims (1)

【特許請求の範囲】[Claims] 0、S−ジメチルN−アセチルホスホロアミドチオニー
1・と0,0−ジメチルS−(α−(工トキシカルホニ
ル)ベンシル〕ホスホロチオロチ第2・−1・とを有効
成分として含有するこ・とを特徴とするツマグロヨコバ
イ防除剤組成物。
Containing 0,S-dimethyl N-acetylphosphoroamide thionyi 1. and 0,0-dimethyl S-(α-(ethoxycarphonyl)benzyl)phosphorothioloti 2.-1. as active ingredients. A characteristic composition for controlling leafhoppers.
JP14312483A 1983-08-06 1983-08-06 Leafhopper control agent Expired JPS6028806B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP14312483A JPS6028806B2 (en) 1983-08-06 1983-08-06 Leafhopper control agent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP14312483A JPS6028806B2 (en) 1983-08-06 1983-08-06 Leafhopper control agent

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
JP48124469A Division JPS5838406B2 (en) 1973-11-07 1973-11-07 Satsuki Yuzai Seibutsu

Publications (2)

Publication Number Publication Date
JPS5946207A true JPS5946207A (en) 1984-03-15
JPS6028806B2 JPS6028806B2 (en) 1985-07-06

Family

ID=15331470

Family Applications (1)

Application Number Title Priority Date Filing Date
JP14312483A Expired JPS6028806B2 (en) 1983-08-06 1983-08-06 Leafhopper control agent

Country Status (1)

Country Link
JP (1) JPS6028806B2 (en)

Also Published As

Publication number Publication date
JPS6028806B2 (en) 1985-07-06

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