JPS5946204B2 - insecticide composition - Google Patents

insecticide composition

Info

Publication number
JPS5946204B2
JPS5946204B2 JP56190670A JP19067081A JPS5946204B2 JP S5946204 B2 JPS5946204 B2 JP S5946204B2 JP 56190670 A JP56190670 A JP 56190670A JP 19067081 A JP19067081 A JP 19067081A JP S5946204 B2 JPS5946204 B2 JP S5946204B2
Authority
JP
Japan
Prior art keywords
parts
insecticide composition
effect
acephate
dmtp
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
JP56190670A
Other languages
Japanese (ja)
Other versions
JPS57118504A (en
Inventor
謙太郎 中臣
公一 石部
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 JP56190670A priority Critical patent/JPS5946204B2/en
Publication of JPS57118504A publication Critical patent/JPS57118504A/en
Publication of JPS5946204B2 publication Critical patent/JPS5946204B2/en
Expired legal-status Critical Current

Links

Landscapes

  • Agricultural Chemicals And Associated Chemicals (AREA)

Description

【発明の詳細な説明】 本発明は、02S−ジメチルN−アセチルホスホロアミ
ドチオエート(以下アセフェートという)と0,0−ジ
メチルS−〔5−メトキシ−2−オキソ−2,3−ジヒ
ドロ−1,3,4−)リアゾリル−(3)−メチル〕ホ
スホロチオロチオネート(以下DMTPという)とを有
効成分として含有してなることを特徴とする殺虫剤組成
物に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention provides 02S-dimethyl N-acetyl phosphoramidothioate (hereinafter referred to as acephate) and 0,0-dimethyl S-[5-methoxy-2-oxo-2,3-dihydro- The present invention relates to an insecticide composition containing 1,3,4-)riazolyl-(3)-methyl]phosphorothiorothionate (hereinafter referred to as DMTP) as an active ingredient.

ニアセフニート :DMTP 従来、有機燐系殺虫剤は、我国では疏菜、果樹の主要害
虫であるヨトウムシ、コカクモンハマキ、クワコナカイ
ガラムシなど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。
Niacefneet: DMTP Conventionally, organic phosphorus insecticides have been used in large quantities in Japan as a specific effective agent for controlling the major pests of cane and fruit trees, such as armyworm, black-spotted beetle, and mulberry mealybug.

しかしながら、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、作物の生育上好ましくない結果が
現われており、これらの主要害虫に対して有力な防除薬
剤の開発が急務となってきた。
However, depending on the compound used, the effect is not always sufficient and undesirable results have appeared in terms of crop growth, and there has been an urgent need to develop effective control agents against these major pests.

本発明者らは、従来の有機燐系殺虫剤では効果の十分で
ないヨトウムシ、コカクモンハマキ、クワコナカイガラ
ムシなどに対しても高い防除効果を奏し得る薬剤を開発
するため種々研究した。
The present inventors have carried out various studies in order to develop a drug that can exhibit a high control effect against armyworms, brown leaf beetles, mulberry scale insects, etc., for which conventional organophosphorus insecticides are not sufficiently effective.

その結果、アセフェートとDMTPとを含有する殺虫剤
組成物が、それぞれ単独の有効成分化合物では効果の十
分でないヨトウムシ、コカクモンハマキ、クワコナカイ
ガラムシなどに対して、極めて高い防除効果を発揮する
ことを見出した。
As a result, it was found that an insecticide composition containing acephate and DMTP exhibits an extremely high control effect against armyworms, brown leaf beetles, mulberry scale insects, etc., for which each active ingredient alone is not sufficiently effective. .

本発明の殺虫剤組成物の防除効果は、各有効成分を単独
で施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、単独成分を施行した場合には見
られない異種の防除効果を発揮する。
The pest control effect of the insecticide composition of the present invention exhibits a synergistic effect that is unimaginable from the additive effect when each active ingredient is applied alone, and is not observed when each active ingredient is applied alone. Demonstrates the effect of controlling different species.

本発明の殺虫剤組成物は、アセフェートとDMTPとを
混合してなるものであるが、アセフェートにDMTPを
少量添加するだけでアセフェートの殺虫効果を相乗的に
増加させることができる。
The insecticide composition of the present invention is a mixture of acephate and DMTP, and the insecticidal effect of acephate can be synergistically increased by simply adding a small amount of DMTP to acephate.

また、DMTPにアセフェートを少量添加して使用すれ
ばDMTPの殺虫効果を相乗的に増加させることができ
る。
Furthermore, if a small amount of acephate is added to DMTP and used, the insecticidal effect of DMTP can be increased synergistically.

さらに、本発明の殺虫剤組成物は、ウンカ・ヨコバイ類
、ニカメイ虫等の水稲害虫、アオムシ、コナガ、ハスモ
ンヨトウ、アブラムシ類などの疏菜害虫ならびにハムグ
リガ、ダニ類などの果樹害虫に対しても単独成分を施用
した場合の効果をはるかに上まわる高い防除効果を発揮
する。
Furthermore, the insecticide composition of the present invention is also effective against paddy rice pests such as planthoppers, leafhoppers, and cutworms; cane pests such as green caterpillars, mealybugs, cutworms, and aphids; and fruit tree pests such as cutworm moths and mites. It exhibits a high pest control effect that far exceeds the effect of applying other ingredients.

本発明の殺虫剤組成物は、公知の処方にて粉剤、乳剤、
粒剤、水和剤、微粒剤などの適宜の形態に調剤すること
ができる。
The insecticide composition of the present invention can be prepared as a powder, emulsion, or
It can be prepared into appropriate forms such as granules, wettable powders, and fine granules.

担体としては、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、特定のものに限定さ
れるものではない。
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 a specific carrier.

例えば、固体担体としては、タルク、クレー、カオリン
、シリカ、けいそう土、ベントナイトなどが挙げられ、
液体担体としては、キジロール、メチルナフタレン、シ
クロヘキサノンなど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。
For example, solid carriers include talc, clay, kaolin, silica, diatomaceous earth, bentonite, etc.
Liquid carriers include, but are not limited to, solvents such as quidylol, methylnaphthalene, and cyclohexanone.

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、分散剤などを添加して効果の確実向
上も期待できる。
Furthermore, by adding auxiliary agents used in agricultural and horticultural chemicals, such as emulsifying agents, wetting agents, spreading agents, and dispersing agents, it is possible to surely improve the effectiveness.

次に、本発明の殺虫剤組成物の実施例を若干挙げるが、
本発明は以下の実施例に限定されるものではない。
Next, some examples of the insecticide composition of the present invention will be listed.
The present invention is not limited to the following examples.

なお、以下実施例中部は重量部を示す。Note that the middle part of the examples below indicates parts by weight.

実施例 1 (水和剤) DMTP25部、アセフェート25部、ナフタレンスル
ホン酸ソーダホルマリン縮金物3部、ドデシルベンゼン
スルホン酸ソーダ5部およびクレー42部を均一に混合
粉砕して水和剤を得る。
Example 1 (Wettable powder) A wettable powder is obtained by uniformly mixing and pulverizing 25 parts of DMTP, 25 parts of acephate, 3 parts of sodium naphthalenesulfonate formalin condensate, 5 parts of sodium dodecylbenzenesulfonate and 42 parts of clay.

実施例 2 (粉剤) DMTPZ部、アセフェート1部、ホワイトカーボン1
部、タルク20部およびクレー76部を均一に混合粉砕
して粉剤を得る。
Example 2 (powder) DMTPZ part, acephate 1 part, white carbon 1 part
1 part, 20 parts of talc, and 76 parts of clay are uniformly mixed and pulverized to obtain a powder.

実施例 3 (微粒剤) DMTPI部、アセフェート1部、PVA1部およびク
レニ97部を均一に混合粉砕して、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 (Fine Granules) A part of DMTPI, 1 part of acephate, 1 part of PVA and 97 parts of Creni are uniformly mixed and pulverized, granulated by rolling while adding water, dried and sieved to obtain a fine granule of 65 to 250 mesh.

実施例 4 (粒剤) DMTP1部、アセフェート4部、ドデシルベ1 ンゼ
゛/スルホン酸ソーダ1.5部、ベントナイト10部お
よびクレー83.5部を均一に混合した後、加水練合し
押出し造粒機にて造粒した後乾燥、整粒および篩別して
粒剤を得る。
Example 4 (Granules) After uniformly mixing 1 part of DMTP, 4 parts of acephate, 1.5 parts of dodecyl bene/sodium sulfonate, 10 parts of bentonite and 83.5 parts of clay, the mixture was kneaded with water and extruded into granules. After being granulated in a machine, it is dried, sized and sieved to obtain granules.

次に、本発明の殺虫剤組成物の有用性を試験例を挙げて
具体的に説明する。
Next, the usefulness of the insecticide composition of the present invention will be specifically explained using test examples.

試験例 1 クワコナ力イガラムシに対する防除効果試験試験方法と
しては、カポチャにクワコナ力イガラムシのト令幼虫を
約50匹寄生させ、そのカポ; チャを細片としてカポ
チャごと所定濃度薬液に10秒間浸漬処理し、その細片
を径9crfLのペトリシャーレに入れ、24時間後の
仰転虫率(至)を調べた。
Test Example 1 Testing the control effect against the Quercus vulgare The test method was to parasitize Kapocha with about 50 instar larvae of the Quercus Quercus larvae, and immerse the Kapocha in small pieces in a chemical solution with a predetermined concentration for 10 seconds. The strips were placed in a Petri dish with a diameter of 9 crfL, and the rate of turning insects after 24 hours was determined.

試験は1区3連制で行い、平均仰転虫率を算出した。The test was conducted in 1 section in triplicate, and the average supine insect rate was calculated.

その試験結果は第1表のとおりである。PMPはジエチ
ル−8−(フタルイミドメチル)ホスホロチオロチオネ
ートを有効成分とする市販の殺虫剤である。
The test results are shown in Table 1. PMP is a commercially available insecticide containing diethyl-8-(phthalimidomethyl)phosphorothiorothionate as an active ingredient.

第1表のデータに基づいて、カーペンタ−の式によりL
C6o値(50%致死薬剤濃度)およびLC9o(90
%致死薬剤濃度)の期待値を求め、実測値との対比から
共力塵を算出した。
Based on the data in Table 1, L is calculated by Carpenter's equation.
C6o value (50% lethal drug concentration) and LC9o (90
The expected value of %lethal drug concentration) was determined, and the synergistic dust was calculated from the comparison with the actual value.

この場合、共力塵が1は相加的な効果を示し、1より小
さい場合は拮抗的な効果を示し、1より大きい場合は相
乗的な効果を示し、特に2以上の場合には相乗的殺虫作
用が顕著であることを示す。
In this case, a synergistic value of 1 indicates an additive effect, a value less than 1 indicates an antagonistic effect, a value greater than 1 indicates a synergistic effect, and a value of 2 or more indicates a synergistic effect. Indicates that the insecticidal effect is significant.

その結果は第2表のとおりである。The results are shown in Table 2.

Claims (1)

【特許請求の範囲】 1式 で表わされる02S−ジメチルN−アセチルホスホロア
ミドチオレートと式 で表わされる0、O−ジメチル5−(5−メトキシ−2
−オキソ−2,3−ジヒドロ−1,3,4−トリアゾリ
ル−(3)−メチル〕ホスホロチオロチオネートとを有
効成分として含有することを特徴とする殺虫剤組成物。
[Scope of Claims] 02S-dimethyl N-acetyl phosphoroamide thiolate represented by the formula 1 and 0,O-dimethyl 5-(5-methoxy-2
-oxo-2,3-dihydro-1,3,4-triazolyl-(3)-methyl]phosphorothiolothionate as an active ingredient.
JP56190670A 1981-11-30 1981-11-30 insecticide composition Expired JPS5946204B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP56190670A JPS5946204B2 (en) 1981-11-30 1981-11-30 insecticide composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56190670A JPS5946204B2 (en) 1981-11-30 1981-11-30 insecticide composition

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
JP48118424A Division JPS5747647B2 (en) 1973-10-20 1973-10-20

Publications (2)

Publication Number Publication Date
JPS57118504A JPS57118504A (en) 1982-07-23
JPS5946204B2 true JPS5946204B2 (en) 1984-11-10

Family

ID=16261934

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56190670A Expired JPS5946204B2 (en) 1981-11-30 1981-11-30 insecticide composition

Country Status (1)

Country Link
JP (1) JPS5946204B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2020057391A1 (en) * 2018-09-20 2020-03-26 周银平 Preparation of pyridazinyl amine compound and application thereof

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2020057391A1 (en) * 2018-09-20 2020-03-26 周银平 Preparation of pyridazinyl amine compound and application thereof

Also Published As

Publication number Publication date
JPS57118504A (en) 1982-07-23

Similar Documents

Publication Publication Date Title
CA1169769A (en) Synergistic insecticidal compositions
EP0163855B1 (en) Nitromethylene derivatives, intermediates, and process for their preparation as insecticides
JPH0629256B2 (en) Nitromethylene-tetrahydropyrimidine derivative, production method and insecticide, acaricide, sentinelicide
JP3086924B2 (en) Insecticidal composition
JPH0791166B2 (en) Insecticidal composition
US4014882A (en) Trifluoromethyl substituted pyrimidine derivatives useful as insecticides
JPS5946204B2 (en) insecticide composition
US3932631A (en) Certain organophosphorus compounds used to control insects
JPS5926634B2 (en) O-ethyl-S-n-propyl-O-2,2,2-trihaloethyl-phosphorothiolate or -thionothiolate, its production method, and insecticide, acaricide, and nematocide containing it as an active ingredient
US2367534A (en) Parasiticides
IL37390A (en) Imidazolyl-alkyl-thiophosphates and thiophosphonates,their manufacture and their use as pesticides
JPH10510299A (en) Hydrazine derivatives
EP0007020A1 (en) Organic phosphoric-acid esters, process for their preparation, their use, pesticides and their preparation
EP0139156B1 (en) Novel phosphoroamido (di) thioate derivatives, pesticidal compositions containing them and the use of the novel derivatives for combating pests
JPS604838B2 (en) Organic phosphoric acid amide ester, its manufacturing process, and insecticide, acaricide, or nematocide
JP3283592B2 (en) Organophosphorus compounds, process for producing the same, and insecticides, miticides and nematicides containing the compounds
CA1047497A (en) Heterocyclic derivative
JPS604839B2 (en) Organic phosphoric acid amide ester, its manufacturing process, and insecticide, acaricide, or nematocide
KR100711325B1 (en) Insecticidal oxadiazine compounds
JPH06227909A (en) Insecticidal composition
CA1050567A (en) Formamidines
JPS5839803B2 (en) insecticide composition
DE69428109T2 (en) Organophosphorus compounds, processes for their preparation and insecticides, acaricides and nematocides containing them
JPS5946203B2 (en) insecticide composition
JP4698729B2 (en) Acaricide triazolidine derivatives