JPS5824505A - Insecticidal composition - Google Patents

Insecticidal composition

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Publication number
JPS5824505A
JPS5824505A JP12346381A JP12346381A JPS5824505A JP S5824505 A JPS5824505 A JP S5824505A JP 12346381 A JP12346381 A JP 12346381A JP 12346381 A JP12346381 A JP 12346381A JP S5824505 A JPS5824505 A JP S5824505A
Authority
JP
Japan
Prior art keywords
composition
insecticidal
compound
present
planthoppers
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
JP12346381A
Other languages
Japanese (ja)
Inventor
Yoji Takahashi
高橋 洋治
Nobuo Okimura
伸夫 興村
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.)
Mitsubishi Kasei Corp
Original Assignee
Mitsubishi Kasei Corp
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 Mitsubishi Kasei Corp filed Critical Mitsubishi Kasei Corp
Priority to JP12346381A priority Critical patent/JPS5824505A/en
Publication of JPS5824505A publication Critical patent/JPS5824505A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:An insecticidal composition, containing a specific oxadiazoline compound and a specific organophosphorus compound, having remarkably improved insecticidal effects by the synergistic effect thereof, and effective for insects, e.g. brown planthopper or rice stem borer. CONSTITUTION:An insecticidal composition containing 2-methoxy-4-(2-methoxyphenyl)-1,3,4-oxadiazolin-5-one and an organophosphorus compound having a dialkylthio or dialkyloxy group, e.g. S,S,S-tributyl phosphorothioate, at a weight ratio of preferably 1:(0.5-2). The resultant composition exhibits excellent insecticidal effects particularly on planthoppers.

Description

【発明の詳細な説明】 本発明は特定のオキサジアゾリン化合物および特定の有
機リン系化合物を含有する殺虫剤組成物に関するもので
ある。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an insecticide composition containing a specific oxadiazoline compound and a specific organophosphorus compound.

オキサジアゾリン化合物が、殺虫、殺ダニ、殺線虫効果
を有することは周知である(特開昭j/−10/91/
号公報)、また、2−メトキシ−亭−(J−メトキシフ
ェニル) −i、s、q−オキナシアゾリン−3−オン
が稲栽培における害虫であるツマグロヨコバイに対して
高い殺虫効果を有することが知られている(特開昭j番
−!りtOS号公報)。
It is well known that oxadiazoline compounds have insecticidal, acaricidal, and nematocidal effects (Japanese Patent Application Laid-Open No. 2003-109003-10/91/
It is also known that 2-methoxy-tei-(J-methoxyphenyl)-i, s, q-okinasiazolin-3-one has a high insecticidal effect against leafhopper, which is a pest in rice cultivation. (Japanese Unexamined Patent Publication No. Shoj-!ritOS).

しかしながら、本発明者等の検討によnば。However, according to the studies of the present inventors.

1−メトキシ−ター(コーメトキシフェニル)−/、j
、亭−オキサジアゾリン−!−オンは、特に、トビイロ
ウンカ、セジ霞ウンカ、ヒメトビウンカ等のウンカ類に
対する殺虫効果が未だ不十分で多った・ 本発明者擲は、かかる点に留意して鋭意検討した結果、
コーメトキシーw−(J−メトキシフェニル) −i、
3.*−オキサジアゾリン−5−することを知得し1本
発l11t−完成するに到った。
1-methoxy-ter(co-methoxyphenyl)-/, j
, Tei - Oxadiazoline -! In particular, the insecticidal effect of on planthoppers against planthoppers such as brown planthoppers, white-legged planthoppers, and brown-bottomed planthoppers was still insufficient.The inventors of the present invention, after careful consideration and consideration of these points, found that
Comethoxyw-(J-methoxyphenyl)-i,
3. *-Oxadiazoline-5- was learned and completed in one batch.

すなわち、本発明の要旨は、コーメトキシー亭−(コー
メトキシフェニル) −/、J、41−オキサジアゾリ
ン−!−オンおよびジアルキルチオ基tたはジアルキル
オキシ基を有する有機リン系化合物を含有することを特
徴とする殺虫剤組成物に存する。
That is, the gist of the present invention is comethoxytei-(comethoxyphenyl)-/, J, 41-oxadiazoline-! An insecticide composition characterized by containing an organophosphorus compound having -one and a dialkylthio group or a dialkyloxy group.

以下1本発明を説明する忙1本発明の殺虫剤組成物(以
下「本発明組成物」という)の第1成分は、J−メトキ
シ−亭−(J−メトキシフェニル)−’eJ*ダーオキ
サジアゾリンー!−オン(以下「化合゛物ム」という)
であり、前述のように殺虫効果を有する。
The first component of the insecticide composition of the present invention (hereinafter referred to as "the composition of the present invention") is J-methoxy-tei-(J-methoxyphenyl)-'eJ*deroxa. Diazoline! -on (hereinafter referred to as "compound")
As mentioned above, it has an insecticidal effect.

iた1本発明組成物の第2成分は、ジアルキルチオ基壇
たはジアルキルオキシ基、を有する有機リン系化合物で
あり1周知の種々のものが使用できる。異体的には1例
えば、8,1.1−)リオエート(x勝F)、$−(メ
チルチオ)フェニル ジブ−ビルホスフェート(Pr@
pak*s)、0・ / 一エテル8.8−ジグロピル ホスホ賞ジテオエート、
参−にトa)フェニル ジプロピルホスフェ−)、I、
II−ジー1−プロピル N−1−プロピル ホスホ−
アミドジチオネート(I)、8.8−ジー鳳−プ・チル
 N−n−プロピル ホスホロア2ドチオエートアルキ
ル 8.11−ジー墓−プロビル N −m−プロピル
 ホスホロアミドトリチオニー)[)、 S、S−ジー
1−ブチル N−1−プロピル ホスホロアミドトリチ
オエート(ト)、0.0−ジ−ミープロピル ドーn−
プ四ピル ホスホ四アミデート、0.0−ジー1−ブチ
ル N−プロピル ホスホロア2ドチオエート等が挙げ
られる。好ましくは、DIF、II?、Propmph
@s I I s I s Iおよび■、特に好ましく
は、DIF、IIIPおよびPropaph*−が挙げ
も詐る。
The second component of the composition of the present invention is an organic phosphorus compound having a dialkylthio group or a dialkyloxy group, and various known compounds can be used. For example, 8,1.1-) lyoate (xKatsu F), $-(methylthio)phenyl dibu-vinyl phosphate (Pr@
pak*s), 0/monoether 8.8-diglopyr phosphor ditheoate,
Reference a) phenyl dipropyl phosphate), I,
II-di-1-propyl N-1-propyl phospho-
Amidodithionate (I), 8.8-Propyl N-n-propyl phosphoro-2-dothioate alkyl 8.11-Propyl N-m-propyl Phosphoramide trithiony) [), S, S-di-1-butyl N-1-propyl phosphoroamide trithioate (t), 0.0-di-1-butyl do n-
Examples include tetrapyl phosphotetraamidate, 0.0-di-1-butyl N-propyl phosphoroa 2-dothioate, and the like. Preferably DIF, II? , Propmph
@s I I s I s I and ■, particularly preferably DIF, IIIP and Propaph*-.

本発明組成物の第1成分は、それ単独でもウンカII岬
に対しある程度の殺虫効果を示すが未だ不十分である。
Although the first component of the composition of the present invention alone exhibits a certain degree of insecticidal effect on Cape Planthopper II, it is still insufficient.

tた。第コ成分は、化合物により殺虫効果の程度は異な
り、はとんど殺與効#− 果を示さないものからある程度の殺虫効果を示すもOま
であるが、いずnもそn単独では十分な殺虫効果とはい
えない。ところが、これら1がみ2られるのである・ 本発明組成物のこの様な相−効果は、トビイロウンカ、
セジロウン力、ヒメトビウンカ岬のウンカ類、その他、
ニカメイチュウやアズキゾウムシ等の昆虫に対して顕著
で″ある。これ忙対し、化合物ムが殺虫効果と同様に殺
ダニ効果を示すことが報告されているKもかかわらず、
後述の比較例に示すように、ナ2ハダニに対して乗 本発明組成物は相鋪効果を示さなかった。仁のことは1
本発明組成物の効果は昆虫に対して特有の現象と思われ
る。
It was. The degree of the insecticidal effect of the third component varies depending on the compound, ranging from almost no insecticidal effect to some degree of insecticidal effect, but it is not sufficient to use it alone. It cannot be said that it has an insecticidal effect. However, these 1 and 2 effects have been observed.Such a synergistic effect of the composition of the present invention is caused by the brown planthopper, brown planthopper,
White-winged planthopper, Cape hopper, and others.
This is particularly true for insects such as the Japanese beetle weevil and the red bean weevil.
As shown in the Comparative Example below, the composition of the present invention did not show any competitive effect on two spider mites. About Jin 1
The effect of the composition of the present invention appears to be a phenomenon unique to insects.

本発v41ili1成物において、上記第1成分および
第1成分の使用割合は、通常、第1成分1重量gK対し
て第1成分aコ〜!重量部、好ましくは、a!〜−重量
部の範囲から選ばれる。
In the v41ili1 composition of the present invention, the above-mentioned first component and the ratio of the first component to be used are usually a to 1 weight gK of the first component! Parts by weight, preferably a! ~- parts by weight.

本発明組成物は、上記第1成分および第1成分の他に、
アセトン、メチルアルコール等の液浸透剤等の公知の種
々の添加剤を含んでいてもよい。
In addition to the first component and the first component, the composition of the present invention includes:
It may contain various known additives such as liquid penetrants such as acetone and methyl alcohol.

本発明組成物の使用形態は特に限定されるものではない
が、通常、乳剤、粉剤、水利剤、粒剤等の形で使用さn
る。特に、乳剤、粉剤の形で使用するのが好ましい赫 本発明組成物の施用量は、使用形態によって異なるが、
通常、有効成分として、20〜コ00f//Da 、好
ましく#i!0〜/コO7710m の範超かも選ばれ
る。特に、乳剤の場合はj0〜10f/10* 、粉剤
の場合は60〜/ J 011/10*の範囲から選ば
れる。
The form of use of the composition of the present invention is not particularly limited, but it is usually used in the form of an emulsion, a powder, an aqueous solution, a granule, etc.
Ru. In particular, the application amount of the composition of the present invention, which is preferably used in the form of an emulsion or a powder, varies depending on the form of use;
Usually, the active ingredient is 20~00f//Da, preferably #i! 0~/ko7710m may also be selected. In particular, it is selected from the range of j0 to 10f/10* for emulsions and from 60 to /J011/10* for powders.

かくして得らnる本発明組成物は、昆虫、特に、稲栽培
における重要害虫であるウンカ類に対し、極めて優f’
L危殺虫効果を示すのである・以下、実施例を挙げて更
に本発明を具体的に説明する。
The composition of the present invention thus obtained is extremely effective against insects, especially planthoppers, which are important pests in rice cultivation.
The present invention will be explained in more detail below with reference to examples.

製剤例1 化合物ムJi7ダをアセトンj−に溶解し、これに1ツ
ルポール”soo!rX(商品名:東邦化学工業製、界
面活性剤)の100 ppm液デ3−を加え、化合物ム
の200ppm*t−得た。
Formulation Example 1 Compound Muji7da was dissolved in acetone j-, 100 ppm liquid De3- of 1Tsurpol "soo! *t-obtained.

製剤例コ 化合物A10ダおよびDIFlolipをアセトンjs
gK溶解し、とnにツルポールJOOIXのJoopν
鵬液をデjm加え、化合物ムとf)CFの組成液(混合
比/:/)のJ 00 ppm液を得友・ 製剤例J 化合物ムI重量部、DEF/重量部及びタレーyt’3
11量部とを乳鉢にて均一に混合粉砕して平均粒径約3
0μの粉剤を得た。
Formulation Example Compound A10 da and DIFlolip in acetone js
Dissolve gK, and joopv of Tsurpol JOOIX to n
Add J00 ppm solution of Compound M and f) CF composition solution (mixing ratio /:/).
11 parts in a mortar and pulverized uniformly to obtain an average particle size of approximately 3.
A powder of 0μ was obtained.

実施例1 トビイロウンカの絡合幼虫10頭を、直径JG、高さ/
1cI11のガラス円筒に稲の苗と共に入n、−〇メツ
シュの金網で蓋をし友。次いで、ガラス円筒内部に製剤
例1またはコに準じて調製し*i!/に示す成分を含有
する薬液(2!rdlt−噴霧し、J#時間後O死虫率
を測定した。この試験IJ回繰ヤ返し、その平均死虫率
を表/に示した。
Example 1 Ten entangled larvae of brown planthopper, diameter JG, height/
Place the rice seedlings in a 1cI11 glass cylinder and cover with a mesh wire mesh. Next, prepare according to Formulation Example 1 or 1 inside the glass cylinder *i! A chemical solution (2!rdlt-) containing the components shown in / was sprayed, and the O insect mortality rate was measured after J# hours. This test was repeated IJ times, and the average mortality rate is shown in Table /.

表  l 実施例コ ニカメイチュウの絡合幼虫!頭を、製剤例1ま友は−で
調製した表2に示す成分を含有する薬液中で30秒間浸
漬処理した。この幼虫を、前記と同じ薬液中で/分間浸
漬後風乾した稲の芽出しを約コO木入っているシャーレ
(l[径ajcs、高さ1Jcts)にスれ、コク時間
後の死生率を測定した。この試験t−ダ回繰り返し、そ
の平均死去率を表JK示した。
Table 1 Example of entangled larvae of Konica Meichu! The head was immersed for 30 seconds in a chemical solution prepared in Formulation Example 1 and containing the ingredients shown in Table 2. The larvae were immersed in the same chemical solution as above for 1 minute, and then the air-dried rice sprouts were placed in a petri dish (diameter: 1 Jcts, height: 1 Jcts) containing about 100 ml of rice, and the mortality rate was measured after the soaking time. did. This test was repeated t times, and the average mortality rate is shown in Table JK.

表  1 実施例3 アズキゾウムシの成虫1084を、直径J1?lI、高
さ/33のガラス円筒に入れ、コ。メツシュの金鋼で蓋
をした0次いで、ガラス円筒内部に製剤例1ま九はコに
準じて調製しt表、7に示す成分を含有する薬液Q!−
を噴霧し、コク時間後の死生率を測定した。この試験t
−−回繰り返し、その平均死去率を表3に示し友。
Table 1 Example 3 Adzuki bean weevil adult 1084 was grown in diameter J1? Place it in a glass cylinder with a height of /33. A drug solution Q containing the ingredients shown in Table 7 was prepared according to Preparation Example 1 and 9, and was then placed inside a glass cylinder with a lid made of mesh gold steel. −
was sprayed, and the mortality rate was measured after a period of time. This test
-- times and the average mortality rate is shown in Table 3.

表  3 比較例1 インゲンの葉に接種したナミハダニ約30頭を、製剤例
/1fI−は2に準じて調製し皮表亭に示す成分を含有
する薬液中Ky秒間葉ごと浸漬した。浸漬後、*が枯れ
ないように水の入った試験管に挿し、2参時間vkK実
体顕微鏡の下で生死1m察して死生率を測定した。この
試験を一回繰シ返し、その平均死去率をfJaに示した
Table 3 Comparative Example 1 Approximately 30 two-spotted spider mites inoculated onto green bean leaves were immersed with the leaves for Ky seconds in a chemical solution prepared according to Formulation Example/1fI-2 and containing the ingredients shown in the table below. After soaking, the specimen was placed in a test tube containing water to prevent it from withering, and the survival rate was measured by observing the specimen for 1 m under a VKK stereomicroscope for 2 hours. This test was repeated once, and the average mortality rate was expressed as fJa.

実施例亭 トビイロウンカの雌成虫10頭を、直径J 3 。Example-tei 10 female adult brown planthoppers, diameter J3.

高さJi7cmの金銅円筒(20メツシユ)に3葉期の
稲の苗と共に入れ几、こnに製剤例3に準じて調製し友
表3に示す成分を含有する粉剤200ダ(ダに#/ /
Daの施用量に相当)を散布し、2時間後およびIり時
間の死生率を測定した。この試験t−e回繰り返し、そ
の平均死去率を表3に示した。
Place the rice seedlings at the 3-leaf stage in a gilt bronze cylinder (20 mesh) with a height of 7 cm, and then add 200 mesh powder (20 mesh) prepared according to Formulation Example 3 and containing the ingredients shown in Table 3. /
(equivalent to the applied amount of Da) was applied, and the mortality rate was measured 2 hours later and after 1 hour. This test was repeated te times, and the average mortality rate is shown in Table 3.

表  3 出願人  三菱化成工業株式会社 C2か l 石Table 3 Applicant: Mitsubishi Chemical Industries, Ltd. C2 or l stone

Claims (1)

【特許請求の範囲】[Claims] (1)2−メトキシ−参−(J−メトキシフエニy )
 −7J、亭−オキサジアゾリン−!−オンおよびジア
ルキルチオ基t7tはジアルキルオキシ基を有する有機
リン系化合物を含有することを特徴とする殺虫剤組成物
(1) 2-Methoxy-(J-methoxyphenyl)
-7J, Tei-Oxadiazoline-! An insecticide composition characterized in that -one and the dialkylthio group t7t contain an organic phosphorus compound having a dialkyloxy group.
JP12346381A 1981-08-06 1981-08-06 Insecticidal composition Pending JPS5824505A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP12346381A JPS5824505A (en) 1981-08-06 1981-08-06 Insecticidal composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP12346381A JPS5824505A (en) 1981-08-06 1981-08-06 Insecticidal composition

Publications (1)

Publication Number Publication Date
JPS5824505A true JPS5824505A (en) 1983-02-14

Family

ID=14861247

Family Applications (1)

Application Number Title Priority Date Filing Date
JP12346381A Pending JPS5824505A (en) 1981-08-06 1981-08-06 Insecticidal composition

Country Status (1)

Country Link
JP (1) JPS5824505A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4562062A (en) * 1983-06-10 1985-12-31 Sumitomo Chemical Company, Limited Insecticidal composition comprising synergistic combinations of 3-(2-methoxyphenyl)-5-methoxy-1,3,4-oxadiazol-2(3H)-one and pyrethroid type compounds

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4562062A (en) * 1983-06-10 1985-12-31 Sumitomo Chemical Company, Limited Insecticidal composition comprising synergistic combinations of 3-(2-methoxyphenyl)-5-methoxy-1,3,4-oxadiazol-2(3H)-one and pyrethroid type compounds

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