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JPH01233201A - Method for strengthening miticidal activity of 2-(acetyloxy)-3-dodecyl-1,4-nephalenedione - Google Patents

Method for strengthening miticidal activity of 2-(acetyloxy)-3-dodecyl-1,4-nephalenedione

Info

Publication number
JPH01233201A
JPH01233201A JP6125588A JP6125588A JPH01233201A JP H01233201 A JPH01233201 A JP H01233201A JP 6125588 A JP6125588 A JP 6125588A JP 6125588 A JP6125588 A JP 6125588A JP H01233201 A JPH01233201 A JP H01233201A
Authority
JP
Japan
Prior art keywords
pts
aqueous suspension
activity
acetyloxy
dodecyl
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
JP6125588A
Other languages
Japanese (ja)
Inventor
Akinori Kariya
苅谷 昭範
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.)
AGURO KANESHO KK
Agro Kanesho Co Ltd
Original Assignee
AGURO KANESHO KK
Agro Kanesho 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 AGURO KANESHO KK, Agro Kanesho Co Ltd filed Critical AGURO KANESHO KK
Priority to JP6125588A priority Critical patent/JPH01233201A/en
Publication of JPH01233201A publication Critical patent/JPH01233201A/en
Pending legal-status Critical Current

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  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

PURPOSE:To remarkably improve residual activity of the above compound and consequently improve the miticidal activity, by using the subject substance in the form of an aqueous suspension. CONSTITUTION:4 pts.wt. of polyoxyethylene phenylphenol phosphate is dissolved as a dispersing agent in a mixture of 61 pts.wt. of water and 5 pts.wt. of propylene glycol. 20 pts.wt. of the subject substance is added to the solution, thoroughly mixed and crushed with a sand mill for 35min in wet state. 10 pts.wt. of a thickener suspended in water is added to the product and crushed by mixing for 5min to obtain the objective aqueous suspension. Although the subject substance has too short residual activity to be used for practical used in the form of emulsion, wettable powder, powder, etc., the above aqueous suspension exhibits excellent residual activity in respect of miticidal activity and is sufficiently usable for practical purposes.

Description

【発明の詳細な説明】 産業上の利用分野 本発明は2−(アセチルオキシ)−3−ドデシル−1,
4−ナフタレンジオン(以下本化合物と称する)を水性
懸濁製剤にすることを特徴とする該化合物の殺ダニ活性
を増強させる方法、更に活性を増強させた殺ダニ剤およ
びその殺ダニ剤を施用することを特徴とする殺ダニ方法
に関するものである。
DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention relates to 2-(acetyloxy)-3-dodecyl-1,
A method for enhancing the acaricidal activity of 4-naphthalenedione (hereinafter referred to as the present compound), which is characterized by preparing the compound into an aqueous suspension preparation, and further application of an acaricide with enhanced activity and the acaricide. The present invention relates to a method for killing mites, which is characterized by:

従来の技術 本化合物は特開昭52−48648号公報に記載されて
いる公知の化合物で、各種のハダニ類に高い効果を有し
、また薬剤抵抗性のハダニ類にも卓効を示す。しかしな
がら、本化合物の乳剤、水和剤、粉剤等の製剤は野外の
圃場試験では施用後急速に効力が低下し、残効性に乏し
いので今日まで実用に供することができなかった。
BACKGROUND OF THE INVENTION The present compound is a known compound described in JP-A-52-48648, and is highly effective against various spider mites, and is also highly effective against drug-resistant spider mites. However, formulations of this compound such as emulsions, wettable powders, and powders have been unable to be put to practical use to date because their efficacy rapidly decreases after application in field tests and they lack residual efficacy.

発明が解決しようとする課題 繁殖力の旺盛なハダニ類を効果的に防除するには残効性
が比較的長期間にわたって維持されることが必要であり
、本化合物の残効性の向上が強く望まれていた。
Problems to be Solved by the Invention In order to effectively control spider mites, which have a high rate of reproduction, it is necessary to maintain residual efficacy for a relatively long period of time, and the improvement in the residual efficacy of this compound is significant. It was wanted.

課題を解決するための手段 本発明者らは本化合物を殺ダニ剤としてより効果的に使
用することを目的として、残効性の向上について鋭意研
究を行った結果、本化合物の乳剤、水和剤、粉剤などで
は残効性が短く、実用性がないにもかかわらず、全く意
外にも本化合物の水性懸濁製剤が殺ダニ活性に関して優
れた残効性を有し、充分実用に供し得ることを見出し、
本発明を完成するに至った。すなわち本発明は本化合物
を水性懸濁製剤にするという手段によって、従来当業者
にも予想もされなかった程度に残効性を著しく向上させ
ることができ、それによって本化合物の殺ダニ活性を増
強させることに成功したことにもとすくものである。
Means for Solving the Problems With the aim of using this compound more effectively as an acaricide, the present inventors conducted intensive research on improving the residual effect, and as a result, we developed an emulsion of this compound, a hydrated Although agents, powders, etc. have short residual effects and are not practical, an aqueous suspension preparation of this compound surprisingly has an excellent residual effect in terms of acaricidal activity and can be put to practical use. I found out that
The present invention has now been completed. In other words, the present invention makes it possible to significantly improve the residual efficacy to an extent previously unforeseeable even by those skilled in the art by making the present compound into an aqueous suspension preparation, thereby enhancing the acaricidal activity of the present compound. I am also very happy that we were able to successfully do this.

以下に実施例をあげて本発明を更に詳しく説明するが、
本発明はこれらの実施例に限定されるものではない。
The present invention will be explained in more detail with reference to Examples below.
The present invention is not limited to these examples.

製剤例 水性懸濁製剤 水61部(重量部、以下同じ)とプロピレングリコール
5部の混合液に分散剤としてポリオキシエチレンフェニ
ルフェノールホスフェート4部を溶解し、これに本化合
物20部を加えてよく混和しサンドミルを用いて35分
分間式粉砕した。つぎに水に懸濁させ、こ増粘剤10部
を加え更に5分間混合粉砕し、水性懸濁製剤を得た。
Formulation Example Aqueous Suspension Formulation 4 parts of polyoxyethylene phenylphenol phosphate as a dispersant may be dissolved in a mixture of 61 parts (by weight, same hereinafter) of water and 5 parts of propylene glycol, and 20 parts of the present compound may be added thereto. The mixture was mixed and pulverized for 35 minutes using a sand mill. Next, the mixture was suspended in water, 10 parts of a thickener was added thereto, and the mixture was further mixed and ground for 5 minutes to obtain an aqueous suspension preparation.

以下の試験例に用いた乳剤および水和剤は下記のように
してm製した。
The emulsions and wettable powders used in the following test examples were prepared as follows.

乳剤 本化合物20部をキシレン75部に溶解し、これに乳化
剤としてポリオキシエチレンアルキルアリルエーテル3
Lアルキルベンゼンスルホン酸塩2部を加え、全体をよ
く混和溶解し、乳剤を得た。
Emulsion 20 parts of the present compound was dissolved in 75 parts of xylene, and 3 parts of polyoxyethylene alkyl allyl ether was added as an emulsifier.
Two parts of L-alkylbenzene sulfonate were added and the whole was thoroughly mixed and dissolved to obtain an emulsion.

水和剤 本化合物20邪にクレー75部、分散剤としてリグニン
スルホン酸ナトリウム3Bおよび高級アルコール硫酸ナ
トリウム2部を加え、全体をよく混合した後粉砕し、水
和剤を得た。
Wettable powder 75 parts of clay, sodium lignin sulfonate 3B and 2 parts of higher alcohol sodium sulfate as dispersants were added to the present compound 20, and the whole was thoroughly mixed and pulverized to obtain a wettable powder.

試験例1 残効性試験 所定濃度の薬液を鉢植えインゲンの初生葉に十分量散布
し、風乾後室内に静置した。散布1日、3日、11日後
に初生葉を切除し、リーフディスク法に準拠してカンザ
ワハダニ雌成虫を1葉片当たり10頭接種した。ハダニ
接種48時間後に雌成虫を除去し、6日後に醇化幼虫の
生虫数、死去数を調べた(2反復)。
Test Example 1 Residual Effect Test A sufficient amount of a chemical solution at a predetermined concentration was sprayed on the first leaves of potted green beans, and after air-drying, the leaves were left indoors. 1, 3, and 11 days after spraying, the primary leaves were excised and inoculated with 10 female Kanzawa spider mites per leaf piece according to the leaf disc method. Adult females were removed 48 hours after inoculation with spider mites, and 6 days later, the number of live and dead larvae was examined (repeat twice).

各薬剤、各経過日数の各々について、得られた死生率を
対数正規確率紙に作図し、LCss値を算出した。
For each drug and each elapsed number of days, the obtained mortality rate was plotted on lognormal probability paper, and the LCss value was calculated.

第1表 0縦軸にLCss値を、横軸に経過日数をそれぞれ対数
値でとり、最小自乗法によって両者間の関係式を算出し
、残効日数(LCssの値が200ppmになる日数)
を求めた。第1表に示すとおり、本化合物の水性懸濁製
剤は乳剤、水和剤に比べて明らかに長い残効性を示した
Table 1 0 Take the LCss value on the vertical axis and the elapsed days on the horizontal axis as logarithmic values, calculate the relational expression between the two using the least squares method, and calculate the number of days after which the LCss value becomes 200 ppm.
I asked for As shown in Table 1, the aqueous suspension formulation of the present compound clearly showed a longer residual effect than the emulsion and wettable powder.

試験例2 野外の圃場試験 神奈川県南足柄市にてミカンハダニに対する圃場での効
果試験を行った。ミカンハダニが発生している15年生
の早生温州に、所定濃度の薬液を動力噴霧機で十分量散
布した。試験区の規模は1区1樹、2連制で行った。調
査は散布前、散布3日、13日、22日、30日後(こ
1樹当たり任意50葉に生息しているミカンハダニ雌成
虫数を数えた。数字は100葉邑九0のミカンハダニ雌
成虫数を示す。
Test Example 2 Outdoor Field Test A field test of efficacy against citrus spider mites was conducted in Minamiashigara City, Kanagawa Prefecture. A sufficient amount of a chemical solution of a predetermined concentration was sprayed with a power sprayer on a 15-year-old early Satsuma tree infested with orange spider mites. The scale of the test plot was one tree per plot, and two consecutive plots were used. The survey was conducted before spraying, 3 days, 13 days, 22 days, and 30 days after spraying (the number of adult female citrus spider mites inhabiting 50 leaves per tree was counted. The numbers indicate the number of female adult citrus spider mites in 90 leaves of 100 leaves). shows.

第2表に示すとおり、本化合物は水性懸濁製剤の50p
pmでも乳剤および水和剤の200ppm、比較薬剤ア
ミトラズ乳剤の2001)I)mより優る効果を示した
As shown in Table 2, this compound is available at 50p in an aqueous suspension formulation.
Even in terms of pm, the emulsion and wettable powder showed a superior effect to 200 ppm and the comparative drug amitraz emulsion 2001)I)m.

発明の効果 本発明の有用性は公知の化合物である本化合物において
、水性懸濁製剤が残効性を著しく向上させる効果を見出
し、本化合物を実用に供し得るほどにまで効果を高めた
点にある。
Effects of the Invention The usefulness of the present invention lies in the fact that in the present compound, which is a known compound, an aqueous suspension preparation was found to be effective in significantly improving the residual efficacy, and the effect was enhanced to the extent that the present compound could be put to practical use. be.

Claims (3)

【特許請求の範囲】[Claims] (1)2−(アセチルオキシ)−3−ドデシル−1,4
−ナフタレンジオンを水性懸濁製剤にすることを特徴と
する該化合物の殺ダニ活性を増強させる方法。
(1) 2-(acetyloxy)-3-dodecyl-1,4
- A method for enhancing the acaricidal activity of naphthalene dione, which comprises preparing the compound into an aqueous suspension.
(2)2−(アセチルオキシ)−3−ドデシル−1,4
−ナフタレンジオンを水性懸濁製剤にすることを特徴と
する殺ダニ剤。
(2) 2-(acetyloxy)-3-dodecyl-1,4
- An acaricide characterized in that naphthalene dione is formed into an aqueous suspension preparation.
(3)2−(アセチルオキシ)−3−ドデシル−1,4
−ナフタレンジオンを水性懸濁製剤にし、該化合物を1
0〜2,000ppmの濃度で植物寄生性のダニに施用
することを特徴とする殺ダニ方法。
(3) 2-(acetyloxy)-3-dodecyl-1,4
- Naphthalenedione is made into an aqueous suspension and the compound is
A method for killing mites, characterized in that it is applied to plant-parasitic mites at a concentration of 0 to 2,000 ppm.
JP6125588A 1988-03-15 1988-03-15 Method for strengthening miticidal activity of 2-(acetyloxy)-3-dodecyl-1,4-nephalenedione Pending JPH01233201A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP6125588A JPH01233201A (en) 1988-03-15 1988-03-15 Method for strengthening miticidal activity of 2-(acetyloxy)-3-dodecyl-1,4-nephalenedione

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP6125588A JPH01233201A (en) 1988-03-15 1988-03-15 Method for strengthening miticidal activity of 2-(acetyloxy)-3-dodecyl-1,4-nephalenedione

Publications (1)

Publication Number Publication Date
JPH01233201A true JPH01233201A (en) 1989-09-19

Family

ID=13165944

Family Applications (1)

Application Number Title Priority Date Filing Date
JP6125588A Pending JPH01233201A (en) 1988-03-15 1988-03-15 Method for strengthening miticidal activity of 2-(acetyloxy)-3-dodecyl-1,4-nephalenedione

Country Status (1)

Country Link
JP (1) JPH01233201A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH09208404A (en) * 1996-02-08 1997-08-12 Agro Kanesho Co Ltd Pesticide aqueous suspension composition having long-term storage stability
CN105076134A (en) * 2012-06-27 2015-11-25 陕西美邦农药有限公司 Pesticide composition

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS50155620A (en) * 1974-05-10 1975-12-16
JPS5248648A (en) * 1975-09-15 1977-04-18 Du Pont 22higher alkyll33hydroxyy 1*44naphthoquinone carboxylic acid ester containing composition and use thereof*

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS50155620A (en) * 1974-05-10 1975-12-16
JPS5248648A (en) * 1975-09-15 1977-04-18 Du Pont 22higher alkyll33hydroxyy 1*44naphthoquinone carboxylic acid ester containing composition and use thereof*

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH09208404A (en) * 1996-02-08 1997-08-12 Agro Kanesho Co Ltd Pesticide aqueous suspension composition having long-term storage stability
CN105076134A (en) * 2012-06-27 2015-11-25 陕西美邦农药有限公司 Pesticide composition

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