JPH10158105A - Acaricide composition - Google Patents

Acaricide composition

Info

Publication number
JPH10158105A
JPH10158105A JP31604796A JP31604796A JPH10158105A JP H10158105 A JPH10158105 A JP H10158105A JP 31604796 A JP31604796 A JP 31604796A JP 31604796 A JP31604796 A JP 31604796A JP H10158105 A JPH10158105 A JP H10158105A
Authority
JP
Japan
Prior art keywords
parts
compound
acaricide
present
acaricide composition
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
JP31604796A
Other languages
Japanese (ja)
Inventor
Ken Kuriyama
研 栗山
Rikio Yamaguchi
力雄 山口
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.)
Nihon Nohyaku Co Ltd
Original Assignee
Nihon Nohyaku 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 Nihon Nohyaku Co Ltd filed Critical Nihon Nohyaku Co Ltd
Priority to JP31604796A priority Critical patent/JPH10158105A/en
Publication of JPH10158105A publication Critical patent/JPH10158105A/en
Pending legal-status Critical Current

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  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

PROBLEM TO BE SOLVED: To obtain an acaricide capable of extraordinarily expressing synergetic effects unexpected from the control effect of a single agent against tetranychidac having developed chemical resistance. SOLUTION: This acaricide composition contains 0.05-20 pts.wt. of 4- bromo-2-(4-chlorophenyl)-1-ethoxymethyl-5-trifluoromethylpyrol-3-carbo nitrile for 1 pt.wt. of t-butyl α-(1,3-dimethyl-5-phenoxypyrazol-4-ylmethyleneaminoxy)-p- toluate.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、t−ブチル α−
(1,3−ジメチル−5−フェノキシビラゾール−4−
イルメチレンアミノオキシ)−p−トルエート(以下化
合物Aという)および4−ブロモ−2−(4−クロロフ
ェニル)−1−エトキシメチル−5−トリフルオロメチ
ルピロール−3−カルボニトリル(以下化合物Bとい
う)を有効成分として含有することを特徴とする殺ダニ
剤組成物に関するものである。さらに詳しくは、薬剤抵
抗性の発達したハダニ類に対して有効な殺ダニ剤組成物
を提供するものである。
[0001] The present invention relates to t-butyl α-
(1,3-dimethyl-5-phenoxyvirazole-4-
Ilmethyleneaminooxy) -p-toluate (hereinafter referred to as compound A) and 4-bromo-2- (4-chlorophenyl) -1-ethoxymethyl-5-trifluoromethylpyrrole-3-carbonitrile (hereinafter referred to as compound B) The present invention relates to an acaricide composition characterized by containing as an active ingredient. More specifically, the present invention provides an acaricide composition that is effective against spider mites that have developed drug resistance.

【0002】[0002]

【従来の技術】果樹、蔬菜、茶、その他の作物、園芸植
物、樹木等に加害するハダニ類は収穫物等に多大の被害
を与えて商品価値を著しく損なうので、これらを防除す
ることは重要なことであることから、ハダニ類に有効な
各種の殺ダニ剤を使用して防除が行なわれている。
2. Description of the Related Art Spider mites that inflict fruit trees, vegetables, tea, other crops, horticultural plants, trees, etc., cause great damage to crops and the like and significantly impair their commercial value, so it is important to control them. For this reason, pests are controlled using various kinds of acaricides effective against spider mites.

【0003】[0003]

【発明が解決しようとする課題】しかし、同一薬剤を多
用することによりハダニ類に薬剤抵抗性の発現が著し
く、既存の殺ダニ剤でも交差抵抗性を示す薬剤があり、
ますますハダニ類に対する防除が困難になってきてい
る。
However, due to the frequent use of the same drug, the occurrence of drug resistance to spider mites is remarkable, and there are drugs that show cross-resistance even with existing acaricides.
Increasingly difficult to control spider mites.

【0004】[0004]

【課題を解決するための手段】本発明者等は上記状況を
鑑み、新規な殺ダニ剤組成物を創出すべく鋭意研究を重
ねた結果、本発明を完成させたものである。本発明は化
合物Aおよび化合物Bの殺ダニ剤を組み合わせて、抵抗
性が発達したハダニ類の防除に使用することにより、各
々単独で使用した場合に比較して予想し得ない顕著な相
乗効果を奏することを見出だし、本発明を完成させたも
のである。
Means for Solving the Problems In view of the above circumstances, the present inventors have conducted intensive studies to create a novel acaricide composition, and as a result, completed the present invention. The present invention uses a compound A and a compound B acaricide and uses them for controlling spider mites that have developed resistance, thereby achieving a remarkable synergistic effect which cannot be expected as compared with the case of using each alone. The present invention has been found to perform.

【0005】[0005]

【発明の実施の形態】本発明の有効成分である化合物A
は特開昭63ー183564号公報によって、また化合
物Bは特開平4ー342552号公報によって殺ダニ剤
としていずれも公知の化合物である。本発明は、化合物
Aおよび化合物Bを適当な割合に配合して、農薬製剤上
の常法に従い、使用に都合の良い剤形に混合調製して使
用すればよく、その剤形としては、例えば乳剤、水和
剤、粉剤、フロアブル剤等が挙げられる。
BEST MODE FOR CARRYING OUT THE INVENTION Compound A which is an active ingredient of the present invention
Is a compound known as an acaricide according to JP-A-63-183564 and Compound B is disclosed in JP-A-4-342552. In the present invention, the compound A and the compound B may be blended in an appropriate ratio, and mixed and prepared into a convenient dosage form according to a conventional method for agrochemical formulation, and the dosage form may be, for example, Emulsions, wettable powders, powders, flowables and the like can be mentioned.

【0006】本発明の殺ダニ剤組成物の各有効成分の割
合は、化合物A 1重量部に対して化合物Bを0.05
〜20重量部の割合で配合すれば良い。本発明の殺ダニ
剤組成物は薬剤抵抗性の発達したナミハダニ (Tetranyc
husurticae Koch) 、カンザワハダニ (Tetranychus kan
zawai Kishida)、オウトウハダニ (Tetranychus Viennen
sis Zacher)、ミカンハダニ(Panonychus citri)等の
ハダニ類に対して顕著な相乗効果を示すものである。
The ratio of each active ingredient of the acaricide composition of the present invention is such that 0.05 parts of compound B are added to 1 part by weight of compound A.
What is necessary is just to mix | blend in the ratio of 20 weight part. The acaricide composition of the present invention is a drug-developed adult spider mite, Tetranyc
husurticae Koch), Kanzawa spider mite (Tetranychus kan)
zawai Kishida), Scotch spider mite (Tetranychus Viennen)
cis Zacher) and red spider mites (Panonychus citri).

【0007】本発明の殺ダニ剤組成物を使用する場合、
目的に応じて製剤形態の組成物をそのまま、または水等
で希釈して使用すれば良く、その使用量は防除対象の果
樹、作物等の種類、大きさにより異なるが、有効成分の
合計として10アール当り有効成分を通常1g〜100
gの範囲で処理すれば良く、好ましくは10g〜70g
の範囲である。
When the acaricide composition of the present invention is used,
Depending on the purpose, the composition in the form of a preparation may be used as it is, or may be diluted with water or the like, and the amount used depends on the type and size of the fruit tree, crop, etc. to be controlled. The active ingredient is usually 1g-100 per are
g, preferably 10 g to 70 g.
Range.

【0008】[0008]

【実施例】以下に本発明の代表的な実施例および試験例
を例示するが、本発明はこれらに限定されるものではな
い。尚、実施例中、部とあるのは重量部を示す。 実施例1 化合物A 3部 化合物B 30部 含水珪酸 30部 ハイテノールM08(第一工業製薬(株)製:界面活性剤) 3部 リグニンスルホン酸カルシウム 2部 水和剤用クレー 32部 化合物Bを含水珪酸に含浸させた後、他の成分と均一に
混合し、水和剤とする。
The present invention will be described in more detail with reference to the following Examples and Test Examples, which by no means limit the present invention. In Examples, “parts” means “parts by weight”. Example 1 Compound A 3 parts Compound B 30 parts Hydrous silica 30 parts Hytenol M08 (Daiichi Kogyo Seiyaku Co., Ltd .: surfactant) 3 parts lignin calcium sulfonate 2 parts Clay for wettable powder 32 parts Compound B After impregnating with hydrous silicic acid, it is uniformly mixed with other components to form a wettable powder.

【0009】実施例2 化合物A 3部 化合物B 21部 含水珪酸 34部 ハイテノールM08(第一工業製薬(株)製:界面活性剤) 3部 デモールT(花王アトラス(株)製:界面活性剤) 2部 炭酸カルシウム粉末 37部 化合物Bを含水珪酸に含浸させた後、他の成分と均一に
混合し、水和剤とする。
Example 2 Compound A 3 parts Compound B 21 parts Hydrous silicic acid 34 parts Hytenol M08 (Daiichi Kogyo Seiyaku Co., Ltd .: surfactant) 3 parts Demol T (Kao Atlas Co., Ltd .: surfactant) 2 parts) Calcium carbonate powder 37 parts After impregnating compound B with hydrous silicic acid, uniformly mix with other components to obtain a wettable powder.

【0010】実施例3 化合物A 10部 化合物B 20部 含水珪酸 30部 SP一3005X(東邦化学(株)製:界面活性剤) 10部 キシレン 30部 以上を均一に混合溶解し、乳剤とする。Example 3 10 parts of compound A 20 parts of compound B 30 parts of hydrous silicic acid 30 parts SP-13005X (manufactured by Toho Chemical Co., Ltd .: surfactant) 10 parts xylene 30 parts The above components are uniformly mixed and dissolved to form an emulsion.

【0011】実施例4 化合物A 5部 化合物B 10部 NPE−100(第一工業製薬(株)製) 2部 プロピレングリコール 5部 ロードポール23 (ローン・プーラン(株)製:増粘剤) 0.5部 水 77.5部 以上を均一に混合し、水に分散させて、フロアブルとす
る。
Example 4 Compound A 5 parts Compound B 10 parts NPE-100 (Daiichi Kogyo Seiyaku Co., Ltd.) 2 parts Propylene glycol 5 parts Road Pole 23 (Lone Poulin Co., Ltd .: thickener) 0 5.5 parts Water 77.5 parts The above components are uniformly mixed and dispersed in water to form a flowable.

【0012】実施例5 化合物A 30部 化合物B 3部 含水珪酸 30部 ハイテノールM08(第一工業製薬(株)製:界面活性剤) 3部 リグニンスルホン酸カルシウム 2部 水和剤用クレー 32部 化合物Bを含水珪酸に含浸させた後、他の成分と均一に
混合し、水和剤とする。
Example 5 30 parts of compound A 3 parts of compound B 30 parts of hydrated silicic acid 3 parts of Hytenol M08 (manufactured by Daiichi Kogyo Seiyaku Co., Ltd .: surfactant) 3 parts of calcium lignin sulfonate 2 parts of clay for wettable powder 32 parts After impregnating Compound B with hydrous silicic acid, it is uniformly mixed with other components to obtain a wettable powder.

【0013】実施例6 化合物A 20部 化合物B 10部 含水珪酸 30部 SP一3005X(東邦化学(株)製製:界面活性剤) 10部 キシレン 30部 以上を均一に混合溶解し、乳剤とする。Example 6 20 parts of compound A 10 parts of compound B 30 parts of hydrous silicic acid 30 parts SP-13005X (manufactured by Toho Chemical Co., Ltd .: surfactant) 10 parts xylene 30 parts The above components are uniformly mixed and dissolved to form an emulsion. .

【0014】試験例1 抵抗性ナミハダニに対する殺成
虫試験 直径8cmのプラスチック製カップに水を満たし、直径l
cmの穴のある蓋をし、該蓋の上に一部切り込みを入れた
濾紙を置き、蓋の中から水中に懸垂させて毛細管現象で
濾紙が常時湿っている状態にした。インゲン初生葉(品
種:トップクロッブ)で直径2cmのリーフディスクを作
成し、雌成虫10頭を接種したリーフディスクを上記濾
紙上に置き、ターンテーブル上で所定濃度の薬液50ml
を均一に散布し、散布後25℃の恒温室に静置した。薬
剤処理2日後に異常虫数および死亡虫数を調査し、下記
式に従って異常および死亡虫の率を算出した。2連制、
結果を第1表に示す。
Test Example 1 Test for Adult Insecticidal Insects Against Resistant Spider Mites A plastic cup having a diameter of 8 cm was filled with water,
A lid with a hole of cm was placed, and a partially cut filter paper was placed on the lid, and the filter paper was suspended in water from the lid to keep the filter paper moist due to capillary action. A leaf disk having a diameter of 2 cm was prepared from the primary leaves of a kidney bean (cultivar: top clob), and a leaf disk inoculated with 10 female adults was placed on the filter paper.
Was sprayed uniformly, and after spraying, it was allowed to stand in a constant temperature room at 25 ° C. Two days after the drug treatment, the numbers of abnormal insects and dead insects were examined, and the ratio of abnormal and dead insects was calculated according to the following formula. Two-part,
The results are shown in Table 1.

【数1】 (Equation 1)

【0015】 [0015]

【0016】試験例2 抵抗性カンザワハダニに対する
殺成虫試験 直径8cmのプラスチック製カップに水を満たし、直径l
cmの穴のある蓋をし、該蓋の上に一部切り込みを入れた
濾紙を置き、蓋の中から水中に懸垂させて毛細管現象で
濾紙が常時湿っている状態にした。インゲン初生葉(品
種:トップクロップ)で直径2cmのリーフディスクを作
成し、雌成虫10頭を接種したリーフディスクを上記濾
紙上に置き、ターンテーブル上で所定濃度の薬液50ml
を均一に散布し、散布後25℃の恒温室に静置した。薬
剤処理2日後に死亡虫数を調査し、試験例1と同様にし
て異常および死亡虫の率を算出した。2連制、結果を第
2表に示す。
Test Example 2 Test for Adult Killing Against Resistant Tetranychus kanzawai A plastic cup having a diameter of 8 cm was filled with water, and the
A lid with a hole of cm was placed, and a partially cut filter paper was placed on the lid, and the filter paper was suspended in water from the lid to keep the filter paper moist due to capillary action. A leaf disc having a diameter of 2 cm was prepared from the primary leaves of a kidney bean (variety: top crop), and a leaf disc inoculated with 10 female adults was placed on the filter paper, and 50 ml of a drug solution having a predetermined concentration was placed on a turntable.
Was sprayed uniformly, and after spraying, it was allowed to stand in a constant temperature room at 25 ° C. Two days after the drug treatment, the number of dead insects was examined, and the rates of abnormal and dead insects were calculated in the same manner as in Test Example 1. Table 2 shows the results of the two-unit control.

【0017】 [0017]

【0018】[0018]

【発明の効果】本発明の殺ダニ剤組成物は薬剤抵抗性の
発達したハダニ類に対して、それぞれ単独での防除効果
からは予想しえない顕著な相乗効果を有しており、防除
が困難な薬剤抵抗性殺ダニ防除組成物として有用であ
る。
EFFECTS OF THE INVENTION The acaricide composition of the present invention has a remarkable synergistic effect on spider mites that have developed drug resistance, which can be expected from the control effect of each alone. It is useful as a difficult drug resistant acaricide control composition.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 t−ブチル α−(1,3−ジメチル−
5−フェノキシビラゾール−4−イルメチレンアミノオ
キシ)−p−トルエートおよび4−ブロモ−2−(4−
クロロフェニル)−1−エトキシメチル−5−トリフル
オロメチルピロール−3−カルボニトリルを有効成分と
して含有することを特徴とする殺ダニ剤組成物。
(1) t-butyl α- (1,3-dimethyl-
5-phenoxyvirazol-4-ylmethyleneaminooxy) -p-toluate and 4-bromo-2- (4-
An acaricide composition comprising (chlorophenyl) -1-ethoxymethyl-5-trifluoromethylpyrrole-3-carbonitrile as an active ingredient.
【請求項2】 t−ブチル α−(1,3−ジメチル−
5−フェノキシビラゾール−4−イルメチレンアミノオ
キシ)−p−トルエート1重量部に対して4−ブロモ−
2−(4−クロロフェニル)−1−エトキシメチル−5
−トリフルオロメチルピロール−3−カルボニトリルを
0.05〜20重量部の割合で含有することを特徴とす
る請求項1記載の殺ダニ剤組成物。
2. t-butyl α- (1,3-dimethyl-
5-phenoxyvirazol-4-ylmethyleneaminooxy) -p-toluate per 1 part by weight of 4-bromo-
2- (4-chlorophenyl) -1-ethoxymethyl-5
2. The acaricide composition according to claim 1, wherein the composition contains 0.05 to 20 parts by weight of -trifluoromethylpyrrole-3-carbonitrile.
JP31604796A 1996-11-27 1996-11-27 Acaricide composition Pending JPH10158105A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP31604796A JPH10158105A (en) 1996-11-27 1996-11-27 Acaricide composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP31604796A JPH10158105A (en) 1996-11-27 1996-11-27 Acaricide composition

Publications (1)

Publication Number Publication Date
JPH10158105A true JPH10158105A (en) 1998-06-16

Family

ID=18072683

Family Applications (1)

Application Number Title Priority Date Filing Date
JP31604796A Pending JPH10158105A (en) 1996-11-27 1996-11-27 Acaricide composition

Country Status (1)

Country Link
JP (1) JPH10158105A (en)

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