JPH0477402A - Acaricidal composition - Google Patents
Acaricidal compositionInfo
- Publication number
- JPH0477402A JPH0477402A JP2192261A JP19226190A JPH0477402A JP H0477402 A JPH0477402 A JP H0477402A JP 2192261 A JP2192261 A JP 2192261A JP 19226190 A JP19226190 A JP 19226190A JP H0477402 A JPH0477402 A JP H0477402A
- Authority
- JP
- Japan
- Prior art keywords
- acaricidal
- compound
- effects
- parts
- compounds
- 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
Links
- 230000000895 acaricidal effect Effects 0.000 title claims abstract description 30
- 239000000203 mixture Substances 0.000 title claims abstract description 17
- 150000001875 compounds Chemical class 0.000 claims abstract description 36
- RAPBNVDSDCTNRC-UHFFFAOYSA-N Chlorobenzilate Chemical compound C=1C=C(Cl)C=CC=1C(O)(C(=O)OCC)C1=CC=C(Cl)C=C1 RAPBNVDSDCTNRC-UHFFFAOYSA-N 0.000 claims abstract 2
- UOAMTSKGCBMZTC-UHFFFAOYSA-N dicofol Chemical compound C=1C=C(Cl)C=CC=1C(C(Cl)(Cl)Cl)(O)C1=CC=C(Cl)C=C1 UOAMTSKGCBMZTC-UHFFFAOYSA-N 0.000 claims abstract 2
- XGWIJUOSCAQSSV-XHDPSFHLSA-N (S,S)-hexythiazox Chemical compound S([C@H]([C@@H]1C)C=2C=CC(Cl)=CC=2)C(=O)N1C(=O)NC1CCCCC1 XGWIJUOSCAQSSV-XHDPSFHLSA-N 0.000 claims description 2
- GLATZGXOBGGISN-UHFFFAOYSA-N C1=CC(C(C)(C)C)=CC=C1OC1C(SCC#C)CCCC1 Chemical compound C1=CC(C(C)(C)C)=CC=C1OC1C(SCC#C)CCCC1 GLATZGXOBGGISN-UHFFFAOYSA-N 0.000 claims description 2
- HOXINJBQVZWYGZ-UHFFFAOYSA-N fenbutatin oxide Chemical compound C=1C=CC=CC=1C(C)(C)C[Sn](O[Sn](CC(C)(C)C=1C=CC=CC=1)(CC(C)(C)C=1C=CC=CC=1)CC(C)(C)C=1C=CC=CC=1)(CC(C)(C)C=1C=CC=CC=1)CC(C)(C)C1=CC=CC=C1 HOXINJBQVZWYGZ-UHFFFAOYSA-N 0.000 claims description 2
- OCLIQMAKECCZNO-UHFFFAOYSA-N 3,6-bis(4-chlorophenyl)-1,2,4,5-tetrazine Chemical compound C1=CC(Cl)=CC=C1C1=NN=C(C=2C=CC(Cl)=CC=2)N=N1 OCLIQMAKECCZNO-UHFFFAOYSA-N 0.000 claims 1
- AXGUBXVWZBFQGA-UHFFFAOYSA-N chloropropylate Chemical compound C=1C=C(Cl)C=CC=1C(O)(C(=O)OC(C)C)C1=CC=C(Cl)C=C1 AXGUBXVWZBFQGA-UHFFFAOYSA-N 0.000 claims 1
- 239000004480 active ingredient Substances 0.000 abstract description 5
- 239000003795 chemical substances by application Substances 0.000 abstract description 4
- 230000002195 synergetic effect Effects 0.000 abstract description 4
- 235000013399 edible fruits Nutrition 0.000 abstract description 3
- 238000002156 mixing Methods 0.000 abstract description 3
- 235000013311 vegetables Nutrition 0.000 abstract description 3
- 230000000694 effects Effects 0.000 abstract 2
- -1 4-[(1,3-dimethyl-5-phenoxypyrazol-4-yl)methyleneiminooxymethyl]benzoate Chemical class 0.000 abstract 1
- 229940126062 Compound A Drugs 0.000 description 9
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 9
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 241000488589 Tetranychus kanzawai Species 0.000 description 3
- 229940125898 compound 5 Drugs 0.000 description 3
- 230000009969 flowable effect Effects 0.000 description 3
- 241000239290 Araneae Species 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- 241001454295 Tetranychidae Species 0.000 description 2
- 239000000642 acaricide Substances 0.000 description 2
- 229940125904 compound 1 Drugs 0.000 description 2
- 229940125782 compound 2 Drugs 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- 241000894007 species Species 0.000 description 2
- 230000004083 survival effect Effects 0.000 description 2
- 239000004563 wettable powder Substances 0.000 description 2
- GHYOCDFICYLMRF-UTIIJYGPSA-N (2S,3R)-N-[(2S)-3-(cyclopenten-1-yl)-1-[(2R)-2-methyloxiran-2-yl]-1-oxopropan-2-yl]-3-hydroxy-3-(4-methoxyphenyl)-2-[[(2S)-2-[(2-morpholin-4-ylacetyl)amino]propanoyl]amino]propanamide Chemical compound C1(=CCCC1)C[C@@H](C(=O)[C@@]1(OC1)C)NC([C@H]([C@@H](C1=CC=C(C=C1)OC)O)NC([C@H](C)NC(CN1CCOCC1)=O)=O)=O GHYOCDFICYLMRF-UTIIJYGPSA-N 0.000 description 1
- OVFJHQBWUUTRFT-UHFFFAOYSA-N 1,2,3,4-tetrahydrotetrazine Chemical compound C1=CNNNN1 OVFJHQBWUUTRFT-UHFFFAOYSA-N 0.000 description 1
- HTSGKJQDMSTCGS-UHFFFAOYSA-N 1,4-bis(4-chlorophenyl)-2-(4-methylphenyl)sulfonylbutane-1,4-dione Chemical compound C1=CC(C)=CC=C1S(=O)(=O)C(C(=O)C=1C=CC(Cl)=CC=1)CC(=O)C1=CC=C(Cl)C=C1 HTSGKJQDMSTCGS-UHFFFAOYSA-N 0.000 description 1
- SHBHYINHXNTBRP-UHFFFAOYSA-N 3-[4-(aminomethyl)-6-(trifluoromethyl)pyridin-2-yl]oxy-N-(2-methylsulfonylethyl)benzamide Chemical group NCC1=CC(=NC(=C1)C(F)(F)F)OC=1C=C(C(=O)NCCS(=O)(=O)C)C=CC=1 SHBHYINHXNTBRP-UHFFFAOYSA-N 0.000 description 1
- 241000238876 Acari Species 0.000 description 1
- 229920001817 Agar Polymers 0.000 description 1
- 241000207199 Citrus Species 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 241000238631 Hexapoda Species 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 241001454293 Tetranychus urticae Species 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000008272 agar Substances 0.000 description 1
- 239000003905 agrochemical Substances 0.000 description 1
- QXAITBQSYVNQDR-UHFFFAOYSA-N amitraz Chemical compound C=1C=C(C)C=C(C)C=1N=CN(C)C=NC1=CC=C(C)C=C1C QXAITBQSYVNQDR-UHFFFAOYSA-N 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- RYAGRZNBULDMBW-UHFFFAOYSA-L calcium;3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Ca+2].COC1=CC=CC(CC(CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O RYAGRZNBULDMBW-UHFFFAOYSA-L 0.000 description 1
- 235000020971 citrus fruits Nutrition 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229940125797 compound 12 Drugs 0.000 description 1
- 229940126214 compound 3 Drugs 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- ZXSBDSGRQIWJPM-UHFFFAOYSA-N dimethylcarbamothioic s-acid Chemical compound CN(C)C(S)=O ZXSBDSGRQIWJPM-UHFFFAOYSA-N 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 244000013123 dwarf bean Species 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
【発明の詳細な説明】
本発明はターツヤリーブチル ４〔（１３−ジメチル−
５−フェノキシピラゾール−４イル）メチレンイミノオ
キシメチル〕ヘンシェード（以下、化合物Ａという、）
と他の殺ダニ化合物から選択される１種又は２種以上の
化合物を含有することを特徴とする殺ダニ組成物に関す
るものである。DETAILED DESCRIPTION OF THE INVENTION The present invention provides tertiary butyl 4[(13-dimethyl-
5-phenoxypyrazol-4yl)methyleneiminooxymethyl] Henshade (hereinafter referred to as compound A)
The present invention relates to an acaricidal composition containing one or more compounds selected from the group consisting of acaricidal compounds and other acaricidal compounds.
ソ菜、果樹、園芸作物の害虫であるハダニ類等に対して
は、近年新規な殺ダニ剤が創出されているが、一方では
作物種の違いによる効果の不安定性、又単一の薬剤の重
複使用により効果を示さない薬剤抵抗性ハダニ類の出現
が頻繁に問題となってきている。New acaricides have been created in recent years for spider mites, which are pests of vegetable crops, fruit trees, and horticultural crops. The emergence of drug-resistant spider mites that are ineffective due to repeated use has become a frequent problem.
本発明者等は作物種による効果の変動がなく、安定した
殺ダニ効果を発揮し、且つ低薬量化を図ることができる
新規殺ダニ組成物の創出に鋭意研究を重ねた結果、化合
物Ａと他の殺ダニ活性を有する化合物から選択される１
種又は２種以上の化合物を混合して使用することにより
、それぞれ単独で使用した場合に比して、想到し得ない
程の相乗効果が得られることを見出し、本発明を完成さ
せたものである。As a result of extensive research into the creation of a new acaricidal composition that does not vary in effectiveness depending on crop species, exhibits a stable acaricidal effect, and is capable of reducing the dosage, the present inventors found that Compound A and 1 selected from other compounds with acaricidal activity
The present invention was completed based on the discovery that by using a species or a mixture of two or more compounds, an unimaginable synergistic effect can be obtained compared to when each is used alone. be.
本発明の一方の有効成分である化合物Ａは特開昭６３−
１８３５６４号公報に記載された、殺ダニ効果を有する
下記構造式で表される公知の化合物である。Compound A, which is one of the active ingredients of the present invention, is
This is a known compound represented by the following structural formula that has an acaricidal effect and is described in Japanese Patent No. 183564.
本発明の化合物ＡはＥ体及び２体の立体異性体を有する
ものであり、本発明はこれらの立体異性体及びこの混合
物をも包含するものであるが、好ましくはＥ〜異性体が
良い。Compound A of the present invention has an E-isomer and two stereoisomers, and the present invention includes these stereoisomers and mixtures thereof, but preferably the E-isomer is preferred.
又、他方の有効成分である他の殺ダニ化合物としては、
特に限定されるものではないが、化合物Ａと混合した場
合に相乗効果を示す化合物であれば良く、例えば以下に
示す公知の化合物から選択される１種又は２種以上の殺
ダニ化合物を使用することができる。In addition, other acaricidal compounds that are the other active ingredients include:
Although not particularly limited, any compound that exhibits a synergistic effect when mixed with Compound A may be used; for example, one or more acaricidal compounds selected from the following known compounds may be used. be able to.
（１）、、２．２−トリクロロ−１．１−ビス（４−ク
ロロフェニル）エタノール（以下、化合物１という）
（２）、エチル ４，４゛ −ジクロロヘンジレートＣ
以下、化合物２という）
■、イソプロピル ４．４゛−ジクロロヘンジレート（
以下、化合物３という）
■、ビス〔トリス（２−メチル−２−フェニルプロピル
）チン］オキサイド（以下、化合物４という）
（５）、２−（４−ターシャリ−ブチルフェノキシ）シ
クロヘキシル ２−プロピニル サルファイド（以下、
化合物５という）
■、 ｔｒａｎｓ−５（４−クロロフェニル）−Ｎ−
シクロヘキシル−４−メチル−２−オキソチアゾリジン
−３−カルボキサミド（以下、化合物６という）。(1), 2,2-trichloro-1,1-bis(4-chlorophenyl)ethanol (hereinafter referred to as compound 1) (2), ethyl 4,4゛-dichlorohendylate C
(hereinafter referred to as compound 2) ■, isopropyl 4.4゛-dichlorohendylate (
(hereinafter referred to as compound 3) ■, bis[tris(2-methyl-2-phenylpropyl)tin] oxide (hereinafter referred to as compound 4) (5), 2-(4-tert-butylphenoxy)cyclohexyl 2-propynyl sulfide (below,
(referred to as compound 5) ■, trans-5(4-chlorophenyl)-N-
Cyclohexyl-4-methyl-2-oxothiazolidine-3-carboxamide (hereinafter referred to as compound 6).
（７）、３，６−ビス（４−クロロフェニル）−１゜２
．４．５−テトラジン（以下、化合物７という）
■、３−クロローα−エトキシイミノ−２，６−シメト
キシベンジル ベンゾエート（以下、化合物８という）
■、Ｎ−メチルビス（２，４−キシリルイミノメチル）
アミン（以下、化合物９という）［相］、 （Ｒ３）
−α−シアノ−３−フェノキシベンジル Ｎ−（２−ク
ロロ−α、α、α−トリフルオローｐ−）リルーＤ−バ
リネート（以下、化合物ＩＯという）
■、５−４−フェノキシブチル Ｎ、Ｎ−ジメチルチオ
カーバメート（以下、化合物ＩＩという）
＠、 （Ｒ３）−α−シンアノ−３−フェノキシヘン
シル２．２，３．３−テトラメチルシクロプロパンカル
ボキシレート（以下、化合物１２という）
以上の殺ダニ化合物を例示することができるが、本発明
はこれらの殺ダニ化合物に限定されるものではない。(7), 3,6-bis(4-chlorophenyl)-1゜2
．． 4.5-tetrazine (hereinafter referred to as compound 7) ■, 3-chloro α-ethoxyimino-2,6-simethoxybenzyl benzoate (hereinafter referred to as compound 8) ■, N-methylbis(2,4-xylylimino methyl)
Amine (hereinafter referred to as compound 9) [phase], (R3)
-α-cyano-3-phenoxybenzyl N-(2-chloro-α,α,α-trifluoro-p-)lylu-D-valinate (hereinafter referred to as compound IO) ■,5-4-phenoxybutyl N,N- Dimethylthiocarbamate (hereinafter referred to as Compound II) @, (R3)-α-synano-3-phenoxyhensyl 2.2,3.3-tetramethylcyclopropanecarboxylate (hereinafter referred to as Compound 12) The above miticides Although these compounds can be exemplified, the present invention is not limited to these acaricidal compounds.
本発明の化合物Ａと組み合わせて使用する上記殺ダニ化
合物のうちで特に好ましい化合物としては、化合物１乃
至７から選択される化合物である。Among the above acaricidal compounds used in combination with Compound A of the present invention, particularly preferred compounds are compounds selected from Compounds 1 to 7.
本発明の殺ダニ組成物はソ菜、果樹、園芸作物を加害す
る各種ダニ類、例えばナミハダニ、ミカンハダニ、カン
ザワハダニ、リンゴハダニ等のハダニ類に対して、単独
の使用からは想到し得ない相乗効果を奏するものである
。The acaricidal composition of the present invention has a synergistic effect against various mites that attack vegetables, fruit trees, and horticultural crops, such as red spider mite, citrus spider mite, Kanzawa spider mite, apple spider mite, etc., which cannot be expected from its use alone. It is something to play.
本発明は、化合物Ａ及び他の殺ダニ活性を有する化合物
から選択される１種又は２種以上の化合物を適当な割合
に配合して、農薬製剤上の常法に従い、使用に都合の良
い剤形に調製して使用すれば良く、例えば乳剤、水和剤
、粉剤、フロアブル剤等に調製して使用すれば良い。The present invention provides a formulation that is convenient for use by blending one or more compounds selected from Compound A and other compounds with acaricidal activity in appropriate proportions and using the conventional method for agricultural chemical formulations. It may be used by preparing it into a form, for example, an emulsion, a wettable powder, a powder, a flowable agent, etc.
本発明の殺ダニ組成物の有効成分の配合割合は、化合物
Ａ１重量部に対して、他の殺ダニ化合物を０．１〜１０
０重量部の範囲の割合で配合すれば良く、好ましくは０
．１〜５０重量部の範囲の割合で配合するのが良い。The blending ratio of the active ingredients in the acaricidal composition of the present invention is 0.1 to 10 parts by weight of other acaricidal compounds to 1 part by weight of compound A.
It may be blended in a proportion within the range of 0 parts by weight, preferably 0 parts by weight.
．． It is preferable to mix it in a proportion ranging from 1 to 50 parts by weight.
本発明の殺ダニ組成物は上記方法により使用に都合の良
い剤形に調製し、使用に際してはそのまま又は水等で所
望の濃度に希釈して使用すれば良い。The acaricidal composition of the present invention may be prepared into a dosage form convenient for use by the above-mentioned method, and may be used as it is or after being diluted with water or the like to a desired concentration.
以下に本発明の代表的な実施例及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。Typical examples and test examples of the present invention are illustrated below, but the present invention is not limited thereto.
尚、実施例中、部とあるのは重量部を示す。In the examples, parts indicate parts by weight.
実施例１゜
化合物Ａ ３部化合物５
３０部
含水珪酸 ３０部ハイテノールＮ
−０８
（第一工業製薬■製） ３部
リグニンスルホン酸カルシウム ２部永和剤用クレー
３２部化合物５を含水珪酸に含浸させ
た後、他の成分と均一に混合して水和剤とする。Example 1゜Compound A 3 parts Compound 5
30 parts hydrated silicic acid 30 parts Hitenol N
-08 (manufactured by Daiichi Kogyo Seiyaku ■) 3 parts calcium lignin sulfonate 2 parts clay for permanent adhesive 32 parts Compound 5 is impregnated with hydrous silicic acid, and then mixed uniformly with other components to form a wettable powder.
実施例２゜
化合物Ａ ３部化合物１
３０部５Ｐ−３００５Ｘ
（東邦化学■製） １０部
キシレン ５７部以上を均一に混
合溶解し乳剤とする。Example 2゜Compound A 3 parts Compound 1
30 parts 5P-3005X (manufactured by Toho Kagaku ■) 10 parts xylene 57 parts or more are uniformly mixed and dissolved to form an emulsion.
実施例３゜
化合物Ａ ３部化合物７
３０部
ＮＰＥ−１００３部
（第一工業製薬■製）
プロピレングリコール ５部ロドポール２３
０．５部（ロース・ブーラン−製）
水 ５８
、５部以上を均一に混合し、水に分散させてフロアブル
剤とする。Example 3゜Compound A 3 parts Compound 7
30 parts NPE-1003 parts (manufactured by Daiichi Kogyo Seiyaku ■) Propylene glycol 5 parts Rhodopol 23
0.5 parts (manufactured by Lois Boulin) Water 58
, 5 parts or more are uniformly mixed and dispersed in water to prepare a flowable agent.
実施例４゜
化合物Ａ ５部化合物２
５部
ＮＰＥ−１００３部
（第−工業製薬味製）
プロピレングリコール ５部ロドポール２３
（ロース・ブーラン−製） ０．５部水
８４．５部以上を均
一に混合し、水に分散させてフロアブル剤とする。Example 4 Compound A 5 parts Compound 2
5 parts NPE-100 3 parts (manufactured by Dai-Kogyo Seiyaku Aji) Propylene glycol 5 parts Rhodopol 23 (manufactured by Loos-Boulin) 0.5 parts water
Mix 84.5 parts or more uniformly and disperse in water to make a flowable agent.
試験例１．カンザワハダニ成虫に対する試験寒天シャー
レに浮かべたインゲン葉のディスクにカンザワハダニの
雌成虫を接種し、所定濃度に希釈した本発明の殺ダニ組
成物の薬液をスプレーガンで５０ｍ１散布した。Test example 1. Test against adult Kanzawa spider mites Female adult Kanzawa spider mites were inoculated onto a disk of green bean leaves floating on an agar petri dish, and 50 ml of the acaricidal composition of the present invention diluted to a predetermined concentration was sprayed with a spray gun.
散布後、２５°Ｃの恒温室に設置し、２日後に生存虫数
を調査し、下記の式に基づいて補正死生率を算出した。After spraying, the plants were placed in a constant temperature room at 25°C, and two days later, the number of surviving insects was investigated, and the corrected mortality rate was calculated based on the following formula.
１デイスクに１０頭接種し、１区当たり３０頭供試した
。Ten animals were inoculated per disk, and 30 animals per area were tested.
但し、Ａ：無処理区の生存率。However, A: survival rate of untreated area.
Ｂ：処理区の生存率。B: Survival rate of treated plot.
結果を第１表に示す。The results are shown in Table 1.
亀−」−一表 結果を第２表に示す。Turtle-”-1 table The results are shown in Table 2.
特許出願人 日本農薬株式会社Patent applicant: Nihon Nohyaku Co., Ltd.
Claims (1)
−５−フェノキシピラゾール−４−イル）メチレンイミ
ノオキシメチル〕ベンゾエートと他の殺ダニ化合物から
選択される１種又は２種以上の化合物を含有することを
特徴とする殺ダニ組成物。 ［２］、他の殺ダニ化合物が以下の化合物から選択され
る１種又は２種以上である請求項第１項記載の殺ダニ組
成物。 （１）、２，２，２−トリクロロ−１，１−ビス（４−
クロロフェニル）エタノール （２）、エチル４，４’−ジクロロベンジレート（３）
、イソプロピル４，４’−ジクロロベンジレート （４）、ビス〔トリス（２−メチル−２−フェニルプロ
ピル）チン〕オキサイド （５）、２−（４−ターシャリ−ブチルフェノキシ）シ
クロヘキシル２−プロピニルサルファイド （６）、ｔｒａｎｓ−５−（４−クロロフェニル）−Ｎ
−シクロヘキシル−４−メチル−２−オキソチアゾリジ
ン−３−カルボキサミド （７）、３，６−ビス（４−クロロフェニル）１，２，
４，５−テトラジン[Scope of Claims] [1] One species selected from tertiary-butyl 4-[(1,3-dimethyl-5-phenoxypyrazol-4-yl)methyleneiminooxymethyl]benzoate and other acaricidal compounds Or an acaricidal composition characterized by containing two or more kinds of compounds. [2] The acaricidal composition according to claim 1, wherein the other acaricidal compound is one or more selected from the following compounds. (1), 2,2,2-trichloro-1,1-bis(4-
chlorophenyl) ethanol (2), ethyl 4,4'-dichlorobenzilate (3)
, isopropyl 4,4'-dichlorobenzilate (4), bis[tris(2-methyl-2-phenylpropyl)tin]oxide (5), 2-(4-tert-butylphenoxy)cyclohexyl 2-propynyl sulfide ( 6), trans-5-(4-chlorophenyl)-N
-cyclohexyl-4-methyl-2-oxothiazolidine-3-carboxamide (7), 3,6-bis(4-chlorophenyl) 1,2,
4,5-tetrazine
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2192261A JP2976234B2 (en) | 1990-07-20 | 1990-07-20 | Acaricidal composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2192261A JP2976234B2 (en) | 1990-07-20 | 1990-07-20 | Acaricidal composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH0477402A true JPH0477402A (en) | 1992-03-11 |
| JP2976234B2 JP2976234B2 (en) | 1999-11-10 |
Family
ID=16288346
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2192261A Expired - Fee Related JP2976234B2 (en) | 1990-07-20 | 1990-07-20 | Acaricidal composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2976234B2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1997039630A1 (en) * | 1996-04-22 | 1997-10-30 | Basf Aktiengesellschaft | Process and agents for controlling harmful fungi |
-
1990
- 1990-07-20 JP JP2192261A patent/JP2976234B2/en not_active Expired - Fee Related
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1997039630A1 (en) * | 1996-04-22 | 1997-10-30 | Basf Aktiengesellschaft | Process and agents for controlling harmful fungi |
| US6143745A (en) * | 1996-04-22 | 2000-11-07 | Basf Aktiengesellschaft | Process and agent for controlling harmful fungi |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2976234B2 (en) | 1999-11-10 |
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| Date | Code | Title | Description |
|---|---|---|---|
| R250 | Receipt of annual fees |
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| LAPS | Cancellation because of no payment of annual fees |