JPH07330516A - Fungicide composition - Google Patents

Fungicide composition

Info

Publication number
JPH07330516A
JPH07330516A JP12630594A JP12630594A JPH07330516A JP H07330516 A JPH07330516 A JP H07330516A JP 12630594 A JP12630594 A JP 12630594A JP 12630594 A JP12630594 A JP 12630594A JP H07330516 A JPH07330516 A JP H07330516A
Authority
JP
Japan
Prior art keywords
compound
parts
formula
fungicide composition
blight
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
JP12630594A
Other languages
Japanese (ja)
Inventor
Yukio Oguri
幸男 小栗
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.)
Sumitomo Chemical Co Ltd
Original Assignee
Sumitomo Chemical 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 Sumitomo Chemical Co Ltd filed Critical Sumitomo Chemical Co Ltd
Priority to JP12630594A priority Critical patent/JPH07330516A/en
Publication of JPH07330516A publication Critical patent/JPH07330516A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To obtain a fungicide composition extremely effective for simultneously controlling sheath blight and blast of rice plant, by using both a specific pyrazole compound and a specific methoxyiminoacetamide compound. CONSTITUTION:This fungicide composition comprises N-(1,1,3-trimethyl-2-oxa-4- indanyl)-5-chloro-1,3-dimethylpyrazole-4-carboxyamide of formula I and N- methyl-alpha-methoxyimino-2-phenoxyphenylacetamide of formula II as active ingredients. The fungicide composition is effective not only for sheath blight of rice plant but also for false sheath blight and helminthosporium leaf spot of rice plant, rust, snow blight, foot rot and loose smut of wheat, Rhizoctonia solani of potato and beet, rust of apple and pear, brown patch of lawn grass, bacterial wilt and stem rot of various crops. The blending ratio of the compound of formula I and the compound of formula II is preferably in the range of 1:0.1 to 100 by weight.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は殺菌剤組成物、特に、イ
ネの病害を防除するのに適した殺菌剤組成物に関するも
のである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a fungicide composition, and more particularly to a fungicide composition suitable for controlling diseases of rice.

【0002】[0002]

【従来の技術および発明が解決しようとする課題】現
在、イネの栽培において紋枯病といもち病とは最も重要
な病害であって、この二病害の防除が安定した米の収穫
をもたらすといえる。
[Background Art] [Technical Problem and Problem to be Solved by the Invention] At present, blight and blast are the most important diseases in rice cultivation, and it can be said that the control of these two diseases results in stable rice harvest. .

【0003】[0003]

【課題を解決するための手段】本発明は、イネの紋枯病
といもち病とを同時に防除する上で、極めて効果的な殺
菌剤組成物を提供するものであり、該殺菌剤組成物は、
有効成分としてN−(1,1,3−トリメチル−2−オ
キサ−4−インダニル)−5−クロロ−1,3−ジメチ
ルピラゾール−4−カルボキシアミド、即ち、式
DISCLOSURE OF THE INVENTION The present invention provides a very effective bactericide composition for simultaneously controlling rice blight and blast of rice, and the bactericide composition is ,
As an active ingredient, N- (1,1,3-trimethyl-2-oxa-4-indanyl) -5-chloro-1,3-dimethylpyrazole-4-carboxamide, that is, the formula

【化3】 で示されるピラゾール化合物(以下、化合物Aと記
す。)とN−メチル−α−メトキシイミノ−2−フェノ
キシフェニルアセトアミド、即ち、式
[Chemical 3] And a N-methyl-α-methoxyimino-2-phenoxyphenylacetamide, that is, a compound represented by the formula:

【化4】 で示されるメトキシイミノ酢酸アミド化合物(以下、化
合物Bと記す。)とを含有するものである。化合物Aは
特開平2−131481号公報に記載の化合物であり、
化合物Bは特開平3−246268号公報に記載の化合
物であって、これらの公報の記載にしたがって化合物A
および化合物Bを得ることができる。
[Chemical 4] And a methoxyiminoacetic acid amide compound (hereinafter referred to as compound B). Compound A is a compound described in JP-A-2-131481,
The compound B is the compound described in JP-A-3-246268, and the compound A according to the description in these publications.
And compound B can be obtained.

【0004】本発明の殺菌剤組成物は、イネの紋枯病
(Rhizoctonia solani)といもち病(Pyricularia oryz
ae)のみならず、イネの擬似紋枯病(Rhizoctonia oryz
ae, R.solani III B 型)、ごま葉枯病(Cochliobolus
miyabeanus )、ムギのさび病(Puccinia striiformis,
P. graminis, P. recondita, P. hordei)、雪腐病(T
yphula incarnata, T. ishikariensis )、株腐病(Rhi
zoctonia cerealis)、裸黒穂病(Ustilago tritici,
U. nuda )、ジャガイモやビートのリゾクトニア病(Rh
izoctonia solani)、リンゴやナシの赤星病(Gymnospo
rangium sp. )、芝生等のブラウンパッチ病(Rhizocto
nia solani)、各種作物の立枯病(Rhizoctonia solan
i)、白絹病(Corticium rolfsii )等の防除において
も有効である。また、イネの紋枯病等のリゾクトニア属
による病害の防除においては、その優れた相乗効果によ
り特に卓効を示すものである。
The fungicidal composition of the present invention is applied to rice blight (Rhizoctonia solani) and blast (Pyricularia oryz).
ae) as well as pseudo-blight of rice (Rhizoctonia oryz)
ae, R.solani III type B), sesame leaf blight (Cochliobolus)
miyabeanus), wheat rust (Puccinia striiformis,
P. graminis, P. recondita, P. hordei), snow rot (T
yphula incarnata, T. ishikariensis), strain rot (Rhi
zoctonia cerealis), naked smut (Ustilago tritici,
U. nuda), potatoes and beets of Rhizoctonia (Rh
izoctonia solani), red scab (Gymnospo) on apples and pears
rangium sp.), brown patch disease (Rhizocto
nia solani), wilt of various crops (Rhizoctonia solan
It is also effective for controlling i) and white silkworm (Corticium rolfsii). Further, in controlling disease caused by Rhizoctonia such as rice blight, it is particularly effective due to its excellent synergistic effect.

【0005】本発明の殺菌剤組成物において、化合物A
と化合物Bとの混合割合は広範囲にわたって変えること
ができるが、通常、重量比で1:0.01〜1000、好ましく
は1:0.1 〜 100の範囲内である。
In the fungicide composition of the present invention, compound A
The mixing ratio of the compound B with the compound B can be varied over a wide range, but it is usually within the range of 1: 0.01 to 1000, preferably 1: 0.1 to 100 by weight.

【0006】本発明の殺菌剤組成物は、通常固体担体、
液体担体、ガス状担体等と混合し、必要により界面活性
剤、その他の製剤用補助剤等を添加して、油剤、乳剤、
水和剤、粒剤、粉剤、エアゾール、懸濁剤、泡沫剤、マ
イクロカプセル製剤、種子用被覆剤、ULV(コールド
ミスト、ウォームミスト)製剤、ペースト剤等に製剤化
して用いられる。これらの製剤中には、化合物Aおよび
化合物Bの合計量が一般に 0.1〜 99.9重量%、好まし
くは 0.2〜 80 重量%含有される。
The fungicide composition of the present invention is usually a solid carrier,
Mixing with a liquid carrier, a gaseous carrier, etc., and optionally adding a surfactant, other auxiliary agents for formulation, etc., an oil solution, an emulsion,
It is used as a wettable powder, granules, powder, aerosol, suspension, foam, microcapsule formulation, seed coating, ULV (cold mist, warm mist) formulation, paste and the like. In these formulations, the total amount of compound A and compound B is generally 0.1-99.9% by weight, preferably 0.2-80% by weight.

【0007】製剤化する際に用いられる固体担体として
は、例えば粘土類(カオリナイト、珪藻土、合成含水酸
化珪素、フバサミクレー、ベントナイト、酸性白土
等)、タルク、その他の無機鉱物(セリサイト、石英粉
末、硫黄粉末、活性炭、炭酸カルシウム等)、化学肥料
(硫安、燐安、硝安、塩安、尿素等)などの微粉末や粒
状物が挙げられ、液体担体としては、例えば水、アルコ
ール類(メタノール、エタノール等)、ケトン類(アセ
トン、メチルエチルケトン、シクロヘキサノン等)、芳
香族炭化水素類(トルエン、キシレン、エチルベンゼ
ン、メチルナフタレン等)、非芳香族炭化水素類(ヘキ
サン、シクロヘキサン、ケロシン等)、エステル類(酢
酸エチル、酢酸ブチル等)、ニトリル類(アセトニトリ
ル、イソブチロニトリル等)、エーテル類(ジオキサ
ン、ジイソプロピルエーテル等)、酸アミド類(ジメチ
ルホルムアミド、ジメチルアセトアミド等)、ハロゲン
化炭化水素類(ジクロロエタン、トリクロロエチレン)
などが挙げられ、ガス状担体、即ち噴射剤としては、例
えば炭酸ガス、ブタンガス、フルオロカーボンなどが挙
げられる。
Examples of solid carriers used for formulation include clays (kaolinite, diatomaceous earth, synthetic hydrous silicon oxide, fubasami clay, bentonite, acid clay, etc.), talc, and other inorganic minerals (sericite, quartz powder). , Sulfur powder, activated carbon, calcium carbonate, etc., chemical fertilizers (ammonium sulphate, ammonium phosphate, ammonium nitrate, ammonium chloride, urea, etc.), etc., and fine powders and granules. Examples of the liquid carrier include water and alcohols (methanol). , Ethanol, etc.), ketones (acetone, methyl ethyl ketone, cyclohexanone, etc.), aromatic hydrocarbons (toluene, xylene, ethylbenzene, methylnaphthalene, etc.), non-aromatic hydrocarbons (hexane, cyclohexane, kerosene, etc.), esters (Ethyl acetate, butyl acetate, etc.), Nitriles (acetonitrile, isobutyronitrile) ), Ethers (dioxane, diisopropyl ether), acid amides (dimethylformamide, dimethylacetamide), halogenated hydrocarbons (dichloroethane, trichlorethylene)
Examples of the gaseous carrier, that is, the propellant include carbon dioxide gas, butane gas, fluorocarbon and the like.

【0008】界面活性剤としては、例えばアルキル硫酸
エステル類、アルキルスルホン酸塩、アルキルアリール
スルホン酸塩、アルキルアリールエーテル類およびその
ポリオキシエチレン化物、ポリエチレングリコールエー
テル類、多価アルコールエステル類、糖アルコール誘導
体などが挙げられる。その他の製剤用補助剤としては、
例えばカゼイン、ゼラチン、多糖類(澱粉、アラビアガ
ム、セルロース誘導体、アルギン酸等)、リグニン誘導
体、ベントナイト、合成水溶性高分子(ポリビニルアル
コール、ポリビニルピロリドン、ポリアクリル酸等)な
どの固着剤や分散剤、PAP(酸性リン酸イソプロピ
ル)、BHT(2,6-ジ-tert-ブチル−4−メチルフェノ
ール)、BHA(2−/3−tert−ブチル−4−メトキ
シフェノール)、植物油、鉱物油、脂肪酸、脂肪酸エス
テルなどの安定剤が挙げられる。
Examples of the surfactant include alkyl sulfates, alkyl sulfonates, alkyl aryl sulfonates, alkyl aryl ethers and polyoxyethylenated products thereof, polyethylene glycol ethers, polyhydric alcohol esters, sugar alcohols. Examples thereof include derivatives. Other auxiliary agents for formulation include
For example, casein, gelatin, polysaccharides (starch, gum arabic, cellulose derivatives, alginic acid, etc.), lignin derivatives, bentonite, synthetic water-soluble polymers (polyvinyl alcohol, polyvinylpyrrolidone, polyacrylic acid, etc.), etc. PAP (isopropyl acid phosphate), BHT (2,6-di-tert-butyl-4-methylphenol), BHA (2- / 3-tert-butyl-4-methoxyphenol), vegetable oil, mineral oil, fatty acid, Examples include stabilizers such as fatty acid esters.

【0009】製剤化された本発明の殺菌剤組成物は、そ
のままでまたは水等で希釈して植物体、水面または土壌
に施用される。施用場所としては、水田、畑地、果樹
園、牧草地、芝生等が挙げられる。また、種子粉衣処
理、種子浸漬処理等の種子処理に用いることもできる。
さらに、他の殺菌剤、殺虫剤、除草剤、肥料、土壌改良
剤等と併用することもできる。
The formulated fungicidal composition of the present invention is applied to a plant, water surface or soil as it is or after diluted with water or the like. Examples of application sites include paddy fields, upland fields, orchards, meadows, lawns and the like. It can also be used for seed treatment such as seed dressing treatment and seed dipping treatment.
Further, it can be used in combination with other fungicides, insecticides, herbicides, fertilizers, soil conditioners and the like.

【0010】本発明の殺菌剤組成物の施用量は、有効成
分化合物である化合物Aおよび化合物Bの混合比、気象
条件、製剤形態、施用時期、施用方法、施用場所、防除
対象病害、対象作物等により異なるが、通常1アール当
たり有効成分化合物量にして0.001〜 1000 g、好まし
くは 0.1〜 100gである。乳剤、水和剤、懸濁剤、液剤
等を水で希釈して施用する場合、その施用濃度は 0.000
1 〜1%、好ましくは0.001〜 0.5%であり、粒剤、粉
剤等は通常希釈することなくそのまま施用する。種子処
理用としては、有効成分化合物量にして種子1kg当たり
通常 0.001〜 50 g、好ましくは 0.01 〜 10 g用いら
れる。土壌処理用としては、通常1アール当たり有効成
分化合物量にして 0.01 〜 1000 g、好ましくは 0.01
〜 100g用いられる。水田の水面処理用としては、通常
1アール当たり有効成分化合物量にして 0.01 〜 400
g、好ましくは1〜 100gであり、イネ育苗箱処理にお
いては、1箱(30cm×60cm×3cm)当たりの有効成分化
合物量にして、通常 0.1〜 100gである。本発明の殺菌
剤組成物は特にイネの病害を防除するのに適し、イネ苗
を育苗箱で育成している時期から田植え後収穫に至る前
までの広範な時期に使用でき、紋枯病、いもち病の防除
に卓効を示すものである。
The application rate of the fungicide composition of the present invention is as follows: mixing ratio of the active ingredient compounds, compound A and compound B, weather conditions, formulation form, application time, application method, application site, disease to be controlled, target crop. The amount is usually 0.001 to 1000 g, preferably 0.1 to 100 g in terms of the amount of the active ingredient compound per are. When emulsions, wettable powders, suspensions, solutions, etc. are diluted with water before application, the application concentration is 0.000.
It is 1 to 1%, preferably 0.001 to 0.5%, and granules, powders and the like are usually applied as they are without dilution. For seed treatment, the amount of the active ingredient compound is usually 0.001 to 50 g, preferably 0.01 to 10 g per 1 kg of seeds. For soil treatment, the amount of the active ingredient compound is usually 0.01 to 1000 g, preferably 0.01 per 1 are.
~ 100g is used. For water surface treatment of paddy fields, the amount of active ingredient compound is usually 0.01 to 400 per are.
g, preferably 1 to 100 g, and in the rice seedling raising box treatment, the amount of the active ingredient compound per box (30 cm × 60 cm × 3 cm) is usually 0.1 to 100 g. The fungicide composition of the present invention is particularly suitable for controlling rice diseases, and can be used in a wide range of times from the time when rice seedlings are grown in a nursery box to the time after harvesting after rice planting, and blight blight, It shows excellent efficacy in controlling blast disease.

【0011】[0011]

【実施例】以下、製剤例および試験例を示す。以下の例
において部は重量部を表す。 製剤例1 化合物A 0.5部、化合物B 8部、合成含水酸化珪素
1部、リグニンスルホン酸カルシウム 2部、ベントナ
イト 30 部およびカオリンクレー 58.5 部をよく粉砕混
合し、水を加えてよく練り合わせた後、造粒、乾燥して
粒剤を得る。 製剤例2 化合物A 1.2部、化合物B 5部、合成含水酸化珪素
1部、リグニンスルホン酸カルシウム 2部、ベントナ
イト 30 部およびカオリンクレー 60.8 部をよく粉砕混
合し、水を加えてよく練り合わせた後、造粒、乾燥して
粒剤を得る。 製剤例3 化合物A 1.5部、化合物B 2部、合成含水酸化珪素
1部、リグニンスルホン酸カルシウム 2部、ベントナ
イト 30 部およびカオリンクレー 63.5 部をよく粉砕混
合し、水を加えてよく練り合わせた後、造粒、乾燥して
粒剤を得る。
[Examples] Formulation examples and test examples are shown below. In the following examples, parts represent parts by weight. Formulation Example 1 Compound A 0.5 part, Compound B 8 parts, synthetic hydrous silicon oxide
1 part, 2 parts of calcium lignin sulfonate, 30 parts of bentonite and 58.5 parts of kaolin clay are well pulverized and mixed, water is added and well kneaded, and then granulated and dried to obtain granules. Formulation Example 2 Compound A 1.2 parts, Compound B 5 parts, synthetic hydrous silicon oxide
1 part, 2 parts of calcium lignin sulfonate, 30 parts of bentonite and 60.8 parts of kaolin clay are well pulverized and mixed, water is added and well kneaded, and then granulated and dried to obtain granules. Formulation Example 3 Compound A 1.5 parts, Compound B 2 parts, synthetic hydrous silicon oxide
1 part, 2 parts of calcium lignin sulfonate, 30 parts of bentonite and 63.5 parts of kaolin clay are thoroughly pulverized and mixed, water is added and the mixture is well kneaded, and then granulated and dried to obtain granules.

【0012】製剤例4 化合物A 2部、化合物B 17 部、合成含水酸化珪素
1部、リグニンスルホン酸カルシウム 2部、ベントナ
イト 25 部およびカオリンクレー 53 部をよく粉砕混合
し、水を加えてよく練り合わせた後、造粒、乾燥して粒
剤を得る。 製剤例5 化合物A 0.3部、化合物B 2.5部、カオリンクレー 86
部およびタルク 11.2部をよく粉砕混合して粉剤を得
る。 製剤例6 化合物A 0.5部、化合物B 1部、カオリンクレー 88
部およびタルク 10.5部をよく粉砕混合して粉剤を得
る。 製剤例7 化合物A 1部、化合物B 1.5部、カオリンクレー 88
部およびタルク 9.5部をよく粉砕混合して粉剤を得る。
Formulation Example 4 Compound A 2 parts, Compound B 17 parts, synthetic hydrous silicon oxide
1 part, 2 parts of calcium lignin sulfonate, 25 parts of bentonite and 53 parts of kaolin clay are well pulverized and mixed, water is added and well kneaded, and then granulated and dried to obtain granules. Formulation Example 5 Compound A 0.3 parts, Compound B 2.5 parts, Kaolin clay 86
Parts and 11.2 parts of talc are well pulverized and mixed to obtain a powder. Formulation Example 6 Compound A 0.5 part, Compound B 1 part, Kaolin clay 88
Parts and 10.5 parts of talc are well pulverized and mixed to obtain a powder. Formulation Example 7 Compound A 1 part, Compound B 1.5 parts, Kaolin clay 88
Parts and 9.5 parts of talc are well pulverized and mixed to obtain a powder.

【0013】製剤例8 化合物A 5部、化合物B 20 部、ポリオキシエチレン
ソルビタンモノオレエート 3部、CMC(カルボキシ
メチルセルロース) 3部および水 69 部を混合し、粒
度が5μ以下になるまで湿式粉砕して懸濁剤を得る。 製剤例9 化合物A 15 部、化合物B 60 部、リグニンスルホン酸
カルシウム 3部、ラウリル硫酸ナトリウム 2部およ
び合成含水酸化珪素 20 部をよく粉砕混合して水和剤を
得る。 製剤例10 化合物A 10 部、化合物B 30 部、ポリオキシエチレン
スチリルフェニルエーテル 14 部、ドデシルベンゼンス
ルホン酸カルシウム 6部およびキシレン 40部を混合
して乳剤を得る。
Formulation Example 8 5 parts of compound A, 20 parts of compound B, 3 parts of polyoxyethylene sorbitan monooleate, 3 parts of CMC (carboxymethyl cellulose) and 69 parts of water are mixed and wet pulverized until the particle size becomes 5 μm or less. To obtain a suspension. Formulation Example 9 15 parts of compound A, 60 parts of compound B, 3 parts of calcium lignin sulfonate, 2 parts of sodium lauryl sulfate and 20 parts of synthetic hydrous silicon oxide are well pulverized and mixed to obtain a wettable powder. Formulation Example 10 10 parts of compound A, 30 parts of compound B, 14 parts of polyoxyethylene styryl phenyl ether, 6 parts of calcium dodecylbenzenesulfonate and 40 parts of xylene are mixed to obtain an emulsion.

【0014】試験例1 プラスチックポットに砂壌土を詰め、イネ(近畿33
号)を播種し、温室内で20日間育成した。製剤例8に
準じて懸濁剤にした供試薬剤を水で希釈して所定濃度に
し、イネ幼苗の葉面に十分付着するように茎葉散布し
た。薬液風乾後、紋枯病菌の菌核を株元に接種した。接
種後、27℃多湿下で10日間保った後、発病度(%)
を調査した。結果を表1に示す。
Test Example 1 A plastic pot was filled with sandy loam soil, and rice (Kinki 33
No.) was sowed and grown in a greenhouse for 20 days. The reagent solution made into a suspension according to Formulation Example 8 was diluted with water to a predetermined concentration and sprayed on foliage so as to adhere sufficiently to the leaf surface of rice seedlings. After air-drying with a chemical solution, the sclerotium of the wilt fungus was inoculated into the strain source. After inoculation, after keeping at 27 ° C and high humidity for 10 days, the degree of disease (%)
investigated. The results are shown in Table 1.

【表1】 [Table 1]

【0015】試験例2 1/10000アールのワグネルポットに砂壌土を詰め
水をはり、2葉期のイネ(近畿33号)を移植し、温室
内で7日間育成した。その後、製剤例2に準じて粒剤に
した供試薬剤を各ポットに水面処理した。処理7日後
に、紋枯病菌の菌核を株元に接種した。接種後、27℃
多湿下で10日間保った後、発病度(%)を調査した。
結果を表2に示す。
Test Example 2 Wagner pots of 1/10000 are were filled with sandy loam soil, watered, and 2-leaf stage rice (Kinki No. 33) was transplanted and grown in a greenhouse for 7 days. Then, each pot was subjected to water surface treatment with a reagent agent made into granules according to Formulation Example 2. Seven days after the treatment, the strain roots were inoculated with the sclerotia of the bacterial wilt disease. 27 ° C after inoculation
After being kept under high humidity for 10 days, the disease severity (%) was investigated.
The results are shown in Table 2.

【表2】 表1および表2の結果に見られるように、本発明の殺菌
剤組成物はその相乗効果により優れた殺菌効力を有す
る。
[Table 2] As can be seen from the results of Table 1 and Table 2, the fungicide composition of the present invention has excellent bactericidal efficacy due to its synergistic effect.

【0016】試験例3 プラスチックポットに砂壌土を詰め、イネ(近畿33
号)を播種し、温室内で20日間育成した。製剤例9に
準じて水和剤にした供試薬剤を水で希釈して所定濃度
(化合物A/化合物B;150ppm/200ppm)にし、イネ幼
苗の葉面に十分付着するように茎葉散布した。薬液風乾
後、いもち病菌の胞子懸濁液を噴霧接種した。接種後、
24℃多湿下で10日間保った後、発病度(%)を調査
したところ、発病度は0%であった。
Test Example 3 A plastic pot was filled with sandy loam, and rice (Kinki 33
No.) was sowed and grown in a greenhouse for 20 days. The reagent solution made into a wettable powder according to Formulation Example 9 was diluted with water to a predetermined concentration (Compound A / Compound B; 150 ppm / 200 ppm) and sprayed on foliage so that it was sufficiently attached to the leaf surface of rice seedlings. After air-drying the drug solution, a spore suspension of blast fungus was spray-inoculated. After inoculation,
After keeping the temperature at 24 ° C. and high humidity for 10 days, the degree of disease (%) was investigated and found to be 0%.

【0017】[0017]

【発明の効果】本発明の殺菌剤組成物は、紋枯病、いも
ち病等イネ病害の防除において極めて有効である。
The fungicidal composition of the present invention is extremely effective in controlling rice diseases such as blight and blast.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】式 【化1】 で示されるピラゾール化合物と式 【化2】 で示されるメトキシイミノ酢酸アミド化合物とを有効成
分として含有することを特徴とする殺菌剤組成物。
1. The formula: And a pyrazole compound represented by the formula: The bactericidal composition comprising a methoxyiminoacetic acid amide compound represented by the formula (1) as an active ingredient.
【請求項2】イネの病害を防除するための請求項1記載
の殺菌剤組成物。
2. The fungicide composition according to claim 1 for controlling rice diseases.
JP12630594A 1994-06-08 1994-06-08 Fungicide composition Pending JPH07330516A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP12630594A JPH07330516A (en) 1994-06-08 1994-06-08 Fungicide composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP12630594A JPH07330516A (en) 1994-06-08 1994-06-08 Fungicide composition

Publications (1)

Publication Number Publication Date
JPH07330516A true JPH07330516A (en) 1995-12-19

Family

ID=14931912

Family Applications (1)

Application Number Title Priority Date Filing Date
JP12630594A Pending JPH07330516A (en) 1994-06-08 1994-06-08 Fungicide composition

Country Status (1)

Country Link
JP (1) JPH07330516A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1997010716A1 (en) * 1995-09-22 1997-03-27 Basf Aktiengesellschaft Harmful fungi control with an active substance inhibiting respiration by inhibiting the cytochrome complex iii, combined with an amide

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1997010716A1 (en) * 1995-09-22 1997-03-27 Basf Aktiengesellschaft Harmful fungi control with an active substance inhibiting respiration by inhibiting the cytochrome complex iii, combined with an amide

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