JP2002255709A - Fungicide for controlling infectious disease and downy mildew - Google Patents

Fungicide for controlling infectious disease and downy mildew

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Publication number
JP2002255709A
JP2002255709A JP2001056363A JP2001056363A JP2002255709A JP 2002255709 A JP2002255709 A JP 2002255709A JP 2001056363 A JP2001056363 A JP 2001056363A JP 2001056363 A JP2001056363 A JP 2001056363A JP 2002255709 A JP2002255709 A JP 2002255709A
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JP
Japan
Prior art keywords
downy mildew
fungicide
disease
parts
infectious disease
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
Application number
JP2001056363A
Other languages
Japanese (ja)
Other versions
JP4676626B2 (en
Inventor
Junro Kishi
淳郎 貴志
Yuji Yanase
勇次 柳瀬
Tomohisa Akese
智久 明瀬
Hideo Kawashima
秀雄 川島
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.)
Mitsui Chemicals Inc
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Mitsui Chemicals Inc
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Priority to JP2001056363A priority Critical patent/JP4676626B2/en
Publication of JP2002255709A publication Critical patent/JP2002255709A/en
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Publication of JP4676626B2 publication Critical patent/JP4676626B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Abstract

PROBLEM TO BE SOLVED: To obtain a fungicide which exhibits excellent control effects on infectious diseases and downy mildew. SOLUTION: This fungicide for controlling infectious diseases and downy mildew is characterized by containing N-(2-chloro-4-nitrophenyl)-3- trifluoromethylbenzenesulfonamide compound. The compound exhibits excellent control effects, when used against infectious diseases and downy mildew.

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】本発明は新規な疫病およびべ
と病防除用殺菌剤に関する。
TECHNICAL FIELD The present invention relates to a novel fungicide for controlling plague and downy mildew.

【0002】[0002]

【従来の技術】従来より、作物栽培上の大きな障害の1
つとして作物の病害がある。病害の中でも特に疫病、べ
と病は、最も難防除な病害の1つになっている。その理
由としては、防除効果の高い薬剤(フェニルアミド系の
薬剤)で耐性菌の発生が認められており、薬剤の防除効
果が低下してきているからである。耐性菌の発生は、結
果的に薬量を高め、環境への負荷も大きくなる。耐性菌
の発生を防ぎ高い防除効果を維持するためには、作用の
異なる既存剤の組み合わせによる混合剤の開発、また薬
剤自身の使用回数の制限などの手段により試みられてい
る。
2. Description of the Related Art Conventionally, one of the major obstacles in crop cultivation is one.
One is crop diseases. Among the diseases, plague and downy mildew are among the most difficult to control. The reason for this is that the generation of resistant bacteria has been observed with a drug having a high control effect (phenylamide-based drug), and the control effect of the drug has been reduced. The occurrence of resistant bacteria results in an increase in the amount of drug and an increase in the burden on the environment. In order to prevent the occurrence of resistant bacteria and maintain a high control effect, attempts have been made by means of developing a mixed agent by combining existing agents having different actions, and limiting the number of times the agent itself is used.

【0003】スルホンアミド系化合物は古くから数多く
の化合物が合成され、その生理活性について多くの研究
がなされている。農業分野においては、除草剤・殺菌剤
はもちろんのこと殺虫剤についても研究がなされてい
る。例えば除草剤としては、特公昭39-29571号公報、特
公昭40−19199号公報があり、殺菌剤としては特公昭44-
9304号公報、特公昭45-6836号公報、特公昭46-6797号公
報、特公昭47-15119号公報、特開昭57-31655号公報、特
開昭58-118558号公報および特開昭58-219159号公報等が
あげられる。また、殺虫剤としては、米国特許3,034,95
5号公報があげられる。
[0003] Many sulfonamide compounds have been synthesized for a long time, and many studies have been made on their physiological activities. In the agricultural field, research is being conducted on pesticides as well as herbicides and fungicides. For example, as herbicides, there are JP-B-39-29571 and JP-B-40-19199.
No. 9304, JP-B-45-6836, JP-B-46-6797, JP-B-47-15119, JP-A-57-31655, JP-A-58-118558 and JP-A-58 -219159 and the like. As insecticides, US Patent 3,034,95
No. 5 gazette.

【0004】また、スルホンアミド系化合物の中でも、
N−(2−クロロ−4−ニトロフェニル)−3−トリフルオ
ロメチルベンゼンスルホンアミド化合物(以下フルスル
ファミドと略す)については、特公平6-27113号公報に
てアブラナ科野菜の根こぶ病、ジャガイモそうか病、ジ
ャガイモ粉状そうか病および各種アファノマイセス菌に
対して優れた防除効果を示すことが記載されている。し
かし、その他の病害への適用については記載も示唆もさ
れていない。
[0004] Among sulfonamide compounds,
N- (2-chloro-4-nitrophenyl) -3-trifluoromethylbenzenesulfonamide compound (hereinafter abbreviated as fursulfamide) is disclosed in Japanese Patent Publication No. Hei 6-27113, the clubroot disease of cruciferous vegetables and potato soybean. It is described that it shows an excellent control effect on scab, potato powder scab and various Aphanomyces fungi. However, there is no mention or suggestion of application to other diseases.

【0005】[0005]

【発明が解決しようとする課題】本発明は新規な疫病、
べと病防除用殺菌剤を提供することを課題とする。
SUMMARY OF THE INVENTION The present invention relates to a novel plague,
It is an object to provide a fungicide for controlling downy mildew.

【0006】[0006]

【課題を解決するための手段】本発明者らは、フルスル
ファミドが公知文献などからは全く予想できない病害で
ある疫病、べと病に対して高い生理活性を有し、作物に
も薬害を発生させないことを見出し、前記課題を解決し
た。
DISCLOSURE OF THE INVENTION The present inventors have found that flusulfamide has high physiological activity against plague and downy mildew, which are diseases that cannot be predicted at all from known literatures, and does not cause phytotoxicity on crops. The present inventors have found that the above problem has been solved.

【0007】すなわち本発明は、N−(2−クロロ−4−
ニトロフェニル)−3−トリフルオロメチルベンゼンス
ルホンアミドを含有する組成物であることを特徴とする
疫病、べと病防除用殺菌剤である。
That is, the present invention relates to N- (2-chloro-4-
A fungicide for controlling plague and downy mildew, which is a composition containing (nitrophenyl) -3-trifluoromethylbenzenesulfonamide.

【0008】[0008]

【発明の実施の形態】本発明に係るN−(2−クロロ−4
−ニトロフェニル)−3−トリフルオロメチルベンゼン
スルホンアミド化合物(フルスルファミド)は、それ自
体公知の化合物であり、公知の製造方法で製造すること
が出来る。
BEST MODE FOR CARRYING OUT THE INVENTION The N- (2-chloro-4) according to the present invention
-Nitrophenyl) -3-trifluoromethylbenzenesulfonamide compound (flusulfamide) is a compound known per se, and can be produced by a known production method.

【0009】フルスルファミドを含有する組成物を疫
病、べと病防除剤として使用する場合は、処理する植物
に対して原体をそのまま使用してもよいが、一般的には
不活性な液体担体、固体担体、界面活性剤と混合し、通
常用いられる製剤形態である、粉剤、水和剤、粒剤、フ
ロアブル剤、乳剤およびその他の一般に慣用される形態
の製剤として使用される。更に製剤上必要ならば補助剤
を添加することもできる。
When the composition containing flusulfamide is used as an agent for controlling plague and downy mildew, the drug substance may be used as it is for the plant to be treated, but generally an inert liquid carrier, It is mixed with a solid carrier and a surfactant and used in the form of powders, wettable powders, granules, flowables, emulsions and other commonly used forms which are usually used. If necessary for the preparation, an auxiliary agent can be added.

【0010】ここでいう担体としては、処理すべき部位
への有効成分の到達を助け、また有効成分化合物の貯
蔵、輸送、取り扱いを容易にするために配合される合成
または天然の無機または有機物質を意味する。担体とし
ては、通常農園園芸用薬剤に使用されるものであるなら
ば固体または液体のいずれでも使用でき、特定のものに
限定されるものではない。例えば、固体担体としては、
モンモリロナイト、カオリナイト等の粘度類、珪藻土、
白土、タルク、バーミキュライト、炭酸カルシウム、シ
リカゲル、硫安などの無機物質、小麦粉、大豆粉、デン
プン、結晶セルロース等の植物性有機質、石油樹脂、ポ
リアルキレングリコール等の高分子化合物、尿素、ワッ
クス類等があげられる。液体担体としては、トルエン、
キシレン、クメンなどの芳香族炭化水素類、ケロシン、
鉱油などのパラフィン系炭化水素類、アセトン、メチル
エチルケトン、ジクロヘキサノンなどのケトン類、ジオ
キサン、ジエチレングリコールジメチルエーテルなどの
エーテル類、メタノール、エタノール、プロパノール、
エチレングリコールなどのアルコール類、ジメチルホル
ムアミド、ジメチルスルホキシドなどの非プロトン性溶
媒および水などがあげられる。
[0010] The carrier used herein is a synthetic or natural inorganic or organic substance incorporated to assist in reaching the active ingredient to the site to be treated and to facilitate storage, transport and handling of the active ingredient compound. Means As the carrier, any solid or liquid carrier can be used as long as it is generally used for agricultural and horticultural medicines, and it is not limited to a specific carrier. For example, as a solid carrier,
Viscosity such as montmorillonite, kaolinite, diatomaceous earth,
Inorganic substances such as clay, talc, vermiculite, calcium carbonate, silica gel, ammonium sulfate, etc., vegetable organic substances such as flour, soy flour, starch, crystalline cellulose, petroleum resins, polymer compounds such as polyalkylene glycol, urea, waxes, etc. can give. As a liquid carrier, toluene,
Aromatic hydrocarbons such as xylene and cumene, kerosene,
Paraffinic hydrocarbons such as mineral oil, ketones such as acetone, methyl ethyl ketone and dicyclohexanone, ethers such as dioxane and diethylene glycol dimethyl ether, methanol, ethanol, propanol,
Examples include alcohols such as ethylene glycol, aprotic solvents such as dimethylformamide and dimethylsulfoxide, and water.

【0011】更に製剤の剤型、適用場面などを考慮して
目的に応じてそれぞれ単独に、または組み合わせて次の
ような補助剤を添加することができる。補助剤として
は、通常使用される界面活性剤、結合剤(例えば、リグ
ニンスルホン酸、アルギン酸、ポリビニルアルコール、
アラビアゴム、CMCナトリウム等)安定化剤(例えば、
酸化防止用としてフェノール系化合物、チオール系化合
物または高級脂肪酸エステルなどを用いたり、pH調整
剤として燐酸塩を用いたり、光安定剤も用いる)などを
必要に応じて単独または組み合わせて使用できる。更に
場合によっては防菌防黴のために工業用殺菌剤、防菌防
黴剤などを添加することもできる。
Further, the following auxiliaries can be added singly or in combination according to the purpose in consideration of the dosage form of the preparation, the application scene, and the like. Examples of the auxiliary include commonly used surfactants and binders (eg, ligninsulfonic acid, alginic acid, polyvinyl alcohol,
Gum arabic, sodium CMC, etc.) stabilizers (eg,
A phenol compound, a thiol compound, a higher fatty acid ester, or the like for antioxidation, a phosphate as a pH regulator, or a light stabilizer may be used alone or in combination as necessary. Further, depending on the case, an industrial bactericide, a bactericidal / antifungal agent or the like may be added for bactericidal / fungicidal purposes.

【0012】本発明の殺菌剤に使用できる界面活性剤と
しては、乳化、分散、拡展、湿潤、結合、安定化などの
目的で使用される化合物であり、例えば、リグニンスル
ホン酸塩、アルキルベンゼンスルホン酸塩、アルキル硫
酸エステル塩、ポリオキシアルキレンアルキル硫酸塩、
ポリオキシアルキレンアルキルリン酸エステル塩などの
アニオン性界面活性剤、ポリオキシアルキレンアルキル
エーテル、ポリオキシアルキレンアルキルアリールエー
テル、ポリオキシアルキレンアルキルアミン、ポリオキ
シアルキレンアルキルアミド、ポリオキシアルキレンア
ルキルアミド、ポリオキシアルキレンアルキルチオエー
テル、ポリオキシアルキレン脂肪酸エステル、グリセリ
ン脂肪酸エステル、ソルビタン脂肪酸エステル、ポリオ
キシアルキレンソルビタン脂肪酸エステル、ポリオキシ
プロピレンポリオキシエチレンブロックポリマーなどの
非イオン性界面活性剤、ステアリン酸、カルシウム、ワ
ックスなどの潤滑剤、イソプロピルヒドロジエンホスフ
ェートなどの安定剤、ホスファチジルエタノールアミ
ン、ホスファチジルセリン、ホスファチジルグリセロー
ル、リゾレシチンなどのセファリンまたはレシチン系の
天然または合成リン脂質、その他メチルセルロース、カ
ルボキシメチルセルロース、カゼイン、アラビアゴムな
どがあげられる。しかし、これらの成分は以上のものに
限定されるものではない。
The surfactant which can be used in the fungicide of the present invention is a compound used for the purpose of emulsification, dispersion, spreading, wetting, binding, stabilization, etc., for example, lignin sulfonate, alkylbenzene sulfone Acid salt, alkyl sulfate salt, polyoxyalkylene alkyl sulfate,
Anionic surfactant such as polyoxyalkylene alkyl phosphate ester salt, polyoxyalkylene alkyl ether, polyoxyalkylene alkyl aryl ether, polyoxyalkylene alkylamine, polyoxyalkylene alkylamide, polyoxyalkylene alkylamide, polyoxyalkylene Lubrication of nonionic surfactants such as alkylthioethers, polyoxyalkylene fatty acid esters, glycerin fatty acid esters, sorbitan fatty acid esters, polyoxyalkylene sorbitan fatty acid esters, polyoxypropylene polyoxyethylene block polymers, stearic acid, calcium, wax, etc. Agents, stabilizers such as isopropylhydrodiene phosphate, phosphatidylethanolamine, phosphatidyl Phosphorus, phosphatidyl glycerol, natural or synthetic phospholipids of the cephalin or lecithin type such as lysolecithin, other cellulose, carboxymethyl cellulose, casein, gum arabic and the like. However, these components are not limited to those described above.

【0013】各種製剤の形態の有効成分は、通常粉剤、
水和剤、粒剤、フロアブル剤共0.1〜80重量%が望まし
い。
The active ingredient in the form of various preparations is usually a powder,
The wettable powder, granule, and flowable are desirably 0.1 to 80% by weight.

【0014】補助剤の含有量は0〜80重量%であり、担
体の含有量は100重量%から有効成分化合物および補助
剤の含有量を差し引いた量である。
The content of the adjuvant is 0 to 80% by weight, and the content of the carrier is 100% by weight minus the content of the active ingredient compound and the adjuvant.

【0015】フルスルファミドを含有する組成物の施用
方法としては、茎葉散布が最も効果を発揮する。
[0015] As a method of applying the composition containing flusulfamide, foliage application is most effective.

【0016】施用量および施用濃度は対象作物、病害の
発生程度、化合物の剤型、施用方法および各種環境条件
などによって変動するが、散布する場合には有効成分量
としてヘクタールあたり0.1〜10kgを処理すればよ
く、望ましくはヘクタールあたり0.5〜5kgである。ま
た水和剤、フロアブル剤または乳剤を使用する場合は、
水で希釈して使用してもかまわない。
The application rate and application concentration vary depending on the target crop, the degree of disease occurrence, the compound dosage form, the application method and various environmental conditions. When spraying, 0.1 to 10 kg of the active ingredient is treated per hectare. And preferably 0.5 to 5 kg per hectare. When using wettable powders, flowables or emulsions,
It may be used after dilution with water.

【0017】フルスルファミドを含有する組成物を使用
する時に、同時に他の農薬、たとえば殺虫剤、殺菌剤、
殺ダニ剤、殺線虫剤、抗ウイルス剤、除草剤、植物調節
剤との混合使用は勿論のこと、これらとの混合製剤も可
能である。
When using a composition containing flusulfamide, at the same time other pesticides such as insecticides, fungicides,
Not only can they be used in combination with miticides, nematicides, antiviral agents, herbicides, and plant regulators, but also mixed preparations with these can be used.

【0018】[0018]

【実施例】次に、フルスルファミドを含有する組成物を
有効成分として含有する殺菌剤の製剤例を示すが、添加
助剤の種類や混合比はこれに限定されるものではない。
また、製剤例中の部は重量部を表す。
EXAMPLES Next, examples of the preparation of a bactericide containing a composition containing flusulfamide as an active ingredient are shown, but the types and mixing ratios of the additives are not limited thereto.
Parts in the preparation examples represent parts by weight.

【0019】製剤例1 フロアブル剤 フルスルファミド5部、プロピレングリコール3部、リ
グニンスルホン酸ナトリウム14部、アラビアゴム1部、
水77部をサンドグラインダーにて混合微粉砕しフロアブ
ル剤を得た。
Formulation Example 1 Flowable agent Flusulfamide 5 parts, propylene glycol 3 parts, sodium ligninsulfonate 14 parts, gum arabic 1 part,
77 parts of water was mixed and pulverized with a sand grinder to obtain a flowable agent.

【0020】製剤例2 フロアブル剤 フルスルファミド10部、ポリエチレンソルビタンモノオ
レエート3部、カルボキシメチルセルロース5部および水
82部をサンドグラインダーにて混合微粉砕しフロアブル
剤を得た。
Formulation Example 2 Flowable agent Flusulfamide 10 parts, polyethylene sorbitan monooleate 3 parts, carboxymethyl cellulose 5 parts and water
82 parts were mixed and pulverized with a sand grinder to obtain a flowable agent.

【0021】製剤例3 水和剤 フルスルファミド5部、ソルポール(東邦化学(株)製
界面活性剤)15部、ラジオライト(昭和化学(株)製焼
成ケイソウ土)80部を均一に粉砕混合し水和剤を得た。
Formulation Example 3 Wettable powder 5 parts of Flusulfamide, 15 parts of Solpol (surfactant manufactured by Toho Chemical Co., Ltd.) and 80 parts of Radiolite (calcined diatomaceous earth manufactured by Showa Chemical Co., Ltd.) are uniformly pulverized and mixed. A sum was obtained.

【0022】製剤例4 水和剤 フルスルファミド5部、カープレックスNo.80(塩
野義製薬(株)製ホワイトカーボン)15部、エマール10
(花王(株)製界面活性剤)10部、クレー70部を均一に
混合粉砕し水和剤を得た。
Formulation Example 4 Wettable powder Flusulfamide 5 parts, Carplex No. 80 (white carbon manufactured by Shionogi & Co., Ltd.) 15 parts, Emar 10
10 parts (surfactant manufactured by Kao Corporation) and 70 parts of clay were uniformly mixed and pulverized to obtain a wettable powder.

【0023】試験例1 トマト疫病予防効果試験 温室内で直径7.5cmのプラスチックポットに5葉期まで
生育させたトマト(品種:世界一)に、製剤例1に準じ
て調製したフロアブル剤を所定濃度に希釈して、4ポッ
ト当たり50mlずつ散布した。薬剤が乾いた後、ジャガ
イモの切片上で培養した疫病菌から遊走子嚢を水で洗い
流し、氷冷して遊走子が出てきた状態(1×105個/m
l)で噴霧接種した。温度18℃、湿度95%以上の温室に
5日間保った後、疫病の病斑が占める面積を次の指標に
従って調査して発病度を求め、下記の式に従って防除価
を算出した。結果を第1表(表1)に示す。 各処理区および無処理区の平均値を発病度とした。
Test Example 1 Test for Preventive Effect on Tomato Blight Disease Tomato (variety: world's best) grown in a greenhouse in a plastic pot having a diameter of 7.5 cm up to the 5th leaf stage has a predetermined concentration of a flowable prepared according to Formulation Example 1. And sprayed 50 ml per 4 pots. After the drug dries, the zoospores are washed off with water from the disease-producing fungus cultured on the potato slices, and the zoospores are emerged after cooling on ice (1 × 10 5 / m).
Spray inoculation in l). For a greenhouse with a temperature of 18 ° C and a humidity of 95% or more
After keeping for 5 days, the area occupied by the disease spot of the plague was investigated according to the following index to determine the degree of disease occurrence, and the control value was calculated according to the following formula. The results are shown in Table 1 (Table 1). The average value of each treated section and the untreated section was defined as the disease severity.

【0024】防除価 = (1−処理区の発病度 /
無処理区の発病度)x100
Control value = (1−Degree of disease in treated plot /
Degree of disease in untreated area) x 100

【0025】[0025]

【表1】 [Table 1]

【0026】試験例2 キュウリべと病予防効果試験 温室内で直径7.5cmのプラスチックポットに1.5葉期まで
生育させたキュウリ(品種:相模半白)に、製剤例2に
準じて調製したフロアブル剤を所定濃度に希釈して、4
ポット当たり50mlずつ散布した。薬剤が乾いた後、キ
ュウリべと病菌の胞子懸濁液(1×105個/ml)を噴霧
接種した。温度25℃、湿度95%以上の温室に7日間保っ
た後、べと病の病斑が占める面積を次の指標に従って調
査して発病度を求め、下記の式に従って防除価を算出し
た。結果を第2表(表2)に示す。 各処理区および無処理区の平均値を発病度とした。
Test Example 2 Test for Preventive Effect of Cucumber Downy Mildew A flowable agent prepared according to Formulation Example 2 on a cucumber (variety: Sagami Hanshiro) grown in a greenhouse in a plastic pot having a diameter of 7.5 cm until the 1.5 leaf stage. Is diluted to a predetermined concentration, and 4
50 ml was sprayed per pot. After the drug was dried, a spore suspension of cucumber downy mildew (1 × 10 5 cells / ml) was spray-inoculated. After being kept in a greenhouse at a temperature of 25 ° C. and a humidity of 95% or more for 7 days, the area occupied by mildew spots was investigated according to the following index to determine the degree of onset, and the control value was calculated according to the following formula. The results are shown in Table 2 (Table 2). The average value of each treated section and the untreated section was defined as the disease severity.

【0027】防除価 = (1−処理区の発病度 /
無処理区の発病度)x100
Control value = (1−Severity of treated plot /
Degree of disease in untreated area) x 100

【0028】[0028]

【表2】 [Table 2]

【0029】試験例3 トマト疫病圃場試験 畝幅1.2mの圃場に2条植えで50cm間隔で5葉期トマト
苗(品種:世界一)を定植した。定植2週間後に製剤例3
に準じて調製した水和剤を所定濃度に希釈して、200L/1
0a相当量の液量でトマト茎葉部に散布した。薬剤が乾い
た後、ジャガイモの切片上で培養した疫病菌から遊走子
嚢を水で洗い流し、氷冷して遊走子が出てきた胞子懸濁
液(1×105個/ml)を茎葉部に45L/10a相当量の液量
で噴霧接種した。発病を促すために潅水チューブを用い
て茎葉部が霧状に濡れるまでに散水した。薬剤処理7日
後に、トマト茎葉部に現れた疫病の病斑が占める面積を
試験例1と同様の指標に従って調査して発病度を求め、
試験例1に記した式に従って防除価を算出した。結果を
第3表(表3)に示す。
Test Example 3 Tomato Blight Field Test A five-leaf tomato seedling (variety: the best in the world) was planted at intervals of 50 cm by two-row planting in a field having a ridge width of 1.2 m. Formulation Example 3 2 weeks after planting
Dilute the wettable powder prepared according to
It was sprayed on the foliage of tomato with a liquid amount equivalent to 0a. After the drug dries, the zoospores are washed off with water and the spore suspension (1 × 10 5 cells / ml) from which the zoospores emerge is washed with water from the disease-causing fungus cultured on the potato slices. Was spray-inoculated with a liquid amount equivalent to 45 L / 10a. In order to promote the onset of the disease, watering was performed until the foliage was sprayed wet using a watering tube. Seven days after the chemical treatment, the area occupied by the disease spot of the plague which appeared on the tomato foliage was investigated according to the same index as in Test Example 1 to determine the degree of disease onset.
The control value was calculated according to the formula described in Test Example 1. The results are shown in Table 3 (Table 3).

【0030】[0030]

【表3】 [Table 3]

【0031】試験例4 ジャガイモ疫病圃場試験 畝幅1.2mの圃場に2条植えで50cm間隔でジャガイモ種
芋(品種:男爵)を植えつけた。植え付け2ヶ月後に製
剤例4に準じて調製した水和剤を所定濃度に希釈して、2
50L/10a相当量の液量でジャガイモ茎葉部に散布した。
薬剤が乾いた後、ジャガイモの切片上で培養した疫病菌
から遊走子嚢を水で洗い流し、氷冷して遊走子が出てき
た胞子懸濁液(1×105個/ml)を茎葉部に45L/10a相
当量の液量で噴霧接種した。発病を促すために潅水チュ
ーブを用いて茎葉部が霧状に濡れるまでに散水した。薬
剤処理7日後に、ジャガイモ茎葉上に現れた疫病の病斑
が占める面積を試験例1と同様の指標に従って調査して
発病度を求め、試験例1に記した式に従って防除価を算
出した。結果を第4表(表4)に示す。
Test Example 4 Potato Blight Field Test A potato seed potato (variety: baron) was planted at intervals of 50 cm by two-row planting in a field having a ridge width of 1.2 m. Two months after planting, the wettable powder prepared according to Formulation Example 4 was diluted to a predetermined concentration,
It was sprayed on the foliage of potatoes with a liquid volume equivalent to 50 L / 10 a.
After the drug dries, the zoospores are washed off with water and the spore suspension (1 × 10 5 cells / ml) from which the zoospores emerge is washed with water from the disease-causing fungus cultured on the potato slices. Was spray-inoculated with a liquid amount equivalent to 45 L / 10a. In order to promote the onset of the disease, watering was performed until the foliage was sprayed wet using a watering tube. Seven days after the chemical treatment, the area occupied by the plague lesions appearing on the potato foliage was examined according to the same index as in Test Example 1 to determine the degree of onset, and the control value was calculated according to the formula described in Test Example 1. The results are shown in Table 4 (Table 4).

【0032】[0032]

【表4】 [Table 4]

【0033】[0033]

【発明の効果】上記試験例の結果より明らかなように、
フルスルファミドを含有する組成物は疫病、べと病に対
して優れた防除効果を示し、作物生産上大いに価値があ
る。
As is clear from the results of the above test examples,
The composition containing flusulfamide shows an excellent control effect against plague and downy mildew, and is of great value in crop production.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 川島 秀雄 千葉県茂原市東郷1144番地 三井化学株式 会社内 Fターム(参考) 4H011 AA01 BA01 BB07 BC03 BC06 BC20 BC22 DA02 DA15 DC01 DC05 DD03 DE15  ────────────────────────────────────────────────── ─── Continued on the front page (72) Inventor Hideo Kawashima 1144 Togo, Mobara-shi, Chiba F-term (reference) 4H011 AA01 BA01 BB07 BC03 BC06 BC20 BC22 DA02 DA15 DC01 DC05 DD03 DE15

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 N−(2−クロロ−4−ニトロフェニル)−
3−トリフルオロメチルベンゼンスルホンアミドを含有
することを特徴とする疫病およびべと病防除用殺菌剤。
1. N- (2-chloro-4-nitrophenyl)-
A fungicide for controlling plague and downy mildew, comprising 3-trifluoromethylbenzenesulfonamide.
JP2001056363A 2001-03-01 2001-03-01 Bactericides for controlling plague and downy mildew Expired - Fee Related JP4676626B2 (en)

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Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61197553A (en) * 1985-02-27 1986-09-01 Mitsui Toatsu Chem Inc N-(2-chloro-4-nitrophenyl)-3-trifluoromethyl benzenesulfonamid e compound and agricultural fungicide
JPS63270658A (en) * 1987-04-30 1988-11-08 Hokko Chem Ind Co Ltd Benzene sulfonanilide derivative and germicide for farm and garden
JPH01272566A (en) * 1988-04-22 1989-10-31 Hokko Chem Ind Co Ltd Sulfonamide derivative and fungicide for agricultural and horticultural use
JPH02212467A (en) * 1989-02-14 1990-08-23 Nippon Tokushu Noyaku Seizo Kk Benzenesulfonic acid anilide and fungicide for agricultural purpose
JPH02231465A (en) * 1988-09-12 1990-09-13 Nippon Tokushu Noyaku Seizo Kk 4-substituted benzene sulfonic acid anilides and agricultural insecticide and fungicide
JPH03227904A (en) * 1990-01-31 1991-10-08 Sumitomo Chem Co Ltd Agricultural and horticultural soil disease controlling agent
JP2001026506A (en) * 1999-04-28 2001-01-30 Takeda Chem Ind Ltd Sulfonamide derivative

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61197553A (en) * 1985-02-27 1986-09-01 Mitsui Toatsu Chem Inc N-(2-chloro-4-nitrophenyl)-3-trifluoromethyl benzenesulfonamid e compound and agricultural fungicide
JPS63270658A (en) * 1987-04-30 1988-11-08 Hokko Chem Ind Co Ltd Benzene sulfonanilide derivative and germicide for farm and garden
JPH01272566A (en) * 1988-04-22 1989-10-31 Hokko Chem Ind Co Ltd Sulfonamide derivative and fungicide for agricultural and horticultural use
JPH02231465A (en) * 1988-09-12 1990-09-13 Nippon Tokushu Noyaku Seizo Kk 4-substituted benzene sulfonic acid anilides and agricultural insecticide and fungicide
JPH02212467A (en) * 1989-02-14 1990-08-23 Nippon Tokushu Noyaku Seizo Kk Benzenesulfonic acid anilide and fungicide for agricultural purpose
JPH03227904A (en) * 1990-01-31 1991-10-08 Sumitomo Chem Co Ltd Agricultural and horticultural soil disease controlling agent
JP2001026506A (en) * 1999-04-28 2001-01-30 Takeda Chem Ind Ltd Sulfonamide derivative

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