JPH0242803B2 - - Google Patents

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Publication number
JPH0242803B2
JPH0242803B2 JP11076782A JP11076782A JPH0242803B2 JP H0242803 B2 JPH0242803 B2 JP H0242803B2 JP 11076782 A JP11076782 A JP 11076782A JP 11076782 A JP11076782 A JP 11076782A JP H0242803 B2 JPH0242803 B2 JP H0242803B2
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Japan
Prior art keywords
leaves
compound
parts
test
seedlings
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.)
Expired
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JP11076782A
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Japanese (ja)
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JPS58174305A (en
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Priority to JP11076782A priority Critical patent/JPS58174305A/en
Publication of JPS58174305A publication Critical patent/JPS58174305A/en
Publication of JPH0242803B2 publication Critical patent/JPH0242803B2/ja
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Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は改善された作用を有する農園芸用殺菌
剤に関する。 農園芸用殺菌剤としては各種の化合物が知られ
ているが、うどんこ病及び炭疽病を完全に防除す
ることは困難である。そのためうどんこ病菌及び
炭疽病菌に対して優れた殺菌効果を有し、しかも
人畜及び作物に対して安全性の高い殺菌剤が要望
されている。 本発明は、下記式で表わされる3−(3,5−
ジクロロフエニル)−1−イソプロピルカーバモ
イルヒダントイン(化合物A)及び塩基性塩化銅
を重量比1:1〜6の割合で有効成分として含有
する農園芸用殺菌剤である。 化合物Aは、特公昭52−42888号公報に記載さ
れている3,5−ジクロロアニリン系の新種の農
園芸用殺菌剤であつて、これらは野菜の灰色かび
病菌、菌核病菌、モリニア病菌等に対して優れた
効果を示すことが知られている。 また塩基性塩化銅は、キユウリの斑点細菌病
菌、べと病菌、ジヤガイモ及びトマトの疫病菌に
対しては効果が認められている。しかしこれらの
殺菌剤は、防除困難な農園芸作物病原菌として知
られているうどんこ病菌及び炭疽病菌に対して
は、ほとんど効果が期待できない。 本発明者らは、種々の比較実験の結果、化合物
Aと塩基性塩化銅を併用することにより、果菜類
のうどんこ病菌及び炭疽病菌に対して予想外の優
れた効果が得られ、これらの病原菌を完全に防除
しうることを見出した。 またこれらの両種の化合物の相乗的作用によ
り、前記の病原菌に対する殺菌力が著しく増大す
るため、各成分の使用量を大幅に減少することが
できる。更にこれらの化合物の併用により、他の
病原菌に対する各成分の効力が消失することがな
いので、広範囲の病原菌を効果的に防除すること
ができる。 本発明の殺菌剤は、化合物A1重量部に対し、
塩基性塩化銅を1〜6重量部(Cuとして)の割
合で含有することが必要である。 本発明の殺菌剤は、化合物Aと塩基性塩化銅と
の混合物をそのまま用いてもよいが、通常は担体
もしくは希釈剤と混合し、場合により補助剤等を
用いて粉剤、水和剤、フローダスト剤(FD剤)
等に製剤化して用いられる。 担体もしくは希釈剤としては、農業において一
般に使用される普通の固体又は液状物が用いられ
る。固体担体としては、例えばクレー、タルク、
カオリン、ベントナイト、珪藻土、ホワイトカー
ボン等又はこれらの混合物、液体担体としては、
例えばアセトン、キシレン、アルコール、DMF,
DMSO等又はこれらの混合物が挙げられる。 また薬剤の分散、懸濁、乳化、付着、固着等の
性質向上を図るための補助剤としては、非イオン
性、陰イオン性、陽イオン性、両性イオン性界面
活性剤、高分子化合物などが用いられる。界面活
性剤としては、例えばポリオキシエチレンアルキ
ルエーテル、ポリオキシエチレンアルキルアリー
ルエーテル、ポリオキシエチレン脂肪酸エステ
ル、アルキルスルホン酸塩、ポリオキシエチレン
アルキル硫酸エステル等、高分子化合物として
は、例えばカルボキシメチルセルロース、ポリビ
ニルアルコール、アラビアゴム等が用いられる。 本発明の殺菌剤の有効成分の含有量は、粉剤で
は2〜20重量%(Cuとして0.5〜10%相当)、好ま
しくは4〜12重量%(Cuとして1.5〜6%相当)
であり、使用に際しては10アール当り3〜4Kgの
範囲で使用する。水和剤では有効成分の含有量
は、20〜90重量%(Cuとして8〜50%相当)、好
ましくは40〜80重量%(Cuとして12〜40%相当)
であり、使用に際しては0.04〜0.20%、好ましく
は0.08〜0.18%の濃度に希釈し、10アール当り
150〜200の範囲で散布する。また、FD剤の場
合は、有効成分の含有量は12〜80重量%(Cuと
して3.5〜40%相当)、好ましくは40〜60重量%
(Cuとして10〜30%相当)であり、使用に際して
は10アール当り200〜300gの範囲で散布するのが
適当である。 本発明の殺菌剤は、使用目的に応じて他の薬
剤、例えば殺菌剤、殺ダニ剤、殺虫剤、除草剤、
植物生長調整剤、肥料等と併用することもでき
る。 下記例中の部は重量部を意味する。また化合物
Bは塩基性塩化銅〔CuCl2・3Cu(OH)2〕を意味
する。 製剤例 1 化合物A 1部 化合物B 3部 イソプロピルアシド ホスフエート 0.3部 クレー 95.7部 前記の成分を均一に混合粉砕して粉剤とする。 製剤例 2 化合物A 20部 化合物B 50部 リグニンスルホン酸 ナトリウム 2部 ポリビニルアルコール 2部 クレー 26部 前記の成分を均一に混合粉砕して水和剤とす
る。 製剤例 3 化合物A 5部 化合物B 15部 ホワイトカーボン 50部 微粉末クレー 30部 前記の成分を均一に混合粉砕してFD剤とする。 試験例 1キユウリうどんこ病防除効果試験 温室内栽培の本葉4葉期のキユウリ幼苗(新光
A号)に7日後及び14日後の2回、製剤例2と同
様にして製造した水和剤を所定濃度に水で希釈懸
濁し、葉に充分に散布した。葉面風乾後、うどん
こ病感染苗を、薬剤処理したキユウリ幼苗のまわ
りに置き、自然感染を促した。 試験は1区、1ポツト、4連制で行つた。調査
は薬剤の最終散布7日後に行い、発病程度を次の
指数により表示し、発病度及び防除価をそれぞれ
次式により算出した。その結果を第1表に示す。 発病指数0:無発病 1:葉の25%未満が発病 2:葉の25〜49%が発病 3:葉の50〜74%が発病 4:葉の75%以上が発病 発病度(%)=Σ(発病指数×葉数)/4×調査葉数×
100 防除価(%)=無処理区発病度−処理区発病度/無処理
区発病度 ×100 更に混合製剤の相乗性の有無を判定するため、
コルビーらの計算式を準用して混合製剤の防除価
期待値(PE)を算出し、実測値(PC)と対比し
た。 PE(%)=Pa+Pb(100−Pa)/100 Pa:化合物Aの防除価実測値(%) Pb:化合物Bの防除価実測値(%) 判定基準 PC>PE:相乗的効果 PC=PE:相加的効果 PC<PE:拮抗的効果
The present invention relates to agricultural and horticultural fungicides with improved action. Although various compounds are known as agricultural and horticultural fungicides, it is difficult to completely control powdery mildew and anthracnose. Therefore, there is a need for a fungicide that has an excellent bactericidal effect against powdery mildew and anthracnose, and is highly safe for humans, livestock, and crops. The present invention provides 3-(3,5-
This is an agricultural and horticultural fungicide containing dichlorophenyl)-1-isopropylcarbamoylhydantoin (compound A) and basic copper chloride in a weight ratio of 1:1 to 6 as active ingredients. Compound A is a new type of 3,5-dichloroaniline type agricultural and horticultural fungicide described in Japanese Patent Publication No. 52-42888. It is known to have excellent effects on Basic copper chloride has also been shown to be effective against bacterial spot and downy mildew of cucumbers, and Phytophthora of potatoes and tomatoes. However, these fungicides are hardly expected to be effective against powdery mildew and anthracnose, which are known as pathogens of agricultural and horticultural crops that are difficult to control. As a result of various comparative experiments, the present inventors found that the combined use of Compound A and basic copper chloride produced unexpectedly excellent effects against powdery mildew and anthracnose on fruit and vegetables. It was discovered that pathogenic bacteria can be completely controlled. Moreover, the synergistic action of these two types of compounds significantly increases the bactericidal activity against the pathogenic bacteria, so the amount of each component used can be significantly reduced. Furthermore, by using these compounds in combination, the efficacy of each component against other pathogenic bacteria is not lost, so that a wide range of pathogenic bacteria can be effectively controlled. The fungicide of the present invention contains 1 part by weight of compound A,
It is necessary to contain basic copper chloride in a proportion of 1 to 6 parts by weight (as Cu). The fungicide of the present invention may be used as a mixture of Compound A and basic copper chloride, but it is usually mixed with a carrier or diluent, and optionally with an adjuvant, etc., to form powders, wettable powders, and powders. Dust agent (FD agent)
It is used in formulations such as As carriers or diluents, the usual solid or liquid substances commonly used in agriculture can be used. Examples of solid carriers include clay, talc,
Kaolin, bentonite, diatomaceous earth, white carbon, etc. or mixtures thereof, liquid carriers include:
For example, acetone, xylene, alcohol, DMF,
Examples include DMSO and mixtures thereof. In addition, nonionic, anionic, cationic, amphoteric surfactants, polymer compounds, etc. are used as auxiliary agents to improve properties such as dispersion, suspension, emulsification, adhesion, and fixation of drugs. used. Examples of surfactants include polyoxyethylene alkyl ether, polyoxyethylene alkylaryl ether, polyoxyethylene fatty acid ester, alkyl sulfonate, and polyoxyethylene alkyl sulfate; examples of polymer compounds include carboxymethyl cellulose, polyvinyl Alcohol, gum arabic, etc. are used. The content of the active ingredient in the disinfectant of the present invention is 2 to 20% by weight (equivalent to 0.5 to 10% as Cu), preferably 4 to 12% by weight (equivalent to 1.5 to 6% as Cu) in the case of powder.
When using it, it is used within the range of 3 to 4 kg per 10 are. In wettable powders, the content of the active ingredient is 20 to 90% by weight (equivalent to 8 to 50% as Cu), preferably 40 to 80% by weight (equivalent to 12 to 40% as Cu).
When used, it is diluted to a concentration of 0.04 to 0.20%, preferably 0.08 to 0.18%, and per 10 ares.
Spray in the range of 150-200. In addition, in the case of FD agents, the content of the active ingredient is 12 to 80% by weight (equivalent to 3.5 to 40% as Cu), preferably 40 to 60% by weight.
(equivalent to 10 to 30% as Cu), and when used, it is appropriate to spray in the range of 200 to 300 g per 10 are. The fungicide of the present invention may be used with other drugs depending on the purpose of use, such as fungicides, acaricides, insecticides, herbicides,
It can also be used in combination with plant growth regulators, fertilizers, etc. Parts in the following examples mean parts by weight. Compound B means basic copper chloride [CuCl 2 .3Cu(OH) 2 ]. Formulation Example 1 Compound A 1 part Compound B 3 parts Isopropyl acid phosphate 0.3 parts Clay 95.7 parts The above ingredients are uniformly mixed and pulverized to form a powder. Formulation Example 2 Compound A 20 parts Compound B 50 parts Sodium ligninsulfonate 2 parts Polyvinyl alcohol 2 parts Clay 26 parts The above ingredients are uniformly mixed and pulverized to prepare a wettable powder. Formulation Example 3 Compound A 5 parts Compound B 15 parts White carbon 50 parts Finely powdered clay 30 parts The above ingredients are mixed and ground uniformly to prepare an FD agent. Test Example 1 Powdery mildew control effect test on cucumber powdery mildew A hydrating powder prepared in the same manner as in Formulation Example 2 was applied twice after 7 days and 14 days to cucumber seedlings (Shinko A) grown in a greenhouse at the 4-leaf stage. The suspension was diluted with water to a predetermined concentration and thoroughly sprayed on leaves. After the leaves were air-dried, powdery mildew-infected seedlings were placed around the chemically treated cucumber seedlings to encourage natural infection. The test was conducted in 1 section, 1 pot, and 4 consecutive sessions. The investigation was conducted 7 days after the final application of the drug, and the degree of disease onset was expressed using the following index, and the degree of disease onset and control value were calculated using the following formulas. The results are shown in Table 1. Disease index: 0: No disease 1: Less than 25% of leaves are affected 2: 25-49% of leaves are affected 3: 50-74% of leaves are affected 4: More than 75% of leaves are affected Disease severity (%) = Σ (infection index x number of leaves) / 4 x number of investigated leaves x
100 Control value (%) = Disease severity in untreated area - Disease severity in treated area / Disease severity in untreated area × 100 In addition, to determine the presence or absence of synergism of the mixed preparation,
The expected pesticidal value (PE) of the mixed preparation was calculated by applying the calculation formula of Colby et al., and compared with the actual value (PC). PE (%) = Pa + Pb (100-Pa) / 100 Pa: Actual pesticidal value of compound A (%) Pb: Actual pesticidal value of compound B (%) Judgment criteria PC>PE: Synergistic effect PC=PE: Additive effect PC<PE: Antagonistic effect

【表】 試験例 2キユウリ炭疽病防除効果試験 温室内栽培の本葉4葉期のキユウリ幼苗(新光
A号)に製剤例2と同様にして製造した水和剤を
所定濃度に水で希釈懸濁し、葉に充分に散布し
た。葉面風乾後、キユウリ葉にキユウリ炭疽病菌
(Colletotrichum lagenarium)胞子懸濁液(オ
リンパス顕微鏡10×10倍で1視野分生胞子数30
個)を噴霧接種し、湿室(温度25±2℃、湿度95
±5%)に1日保ち、翌日から温室で発病を促し
た。 試験は1区、1ポツト、4連制で行つた。調査
は薬剤の散布5日後に行い、発病度(%)及び防
除価(%)を試験例1に準じて算出した。その結
果を第2表に示す。
[Table] Test Example 2 Anthracnose control effect test on cucumber Anthracnose control effect A wettable powder prepared in the same manner as Formulation Example 2 was diluted with water to a predetermined concentration on young cucumber seedlings (Shinko A) grown in a greenhouse at the 4-leaf stage. The mixture was made cloudy and thoroughly sprayed on the leaves. After the leaves were air-dried, a spore suspension of Colletotrichum lagenarium was placed on the cucumber leaves (30 conidia per field using an Olympus microscope at 10x10 magnification).
) was spray-inoculated, and the humidity chamber (temperature 25±2℃, humidity 95℃) was inoculated.
±5%) for one day, and the next day, the disease was induced in a greenhouse. The test was conducted in 1 section, 1 pot, and 4 consecutive sessions. The investigation was conducted 5 days after the application of the drug, and the disease severity (%) and control value (%) were calculated according to Test Example 1. The results are shown in Table 2.

【表】【table】

【表】 試験例3 ピーマンうどんこ病防除効果試験 温室内栽培の本葉5葉期のピーマン幼苗(エー
スピーマン)に、7日間隔で2回、製剤例2と同
様にして製造した水和剤を所定濃度に水で希釈懸
濁して、葉に充分に散布した。葉面風乾後、うど
んこ病感染苗を薬剤処理したピーマン幼苗のまわ
りに置き、自然感染を促した。 試験は1区、1ポツト、5連制で行つた。調査
は薬剤の最終散布7日後に行い、発病度(%)及
び防除価(%)を試験例1に準じて算出した。そ
の結果を第3表に示す。
[Table] Test Example 3 Powdery mildew control effect test on green pepper A hydrating powder prepared in the same manner as Formulation Example 2 was applied twice at 7-day intervals to young green pepper seedlings (ace pepper) at the 5th true leaf stage grown in a greenhouse. was diluted and suspended in water to a predetermined concentration and thoroughly sprayed on the leaves. After the leaves were air-dried, powdery mildew-infected seedlings were placed around the chemically treated green pepper seedlings to encourage natural infection. The test was conducted in 1 section, 1 pot, and 5 consecutive sessions. The investigation was conducted 7 days after the final application of the drug, and the disease severity (%) and control value (%) were calculated according to Test Example 1. The results are shown in Table 3.

【表】 試験例4 ナスうどんこ病防除効果試験 温室内栽培の本葉5葉期のナス幼苗(千両2
号)に、7日間隔で2回、製剤例2と同様にして
製造した水和剤を所定濃度に希釈懸濁して、葉に
充分散布した。葉面風乾後、うどんこ病感染苗を
薬剤処理したナス幼苗のまわりに置き自然感染を
促した。 試験は1区、1ポツト、5連制で行つた。調査
は薬剤の最終散布7日後に行い、発病度(%)及
び防除価(%)を試験例1に準じて算出した。そ
の結果を第4表に示す。
[Table] Test Example 4 Eggplant powdery mildew control effect test
No. 2), a wettable powder prepared in the same manner as in Formulation Example 2 was diluted and suspended to a predetermined concentration, and thoroughly sprayed on the leaves twice at 7-day intervals. After the leaves were air-dried, powdery mildew-infected seedlings were placed around the chemically treated eggplant seedlings to encourage natural infection. The test consisted of 1 section, 1 pot, and 5 consecutive sessions. The investigation was conducted 7 days after the final application of the drug, and the disease severity (%) and control value (%) were calculated according to Test Example 1. The results are shown in Table 4.

【表】【table】

【表】 試験例5 スイカ炭疽病防除効果試験 本葉15葉期のスイカ苗(縞玉)に、7日間隔で
3回、製剤例2と同様にして製造した水和剤を所
定濃度に希釈懸濁し、葉に充分散布した。葉面風
乾後、炭疽病感染苗を薬剤処理したスイカ苗のま
わりに置き、自然感染を促した。 試験は1区、10株(20m2)、3連制で行つた。
調査は薬剤の最終散布10日後に行い、発病度
(%)及び防除価(%)を試験例1に準じて算出
した。その結果を第5表に示す。
[Table] Test Example 5 Watermelon anthracnose control effect test Watermelon seedlings (striped balls) at the 15th true leaf stage were diluted with a wettable powder prepared in the same manner as Formulation Example 2 to the specified concentration three times at 7-day intervals. Suspended and thoroughly sprayed on leaves. After the leaves were air-dried, anthracnose-infected seedlings were placed around the chemically treated watermelon seedlings to encourage natural infection. The test was conducted in 1 area, 10 plants (20 m 2 ), and in triplicate.
The investigation was conducted 10 days after the final application of the drug, and the disease severity (%) and control value (%) were calculated according to Test Example 1. The results are shown in Table 5.

【表】【table】

Claims (1)

【特許請求の範囲】[Claims] 1 3−(3,5−ジクロロフエニル)−1−イソ
プロピルカーバモイルヒダントインと塩基性塩化
銅を重量比1:1〜6の割合で有効成分として含
有することを特徴とする農園芸用殺菌剤。
1. An agricultural and horticultural fungicide characterized by containing 3-(3,5-dichlorophenyl)-1-isopropylcarbamoylhydantoin and basic copper chloride as active ingredients in a weight ratio of 1:1 to 6. .
JP11076782A 1982-06-29 1982-06-29 Agricultural and horticultural fungicide Granted JPS58174305A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11076782A JPS58174305A (en) 1982-06-29 1982-06-29 Agricultural and horticultural fungicide

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11076782A JPS58174305A (en) 1982-06-29 1982-06-29 Agricultural and horticultural fungicide

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
JP57030527 Division

Publications (2)

Publication Number Publication Date
JPS58174305A JPS58174305A (en) 1983-10-13
JPH0242803B2 true JPH0242803B2 (en) 1990-09-26

Family

ID=14544058

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11076782A Granted JPS58174305A (en) 1982-06-29 1982-06-29 Agricultural and horticultural fungicide

Country Status (1)

Country Link
JP (1) JPS58174305A (en)

Also Published As

Publication number Publication date
JPS58174305A (en) 1983-10-13

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