JPS597105A - Agricultural and horticultural germicide - Google Patents

Agricultural and horticultural germicide

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Publication number
JPS597105A
JPS597105A JP57114795A JP11479582A JPS597105A JP S597105 A JPS597105 A JP S597105A JP 57114795 A JP57114795 A JP 57114795A JP 11479582 A JP11479582 A JP 11479582A JP S597105 A JPS597105 A JP S597105A
Authority
JP
Japan
Prior art keywords
compound
agricultural
diseases
sprayed
control
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
JP57114795A
Other languages
Japanese (ja)
Other versions
JPH023764B2 (en
Inventor
Takuo Wada
和田 拓雄
Katsumi Sato
克己 佐藤
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.)
Hokko Chemical Industry Co Ltd
Original Assignee
Hokko Chemical Industry 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 Hokko Chemical Industry Co Ltd filed Critical Hokko Chemical Industry Co Ltd
Priority to JP57114795A priority Critical patent/JPS597105A/en
Publication of JPS597105A publication Critical patent/JPS597105A/en
Publication of JPH023764B2 publication Critical patent/JPH023764B2/ja
Granted legal-status Critical Current

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Abstract

PURPOSE:A safe agricultural and horticultural germicide, containing a 1,2,4-triazole derivative and N-(3,5-dichlorophenyl)-1,2-dimethylcyclopropane-1,2-dicarboximide, and having a powerful activity and general-purpose properties. CONSTITUTION:An agricultural and horticultural germicide containing a 1,2,4- triazole derivative of formula (X is <=2 halogens or halogenated alkyl; Y is <=2 halogens), e.g. the compound of formula II, and N-(3,5-dichlorophenyl)-1,2- dimethylcyclopropane-1,2-dicarboximide preferably at 1:(0.1-10) weight ratio. EFFECT: The potentiating or synergistic enhancing action on the controlling effects of blights permits the application in a small amount of the chemical.

Description

【発明の詳細な説明】 本発明は一般式(I) (但し式中Xは2個までの同一または相異なるハロゲン
原子またはハロゲン化低級アルキル基を示しYは2個ま
でのハロゲン原子を示す。)で表わされる1、2.4’
−)リアゾール誘導体の1sとN−(3,5−ジクロロ
フェニル) −1,2−ジメチルシフo 7’ oパン
−1,2−ジカルボキシイミド(以下化合物Aと称する
。)を有効成分として含有する農園芸用殺菌剤に関する
DETAILED DESCRIPTION OF THE INVENTION The present invention is based on the general formula (I) (wherein X represents up to two identical or different halogen atoms or halogenated lower alkyl groups, and Y represents up to two halogen atoms. ) 1, 2.4'
-) An agricultural product containing 1s of a lyazole derivative and N-(3,5-dichlorophenyl)-1,2-dimethylsifuo7'opan-1,2-dicarboximide (hereinafter referred to as compound A) as an active ingredient. Regarding horticultural fungicides.

近年、全国的に施設固装が普及し、ガラス温室やビニー
ルハウスなどで年間を通じて各種野菜、花弁類、果樹な
どの栽培が盛んに行われている。
In recent years, hardened facilities have become popular throughout the country, and various vegetables, flower petals, fruit trees, and other crops are now actively cultivated year-round in glass greenhouses and plastic greenhouses.

こうした施設環境は有害病原菌の感染と増殖に好適な温
度・湿度条件を提供するために各種の病害が多発してい
る。現在こうした有害病害防除を目的として各種殺菌剤
が開発され使用されている。
These facility environments provide temperature and humidity conditions suitable for the infection and proliferation of harmful pathogens, and as a result, various diseases frequently occur. Various fungicides are currently being developed and used for the purpose of controlling these harmful diseases.

しかしながら、いずれの薬剤においてもその効果は従来
の水銀剤などに比べて甘く、多発するこれら病害を防除
しきれないのが現状である。また、これら薬剤は、その
適用病害幅が狭いものが多く、各種病害の併発する施設
内での使用には、はなはだ不便である。こうした実情か
ら、農家は、多数回に亘って各種薬剤の高薬量散布を繰
り返し行って病害防除に努めている。しかしながら、ガ
ラス温室あるいはビニールハウスでのこうした多量の薬
剤使用は屋外に比べ特に降雨による流亡や光分解などを
受けにくいことから作物上の残留あるいは薬害などの問
題を引き起している。したがって強力な防除活性を示し
、併発する各種病害を同時防除できる防除活性スペクト
ラムの広い薬剤であって、しかも少薬量散布で有効であ
り、残留毒性や薬害などの心配のない薬剤の早期開発が
強く望まれている。
However, the effectiveness of any of these drugs is weaker than that of conventional mercury drugs, and the current situation is that they cannot fully control these frequently occurring diseases. In addition, these drugs are often applicable to a narrow range of diseases, making it extremely inconvenient to use them in facilities where various diseases coexist. Under these circumstances, farmers try to control diseases by repeatedly spraying various chemicals at high doses many times. However, the use of such large amounts of chemicals in glass greenhouses or plastic greenhouses causes problems such as residues on crops and chemical damage, as they are less susceptible to washing away by rain and photodegradation compared to outdoors. Therefore, there is an urgent need for the early development of a drug that exhibits strong pesticidal activity, has a wide spectrum of pesticidal activity that can simultaneously control various diseases that occur, is effective when sprayed in small doses, and has no concerns about residual toxicity or drug damage. Highly desired.

本発明者らは、このような観点から、強力で汎用性があ
り、しかも安全性の高い農園芸用殺菌剤を開発するため
に各種試験を重ねた。その結果、前記一般式(I)で示
すトリアゾール舖導体の1種以上と化合物Aを配合する
ことにより、主要な作物病害の#1とんどすべてを完全
に防除することかで負、シかも各単剤で使用する場合よ
りも使用薬量を大幅に減することができるという新規で
有用な農園芸用殺菌剤を創製するに至りた。
From this viewpoint, the present inventors conducted various tests in order to develop a strong, versatile, and highly safe agricultural and horticultural fungicide. As a result, by blending Compound A with one or more of the triazole conductors represented by the general formula (I), it was found that almost all of the major crop diseases (#1) could be completely controlled. We have now created a novel and useful agricultural and horticultural fungicide that can be used in significantly lower amounts than when each agent is used alone.

本発明の有効成分の1つである一般式(I)で示される
1、2.4− )リアゾール誘導体は特ilt昭56−
163409号明細書に記載された化合物である◎そし
て、これら誘導体は、各種野菜、花弁類、果樹のうどん
ζ病、銹病に対して低薬量散布で優れた活性を示し、薬
害もないがその他病害を防除するためには高薬量散布し
ても十分な効果が得られない。一方、化合物Aは、各種
野菜、花弁、果樹の灰色かび病、菌核病、火星病に優れ
た防除効果を示す特公昭47−43813号公報に記載
されている化合物である。しかし本化合物の防除活性ス
ペクトラムも上記病害な含む少数の病害に限定されてお
り、またこれら病害の防除に当っては高薬量散布が必要
であるなどから多数回散布すると薬害を発生するなどの
欠点がある。
The 1,2,4-) lyazole derivative represented by general formula (I), which is one of the active ingredients of the present invention, is specially
These derivatives are compounds described in the specification of No. 163409.These derivatives show excellent activity against udon zeta disease and rust disease on various vegetables, flower petals, and fruit trees when sprayed at low doses, and have no phytotoxicity, but are not harmful to other plants. In order to control diseases, even high-dose spraying is not effective enough. On the other hand, Compound A is a compound described in Japanese Patent Publication No. 47-43813 which shows excellent control effects on botrytis, sclerotium, and Mars' disease on various vegetables, flower petals, and fruit trees. However, the spectrum of control activity of this compound is limited to a small number of diseases, including the above-mentioned diseases, and in order to control these diseases, it is necessary to spray at high doses, so repeated spraying may cause chemical damage. There are drawbacks.

本発明者らは、こうした欠点を有する2系統の化合物す
なわち、一般式(I)で示される1、2.4−トリアゾ
ール誘導体と化合物Aを配合して散布することKよって
各種病害に対して予期し難い共力的または相乗的な病害
防除効果の増強作用があることを見出し・た。す・なわ
ち低薬量散布した場合に単独使用ではtlとんど防除活
性の認められない病害に対しても混合使用により顕著な
防除活性を発揮する。このような事実は従来の混合斉j
の既成概念を打ち破るものであり全く予期し得な力・つ
た新知見でおる。
The present inventors have proposed that they can prevent various diseases by combining and spraying two types of compounds having these drawbacks, namely, the 1,2,4-triazole derivative represented by the general formula (I) and the compound A. It was discovered that this compound has a synergistic or synergistic effect of enhancing the disease control effect. In other words, when sprayed in low doses, they exert remarkable control activity against diseases for which TL control activity is not observed when used alone, when used in combination. This fact is based on the conventional mixed symmetry
It is a completely unexpected power and new knowledge that breaks the preconceptions of the world.

本発明の農園芸用殺菌剤・は前述のような優れた作用を
有するため薬剤の使用量を各々の薬剤を単独使用した場
合の4分の1から10分の1に減らしても十分な防除効
果が得られる。また、本発明の農園芸用殺菌剤の使用に
よりて効果の期待できるのは、ウリ類のうどんこ病、炭
そ病、つる枯病、灰色かび病、菌核病、トマト・ナスの
葉力・び病、輪紋病、灰色かび病、ネギの灰色腐敗病、
銹病、レタスの灰色かび病、鉋核病、インゲンマメの菌
核病、炭そ病、イチゴのうどんこ病、ソラマメの銹病、
輪紋病1.花弁類のうどんこ病、銹病、黒星病、リンゴ
の赤星病、うどんと病、黒星病、斑点落葉病、ナシの赤
星病、黒星病、黒斑病、モモの火星病、ブドウのうどん
と病、銹病、灰色かび病、黒とり病、ダイス、アズキの
菌核病、銹病、ムギ類のうどんこ病、銹病、雪腐病、イ
ネのごま葉枯病などの幅広い病害である。
The agricultural and horticultural fungicide of the present invention has the excellent action described above, so it can provide sufficient control even if the amount of the fungicide used is reduced to one-fourth to one-tenth of the amount when each agent is used alone. Effects can be obtained. In addition, the agricultural and horticultural fungicides of the present invention can be expected to be effective against powdery mildew of cucurbits, anthracnose, vine blight, gray mold, sclerotinia, and tomato/eggplant leaf vigor. - Mildew, ring spot, gray mold, gray onion rot,
Mildew, gray mold of lettuce, sclerotia, sclerotium of kidney beans, anthracnose, powdery mildew of strawberries, rust of broad beans,
Ring-shaped disease 1. Powdery mildew, mildew, scab of petals, powdery mildew of apple, powdery mildew, powdery mildew, scab, leaf spot, powdery mildew of pear, scab, black spot, mars of peach, powdery mildew of grapes , rust, gray mold, black mold, sclerotinia of soybeans, adzuki bean, powdery mildew of wheat, rust, snow rot, and sesame leaf blight of rice.

次に本発明で使用できる1、2.4−) 1ノアゾ一ル
誘導体の代表化合物を例示すると以下のとお9であるが
、これら化合物のみに限定されるもので社ない。なお化
合物陰は以下の実施例および試験PIにおいても参照さ
れる。
Next, representative compounds of the 1,2,4-)1 noazole derivatives that can be used in the present invention are exemplified by the following 9, but the present invention is not limited to these compounds. In addition, compound Yin is also referred to in the following examples and test PI.

本発明を実施するに際しては、有効成分化合物を担体で
希釈して通常使用される形態、例えに、水利剤、乳剤、
粉剤、DL型粉剤、フロアブル、粒剤、微粒剤、錠剤な
どKm剤して公知の方法に準じて使用すればよい。本発
明で使用される担体とは、クレー、タルク、べ/トナイ
ト、カオリン、叶いそう土、シリカなど固体担体あるい
はベンゼン、キシレン、トルエン、ケロシン、アルコー
ル類(メタノール、エタノール、イソプロパツール、n
−ブタノールなど)、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hと)などの液体担体が使
用できる。これらに適当な界面活性剤、産着剤などを適
量配合して製剤化して使用できる。本発明における有効
成分の配合割合は、ぐ− 重量比でトリアゾール誘導体の1種1部に対して化合物
Aを0.1〜10部配合するのが適当であるが、施用時
の条件や病害発生状況に応じて配合割合を適宜変更して
使用することができる。また、本発明の有効成分の#1
かに他の殺菌剤、殺虫剤、除草剤などを配合して使用す
ることもできる。
When carrying out the present invention, the active ingredient compound is diluted with a carrier and used in a commonly used form, for example, an aquarium, an emulsion, or
It may be used in the form of powders, DL-type powders, flowables, granules, fine granules, tablets, etc. according to known methods. The carriers used in the present invention include solid carriers such as clay, talc, betonite, kaolin, soybean earth, and silica, or benzene, xylene, toluene, kerosene, and alcohols (methanol, ethanol, isopropanol,
-butanol, etc.), ketones (acetone, methyl ethyl ketone, cyclohexanone, etc.) can be used. These can be used by blending appropriate amounts of suitable surfactants, adhesives, etc. into formulations. The appropriate blending ratio of the active ingredients in the present invention is 0.1 to 10 parts by weight of Compound A to 1 part of each type of triazole derivative, but depending on the conditions during application and the occurrence of disease. The blending ratio can be changed as appropriate depending on the situation. In addition, #1 of the active ingredients of the present invention
Crab may also be used in combination with other fungicides, insecticides, herbicides, etc.

次に本発明の貴園芸用殺菌剤について実施例を示すが、
本発明は以下の実施例のみに限定されるものではない。
Next, examples will be shown regarding the fungicide for gardening of the present invention.
The present invention is not limited only to the following examples.

実施例1 水和剤 化合物1の化合物10部、化合物A20部、ポリオキシ
エチレンアルキルアリールエーテル5部、リグニンスル
ホン酸カルシウム3部およびけいそう土62部を均一に
混合粉砕して水和剤を得る。
Example 1 Wettable powders 10 parts of Compound 1, 20 parts of Compound A, 5 parts of polyoxyethylene alkylaryl ether, 3 parts of calcium lignin sulfonate, and 62 parts of diatomaceous earth are uniformly mixed and ground to obtain a wettable powder. .

実施例2 粉剤 化合物3の化合物1部、化合物A2部、無水珪酸微粉末
0.5部、ステアリン酸カルシウム0.5部、クレー5
0部およびタルク46部を均一に混合して粉剤を得る。
Example 2 1 part of powder compound 3, 2 parts of compound A, 0.5 part of silicic anhydride fine powder, 0.5 part of calcium stearate, clay 5
0 parts and 46 parts of talc are uniformly mixed to obtain a powder.

実施例3 乳剤 化合物4の化合物10部、化合物A20部、メチルエチ
ルケト750部およびポリオキシエチレンノニルフェニ
ルエーテル20部を混合して溶解すれは有効成分30%
を含有する乳剤を得る。このものを使用する場合は、水
で500倍〜10000倍に希釈して植物に散布する。
Example 3 10 parts of Emulsion Compound 4, 20 parts of Compound A, 750 parts of methyl ethyl keto and 20 parts of polyoxyethylene nonylphenyl ether were mixed and dissolved to give 30% active ingredient.
An emulsion containing . When using this product, dilute it 500 to 10,000 times with water and spray it on plants.

次に本発明の化合物を農@苺用殺菌剤として使用する場
合の防除効果を試験例によって説明する。
Next, the pesticidal effect when the compound of the present invention is used as a fungicide for agriculture@strawberries will be explained using test examples.

試験例1 キエウリクる枯病に対する防除効果温室内で
直径9 Cmの素焼体で土耕栽培したキュウリ (品種
 相撲半白)の第1本葉期苗に、水利剤の所定濃度希釈
液を2鉢当り201d宛スズレーガンで散布した。笠日
子めPSA培地上で24で74日間培養したキーウリつ
る枯病菌(マ°イコ狐7アエレラ メロニス: Myc
ospho@rslla melonis )の菌叢先
端部を直径8寵のコルクポーラ−で打ち抜いた食菌寒天
片を接極源として散布葉上に接゛種した。接種後は24
℃の温室内に3日間格納して発病を促した。発病調査社
病斑径をノギスを用いて測定し、無処理区との対比から
防除価(チ)を求めた。また下記の指標により薬害を調
査した。
Test Example 1 Control effect on K. blight I sprayed it with a tin gun aimed at 201d. Myc vine blight fungus (Myc fox 7 Aerella melonis: Myc
The seeds were inoculated onto the sprayed leaves using a piece of edible fungi agar obtained by punching out the tip of a bacterial colony of Ospho@rslla melonis with a cork polarizer with a diameter of 8 holes as an electrode source. 24 days after vaccination
The seeds were stored in a greenhouse at ℃ for 3 days to promote disease onset. The diameter of the lesions was measured using a vernier caliper, and the control value (chi) was determined from comparison with the untreated area. In addition, drug damage was investigated using the following indicators.

薬害の調査指標 5:@甚  4:甚  3:多 2:少    1:微少  0:なし 第  1  表 チオファネートメチルは、4.4’−O−フ二二しンピ
ス(3−4オフロアアン酸)ジメチルを示す。また、無
散布区のかっこ内数値は、無散布の平均病斑径を示す。
Drug damage investigation index 5: @ Significant 4: Significant 3: Much 2: Little 1: Slight 0: None Table 1 Thiophanate methyl is 4.4'-O-phenyl dimethyl show. Furthermore, the value in parentheses in the non-sprayed area indicates the average lesion diameter in the non-sprayed area.

試験例2 ナシ赤星病に対する防除効果(#1場防除試
験) 二十世紀の15年生樹を用い1区1樹3i!制で試験し
た。多発病状態にするため、ナシ赤星病菌(ギムノスボ
ランギウム ハラエアヌム: Gymno−8pora
ngium haraeanum)の冬胞子推が密生し
たカイズカイプキをt′!場内に移植し感染源とした。
Test Example 2 Control effect on pear blight (#1 field control test) Using 15-year-old trees from the 20th century, 1 plot, 1 tree, 3 i! Tested under the system. Gymno-8pora (Gymnosborangium halaeanum) is used to cause multiple diseases.
T'! It was transplanted into the field and used as a source of infection.

薬剤散布は、水和剤の所定濃度希釈液をlOアール当り
3001の割合で簡易噴霧器を用いて4月16日からl
O日間隔で3回散布した。発病調査は、最終散布20日
後に任意に1樹300葉の1葉当りの病斑数を調査し、
次式により防除価(@を算出した。また葉、果実に対す
る薬害を下記の指標により調査した。
The drug was sprayed from April 16th using a simple sprayer with a diluted solution of a predetermined concentration of hydrating powder at a rate of 3,001 liters per liter.
It was sprayed 3 times with an interval of O days. To investigate the onset of disease, 20 days after the final spraying, we arbitrarily investigated the number of lesions per leaf on 300 leaves per tree.
The control value (@) was calculated using the following formula. In addition, phytotoxicity on leaves and fruits was investigated using the following indicators.

薬害の調査指標 5:激甚   4:甚   3:多 2:少    1:微少  0:なし 第  2  表 ビスダイセンは、ビス(ジメチルジチオカルバミド酸)
 エチレンビス〈ジチオカルバミド酸)二亜鉛を示す。
Drug damage investigation index 5: Severe 4: Severe 3: Much 2: Little 1: Slight 0: None Table 2 Bisdaicene is bis(dimethyldithiocarbamic acid)
Indicates ethylene bis(dithiocarbamic acid) dizinc.

また、無散布区のかっこ内数値は、無散布区の1葉あた
りの病斑数を示す。
Furthermore, the numbers in parentheses in the non-sprayed plot indicate the number of lesions per leaf in the non-sprayed plot.

試験例3 イネごま葉枯病に対する防除効果(ボ・ソト
) 温室内で直径9 Cmの素焼鉢で土耕栽培したイネ(品
種:朝日)の第4本葉朗苗に所定濃度に希釈した薬液を
散布した。散布1日後にイネごま葉枯病菌(コクリオボ
ルス ミャベアヌス: Cochlj−obolua 
m1yabeanus )の分生胞子懸濁液を噴霧し、
24℃の温室内に一夜格納したのち発病温室に移した。
Test Example 3 Control effect on rice sesame leaf blight (Bo Soto) A chemical solution diluted to a predetermined concentration was applied to the fourth true-leaf seedlings of rice (variety: Asahi) cultivated in clay pots with a diameter of 9 cm in a greenhouse. was scattered. One day after spraying, rice sesame leaf blight fungus (Cochlj-obolua) was detected.
mlyabeanus) by spraying a conidial suspension of
After being stored in a greenhouse at 24°C overnight, it was transferred to an infection greenhouse.

接種5日後に第4葉の1葉当りの病斑数を調査して次式
により防除価(%)を算出した。また、試験例1と同様
な方法によりイネに対する薬害を調査した。
Five days after inoculation, the number of lesions per leaf on the fourth leaf was investigated, and the control value (%) was calculated using the following formula. In addition, chemical damage to rice was investigated using the same method as Test Example 1.

試験結果は、第3表のとおりである。The test results are shown in Table 3.

第  3  表 ジマンダイセンは、亜鉛・マンネブ錯化合物である。ま
た、無散布区のかっこ内数値は、無散布区の1葉あたシ
の平均病斑数を示す。
Table 3 Dimandycene is a zinc-maneb complex compound. Furthermore, the numbers in parentheses in the non-sprayed plots indicate the average number of lesions per leaf in the non-sprayed plots.

手続補正書 昭和57年9月9 日 特許庁長官 若杉和夫 殿 1、事件の表示 昭Nll b 7年特許願第11LF”795  号2
、発明の名称 6、補正をする者 事件との関係 1)第15頁第6表中の1化合物1+化合物A」の散布
調度が1”25+25   とあるのを1−2512.
5+12.5 J       12.5+12.5 
 と補正する。
Procedural amendment September 9, 1981 Kazuo Wakasugi, Commissioner of the Patent Office 1, Indication of the case 1982 Patent Application No. 11LF”795 2
, Title of the Invention 6, Relationship with the person making the amendment 1) In Table 6 on page 15, the dispersion rate of 1 compound 1 + compound A'' is 1''25+25.1-2512.
5+12.5 J 12.5+12.5
and correct it.

+6.3J 2)同頁同表中の1−化合物2・十化合物A」の散布濃
度がr25  +25   とあるのをr−25+12
.512.5+12.5 J        12.5
−1− 6.64と補正する。
+6.3J 2) In the same table on the same page, the spray concentration of 1-Compound 2.
.. 512.5+12.5 J 12.5
-1- Corrected to 6.64.

Claims (1)

【特許請求の範囲】[Claims] ン原子またはハロゲン化低級アルキル基を示し、Yは2
個までのハロゲン原子を示す。)で示される1、2.4
− トリアゾール誘導体とN−(3,5−ジクロロフェ
ニル) −1,2−ジメチルシクロプロパン−1,2−
ジカルボキシイミドを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。
represents an atom or a halogenated lower alkyl group, and Y is 2
Indicates up to halogen atoms. ) 1, 2.4
- Triazole derivative and N-(3,5-dichlorophenyl)-1,2-dimethylcyclopropane-1,2-
An agricultural and horticultural fungicide characterized by containing dicarboximide as an active ingredient.
JP57114795A 1982-07-03 1982-07-03 Agricultural and horticultural germicide Granted JPS597105A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57114795A JPS597105A (en) 1982-07-03 1982-07-03 Agricultural and horticultural germicide

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57114795A JPS597105A (en) 1982-07-03 1982-07-03 Agricultural and horticultural germicide

Publications (2)

Publication Number Publication Date
JPS597105A true JPS597105A (en) 1984-01-14
JPH023764B2 JPH023764B2 (en) 1990-01-24

Family

ID=14646875

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57114795A Granted JPS597105A (en) 1982-07-03 1982-07-03 Agricultural and horticultural germicide

Country Status (1)

Country Link
JP (1) JPS597105A (en)

Also Published As

Publication number Publication date
JPH023764B2 (en) 1990-01-24

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