JP2568099B2 - Disinfectant composition - Google Patents
Disinfectant compositionInfo
- Publication number
- JP2568099B2 JP2568099B2 JP63060486A JP6048688A JP2568099B2 JP 2568099 B2 JP2568099 B2 JP 2568099B2 JP 63060486 A JP63060486 A JP 63060486A JP 6048688 A JP6048688 A JP 6048688A JP 2568099 B2 JP2568099 B2 JP 2568099B2
- Authority
- JP
- Japan
- Prior art keywords
- disease
- blight
- tpn
- spot
- composition
- 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 - Fee Related
Links
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
- A01N43/76—1,3-Oxazoles; Hydrogenated 1,3-oxazoles
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
- A01N25/04—Dispersions, emulsions, suspoemulsions, suspension concentrates or gels
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/34—Nitriles
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/36—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
Landscapes
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Zoology (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Environmental Sciences (AREA)
- Dispersion Chemistry (AREA)
- Toxicology (AREA)
- Chemical & Material Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
Description
【発明の詳細な説明】 (1) 発明の目的 産業上の利用分野 本発明は、殺菌剤組成物に関し、ことに植物の病害防
除効果が向上した農園芸用殺菌剤組成物に関するもので
ある。DETAILED DESCRIPTION OF THE INVENTION (1) Object of the Invention Industrial Field of the Invention The present invention relates to a fungicide composition, and more particularly to an agricultural / horticultural fungicide composition having an improved disease control effect on plants.
従来の技術 テトラクロロイソフタロニトリル(以下TPNとい
う。)を有効成分として含有する殺菌剤は保護作用の強
い薬剤として実用化されており特に農園芸用殺菌剤とし
て果樹・野菜の病害防除を目的として植物に散布或い
は、土壌に混和したりして広く一般に使用されている。BACKGROUND ART A bactericide containing tetrachloroisophthalonitrile (hereinafter referred to as TPN) as an active ingredient has been put to practical use as a chemical with a strong protective action, and especially for the purpose of controlling disease of fruits and vegetables as a bactericide for agriculture and horticulture. It is widely used by being sprayed on plants or mixed with soil.
一方、一般式〔I〕 〔式中、Zは2−オキソ−1,3−オキサゾリジン−3−
イル、1−(メトキシカルボニル)エチルまたは2−オ
キソ−チオラン−3−イルを示す。〕で表わされる化合
物(以下フェニルアミド化合物という。)は特に果樹・
野菜に大きな被害をもたらすべと病・えき病に優れた防
除効果を示し、また植物体内に浸透移行するため、予防
効果だけでなく、植物の組織内に侵入した病原菌にも作
用して、病害が広がるのを防ぐことができるものとして
知られている。On the other hand, the general formula [I] [In the formula, Z is 2-oxo-1,3-oxazolidine-3-
Represents 1- (methoxycarbonyl) ethyl or 2-oxo-thiolan-3-yl. ] The compound (hereinafter referred to as phenylamide compound) represented by
It has an excellent control effect against downy mildew and blight that cause great damage to vegetables, and because it penetrates into the plant body, it not only has a preventive effect, but also acts on pathogenic bacteria that have invaded into the tissues of the plant and Is known to be able to prevent the spread of.
殺菌スペクトルを広げ、同時防除を可能にするために
TPNとその他の殺菌活性化合物との混合殺菌剤、例えば
メチル3−(ブチルカルバモイル)−3H−ベンズイミダ
ゾール−2−イルカーバメート(一般名ベノミル)との
混合殺菌剤などが使用されている。また、フェニルアミ
ド化合物に関しても殺菌スペクトルを広げるため、及び
耐性菌対策としても各種の混合殺菌剤、例えば塩基性塩
化銅、マンゼブとの混合殺菌剤などが使用されている。To broaden the sterilization spectrum and enable simultaneous control
A mixed bactericide of TPN and other bactericidal active compounds, for example, a mixed bactericide of methyl 3- (butylcarbamoyl) -3H-benzimidazol-2-ylcarbamate (general name benomyl) is used. Further, in order to broaden the sterilization spectrum of phenylamide compounds and as a countermeasure against resistant bacteria, various mixed bactericides such as basic copper chloride and mixed bactericide with manzeb are used.
TPNとフェニルアミド化合物である2−メトキシ−N
−(2−オキソ−1,3−オキサゾリジン−3−イル)ア
セト−2′,6′−キシリジン(一般名オキサジキシル)
との混合使用については、Trans.Br.mycol.Soc.85,299
〜306(1985)に記載されている。しかし、上記文献で
はTPNとオキサジキシルと相乗効果が充分あるとは開示
されていない。しかも使用されたTPNは水和剤として使
用され、オキサジキシルとTPNとの混合比は1:3の例が示
されているに過ぎない。2-methoxy-N which is a phenylamide compound with TPN
-(2-oxo-1,3-oxazolidin-3-yl) aceto-2 ', 6'-xylidine (generic name oxadixyl)
The mixed use with, Trans.Br.mycol.Soc. 85, 299
~ 306 (1985). However, the above document does not disclose that TPN and oxadixyl have a sufficient synergistic effect. Moreover, the TPN used is used as a wettable powder, and the mixing ratio of oxadixyl and TPN is only 1: 3.
発明が解決しようとする問題点 現在市販されている農薬は現在の投下薬量で、優れた
防除効果を示すものであり、環境に対する悪影響も少な
いものであるが、環境に対する安全性をさらに高めるた
め、有効成分の効率的な利用により、投下薬量を減少さ
せることが望まれている。TPN剤についても環境に対す
る安全性をさらに高めるため作物に対する投下薬量をさ
らに減少するための研究が進められているが、従来知ら
れている組成物では投下薬量を減少させると防除効力が
低下するという問題点があった。Problems to be Solved by the Invention Agricultural chemicals currently on the market have excellent control effects at the current doses, and have little adverse effect on the environment, but to further enhance safety to the environment. Therefore, it is desired to reduce the amount of drug to be dropped by efficiently using the active ingredient. Regarding TPN agents as well, research is underway to further reduce the amount of drug applied to crops in order to further enhance the safety to the environment.However, the control efficacy of previously known compositions decreases when the amount of drug applied is decreased. There was a problem to do.
一般に二種以上の殺菌性有効成分を混合使用する場
合、その殺菌効果は単なる相加的作用にとどまるか、あ
るいは拮抗作用又は相乗作用を示すかに分類される。そ
して相乗作用を示す場合、投下薬量の低減につながり、
安全性のより高く、且つ経済的な薬剤を提供することが
期待できる。Generally, when two or more kinds of bactericidal active ingredients are mixed and used, the bactericidal effect is classified into a mere additive effect, an antagonistic effect or a synergistic effect. And when it shows a synergistic effect, it leads to the reduction of the amount of drug dropped,
It can be expected to provide a more safe and economical drug.
特に、上記のTPNとオキサジキシルの各々の優れた特
徴を兼ね備え、しかも相乗効果を有する殺菌剤組成物が
強く求められているにも拘わらず、これまで知られてい
なかったという問題点があった。In particular, there has been a problem that a bactericidal composition having the excellent characteristics of each of the above TPN and oxadixyl and having a synergistic effect has not been known so far in spite of strong demand.
(2) 発明の構成 問題点を解決するための手段 本発明者は、斯かる実状において鋭意研究を重ねた結
果、フェニルアミド化合物及びTPNを有効成分として1:3
乃至1:13の比率で含有し、かつ、その固形成分の粒度分
布が体積累積50%点の粒径(以下VMDという。)で0.8乃
至2.5μmの間にあるフロアブル製剤である殺菌剤組成
物がTPNとフェニルアミド化合物の各々の優れた特徴を
兼ね備え、驚くべきことに極めて強い相乗効果を有する
ことを見い出し本発明を完成するに至った。(2) Structure of the Invention Means for Solving Problems The present inventors have conducted earnest studies in such an actual situation, and as a result, 1: 3 with a phenylamide compound and TPN as active ingredients.
To a 1:13 ratio, and the particle size distribution of the solid component is a flowable formulation having a particle size distribution at a 50% volume cumulative point (hereinafter referred to as VMD) of 0.8 to 2.5 μm. It has been found that the compound has excellent characteristics of each of TPN and a phenylamide compound, and surprisingly has an extremely strong synergistic effect, and thus completed the present invention.
本発明の殺菌剤組成物を製造する方法には特に制限は
ない。従来より用いられた粉砕機を用い、一般的な配合
によって製造することができる。There is no particular limitation on the method for producing the disinfectant composition of the present invention. It can be produced by a general blending using a crusher that has been used conventionally.
粉砕機としては効率の良い粉砕機を用いると容易に製
造できる。The crusher can be easily manufactured by using an efficient crusher.
これらの粉砕機としては、ボールミル、衝撃式粉砕
機、ジェット粉砕機、湿式粉砕機などを挙げることがで
きる。Examples of these crushers include a ball mill, an impact crusher, a jet crusher, and a wet crusher.
VMDはコールターカウンター モデルTA−11(株式会
社日科機)で測定されたものである。VMDは0.8μm乃至
2.5μmが好ましいが、0.8μm乃至1.8μmが特に好ま
しい。 VMD is a coulter counter Model TA-11 (Stock Association
Company Nikkaki) was measured. VMD is 0.8μm or more
2.5 μm is preferable, but 0.8 μm to 1.8 μm is particularly preferable.
New
また本発明組成物中のTPNとフェニルアミド化合物の
含有量は特に制限されるものではないが、1%乃至98%
程度で使用されることが望ましい。TPNとフェニルアミ
ド化合物の含有比は1:3乃至1:13が好ましいが、1:4乃至
1:11が特に好ましい。The content of TPN and phenylamide compound in the composition of the present invention is not particularly limited, but is 1% to 98%.
It is desirable to be used in a degree. The content ratio of TPN and phenylamide compound is preferably 1: 3 to 1:13, but 1: 4 to
1:11 is particularly preferred.
散布量については必ずしも制限はないが、通常は作物
の生育する圃場に散布する場合には、有効成分化合物
(A.I.)として1〜500g/10a、又、土壌中に施用する場
合には0.1〜5kg(A.l.)/10a程度が適当である。The application amount is not necessarily limited, but usually 1 to 500 g / 10a as an active ingredient compound (AI) when applied to a field where a crop grows, and 0.1 to 5 kg when applied to soil. (Al) / 10a is suitable.
勿論、これは一つの目安であり、作物の種類、病害の
種類、及びひがいの程度、時期、天候、薬剤の剤型等の
要因を考慮して、必要に応じて適宜加減される。Of course, this is one guideline, and is appropriately adjusted as necessary in consideration of factors such as the type of crop, the type of disease, the degree of strain, the season, the weather, and the dosage form of the drug.
次に本発明組成物の製剤実施例を挙げて説明するが、
これにのみ限定されるものでないことは言うまでもな
い。Next, formulation examples of the composition of the present invention will be described.
It goes without saying that the present invention is not limited to this.
実施例 1 メタラキシル((±)−methyl N−(2−methoxyace
tyl)−N−(2,6−xylyl)−DL−alaniate) 25部 ノニポール100(三洋化成工業株式会社) 1部 デモール N(花王株式会社) 2部 水 72部 を混合し、湿式粉砕機アイガーモーターミル(アイガー
ジャパン株式会社)を用い粉砕する。粉砕時間を調整し
て、VMD1.5μmのサンプルを作成した。Example 1 Metalaxyl ((±) -methyl N- (2-methoxyace
tyl) -N- (2,6-xylyl) -DL-alaniate) 25 parts Nonipol 100 (Sanyo Kasei Co., Ltd.) 1 part Demol N (Kao Co., Ltd.) 2 parts 72 parts water Wet crusher Eiger Grind using a motor mill (Eiger Japan Co., Ltd.). The crushing time was adjusted to prepare a sample having a VMD of 1.5 μm.
実施例 2 オキサジキシル(2−メトキシ−N−(2−オキソ−1,
3−オキサゾリジン−3−イル)アセト−2′,6′−キ
シリジド) 25部 ノニポール100(三洋化成工業株式会社) 1部 デモール N(花王株式会社) 2部 水 72部 を混合し、実施例1と同様に、VMD1.5μmのサンプルを
作成した。Example 2 Oxadixyl (2-methoxy-N- (2-oxo-1,
3-oxazolidin-3-yl) aceto-2 ', 6'-xylidide) 25 parts Nonipol 100 (Sanyo Kasei Co., Ltd.) 1 part Demol N (Kao Co., Ltd.) 2 parts Water 72 parts were mixed, and Example 1 A sample with a VMD of 1.5 μm was prepared in the same manner as in.
実施例 3〜6 TPN(テトラクロロイソフタロニトリル) 50 部 ノニポール100 1.5部 デモール N 3 部 水 45.5部 を混合し、アイガーモーターミルの粉砕時間を調整し
て、VMDを種々に変化させたフロアブル剤のサンプルを
調整した。Examples 3 to 6 TPN (tetrachloroisophthalonitrile) 50 parts Nonipol 100 1.5 parts Demol N 3 parts Water 45.5 parts were mixed, and the pulverization time of the Eiger motor mill was adjusted to obtain various flowable agents with different VMD. Samples were prepared.
実施例 3 VMD 0.5μm 実施例 4 VMD 1.0μm 実施例 5 VMD 1.5μm 実施例 6 VMD 5 μm 実施例 7 オキサジキシル 6.4部 TPN 32.0部 ノニポール100 1.5部 デモール N 3 部 水 57.1部 を混合し、アイガーモーターミルの粉砕時間を調整し
て、VMD1.0μmのフロアブル剤のサンプルを調整した。Example 3 VMD 0.5 μm Example 4 VMD 1.0 μm Example 5 VMD 1.5 μm Example 6 VMD 5 μm Example 7 Oxadixyl 6.4 parts TPN 32.0 parts Nonipol 100 1.5 parts Demol N 3 parts Water 57.1 parts are mixed to form an Eiger motor. The milling time of the mill was adjusted to prepare a sample of VMD 1.0 μm flowable agent.
(3) 発明の効果 本発明組成物に広汎な農園芸作物の病害の防除に効果
的であり、その主なものを例示すれば以下のものが挙げ
られる。(3) Effects of the Invention The composition of the present invention is effective for controlling diseases of a wide range of agricultural and horticultural crops, and the main ones are as follows.
水稲:いもち病、ごま葉枯病、紋枯病、馬鹿苗病、苗立
枯病等 小麦:赤さび病、黄さび病、裸黒穂病、葉枯病、斑点
病、褐色雪腐病、うどんこ病等 ジャガ芋:疫病、夏疫病、黒あざ病等 豆類 大豆:べと病、斑点病、褐斑病、菌核病、さび
病、紫斑病等 小豆:褐斑病、さび病、すす紋病、うどんこ病等 落花生:褐斑病、黒渋病、菌核病等 タバコ:赤星病、疫病、菌核病、腰折病、舞病、白星
病、うどんこ病等 ビート:べと病、褐斑病、苗立枯病等 野菜トマト:灰色かび病、葉かび病、疫病、菌核病、輪
紋病、すすかび病、萎凋病、苗立枯病等 ナス:灰色かび病、半身萎凋病、褐色腐敗病、黒枯病、
うどんこ病、すすかび病等 ウリ類:べと病、灰色疫病、灰色かび病、菌核病、黒星
病、炭そ病、つる枯病、つる割病、うどんこ病、苗立枯
病等 白菜:べと病、白斑病、菌核病、根こぶ病等 玉ネギ:白色疫病、べと病、灰色腐敗病、炭そ病等 レタス:べと病、灰色かび病、褐斑病、菌核病等 イチゴ:灰色かび病、うどんこ病、輪斑病等 鑑賞植物菊:白さび病、うどんこ病、等 シクラメン:灰色かび病等 バラ:黒星病、うどんこ病等 果樹カンキツ:青かび病、灰色かび病、黒点病、そうか
病等 リンゴ:赤星病、斑点落葉病、黒星病、モニリア病、う
どんこ病等 ナシ:赤星病、黒斑病、黒星病等 モモ:灰星病、黒星病、フォモプレス腐敗病、縮葉病等 ブドウ:べと病、灰色かび病、褐斑病、黒とう病、晩腐
病、さび病、ペスタロチアつる枯病、つる割病、うどん
こ病等 また本発明組成物はフロアブル製剤組成物であること
により次のことが考えられる。Paddy rice: Rice blast, sesame leaf blight, leaf blight, scab seedling disease, seedling blight, etc. Wheat: Red rust, Yellow rust, Naked smut, Leaf blight, Spot disease, Brown snow rot, Udon Diseases, etc. Potato: Late blight, summer blight, black blight, etc. Beans Soybeans: downy mildew, leaf spot, brown spot, sclerotial disease, rust, purple spot, etc. Red beans: brown spot, rust, soot spot disease , Powdery mildew, etc. Peanut: brown spot, black spot, sclerotium, etc. Tobacco: red scab, epidemic, sclerotium, hip fracture, dance, white scab, powdery mildew etc. Beat: downy mildew Brown spot disease, seedling blight, etc. Vegetable tomato: Gray mold, leaf mold, plague, sclerotial disease, ring spot disease, rust mold, wilt disease, seed blight etc. Eggplant: Gray mold, half body wilt Disease, brown rot, black spot,
Powdery mildew, scab, etc. Cucurbits: downy mildew, gray blight, gray mold, sclerotium disease, scab, anthracnose, vine blight, vine wilt, powdery mildew, seedling blight, etc. Chinese cabbage: downy mildew, white spot, sclerotium, root rot, etc. Onion: white blight, downy mildew, gray rot, anthracnose, etc. lettuce: downy mildew, gray mold, brown spot, fungus Nuclear disease, etc. Strawberry: Gray mold, powdery mildew, ring spot disease, etc. Appreciation plant chrysanthemum: White rust, powdery mildew, etc. Cyclamen: Gray mold, etc. Rose: Black scab, powdery mildew Citrus: Blue mold , Gray mold, Black spot, Scab, etc. Apple: Red scab, Spotted leaf spot, Black scab, Monilia disease, Powdery mildew, etc. Pear: Red scab, Black spot, Black scab, etc. Peach: Ash sterility, Black star Disease, phomopress rot, leaf rot, etc. Grape: downy mildew, gray mold, brown spot, black rot, late rot, rust, pestalothia vine Disease, Fusarium wilt, powdery mildew, etc. Further, since the composition of the present invention is a flowable pharmaceutical composition, the following can be considered.
既に液中に分散させているため希釈水中での凝集がお
きにくく、最適化した粒径がそのまま維持できる。Since it is already dispersed in the liquid, aggregation in diluting water is unlikely to occur and the optimized particle size can be maintained as it is.
剤希釈物として他に固形物を加える必要がないため固
形物による分解作用を回避できる。Since it is not necessary to add another solid substance as the agent diluent, the decomposition action by the solid substance can be avoided.
これらのことにより有効成分が著るしく効率的に作用
でき、防除効果が向上する。実際に使用する場合、水中
分散性が優れているので、水に混ざりやすく、散布液の
調製が簡単である。懸垂性も優れているので、調製後の
薬液は長時間にわたって均一な懸濁状態を保つことがで
きるので散布開始から終了まで所定の濃度で散布でき、
散布時の目づまりも問題にならなくなる。水和剤を散布
した後、果実や葉に汚れ(散布液の跡)が残るが、本発
明組成物はこの汚れの原因である鉱物質を含まないので
極めて汚れの少い収穫物が得られる。さらに粉末ではな
いので、ほこり立ちもなくなり、より安全な使用が可能
となる。By these, the active ingredient can act remarkably and efficiently, and the control effect is improved. When it is actually used, since it has excellent dispersibility in water, it is easily mixed with water and the spray solution can be easily prepared. Since the suspension is also excellent, the drug solution after preparation can maintain a uniform suspension state for a long time, so it can be sprayed at a predetermined concentration from the start to the end of spraying.
The clogging at the time of spraying does not become a problem. After spraying the wettable powder, stains (traces of spray liquid) remain on the fruits and leaves, but since the composition of the present invention does not contain the mineral substances that cause this stain, a crop with very little stain can be obtained. . Furthermore, since it is not a powder, it does not become dusty and can be used more safely.
以下、本発明組成物の効果を具体的に説明するため、
代表的な試験例を示す。Hereinafter, in order to specifically describe the effects of the composition of the present invention,
A representative test example is shown.
但し、これらは単なる例示であり、本発明の適用例は
これらのみに限らないことは言うまでもない。However, it goes without saying that these are merely examples and the application examples of the present invention are not limited to these.
試験例 1 各剤の所定濃度散布液(有効成分濃度20,10,5,2,1,0.
5ppm)を作り第5本葉期のトマト(品種:レッドチェリ
ー)に薬液の200/10a相当量を噴霧した。薬剤散布風
乾後(約2時間後)トマト疫病(Phytophthora infesta
ns)の遊走子懸濁液を接種した。Test example 1 Spray solution of each agent at the specified concentration (concentration of active ingredient 20,10,5,2,1,0.
5 ppm) was prepared and the tomato (variety: red cherry) in the fifth true leaf stage was sprayed with 200 / 10a of the chemical solution. After spray-drying chemicals (after about 2 hours) Tomato blight (Phytophthora infesta)
ns) zoospore suspension.
その後2日間21℃の湿室に保持し、この後温室内に2
日間放置した。Then, keep it in a humid chamber at 21 ° C for 2 days, and then put it in a greenhouse for 2 days.
Left for days.
接種5日後に第3,第4及び第5本葉につき病斑面積を
調査し、防除価 を求めEC90を算出した。Five days after the inoculation, the lesion area of the third, fourth and fifth true leaves was investigated and the control value was determined. Then, EC 90 was calculated.
試験例 2 各剤の所定濃度散布液(有効成分濃度20,10,5,2,1,0.
5ppm)を作り第2本葉期のキュウリ(品種:ときわ光3
号P型)に薬液の200/10a相当量を噴霧した。薬剤散
布風乾後(約2時間後)キュウリベと病(Pseudoperono
sporacubensis)の遊走子のう懸濁液を接種した。Test Example 2 Dispersion liquid of specified concentration of each agent (active ingredient concentration 20,10,5,2,1,0.
5ppm) cucumber in the second true leaf stage (variety: Tokiwa Hikari 3)
No. P type) was sprayed with an amount equivalent to 200 / 10a of the drug solution. After spray-drying chemicals (after about 2 hours) Cucumber bean and disease (Pseudoperono
sporacubensis).
その後2日間21℃の湿室に保持し、その後湿室内に2
日間放置した。Then, keep it in a humid chamber at 21 ° C for 2 days, and then keep it in the humid chamber for 2 days.
Left for days.
接種5日後に第1,第2本葉につき病斑面積を調査し、
防除価 を求めEC90を算出した。Five days after the inoculation, the lesion area of the first and second true leaves was investigated,
Control value Then, EC 90 was calculated.
試験例 3 試験例1と同様の方法でトマトに薬液を散布した。散
布24時間後に人工降雨装置により1時間40mm/hrの雨を
降らせた。さらに3時間後にトマト疫病菌の遊走子懸濁
液を接種し以降は試験例1と同様に行ない各薬剤のEC90
を求めた。Test Example 3 In the same manner as in Test Example 1, tomatoes were sprayed with the drug solution. Twenty-four hours after spraying, 40 mm / hr of rain was applied for one hour using an artificial rainfall device. Further 3 hours after the tomato late blight since inoculated with zoospore suspension of the fungus for each drug a similar manner to Test Example 1 EC 90
I asked.
次に試験結果を表に示す。試験例1の結果は表−1〜
表−7に、試験例2の結果は表−1,表−8〜表−13に、
試験例3の結果は表−〜表−に示される。但し、表中の
メタラキシルはメチルN−(2−メトキシアセチル)−
N−(2,6−キシリル)アラニエートを示し、粒径はVMD
を示し、FLはフロアブル製剤を示し、WPは水和剤を示
し、SFは次式により計算された相乗効果を表わす指数で
ある。SFが1より大きい時は相乗効果があることが示さ
れる。Next, the test results are shown in the table. The results of Test Example 1 are shown in Table-1.
The results of Test Example 2 are shown in Table-7 and Table-1, Table-8 to Table-13.
The results of Test Example 3 are shown in Table. However, metalaxyl in the table is methyl N- (2-methoxyacetyl)-
N- (2,6-xylyl) alaniate, particle size is VMD
, FL represents a flowable formulation, WP represents a wettable powder, and SF is an index representing the synergistic effect calculated by the following formula. When SF is larger than 1, it is shown that there is a synergistic effect.
SF=EC90(理論値)/EC90(測定値) 〔式中、X,Yは各々、組成物中の有効成分a,bの含有比を
示す。〕 以上の試験結果から本発明組成物は優れた殺菌効力及
び充分な相乗効果を有することが示される。 SF = EC 90 (theoretical value) / EC 90 (measured value) [In the formula, X and Y respectively represent the content ratios of the active ingredients a and b in the composition. ] From the above test results, it is shown that the composition of the present invention has an excellent bactericidal effect and a sufficient synergistic effect.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 小島 一弘 東京都大田区多摩川2丁目24番25号 株 式会社エス・ディー・エスバイオテック 東京研究所内 審査官 平山 美千恵 (56)参考文献 特開 昭62−19501(JP,A) 特開 昭59−51203(JP,A) ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Kazuhiro Kojima 2-24-25 Tamagawa, Ota-ku, Tokyo SDS Biotech Co., Ltd. Tokyo Research Laboratory Examiner Michie Hirayama (56) References Sho 62-19501 (JP, A) JP-A-59-51203 (JP, A)
Claims (1)
イル、1−(メトキシカルボニル)エチルまたは2−オ
キソ−チオラン−3−イルを示す。〕で表わされる化合
物及びテトラクロロイソフタロニトリルを有効成分とし
て、1:3乃至1:13の比率で含有し、かつ、その固形成分
の粒度分布が体積累積50%の粒径で0.8μm乃至2.5μm
の間にあるフロアブル製剤である殺菌剤組成物。1. A general formula [I] [In the formula, Z is 2-oxo-1,3-oxazolidine-3-
Represents 1- (methoxycarbonyl) ethyl or 2-oxo-thiolan-3-yl. ] The compound represented by and tetrachloroisophthalonitrile are contained as an active ingredient in a ratio of 1: 3 to 1:13, and the particle size distribution of the solid component is 0.8 μm to 2.5 at a particle size with a volume cumulative 50%. μm
A bactericidal composition which is a flowable formulation between.
Priority Applications (9)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63060486A JP2568099B2 (en) | 1988-03-16 | 1988-03-16 | Disinfectant composition |
GB8905713A GB2216798B (en) | 1988-03-16 | 1989-03-13 | Fungicidal compositions containing tetrachloroisophthalonitrile and an n-phenyl -carboxamide |
KR1019890003026A KR920002221B1 (en) | 1988-03-16 | 1989-03-13 | Germicidal agent composition |
FR8903368A FR2628604B1 (en) | 1988-03-16 | 1989-03-13 | |
IT8947739A IT1232821B (en) | 1988-03-16 | 1989-03-14 | IMPROVEMENTS IN ORGANIC COMPOUNDS WITH FUNGICIDE ACTION |
PH38334A PH26831A (en) | 1988-03-16 | 1989-03-15 | Fungicidal composition |
DE3908460A DE3908460C2 (en) | 1988-03-16 | 1989-03-15 | New fungicidal formulations |
ES8900968A ES2013120A6 (en) | 1988-03-16 | 1989-03-16 | Fungicidal compositions containing tetrachloroisophthalonitrile and an N-phenyl-carboxamide |
NL8900641A NL194985C (en) | 1988-03-16 | 1989-03-16 | Preparations with fungicidal action and method for the preparation thereof. |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63060486A JP2568099B2 (en) | 1988-03-16 | 1988-03-16 | Disinfectant composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH01238504A JPH01238504A (en) | 1989-09-22 |
JP2568099B2 true JP2568099B2 (en) | 1996-12-25 |
Family
ID=13143656
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63060486A Expired - Fee Related JP2568099B2 (en) | 1988-03-16 | 1988-03-16 | Disinfectant composition |
Country Status (9)
Country | Link |
---|---|
JP (1) | JP2568099B2 (en) |
KR (1) | KR920002221B1 (en) |
DE (1) | DE3908460C2 (en) |
ES (1) | ES2013120A6 (en) |
FR (1) | FR2628604B1 (en) |
GB (1) | GB2216798B (en) |
IT (1) | IT1232821B (en) |
NL (1) | NL194985C (en) |
PH (1) | PH26831A (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5496845A (en) * | 1994-05-25 | 1996-03-05 | American Cyanamid Co. | Suspension concentrate compositions of arylpyrrole insecticidal and acaricidal agents |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IT1114941B (en) * | 1977-12-27 | 1986-02-03 | Sipcam Spa | FUMERO - PATENT CONSULTING STUDY S.N.C. VIA S.AGNESE, 12 MILAN |
IT1096345B (en) * | 1978-05-26 | 1985-08-26 | Sipcam | FUNGICIDE COMPOUND |
-
1988
- 1988-03-16 JP JP63060486A patent/JP2568099B2/en not_active Expired - Fee Related
-
1989
- 1989-03-13 FR FR8903368A patent/FR2628604B1/fr not_active Expired - Fee Related
- 1989-03-13 GB GB8905713A patent/GB2216798B/en not_active Expired - Lifetime
- 1989-03-13 KR KR1019890003026A patent/KR920002221B1/en not_active IP Right Cessation
- 1989-03-14 IT IT8947739A patent/IT1232821B/en active
- 1989-03-15 PH PH38334A patent/PH26831A/en unknown
- 1989-03-15 DE DE3908460A patent/DE3908460C2/en not_active Expired - Fee Related
- 1989-03-16 ES ES8900968A patent/ES2013120A6/en not_active Expired - Lifetime
- 1989-03-16 NL NL8900641A patent/NL194985C/en not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
DE3908460C2 (en) | 2003-12-04 |
GB8905713D0 (en) | 1989-04-26 |
GB2216798B (en) | 1991-10-02 |
KR890013986A (en) | 1989-10-21 |
ES2013120A6 (en) | 1990-04-16 |
NL8900641A (en) | 1989-10-16 |
NL194985B (en) | 2003-06-02 |
IT1232821B (en) | 1992-03-05 |
FR2628604B1 (en) | 1996-05-31 |
DE3908460A1 (en) | 1989-09-28 |
PH26831A (en) | 1992-11-05 |
FR2628604A1 (en) | 1989-09-22 |
JPH01238504A (en) | 1989-09-22 |
GB2216798A (en) | 1989-10-18 |
KR920002221B1 (en) | 1992-03-20 |
IT8947739A0 (en) | 1989-03-14 |
NL194985C (en) | 2003-10-03 |
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