FR2599942A1 - PROCESS FOR COMBATTING FUNGAL DISEASES OF PLANTS USING A COMPOSITION BASED ON PROCHLORAZ AND TRIAZOLE. - Google Patents
PROCESS FOR COMBATTING FUNGAL DISEASES OF PLANTS USING A COMPOSITION BASED ON PROCHLORAZ AND TRIAZOLE. Download PDFInfo
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- FR2599942A1 FR2599942A1 FR8708035A FR8708035A FR2599942A1 FR 2599942 A1 FR2599942 A1 FR 2599942A1 FR 8708035 A FR8708035 A FR 8708035A FR 8708035 A FR8708035 A FR 8708035A FR 2599942 A1 FR2599942 A1 FR 2599942A1
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- France
- Prior art keywords
- compound
- formula
- plants
- prochloraz
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- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/38—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< where at least one nitrogen atom is part of a heterocyclic ring; Thio analogues thereof
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- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
L'INVENTION A POUR OBJET UN PROCEDE POUR COMBATTRE LES MALADIES FONGIQUES DES PLANTES QUI CONSISTE A APPLIQUER SUR LES PLANTES: A)LE COMPOSE DE FORMULE I (CF DESSIN DANS BOPI) ET B)LE COMPOSE DE FORMULE II (CF DESSIN DANS BOPI) EN UNE QUANTITE EFFICACE DU POINT DE VUE FONGICIDE.THE SUBJECT OF THE INVENTION IS A PROCESS FOR COMBATTING FUNGAL DISEASES OF PLANTS WHICH CONSISTS OF APPLYING ON PLANTS: A) THE COMPOUND OF FORMULA I (CF DRAWING IN BOPI) AND B) THE COMPOUND OF FORMULA II (CF DRAWING IN BOPI) IN A FUNGICIDE EFFECTIVE QUANTITY.
Description
-1 La présente invention a pour objet un procédé pour combattre lesThe subject of the present invention is a method for combating
maladies fongiques des plantes ainsi que les compositions fungal diseases of plants as well as compositions
fongicides utilisables dans ce procédé. fungicides for use in this process.
Selon un premier aspect, l'invention concerne un procédé pour combattre les maladies fongiques des plantes au moyen a) du composé de formule I According to a first aspect, the invention relates to a method for combating fungal diseases of plants by means of a) the compound of formula I
OH NOH N
Cl- ( -CH-CH-3) ICl- (-CH-CH-3) I
33
désigné ci-après composé A, et b) du composé de formule II hereinafter referred to as compound A, and b) of the compound of formula II
/N/NOT
Cl- O-CH2-CH2- N-CO-N IICl-O-CH 2 -CH 2 -N-CO-N II
1 5H2-CH31 5H2-CH3
désigné ci-après sous son nom commun de "prochloraz". hereinafter referred to as "prochloraz".
Le composé A est un fongicide connu permettant de combattre efficacement les champignons des cultures comme les céréales, y compris le riz, spécialement le blé et l'orge. Il est extrêmement efficace contre les rouilles (comme Puccinia spp.) et son activité est bonne contre les oidiums (comme Erysiphe), Septoria et Rhizoc25 tonia. Le prochloraz est un fongicide connu ayant une bonne activité contre Pseudocercosporella, Septoria, Pyrenophora, les oidiums Compound A is a known fungicide for effectively controlling fungi in crops such as cereals, including rice, especially wheat and barley. It is extremely effective against rust (such as Puccinia spp.) And has good activity against oidiums (such as Erysiphe), Septoria and Rhizoc25 tonia. Prochloraz is a known fungicide with good activity against Pseudocercosporella, Septoria, Pyrenophora, Oidiums
et Pyricularia.and Pyricularia.
On a maintenant trouvé que l'utilisation du prochloraz en association avec le composé A permet, de façon suprenante, de com30 battre efficacement les champignons phytopathogènes. Cette association est particulièrement appropriée pour l'utilisation pendant toute la durée végétative contre les viétins,1es maladies foliaireset les maladies des épis, en particulier les piétins dans It has now been found that the use of prochloraz in combination with compound A makes it possible, surprisingly, to effectively control phytopathogenic fungi. This combination is particularly suitable for use throughout the vegetative period against vietins, foliar diseases and ear diseases, especially
les céréales.the cereals.
La présente invention concerne par conséquent un procédé amélioré pour combattre les maladies fongiques des plantes, en particulier des céréales (y compris le riz), procédé selon lequel, en particulier pour le blé et l'orge, on applique sur les plantes le 5 composé A et le prochloraz, en mélange ou séparément, en une quantité efficace du point de vue fongicide. Le procédé est extrêmement The present invention therefore relates to an improved method for combating plant fungal diseases, in particular cereals (including rice), in which process, particularly for wheat and barley, the compound is applied to the plants. A and prochloraz, as a mixture or separately, in a fungicidally effective amount. The process is extremely
bien toléré par les plantes. On observe un effet supérieur à celui résultant de la simple addition des effets obtenus avec chacun des constituants pris séparément, entre autres contre Septoria dans le 10 blé et contre Helminthosporium dans l'orge. well tolerated by plants. A greater effect is observed than that resulting from the simple addition of the effects obtained with each of the constituents taken separately, inter alia against Septoria in wheat and against Helminthosporium in barley.
De façon appropriée, le composé A sera utilisé à une dose de l'ordre de 50 à 100 g, en particulier de 60 à 80 g par hectare et le prochloraz à une dose de 250 à 500 g, en particulier de 300 Suitably, compound A will be used at a dose in the range of 50 to 100 g, in particular 60 to 80 g per hectare and prochloraz at a dose of 250 to 500 g, in particular 300 g.
450 g par hectare de culture. Le rapport pondéral du composé A au 15 prochloraz est de préférence compris entre 1:2 et 1:8, plus particulièrement entre 1:3,5 et 1:8, spécialement entre 1:3,75 et 1:6. 450 g per hectare of culture. The weight ratio of compound A to prochloraz is preferably from 1: 2 to 1: 8, more preferably from 1: 3.5 to 1: 8, especially from 1: 3.75 to 1: 6.
Un rapport pondéral approprié est par exemple 1:3,75, 1:5 et 1:7,5. Les composés sont appliqués de préférence par pulvérisatUon en utilisant en général un volume d'application compris entre 0,05 20 et 0,5 hl par hectare, par exemple entre 0,05 à 0,1 hl pour une application aérienne et entre 0,2 et 0,4 hl pour une application An appropriate weight ratio is for example 1: 3.75, 1: 5 and 1: 7.5. The compounds are preferably applied by spraying, generally using an application volume of between 0.05 and 0.5 hl per hectare, for example between 0.05 to 0.1 hl for aerial application and between 0.degree. 2 and 0.4 hl for one application
terrestre classique.classical earth.
Selon un autre aspect, l'invention concerne également une According to another aspect, the invention also relates to a
composition fongicide comprenant le composé A et le prochloraz, de 25 préférence dans le rapport pondéral défini ci-dessus. fungicidal composition comprising compound A and prochloraz, preferably in the weight ratio defined above.
La composition de l'invention peut être formulée sous une forme classique quelconque, par exemple sous forme d'un emballage jumelé, ou sous forme de concentrés émulsionnables, de poudres mouillables ou de granulés à dissoudre dans l'eau, de préférence sous forme de concentrés émulsionnables. On peut préparer de telles formulations selon les méthodes connues, par exemple en mélangeant le composé A et le prochloraz avec des adjuvants appropriés comme The composition of the invention may be formulated in any conventional form, for example in the form of a twin package, or in the form of emulsifiable concentrates, wettable powders or granules for dissolving in water, preferably in the form of emulsifiable concentrates. Such formulations can be prepared according to known methods, for example by mixing compound A and prochloraz with appropriate adjuvants such as
des diluants, et éventuellement avec d'autres ingrédients de formulation comme des agents tensio-actifs. diluents, and optionally with other formulation ingredients such as surfactants.
Par diluant, on entend dans la présente demande de brevet n'importe quelle matière solide ou liquide acceptable en agriculture - y compris les charges - pouvant être ajoutée aux matières actives pour faciliter ou améliorer leur application, ou respecti5 vement pour leur conférer une activité utilisable ou désirable. Il peut s'agir par exemple de talc, de kaolin, de terre de diatomées, By diluent is meant in this patent application any agriculturally acceptable solid or liquid material - including fillers - which may be added to the active ingredients to facilitate or improve their application, or respectively to give them a usable activity. or desirable. It may be for example talc, kaolin, diatomaceous earth,
de xylène ou d'eau.xylene or water.
En particulier les formulations destinées à être appliquées par pulvérisation, comme les suspensions concentrées ou les 10 poudres mouillables, peuvent contenir des agents tensio-actifs tels que des agents mouillants et des agents de dispersion, par exemple le produit de condensation du formaldéhyde avec un naphtalènesulfonate, un alkylarylsulfonate, un lignine-sulfonate, un sulfate d'alcool gras, unalkylphénol éthoxylé et un alcool gras éthoxylé. 15 Généralement, les formulations contiennent de 0,01 à 90% en poids de matière active, de 0 à 20% d'un agent tensio-actif acceptable en agriculture et de 10 à 99,99% d'un ou de plusieurs adjuvants solides ou liquides, la matière active étant constituée du In particular, formulations intended to be applied by spraying, such as concentrated suspensions or wettable powders, may contain surfactants such as wetting agents and dispersing agents, for example the condensation product of formaldehyde with a naphthalenesulphonate. an alkylarylsulfonate, a lignin sulfonate, a fatty alcohol sulfate, an ethoxylated alkylphenol and an ethoxylated fatty alcohol. Generally, the formulations contain from 0.01 to 90% by weight of active ingredient, from 0 to 20% of an agriculturally acceptable surfactant and from 10 to 99.99% of one or more solid adjuvants. or liquids, the active ingredient consisting of
composé A, du prochloraz et éventuellement d'autres matières ac20 tives. compound A, prochloraz and possibly other active materials.
Les formes concentrées contiennent en général entre environ 2 et 80%, de préférence entre environ 5 et 70% en poids de matière active. Les formes prêtes à l'emploi peuvent contenir par The concentrated forms generally contain between about 2 and 80%, preferably between about 5 and 70% by weight of active ingredient. Ready-to-use shapes may contain by
exemple entre 0,01 et 45% en poids de matière active. example between 0.01 and 45% by weight of active ingredient.
Les exemples suivants illustrent la présente invention The following examples illustrate the present invention
sans aucunement en limiter la portée. Dans ces exemples, les parties et les pourcentages sont indiqués en poids. without in any way limiting its scope. In these examples, parts and percentages are by weight.
- 4 Concentrés émulsionnables Composition A B Composé A techn, (95,5%) 6, 2 8,2 Prochloraz techn. (97,4%) 29,7 29,7 Emulsifiant 1 15,0 15,0 Solvant 2 49,1 47,1 Total 100 100 (1) par exemple un mélange composé de 7 parties d'un mélange de 10 triglycérides éthoxylés et d'alkylaryl-sulfonate de calcium - 4 Emulsifiable concentrates Composition A B Compound A techn., (95.5%) 6, 2 8,2 Prochloraz techn. (97.4%) 29.7 29.7 Emulsifier 1 15.0 15.0 Solvent 2 49.1 47.1 Total 100 100 (1) for example a mixture consisting of 7 parts of a mixture of 10 ethoxylated triglycerides and calcium alkylarylsulfonate
ramifié dans de l'iso-butanol et de 8 parties d'éther polyglycolique du tributylphénol. branched in iso-butanol and 8 parts of polyglycolic ether tributylphenol.
(2) par exemple un mélange composé de 15 parties d'éther monométhylique du propylèneglycol et de 34,1 parties (pour la com15 position A) ou de 32, 1 parties (pour la composition B) de xylène. (2) for example, a mixture of 15 parts of propylene glycol monomethyl ether and 34.1 parts (for A) or 32.1 parts (for composition B) of xylene.
Claims (9)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB868614367A GB8614367D0 (en) | 1986-06-12 | 1986-06-12 | Fungicides |
Publications (2)
Publication Number | Publication Date |
---|---|
FR2599942A1 true FR2599942A1 (en) | 1987-12-18 |
FR2599942B1 FR2599942B1 (en) | 1991-03-29 |
Family
ID=10599383
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FR878708035A Expired - Lifetime FR2599942B1 (en) | 1986-06-12 | 1987-06-09 | METHOD FOR COMBATING FUNGAL DISEASES OF PLANTS USING A COMPOSITION BASED ON PROCHLORAZ AND A TRIAZOLE. |
Country Status (15)
Country | Link |
---|---|
AU (1) | AU599986B2 (en) |
BE (1) | BE1001743A4 (en) |
CA (1) | CA1329117C (en) |
CH (1) | CH670932A5 (en) |
DE (1) | DE3718695C2 (en) |
DK (1) | DK295787A (en) |
FR (1) | FR2599942B1 (en) |
GB (2) | GB8614367D0 (en) |
GR (1) | GR870908B (en) |
HU (1) | HU206599B (en) |
IE (1) | IE60413B1 (en) |
IT (1) | IT1216820B (en) |
SE (1) | SE468233B (en) |
TR (1) | TR24875A (en) |
ZA (1) | ZA874258B (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0687703A (en) * | 1992-07-31 | 1994-03-29 | Shell Internatl Res Maatschappij Bv | Bactericidal composition |
GB9424373D0 (en) * | 1994-12-02 | 1995-01-18 | Sandoz Ltd | Novel combinations |
US5651587A (en) † | 1995-06-09 | 1997-07-29 | P.L. Porter Co. | Vehicle seat and system for controlling the same |
JP5940369B2 (en) * | 2011-05-27 | 2016-06-29 | 石原産業株式会社 | How to control plant diseases |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0040007A2 (en) * | 1980-04-24 | 1981-11-18 | Fbc Limited | Fungicidal compositions |
GB2136423A (en) * | 1983-03-04 | 1984-09-19 | Sandoz Ltd | Fungicidal 1h-azole-1-ethanol derivatives |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IT1196465B (en) * | 1986-07-07 | 1988-11-16 | Montedison Spa | FUNGICIDE MIXTURES |
-
1986
- 1986-06-12 GB GB868614367A patent/GB8614367D0/en active Pending
-
1987
- 1987-06-01 HU HU872508A patent/HU206599B/en unknown
- 1987-06-04 DE DE3718695A patent/DE3718695C2/en not_active Expired - Lifetime
- 1987-06-05 CH CH2137/87A patent/CH670932A5/de not_active IP Right Cessation
- 1987-06-08 GB GB8713348A patent/GB2191401B/en not_active Expired - Lifetime
- 1987-06-09 FR FR878708035A patent/FR2599942B1/en not_active Expired - Lifetime
- 1987-06-09 BE BE8700639A patent/BE1001743A4/en not_active IP Right Cessation
- 1987-06-10 AU AU74068/87A patent/AU599986B2/en not_active Expired
- 1987-06-10 DK DK295787A patent/DK295787A/en not_active Application Discontinuation
- 1987-06-10 SE SE8702422A patent/SE468233B/en not_active IP Right Cessation
- 1987-06-10 GR GR870908A patent/GR870908B/en unknown
- 1987-06-11 TR TR87/0426A patent/TR24875A/en unknown
- 1987-06-11 IE IE154487A patent/IE60413B1/en not_active IP Right Cessation
- 1987-06-11 IT IT8748046A patent/IT1216820B/en active
- 1987-06-11 CA CA000539451A patent/CA1329117C/en not_active Expired - Fee Related
- 1987-06-12 ZA ZA874258A patent/ZA874258B/en unknown
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0040007A2 (en) * | 1980-04-24 | 1981-11-18 | Fbc Limited | Fungicidal compositions |
GB2136423A (en) * | 1983-03-04 | 1984-09-19 | Sandoz Ltd | Fungicidal 1h-azole-1-ethanol derivatives |
Also Published As
Publication number | Publication date |
---|---|
TR24875A (en) | 1992-07-07 |
DE3718695C2 (en) | 1997-02-06 |
IT8748046A0 (en) | 1987-06-11 |
AU599986B2 (en) | 1990-08-02 |
HUT44417A (en) | 1988-03-28 |
GR870908B (en) | 1987-10-12 |
SE8702422D0 (en) | 1987-06-10 |
IE60413B1 (en) | 1994-07-13 |
GB2191401B (en) | 1990-10-31 |
GB8614367D0 (en) | 1986-07-16 |
DK295787D0 (en) | 1987-06-10 |
CH670932A5 (en) | 1989-07-31 |
IE871544L (en) | 1987-12-12 |
FR2599942B1 (en) | 1991-03-29 |
SE8702422L (en) | 1987-12-13 |
AU7406887A (en) | 1987-12-17 |
GB8713348D0 (en) | 1987-07-15 |
SE468233B (en) | 1992-11-30 |
IT1216820B (en) | 1990-03-14 |
HU206599B (en) | 1992-12-28 |
CA1329117C (en) | 1994-05-03 |
ZA874258B (en) | 1989-01-25 |
DE3718695A1 (en) | 1987-12-17 |
GB2191401A (en) | 1987-12-16 |
BE1001743A4 (en) | 1990-02-27 |
DK295787A (en) | 1987-12-13 |
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