EP1670312A1

EP1670312A1 - Fungicide mixtures

Info

Publication number: EP1670312A1
Application number: EP04765706A
Authority: EP
Inventors: Jordi Tormo I Blasco; Thomas Grote; Maria Scherer; Reinhard Stierl; Siegfried Strathmann; Ulrich Schöfl
Original assignee: BASF SE
Current assignee: BASF SE
Priority date: 2003-10-01
Filing date: 2004-09-30
Publication date: 2006-06-21
Also published as: CO5670322A2; EA009084B1; KR100751612B1; TW200520691A; CA2539732A1; CN1863460A; NO20061356L; WO2005032255A1; JP2007507453A; ZA200603380B; CN100348105C; MXPA06002925A; US20060293346A1; AR045851A1; UA79402C2; BRPI0414836A; EA200600610A1; KR20060063980A; AU2004277340A1; IL174223A0

Abstract

The invention relates to fungicide mixtures, containing the following as active ingredients 1) the triazolopyrimidine derivative of formula (I) and 2) quinoxyfen of formula (II), in synergistically effective amounts, a method for the control of fungal pests of the class Oomycete with mixtures of compound (I) and compound (II), the use of compound (I) and compound (II) for the production of such mixtures and agents comprising said mixtures.

Description

Fungicidal mixtures

description

The present invention relates to fungicidal mixtures containing as active components

1) the triazolopyrimidine derivative of the formula I,

and

2) quinoxyfen of the formula II,

in a synergistically effective amount.

In addition, the invention relates to a method for controlling harmful fungi from the class of the Oomycetes with mixtures of the compound I with the compound II and the use of the compound I with the compound II for the preparation of such mixtures and agents which contain these mixtures.

The compound I, 5-chloro-7- (4-methyl-piperidin-1-yl) -6- (2,4,6-trifluorophenyl) - [1,2,4] tri-azolo [1,5 -a] pyrimidine, its preparation and its action against harmful fungi is known from the literature (WO 98/46607).

The compound II, 5,7-dichloro-4- (4-fluorophenoxy) quinoline, its preparation and its action against harmful fungi is also known from the literature (US Pat. No. 5,240,940; common name: Quinoxyfen). Quinoxyfen is established as a fungicide against mildew diseases in the market. Mixtures of triazolopyrimidine derivatives with quinoxyfen are generally known from EP-A 988 790. Compound I is included in the general disclosure of this document, but is not explicitly mentioned. The combination of compound I with quinoxyfen is therefore new.

The synergistic mixtures of triazolopyrimidines described in EP-A 988 790 are described as being fungicidally active against various diseases of cereals, fruits and vegetables, in particular mildew on wheat and barley or gray mold on apples. However, the fungicidal activity of these mixtures against harmful fungi from the Oomycetes class leaves something to be desired.

The biological behavior of Oomycetes differs significantly from that of Ascomycetes, Deuteromycetes, and Basidiomycetes, because Oomycetes are biologically more related to algae than to fungi. Therefore, knowledge about the fungicidal activity of active substances against "real fungi", such as Ascomycetes, Deuteromycetes, and Basidiomycetes can only be transferred to Oomycetes to a very limited extent.

Oomycetes cause economically significant damage to various crops. In many regions, infections caused by Phytophthora infestans are the most important plant diseases in potato and tomato cultivation. In viticulture, considerable damage is caused by vine peronospora.

There is an ongoing need for new Oθ / r.yce, etj agents in agriculture, since the harmful fungi against the products established in the market, such as e.g. Metalaxyl and structurally similar active ingredients, have already developed widespread resistance.

Practical experience in agriculture has shown that the repeated and exclusive use of a single active ingredient in the control of harmful fungi in many cases leads to the rapid selection of those fungal strains that have developed a natural or adapted resistance to the active ingredient in question. An effective control of these fungi with the active ingredient in question is then no longer possible.

In order to reduce the risk of selection of resistant fungal strains, mixtures of different active ingredients are preferably used today to combat harmful fungi. Combining active ingredients with different mechanisms of action can ensure long-term control success.

With regard to effective resistance management and an effective control of harmful fungi from the Oomycetes class with the least possible effort The object of the present invention was to provide mixtures which, with the total amount of active ingredients applied being as small as possible, have a sufficient action against the harmful fungi.

Accordingly, the mixtures defined at the outset were found. It has also been found that when the compound I and the compound II are used simultaneously or separately or when the compounds I and the compound II are used in succession, Oomycetes can be controlled more effectively than with the individual compounds (synergistic mixtures).

The mixtures of the compound I and the compound II or the simultaneous joint or separate use of the compound I and the compound II are distinguished by an excellent activity against phytopathogenic fungi from the Oomycetes class, in particular from Phytophthora infestans on potatoes and tomatoes, and Plasmopara viticola on vines. They can be used in plant protection as leaf and soil fungicides.

They are of particular importance for the control of Oomycetes on various crops such as vegetables (e.g. cucumbers, lettuce and pumpkin plants), potatoes, tomatoes, vines and corresponding seeds.

In particular, they are suitable for combating late blight on tomatoes and potatoes caused by Phytophthora infestans, as well as false downy mildew (vine peronospora) caused by Plasmopara viticola.

In addition, the combination of compounds I and II according to the invention is also suitable for controlling other pathogens, such as, for. B. Septoria and Puccinia Aήen in cereals and Alternaria and Boyt tis species in vegetables, fruits and wine.

In the preparation of the mixtures, preference is given to using the pure active ingredients I and II, to which, as required, further active ingredients against harmful fungi or other pests such as insects, arachnids or nematodes, or else herbicidal or growth-regulating active ingredients or fertilizers can be admixed.

Fungicides selected from the following group are particularly suitable as further active ingredients in the above sense: i

Acylalanines such as benalaxyl, metalaxyl, ofurace, oxadixyl,

Amine derivatives such as aldimorph, dodemorph, fenpropidine, guazatine, iminoctadine, tridemorph, Antibiotics such as cycloheximide, griseofulvin, kasugamycin, natamycin, polyoxin or streptomycin,

Azoles such as bitertanol, bromoconazole, cyproconazole, difenoconazole, dinitroconazole, enilconazole, fenbuconazole, fluquiconazole, flusilazole, flutriafol, hexaconazole, imazalil, ipazazol, myclobutanil, penconazole, propicon , Triadimenol, triflumizole, triticonazole,

Dicarboximides such as myclozolin, procymidone,

Dithiocarbamates such as Ferbam, Nabam, Metam, Propineb, Polycarbamat, Ziram, Zineb,

• Heterocyclic compounds such as anilazine, boscalid, carbendazim, carboxin, oxycarboxin, cyazofamid, Dazomet, famoxadone, fenamidone, fuberidazole, flutolanil, furametpyr, isoprothiolan, mepronil, nuarimol, probenazole, pyroofilamol, thiazilazililililililililililililililililililililililililililililinilililililililililililililililililililililililililililinililililililililililililililililinililililililililililililililililililzilililililililililililzilililililililililililzolzilazilzilazilazoladil Triforins, • nitrophenyl derivatives such as binapacryl, dinocap, dinobutone, nitrophthal-isopropyl,

Phenylpyrroles such as fenpiclonil or fludioxonil,

• sulfur,

• Other fungicides such as acibenzolar-S-methyl, carpropamide, chlorothalonil, cyflufamid, cymoxanil, diclomezin, diclocymet, diethofencarb, edifenphos, ethaboxam, fenhexamide, fentin acetate, fenoxanil, Ferimzone, fluazinam, fosetlorobenzene Metrafenone, pencycuron, propamocarb, phthalide, toloclofos-methyl, quintozene, zoxamide,

Strobilurins such as fluoxastrobin, metominostrobin, orysastrobin, pyraclostrobin or trifloxystrobin, sulfenic acid derivatives such as captafol,

• Cinnamic acid amides and analogues such as Flumetover.

In one embodiment of the mixtures according to the invention, a further fungicide III or two fungicides IM and IV are added to the compounds I and II. Mixtures of the compounds I and II with a component III are preferred. Mixtures of compounds I and II are particularly preferred.

The compound I and the compound II can be applied simultaneously together or separately or in succession, the sequence in the case of separate application generally not having any effect on the success of the control.

In the control of harmful pathogens for plants, the separate or joint application of the compound I and the compound II or the mixtures of the compound I and the compound II is carried out by spraying or dusting the seeds, the plants or the soil before or after sowing of the plants or before or after the plants emerge. The mixtures are preferably applied by spraying the leaves.

The compound I and the compound II are usually used in a weight ratio of 100: 1 to 1: 100, preferably 50: 1 to 1:10, in particular 10: 1 to 1: 5.

If desired, components III and, if appropriate, IV are mixed in a ratio of 20: 1 to 1:20 to compound I.

Depending on the type of compound and the desired effect, the application rates of the mixtures according to the invention are 5 g / ha to 2000 g / ha, preferably 50 to 1500 g / ha, in particular 50 to 750 g / ha.

Accordingly, the application rates for the compound I are generally from 1 to 1000 g / ha, preferably from 10 to 750 g / ha, in particular from 20 to 500 g / ha.

Correspondingly, the application rates for the compound II are generally 5 to 2000 g / ha, preferably 10 to 1000 g / ha, in particular 50 to 750 g / ha.

In the case of seed treatment, application rates of the mixture of 1 to 1000 g / 100 kg of seed, preferably 1 to 750 g / 100 kg, in particular 5 to 500 g / 100 kg, are generally used.

The mixtures according to the invention, or the compounds I and II, can be converted into the customary formulations, e.g. Solutions, emulsions, suspensions, dusts, powders, pastes and granules. The form of application depends on the respective purpose; in any case, it should ensure a fine and uniform distribution of the compound according to the invention.

The formulations are prepared in a known manner, for example by stretching the active ingredient with solvents and / or carriers, if desired using emulsifiers and dispersants. The following are essentially suitable as solvents / auxiliaries: water, aromatic solvents (for example Solvesso products, xylene), paraffins (for example petroleum fractions), alcohols (for example methanol, butanol, pentanol, benzyl alcohol), ketones (for example cyclohexanone, gamma-butryolactone) , Pyrrolidones (NMP, NOP), acetates (glycol diacetate), glycols, dimethyl fatty acid amides, fatty acids and fatty acid esters. In principle, solvent mixtures can also be used, carriers such as natural stone powder (eg kaolins, clays, talc, chalk) and synthetic stone powder (eg highly disperse silica, silicates); Emulsifiers such as nonionic and anionic emulsifiers (eg polyoxyethylene fatty alcohol ethers, alkyl sulfonates and aryl sulfonates) and dispersants such as lignin sulfite waste liquors and methyl cellulose.

Alkali, alkaline earth, and ammonium salts of lignosulfonic acid, naphthalenesulfonic acid, phenolsulfonic acid, dibutylnaphthalenesulfonic acid, alkylarylsulfonates, alkyl sulfates, alkyl sulfonates, fatty alcohol sulfates, fatty acids and sulfated naphthalene naphthalene and sulfonated dehydrogenated naphthalene derivatives of sulfonated formaldehyde derivatives and sulfonated dehydrogenated naphthalenedaphthalene from sulfonates, as well as condensation products with sulfated naphthalenedaphthalene and sulfonated dehydrogenated naphthalenedaphthalene and sulfonated dehydrogenated naphthalenedaphthalene and sulfonated dehydrogenated naphthalenedaphthalene and sulfonated dehydrogenated naphthalenedaphthalene ether and condensation products , Condensation products of naphthalene or of naphthalene sulfonic acid with phenol and formaldehyde, polyoxyethylene octylphenol ether, ethoxylated isooctylphenol, octylphenol, nonylphenol, alkylphenol polyglycol ether, tri-butylphenyl polyglycol ether, trihylphenyl polyglycol ether, alkyl alcoholoxy ethoxylated alcohol, alkyl alcoholoxy ethoxylated alcohol , Laurylalkoholpolyglykoletheracetal, sorbitol ester, lignin sulfite waste liquors and methyl cellulose into consideration.

For the production of directly sprayable solutions, emulsions, pastes or oil dispersions, mineral oil fractions from medium to high boiling points, such as kerosene or diesel oil, furthermore coal tar oils as well as oils of vegetable or animal origin, aliphatic, cyclic and aromatic hydrocarbons, e.g. Toluene, xylene, paraffin, tetrahydronaphthalene, alkylated naphthalenes or their derivatives, methanol, ethanol, propanol, butanol, cyclohexanol, cyclohexanone, isophorone, strongly polar solvents, e.g. Dimethyl sulfoxide, N-methylpyrrolidone or water into consideration.

Powders, materials for broadcasting and dusts can be prepared by mixing or grinding the active substances together with a solid carrier.

Granules, e.g. Coating, impregnation and homogeneous granules can be produced by binding the active ingredients to solid carriers. Solid carriers are e.g. Mineral earths, such as silica gels, silicates, talc, kaolin, attack clay, limestone, lime, chalk, bolus, loess, clay, dolomite, diatomaceous earth, calcium and magnesium sulfate, magnesium oxide, ground plastics, fertilizers, e.g. Ammonium sulfate, ammonium phosphate, ammonium nitrate, ureas and vegetable products such as cereal flour, tree bark, wood and nutshell flour, cellulose powder and other solid carriers.

The formulations generally contain between 0.01 and 95% by weight, preferably between 0.1 and 90% by weight, of the active ingredients. The active ingredients are used in a purity of 90% to 100%, preferably 95% to 100% (according to the NMR spectrum). Examples of formulations are: 1. Products for dilution in water

A) Water-soluble concentrates (SL) 10 parts by weight of the active ingredients are dissolved in water or a water-soluble solvent. Alternatively, wetting agents or other aids are added. The active ingredient dissolves when diluted in water.

B) Dispersible concentrates (TLC) 20 parts by weight of the active ingredients are dissolved in cyclohexanone with the addition of a dispersant e.g. Dissolved polyvinyl pyrrolidone. When diluted in water, a dispersion results.

C) Emulsifiable concentrates (EC) 15 parts by weight of the active compounds are dissolved in xylene with the addition of calcium dodecylbenzenesulfonate and castor oil ethoxylate (5% each). Dilution in water results in an emulsion.

D) Emulsions (EW, EO) 40 parts by weight of the active ingredients are dissolved in xylene with the addition of calcium dodecylbenzenesulfonate and castor oil ethoxylate (5% each). This mixture is introduced into water using an emulsifying machine (Ultraturax) and brought to a homogeneous emulsion. Dilution in water results in an emulsion.

E) suspensions (SC, OD)

20 parts by weight of the active ingredients are comminuted in a stirred ball mill to form a fine active ingredient suspension with the addition of dispersing and wetting agents and water or an organic solvent. Dilution in water results in a stable suspension of the active ingredient.

F) Water-dispersible and water-soluble granules (WG, SG)

50 parts by weight of the active ingredients are finely ground with the addition of dispersing and wetting agents and produced using technical equipment (e.g. extrusion, spray tower, fluidized bed) as water-dispersible or water-soluble granules. Dilution in water results in a stable dispersion or solution of the active ingredient.

G) Water-dispersible and water-soluble powders (WP, SP)

75 parts by weight of the active ingredients are ground in a rotor-strator mill with the addition of dispersing and wetting agents and silica gel. Dilution in water results in a stable dispersion or solution of the active ingredient. 2. Products for direct application

H) Dusts (DP) 5 parts by weight of the active ingredients are finely ground and intimately mixed with 95% finely divided kaolin. This gives a dust.

I) Granules (GR, FG, GG, MG)

0.5 part by weight of the active ingredients are finely ground and combined with 95.5% carriers. Common processes are extrusion, spray drying or fluidized bed. This gives granules for direct application.

J) ULV solutions (UL)

10 parts by weight of the active ingredients are dissolved in an organic solvent e.g. Xylene dissolved. This gives you a product for direct application.

The active ingredients as such, in the form of their formulations or the use forms prepared therefrom, e.g. in the form of directly sprayable solutions, powders, suspensions or dispersions, emulsions, oil dispersions, pastes, dusts, sprinkling agents, granules by spraying, atomizing, dusting, scattering or pouring. The application forms depend entirely on the purposes; in any case, they should ensure the finest possible distribution of the active compounds according to the invention.

Aqueous application forms can be prepared from emulsion concentrates, pastes or wettable powders (wettable powders, oil dispersions) by adding water. To prepare emulsions, pastes or oil dispersions, the substances as such or dissolved in an oil or solvent can be homogenized in water by means of wetting agents, adhesives, dispersants or emulsifiers. However, it is also possible to prepare concentrates composed of an active substance, wetting agents, adhesives, dispersants or emulsifiers and possibly solvents or oil, which are suitable for dilution with water.

The active ingredient concentrations in the ready-to-use preparations can be varied over a wide range. In general, they are between 0.0001 and 10%, preferably between 0.01 and 1%.

The active ingredients can also be used with great success in the ultra-low-volume process (ULV), it being possible to apply formulations with more than 95% by weight of active ingredient or even the active ingredient without additives. Oils of various types, wetting agents, adjuvants, herbicides, fungicides, other pesticides, bactericides can be added to the active compounds, if appropriate also only immediately before use (tank mix). These agents can be added to the agents according to the invention in a weight ratio of 1:10 to 10: 1.

The compounds I and II, or the mixtures or the corresponding formulations, are used in that the harmful fungi, the plants, seeds, soils, areas, materials or spaces to be kept free from them are mixed with a fungicidally effective amount of the mixture or the compounds I and II when applied separately. The application can take place before or after the infestation by the harmful fungi.

The fungicidal activity of the compound and the mixtures can be demonstrated by the following tests:

The active ingredients were prepared separately or together as a stock solution with 0.25% by weight of active ingredient in acetone or DMSO. 1% by weight of emulsifier Uniperol® EL (wetting agent with emulsifying and dispersing action based on ethoxylated alkylphenols) was added to this solution and diluted with water to the desired concentration.

Example of use - effectiveness against vine peronospora caused by Plasmopara viticola

Leaves of potted vines of the "Riesling" variety were sprayed to runoff point with an aqueous suspension in the active compound concentration given below. The following day, the undersides of the leaves were inoculated with an aqueous zoospore suspension of Plasmopara viticola. The vines were then placed for 48 hours in a steam-saturated chamber at 24 ° C and then for 5 days in a greenhouse at temperatures between 20 and 30 ° C. After this time, the plants were again placed in a moist chamber for 16 hours in order to accelerate the sporangium carrier outbreak. The extent of the development of the infestation on the undersides of the leaves was then determined visually.

The visually determined values for the percentage of leaf areas affected were converted into efficiencies as% of the untreated control. Efficiency (W) is calculated using Abbot's formula as follows:

W = (1 - α / β) 100

α corresponds to the fungal attack of the treated plants in% and ß corresponds to the fungal attack of the untreated (control) plants in%

With an efficiency of 0, the infestation of the treated plants corresponds to that of the untreated control plants; with an efficiency of 100, the treated plants show no infection.

The expected efficacies for combinations of active ingredients were determined using the Colby formula (Colby, S.R. (Calculating synergistic and antagonistic responses of herbicide combinations ", Weeds, 15, pp. 20-22, 1967) and compared with the observed efficacies.

Colby formula: E = x + y - x y / 100

E expected efficiency, expressed in% of the untreated control, when using the mixture of active ingredients A and B in concentrations a and b

x the efficiency, expressed in% of the untreated control, when using the active ingredient A in the concentration a

y the efficiency, expressed in% of the untreated control, when using the active ingredient B in the concentration b

As comparison compounds, those of those described in EP-A 988 790 were used

Quinoxyfen mixtures known compounds A and B used:

Table A - Individual substances

Table B - mixtures according to the invention

*) Efficiency calculated according to the Colby formula

Table C - Comparative experiments - mixtures known from EP-A 988 780

*) Efficiency calculated according to the Colby formula The results of the experiments show that the mixtures according to the invention are considerably more effective than the quinoxyfen mixtures known from EP-A 988780 due to the strong synergism against vine peronospora.

Claims

claims

1. Fungicidal mixtures containing as active components

1) the triazolopyrimidine derivative of the formula I,

and

2) quinoxyfen of the formula II,

in a synergistically effective amount.

2. Fungicidal mixtures comprising the compound of the formula I and the compound of the formula II in a weight ratio of 100: 1 to 1: 100.

3. Fungicidal composition comprising a liquid or solid carrier and a mixture according to claim 1 or 2.

4. A method for controlling harmful fungi from the class of the Oomycetes, characterized in that the fungi, their habitat or the plants to be protected against fungal attack, the soil or seeds with an effective amount of the compound I and the compound II according to claim 1 treated.

5. The method according to claim 4, characterized in that the compounds I and II according to claim 1 are applied simultaneously, that is jointly or separately, or in succession.

6. The method according to claim 4, characterized in that the mixture according to claims 1 or 2 is applied to the plants to be protected against fungal attack or the soil in an amount of 5 g / ha to 2000 g / ha.

7. Process according to claims 4 and 5, characterized in that the mixture according to claims 1 or 2 is used in an amount of 1 to 1000 g / 100 kg of seed.

8. The method according to claims 4 to 7, characterized in that the harmful fungus Plasmopara viticola is controlled.

9. Seed containing the mixture according to claims 1 or 2 in an amount of 1 to 1000 g / 100 kg.

10. Use of the compound I and the compound II according to claim 1 for the preparation of an agent suitable for controlling oomycetes.