EP1681930A1

EP1681930A1 - Fungicidal mixtures

Info

Publication number: EP1681930A1
Application number: EP04817271A
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: 2003-10-29
Filing date: 2004-10-27
Publication date: 2006-07-26
Also published as: CR8365A; IL174791A0; NZ546401A; WO2005039295A1; BRPI0416015A; NO20062011L; JP2007509879A; KR20060105753A; AU2004283042A1; ECSP066537A; EA200600832A1; AR046215A1; CA2543297A1; ZA200604335B; TW200528026A; US20070129384A1; UA80368C2; CO5670339A2; CN1874682A

Abstract

The invention relates to fungicidal mixtures, comprising the active components 1) the triazolopyrimidine of formula I and 2) carbendazime of formula II, in synergistically effective amounts, methods for the treatment of harmful fungi with mixtures of compound I and compound II, the use of compound I with 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 of the formula I,

and

2) carbendazim of the formula II,

in a synergistically effective amount.

In addition, the invention relates to a method for controlling harmful fungi with mixtures of the compound I with the compound II and the use of the compound I with the compound II for the production 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).

Mixtures of triazolopyrimidines with other active ingredients are known from EP-A 988 790 and US 6 268371.

The compound of the formula II, (1H-benzimidazol-2-yI) carbamic acid methyl ester, its preparation and its action against harmful fungi is also known (common name: carbendazim; US 3657443). In view of an effective control of phytopathogenic harmful fungi with the lowest possible application rates, the present invention was based on mixtures which, with a reduced total amount of active compounds applied, have an improved activity against a broad spectrum of harmful fungi (synergistic mixtures).

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, harmful fungi can be better controlled than with the individual compounds.

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 outstanding activity against a broad spectrum of phytopathogenic fungi, in particular from the class of the Ascomycetes, Deuteromyces ten, Oomycetes and Basidiomycetes. They can be used in plant protection as leaf and soil fungicides.

They are particularly important for combating a large number of fungi on various crops such as bananas, cotton, vegetables (e.g. cucumbers, beans and squashes), barley, grass, oats, coffee, potatoes, corn, fruit plants, rice, rye, soybeans, tomatoes , Wine, wheat, ornamental plants, sugar cane and a variety of seeds.

They are particularly suitable for combating the following phytopathogenic fungi: Blumeria graminis (powdery mildew) on cereals, Erysiphe cichoracearum and Sphaerotheca fuliginea on pumpkin plants, Podosphaera leucotricha on apples, Uncinula necatoran vines, Puccinia A -en on cereals, rhizomes , Rice and lawn, Ustilago species on cereals and sugar cane, Venturia inaequalis on apples, Bipolaris and Drechslera species on cereals, rice and lawn, Septoria nodumrum on wheat, Botrytis cinerea on strawberries, vegetables, ornamental plants and vines, my - cosphaerella arl on bananas, peanuts and cereals, Pseudocercosporella her- potrichoides on wheat and barley, Pyricularia oryzae on rice, Phytophthora infestans on potatoes and tomatoes, Pseudoperonospora species on squashes and hops, Plasmopara viticola on vegetables, Alternaria species on vegetables and fruit as well as Fusaria and Verticillium species. Due to the special cultivation conditions of rice plants, there are significantly different requirements for a rice fungicide than for fungicides that are used in cereal or fruit growing. There are differences in the method of application: in addition to the foliar application used in many places, in modern rice cultivation the fungicide is applied directly to the soil or shortly after sowing. The fungicide is absorbed into the plant via the roots and transported in the plant sap in the plant to the parts of the plant to be protected. In cereal or fruit growing, on the other hand, the fungicide is usually applied to the leaves or the fruit, so the systemics of the active ingredients play a significantly smaller role in these crops.

Other pathogens are also typical in rice than in cereals or fruit. Pyricularia oryzae and Corticium sasakii (syn. Rhizoctonia solani) are the causative agents of the most important diseases of rice plants. Rhizoctonia solani is the only agronomically important pathogen within the Agaricomycetidae subclass. This fungus does not attack the plant via spores like most other fungi, but via a mycelial infection.

They are of particular importance for controlling harmful fungi on rice plants and on their seeds, such as bipolaris and Drechslera arias, and Pyricularia oryzae. They are particularly suitable for combating the rice blight caused by Pyricularia oryzae.

They can also be used in material protection (e.g. wood protection), for example against Paecilomyces variotii.

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 measures.

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:

Acylalanines such as benalaxyl, ofurace, oxadixyl, Amine derivatives such as aldimorph, dodemorph, fenpropidine, guazatine, iminoctadine, tridemorph,

Anilinopyrimidines such as pyrimethanil, mepanipyrim or cyprodinil,

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, priazolone, propazole, propicon , Triflumizole, tritico-nazole,

Dicarboximides such as myclozolin, procymidone,

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

Heterocyclic compounds such as anilazine, boscalid, oxycarboxin, cyazofamid, Dazomet, famoxadone, fenamidone, fuberidazole, flutolanil, furametpyr, isoprothiolan, mepronil, nuarimol, probenazole, pyroquilon, silthiololamide, thifluorozolamide, thifluorozolamide, thifluorozolamide, thifluorozolamide, thifluorozolamide, thifluizolicyle

Nitrophenyl derivatives such as binapacryl, dinocap, dinobuton, nitrophthal-isopropyl,

• phenylpyrroles such as fenpiclonil, • other fungicides such as acibenzolar-S-methyl, carpropamide, chlorothalonil, cyflufamid, cymoxanil, diclomezin, diclocymet, diethofencarb, edifenphos, ethaboxam, fentin acetate, fenoxanosetyl, ferylzone, ferimzone, ferim zone , Pencycuron, propamocarb, phthalide, toloclofos-methyl, quintozene, zoxamide,

Strobilurins such as fluoxastrobin, metominostrobin, orysastrobin or pyraclostrobin, 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 III 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 are usually used in a weight ratio of 100: 1 to 1: 100, preferably 10: 1 to 1:20, in particular 10: 1 to 1: 2.

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

The application rates for the compound I are accordingly generally from 1 to 1000 g / ha, preferably from 10 to 900 g / ha, in particular from 20 to 750 g / ha.

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

In the case of seed treatment, application rates of mixture of 1 to 1000 g / 100 kg of seed, preferably 1 to 200 g / 100 kg, in particular 5 to 100 g / 100 kg, are generally used.

If pathogenic harmful fungi are to be combated 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 emergence of the plants. Compounds I and II are preferably applied by spraying the leaves.

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 (e.g. 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 (DC)

20 parts by weight of the active ingredients are dissolved in cyclohexanone with the addition of a dispersing agent e.g. Dissolved polyvinyl pyrrolidone. When diluted in water, a dispersion results.

C) Emulsifiable concentrates (EC)

15 parts by weight of the active ingredients 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 mixed internally 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, oldispersions, 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, old dispersions) by adding water. To prepare emulsions, pastes or old 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 agent, tackifier, dispersant or emulsifier and possibly solvent 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. Various types of oils, wetting agents, adjuvants, herbicides,

Fungicides, other pesticides, bactericides, if appropriate also only immediately before use (tank mix), are added. These agents are usually 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, surfaces, materials or spaces to be kept free of them are mixed with a fungicidally effective amount of the mixture or Compounds I and II treated 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 Emulator 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 - Protective activity against rice blight caused by Pyricularia oryzae

Leaves of rice seedlings of the "Tai-Nong 67" variety, grown in pots, were sprayed to runoff point with an aqueous suspension in the active compound concentration given below. The following day, the plants were inoculated with an aqueous spore suspension of Pyricularia oryzae. The test plants were then placed in climatic chambers at 22-24 ° C and 95-99% relative humidity for 6 days. The extent of the development of the infestation on the leaves was then determined visually.

The evaluation is carried out by determining the affected leaf areas in percent. These percentages were converted into efficiencies. Efficiency (W) is calculated using Abbot's formula as follows:

W = (1 - σ / yff) - 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 infection 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 of the active ingredient mixtures are calculated according to the Colby formula [R.S. Colby, Weeds 15, 20-22 (1967)] and compared with the observed efficiencies.

Colby formula: E = x + y - xy / 100 expected efficiency, expressed in% of the untreated control, when using the mixture of active ingredients A and B in concentrations a and b, the efficiency, expressed in% of the untreated control, when Use of the active ingredient A in the concentration a the efficiency, expressed in% of the untreated control, when using the active ingredient B in the concentration b

Table A - Individual substances

Table B - mixtures according to the invention

*) Efficiency calculated according to the Colby formula

The results of the experiments show that the observed efficiency in all mixing ratios is higher than calculated using the Colby formula.

Claims

claims

1. Containing fungicidal mixtures for controlling harmful fungi

1) the triazolopyrimidine derivative of the formula I,

and

2) carbendazim of the formula II,

in a synergistically effective amount.

2. Fungicidal mixtures according to claim 1, 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 one of claims 1 or 2.

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

5. The method according to claim 4, characterized in that the compounds I and II according to claim 1 simultaneously, 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 used in an amount of 5 g / ha to 2000 g / ha.

7. The method according to claims 4 to 6, characterized in that rice pathogenic harmful fungi are combated.

8. The method 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.

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 compounds I and II according to claim 1 for the preparation of an agent suitable for combating harmful fungi.