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
  • A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system

Definitions

• the present invention relates to fungicidal mixtures for controlling rice pathogens containing as active components
• the invention relates to a method for controlling rice pathogens 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 compositions containing these mixtures.
• EP-A 988 790 synergistic mixtures are fungicidally effective against various diseases of cereals, fruits and vegetables, such as. As mildew on wheat and barley or gray mold on apples.
• Rhizoctonia solani is the causative agents of the most important diseases of rice plants. Rhizoctonia solani is the only agriculturally significant pathogen within the subclass Agaricomycetidae. This fungus does not attack the plant like most other fungi via spores, but via a mycelial infection.
• the mixtures of the compounds I and II or the simultaneous joint or separate use of the compounds I and the compound II are distinguished by an outstanding activity against rice pathogens from the class of the Ascomycetes, Deuteromycetes and Basidiomycetes. They can be used for seed treatment, as well as foliar and soil fungicides.
• the application of the compounds I and II is preferably carried out by spraying the leaves.
• the application of the compounds can also be carried out by granule application or dusting of the soil.
• inventive combination of compounds I and II is also suitable for controlling other pathogens, such.
• the pure active ingredients I and II which can be added as needed further active against harmful fungi or other pests such as insects, spider animals or nematodes, or herbicidal or growth-regulating agents or fertilizers.
• fungicides selected from the following group are suitable as further active ingredients in the above sense: Acylalanines such as benalaxyl, metalaxyl, ofurace, oxadixyl,
• Amine derivatives such as aldimorph, dodemorph, fenpropidin, 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, ipconazole, myclobutanil, penconazole, propiconazole, prochlorazole, prothio- conazole, simeconazole, tetraconazole, triadimefon, triadimenol , Triflumizole, triticonazole,
• Dicarboximides such as mycoclin, procymidone,
• Dithiocarbamates such as Ferbam, Nabam, Metam, Propineb, Polycarbamate, Ziram, Zinc,
• Heterocyclic compounds such as anilazine, boscalid, carbendazim, carboxin, oxycarboxine, cyazofamide, dazomet, famoxadone, fenamidone, fuberidazole, flutolanil, furametpyr, isoprothiolane, mepronil, nuarimol, probenazole, pyroquilon, silthiofam, thiabendazole, thifluzamide, tiadinil, tricyclazole, triforine,
• Nitrophenyl derivatives such as binapacryl, dinocap, dinobutone, nitrophthalic-isopropyl,
• phenylpyrroles such as fenpiclonil or fludioxonil, • sulfur,
• fungicides such as acibenzolar-S-methyl, carpropamide, chlorothalonil, cyfluhenamide, cymoxanil, diclomethine, diclocymet, diethofencarb, edifenphos, ethaboxam, fentin acetate, fenoxanil, ferimzone, fosetyl, hexachlorobenzene, metrafenone, pencycuron, propamocarb, Phthalide, toloclofos-methyl, quintozene, zoxamide, • strobilurins such as fluoxastrobin, metominostrobin, orysastrobin or pyraclostrobin,
• Cinnamic acid amides and analogues such as Flumetover.
• fertilizers I and II are admixed with another fungicide III or two fungicides III and IV.
• Mixtures of compounds I and II with a component III are preferred. Particular preference is given to mixtures of the compounds I and II.
• 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 having no effect on the control result.
• the compound I and the compound II are usually used in a weight ratio of 100: 1 to 1: 100, preferably 20: 1 to 1:50, especially 10: 1 to 1:10 applied. If desired, components III and, if appropriate, IV are admixed to compound I in a ratio of from 20: 1 to 1:20.
• the application rates of the mixtures according to the invention are from 5 g / ha to 2000 g / ha, preferably from 50 to 1500 g / ha, in particular from 50 to 750 g / ha.
• the application rates for the compound I are accordingly generally 1 to 1000 g / ha, preferably 10 to 750 g / ha, in particular 20 to 500 g / ha.
• the application rates for the compound II are accordingly generally 1 to 1000 g / ha, preferably 10 to 750 g / ha, in particular 20 to 500 g / ha.
• application rates of 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 separate or combined application of the compounds I and II or the mixtures of the compounds I and II by spraying or dusting the seeds, seedlings, plants or soils before or after sowing of the Plants or before or after emergence of the plants.
• 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 application form depends on the respective purpose; It should in any case 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 excipients, if desired using emulsifiers and dispersants.
• Suitable solvents / auxiliaries are essentially: water, aromatic solvents (eg Solvesso products, xylene), paraffins (eg petroleum fractions), alcohols (eg methanol, butanol, pentanol, benzyl alcohol), ketones (eg cyclohexanone, gamma-butyrololactone) , Pyrrolidones (NMP, NOP), acetates (glycol diacetate), glycols, dimethyl fatty acid amides, fatty acids and fatty acid esters.
• aromatic solvents eg Solvesso products, xylene
• paraffins eg petroleum fractions
• alcohols eg methanol, butanol, pentanol, benzyl alcohol
• ketones eg
• solvent mixtures can also be used, excipients such as ground natural minerals (eg kaolins, clays, talc, chalk) and ground synthetic minerals (eg finely divided silica, silicates); Emulsifiers such as nonionic and anionic emulsifiers (eg polyoxyethylene fatty alcohol ethers, alkyl sulfonates and arylsulfonates) and dispersants such as lignin liquors and methylcellulose.
• ground natural minerals eg kaolins, clays, talc, chalk
• ground synthetic minerals eg finely divided silica, silicates
• Emulsifiers such as nonionic and anionic emulsifiers (eg polyoxyethylene fatty alcohol ethers, alkyl sulfonates and arylsulfonates) and dispersants such as lignin liquors and methylcellulose.
• the surface-active substances used are alkali metal, alkaline earth metal, ammonium salts of lignin sulfonic acid, naphthalenesulfonic acid, phenolsulfonic acid, dibutylnaphthalenesulfonic acid, alkylarylsulfonates, alkyl sulfates, alkyl sulfonates, fatty alcohol sulfates, fatty acids and sulfated fatty alcohol glycol ethers, and condensation products of sulfonated naphthalene and naphthalene derivatives with formaldehyde , Condensation products of naphthalene or naphthalenesulfonic acid with phenol and formaldehyde, polyoxyethylene octylphenol ether, ethoxylated isooctylphenol, octylphenol, nonylphenol, alkylphenol polyglycol ethers, tributylphenyl
• mineral oil fractions of medium to high boiling point such as kerosine or diesel oil, coal tar oils and 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, strong polar solvents, e.g. Dimethylsulfoxide, N-methylpyrrolidone or water into consideration.
• mineral oil fractions of medium to high boiling point such as kerosine or diesel oil, coal tar oils and oils of vegetable or animal origin, aliphatic, cyclic and aromatic hydrocarbons, e.g. Toluene, xylene, paraffin, tetrahydronaphthalene, alkylated naphthalenes or their derivative
• Powders, dispersants and dusts may be prepared by mixing or co-grinding the active substances with a solid carrier.
• Granules e.g. Coated, impregnated and homogeneous granules can be prepared by binding the active compounds to solid carriers.
• Solid carriers are e.g. Mineral earths, such as silica gels, silicates, talc, kaolin, attaclay, limestone, lime, chalk, bolus, loess, clay, dolomite, diatomaceous earth, calcium and magnesium sulphate, 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 meal, cellulose powder and other solid carriers.
• Mineral earths such as silica gels, silicates, talc, kaolin, attaclay, limestone, lime, chalk, bolus, loess, clay, dolomite, diatomaceous earth, calcium and magnesium sulphate, magnesium oxide, ground plastics
• the formulations generally contain between 0.01 and 95 wt .-%, preferably between 0.1 and 90 wt .-% of the active ingredients.
• the active ingredients are used in a purity of 90% to 100%, preferably 95% to 100% (according to NMR spectrum). Examples of formulations are: 1. Products for dilution in water
• the active ingredients 10 parts by weight of the active ingredients are dissolved in water or a water-soluble solvent. Alternatively, wetting agents or other adjuvants are added. When diluted in water, the active ingredient dissolves.
• Suspensions 20 parts by weight of the active ingredients are comminuted with the addition of dispersants and wetting agents and water or an organic solvent in a stirred ball mill to give a fine active substance suspension. Dilution in water results in a stable suspension of the active ingredient.
• the active ingredients 50 parts by weight of the active ingredients are finely ground with the addition of dispersing and wetting agents and prepared by means of technical equipment (for example 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.
• the active compounds may be used as such, in the form of their formulations or the forms of use prepared therefrom, e.g. in the form of directly sprayable solutions, powders, suspensions or dispersions, emulsions, Oldispersionen, pastes, dusts, scattering agents, granules by spraying, atomizing, dusting, scattering or pouring are applied.
• the forms of application depend entirely on the intended use; 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 (spray powder, old dispersions) by adding water.
• the substances as such or dissolved in an oil or solvent, can be homogenized in water by means of wetter, tackifier, dispersant or emulsifier.
• the active compound concentrations in the ready-to-use preparations can be varied within wide ranges. 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 (ULV) process, it being possible to apply formulations containing more than 95% by weight of active ingredient or even the active ingredient without additives.
• UUV ultra-low-volume
• wetting agents, adjuvants, herbicides, fungicides, other pesticides, bactericides, optionally also just before use (tank mix) are added. These agents are added to the compositions of the invention usually in a weight ratio of 1: 10 to 10: 1.
• the compounds I and II, or the mixtures or the corresponding formulations are applied by mixing the harmful fungi, the plants, seeds, soils, surfaces, materials or spaces to be kept free of them with a fungicidally effective amount of the mixture Compounds I and II in separate application, treated.
• the application can be made before or after the attack by the harmful fungi.
• the active compounds were prepared separately or together as a stock solution with 0.25% by weight of active ingredient in acetone or DMSO. To this solution was added 1% by weight of emulsifier Uniperol® EL (wetting agent with emulsifying and dispersing action based on ethoxylated alkylphenols) and diluted with water according to the desired concentration.
• emulsifier Uniperol® EL wetting agent with emulsifying and dispersing action based on ethoxylated alkylphenols
• Leaves of potted rice seedlings of the cultivar "Tai-Nong 67" were sprayed to drip point with aqueous suspension in the concentration of active compound specified below. The following day, the plants were inoculated with an aqueous spore suspension of Cochliobolus miyabeanus. The test plants were then placed in climatic chambers at 22-24 ° C and 95-99% relative humidity for six days. Then the extent of infestation on the leaves was visually determined.
• the evaluation is carried out by determining the affected plants in percent. These percentages were converted into efficiencies.
• the efficiency (W) is calculated according to the formula of Abbot as follows:
• W (1- ⁇ / ⁇ ) -100 ⁇ corresponds to the fungal infestation of the treated plants in% and ⁇ corresponds to the fungal infestation of the untreated (control) plants in%
• the infestation of the treated plants corresponds to that of the untreated control plants; at an efficiency of 100, the treated plants have no infestation.
• the expected efficiencies of the drug mixtures are according to the Colby formula [R.S. Colby, Weeds 15, 20-22 (1967)] and compared with the observed efficiencies.
• the comparative compounds which were used were the compounds A and B known from the fluazinamine mixtures described in EP-A 988 790:

Landscapes

• 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)
• Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Applications Claiming Priority (2)

Publications (1)

Family

ID=34428383

Family Applications (1)

Country Status (23)

Families Citing this family (2)

Family Cites Families (6)

• 2004
  • 2004-07-10 UA UAA200605000A patent/UA80364C2/uk unknown
  • 2004-09-30 PE PE2004000959A patent/PE20050514A1/es not_active Application Discontinuation
  • 2004-10-07 CA CA002540296A patent/CA2540296A1/en not_active Abandoned
  • 2004-10-07 JP JP2006530109A patent/JP2007533629A/ja not_active Withdrawn
  • 2004-10-07 EA EA200600659A patent/EA200600659A1/ru unknown
  • 2004-10-07 CN CNA2004800284296A patent/CN1859848A/zh active Pending
  • 2004-10-07 EP EP04765861A patent/EP1672979A1/de not_active Withdrawn
  • 2004-10-07 MX MXPA06003232A patent/MXPA06003232A/es unknown
  • 2004-10-07 BR BRPI0415093-7A patent/BRPI0415093A/pt not_active IP Right Cessation
  • 2004-10-07 US US10/574,083 patent/US20060264447A1/en not_active Abandoned
  • 2004-10-07 NZ NZ546481A patent/NZ546481A/en unknown
  • 2004-10-07 UY UY28552A patent/UY28552A1/es unknown
  • 2004-10-07 AU AU2004280080A patent/AU2004280080A1/en not_active Abandoned
  • 2004-10-07 KR KR1020067006777A patent/KR20060123110A/ko not_active Application Discontinuation
  • 2004-10-07 WO PCT/EP2004/011184 patent/WO2005034630A1/de not_active Application Discontinuation
  • 2004-10-08 AR ARP040103674A patent/AR046099A1/es not_active Application Discontinuation
  • 2004-10-08 TW TW093130643A patent/TW200522864A/zh unknown
• 2006
  • 2006-03-21 IL IL174440A patent/IL174440A0/en unknown
  • 2006-03-27 NO NO20061384A patent/NO20061384L/no not_active Application Discontinuation
  • 2006-04-07 CO CO06034501A patent/CO5670335A2/es not_active Application Discontinuation
  • 2006-04-11 EC EC2006006502A patent/ECSP066502A/es unknown
  • 2006-04-25 CR CR8361A patent/CR8361A/es unknown
  • 2006-05-05 ZA ZA200603576A patent/ZA200603576B/en unknown

Non-Patent Citations (1)

Also Published As

Similar Documents

Legal Events