EP1830647A2 - Procede pour lutter contre les mycoses chez les legumineuses - Google Patents

Procede pour lutter contre les mycoses chez les legumineuses

Info

Publication number
EP1830647A2
EP1830647A2 EP05817599A EP05817599A EP1830647A2 EP 1830647 A2 EP1830647 A2 EP 1830647A2 EP 05817599 A EP05817599 A EP 05817599A EP 05817599 A EP05817599 A EP 05817599A EP 1830647 A2 EP1830647 A2 EP 1830647A2
Authority
EP
European Patent Office
Prior art keywords
orysastrobin
active ingredient
active
weight
seed
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.)
Withdrawn
Application number
EP05817599A
Other languages
German (de)
English (en)
Inventor
Ulf Groeger
Dirk Voeste
Egon Haden
Matthias NIEDENBRÜCK
Peter Dombo
Siegfried Strathmann
Reinhard Stierl
John-Bryan Speakman
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BASF SE
Original Assignee
BASF SE
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by BASF SE filed Critical BASF SE
Publication of EP1830647A2 publication Critical patent/EP1830647A2/fr
Withdrawn legal-status Critical Current

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
    • A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
    • A01N33/16—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds containing nitrogen-to-oxygen bonds
    • A01N33/18—Nitro compounds
    • A01N33/20—Nitro compounds containing oxygen or sulfur attached to the carbon skeleton containing the nitro group
    • A01N33/22—Nitro compounds containing oxygen or sulfur attached to the carbon skeleton containing the nitro group having at least one oxygen or sulfur atom and at least one nitro group directly attached to the same aromatic ring system
    • 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
    • A01N37/44—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 nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
    • A01N37/50—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 nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids the nitrogen atom being doubly bound to the carbon skeleton
    • 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

Definitions

  • the invention relates to a method for controlling rust attack in legumes.
  • Orysastrobin (2 lbs) -2- (methoxyimino) -2- ⁇ 2 - [(3E, 5E, 6E) -5- (methoxyimino) -4,6-dimethyl-2,8-dioxa-3,7- diazanona-3,6-dien-1-yl] phenyl ⁇ - ⁇ / -methylacetamide is known as a particularly effective against rice pathogens fungicide from WO-A 97/15552 known (see also www.hclrss.demon.co.uk).
  • Synergistic mixtures of orysastrobin specially adapted to rice diseases are known from WO 99/48365, WO 99/48366, WO 99/48367, WO 99/48368, WO 99/48369 and WO 99/48370.
  • the active substances described as mixing partners in the present invention are generally known to the person skilled in the art (cf., http://www.hclrss.demon.co.uk/) and are commercially available.
  • the control of harmful fungi is carried out by application of orysastrobin by seed treatment, spraying or dusting of the plants or the soil before or after the sowing of the plants or before or after emergence of the plants.
  • the control of rust diseases in legumes is advantageously carried out by applying an aqueous preparation of a formulation containing orysastrobin on the above-ground parts of plants especially leaves, or, as prophylaxis due to the high systemic effect by seed or soil treatment done.
  • Azoles such as bromoconazole, cyproconazole, difenoconazole, epoxiconazole, fluquinconazole, flusilazole, flutriafol, hexaconazole, imazalil, metconazole, myclobutanil, penconazole, propiconazole, prochloraz, prothioconazole, tebuconazole, tetraconazole, triadimefon, triadimol, triticonazole,
  • Acylalanines such as benalaxyl, metalaxyl, mefenoxam, ofurace, oxadixyl, amine derivatives such as guazatine,
  • Anilinopyrimidines such as pyrimethanil, mepanipyrim or cyprodinil,
  • Dicarboximides such as iprodione, procymidone, vinclozolin,
  • Heterocyclic compounds such as benomyl, boscalid, carbendazim, carboxin, oxycarboxin, fuberidazole, picobenzamide, penthiopyrad, proquinazide, thiabendazole, thiophanate-methyl,
  • Phenylpyrroles such as fenpiclonil or fludioxonil
  • the invention therefore also relates to fungicidal mixtures for controlling rust fungi containing as active components
  • an active ingredient II as defined above in synergistically effective amounts an active ingredient II as defined above in synergistically effective amounts.
  • Orysastrobin and the active ingredient 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 compounds I and II are usually employed in a weight ratio of 100: 1 to 1: 100, preferably 20: 1 to 1:20, in particular 10: 1 to 1:10.
  • Orysastrobin can advantageously be used in the process according to the invention together with other active ingredients IM, in addition to the active compounds II also with herbicides, insecticides, growth regulators, other fungicides or else with fertilizers.
  • active ingredients IM in addition to the active compounds II also with herbicides, insecticides, growth regulators, other fungicides or else with fertilizers.
  • these other mixing partners III are in particular:
  • the compounds I and III are usually used in a weight ratio of 100: 1 to 1: 100, preferably 20: 1 to 1:20, in particular 10: 1 to 1:10 applied.
  • orysastrobin in soybean has led to a significant increase in yield.
  • the use of orysastrobin can thus also be done for the purpose of increasing the yield.
  • the increase in earning power in combination with the excellent effect of orysastrobin against rust diseases in legumes renders the method according to the invention valuable for the farmer.
  • Excellent results can be achieved with the use of Orysastrobin in combination with an active ingredient II.
  • Orysastrobin or the mixtures described above are also suitable for controlling the o.g. Diseases.
  • Orysastrobin, or mixtures of the invention are also highly effective against Blumeria graminis (powdery mildew) to cereals, Erysiphe cichoracearum and Sphaerotheca fuliginea on cucurbits, Podosphaera leucot ⁇ cha on apples, Uncinula necator on vines, Puccinia species on cereals, Rhizoctonia arias on tree - wool and turf, Ustilago species on cereals and sugarcane, Venturia inaequalis on apples, Bipolaris and Drechslera species on cereals and turf, Septoria arias on wheat, Botrytis cinerea on strawberries, vegetables, ornamental plants and vines, mycosphaerella Bananas, peanuts and cereals, Pseudocercosporella her- potrichoides on wheat and barley, Phytophthora infestans on potatoes and tomatoes, Pseudoperonospora on cucurbits and
  • mixtures of orysastrobin with one of the abovementioned fungicidal active compounds II are particularly suitable.
  • mixtures of orysastrobin with an azole such as cyproconazole, epoxiconazole, flutriafol, metconazole, tebuconazole, triticonazole, metalaxyl, pyrimethanil, iprodione, dimethomorph, metiram, boscalid, thiophanate-methyl, penthiopyrad, fludioxonil, metrafenone, cyflufenamid or Proquinazid particularly suitable.
  • an azole such as cyproconazole, epoxiconazole, flutriafol, metconazole, tebuconazole, triticonazole, metalaxyl, pyrimethanil, iprodione, dimethomorph, metiram, boscalid, thiophanate-methyl, penthiopyrad, fludioxonil, metrafenone, cyflu
  • Orysastrobin or the Orysastrobin mixtures are applied by treating the fungi or the fungi to be protected plants, materials or the soil with a fungicidally effective amount of the active ingredients.
  • the application can take place both before and after the infection of the materials or plants by the fungi.
  • the treatment preferably takes place before the infection.
  • the fungicidal compositions generally contain between 0.1 and 95, preferably between 0.5 and 90 wt .-% of active ingredient.
  • the application rates in the process according to the invention are between 0.01 and 1.5 kg of active ingredient per ha, depending on the nature of the desired effect.
  • amounts of active ingredient of 1 to 1500 g of orysastrobin, preferably 10 to 500 g per 100 kilograms of seed are needed.
  • the application rates of the mixtures according to the invention are, depending on the nature of the active compound II and the desired effect at 10 g / ha to 2500 g / ha, preferably 50 to 2000 g / ha, in particular 100 to 1500 g / ha.
  • the application rates for oryastrobin 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 active compound II are accordingly generally 1 to 1500 g / ha, preferably 10 to 1250 g / ha, in particular 20 to 1000 g / ha.
  • application rates of mixture of 1 to 2000 g / 100 kg of seed preferably 1 to 1500 g / 100 kg, in particular 5 to 1000 g / 100 kg, are generally used.
  • the compounds may be converted into the usual 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 Butyrolactone), 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 cyclohe
  • solvent mixtures can also be used, - carriers 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 flour, 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% by weight, preferably between 0.1 and 90% by weight of the active ingredient.
  • 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
  • a Water-soluble concentrates (SL, LS)
  • DC Dispersible Concentrates
  • Emulsifiable Concentrates 15 parts by weight of the active compounds are dissolved in 75 parts by weight of xylene with addition of calcium dodecylbenzenesulfonate and castor oil ethoxylate (in each case 5 parts by weight). Dilution in water results in an emulsion.
  • the formulation has 15% by weight active ingredient content.
  • the active compounds 25 parts by weight of the active compounds are dissolved in 35 parts by weight of xylene with addition of calcium dodecylbenzenesulfonate and castor oil ethoxylate (in each case 5 parts by weight).
  • This mixture is added to water by means of an emulsifying machine (e.g., Ultraturax) in 30 parts by weight and made into a homogeneous emulsion. Dilution in water results in an emulsion.
  • the formulation has an active ingredient content of 25% by weight.
  • the active ingredients 20 parts by weight of the active ingredients are comminuted with the addition of 10 parts by weight of dispersants and wetting agents and 70 parts by weight of water or an organic solvent in a stirred ball mill to a fine active substance suspension. Dilution in water results in a stable suspension of the active ingredient.
  • the active ingredient content in the formulation is 20% by weight.
  • Water-dispersible and water-soluble granules 50 parts by weight of the active ingredients are finely ground with the addition of 50 parts by weight of dispersants and wetting agents and prepared by means of technical equipment (eg 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 formulation has an active ingredient content of 50% by weight.
  • G Water-dispersible and water-soluble powders (WP, SP, SS, WS) 75 parts by weight of the active compounds are ground in a rotor-stator mill with the addition of 25 parts by weight of dispersing and wetting agents and silica gel. Dilution in water results in a stable dispersion or solution of the active ingredient.
  • the active ingredient content of the formulation is 75% by weight.
  • 0.5 parts by weight of the active ingredients are finely ground and combined with 99.5 parts by weight of carriers. Common processes are extrusion, spray drying or fluidized bed. This gives a granulate for direct application with 0.5 wt .-% active ingredient content.
  • LS water-soluble concentrates
  • FS suspensions
  • DS dusts
  • WS water-dispersible and water-soluble powders
  • ES emulsions
  • EC emulsifiable concentrates
  • gel formulations GF
  • FS formulations for seed treatment typically contain 1 to 800 g / l active ingredient, 1 to 200 g / l surfactants, 0 to 200 g / l antifreeze, 0 to 400 g / l binder, 0 to 200 g / l dyes and solvents, preferably water
  • the active compounds can be used as such, in the form of their formulations or the use forms prepared therefrom, for example in the form of directly sprayable solutions, powders, suspensions or dispersions, emulsions, oil dispersions, pastes, dusts, scattering agents, granules by spraying, atomizing, dusting, scattering or Pouring be 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 (wettable powders, oil 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. But it can also be made of effective substance wetting, adhesion, dispersing or emulsifying and possibly solvent or oil concentrates, which are suitable for dilution with water.
  • 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 To the active ingredients oils of various types, wetting agents, adjuvants, herbicides, fungicides, other pesticides, bactericides, optionally also just before use (tank mix), are added. These agents can be added to the compositions according to the invention in a weight ratio of 1: 100 to 100: 1, preferably 1:10 to 10: 1.
  • adjuvants in this sense are in particular: organically modified polysiloxanes, eg Break Thru S 240 ® ; Alcohol alkoxylates, eg. As Atplus 245 ®, Atplus MBA 1303 ®, Plurafac LF 300 ® and Lutensol ON 30 ®; EO-PO block polymers, eg. B. Pluro- nic RPE 2035 ® and Genapol B ®; Alcohol ethoxylates, eg. As Lutensol XP 80 ®; and sodium dioctylsulfosuccinate, e. B. Leophen RA ®.
  • organically modified polysiloxanes eg Break Thru S 240 ®
  • Alcohol alkoxylates eg. As Atplus 245 ®, Atplus MBA 1303 ®, Plurafac LF 300 ® and Lutensol ON 30 ®
  • EO-PO block polymers eg. B. Pluro
  • Seeds of soybean BRS 133 were treated with 1000g orysastrobin / 100 kg of seed, formulated as SC with 250g of active ingredient per liter, as a wet pickle, then seeded in pots and cultured in the greenhouse at about 22 ° C. 3 weeks after sowing, the plants were inoculated with soybean rust, for 24 hours at 100% rel. Humidity incubated and then cultivated again in the greenhouse. At the time of inoculation, the first pair of leaves and a follow-up blade were developed. 11 days after the inoculation, the infestation of the leaves was evaluated.

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Plant Pathology (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • Pest Control & Pesticides (AREA)
  • Agronomy & Crop Science (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Toxicology (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Pretreatment Of Seeds And Plants (AREA)
  • Cultivation Of Plants (AREA)
  • Catching Or Destruction (AREA)

Abstract

L'invention concerne un procédé servant à combattre la rouille chez les légumineuses par utilisation d'orysastrobine. L'invention concerne également des mélanges d'orysastrobine avec un principe actif fongicide II du groupe des azoles, acylalanines, dérivés d'amine, anilinopyrimidines, dicarboximides, dithiocarbamates, composés hétérocycliques, phénylpyrroles, amides de l'acide cinnamique et analogues, ou d'autres fongicides selon la description. L'invention concerne en outre des agents et des semences contenant ces mélanges.
EP05817599A 2004-12-20 2005-12-16 Procede pour lutter contre les mycoses chez les legumineuses Withdrawn EP1830647A2 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102004062455 2004-12-20
PCT/EP2005/013552 WO2006066810A2 (fr) 2004-12-20 2005-12-16 Procede pour lutter contre les mycoses chez les legumineuses

Publications (1)

Publication Number Publication Date
EP1830647A2 true EP1830647A2 (fr) 2007-09-12

Family

ID=36463326

Family Applications (1)

Application Number Title Priority Date Filing Date
EP05817599A Withdrawn EP1830647A2 (fr) 2004-12-20 2005-12-16 Procede pour lutter contre les mycoses chez les legumineuses

Country Status (20)

Country Link
US (1) US20080153824A1 (fr)
EP (1) EP1830647A2 (fr)
JP (1) JP2008524150A (fr)
KR (1) KR20070089866A (fr)
CN (1) CN101080170A (fr)
AP (1) AP2007004082A0 (fr)
AR (1) AR052270A1 (fr)
AU (1) AU2005318481A1 (fr)
BR (1) BRPI0519162A2 (fr)
CA (1) CA2589646A1 (fr)
EA (1) EA012612B1 (fr)
IL (1) IL183569A0 (fr)
MA (1) MA29156B1 (fr)
MX (1) MX2007006474A (fr)
NZ (1) NZ555623A (fr)
TW (1) TW200637487A (fr)
UA (1) UA87722C2 (fr)
UY (1) UY29261A1 (fr)
WO (1) WO2006066810A2 (fr)
ZA (1) ZA200704453B (fr)

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CN102630679B (zh) * 2012-04-05 2014-05-21 广西田园生化股份有限公司 一种含肟醚菌胺的农药组合物
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CN104996432A (zh) * 2012-09-07 2015-10-28 陕西美邦农药有限公司 一种含吡噻菌胺与甲氧基丙烯酸酯类的杀菌组合物
CN103651425B (zh) * 2012-09-18 2015-12-16 陕西美邦农药有限公司 一种含醚菌胺的农药组合物
CN105815314B (zh) * 2012-12-12 2018-08-03 陕西美邦农药有限公司 一种含苯菌酮与甲氧基丙烯酸酯类的杀菌组合物
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CN103210920A (zh) * 2013-03-24 2013-07-24 广东中迅农科股份有限公司 肟醚菌胺水分散粒剂及其制备方法
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UY29261A1 (es) 2006-07-31
WO2006066810A2 (fr) 2006-06-29
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AP2007004082A0 (en) 2007-08-31
EA200701224A1 (ru) 2008-02-28
AR052270A1 (es) 2007-03-07
KR20070089866A (ko) 2007-09-03
BRPI0519162A2 (pt) 2008-12-30
MA29156B1 (fr) 2008-01-02
US20080153824A1 (en) 2008-06-26
JP2008524150A (ja) 2008-07-10
NZ555623A (en) 2009-04-30
CN101080170A (zh) 2007-11-28
WO2006066810A3 (fr) 2006-09-21
IL183569A0 (en) 2007-09-20
TW200637487A (en) 2006-11-01
ZA200704453B (en) 2008-09-25
EA012612B1 (ru) 2009-10-30
UA87722C2 (ru) 2009-08-10
CA2589646A1 (fr) 2006-06-29

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