WO2005074685A1 - Compositions de protection des plantes et utilisation associee - Google Patents

Compositions de protection des plantes et utilisation associee Download PDF

Info

Publication number
WO2005074685A1
WO2005074685A1 PCT/EP2005/000959 EP2005000959W WO2005074685A1 WO 2005074685 A1 WO2005074685 A1 WO 2005074685A1 EP 2005000959 W EP2005000959 W EP 2005000959W WO 2005074685 A1 WO2005074685 A1 WO 2005074685A1
Authority
WO
WIPO (PCT)
Prior art keywords
rice
methyl
plant protection
active substance
protection composition
Prior art date
Application number
PCT/EP2005/000959
Other languages
English (en)
Other versions
WO2005074685A8 (fr
Inventor
Claude Taranta
Rainer Buckpesch
Original Assignee
Bayer Cropscience Gmbh
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 Bayer Cropscience Gmbh filed Critical Bayer Cropscience Gmbh
Priority to JP2006551780A priority Critical patent/JP2007520511A/ja
Priority to KR1020067017372A priority patent/KR101196233B1/ko
Priority to CN200580007199XA priority patent/CN1929735B/zh
Publication of WO2005074685A1 publication Critical patent/WO2005074685A1/fr
Publication of WO2005074685A8 publication Critical patent/WO2005074685A8/fr

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
    • A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
    • A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
    • A01N57/20—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing acyclic or cycloaliphatic radicals
    • 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
    • A01N25/02—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 containing liquids as carriers, diluents or solvents
    • 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
    • A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds

Definitions

  • the invention relates to uses of plant protection compositions comprising 2- ethylhexyl lactate (EHL), and specific plant protection compositions comprising EHL.
  • EHL 2- ethylhexyl lactate
  • the rice plants and/or harmful organisms present in the water either have to come into contact in a direct and timely fashion with the active substance to be applied or the active substance has to be evenly and extensively distributed over the entire rice paddy field.
  • the application of known spray solutions or granules as standard application processes is costly.
  • Processes in which the active substances, in water-soluble containers, such as bottles, disclosed in JP-A-10175804, or bags, disclosed in US-5439 683, are positioned on the edge of the rice field are more economical. After the release from the containers, the even distribution of the active substances over the surface of the water is dependent on several factors and can be improved or indeed even guaranteed by suitable additives.
  • Special compositions can be used for sparingly water-soluble active substances, as disclosed in JP-A-10017410, or the water-insoluble active substance is, as disclosed in JP-A-05339103, dissolved directly in aprotic solvents, such as (C 8 - C- ⁇ 3 )-alkyl phthalates.
  • aprotic solvents such as (C 8 - C- ⁇ 3 )-alkyl phthalates.
  • vegetable oil is added to the active substances, and the active substance content in the oil could be further increased by further addition of an aprotic solvent.
  • the active substance is then evenly distributed in the rice paddy field via the formation of an oil film.
  • the oil film may also prevent the exchange of oxygen between air and water and the additional introduction of certain solubility promoters may in consequence lead to negative effects ecologically.
  • the plant protection composition used according to the invention and its application according to the invention are simple and safe to operate for the user, exhibit favorable properties with regard to toxicity and are reliable in the effect for the control of harmful organisms in rice paddy fields.
  • the behavior with regard to the environment is also improved since EHL, as solvent, can be completely decomposed biologically to CO2 and water.
  • the solvent film formed at the beginning distributes the active substance evenly in the rice paddy field but subsequently disintegrates into thousands of small droplets, with the result that there is no longer the danger of oxygen exchange between air and water being prevented by the surface of the water being completely covered.
  • WO-A-91/14366 discloses EHL as an active substance which regulates the growth of grapes.
  • EHL is here charged directly to water in a fixed dosage without additional additives and is used as leaf spray solution in an early growth stage of the grapes.
  • the use of EHL as solvent is neither revealed nor suggested in this document.
  • EHL is disclosed as suspending agent for insoluble agrochemical active substances in nonaqueous suspension concentrates.
  • EHL is disclosed as an agent for preventing crystallization of pesticidal compositions, particularly compositions comprising azole fungicides, during application. None of these documents suggests the particular advantages of using EHL containing plant protection compositions for application in paddy rice crops.
  • a plant protection composition comprising a) 2-ethylhexal lactate, b) one or more agrochemical active substances dissolved therein, and c) optionally one or more formulation aids, for the control of harmful organisms in paddy rice crops.
  • a plant protection composition comprising a) 2-ethyl lactate, b) one or more agrochemical active substances dissolved therein, and c) optionally one or more formulation aids, is applied in or on the water of paddy rice fields.
  • Plant protection composition within the meaning of the invention is the formulation of agrochemical active substances, i.e. either an active substance concentrate, comprising EHL and one or more agrochemical active substance, or such an active substance concentrate and formulation aids.
  • formulation aids are additives and aids conventional in formulation technology which are typical of the most varied formulation types, such as emulsifiers (e.g., for the formulation types emulsifiable concentrate (EC) and microemulsion (ME)), wetting agents (e.g., for the formulation type ready-to-use liquid formulation (AL)), inert materials (e.g., for the formulation types granule (GR) and emulsifiable granule (EG)), dispersing agents (e.g., for the formulation types oil-in-water emulsion (EW) and suspoemulsion (SE)) and surfactants (e.g., for the formulation type soluble concentrate (SL)), and also additional solvents, thickeners, flow
  • formulation aids which may be necessary, such as emulsifiers, wetting agents, inert materials, dispersing agents, surfactants, solvents and additional additives, are known to a person skilled in the art and are described, for example, in: Watkins, "Handbook of Insecticide Dust Diluents and Carriers", 2nd Ed., Darland Books, Caldwell, N.J.; H.v. Olphen, "Introduction to Clay Colloid Chemistry", 2nd Ed., J. Wiley & Sons, N.Y.; C.
  • the solvent EHL 2-ethylhexyl lactate
  • lactic acid preferably L-(+)-lactic acid
  • lactic acid preferably L-(+)-lactic acid
  • Additional terms for EHL are: 2-ethylhexyl S- lactate; 2-ethylhexyl L-lactic acid, L-lactic acid 2-ethylhexyl ester; CAS-No. 186817- 80-1; EC-No. 228-503-2.
  • EHL exhibits good solvent properties, it can be completely decomposed biologically to CO2 and water in the environment and does not have any ozone-reducing action.
  • EHL with LD50 values (rats, oral) in concentrations of over 2000 mg per kg of body weight, is toxicologically harmless.
  • the ester bond in EHL is quickly degraded and EHL is decomposed by enzymatic hydrolysis to CO2 and water. Because of these convenient properties, EHL is accordingly frequently used in metal working to degrease materials and the printing industry as additive in colorants and inks.
  • EHL in plant protection compositions, as well as for supporting the activity of agrochemical active substances against harmful organisms, whereby also undesired side effects, such as, e.g., plant damage (phytotoxicity) when insecticides are used, can occur to a reduced extent.
  • Additional advantages by the use of EHL are the possibility of obtaining plant protection compositions with a favourable flash point, whereby restrictions with regard to transportation and storage which may be necessary can be reduced or completely abolished.
  • the storage stability of plant protection compositions can also be improved by the use of EHL.
  • EHL can keep agrochemical active substances in solution at low temperatures and consequently ensures the stability toward freezing of plant protection compositions.
  • EHL may already be advantageous in an active substance concentrate, e.g. by increasing the stability of agrochemical active substances before the preparation of plant protection compositions by wetting the active substance surface.
  • EHL may however also contribute to an improved homogeneity of the active substance in the preparation of the plant protection composition.
  • agrochemical active substances comprises all substances which are used in the fields of agriculture, horticulture, forestry and veterinary medicine, as well as in the domestic sphere and in stock-keeping, such as herbicides, insecticides, fungicides, bactericides, nematicides, algicides, molluscicides, virucides, resistance- inducing substances, substances active as repellants and substances active as growth regulators, compositions with and without biological organisms, and also fertilizers which supply trace elements and nutrients.
  • Herbicidally, insecticidally, fungicidally, bactericidally and virucidally active substances and substances active as growth regulators are preferred.
  • Herbicidal, insecticidal and fungicidal active substances are particularly preferred.
  • herbicidal active substances aclonifen, amidosulfuron, anilofos, asulam, benfuresate, byspiribac-sodium, bromoxynil, chlotoluron, cyclanilide, desmedipham, diclofop-methyl, diflufenican, diuron, ethephon, ethofumesate, ethoxysulfuron, fenoxaprop-P-ethyl, fentrazamide, flucarbazone-sodium, flufenacet, flurtamone, foramsulfuron, glufosinate-ammonium, glyphosate, iodosulfuron, ioxynil, isoproturon, isoxaflutole, linuron, mefenacet, mesosulfuron-methyl, metamitron, metosulam, metribuzin, ox
  • insecticidal active substances acetamiprid, acrinathrin, aldicarb, amitraz, azinphos-methyl, beta-cyfluthrin, carbaryl, clothianidin, cyfluthrin, cypermethrin, deltamethrin, endosulfan, ethiprole, ethoprophos, fenamiphos, fenthion, fipronil, imidacloprid, methamidophos, methiocarb, niclosamide, oxydemeton-methyl, permethrin, phosalone, prothiofos, silafluofen, spirodiclofen, spiromesifen, thiacloprid, thiodicarb, tralomethrin, triazophos, thrichlorfon and triflumuron.
  • fungicidal active substances bitertanol, bromuconazole, carbendazim, carpropamid, cyproconazole, edifenphos, fenamidone, fenhexamid, fentin, fluoxastrobin, fluquinconazole, fosetyl-aluminum, iprodione, iprovalicarb, pencycuron, prochloraz, propamocarb HCI, propineb, prothioconazole, pyrimethanil, spiroxamine, tebuconazole, tolylfluanid-dichlofluanid, triadimefon, triadimenol, trifloxystrobin and triticonazole.
  • herbicidal and insecticidal active substances are herbicidal and insecticidal active substances. More preferred are insecticidal active substances, in particular ethiprole and fipronil.
  • concentrations of the abovementioned active substances in the active substance concentrate vary within a wide range and are dependent on the respective end uses. Use is generally made of concentrations which are known to a person skilled in the art as conventional for active substance concentrates and for their respective end uses. Preference is given to concentrations of 0.1% by weight to 95% by weight, particularly preferably of 0.2% by weight to 85% by weight.
  • compounds from the group consisting of polydimethylsiloxanes which are supposed to prevent foam formation (so-called "antifoam agents"), such as Break Thru® (Goldschmidt, Essen, GER), Dow Corning® (Dow Chemicals, Wiesbaden, GER) and Silwet® (Osi Specialities/Akzo Nobel, Frankfurt, GER), are included as additional component of the plant protection composition according to the invention.
  • foam agents such as Break Thru® (Goldschmidt, Essen, GER), Dow Corning® (Dow Chemicals, Wiesbaden, GER) and Silwet® (Osi Specialities/Akzo Nobel, Frankfurt, GER).
  • the polydimethylsiloxanes inter alia, improve the distribution behavior on the surface of the water.
  • concentration of polydimethylsiloxanes varies within a wide range and is dependent on the desired distribution effect of the plant protection composition. Generally, use is made of concentrations which are known to a person skilled in the art as conventional for the distribution effect desired each time. Preference is given to concentrations of 0.5% by weight to 30% by weight, particularly preferably of 3% by weight to 10% by weight.
  • Polydimethylsiloxanes are prefereably used in liquid formulations, particularly of the AL type (as explained below).
  • additional substances can be used in formulations according to the invention, according to the chemical nature of the agrochemical active substances.
  • agrochemical active substances such as butylated hydroxytoluene (BHT), citric acid or acetic acid, the selection and concentration of which may vary within a wide range and are dependent on the stability of the agrochemical active substance.
  • BHT butylated hydroxytoluene
  • concentrations which are known to a person skilled in the art as conventional for the agrochemical active substance to be dissolved each time. Preference is given to concentrations of 0.01% by weight to 1 % by weight, particularly preferably of 0.1 % by weight to 0.2% by weight.
  • solvents from the group consisting of nonpolar or polar and aprotic or protic solvents such as benzyl alcohol, dimethylsulfoxide (DMSO), C12-
  • N-octylpyrrolidone NOP
  • DMAc dimethylacetamide
  • concentrations which are known to a person skilled in the art as conventional for the agrochemical active substance to be dissolved each time. Preference is given to concentrations of 50% by weight to 95% by weight, particularly preferably of 75% by weight to 85% by weight.
  • formulation types are (use each time of the GCPF formulation code with abbreviation and description): AE Aerosol dispenser; AL Any other liquid; CG Encapsulated granule; CL Contact liquid or gel; CS Capsule suspension; DC Dispersible concentrate; DP Dustable powder; DT Tablet for direct application; EC Emulsifiable concentrate; ED Electrochargeable liquid; EG Emulsifiable Granule; EO Emulsion, water in oil; EW Emulsion, oil in water; FG Fine granule; FS Flowable concentrate for seed treatment; GG Macrogranule; GL Emulsifiable gel; GP Flo-dust; GR Granule; GW Water soluble gel; ME Micro-emulsion; MG Microgranule; OF Oil miscible flowable concentrate/oil miscible suspension; OL Oil miscible liquid; OP Oil dispersible powder; PC Gel or paste concentrate; SE Suspo-emulsion; SG Water soluble granule;
  • liquid formulation types and solid formulation types which can be obtained via an active substance concentrate.
  • formulation types EC GCPF formulation code for emulsifiable concentrate
  • GR GCPF formulation code for granule
  • EW GCPF formulation code for oil-in-water emulsion
  • ME GCPF formulation code for microemulsion
  • EG GCPF formulation code for emulsifiable granule
  • SE GCPF formulation code for suspoemulsion
  • SL GCPF formulation code for soluble concentrate
  • CS GCPF formulation code for capsule suspension
  • AL GCPF formulation code for ready-to-use liquid formulation.
  • Special preference is given to liquid formulations in particular to ready-to-use liquid formulations (formulation type AL).
  • concentration of the active substance concentrate comprising EHL and one or more agrochemically active substances, in the respective formulation type varies within a wide range and is dependent on the corresponding type of the formulation. Generally, use is made of concentrations which are known to a person skilled in the art as conventional for the respective formulation type. Preference is given to concentrations of 2% by weight to 95% by weight, particularly preferably of 10% by weight to 90% by weight.
  • the invention also includes the preparation of an active substance concentrate, comprising EHL and one or more agrochemically active substances, and the preparation of plant protection compositions from the active substance concentrate.
  • an active substance concentrate comprising EHL and one or more agrochemically active substances
  • plant protection compositions from the active substance concentrate.
  • An active substance concentrate according to the invention is a true solution, i.e. the agrochemical active substances of this liquid concentrate are present in dissolved form at ambient temperature (20°C).
  • the respective amounts of the plant protection compositions of various formulation types according to the invention expended per unit area and/or test subject for the control of harmful organisms vary very greatly.
  • the application media known to a person skilled in the art as conventional for the respective field of use are used in the conventional amounts, such as, for example, from several hundred liters of water per hectare with standard spray processes via a few liters of oil per hectare with the ultralow volume aircraft application down to a few milliliters of a physiological solution with injection processes.
  • concentrations of the plant protection compositions according to the invention in the corresponding application media consequently vary within a wide range and are dependent on the respective fields of use.
  • concentrations are used which are known to a person skilled in the art as conventional for the respective fields of use. Preference is given to concentrations of 0.01% by weight to 99% by weight, particularly preferably of 0.1% by weight to 90% by weight.
  • the active substance concentrate according to the invention or the plant protection compositions of the varied formulation types prepared therefrom directly with additional plant protection compositions/formulations which in turn can also comprise agrochemical active substances and additional formulation aids.
  • additional plant protection compositions/formulations which in turn can also comprise agrochemical active substances and additional formulation aids.
  • the processes used in this connection, and also the formulation aids which may be necessary and plant protection compositions/formulations are generally familiar to a person skilled in the art and are described, for example, in the literature cited with the various formulation types (see above), and in: Watkins, "Handbook of Insecticide Dust Diluents and Carriers", 2nd Ed., Darland Books, Caldwell, New Jersey; H.v. Olphen, "Introduction to Clay Colloid Chemistry", 2nd Ed., J. Wiley & Sons, New York; C. Marsden,
  • the abovementioned agrochemical active substances and/or formulation types are preferred as additional mixing partners.
  • the mixing ratios of the abovementioned mixing partners vary within a wide range and are dependent on the respective end uses. Generally, use is made of mixing ratios which are known to a person skilled in the art as conventional for the respective end uses. These are mixing ratios of 1-10 000 (plant protection composition/formulation comprising active substance concentrate):1-10 000 (plant protection composition/formulation not comprising active substance concentrate), preferably 1-1000:1-1000, particularly preferably 1- 100:1-100.
  • a preferred embodiment of the invention is the use of a plant protection composition, which is a liquid formulation, preferably an AL formulation, which comprises EHL, optionally one or more solvents from the group consisting of nonpolar or polar aprotic or protic solvents, one or more antifoam agents from the group consisting of polydimethylsiloxanes, one or more agrochemical active substances and optionally substances for the stabilization thereof.
  • a plant protection composition which is a liquid formulation, preferably an AL formulation, which comprises EHL, optionally one or more solvents from the group consisting of nonpolar or polar aprotic or protic solvents, one or more antifoam agents from the group consisting of polydimethylsiloxanes, one or more agrochemical active substances and optionally substances for the stabilization thereof.
  • a plant protection composition which is a liquid formulation, preferably an AL formulation, which comprises EHL, optionally one or more solvents from the group consisting of nonpolar or polar aprotic or protic solvents,
  • the plant protection compositions used according to the invention are partly known and partly new.
  • a plant protection composition comprising a) 2-ethylhexyl lactate, b) dissolved therein one or more agrochemical active substances from the group consisting of 1) aclonifen, amidosulfuron, anilofos, asulam, benfuresate, byspiribac- sodium, bromoxynil, chlotoluron, cyclanilide, desmedipham, diclofop- methyl, diflufenican, diuron, ethephon, ethofumesate, ethoxysulfuron, fenoxaprop-P-ethyl, fentrazamide, flucarbazone-sodium, flufenacet, flurtamone, foramsulfuron, glufosinate-ammonium, glyphosate, iodosulfuron, ioxynil, isoproturon, isoxa
  • agrochemical active substances from the group consisting
  • compositions comprising one or more agrochemical substances from groups 1) and 2), more preferred from group 2), in particular fipronil and/or ethiprole.
  • compositions comprising as a component c) one or more polydimethyl siloxanes (as described above).
  • compositions comprising substances for the stabilization of the agrochemical active substances, in particular butylated hydroxytoluene, citric acid or acetic acid.
  • compositions comprising additional nonpolar, polar aproctic or protic solvents, in particular benzylaclcohol, DMSO, C- ⁇ 2 - 5 alkyl benzoates, diisopropyl adipate, N-octylpyrrolidone, and dimethylacetamide.
  • compositions comprising two or more of the additional formulation aids.
  • an active substance concentrate comprising (a) 2-ethylhexyl lactate and (b) one or more agrochemical active compounds from groups 1 ), 2) and/or 3).
  • a water-soluble container comprising a composition as described above.
  • harmful organisms comprises all forms of organisms which cause economic damage and/or damage to the health in the relevant field of use. Preference is given to harmful plant and animal organisms and to organisms which cause diseases; particular preference is given to terrestrial and aquatic weeds, including grass weeds, algae, mosses, arthropods, including insects and arachnids (such as mites), helminths, including nematodes, rodents, fungi, bacteria and viruses.
  • harmful organisms means harmful arthropods, including insects and arachnids, and helminths, including nemathodes.
  • Examples of harmful organisms in paddy rice crops are (use each time of the taxonomic and English term): Acanthospermum hispidum (star burr); Acidovorax avenae subsp. avenae (bacterial leaf blight); Acrida cinerea; Acrida exaltata; Aeneolamia contigua (spotted spittlebug of pastures); Aeneolamia flavilatera (yellow- sided froghopper); Aeneolamia varia (froghopper); Aeschynomene indica (Northern jointvetch); Ageratum conyzoides (goat weed); Agromyz-a oryzae (rice leaf miner); Agrotis segetum (turnip moth); Ahasverus advena (foreign grain beetle);
  • Aleurocybotus indicus Aleuroglyphus ovatus (brownlegged grain mite); Alphitobius diaperinus (lesser mealworm); Alternanthera philoxeroides (alligator weed); Altemanthera sessilis (sessile joyweed); Alternaria alternata f.sp.
  • lycopersici (alternaria leaf spot); Alternaria padwickii (stackburn disease); Amaranthus retroflexus (redroot); Amaranthus spinosus (spiny amaranthus); Anadastus filiformis; Anadastus scutellatus; Anagallis arvensis (scarlet pimpernel); Anaphothrips obscurus (grass thrips); Anaphothrips sudanensis; Anisopteromalus calandrae; Anomala antiqua (groundnut chafer); Anomala dimidiata; Anomala pallida; Aphelenchoides besseyi (rice leaf nematode); Arthrinium phaeospermum; Aspavia armigera; Aspergillus parasiticus; Aspergillus terreus; Aspergillus ustus; Atherigona oryzae (shoot fly); Atractomorpha crenulata; Atta
  • Coptotermes (termites); Corchorus aestuans; Corcyra cephalonica (rice meal moth); Corticium rolfsii (sclerotium rot); Crassocephalum crepidioides; Criconemella (ring nematode); Cricotopus bicinctus; Cricotopus sylvestris; Cricotopus trifasciatus; Cryptolestes ferrugineus (rusty grain beetle); Cryptolestes pusillus (flat grain beetle); Culicoides furens; Curvularia (black kernel); Cymoninus notabilis; Cynodon dactylon (Bermuda grass); Cyperus brevifolius (sedge); Cyperus compressus (annual sedge); Cyperus difformis (small-flowered nutsedge); Cyperus esculentus (yellow nutsedge); Cyperus iria (grasshopper's cyperus); Cyperus rotund
  • Neoconocephalus maxillosus (longhorned grasshopper); Nephotettix; Nephotettix cincticeps (rice green leafhopper); Nephotettix malayanus; Nephotettix nigropictus (rice green leafhopper); Nephotettix parvus; Nephotettix virescens (green paddy leafhopper); Nezara viridula (green stink bug); Nilaparvata bakeri; Nilaparvata lugens (brown-backed rice plant hopper; BPH); Nilaparvata maeander; Nisaga simplex;
  • Nisia nervosa grey planthopper; Nomadacris septemfasciata (red locust); Oebalus insularis (island stinkbug); Oebalus ornatus (rice stink bug); Oebalus poecilus; Oebalus pugnax (rice stinkbug); Oebalus ypsiloinoides (paddy bug); Oebalus ypsilongriseus; Oligonychus oryzae; Omalonyx felina (slug); Orphulella punctata; Orseolia oryzae (rice stem gall midge); Orseolia oryzivora (African rice gall midge); Oryza longistaminata (perennial wild rice); Oryza rufipogon (red rice); Oiyzaephilus surinamensis (saw toothed grain beetle); Oryzophagus oryzae; Oulema oryzae (rice leaf be
  • zizaniae bacterial leaf streak
  • Pseudomonas syringae Pyralis farinalis (meal moth); Pythium arrhenomanes (cereals root rot); Pythium graminicola (gramineae seedling blight); Pythium irregulare (black: beet vascular necrosis); Pythium spinosum (root rot: ornamentals); Pythium ultimum; Rattus argentiventer (rice field rat); Rattus exulans (bush rat); Rattus norvegicus (brown rat); Rattus rattus (black rat); Rattus rattus diardii (Malaysian house rat); Rattus rattus mindanensis (common Philippine field rat); Recilia dorsalis (zigzag leafhopper); Rhizoctonia; Rhizoctonia oryzae (sheath spot); Rhizoglyphus robini; Rhopalosiphum
  • Sitophilus zeamais greater grain weevil
  • Sitotroga cerealella grain moth
  • Sogata wallicci Sogatella furcifera (white-backed planthopper; WBPH); Sogatella vibix (white-backed planthopper);
  • Sorghum halepense Johnson grass
  • Sphaerulina oryzina no brown leaf spot
  • Sphenoclea zeylanica wedgewort
  • Spodoptera cilium caterpillar, lawn
  • Spodoptera exempta black armyworm
  • Spodoptera exigua beet armyworm
  • Spodoptera frugiperda fall armyworm
  • Spodoptera littoralis leafworm, Egyptian cotton
  • Spodoptera litura taro caterpillar
  • Spodoptera mauritia piaddy swarming caterpillar
  • Spodoptera mauritia acronyctoides armyworm
  • Spodoptera ornithogalli yellow striped armyworm
  • oryzae rice leaf blight
  • Xanthomonas oryzae pv. oryzicola bacterial leaf streak of rice
  • Xiphinema (dagger nematode); Xiphinema americanum (dagger nematode); Xiphinema ifacolum (dagger nematode); Zeros orientalis; Zulia entreriana.
  • An additional aspect is processes for applying plant protection composition according to the invention of liquid AL formulation type.
  • the suitable standard processes for this are known to a person skilled in the art.
  • it is advantageous to apply the plant protection composition by use of water-soluble bottles, sheet bags or other containers on the edge of rice paddy fields or to apply it on the surface of the water of the rice paddy fields, either dropwise from special shake bottles or by spraying with knapsack sprayers or similar devices.
  • the active substance concentrate was prepared and was subsequently mixed with solvents and wetting agents.
  • the active substance concentrate was prepared and was subsequently mixed with solvents and wetting agents.
  • the active substance concentrate was prepared and was subsequently mixed with solvents and wetting agents.
  • the active substance concentrate was prepared and was subsequently mixed with solvents and wetting agents.
  • the active substance concentrate was prepared and was subsequently mixed with solvents and wetting agents.
  • the active substance concentrate was prepared and was subsequently adsorbed on an inert material.
  • the active substance concentrate was prepared and was subsequently mixed with emulsifiers.
  • the active substance concentrate was prepared and was subsequently emulsified in water. The concentrated emulsion was then stabilized.
  • the active substance concentrate was prepared and was subsequently emulsified in water to give a microemulsion.
  • the active substance concentrate was prepared. Subsequently, an emulsion of the active substance concentrate was sprayed over inert materials in a granulation apparatus.
  • the active substance concentrate was prepared.
  • An emulsion of the active substance concentrate was pulverized in an aqueous composition with a second agrochemical active substance, the solid particles of which were subsequently dispersed.
  • the active substance concentrate was prepared and was subsequently mixed with solvents and surfactants.
  • Luviskol K90 Luviskol K90; BASF, Ludwigshafen, GER), citric acid (various suppliers), Rhodorsil 416® (antifoam; Rhodia, Frankfurt, GER), Rhodorsil 426R® (antifoam; Rhodia, Frankfurt, GER), anisole (e.g. Rhodiasolv MPE®, Rhodia, Frankfurt, GER), hexylene glycol (Sigma-Aldrich, Tauf Wegn, GER), Soprophor BSU® (tristyrylphenol + 16 EO; Rhodia, Frankfurt, GER), Solvesso 200® (aromatic hydrocarbon fluid; Exxon, Cologne, GER), tributyl phosphate (e.g.
  • the formulations AL1 and AL2 were tested.
  • the rice paddy field harmful organism controlled was the rice cicada Nilaparvata lugens (brown-backed rice plant hopper; BPH).
  • the application was carried out by pipetting a fixed amount onto the surface of the water.
  • the dosages tested were equivalent to 3, 4 and 5 l/ha.
  • the following individual results are based on 2 repetitions, consisting each time of 4 pots with rice plants.
  • the plant damage was determined 7 and 13 days after application (DAA).
  • DAA The plant damage was determined 7 and 13 days after application.
  • the growth and phenotype of the rice plants were rated in % plant damage (high % values in this connection characterize serious plant damage).
  • the formulation AL1 (see preparation example 1 for the preparation and composition) was tested in comparison with a standard EC formulation: AL1 with 3% by weight of ethiprole in the dosages 50 (dose 1), 83 (dose 2), 1 17 (dose 3) and 150 (dose 4) g/ha and standard EC with 10% by weight of ethiprole in the dosages 15 (dose 1 ), 25 (dose 2), 35 (dose 3) and 45 (dose 4) g/ha, doses 1 to 4 each time comprising identical amounts of the agrochemical active substance ethiprole.
  • the field trial locations were JiangSu-RF, HuN-IPP and Xiushan PPS-CQ in China.
  • the formulations comprising active substance were applied in the rice paddy fields by hand spraying with a knapsack sprayer.
  • Test plot layout was according to the 2 RCB method with a plot size of 30 m each time. The following individual results per location are based on 3 repetitions each time.
  • the rice paddy field harmful, organisms controlled were the rice cicadas Nilaparvata lugens (brown-backed rice plant hopper; BPH) and Sogatella furcifera (white-backed plant hopper; WBPH), which occurred at the infestation level naturally present at the location. In addition, the secondary action on useful spiders was ascertained.
  • the activity against the two harmful organisms of the agrochemical active substance ethiprole in the AL1 formulation was, in comparison with the standard EC formulation, clearly increased on average.
  • the secondary action on useful spiders by the use of the AL1 formulation was, in comparison with the standard EC formulation, not increased.
  • favorable flash points of the formulation types such as, for example, 95°C for AL1 and 96°C for AL3, may make possible simplified storage of the plant protection compositions, since expenditures on special safety measures may disappear or be reduced.

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Dentistry (AREA)
  • Plant Pathology (AREA)
  • Engineering & Computer Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Agronomy & Crop Science (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Toxicology (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

L'invention concerne des compositions de protection des plantes et leur utilisation. Elle porte sur l'utilisation d'une composition de protection des plantes contenant : a) 2-ethylehxyl lactate, b) une ou plusieurs substances actives agrochimiques dissoutes dedans, et c) facultativement un ou plusieurs adjuvants de formulation, pour le contrôle d'organismes nocifs dans des cultures de rizières. Elle se rapporte aussi à des compositions de protection des plantes contenant 2-ethylhexyl lactate et une substance active agrochimique.
PCT/EP2005/000959 2004-02-06 2005-02-01 Compositions de protection des plantes et utilisation associee WO2005074685A1 (fr)

Priority Applications (3)

Application Number Priority Date Filing Date Title
JP2006551780A JP2007520511A (ja) 2004-02-06 2005-02-01 植物保護組成物およびその使用
KR1020067017372A KR101196233B1 (ko) 2004-02-06 2005-02-01 식물 보호 조성물 및 그 용도
CN200580007199XA CN1929735B (zh) 2004-02-06 2005-02-01 植物保护组合物及其用途

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102004006107.6 2004-02-06
DE102004006107 2004-02-06

Publications (2)

Publication Number Publication Date
WO2005074685A1 true WO2005074685A1 (fr) 2005-08-18
WO2005074685A8 WO2005074685A8 (fr) 2005-10-27

Family

ID=34832558

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2005/000959 WO2005074685A1 (fr) 2004-02-06 2005-02-01 Compositions de protection des plantes et utilisation associee

Country Status (5)

Country Link
JP (1) JP2007520511A (fr)
KR (1) KR101196233B1 (fr)
CN (1) CN1929735B (fr)
TW (1) TW200529745A (fr)
WO (1) WO2005074685A1 (fr)

Cited By (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1625791A1 (fr) * 2003-05-19 2006-02-15 Nippon Soda Co., Ltd. Composition insecticide
EP1787516A1 (fr) * 2005-11-09 2007-05-23 Agrichem B.V. Composition inhibitrice de germination
WO2008001783A1 (fr) * 2006-06-28 2008-01-03 Nihon Nohyaku Co., Ltd. Agent de régulation de bryophyte et ses applications
JP2009507799A (ja) * 2005-09-09 2009-02-26 バイエル・クロツプサイエンス・アクチエンゲゼルシヤフト 農薬の効果を改善するための乳酸エステルの使用
JP2009530349A (ja) * 2006-03-24 2009-08-27 ビーエーエスエフ ソシエタス・ヨーロピア 農薬製剤
US20100285960A1 (en) * 2008-01-04 2010-11-11 Endura S.P.A. method for modulating the release rate of microencapsulated actives
WO2011012493A2 (fr) 2009-07-28 2011-02-03 Basf Se Compositions de suspo-émulsions pesticides
WO2011098419A2 (fr) 2010-02-12 2011-08-18 Basf Se Composition anhydre comprenant un pesticide en solution et un pesticide en suspension, un lactate d'alkyle et un alcool
EP2387886A1 (fr) * 2010-05-18 2011-11-23 Cognis IP Management GmbH Compositions de biocide comportant du lactate isoamylique
JP2012214520A (ja) * 2006-03-29 2012-11-08 Bayer Cropscience Ag ジフルフェニカンおよびフルルタモンを含む分散液としての除草剤組成物
CN103073634A (zh) * 2011-10-25 2013-05-01 天津科技大学 一种抗除草剂莎稗磷的特异性抗体
WO2013083372A1 (fr) * 2011-12-05 2013-06-13 Basf Se Concentré émulsionnable comprenant un pesticide, du diméthylsulfoxyde, de l'alcool benzylique et un lactate d'alkyle
WO2013083405A1 (fr) * 2011-12-05 2013-06-13 Basf Se Concentré émulsionnable comprenant un pesticide, du diméthylsulfoxyde, de l'alcool benzylique, un lactate d'alkyle et un diester
CN103190411A (zh) * 2013-04-03 2013-07-10 北京颖泰嘉和生物科技有限公司 一种除草剂组合物及其制剂和应用
WO2014154447A1 (fr) * 2013-03-27 2014-10-02 Basf Se Concentré émulsionnable comprenant un pesticide, un lactate d'alkyle et un amide gras
US20140357489A1 (en) * 2011-12-05 2014-12-04 Basf Se Emulsifiable concentrate comprising pesticide, dimethyl sulfoxide, benzyl alcohol, alkyl lactate
WO2015007573A1 (fr) * 2013-07-18 2015-01-22 Basf Se Concentré émulsionnable comprenant un pesticide, un lactate d'alkyle, un amide gras et de l'acétophénone
CN104316688A (zh) * 2014-10-16 2015-01-28 江南大学 一种检测水稻细菌性条斑病菌的双抗体夹心酶联免疫法
US20150150254A1 (en) * 2011-05-21 2015-06-04 Ensystex Inc. Control of bed bugs
US20170280710A1 (en) * 2014-09-02 2017-10-05 Basf Se Aqueous pesticide microemulsion
CN118064455A (zh) * 2024-04-22 2024-05-24 中国热带农业科学院三亚研究院 一种油莎豆CeWRI3基因、表达载体及其在植物油脂调控方面的应用

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1878345A1 (fr) * 2006-07-13 2008-01-16 Sygenta Participations AG. Composition herbicide
EP2067403A1 (fr) * 2007-12-03 2009-06-10 Bayer CropScience AG Mélanges de composés pesticides contenant d'ethiprole et des carbamates spécifiques
JP5590484B2 (ja) * 2009-05-25 2014-09-17 住友化学株式会社 殺虫組成物及び害虫防除方法
CN102210314B (zh) * 2010-04-02 2013-03-13 海利尔药业集团股份有限公司 一种含有杀螺胺和甲萘威的杀软体动物组合物
PT2809154T (pt) * 2012-01-30 2017-11-15 Basf Se Adjuvante com poliorganossiloxano e solvente orgânico para preparar uma mistura de tanque larvicida
JP6102912B2 (ja) * 2012-02-29 2017-03-29 住友化学株式会社 サスポエマルジョン
KR101459548B1 (ko) * 2012-10-11 2014-11-12 대한민국 글로포시네이트 암모니움을 포함하는 흰잎마름병 방제용 조성물
CN102899280B (zh) * 2012-11-14 2013-08-21 中国热带农业科学院热带生物技术研究所 枯草芽孢杆菌has及其在防治甘蔗黑穗病中的应用
CN103031309B (zh) * 2012-12-19 2014-05-14 中国热带农业科学院热带生物技术研究所 一种抗菌蛋白has1编码基因的克隆、表达及其应用
CN108601342A (zh) * 2016-02-02 2018-09-28 赢创德固赛有限公司 在固体水溶性载体上具有表面活性物质的粉末状配制物、其生产方法和其用途
CN106332899A (zh) * 2016-08-25 2017-01-18 安徽美兰农业发展股份有限公司 一种氟唑磺隆和异丙隆复配悬浮剂及其制备方法
JP6871591B2 (ja) * 2016-10-11 2021-05-12 フマキラー株式会社 除草剤
CN109717031A (zh) * 2018-12-24 2019-05-07 淮安市植保植检站 稻田丙森锌结合除草剂混施植保方法
CN112913605B (zh) * 2021-01-22 2022-04-19 阳江职业技术学院 一种以禾虫增殖为主的虫稻共生综合种养方法
CN114480141B (zh) * 2022-01-19 2023-08-25 青岛中尚奇生物科技有限公司 一株赤霉菌qjp2及其在除草中的应用
CN116530410A (zh) * 2023-05-22 2023-08-04 甘肃省农业科学院作物研究所 一种隐性单基因调控的光叶性状高光效油菜种质的创制方法
CN116904327B (zh) * 2023-09-13 2023-11-14 中国农业科学院草原研究所 一株能够防除长刺蒺藜草的互隔交链孢霉、菌剂及其应用

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1991014366A1 (fr) * 1990-03-20 1991-10-03 Union Oil Company Of California Regulation de la croissance des plantes
WO2000018227A1 (fr) * 1998-09-25 2000-04-06 American Cyanamid Company Suspension concentree non aqueuse
WO2003075657A1 (fr) * 2002-03-14 2003-09-18 Makhteshim Chemical Works Ltd. Composition pesticide comprenant un ester de lactate comme inhibiteur de la croissance des cristaux

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003055115A (ja) * 2001-08-14 2003-02-26 Meiji Seika Kaisha Ltd 水稲用殺虫殺菌混合組成物

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1991014366A1 (fr) * 1990-03-20 1991-10-03 Union Oil Company Of California Regulation de la croissance des plantes
WO2000018227A1 (fr) * 1998-09-25 2000-04-06 American Cyanamid Company Suspension concentree non aqueuse
WO2003075657A1 (fr) * 2002-03-14 2003-09-18 Makhteshim Chemical Works Ltd. Composition pesticide comprenant un ester de lactate comme inhibiteur de la croissance des cristaux

Cited By (38)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1625791A1 (fr) * 2003-05-19 2006-02-15 Nippon Soda Co., Ltd. Composition insecticide
EP1625791A4 (fr) * 2003-05-19 2006-06-14 Nippon Soda Co Composition insecticide
JP2009507799A (ja) * 2005-09-09 2009-02-26 バイエル・クロツプサイエンス・アクチエンゲゼルシヤフト 農薬の効果を改善するための乳酸エステルの使用
EP1926369B1 (fr) 2005-09-09 2015-06-17 Bayer Intellectual Property GmbH Utilisation d'esters de lactate pour ameliorer l'action de produits phytosanitaires
EP1787516A1 (fr) * 2005-11-09 2007-05-23 Agrichem B.V. Composition inhibitrice de germination
JP2009530349A (ja) * 2006-03-24 2009-08-27 ビーエーエスエフ ソシエタス・ヨーロピア 農薬製剤
JP2012214520A (ja) * 2006-03-29 2012-11-08 Bayer Cropscience Ag ジフルフェニカンおよびフルルタモンを含む分散液としての除草剤組成物
WO2008001783A1 (fr) * 2006-06-28 2008-01-03 Nihon Nohyaku Co., Ltd. Agent de régulation de bryophyte et ses applications
US20100285960A1 (en) * 2008-01-04 2010-11-11 Endura S.P.A. method for modulating the release rate of microencapsulated actives
WO2011012493A3 (fr) * 2009-07-28 2011-10-13 Basf Se Compositions de suspo-émulsions pesticides
US8703649B2 (en) 2009-07-28 2014-04-22 Basf Se Pesticidal suspo-emulsion compositions
WO2011012493A2 (fr) 2009-07-28 2011-02-03 Basf Se Compositions de suspo-émulsions pesticides
EA020385B1 (ru) * 2009-07-28 2014-10-30 Басф Се Пестицидные суспоэмульсионные композиции
KR101869107B1 (ko) * 2010-02-12 2018-06-19 바스프 에스이 용해된 살충제 및 현탁된 살충제, 알킬 락테이트 및 알콜을 포함하는 무수 조성물
KR20130030250A (ko) * 2010-02-12 2013-03-26 바스프 에스이 용해된 살충제 및 현탁된 살충제, 알킬 락테이트 및 알콜을 포함하는 무수 조성물
WO2011098419A3 (fr) * 2010-02-12 2011-12-01 Basf Se Composition anhydre comprenant un pesticide en solution et un pesticide en suspension, un lactate d'alkyle et un alcool
EA021744B1 (ru) * 2010-02-12 2015-08-31 Басф Се Безводная композиция, включающая растворенный и суспендированный пестицид, алкиллактат и спирт
WO2011098419A2 (fr) 2010-02-12 2011-08-18 Basf Se Composition anhydre comprenant un pesticide en solution et un pesticide en suspension, un lactate d'alkyle et un alcool
WO2011144273A1 (fr) * 2010-05-18 2011-11-24 Cognis Ip Management Gmbh Compositions biocides comprenant le lactate d'isoamyle
EP2387886A1 (fr) * 2010-05-18 2011-11-23 Cognis IP Management GmbH Compositions de biocide comportant du lactate isoamylique
US20150150254A1 (en) * 2011-05-21 2015-06-04 Ensystex Inc. Control of bed bugs
US9763443B2 (en) * 2011-05-21 2017-09-19 Ensystex Inc. Control of bed bugs
CN103073634B (zh) * 2011-10-25 2014-07-02 天津科技大学 一种抗除草剂莎稗磷的特异性抗体
CN103073634A (zh) * 2011-10-25 2013-05-01 天津科技大学 一种抗除草剂莎稗磷的特异性抗体
US20140357489A1 (en) * 2011-12-05 2014-12-04 Basf Se Emulsifiable concentrate comprising pesticide, dimethyl sulfoxide, benzyl alcohol, alkyl lactate
CN103974615A (zh) * 2011-12-05 2014-08-06 巴斯夫欧洲公司 包含农药、二甲亚砜、苄醇、乳酸烷基酯和二酯的可乳化浓缩物
WO2013083405A1 (fr) * 2011-12-05 2013-06-13 Basf Se Concentré émulsionnable comprenant un pesticide, du diméthylsulfoxyde, de l'alcool benzylique, un lactate d'alkyle et un diester
WO2013083372A1 (fr) * 2011-12-05 2013-06-13 Basf Se Concentré émulsionnable comprenant un pesticide, du diméthylsulfoxyde, de l'alcool benzylique et un lactate d'alkyle
WO2014154447A1 (fr) * 2013-03-27 2014-10-02 Basf Se Concentré émulsionnable comprenant un pesticide, un lactate d'alkyle et un amide gras
EA030150B1 (ru) * 2013-03-27 2018-06-29 Басф Се Эмульгируемый концентрат, включающий пестицид, алкиллактат и жирный амид
CN105188363A (zh) * 2013-03-27 2015-12-23 巴斯夫欧洲公司 包含农药、乳酸烷基酯和脂肪酰胺的可乳化浓缩物
CN103190411A (zh) * 2013-04-03 2013-07-10 北京颖泰嘉和生物科技有限公司 一种除草剂组合物及其制剂和应用
WO2015007573A1 (fr) * 2013-07-18 2015-01-22 Basf Se Concentré émulsionnable comprenant un pesticide, un lactate d'alkyle, un amide gras et de l'acétophénone
US20170280710A1 (en) * 2014-09-02 2017-10-05 Basf Se Aqueous pesticide microemulsion
US10785973B2 (en) * 2014-09-02 2020-09-29 Basf Se Aqueous pesticide microemulsion
CN104316688B (zh) * 2014-10-16 2016-06-22 江南大学 一种检测水稻细菌性条斑病菌的双抗体夹心酶联免疫法
CN104316688A (zh) * 2014-10-16 2015-01-28 江南大学 一种检测水稻细菌性条斑病菌的双抗体夹心酶联免疫法
CN118064455A (zh) * 2024-04-22 2024-05-24 中国热带农业科学院三亚研究院 一种油莎豆CeWRI3基因、表达载体及其在植物油脂调控方面的应用

Also Published As

Publication number Publication date
KR20060133594A (ko) 2006-12-26
TW200529745A (en) 2005-09-16
CN1929735A (zh) 2007-03-14
JP2007520511A (ja) 2007-07-26
CN1929735B (zh) 2011-06-15
KR101196233B1 (ko) 2012-11-05
WO2005074685A8 (fr) 2005-10-27

Similar Documents

Publication Publication Date Title
KR101196233B1 (ko) 식물 보호 조성물 및 그 용도
JP6731351B2 (ja) 農園芸用有害生物防除剤組成物及びその使用方法
CN106035349A (zh) 农园艺用有害生物防除剂组合物及其使用方法
KR101607222B1 (ko) 알파-알콕시페닐아세트산 유도체 및 네오니코티노이드 화합물을 함유하는 유해생물 방제용 조성물
JP2018024669A (ja) 有害生物防除組成物及びその用途
WO2016002594A1 (fr) Composition pesticide et son application
KR101840487B1 (ko) 유해 생물 방제 조성물 및 그의 용도
JP6683804B2 (ja) 農園芸用組成物
KR101811898B1 (ko) 유해 생물 방제 조성물 및 그의 용도
JP2014224067A (ja) 農園芸用殺菌剤組成物及びその使用方法
BR112019001364B1 (pt) Método de controle de pragas de culturas agrícolas e composição herbicida
JP2016056197A (ja) 有害生物防除組成物及びその用途
JP5787545B2 (ja) 有害生物防除組成物
RU2513531C2 (ru) Композиции для борьбы с вредителями растений и способ борьбы с вредителями растений
JP2016199589A (ja) 有害生物の防除方法及び作物の栽培方法
JP2017122055A (ja) フルオロピリミジン化合物を含有する有害生物防除剤組成物及びその使用方法
JP2013032310A (ja) 有害生物防除組成物
JP2012106994A (ja) 有害生物防除組成物
JP2011246436A (ja) 有害生物防除組成物
JP2016088852A (ja) 有害生物防除剤組成物及びその使用方法
JP2017122066A (ja) 有害生物防除剤組成物及びその使用方法
KR101800907B1 (ko) 해충 방제용 조성물 및 방법
JP2018095579A (ja) 有害生物防除剤組成物およびその使用方法
JP2022030061A (ja) 親水性でかつ酸又は塩基による変性を特徴とする、ｉｐｍ用組成物
ES2355457B1 (es) Composición y método para controlar plagas, ácaros o ambos.

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BW BY BZ CA CH CN CO CR CU CZ DK DM DZ EC EE EG ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NA NI NO NZ OM PG PH PL PT RO RU SC SD SE SG SK SL SY TJ TM TN TR TT TZ UA UG US UZ VC VN YU ZA ZM ZW

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): GM KE LS MW MZ NA SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LT LU MC NL PL PT RO SE SI SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG

121 Ep: the epo has been informed by wipo that ep was designated in this application
CFP Corrected version of a pamphlet front page
CR1 Correction of entry in section i

Free format text: IN PCT GAZETTE 33/2005 UNDER (72,75) THE NAME OF "BUCKESPACH, RAINER" SHOULD READ "BUCKPESCH, RAINER"

WWE Wipo information: entry into national phase

Ref document number: 2006551780

Country of ref document: JP

WWE Wipo information: entry into national phase

Ref document number: 1020067017372

Country of ref document: KR

WWE Wipo information: entry into national phase

Ref document number: 200580007199.X

Country of ref document: CN

WWP Wipo information: published in national office

Ref document number: 1020067017372

Country of ref document: KR

122 Ep: pct application non-entry in european phase