EP4387452A1 - Method of controlling pests on tea plants - Google Patents
Method of controlling pests on tea plantsInfo
- Publication number
- EP4387452A1 EP4387452A1 EP22765559.4A EP22765559A EP4387452A1 EP 4387452 A1 EP4387452 A1 EP 4387452A1 EP 22765559 A EP22765559 A EP 22765559A EP 4387452 A1 EP4387452 A1 EP 4387452A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- active ingredient
- methyl
- per hectare
- spiropidion
- tea plant
- 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.)
- Pending
Links
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01P—BIOCIDAL, PEST REPELLANT, PEST ATTRACTANT OR PLANT GROWTH REGULATORY ACTIVITY OF CHEMICAL COMPOUNDS OR PREPARATIONS
- A01P7/00—Arthropodicides
- A01P7/04—Insecticides
-
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom
- A01N47/06—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom containing —O—CO—O— groups; Thio analogues thereof
Definitions
- the present invention generally relates to the use of certain compounds as a pesticidal active ingredient (Al) in methods of application to tea plants of the genus Camellia, and in particular Camellia sinensis.
- Tea is an important agricultural crop globally, in particular, in many parts of Eastern and Southern Asia, with many different varieties grown which may be vulnerable to attack by insect pests, often at great commercial cost.
- Compounds used in accordance with the present invention belong in the IRAC MoA Classification 23 relating to inhibitors of acetyl CoA Carboxylase (ACCase) inhibitors, eg, spiropidion, spirotetramat, spiromesifen and spirodiclofen.
- ACCase acetyl CoA Carboxylase
- Spiropidion (CAS no.: 1229023-00-0), which is known to be effective for the control of insect pests, including the so-called sucking insect pests (such as aphids, white flies, scales and mites) is described inter alia in WO 2010/066780, WO 2018/114648 and WO 2018/114649.
- Pesticidal formulations comprising spiropidion are described in WO 2020/208098.
- Spirotetramat (CAS no.: 203313-25-1) is described inter alia in WO 98/05638 and WO 2004/007448.
- Spiromesifen (CAS no.: 283594-90-1) and spirodiclofen (CAS no.: 148477-71-8) are described inter alia in EP 0 528 156.
- Other active ingredient compounds include spidoxamat (CAS no.: 907187-07-9), which is disclosed inter alia in WO 2006/089633.
- Achieving full plant coverage of the spray application of a pesticidal composition to tea plants is often hindered by the thick canopy of leaves of the plant.
- the canopy acts as a physical barrier limiting the effective application to the stem (trunk) or branches, which indeed may be the main habitat of an insect pest, such as a scale.
- this problem may at least be partially overcome by washing the active ingredient spray composition through the canopy and into the harder to access parts of the plant below the canopy.
- the downside of this being that generally large volumes (water dilution) of the pesticidal composition are required for full coverage of the plant crop. These volumes can be as much as 10,000 litre per hectare (L/ha) or more and so result in an undesirable high water usage requirement.
- the spray applicator eg, tea plantation worker
- a method of controlling an insect pest on a tea plant comprises a spray application to the leaf canopy of the tea plant with a pesticidal composition comprising an insecticidal active ingredient selected from spiropidion, spirotetramat, spirodiclofen, spiromesifen or spidoxamat.
- the spray application preferably (substantially) avoids the application of the pesticidal composition to the non-foliar parts (trunk, branches, stem, roots) of the tea plant.
- the method of the invention may be for curative or preventative control of insects pests.
- the active ingredient is spiropidion or spirotetramat. Most preferably, the active ingredient is spiropidion.
- the active ingredient such as spiropidion
- the liquid composition is a dilution of a concentrated active ingredient composition (such as a suspension concentrate (SC) formulation, eg SC100 or SC300) in water.
- SC suspension concentrate
- the liquid composition may comprise an adjuvant (built-in or tank mixed), preferably an adjuvant selected from a mineral oil, a vegetable oil or a trans-esterified vegetable oil.
- adjuvant classes which may be used in accordance with the present invention include a mineral oil, a vegetable oil, an esterified vegetable oil, a methylated vegetable oil or an alkyl ester phosphate-based adjuvant.
- Commercially-available adjuvant products which may be tank-mixed to yield a spray fomulation with the composition of the present invention include HASTENTM (Victorian Chemical Co. Pty. Ltd.
- the tea plant is Camellia sinensis.
- the pest is a scale insect.
- white peach scale Pseudaulacaspis pentagona
- Indian wax scale Ceroplastes ceriferus
- the pest is white peach scale.
- the spray application volume per hectare of the pesticidal composition is in the range of 100 to 5000 litres per hectare (L/ha), more preferably in the range of 200 to 4000 litres per hectare (L/ha), and still more preferably in the range of 500 to 1500 litres per hectare (L/ha).
- the application rate of the active ingredient, such as spiropidion, in accordance with the invention may be at a rate of 500 to 2000 grams per hectare, and preferably a rate of 1000 to 1500 grams per hectare.
- the application is as a single treatment prior to the onset of an infestation of an insect pest, eg, at 7 to 28 days before infestation (DBI) or more preferably, at at 14 to 21 days before infestation.
- controlling an insect pest in accordance with the invention, it is meant inter alia the killing of such insect pests, retarding the growth or reproduction of insects, reducing an insect population, and/or reducing damage to plants caused by insects.
- the active ingredient such as spriopidion
- a pesticidal composition as the sole pesticidal active ingredient.
- additional pesticidal active ingredients either in the same composition or separate compositions.
- This may include pesticidal active ingredient compositions comprising spiropidion (represented by “(I)”) and another active ingredient as follows:
- compositions comprising an adjuvant include (I) + compounds selected from the group of substances consisting of petroleum oils.
- compositions comprising an acaricide include (I) + 1 ,1-bis(4-chlorophenyl)-2-ethoxyethanol, (I) + 2,4-dichlorophenyl benzenesulfonate, (I) + 2-fluoro-N-methyl-N-1 -naphthylacetamide, (I) + 4- chlorophenyl phenyl sulfone, (I) + abamectin, (I) + acequinocyl, (I) + acetoprole, (I) + acrinathrin, (I) + aldicarb, (I) + aldoxycarb, (I) + alpha-cypermethrin, (I) + amidithion, (I) + amidoflumet, (I) + amidothioate, (I) + amiton, (I) + amiton hydrogen oxalate, (I) + amitraz, (I) + aramite,
- Compositions comprising an anthelmintic include (I) + abamectin, (I) + crufomate, (I) + doramectin, (I) + emamectin, (I) + emamectin benzoate, (I) + eprinomectin, (I) + ivermectin, (I) + milbemycin oxime, (I) + moxidectin, (I) + piperazine, (I) + selamectin, (I) + spinosad and (I) + thiophanate.
- Compositions comprising a biological control agent include (I) + Adoxophyes orana GV, (I) + Agrobacterium radiobacter, (I) + Amblyseius spp., (I) + Anagrapha falcifera NPV, (I) + Anagrus atomus, (I) + Aphelinus abdominalis, (I) + Aphidius colemani, (I) + Aphidoletes aphidimyza, (I) + Autographa californica NPV, (I) + Bacillus firmus, (I) + Bacillus sphaericus Neide, (I) + Bacillus thuringiensis Kirk, (I) + Bacillus thuringiensis subsp.
- lecontei NPV lecontei NPV
- Orius spp. Orius spp.
- Paecilomyces fumosoroseus Orius spp.
- I) + Phytoseiulus persimilis Orius spp.
- I) + Phytoseiulus persimilis SBA
- Spodoptera exigua multicapsid nuclear polyhedrosis virus (I) + Steinernema bibionis, (I) + Steinernema carpocapsae, (I) + Steinernema feltiae, (I) + Steinernema glaseri, (I) + Steinernema riobrave, (I) + Steinernema riobravis, (I) + Steinernema scapterisci, (I) + Steinernema spp., (I) + Trichogramma spp., (I) + Typhlodromus
- compositions comprising a soil sterilant include (I) + iodomethane and methyl bromide.
- Compositions comprising a chemosterilant include (I) + apholate, (I) + bisazir, (I) + busulfan, (I) + diflubenzuron, (I) + dimatif, (I) + hemel, (I) + hempa, (I) + metepa, (I) + methiotepa, (I) + methyl apholate, (I) + morzid, (I) + penfluron, (I) + tepa, (I) + thiohempa, (I) + thiotepa, (I) + tretamine and (I) + uredepa.
- compositions comprising an insect pheromone include (I) + (E)-dec-5-en-1-yl acetate with (E)- dec-5-en-1-ol, (I) + (E)-tridec-4-en-1-yl acetate, (I) + (E)-6-methylhept-2-en-4-ol, (I) + (E.Z)-tetradeca- 4, 10-dien-1 -yl acetate, (I) + (Z)-dodec-7-en-1-yl acetate, (I) + (Z)-hexadec-l 1-enal, (I) + (Z)-hexadec- 11-en-1-yl acetate, (I) + (Z)-hexadec-13-en-11-yn-1-yl acetate, (I) + (Z)-icos-13-en-10-one, (I) + (Z)- tetradec-7-en-1 -al, (I) +
- compositions comprising an insect repellent include (I) + 2-(octylthio)ethanol, (I) + butopyronoxyl, (I) + butoxy(polypropylene glycol), (I) + dibutyl adipate, (I) + dibutyl phthalate, (I) + dibutyl succinate, (I) + diethyltoluamide, (I) + dimethyl carbate, (I) + dimethyl phthalate, (I) + ethyl hexanediol, (I) + hexamide, (I) + methoquin-butyl, (I) + methylneodecanamide, (I) + oxamate and (I) + picaridin.
- compositions comprising an insecticide include (I) + 1-dichloro-1 -nitroethane, (I) + 1 , 1 -dichloro- 2,2-bis(4-ethylphenyl)ethane , (I) +, (I) + 1 ,2-dichloropropane, (I) + 1 ,2-dichloropropane with 1 ,3- dichloropropene, (I) + 1 -bromo-2-chloroethane, (I) + 2,2,2-trichloro-1-(3,4-dichlorophenyl)ethyl acetate, (I) + 2,2-dichlorovinyl 2-ethylsulfinylethyl methyl phosphate, (I) + 2-(1 ,3-dithiolan-2-yl)phenyl dimethylcarbamate, (I) + 2-(2-butoxyethoxy)ethyl thiocyanate, (I) + 2-(4,5-
- Compositions comprising a molluscicide include (I) + bis(tributyltin) oxide, (I) + bromoacetamide, (I) + calcium arsenate, (I) + cloethocarb, (I) + copper acetoarsenite, (I) + copper sulfate, (I) + fentin, (I) + ferric phosphate, (I) + metaldehyde, (I) + methiocarb, (I) + niclosamide, (I) + niclosamide-olamine, (I) + pentachlorophenol, (I) + sodium pentachlorophenoxide, (I) + tazimcarb, (I) + thiodicarb, (I) + tributyltin oxide, (I) + trifenmorph, (I) + trimethacarb, (I) + triphenyltin acetate and triphenyltin hydroxide, (I)
- compositions comprising a nematicide include (I) + AKD-3088, (I) + 1 ,2-dibromo-3- chloropropane, (I) + 1 ,2-dichloropropane, (I) + 1 ,2-dichloropropane with 1 ,3-dichloropropene, (I) + 1 ,3- dichloropropene, (I) + 3,4-dichlorotetrahydrothiophene 1 ,1-dioxide, (I) + 3-(4-chlorophenyl)-5- methylrhodanine, (I) + 5-methyl-6-thioxo-1 ,3,5-thiadiazinan-3-ylacetic acid, (I) + 6- isopentenylaminopurine, (I) + abamectin, (I) + acetoprole, (I) + alanycarb, (I) + aldicarb, (I) + aldoxycarb, (I)
- compositions comprising a synergist include (I) + 2-(2-butoxyethoxy)ethyl piperonylate, (I) + 5- (1 ,3-benzodioxol-5-yl)-3-hexylcyclohex-2-enone, (I) + farnesol with nerolidol, (I) + MB-599, (I) + MGK 264, (I) + piperonyl butoxide, (I) + piprotal, (I) + propyl isomer, (I) + S421 , (I) + sesamex, (I) + sesasmolin and (I) + sulfoxide.
- Compositions comprising an animal repellent include (I) + anthraquinone, (I) + chloralose, (I) + copper naphthenate, (I) + copper oxychloride, (I) + diazinon, (I) + dicyclopentadiene, (I) + guazatine, (I) + guazatine acetates, (I) + methiocarb, (I) + pyridin-4-amine, (I) + thiram, (I) + trimethacarb, (I) + zinc naphthenate and (I) + ziram.
- compositions include (I) + brofluthrinate, (I) + cycloxaprid, (I) + diflovidazine, (I) + flometoquin, (I) + fluhexafon, (I) + Guadipyr, (I) + Plutella xylostella Granulosis virus, (I) + Cydia pomonella Granulosis virus, (I) + harpin, (I) + imicyafos, (I) + Heliothis virescens Nucleopolyhedrovirus, (I) + Heliothis punctigera Nucleopolyhedrovirus, (I) + Helicoverpa armigera Nucleopolyhedrovirus, (I) + Helicoverpa zea Nucleopolyhedrovirus, (I) + Spodoptera frugiperda Nucleopolyhedrovirus, (I) + Plutella xylostella
- the weight ratio of spiropidion and another pesticidal active ingredient is generally between 1000:1 and 1 :100, more preferably between 500:1 and 1 :100, for example between 250:1 and 1 :66, between 125:1 and 1 :33, between 100:1 and 1 :25, between 66:1 and 1 :10, between 33:1 and 1 :5, between 8:1 and 1 :3, and between 2:1 to 1 :2.
- pesticidal compositions used in accordance with the invention are applied as a formulation containing other formulation components known to or used in the industry.
- formulations can be in various physical forms, e.g. in the form of dusting powders, gels, wettable powders, water-dispersible granules, water-dispersible tablets, effervescent pellets, emulsifiable concentrates, microemulsifiable concentrates, oil-in-water emulsions, oil-flowables, aqueous dispersions, oily dispersions, suspo-emulsions, capsule suspensions, emulsifiable granules, soluble liquids, water-soluble concentrates (with water or a water-miscible organic solvent as carrier), impregnated polymer films or in other forms known e.g.
- Such formulations are typically diluted prior to use.
- the dilutions can be made, for example, with water, liquid fertilisers, micronutrients, biological organisms, oil or solvents.
- the formulations may be prepared by mixing the active ingredient with the formulation adjuvants in order to obtain formulations in the form of finely divided solids, granules, solutions, dispersions or emulsions.
- the active ingredient can also be formulated with other adjuvants, such as finely divided solids, mineral oils, oils of vegetable or animal origin, modified oils of vegetable or animal origin, organic solvents, water, surface-active substances or combinations thereof.
- liquid carriers there may be used: water, toluene, xylene, petroleum ether, vegetable oils, acetone, methyl ethyl ketone, cyclohexanone, acid anhydrides, acetonitrile, acetophenone, amyl acetate, 2-butanone, butylene carbonate, chlorobenzene, cyclohexane, cyclohexanol, alkyl esters of acetic acid, diacetone alcohol, 1 ,2-dichloropropane, diethanolamine, p- diethylbenzene, diethylene glycol, diethylene glycol abietate, diethylene glycol butyl ether, diethylene glycol ethyl ether, diethylene glycol methyl ether, /V,/V-dimethylformamide, dimethyl sulfoxide, 1 ,4- dioxane,
- Suitable solid carriers are, for example, talc, titanium dioxide, pyrophyllite clay, silica, attapulgite clay, kieselguhr, limestone, calcium carbonate, bentonite, calcium montmorillonite, cottonseed husks, wheat flour, soybean flour, pumice, wood flour, ground walnut shells, lignin and similar substances.
- a large number of surface-active substances can advantageously be used in both solid and liquid formulations, especially in those formulations which can be diluted with a carrier prior to use.
- Surfaceactive substances may be anionic, cationic, non-ionic or polymeric and they can be used as emulsifiers, wetting agents or suspending agents or for other purposes.
- Typical surface-active substances include, for example, salts of alkyl sulfates, such as diethanolammonium lauryl sulfate; salts of alkylarylsulfonates, such as calcium dodecylbenzenesulfonate; alkylphenol/alkylene oxide addition products, such as nonylphenol ethoxylate; alcohol/alkylene oxide addition products, such as tridecylalcohol ethoxylate; soaps, such as sodium stearate; salts of alkylnaphthalenesulfonates, such as sodium dibutylnaphthalenesulfonate; dialkyl esters of sulfosuccinate salts, such as sodium di(2- ethylhexyl)sulfosuccinate; sorbitol esters, such as sorbitol oleate; quaternary amines, such as lauryltrimethylammonium chloride, polyethylene glycol esters of
- Further adjuvants that can be used in pesticidal formulations include crystallisation inhibitors, viscosity modifiers, suspending agents, dyes, anti-oxidants, foaming agents, light absorbers, mixing auxiliaries, antifoams, complexing agents, neutralising or pH-modifying substances and buffers, corrosion inhibitors, fragrances, wetting agents, take-up enhancers, micronutrients, plasticisers, glidants, lubricants, dispersants, thickeners, antifreezes, microbicides, and liquid and solid fertilisers.
- the formulations/compositions used according to the invention can include an additive comprising an oil of vegetable or animal origin, a mineral oil, alkyl esters of such oils or mixtures of such oils and oil derivatives.
- the amount of oil additive in the formulations according to the invention is generally from 0.01 to 10 %, based on the mixture to be applied.
- the oil additive can be added to a spray tank in the desired concentration after a spray mixture has been prepared.
- Preferred oil additives comprise mineral oils or an oil of vegetable origin, for example rapeseed oil, olive oil or sunflower oil, emulsified vegetable oil, alkyl esters of oils of vegetable origin, for example the methyl derivatives, or an oil of animal origin, such as fish oil or beef tallow.
- Preferred oil additives comprise alkyl esters of C8-C22 fatty acids, especially the methyl derivatives of C12-C18 fatty acids, for example the methyl esters of lauric acid, palmitic acid and oleic acid (methyl laurate, methyl palmitate and methyl oleate, respectively).
- Many oil derivatives are known from the Compendium of Herbicide Adjuvants, 10 th Edition, Southern Illinois University, 2010.
- a preferred formulation can have the following composition (weight %):
- Suspension concentrates active ingredient: 5 to 75 %, preferably 10 to 50 % water: 94 to 24 %, preferably 88 to 30 % surface-active agent: 1 to 40 %, preferably 2 to 30 %
- Wettable powders active ingredient: 0.5 to 90 %, preferably 1 to 80 % surface-active agent: 0.5 to 20 %, preferably 1 to 15 % solid carrier: 5 to 95 %, preferably 15 to 90 %
- Granules active ingredient: 0.1 to 30 %, preferably 0.1 to 15 % solid carrier: 99.5 to 70 %, preferably 97 to 85 %
- spiropidion 3-(4-chloro-2,6-dimethyl-phenyl)-8-methoxy- 1-methyl-2-oxo-1 ,8-diazaspiro[4.5]dec-3-en-4-yl] ethyl carbonate.
- CAS no.: 1229023-00-0 are described in WO 2010/066780, WO 2018/114648 and WO 2018/114649, and references cited therein.
- a spiropidion suspension concentrate formulation (SC300) was diluted in water and mixed with the paraffinic oil adjuvant Atplus® 463 (0.1% of the dilution).
- Test compositions comprising the spiropidion dilutions at the application volumes and rates defined for test compositions 1 to 9 in the Table were sprayed on the trunk (Test composition 1) or canopy (Test compositions 2 to 9) of three tea plants (Camellia sinensis) - 27 plants in total.
- the application was made at varying days before infestation (DBI) of white peach scale.
- the infestation site was on the trunk of the tea plant.
- Percentage control of white peach scale was measured at 30 days after infestation (DAI).
- DAI days after infestation
- test composition 1 show that the water- and labour-intensive application of a spiropidion composition to the trunk of a tea plant (adhesion of Al to plant) using high volumes of the composition per hectare provided 100% control 30 days after infestation against white peach scale.
- test compositions 2 to 9 show the surprising effect of test compositions 2 to 9 that for tea plant canopy applications when the application volume is reduced 10-fold (1000 L/ha) or even 50-fold (200 L/ha) over test composition 1 at equivalent doses , similarly high levels of pest control are observed (systemic effect through translaminar action and phloem transport). This was not expected.
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- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Dentistry (AREA)
- Agronomy & Crop Science (AREA)
- Insects & Arthropods (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
Claims
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP21192374 | 2021-08-20 | ||
| PCT/EP2022/073069 WO2023021136A1 (en) | 2021-08-20 | 2022-08-18 | Method of controlling pests on tea plants |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP4387452A1 true EP4387452A1 (en) | 2024-06-26 |
Family
ID=77431205
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP22765559.4A Pending EP4387452A1 (en) | 2021-08-20 | 2022-08-18 | Method of controlling pests on tea plants |
Country Status (4)
| Country | Link |
|---|---|
| EP (1) | EP4387452A1 (en) |
| JP (1) | JP2024529761A (en) |
| CN (1) | CN117794372A (en) |
| WO (1) | WO2023021136A1 (en) |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4216814A1 (en) | 1991-07-16 | 1993-01-21 | Bayer Ag | 3-ARYL-4-HYDROXY- (DELTA) (UP ARROW) 3 (UP ARROW) -DIHYDROFURANONE- AND 3-ARYL-4-HYDROXY- (DELTA) (UP ARROW) 3 (UP ARROW) -DIHYDROTHIOPHENONE DERIVATIVES |
| DK1277734T3 (en) | 1996-08-05 | 2007-06-04 | Bayer Cropscience Ag | 2- and 2,5-substituted phenylketoenols |
| DE10231333A1 (en) | 2002-07-11 | 2004-01-22 | Bayer Cropscience Ag | Cis-alkoxy-substituted 1-H-pyrrolidine-2,4-dione spirocyclic derivatives |
| DE102005008021A1 (en) | 2005-02-22 | 2006-08-24 | Bayer Cropscience Ag | New spiroketal-substituted cyclic ketoenol compounds used for combating animal parasites, undesired plant growth and/or undesired microorganisms |
| MX2011005795A (en) | 2008-12-12 | 2011-06-20 | Syngenta Participations Ag | Spiroheterocyclic n-oxypiperidines as pesticides. |
| CN110099897A (en) | 2016-12-22 | 2019-08-06 | 先正达参股股份有限公司 | Polymorph |
| GB201622007D0 (en) | 2016-12-22 | 2017-02-08 | And See Cambridge Display Tech Ltd Syngenta Participations Ag | Polymorphs |
| EA202192734A1 (en) | 2019-04-10 | 2022-02-15 | Сингента Кроп Протекшн Аг | PESTICIDE COMPOSITIONS |
-
2022
- 2022-08-18 EP EP22765559.4A patent/EP4387452A1/en active Pending
- 2022-08-18 CN CN202280053990.8A patent/CN117794372A/en active Pending
- 2022-08-18 JP JP2024510339A patent/JP2024529761A/en active Pending
- 2022-08-18 WO PCT/EP2022/073069 patent/WO2023021136A1/en not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| WO2023021136A1 (en) | 2023-02-23 |
| CN117794372A (en) | 2024-03-29 |
| JP2024529761A (en) | 2024-08-08 |
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