UA73820C2 - Oil-in-water emulsion formulation and a method for controlling pests - Google Patents
Oil-in-water emulsion formulation and a method for controlling pests Download PDFInfo
- Publication number
- UA73820C2 UA73820C2 UA2003066037A UA2003066037A UA73820C2 UA 73820 C2 UA73820 C2 UA 73820C2 UA 2003066037 A UA2003066037 A UA 2003066037A UA 2003066037 A UA2003066037 A UA 2003066037A UA 73820 C2 UA73820 C2 UA 73820C2
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- UA
- Ukraine
- Prior art keywords
- esters
- acid
- oil
- acids
- water
- Prior art date
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- 239000000203 mixture Substances 0.000 title abstract description 30
- 241000607479 Yersinia pestis Species 0.000 title abstract description 5
- 239000007764 o/w emulsion Substances 0.000 title abstract description 3
- 238000009472 formulation Methods 0.000 title abstract 2
- 238000000034 method Methods 0.000 title description 6
- -1 aliphatic monocarboxylic acids Chemical class 0.000 abstract description 40
- 150000002148 esters Chemical class 0.000 abstract description 30
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 19
- 239000003995 emulsifying agent Substances 0.000 abstract description 12
- 239000002904 solvent Substances 0.000 abstract description 10
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- 239000002917 insecticide Substances 0.000 abstract description 7
- 239000002562 thickening agent Substances 0.000 abstract description 6
- 239000002736 nonionic surfactant Substances 0.000 abstract description 2
- 239000003945 anionic surfactant Substances 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 14
- 239000000194 fatty acid Substances 0.000 description 13
- 239000002253 acid Substances 0.000 description 12
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- 239000006184 cosolvent Substances 0.000 description 9
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- 229910019142 PO4 Inorganic materials 0.000 description 5
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- 125000003229 2-methylhexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 2
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- 125000004494 ethyl ester group Chemical group 0.000 description 2
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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
- 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
- A01N25/04—Dispersions, emulsions, suspoemulsions, suspension concentrates or gels
-
- 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
- A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof
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)
- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Toxicology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP00126276A EP1210877A1 (en) | 2000-12-01 | 2000-12-01 | Oil-in-water emulsion formulation of insecticides |
| PCT/EP2001/013658 WO2002043488A1 (en) | 2000-12-01 | 2001-11-23 | Oil-in-water emulsion formulation of insecticides |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| UA73820C2 true UA73820C2 (en) | 2005-09-15 |
Family
ID=8170545
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| UA2003066037A UA73820C2 (en) | 2000-12-01 | 2001-11-23 | Oil-in-water emulsion formulation and a method for controlling pests |
Country Status (34)
| Country | Link |
|---|---|
| US (2) | US20020098221A1 (bg) |
| EP (2) | EP1210877A1 (bg) |
| JP (1) | JP4303963B2 (bg) |
| CN (1) | CN1286366C (bg) |
| AR (1) | AR031444A1 (bg) |
| AT (1) | ATE272941T1 (bg) |
| AU (2) | AU2002234523B2 (bg) |
| BG (1) | BG66227B1 (bg) |
| BR (1) | BR0115873A (bg) |
| CA (1) | CA2436199C (bg) |
| CU (1) | CU23192A3 (bg) |
| CZ (1) | CZ300087B6 (bg) |
| DE (1) | DE60104887T2 (bg) |
| DK (1) | DK1339281T3 (bg) |
| DZ (1) | DZ3432A1 (bg) |
| EC (1) | ECSP034633A (bg) |
| ES (1) | ES2223935T3 (bg) |
| HU (1) | HU229964B1 (bg) |
| IL (1) | IL156215A0 (bg) |
| MA (1) | MA25858A1 (bg) |
| MD (1) | MD3068C2 (bg) |
| MX (1) | MXPA03004877A (bg) |
| MY (1) | MY127187A (bg) |
| PL (1) | PL203263B1 (bg) |
| PT (1) | PT1339281E (bg) |
| RU (1) | RU2284107C2 (bg) |
| SI (1) | SI1339281T1 (bg) |
| SK (1) | SK287502B6 (bg) |
| TR (1) | TR200402144T4 (bg) |
| TW (1) | TWI280099B (bg) |
| UA (1) | UA73820C2 (bg) |
| UY (1) | UY27048A1 (bg) |
| WO (1) | WO2002043488A1 (bg) |
| ZA (1) | ZA200303850B (bg) |
Families Citing this family (58)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2002257116A1 (en) * | 2001-03-30 | 2002-10-15 | Trustees Of Princeton University | A process and apparatuses for preparing nanoparticle compositions with amphiphilic copolymers and their use |
| IL148684A (en) * | 2002-03-14 | 2006-12-31 | Yoel Sasson | Pesticidal composition |
| US20040166083A1 (en) * | 2003-02-26 | 2004-08-26 | The Andrew Jergens Company | Personal care water-in-oil emulsion products |
| DE102004026938A1 (de) | 2004-06-01 | 2005-12-22 | Bayer Cropscience Gmbh | Schaumarme wäßrige Formulierungen für den Pflanzenschutz |
| AU2005239726C1 (en) * | 2004-12-14 | 2010-11-18 | Sumitomo Chemical Company, Limited | Pesticidal composition comprising pyriproxyfen |
| WO2006069580A1 (en) * | 2004-12-30 | 2006-07-06 | Cheminova A/S | Oil-in-water formulation of avermectins |
| TWI402034B (zh) * | 2005-07-28 | 2013-07-21 | Dow Agrosciences Llc | 具有被層狀液晶覆膜包覆之油球之水包油乳化劑之農用組成物 |
| TWI444140B (zh) * | 2005-11-18 | 2014-07-11 | Cheminova As | 艾維菌素類之水包油調配物 |
| WO2007110355A2 (en) * | 2006-03-24 | 2007-10-04 | Basf Se | Liquid non aqueous agrochemical formulations comprising distyrylphenol ethoxylate |
| CN101541167A (zh) | 2006-11-22 | 2009-09-23 | 巴斯夫欧洲公司 | 基于水的液体农业化学配制剂 |
| TW200915984A (en) * | 2007-08-08 | 2009-04-16 | Basf Se | Aqueous microemulsions containing organic insecticide compounds |
| EP2070415A1 (en) * | 2007-12-11 | 2009-06-17 | Bayer CropScience AG | Active compound combinations |
| DK2252145T3 (en) * | 2008-02-04 | 2016-07-18 | Dow Agrosciences Llc | STABILIZED OILE-in-water emulsions, WHICH COVERS THE AGRICULTURAL RESPONSE ACTIVE INGREDIENTS |
| ES2558711T3 (es) | 2008-03-25 | 2016-02-08 | Dow Agrosciences Llc | Emulsiones estabilizadas de aceite en agua que incluyen principios agrícolamente activos |
| EP2285212B1 (en) * | 2008-04-30 | 2016-02-17 | Sumitomo Chemical Company, Limited | Novel pyriproxyfen compositions |
| AU2009242072A1 (en) | 2008-05-02 | 2009-11-05 | Basf Se | Improved microemulsion having wide application range |
| EP2309847A2 (de) * | 2008-07-24 | 2011-04-20 | Basf Se | Öl-in-wasser emulsion umfassend lösungsmittel, wasser, tensid und pestizid |
| US9149416B1 (en) * | 2008-08-22 | 2015-10-06 | Wellmark International | High deposition cleansing system |
| US8747875B2 (en) * | 2008-09-29 | 2014-06-10 | The Hartz Mountain Corporation | Photo-stable pest control |
| TW201018400A (en) * | 2008-10-10 | 2010-05-16 | Basf Se | Liquid aqueous plant protection formulations |
| UA106213C2 (ru) | 2008-10-10 | 2014-08-11 | Басф Се | Жидкие препараты для защиты растений, содержащие пираклостробин |
| EP2470662B1 (en) | 2009-08-28 | 2016-08-10 | E. I. du Pont de Nemours and Company | Compositions and methods to control insect pests |
| CN201712857U (zh) | 2010-05-10 | 2011-01-19 | S.C.约翰逊父子公司 | 用于挥发性材料的散发装置及其壳体和散发片 |
| UY33443A (es) * | 2010-06-19 | 2012-01-31 | Bayer Animal Health Gmbh | Preparacion que contiene ectoparasiticida para la formacion de emulsion espontanea |
| WO2012028583A1 (de) | 2010-09-03 | 2012-03-08 | Bayer Cropscience Ag | Deltamethrin enthaltende formulierungen |
| EP2446743B1 (en) * | 2010-10-26 | 2014-06-04 | Cognis IP Management GmbH | Biocide compositions comprising esters of ethoxylated alcohols |
| JP5620230B2 (ja) * | 2010-11-09 | 2014-11-05 | 住友化学株式会社 | 動物外部寄生虫防除組成物 |
| EP2457890A1 (en) * | 2010-11-29 | 2012-05-30 | Cognis IP Management GmbH | Biocide compositions comprising alkoxylation products of isoamyl alcohol derivatives |
| CA2818425C (en) * | 2010-12-03 | 2019-04-09 | Huntsman Petrochemical Llc | Low toxicity, low odor, low volatility solvent for agricultural chemical formulations |
| GB201107039D0 (en) * | 2011-04-26 | 2011-06-08 | Syngenta Ltd | Formulation component |
| GB201107040D0 (en) | 2011-04-26 | 2011-06-08 | Syngenta Ltd | Formulation component |
| WO2013054194A1 (en) | 2011-10-13 | 2013-04-18 | Amril Ag | A formulated solvent composition for pesticide |
| EP2797419A4 (en) * | 2011-12-28 | 2015-10-07 | Sumitomo Chemical Co | COMPOSITION FOR CONTROLLING PESTS |
| JP2013230992A (ja) * | 2012-04-27 | 2013-11-14 | Osaka Seiyaku:Kk | 水系動物用害虫阻害剤 |
| WO2013171201A1 (de) | 2012-05-16 | 2013-11-21 | Bayer Cropscience Ag | Insektizide öl-in-wasser (o/w) formulierung |
| US9205163B2 (en) | 2012-11-27 | 2015-12-08 | S.C. Johnson & Son, Inc. | Volatile material dispenser |
| US9278151B2 (en) | 2012-11-27 | 2016-03-08 | S.C. Johnson & Son, Inc. | Volatile material dispenser |
| CN104955331A (zh) * | 2013-01-29 | 2015-09-30 | 日产化学工业株式会社 | 乳化稳定性优异的农药乳化性组合物 |
| GB2533685B (en) * | 2013-02-27 | 2017-07-19 | Rotam Agrochem Int Co Ltd | Agrochemical composition with polyether adhesion promoter |
| CN105339380A (zh) | 2013-03-14 | 2016-02-17 | 先锋国际良种公司 | 用以防治昆虫害虫的组合物和方法 |
| RU2548500C2 (ru) * | 2013-08-21 | 2015-04-20 | Биогард Инвестментс Лтд. | Инсектицидная композиция |
| US20160309708A1 (en) * | 2013-12-11 | 2016-10-27 | Oxiteno S.A. Indústria E Comércio | Polycarboxylic acid ester alkyl derived from branched and straight alcohol of plant origin, and use of an alkyl ester in agrochemical formulations |
| US20170247719A1 (en) | 2014-09-17 | 2017-08-31 | Pioneer Hi-Bred International, Inc. | Compositions and methods to control insect pests |
| US9497971B2 (en) * | 2015-02-24 | 2016-11-22 | Bayer Cropscience Lp | Non-volatile organic compound pesticide formulations |
| WO2016144688A1 (en) | 2015-03-11 | 2016-09-15 | Pioneer Hi Bred International Inc | Insecticidal combinations of pip-72 and methods of use |
| CA2986265A1 (en) | 2015-06-16 | 2016-12-22 | Pioneer Hi-Bred International, Inc. | Compositions and methods to control insect pests |
| FR3048852B1 (fr) * | 2016-03-17 | 2019-09-06 | Oleon Nv | Concentre comprenant un mel et un ester d'acide gras et de polyethylene glycol de hlb superieur ou egal a 12 |
| CA3022858A1 (en) | 2016-06-16 | 2017-12-21 | Pioneer Hi-Bred International, Inc. | Compositions and methods to control insect pests |
| WO2018013333A1 (en) | 2016-07-12 | 2018-01-18 | Pioneer Hi-Bred International, Inc. | Compositions and methods to control insect pests |
| MX2019009371A (es) | 2017-02-08 | 2019-09-23 | Pionner Hi Bred Int Inc | Combinaciones insecticidas de proteinas insecticidas derivadas de plantas y metodos para su uso. |
| US10172359B2 (en) * | 2017-05-17 | 2019-01-08 | Sergeant's Pet Care Products, Inc. | Solvent system for use with spot-on pesticide compositions |
| AR111838A1 (es) * | 2017-05-30 | 2019-08-21 | Arysta Lifescience Inc | Dispersión oleosa herbicida que contiene un fitoprotector |
| WO2019074598A1 (en) | 2017-10-13 | 2019-04-18 | Pioneer Hi-Bred International, Inc. | VIRUS-INDUCED GENETIC SILENCING TECHNOLOGY FOR THE CONTROL OF INSECTS IN MAIZE |
| WO2020049493A1 (en) | 2018-09-06 | 2020-03-12 | Pi Industries Ltd. | Stable agrochemical composition |
| WO2022118814A1 (ja) * | 2020-12-01 | 2022-06-09 | 住友化学株式会社 | 液体農薬組成物 |
| US20240324606A1 (en) * | 2021-09-29 | 2024-10-03 | Firmenich Sa | Arthropod control products |
| WO2023176613A1 (ja) * | 2022-03-14 | 2023-09-21 | 日本化薬株式会社 | 農薬乳化性組成物 |
| EP4245139A1 (en) * | 2022-03-15 | 2023-09-20 | Centre national de la recherche scientifique | Compositions comprising a botanical extract as insecticidal agent |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4469675A (en) * | 1981-11-30 | 1984-09-04 | Zoecon Corporation | Pesticidal formulation |
| FR2624761B1 (fr) * | 1987-12-17 | 1993-10-08 | Roussel Uclaf | Granules a base de polymeres hydrophiles sur lesquels sont absorbes une formulation aqueuse renfermant un ou plusieurs principes actifs |
| FR2643223B1 (fr) * | 1989-02-17 | 1991-12-13 | Roussel Uclaf | Nouvelles emulsions aqueuses concentrees, leur procede de preparation et leur application dans le domaine pesticide |
| US5466458A (en) * | 1992-03-09 | 1995-11-14 | Roussel Uclaf | Emulsified spray formulations |
| FR2689729B1 (fr) * | 1992-04-09 | 1994-06-03 | Roussel Uclaf | Nouvelles compositions pesticides renfermant un pyrethrinouide. |
| FR2721800B1 (fr) * | 1994-07-01 | 1997-12-26 | Roussel Uclaf | Nouveaux concentres emulsionnables renfermant un u plussieurs pesticides |
| US6068849A (en) * | 1997-07-14 | 2000-05-30 | Henkel Corporation | Surfactants for use in agricultural formulations |
| ES2250074T3 (es) * | 1999-01-29 | 2006-04-16 | Basf Agro B.V., Arnhem (Nl), Wadenswil-Branch | Concentrado emulsificable para la proteccion de cultivos que contiene agentes desespumantes. |
-
2000
- 2000-12-01 EP EP00126276A patent/EP1210877A1/en not_active Withdrawn
-
2001
- 2001-11-23 IL IL15621501A patent/IL156215A0/xx not_active IP Right Cessation
- 2001-11-23 UA UA2003066037A patent/UA73820C2/uk unknown
- 2001-11-23 ES ES01985335T patent/ES2223935T3/es not_active Expired - Lifetime
- 2001-11-23 MD MDA20030132A patent/MD3068C2/ro not_active IP Right Cessation
- 2001-11-23 CN CNB018198341A patent/CN1286366C/zh not_active Expired - Fee Related
- 2001-11-23 MX MXPA03004877A patent/MXPA03004877A/es active IP Right Grant
- 2001-11-23 DE DE60104887T patent/DE60104887T2/de not_active Expired - Lifetime
- 2001-11-23 WO PCT/EP2001/013658 patent/WO2002043488A1/en active IP Right Grant
- 2001-11-23 SK SK665-2003A patent/SK287502B6/sk not_active IP Right Cessation
- 2001-11-23 TW TW090129087A patent/TWI280099B/zh not_active IP Right Cessation
- 2001-11-23 DZ DZ013432A patent/DZ3432A1/fr active
- 2001-11-23 HU HU0303290A patent/HU229964B1/hu unknown
- 2001-11-23 CZ CZ20031482A patent/CZ300087B6/cs not_active IP Right Cessation
- 2001-11-23 BR BR0115873-2A patent/BR0115873A/pt not_active Application Discontinuation
- 2001-11-23 JP JP2002545478A patent/JP4303963B2/ja not_active Expired - Fee Related
- 2001-11-23 AT AT01985335T patent/ATE272941T1/de active
- 2001-11-23 CA CA002436199A patent/CA2436199C/en not_active Expired - Fee Related
- 2001-11-23 PT PT01985335T patent/PT1339281E/pt unknown
- 2001-11-23 RU RU2003119547/15A patent/RU2284107C2/ru active
- 2001-11-23 DK DK01985335T patent/DK1339281T3/da active
- 2001-11-23 AU AU2002234523A patent/AU2002234523B2/en not_active Ceased
- 2001-11-23 EP EP01985335A patent/EP1339281B1/en not_active Expired - Lifetime
- 2001-11-23 AU AU3452302A patent/AU3452302A/xx active Pending
- 2001-11-23 SI SI200130210T patent/SI1339281T1/xx unknown
- 2001-11-23 TR TR2004/02144T patent/TR200402144T4/xx unknown
- 2001-11-23 PL PL366224A patent/PL203263B1/pl unknown
- 2001-11-29 US US09/997,043 patent/US20020098221A1/en not_active Abandoned
- 2001-11-29 AR ARP010105564A patent/AR031444A1/es unknown
- 2001-11-30 UY UY27048A patent/UY27048A1/es unknown
- 2001-11-30 MY MYPI20015472A patent/MY127187A/en unknown
-
2003
- 2003-05-19 ZA ZA200303850A patent/ZA200303850B/en unknown
- 2003-05-21 BG BG107833A patent/BG66227B1/bg unknown
- 2003-05-23 MA MA27176A patent/MA25858A1/fr unknown
- 2003-05-27 CU CU20030124A patent/CU23192A3/es not_active IP Right Cessation
- 2003-05-30 EC EC2003004633A patent/ECSP034633A/es unknown
-
2004
- 2004-09-08 US US10/936,238 patent/US20050042245A1/en not_active Abandoned
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