TWI241887B - Active compound combinations having insecticidal and acaricidal properties - Google Patents
Active compound combinations having insecticidal and acaricidal properties Download PDFInfo
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- TWI241887B TWI241887B TW090106531A TW90106531A TWI241887B TW I241887 B TWI241887 B TW I241887B TW 090106531 A TW090106531 A TW 090106531A TW 90106531 A TW90106531 A TW 90106531A TW I241887 B TWI241887 B TW I241887B
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- WIBFFTLQMKKBLZ-SEYXRHQNSA-N n-butyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCCCC WIBFFTLQMKKBLZ-SEYXRHQNSA-N 0.000 description 1
- 229940042880 natural phospholipid Drugs 0.000 description 1
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- 239000005645 nematicide Substances 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
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- 239000003973 paint Substances 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 244000045947 parasite Species 0.000 description 1
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- RLBIQVVOMOPOHC-UHFFFAOYSA-N parathion-methyl Chemical compound COP(=S)(OC)OC1=CC=C([N+]([O-])=O)C=C1 RLBIQVVOMOPOHC-UHFFFAOYSA-N 0.000 description 1
- MOQRZWSWPNIGMP-UHFFFAOYSA-N pentyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCCCC MOQRZWSWPNIGMP-UHFFFAOYSA-N 0.000 description 1
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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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/06—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings
- A01N43/08—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings with oxygen as the ring hetero atom
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/06—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings
- A01N43/12—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings condensed with a carbocyclic ring
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
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|---|---|---|---|
| DE10015310A DE10015310A1 (de) | 2000-03-28 | 2000-03-28 | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
Publications (1)
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|---|---|
| TWI241887B true TWI241887B (en) | 2005-10-21 |
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| TW090106531A TWI241887B (en) | 2000-03-28 | 2001-03-21 | Active compound combinations having insecticidal and acaricidal properties |
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| EP (1) | EP1267619B1 (https=) |
| JP (1) | JP5002106B2 (https=) |
| KR (1) | KR100730001B1 (https=) |
| CN (2) | CN1853469A (https=) |
| AT (1) | ATE279861T1 (https=) |
| AU (1) | AU2001242473A1 (https=) |
| BR (1) | BR0109541A (https=) |
| DE (2) | DE10015310A1 (https=) |
| EG (1) | EG23185A (https=) |
| GT (1) | GT200100046A (https=) |
| HU (1) | HUP0301516A2 (https=) |
| IL (2) | IL151750A0 (https=) |
| MX (1) | MXPA02009530A (https=) |
| PT (1) | PT1267619E (https=) |
| TW (1) | TWI241887B (https=) |
| WO (1) | WO2001072125A2 (https=) |
| ZA (1) | ZA200206765B (https=) |
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| DE19948129A1 (de) * | 1999-10-07 | 2001-04-12 | Bayer Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE19953775A1 (de) * | 1999-11-09 | 2001-05-10 | Bayer Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE10017881A1 (de) * | 2000-04-11 | 2001-10-25 | Bayer Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE10018370A1 (de) * | 2000-04-14 | 2001-10-18 | Bayer Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| US20040185212A1 (en) * | 2003-03-20 | 2004-09-23 | Bogrett Blake Boyd | Fungi resistant sheet, facing and faced insulation assembly |
| US20040192132A1 (en) * | 2003-03-20 | 2004-09-30 | Fay Ralph Michael | Fungi resistant asphalt and asphalt sheet materials |
| DE10330723A1 (de) * | 2003-07-08 | 2005-02-03 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE10353281A1 (de) * | 2003-11-14 | 2005-06-16 | Bayer Cropscience Ag | Wirkstoffkombination mit insektiziden und akariziden Eigenschaften |
| WO2005053405A1 (de) † | 2003-12-04 | 2005-06-16 | Bayer Cropscience Aktiengesellschaft | Wirkstoffkombinationen mit insektiziden und akariziden eigenschaften |
| DE102004001112A1 (de) * | 2004-01-07 | 2005-08-18 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektizide und akariziden Eigenschaften |
| DE102006014480A1 (de) * | 2006-03-29 | 2007-10-04 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE102006014489A1 (de) * | 2006-03-29 | 2007-10-04 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE102006027732A1 (de) * | 2006-06-16 | 2008-01-10 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE102006027730A1 (de) * | 2006-06-16 | 2007-12-20 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| US8110608B2 (en) | 2008-06-05 | 2012-02-07 | Ecolab Usa Inc. | Solid form sodium lauryl sulfate (SLS) pesticide composition |
| EP2525658B1 (de) | 2010-01-22 | 2017-03-01 | Bayer Intellectual Property GmbH | Akarizide und/oder insektizide wirkstoffkombinationen |
| US8968757B2 (en) | 2010-10-12 | 2015-03-03 | Ecolab Usa Inc. | Highly wettable, water dispersible, granules including two pesticides |
| CN103621509B (zh) * | 2012-08-28 | 2015-10-21 | 陕西美邦农药有限公司 | 一种含螺甲螨酯的农药组合物 |
| CN103651499A (zh) * | 2012-08-31 | 2014-03-26 | 陕西美邦农药有限公司 | 一种含螺甲螨酯与新烟碱类的杀虫组合物 |
| CN104738064B (zh) * | 2012-08-31 | 2017-03-01 | 陕西美邦农药有限公司 | 一种含螺甲螨酯与氨基甲酸酯类的农药组合物 |
| JP7110360B2 (ja) | 2017-10-09 | 2022-08-01 | テルモ ビーシーティー バイオテクノロジーズ，エルエルシー | 凍結乾燥方法 |
| CN113614477B (zh) | 2019-03-14 | 2023-04-28 | 泰尔茂比司特生物技术有限公司 | 冷冻干燥装载托盘组件及系统 |
Family Cites Families (101)
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| BE552284A (https=) | ||||
| DE814152C (de) | 1951-07-26 | I arbenfabriken Bayer | everkusen I Verfahren zur Herstellung von Estern der Phosphorsaure und Thiophosphor saure | |
| US2498283A (en) * | 1945-01-30 | 1950-02-21 | United Aircraft Corp | Drive for helicopters |
| NL65075C (https=) | 1947-05-21 | |||
| CA494562A (en) * | 1948-02-04 | 1953-07-21 | American Cyanamid Company | Carbamylalkyl phosphates and method of preparation |
| US2586655A (en) * | 1948-03-26 | 1952-02-19 | American Cyanamid Co | S-alkoxymethyl-o, o'-dialkyldithiophosphates |
| NL80825C (https=) * | 1950-03-02 | |||
| ZA15258B (https=) * | 1951-04-20 | 1900-01-01 | ||
| GB775085A (en) | 1951-09-25 | 1957-05-22 | Ciba Ltd | Preparations for combating pests |
| US2754246A (en) * | 1952-02-25 | 1956-07-10 | Phillips Petroleum Co | Stripping still control according to specific gravity of liquid and vapors introduced into column |
| US2685552A (en) * | 1952-02-29 | 1954-08-03 | Shell Dev | Dimethyl 1-carbomethoxy-1-propen-2-yl phosphate |
| DE917668C (de) | 1952-08-01 | 1954-09-09 | Bayer Ag | Verfahren zur Herstellung von neutralen Estern der Dithiophosphorsaeure |
| NL181407B (nl) * | 1952-09-20 | Merck & Co Inc | Verbetering van een werkwijze ter bereiding van een farmaceutisch preparaat met antibacteriele werking, dat een combinatie van een verbinding van het 3-fluor-d-alaninetype en een cycloserineverbinding bevat. | |
| DE947368C (de) | 1954-11-06 | 1956-08-16 | Bayer Ag | Verfahren zur Herstellung von Sulfoxydgruppen enthaltenden Estern der Phosphor- und Thiophosphorsaeuren |
| US2758115A (en) * | 1955-02-10 | 1956-08-07 | Bayer Ag | Derivatives of thiophosphoric acid |
| US2767194A (en) * | 1955-03-18 | 1956-10-16 | Stauffer Chemical Co | Compositions of matter |
| GB834814A (en) | 1955-06-14 | 1960-05-11 | Montedison Spa | ª‡-substituted o, o-dialkyl-dithiophosphorylacetic esters and process for their preparation |
| US2908605A (en) * | 1955-11-03 | 1959-10-13 | Ciba Ltd | New organic phosphorus compounds and process for their manufacture |
| DE1116656B (de) | 1958-05-28 | 1961-11-09 | Bayer Ag | Verfahren zur Herstellung von Thionophosphorsaeureestern |
| US2873228A (en) * | 1956-07-16 | 1959-02-10 | Fmc Corp | Pesticidal phosphorus esters |
| BE587481A (https=) * | 1958-08-07 | |||
| BE593564A (https=) | 1959-07-31 | |||
| NL105160C (https=) | 1959-09-03 | |||
| NL258661A (https=) | 1959-12-05 | |||
| US2956073A (en) * | 1960-04-13 | 1960-10-11 | Shell Oil Co | Insecticidally active esters of phosphorus acids and preparation of the same |
| NL125457C (https=) * | 1962-04-30 | 1965-07-12 | ||
| BE635767A (https=) | 1962-08-02 | |||
| US3264177A (en) * | 1964-02-17 | 1966-08-02 | Dow Chemical Co | Methods for the control of arachnids |
| DE1238902B (de) * | 1965-06-26 | 1967-04-20 | Bayer Ag | Verfahren zur Herstellung von Phosphor-, Phosphon- bzw. Thionophosphor-, -phosphon-saeureestern |
| US3309266A (en) * | 1965-07-01 | 1967-03-14 | Chevron Res | Insecticidal compositions containing oalkyl-s-alkyl phosphoroamidothioates and methods for killing insects therewith |
| DE1793838C2 (de) * | 1965-08-20 | 1978-08-31 | Sankyo Co., Ltd., Tokio | 3-Isoxazolylthiono-phosphorsäure-(-phosphonsäure-Werivate und Verfahren zu ihrer Herstellung |
| GB1181657A (en) | 1966-03-31 | 1970-02-18 | Ici Ltd | Pyrimidine Derivatives and Compositions Containing them |
| CH478152A (de) | 1966-07-05 | 1969-09-15 | Agripat Sa | Verfahren zur Herstellung heterozyklischer Thiophosphor- und Thiophosphonsäureester |
| NL136285C (https=) * | 1967-06-03 | 1900-01-01 | ||
| US3763143A (en) * | 1967-06-19 | 1973-10-02 | Du Pont | 1 - (alkyleneiminocarbonyl)-n-(substituted carbamoyloxy)thioformimidates |
| US3530220A (en) * | 1967-06-19 | 1970-09-22 | Du Pont | Pesticidal composition and method containing alkyl 1 - carbamoyl - n - (substituted carbamoyloxy)thioformimidates |
| US3689648A (en) * | 1968-10-24 | 1972-09-05 | Bayer Ag | Phosphorus acid ester-containing pesticidal composition and methods of combating pests |
| US3632694A (en) * | 1968-12-26 | 1972-01-04 | Shell Oil Co | Process for the production of dimethyl 1 - methyl - 2-(methylcarbamoyl) vinyl phosphate |
| US3801680A (en) * | 1970-02-24 | 1974-04-02 | Chevron Res | O(s),s-dihydrocarbyl-n-acylphosphoroamidothio,dithoates |
| US3825634A (en) * | 1970-02-24 | 1974-07-23 | Chevron Res | N-aralkanoyl and n-aralkenoyl derivatives of o,s-dihydrocarbylphosphoroamidothioates and s,s-dihydrocarbylphosphoroamidodithioates |
| JPS4924656B1 (https=) * | 1970-03-13 | 1974-06-25 | ||
| US4013793A (en) | 1970-03-13 | 1977-03-22 | Nihon Tokushu Noyaku Seizo Kabushiki Kaisha | Combating pests with o-ethyl-s-propyl-thionothiol or dithiophosphoric acid phenyl or naphthyl esters |
| US3947529A (en) * | 1970-03-13 | 1976-03-30 | Bayer Aktiengesellschaft | O-ethyl-S-propyl-dithiophosphoric acid phenyl or naphthyl esters |
| US3898334A (en) * | 1970-03-13 | 1975-08-05 | Bayer Ag | Pesticidal o-ethyl-S-propyl-dithiophosphoric acid phenyl or naphthyl esters |
| US3685200A (en) | 1970-09-14 | 1972-08-22 | Evelyn Noll | Electronically and manually animated talking doll |
| US3845172A (en) * | 1971-05-28 | 1974-10-29 | Chevron Res | N-hydrocarboyl phosphoroamido-thioates and phosphoroamidodithioates |
| US3992533A (en) * | 1971-10-12 | 1976-11-16 | Ciba-Geigy Corporation | O-ethyl-S-N-propyl-O-(2-chloro-4-bromophenyl)-thiophosphate |
| US4049679A (en) * | 1972-02-24 | 1977-09-20 | Chevron Research Company | Insecticidal O,S-dihydrocarbyl-N-haloacylphosphoroamidothioates and S,S-dihydrocarbyl-N-haloacylphosphoroamidodithioates |
| US3914417A (en) * | 1972-12-21 | 1975-10-21 | Chevron Res | Insectidical N-hydrocarboyl phosphoroamidothioates and phosphoroamidodithioates |
| US4110443A (en) * | 1972-12-21 | 1978-08-29 | Chevron Research Company | Insecticidal o,s-dihydrocarbyl-n-haloacylphosphoroamidothioates and s,s-dihydrocarbyl-n-haloacylphosphoroamidodithioates |
| US3868449A (en) * | 1972-12-21 | 1975-02-25 | Philip S Magee | Insecticidal o,s-dihydrocarbyl-n-acylphosphoroamidothioates and s,s-dihydrocarbyl-n-acylphosphoroamidodithioates |
| US3885032A (en) * | 1972-12-21 | 1975-05-20 | Chevron Res | Insecticidal N-aralkanoyl and N-aralkenoyl derivatives of O,S-dihydrocarbylphosphoroamidothioates and S,S-dihydrocarbylphosphoroamidodithioates |
| FR2235129B1 (https=) * | 1973-06-28 | 1976-04-30 | Rhone Poulenc Ind | |
| US4148918A (en) * | 1974-05-10 | 1979-04-10 | E. I. Du Pont De Nemours And Company | Substituted 2-higher alkyl-3-hydroxy-1,4-naphthoquinone carboxylic acid esters and their use as miticides |
| US4055661A (en) * | 1974-12-11 | 1977-10-25 | E. I. Du Pont De Nemours And Company | Miticidal and aphicidal method utilizing 2-higher alkyl-3-hydroxy-1,4-naphthoquinone carboxylic acid esters |
| US4070481A (en) * | 1975-09-15 | 1978-01-24 | E. I. Du Pont De Nemours And Company | Substituted 2-higher alkyl-3-hydroxy-1,4-naphthoquinone carboxylic acid esters and their use as miticides |
| US4053634A (en) * | 1975-09-15 | 1977-10-11 | E. I. Du Pont De Nemours And Company | Miticidal and aphicidal method utilizing 2-higher alkyl-3-hydroxy-1,4-naphthoquinone carboxylic acid esters |
| US4013378A (en) * | 1976-03-26 | 1977-03-22 | General Electric Company | Axial flow turbine exhaust hood |
| SE7610038L (sv) * | 1976-03-29 | 1977-09-20 | Du Pont | Miticida och aficida karboxylsyraestrar |
| US4143157A (en) * | 1977-08-25 | 1979-03-06 | E. I. Du Pont De Nemours And Company | Miticidal and aphicidal method utilizing 2-higher alkyl-3-hydroxy-1'4-naphthoquinone carboxylic acid esters |
| CA1137506A (en) * | 1978-03-17 | 1982-12-14 | Ulf Fischer | Carbamic acid derivatives |
| DE3317824A1 (de) * | 1983-05-17 | 1984-11-22 | Bayer Ag, 5090 Leverkusen | Phosphorsaeureester |
| DD235019A1 (de) * | 1985-03-04 | 1986-04-23 | Bitterfeld Chemie | Insektizid/symbiontizide mittel zur bekaempfung schaedlicher arthropoden |
| IL79360A (en) * | 1985-07-12 | 1993-02-21 | Ciba Geigy Ag | Aleyrodidae-controlling compositions containing n-(4-phenoxy-2,6- diisopropylphenyl) -n)-tert- butylthiourea as active agent |
| US4843068A (en) * | 1985-12-27 | 1989-06-27 | Nihon Nohyaku Co., Ltd. | Pyrazole oxime derivatives and compositions |
| US5455263A (en) * | 1987-07-29 | 1995-10-03 | American Cyanamid Company | Methods for the control and the protection of warm-blooded animals against infestation and infection by helminths, acarids and arthropod endo- and ectoparasites |
| US5010098A (en) * | 1987-07-29 | 1991-04-23 | American Cyanamid Company | Arylpyrrole insecticidal acaricidal and nematicidal agents and methods for the preparation thereof |
| DE4216814A1 (de) * | 1991-07-16 | 1993-01-21 | Bayer Ag | 3-aryl-4-hydroxy-(delta)(pfeil hoch)3(pfeil hoch)-dihydrofuranon- und 3-aryl-4-hydroxy-(delta)(pfeil hoch)3(pfeil hoch)-dihydrothiophenon-derivate |
| BR9206803A (pt) * | 1991-11-22 | 1995-05-02 | Uniroyal Chemical Ltd | Derivados inseticidas de fenilhidrazina |
| SK282306B6 (sk) * | 1991-11-22 | 2002-01-07 | Uniroyal Chemical Company, Inc. | Fenylhydrazínové deriváty, pesticídny prostriedok obsahujúci tieto zlúčeniny a spôsob kontrolovania nežiaduceho hmyzu |
| WO1993022297A1 (fr) * | 1992-04-28 | 1993-11-11 | Yashima Chemical Industrial Co., Ltd. | 2-(2,6-difluorophenyle)-4-(2-ethoxy-4-tert-butylphenyle)-2-oxazoline |
| CN1129444A (zh) * | 1993-07-05 | 1996-08-21 | 拜尔公司 | 取代的芳基酮-烯醇杂环类化合物 |
| AU7159994A (en) * | 1993-09-17 | 1995-03-30 | Bayer Aktiengesellschaft | 3-aryl-4-hydroxy-delta3-dihydrofuranone derivatives |
| EP0792272A1 (de) * | 1994-11-17 | 1997-09-03 | Bayer Ag | Substituierte thiophenderivate als schädlingsbekämpfungsmittel und herbizide |
| AU4342096A (en) * | 1994-12-23 | 1996-07-19 | Bayer Aktiengesellschaft | 3-aryl-tetronic acid derivatives, the production thereof and the use thereof as anti-parasitic agents |
| US6358887B1 (en) * | 1995-02-13 | 2002-03-19 | Bayer Aktiengesellschaft | 2-Phenyl-substituted heterocyclic 1,3-ketonols as herbicides and pesticides |
| CN1131209C (zh) * | 1995-05-09 | 2003-12-17 | 拜尔公司 | 可用作杀虫剂和除草剂的烷基－二卤代苯基取代的酮烯醇 |
| MX9710373A (es) * | 1995-06-28 | 1998-07-31 | Bayer Ag | Fenilcetoenoles 2,4,5-trisubstituidos para el empleo como pesticidas y herbicidas. |
| CN1152860C (zh) * | 1995-06-30 | 2004-06-09 | 拜尔公司 | 二烷基-卤代苯基取代的酮-烯醇 |
| CN1215390A (zh) * | 1996-04-02 | 1999-04-28 | 拜尔公司 | 取代的苯基酮烯醇杀虫剂及除草剂 |
| ES2251022T3 (es) * | 1996-05-10 | 2006-04-16 | Bayer Cropscience Ag | Nuevos piridilcetoenoles sustituidos. |
| ES2275796T3 (es) * | 1996-08-05 | 2007-06-16 | Bayer Cropscience Ag | Fenilcetoenoles 2- y 2,5-substituidos. |
| DE19632126A1 (de) * | 1996-08-09 | 1998-02-12 | Bayer Ag | Phenylsubstituierte cyclische Ketoenole |
| DE19742492A1 (de) * | 1997-09-26 | 1999-04-01 | Bayer Ag | Spirocyclische Phenylketoenole |
| DE19808261A1 (de) * | 1998-02-27 | 1999-10-28 | Bayer Ag | Arylphenylsubstituierte cyclische Ketoenole |
| DE19813354A1 (de) * | 1998-03-26 | 1999-09-30 | Bayer Ag | Arylphenylsubstituierte cyclische Ketoenole |
| DE19818732A1 (de) * | 1998-04-27 | 1999-10-28 | Bayer Ag | Arylphenylsubstituierte cyclische Ketoenole |
| BR0017605B1 (pt) * | 1999-03-12 | 2013-01-22 | composiÇço inseticida sinÉrgica, processo para controle de insetos e processo para proteger plantas contra infestaÇço e ataque de insetos. | |
| DE19913174A1 (de) * | 1999-03-24 | 2000-09-28 | Bayer Ag | Synergistische insektizide Mischungen |
| DE19953775A1 (de) * | 1999-11-09 | 2001-05-10 | Bayer Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE10007411A1 (de) * | 2000-02-18 | 2001-08-23 | Bayer Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE10013914A1 (de) * | 2000-03-21 | 2001-09-27 | Bayer Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| CL2007003748A1 (es) * | 2006-12-22 | 2008-07-18 | Bayer Cropscience Ag | Composicion pesticida que comprende fosetil-al, propamocarb-hcl y una sustancia insecticida activa; y metodo para controlar hongos fitopatogenos o insecticidas daninos de las plantas, cultivos o semillas que comprende aplicar dicha composicion. |
| CL2007003747A1 (es) * | 2006-12-22 | 2008-07-18 | Bayer Cropscience Ag | Composicion pesticida que comprende fosetil-al y un compuesto insecticida; y metodo para controlar hongos fitopatogenos o insecticidas daninos de las plantas, cultivos o semillas que comprende aplicar dicha composicion. |
| CL2007003746A1 (es) * | 2006-12-22 | 2008-07-18 | Bayer Cropscience Ag | Composicion pesticida que comprende propamocarb-hcl y un compuesto insecticida; y metodo para controlar hongos fitopatogenos o insecticidas daninos de las plantas, cultivos o semillas que comprende aplicar dicha composicion. |
| CL2007003743A1 (es) * | 2006-12-22 | 2008-07-11 | Bayer Cropscience Ag | Composicion que comprende fenamidona y un compuesto insecticida; y metodo para controlar de forma curativa o preventiva hongos fitopatogenos de cultivos e insectos. |
| DE102007018452A1 (de) * | 2007-04-17 | 2008-10-23 | Bayer Cropscience Ag | Verfahren zur verbesserten Nutzung des Produktionspotentials transgener Pflanzen |
| TW200904331A (en) * | 2007-06-15 | 2009-02-01 | Bayer Cropscience Sa | Pesticidal composition comprising a strigolactone derivative and an insecticide compound |
| MX2010012024A (es) * | 2008-05-07 | 2010-12-07 | Bayer Cropscience Ag | Combinaciones sinergicas de compuestos activos. |
| KR20120027265A (ko) * | 2009-04-27 | 2012-03-21 | 다우 아그로사이언시즈 엘엘씨 | 살충성 피리딘 화합물 |
| RU2565081C2 (ru) * | 2009-11-17 | 2015-10-20 | Байер Кропсайенс Аг | Комбинации активных соединений |
-
2000
- 2000-03-28 DE DE10015310A patent/DE10015310A1/de not_active Withdrawn
-
2001
- 2001-03-15 DE DE50104210T patent/DE50104210D1/de not_active Expired - Fee Related
- 2001-03-15 HU HU0301516A patent/HUP0301516A2/hu unknown
- 2001-03-15 JP JP2001570094A patent/JP5002106B2/ja not_active Expired - Fee Related
- 2001-03-15 CN CNA2006100847210A patent/CN1853469A/zh active Pending
- 2001-03-15 CN CNB018072038A patent/CN1267004C/zh not_active Expired - Lifetime
- 2001-03-15 MX MXPA02009530A patent/MXPA02009530A/es active IP Right Grant
- 2001-03-15 WO PCT/EP2001/002977 patent/WO2001072125A2/de not_active Ceased
- 2001-03-15 US US10/239,332 patent/US6900190B2/en not_active Expired - Fee Related
- 2001-03-15 AU AU2001242473A patent/AU2001242473A1/en not_active Abandoned
- 2001-03-15 AT AT01915355T patent/ATE279861T1/de not_active IP Right Cessation
- 2001-03-15 IL IL15175001A patent/IL151750A0/xx active IP Right Grant
- 2001-03-15 KR KR1020027012220A patent/KR100730001B1/ko not_active Expired - Fee Related
- 2001-03-15 BR BR0109541-2A patent/BR0109541A/pt not_active Application Discontinuation
- 2001-03-15 PT PT01915355T patent/PT1267619E/pt unknown
- 2001-03-15 EP EP01915355A patent/EP1267619B1/de not_active Expired - Lifetime
- 2001-03-21 TW TW090106531A patent/TWI241887B/zh not_active IP Right Cessation
- 2001-03-23 GT GT200100046A patent/GT200100046A/es unknown
- 2001-03-27 EG EG20010302A patent/EG23185A/xx active
-
2002
- 2002-08-23 ZA ZA200206765A patent/ZA200206765B/en unknown
- 2002-09-12 IL IL151750A patent/IL151750A/en not_active IP Right Cessation
-
2005
- 2005-03-07 US US11/074,156 patent/US20050147639A1/en not_active Abandoned
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- 2009-08-27 US US12/548,731 patent/US20090318386A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| IL151750A (en) | 2006-08-20 |
| CN1419412A (zh) | 2003-05-21 |
| EP1267619A2 (de) | 2003-01-02 |
| BR0109541A (pt) | 2003-06-10 |
| JP5002106B2 (ja) | 2012-08-15 |
| ZA200206765B (en) | 2003-08-25 |
| HUP0301516A2 (hu) | 2003-08-28 |
| US6900190B2 (en) | 2005-05-31 |
| CN1853469A (zh) | 2006-11-01 |
| US20090318386A1 (en) | 2009-12-24 |
| WO2001072125A2 (de) | 2001-10-04 |
| JP2003528116A (ja) | 2003-09-24 |
| MXPA02009530A (es) | 2003-05-14 |
| US20030100604A1 (en) | 2003-05-29 |
| PT1267619E (pt) | 2005-03-31 |
| KR100730001B1 (ko) | 2007-06-20 |
| EP1267619B1 (de) | 2004-10-20 |
| CN1267004C (zh) | 2006-08-02 |
| WO2001072125A8 (de) | 2004-03-04 |
| US20050147639A1 (en) | 2005-07-07 |
| DE50104210D1 (de) | 2004-11-25 |
| EG23185A (en) | 2004-07-31 |
| AU2001242473A1 (en) | 2001-10-08 |
| GT200100046A (es) | 2002-01-11 |
| WO2001072125A3 (de) | 2002-02-28 |
| IL151750A0 (en) | 2003-04-10 |
| KR20020084209A (ko) | 2002-11-04 |
| ATE279861T1 (de) | 2004-11-15 |
| DE10015310A1 (de) | 2001-10-04 |
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| MM4A | Annulment or lapse of patent due to non-payment of fees |