HU217371B - Fluroxipir-észtert tartalmazó herbicid készítmény és a felhasználásán alapuló gyomirtási eljárás - Google Patents
Fluroxipir-észtert tartalmazó herbicid készítmény és a felhasználásán alapuló gyomirtási eljárás Download PDFInfo
- Publication number
- HU217371B HU217371B HU9403753A HU9403753A HU217371B HU 217371 B HU217371 B HU 217371B HU 9403753 A HU9403753 A HU 9403753A HU 9403753 A HU9403753 A HU 9403753A HU 217371 B HU217371 B HU 217371B
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- HU
- Hungary
- Prior art keywords
- ester
- fluroxypyr
- weight
- butoxy
- propyl
- Prior art date
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- IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 description 1
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- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical class OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- WYEHFWKAOXOVJD-UHFFFAOYSA-N diflufenican Chemical compound FC1=CC(F)=CC=C1NC(=O)C1=CC=CN=C1OC1=CC=CC(C(F)(F)F)=C1 WYEHFWKAOXOVJD-UHFFFAOYSA-N 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 239000003623 enhancer Substances 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000004494 ethyl ester group Chemical group 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 229940100242 glycol stearate Drugs 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 description 1
- 229940097068 glyphosate Drugs 0.000 description 1
- 229920000578 graft copolymer Polymers 0.000 description 1
- MNWFXJYAOYHMED-UHFFFAOYSA-N heptanoic acid Chemical compound CCCCCCC(O)=O MNWFXJYAOYHMED-UHFFFAOYSA-N 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 238000000265 homogenisation Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 229920003063 hydroxymethyl cellulose Polymers 0.000 description 1
- 229940031574 hydroxymethyl cellulose Drugs 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- NRXQIUSYPAHGNM-UHFFFAOYSA-N ioxynil Chemical compound OC1=C(I)C=C(C#N)C=C1I NRXQIUSYPAHGNM-UHFFFAOYSA-N 0.000 description 1
- 238000003973 irrigation Methods 0.000 description 1
- 230000002262 irrigation Effects 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- PUIYMUZLKQOUOZ-UHFFFAOYSA-N isoproturon Chemical compound CC(C)C1=CC=C(NC(=O)N(C)C)C=C1 PUIYMUZLKQOUOZ-UHFFFAOYSA-N 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 235000019645 odor Nutrition 0.000 description 1
- 229940049964 oleate Drugs 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 239000003209 petroleum derivative Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 229920001983 poloxamer Polymers 0.000 description 1
- 229920000233 poly(alkylene oxides) Polymers 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 238000013207 serial dilution Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000008247 solid mixture Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 238000007619 statistical method Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- 150000003456 sulfonamides Chemical class 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- LOQQVLXUKHKNIA-UHFFFAOYSA-N thifensulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C2=C(SC=C2)C(O)=O)=N1 LOQQVLXUKHKNIA-UHFFFAOYSA-N 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- BQZXUHDXIARLEO-UHFFFAOYSA-N tribenuron Chemical compound COC1=NC(C)=NC(N(C)C(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 BQZXUHDXIARLEO-UHFFFAOYSA-N 0.000 description 1
- REEQLXCGVXDJSQ-UHFFFAOYSA-N trichlopyr Chemical compound OC(=O)COC1=NC(Cl)=C(Cl)C=C1Cl REEQLXCGVXDJSQ-UHFFFAOYSA-N 0.000 description 1
- 229940087291 tridecyl alcohol Drugs 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/72—Nitrogen atoms
- C07D213/73—Unsubstituted amino or imino 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Catching Or Destruction (AREA)
- Processing Of Solid Wastes (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/052,446 US5374603A (en) | 1993-04-23 | 1993-04-23 | Agricultural formulations comprising fluroxypyr esters which are liquid at 25° C. |
Publications (2)
Publication Number | Publication Date |
---|---|
HUT69008A HUT69008A (en) | 1995-08-28 |
HU217371B true HU217371B (hu) | 2000-01-28 |
Family
ID=21977661
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HU9403753A HU217371B (hu) | 1993-04-23 | 1994-04-08 | Fluroxipir-észtert tartalmazó herbicid készítmény és a felhasználásán alapuló gyomirtási eljárás |
Country Status (24)
Families Citing this family (26)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5965487A (en) * | 1995-03-15 | 1999-10-12 | Dow Agrosciences Llc | Mixed herbicidal compositions |
GB9505204D0 (en) * | 1995-03-15 | 1995-05-03 | Dowelanco | Mixed herbicidal compositions |
US5834400A (en) * | 1997-04-29 | 1998-11-10 | Isp Investments Inc. | Emulsifiable concentrate for a low dosage fluorinated agricultural chemical |
US6566308B1 (en) * | 1999-01-29 | 2003-05-20 | Basf Aktiengesellschaft | Emulsifiable concentrate containing one or more pesticides and adjuvants |
US6825151B2 (en) * | 2002-01-30 | 2004-11-30 | Nufarm Americas Inc. | Liquid herbicidal compositions and use thereof in a granular herbicide |
DE10209478A1 (de) * | 2002-03-05 | 2003-09-18 | Bayer Cropscience Gmbh | Herbizid-Kombinationen mit speziellen Sulfonylharnstoffen |
US20050026781A1 (en) | 2003-04-22 | 2005-02-03 | Monsanto Technology Llc | Herbicidal compositions containing glyphosate and a pyridine analog |
ATE517548T1 (de) | 2004-03-10 | 2011-08-15 | Monsanto Technology Llc | Herbizide zusammensetzungen, die n- phosphonomethylglycin und ein auxinherbizid enthalten |
MY141272A (en) * | 2006-06-29 | 2010-04-16 | Dow Agrosciences Llc | High-strength, low-temperature stable herbicidal formulations of fluroxypyr esters |
JP5125126B2 (ja) * | 2007-01-31 | 2013-01-23 | 住友化学株式会社 | 疎水性農薬活性化合物を含有する農薬液剤 |
US20090054239A1 (en) * | 2007-08-22 | 2009-02-26 | Dow Agrosciences Llc | High-strength, low-temperature stable herbicidal formulations of fluroxypyr meptyl ester |
JP5256749B2 (ja) * | 2008-01-23 | 2013-08-07 | 住友化学株式会社 | 乳剤組成物 |
JP2009173578A (ja) * | 2008-01-24 | 2009-08-06 | Sumitomo Chemical Co Ltd | 乳剤組成物 |
JP5262131B2 (ja) * | 2008-01-24 | 2013-08-14 | 住友化学株式会社 | 乳剤組成物 |
EP2252146A2 (en) * | 2008-02-05 | 2010-11-24 | Arysta LifeScience North America, LLC | Solid formulation of low melting active compound |
WO2010053784A2 (en) * | 2008-10-29 | 2010-05-14 | Dow Agrosciences Llc | Stable emulsifiable concentrates containing a first herbicidal carboxylic acid salt and a second herbicidal carboxylic acid ester |
AU2010339608B2 (en) * | 2009-12-29 | 2015-07-30 | Syngenta Participations Ag | Pesticidal composition |
BR122019001044B1 (pt) | 2011-10-26 | 2019-08-27 | Monsanto Technology Llc | sais herbicidas de auxina, mistura de aplicação herbicida compreendendo os mesmos para uso na eliminação e controle do crescimento de plantas indesejadas, bem como métodos de controle de plantas indesejadas e de plantas suscetíveis ao herbicida de auxina |
US10736322B2 (en) | 2012-06-04 | 2020-08-11 | Monsanto Technology Llc | Aqueous concentrated herbicidal compositions containing glyphosate salts and dicamba salts |
EP2934113B1 (en) * | 2012-12-20 | 2019-08-21 | Dow AgroSciences LLC | Herbicidal compositions comprising fluroxypyr and flumetsulam |
CA2901680C (en) | 2013-02-27 | 2021-09-07 | Monsanto Technology Llc | Glyphosate composition for dicamba tank mixtures with improved volatility |
NZ741721A (en) | 2015-10-26 | 2019-08-30 | Dow Agrosciences Llc | Solid herbicide compositions containing fluroxypyr-meptyl |
WO2022152760A1 (en) | 2021-01-13 | 2022-07-21 | Nutrition & Biosciences Usa 1, Llc | Improved method for the preparation of colloidal microcrystalline cellulose |
EP4307890A1 (en) | 2021-03-17 | 2024-01-24 | Globachem NV | Herbicidal compositions of fluroxypyr |
WO2023110585A1 (en) | 2021-12-14 | 2023-06-22 | Nutrition & Biosciences Usa 1, Llc | Process for reducing nitrite in microcrystalline cellulose |
US11999684B1 (en) * | 2023-10-09 | 2024-06-04 | King Faisal University | Ethyl {[N'-(3-chlorophenyl)-N-(2,4-dichlorobenzoyl) carbamimidoyl]sulfanyl}acetate as an eco-friendly insecticidal agent against Spodoptera littoralis (boisd.) |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3755339A (en) * | 1971-07-26 | 1973-08-28 | Dow Chemical Co | Esters of aminohalopyridyloxy acids |
US4108629A (en) * | 1973-03-19 | 1978-08-22 | The Dow Chemical Company | Herbicidal use of esters of aminohalopyridyloxy acids |
US4542221A (en) * | 1981-05-18 | 1985-09-17 | The Dow Chemical Company | Exchanging fluorine for chlorine in a chlorinated pyridine with an alkali metal fluoride |
GB2100128B (en) * | 1981-06-15 | 1984-08-08 | Dow Chemical Co | A herbicidal composition |
GB2100129B (en) * | 1981-06-15 | 1984-08-30 | Dow Chemical Co | Composition for a herbicide |
GB8304829D0 (en) * | 1983-02-22 | 1983-03-23 | Fbc Ltd | Herbicide |
EP0441459A1 (en) * | 1985-07-02 | 1991-08-14 | Pioneer Electronic Corporation | Pulse-width modulation drive circuit |
WO1989003175A1 (en) * | 1987-10-14 | 1989-04-20 | Dow Chemical Company Limited | Agricultural compositions containing latexes |
BR9100532A (pt) * | 1990-02-09 | 1991-10-29 | Dowelanco | Processo para a preparacao de um ester de acido(4-amino-3,5-dicloro-6-fluoro-2-piridimilox)acetico e um alcool alifatico |
GB9109600D0 (en) * | 1991-05-03 | 1991-06-26 | Dow Chemical Co | Synergistic herbicidal compositions |
-
1993
- 1993-04-23 US US08/052,446 patent/US5374603A/en not_active Expired - Fee Related
- 1993-08-18 TW TW082106650A patent/TW272932B/zh active
- 1993-08-26 CO CO93404646A patent/CO4560532A1/es unknown
-
1994
- 1994-04-08 AU AU65569/94A patent/AU668472B2/en not_active Ceased
- 1994-04-08 CZ CZ19943283A patent/CZ287100B6/cs not_active IP Right Cessation
- 1994-04-08 DE DE69412200T patent/DE69412200T2/de not_active Expired - Fee Related
- 1994-04-08 RU RU95105586A patent/RU2139659C1/ru active
- 1994-04-08 WO PCT/US1994/003880 patent/WO1994024866A1/en active IP Right Grant
- 1994-04-08 HU HU9403753A patent/HU217371B/hu not_active IP Right Cessation
- 1994-04-08 KR KR1019940704681A patent/KR100232246B1/ko not_active Expired - Fee Related
- 1994-04-08 CA CA002138965A patent/CA2138965A1/en not_active Abandoned
- 1994-04-08 JP JP6524295A patent/JPH08501320A/ja not_active Ceased
- 1994-04-08 RO RO94-02086A patent/RO112425B1/ro unknown
- 1994-04-08 PL PL94306837A patent/PL177145B1/pl unknown
- 1994-04-08 ES ES94913390T patent/ES2122268T3/es not_active Expired - Lifetime
- 1994-04-08 CN CN94190218A patent/CN1068171C/zh not_active Expired - Fee Related
- 1994-04-08 DK DK94913390T patent/DK0647096T3/da active
- 1994-04-08 BR BR9405242-5A patent/BR9405242A/pt not_active Application Discontinuation
- 1994-04-08 EP EP94913390A patent/EP0647096B1/en not_active Expired - Lifetime
- 1994-04-21 IL IL109362A patent/IL109362A/en not_active IP Right Cessation
- 1994-04-21 MY MYPI94000985A patent/MY110710A/en unknown
- 1994-04-22 ZA ZA942814A patent/ZA942814B/xx unknown
- 1994-04-26 US US08/233,207 patent/US5436223A/en not_active Expired - Fee Related
- 1994-08-04 UA UA95018061A patent/UA39874C2/uk unknown
- 1994-12-22 FI FI946037A patent/FI107012B/fi active
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
DGB9 | Succession in title of applicant |
Owner name: DOW AGROSCIENCES LLC, US |
|
HMM4 | Cancellation of final prot. due to non-payment of fee |