SK5202003A3 - Agrochemical composition in the form of a suspension concentrate comprising a surface-active compound and a quinoline antidote, use thereof for the growth control of undesirable plants, and a quinoline antidote - Google Patents

Agrochemical composition in the form of a suspension concentrate comprising a surface-active compound and a quinoline antidote, use thereof for the growth control of undesirable plants, and a quinoline antidote Download PDF

Info

Publication number: SK5202003A3
Authority: SK; Slovakia
Prior art keywords: antidote; quinoline; composition according; herbicide; formula
Prior art date: 2000-11-01

Application number

SK520-2003A

Other languages

English (en)

Slovak (sk)

Inventor

Hans Walter Haesslin

Fritz Blatter

Original Assignee

Syngenta Participations Ag

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.)

2000-11-01

Filing date

2001-10-29

Publication date

2004-03-02

2001-10-29 Application filed by Syngenta Participations Ag filed Critical Syngenta Participations Ag

2004-03-02 Publication of SK5202003A3 publication Critical patent/SK5202003A3/sk

Links

239000004094 surface-active agent Substances 0.000 title claims abstract description 35
SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 title claims abstract description 18
239000004546 suspension concentrate Substances 0.000 title claims abstract description 10
239000012872 agrochemical composition Substances 0.000 title claims abstract description 4
239000000729 antidote Substances 0.000 title claims description 45
239000000203 mixture Substances 0.000 claims abstract description 50
238000009472 formulation Methods 0.000 claims abstract description 4
239000004009 herbicide Substances 0.000 claims description 33
230000002363 herbicidal effect Effects 0.000 claims description 25
150000001875 compounds Chemical class 0.000 claims description 15
239000002736 nonionic surfactant Substances 0.000 claims description 12
238000000034 method Methods 0.000 claims description 10
239000002671 adjuvant Substances 0.000 claims description 7
239000003945 anionic surfactant Substances 0.000 claims description 6
229920000058 polyacrylate Polymers 0.000 claims description 6
239000003093 cationic surfactant Substances 0.000 claims description 5
239000003085 diluting agent Substances 0.000 claims description 5
229920000728 polyester Polymers 0.000 claims description 5
239000000654 additive Substances 0.000 claims description 4
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims description 4
239000000843 powder Substances 0.000 claims description 4
239000007859 condensation product Substances 0.000 claims description 3
QQVIHTHCMHWDBS-UHFFFAOYSA-L isophthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC(C([O-])=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-L 0.000 claims description 3
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125000002091 cationic group Chemical group 0.000 claims description 2
238000010790 dilution Methods 0.000 claims 2
239000012895 dilution Substances 0.000 claims 2
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125000000129 anionic group Chemical group 0.000 claims 1
WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 claims 1
VFNGKCDDZUSWLR-UHFFFAOYSA-M sulfo sulfate Chemical compound OS(=O)(=O)OS([O-])(=O)=O VFNGKCDDZUSWLR-UHFFFAOYSA-M 0.000 claims 1
-1 carbazones Chemical class 0.000 description 29
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125000004432 carbon atom Chemical group C* 0.000 description 13
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PRXRUNOAOLTIEF-ADSICKODSA-N Sorbitan trioleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@@H](OC(=O)CCCCCCC\C=C/CCCCCCCC)[C@H]1OC[C@H](O)[C@H]1OC(=O)CCCCCCC\C=C/CCCCCCCC PRXRUNOAOLTIEF-ADSICKODSA-N 0.000 description 2
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JTHMVYBOQLDDIY-UHFFFAOYSA-N methyl 2-[(4-methyl-5-oxo-3-propoxy-1,2,4-triazole-1-carbonyl)sulfamoyl]benzoate Chemical compound O=C1N(C)C(OCCC)=NN1C(=O)NS(=O)(=O)C1=CC=CC=C1C(=O)OC JTHMVYBOQLDDIY-UHFFFAOYSA-N 0.000 description 2
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244000098338 Triticum aestivum Species 0.000 description 1
239000005629 Tritosulfuron Substances 0.000 description 1
240000001260 Tropaeolum majus Species 0.000 description 1
235000004424 Tropaeolum majus Nutrition 0.000 description 1
240000005592 Veronica officinalis Species 0.000 description 1
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
241000405217 Viola <butterfly> Species 0.000 description 1
241001506766 Xanthium Species 0.000 description 1
240000008042 Zea mays Species 0.000 description 1
235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 1
235000002017 Zea mays subsp mays Nutrition 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
125000005907 alkyl ester group Chemical group 0.000 description 1
229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
150000008052 alkyl sulfonates Chemical class 0.000 description 1
230000003042 antagnostic effect Effects 0.000 description 1
239000002518 antifoaming agent Substances 0.000 description 1
229940111121 antirheumatic drug quinolines Drugs 0.000 description 1
239000007900 aqueous suspension Substances 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
XOEMATDHVZOBSG-UHFFFAOYSA-N azafenidin Chemical compound C1=C(OCC#C)C(Cl)=CC(Cl)=C1N1C(=O)N2CCCCC2=N1 XOEMATDHVZOBSG-UHFFFAOYSA-N 0.000 description 1
235000015278 beef Nutrition 0.000 description 1
PPWBRCCBKOWDNB-UHFFFAOYSA-N bensulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)CC=2C(=CC=CC=2)C(O)=O)=N1 PPWBRCCBKOWDNB-UHFFFAOYSA-N 0.000 description 1
150000001556 benzimidazoles Chemical class 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
239000011575 calcium Substances 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
159000000007 calcium salts Chemical class 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
235000013339 cereals Nutrition 0.000 description 1
NNKKTZOEKDFTBU-YBEGLDIGSA-N cinidon ethyl Chemical group C1=C(Cl)C(/C=C(\Cl)C(=O)OCC)=CC(N2C(C3=C(CCCC3)C2=O)=O)=C1 NNKKTZOEKDFTBU-YBEGLDIGSA-N 0.000 description 1
HUBANNPOLNYSAD-UHFFFAOYSA-N clopyralid Chemical compound OC(=O)C1=NC(Cl)=CC=C1Cl HUBANNPOLNYSAD-UHFFFAOYSA-N 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
238000002425 crystallisation Methods 0.000 description 1
230000008025 crystallization Effects 0.000 description 1
230000000254 damaging effect Effects 0.000 description 1
229910003460 diamond Inorganic materials 0.000 description 1
239000010432 diamond Substances 0.000 description 1
IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 description 1
238000002050 diffraction method Methods 0.000 description 1
238000007598 dipping method Methods 0.000 description 1
229940060296 dodecylbenzenesulfonic acid Drugs 0.000 description 1
238000001035 drying Methods 0.000 description 1
230000000694 effects Effects 0.000 description 1
239000004495 emulsifiable concentrate Substances 0.000 description 1
230000001804 emulsifying effect Effects 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
150000002171 ethylene diamines Chemical class 0.000 description 1
GINFBXXYGUODAT-UHFFFAOYSA-N flucarbazone Chemical compound O=C1N(C)C(OC)=NN1C(=O)NS(=O)(=O)C1=CC=CC=C1OC(F)(F)F GINFBXXYGUODAT-UHFFFAOYSA-N 0.000 description 1
IANUJLZYFUDJIH-UHFFFAOYSA-N flufenacet Chemical compound C=1C=C(F)C=CC=1N(C(C)C)C(=O)COC1=NN=C(C(F)(F)F)S1 IANUJLZYFUDJIH-UHFFFAOYSA-N 0.000 description 1
WFZSZAXUALBVNX-UHFFFAOYSA-N flufenpyr Chemical compound O=C1C(C)=C(C(F)(F)F)C=NN1C1=CC(OCC(O)=O)=C(Cl)C=C1F WFZSZAXUALBVNX-UHFFFAOYSA-N 0.000 description 1
MEFQWPUMEMWTJP-UHFFFAOYSA-N fluroxypyr Chemical compound NC1=C(Cl)C(F)=NC(OCC(O)=O)=C1Cl MEFQWPUMEMWTJP-UHFFFAOYSA-N 0.000 description 1
PXDNXJSDGQBLKS-UHFFFAOYSA-N foramsulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=C(NC=O)C=2)C(=O)N(C)C)=N1 PXDNXJSDGQBLKS-UHFFFAOYSA-N 0.000 description 1
239000008098 formaldehyde solution Substances 0.000 description 1
229910052733 gallium Inorganic materials 0.000 description 1
238000000227 grinding Methods 0.000 description 1
230000009931 harmful effect Effects 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
239000012669 liquid formulation Substances 0.000 description 1
235000009973 maize Nutrition 0.000 description 1
239000011785 micronutrient Substances 0.000 description 1
235000013369 micronutrients Nutrition 0.000 description 1
235000019713 millet Nutrition 0.000 description 1
239000011707 mineral Substances 0.000 description 1
235000010446 mineral oil Nutrition 0.000 description 1
PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
RTCOGUMHFFWOJV-UHFFFAOYSA-N nicosulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CN=2)C(=O)N(C)C)=N1 RTCOGUMHFFWOJV-UHFFFAOYSA-N 0.000 description 1
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical class CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Chemical class CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical class CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
235000021317 phosphate Nutrition 0.000 description 1
150000003904 phospholipids Chemical class 0.000 description 1
150000003014 phosphoric acid esters Chemical class 0.000 description 1
230000000885 phytotoxic effect Effects 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920001983 poloxamer Polymers 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
229920000136 polysorbate Polymers 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
159000000001 potassium salts Chemical class 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
239000003755 preservative agent Substances 0.000 description 1
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
YXIIPOGUBVYZIW-UHFFFAOYSA-N pyraflufen Chemical compound ClC1=C(OC(F)F)N(C)N=C1C1=CC(OCC(O)=O)=C(Cl)C=C1F YXIIPOGUBVYZIW-UHFFFAOYSA-N 0.000 description 1
150000003248 quinolines Chemical class 0.000 description 1
238000010188 recombinant method Methods 0.000 description 1
235000009566 rice Nutrition 0.000 description 1
MEFOUWRMVYJCQC-UHFFFAOYSA-N rimsulfuron Chemical compound CCS(=O)(=O)C1=CC=CN=C1S(=O)(=O)NC(=O)NC1=NC(OC)=CC(OC)=N1 MEFOUWRMVYJCQC-UHFFFAOYSA-N 0.000 description 1
235000019512 sardine Nutrition 0.000 description 1
229920005552 sodium lignosulfonate Polymers 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000003549 soybean oil Substances 0.000 description 1
235000012424 soybean oil Nutrition 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
239000008117 stearic acid Chemical class 0.000 description 1
125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 1
229940124530 sulfonamide Drugs 0.000 description 1
150000003456 sulfonamides Chemical class 0.000 description 1
150000003460 sulfonic acids Chemical class 0.000 description 1
239000002600 sunflower oil Substances 0.000 description 1
150000004685 tetrahydrates Chemical class 0.000 description 1
ZFXYFBGIUFBOJW-UHFFFAOYSA-N theophylline Chemical compound O=C1N(C)C(=O)N(C)C2=C1NC=N2 ZFXYFBGIUFBOJW-UHFFFAOYSA-N 0.000 description 1
229960000278 theophylline Drugs 0.000 description 1
DQFPEYARZIQXRM-LTGZKZEYSA-N tralkoxydim Chemical compound C1C(=O)C(C(/CC)=N/OCC)=C(O)CC1C1=C(C)C=C(C)C=C1C DQFPEYARZIQXRM-LTGZKZEYSA-N 0.000 description 1
XOPFESVZMSQIKC-UHFFFAOYSA-N triasulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)OCCCl)=N1 XOPFESVZMSQIKC-UHFFFAOYSA-N 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
KVEQCVKVIFQSGC-UHFFFAOYSA-N tritosulfuron Chemical compound FC(F)(F)C1=NC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(F)(F)F)=N1 KVEQCVKVIFQSGC-UHFFFAOYSA-N 0.000 description 1
239000004563 wettable powder Substances 0.000 description 1
238000009736 wetting Methods 0.000 description 1
239000000230 xanthan gum Substances 0.000 description 1
235000010493 xanthan gum Nutrition 0.000 description 1
229920001285 xanthan gum Polymers 0.000 description 1
229940082509 xanthan gum Drugs 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms 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
- C07D215/20—Oxygen atoms
- C07D215/24—Oxygen atoms attached in position 8
- C07D215/26—Alcohols; Ethers thereof
- C07D215/28—Alcohols; Ethers thereof with halogen atoms or nitro radicals in positions 5, 6 or 7
- 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
- A01N43/42—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 condensed with carbocyclic rings

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
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)
Quinoline Compounds (AREA)

SK520-2003A 2000-11-01 2001-10-29 Agrochemical composition in the form of a suspension concentrate comprising a surface-active compound and a quinoline antidote, use thereof for the growth control of undesirable plants, and a quinoline antidote SK5202003A3 (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
CH21352000		2000-11-01
PCT/EP2001/012482 WO2002036566A1 (en)	2000-11-01	2001-10-29	Agrochemical composition

Publications (1)

Publication Number	Publication Date
SK5202003A3 true SK5202003A3 (en)	2004-03-02

Family

ID=4567645

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SK520-2003A SK5202003A3 (en)	2000-11-01	2001-10-29	Agrochemical composition in the form of a suspension concentrate comprising a surface-active compound and a quinoline antidote, use thereof for the growth control of undesirable plants, and a quinoline antidote

Country Status (17)

Country	Link
US (1)	US20040038824A1 (pl)
EP (1)	EP1330438A1 (pl)
JP (1)	JP2004513115A (pl)
CN (1)	CN1471513A (pl)
AR (1)	AR034419A1 (pl)
AU (1)	AU2002221774A1 (pl)
BR (1)	BR0115026A (pl)
CA (1)	CA2425023A1 (pl)
EA (1)	EA200300505A1 (pl)
GT (1)	GT200100218A (pl)
HU (1)	HUP0301593A3 (pl)
MX (1)	MXPA03003747A (pl)
PL (1)	PL362967A1 (pl)
SK (1)	SK5202003A3 (pl)
TR (1)	TR200300551T2 (pl)
WO (1)	WO2002036566A1 (pl)
ZA (1)	ZA200302583B (pl)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US6911421B2 (en) *	2002-11-01	2005-06-28	Nicca Usa, Inc.	Surfactant blends for removing oligomer deposits from polyester fibers and polyester processing equipment
UA109416C2 (xx)	2009-10-06	2015-08-25		Стабільні емульсії типу "масло в воді"
NZ603014A (en) *	2010-04-26	2014-10-31	Dow Agrosciences Llc	Stabilized agricultural oil dispersions
WO2012108873A1 (en) *	2011-02-11	2012-08-16	Dow Agrosciences Llc	Stable agrochemical oil dispersions
ES2716878T3 (es) *	2012-12-21	2019-06-17	Dow Agrosciences Llc	Composiciones acuosas de cloquintocet-mexil termoestables
JP2016145188A (ja) *	2015-12-28	2016-08-12	ダウアグロサイエンシィズエルエルシー	安定な農薬油分散体
EP3278666A1 (de) *	2016-08-04	2018-02-07	Bayer CropScience Aktiengesellschaft	Wässrige kapselsuspensionskonzentrate auf basis von 2-(2,4-dichlorbenzyl)-4,4-dimethyl-1,2-oxazolidin-3-on
WO2021055314A1 (en) *	2019-09-16	2021-03-25	Eastman Chemical Company	Substantially non-phytotoxic formulation containing a sulfopolymer
US20220361484A1 (en) *	2019-09-16	2022-11-17	Eastman Chemical Company	Rapid dispersal formulation containing a sulfopolymer
WO2021055316A1 (en) *	2019-09-16	2021-03-25	Eastman Chemical Company	Agricultural inert package formulation containing a sulfopolymer
CN119632025B (zh) *	2024-11-27	2025-10-31	深圳诺普信作物科学股份有限公司	干悬浮剂及其制备方法和应用

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4505743A (en) *	1981-12-31	1985-03-19	Ciba-Geigy Corporation	α-[4-(3-Fluoro-5'-halopyridyl-2'-oxy)-phenoxy]-propionic acid derivatives having herbicidal activity
EP0551650B1 (de) *	1991-12-31	1999-10-13	Hoechst Schering AgrEvo GmbH	Kombinationen aus Herbiziden und pflanzenschützenden Stoffen
WO1994000987A2 (en) *	1992-07-08	1994-01-20	Ciba-Geigy Ag	Selective herbicidal composition
US5674514A (en) *	1992-09-21	1997-10-07	Ciba-Geigy Corporation	Storage stable pesticidal aqueous emulsions
AU3183199A (en) *	1998-05-14	1999-11-29	E.I. Du Pont De Nemours And Company	Crop-safened herbicidal mixtures

2001
- 2001-10-29 WO PCT/EP2001/012482 patent/WO2002036566A1/en not_active Ceased
- 2001-10-29 CA CA002425023A patent/CA2425023A1/en not_active Abandoned
- 2001-10-29 CN CNA018181988A patent/CN1471513A/zh active Pending
- 2001-10-29 AU AU2002221774A patent/AU2002221774A1/en not_active Abandoned
- 2001-10-29 MX MXPA03003747A patent/MXPA03003747A/es not_active Application Discontinuation
- 2001-10-29 PL PL01362967A patent/PL362967A1/pl not_active Application Discontinuation
- 2001-10-29 JP JP2002539326A patent/JP2004513115A/ja active Pending
- 2001-10-29 BR BR0115026-0A patent/BR0115026A/pt not_active Application Discontinuation
- 2001-10-29 HU HU0301593A patent/HUP0301593A3/hu unknown
- 2001-10-29 EA EA200300505A patent/EA200300505A1/ru unknown
- 2001-10-29 SK SK520-2003A patent/SK5202003A3/sk unknown
- 2001-10-29 US US10/415,565 patent/US20040038824A1/en not_active Abandoned
- 2001-10-29 EP EP01992701A patent/EP1330438A1/en not_active Withdrawn
- 2001-10-29 TR TR2003/00551T patent/TR200300551T2/xx unknown
- 2001-10-30 AR ARP010105070A patent/AR034419A1/es unknown
- 2001-10-31 GT GT200100218A patent/GT200100218A/es unknown
2003
- 2003-04-02 ZA ZA200302583A patent/ZA200302583B/en unknown

Also Published As

Publication number	Publication date
EA200300505A1 (ru)	2003-10-30
HUP0301593A2 (hu)	2003-10-28
EP1330438A1 (en)	2003-07-30
CA2425023A1 (en)	2002-05-10
BR0115026A (pt)	2003-12-23
JP2004513115A (ja)	2004-04-30
TR200300551T2 (tr)	2003-09-22
AU2002221774A1 (en)	2002-05-15
AR034419A1 (es)	2004-02-25
GT200100218A (es)	2002-06-13
PL362967A1 (pl)	2004-11-02
MXPA03003747A (es)	2003-07-28
US20040038824A1 (en)	2004-02-26
WO2002036566A1 (en)	2002-05-10
HUP0301593A3 (en)	2004-11-29
ZA200302583B (en)	2004-04-28
CN1471513A (zh)	2004-01-28

Publication	Publication Date	Title
SK4722003A3 (en)	2003-09-11	Agrochemical compositions with quinoline safeners and use thereof
ES2259425T3 (es)	2006-10-01	Nuevos herbicidas.
EP1128729B1 (en)	2003-05-21	Herbicidal composition
US6770594B2 (en)	2004-08-03	Herbicidal compositions
KR20050088183A (ko)	2005-09-02	미세유제 농축액
AU2004260586B2 (en)	2009-08-06	Ternary herbicidal combinations comprising special sulphonamides
BG64030B1 (bg)	2003-11-28	Хербицидни средства с n-[(4,6-диметоксипиримидин-2-ил) аминокарбонил]-5-метилсулфонамидометил-2-алкоксикарбо- нилбензенсулфонамиди
MXPA04008676A (es)	2004-12-06	Combinaciones de herbicidas con sulfonilureas especiales.
CA3011264C (en)	2024-04-09	Aqueous dispersions containing aclonifen and flufenacet
KR20050021461A (ko)	2005-03-07	액체 애주번트
US20040038824A1 (en)	2004-02-26	Agrochemical composition
US6017850A (en)	2000-01-25	Herbicidal composition and method of weed control
US6511941B2 (en)	2003-01-28	Herbicidal synergistic composition, and method of controlling weeds
US20050026783A1 (en)	2005-02-03	Herbicide combinations comprising specific sulfonamides
AU2004259166B2 (en)	2010-06-10	Herbicide combinations with specific sulfonamides
KR20050021460A (ko)	2005-03-07	고체 애주번트