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
150000002790 naphthalenes Chemical class 0.000 claims description 3
229920000036 polyvinylpyrrolidone Polymers 0.000 claims description 3
235000013855 polyvinylpyrrolidone Nutrition 0.000 claims description 3
150000003467 sulfuric acid derivatives Chemical class 0.000 claims description 3
TVFWYUWNQVRQRG-UHFFFAOYSA-N 2,3,4-tris(2-phenylethenyl)phenol Chemical compound C=1C=CC=CC=1C=CC1=C(C=CC=2C=CC=CC=2)C(O)=CC=C1C=CC1=CC=CC=C1 TVFWYUWNQVRQRG-UHFFFAOYSA-N 0.000 claims description 2
125000002091 cationic group Chemical group 0.000 claims description 2
238000010790 dilution Methods 0.000 claims 2
239000012895 dilution Substances 0.000 claims 2
244000045561 useful plants Species 0.000 claims 2
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
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 20
125000004432 carbon atom Chemical group C* 0.000 description 13
125000000217 alkyl group Chemical group 0.000 description 12
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
241000196324 Embryophyta Species 0.000 description 10
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 10
235000014113 dietary fatty acids Nutrition 0.000 description 10
239000000194 fatty acid Substances 0.000 description 10
229930195729 fatty acid Natural products 0.000 description 10
229940075522 antidotes Drugs 0.000 description 7
150000004665 fatty acids Chemical class 0.000 description 7
239000000725 suspension Substances 0.000 description 6
235000015112 vegetable and seed oil Nutrition 0.000 description 6
239000008158 vegetable oil Substances 0.000 description 6
239000002253 acid Substances 0.000 description 5
COYBRKAVBMYYSF-UHFFFAOYSA-N heptan-2-yl [(5-chloroquinolin-8-yl)oxy]acetate Chemical compound C1=CN=C2C(OCC(=O)OC(C)CCCCC)=CC=C(Cl)C2=C1 COYBRKAVBMYYSF-UHFFFAOYSA-N 0.000 description 5
229910052757 nitrogen Inorganic materials 0.000 description 5
239000003921 oil Substances 0.000 description 5
235000019198 oils Nutrition 0.000 description 5
238000000634 powder X-ray diffraction Methods 0.000 description 5
239000000126 substance Substances 0.000 description 5
LQIAZOCLNBBZQK-UHFFFAOYSA-N 1-(1,2-Diphosphanylethyl)pyrrolidin-2-one Chemical compound PCC(P)N1CCCC1=O LQIAZOCLNBBZQK-UHFFFAOYSA-N 0.000 description 4
IGFHQQFPSIBGKE-UHFFFAOYSA-N 4-nonylphenol Chemical compound CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 4
229920001214 Polysorbate 60 Polymers 0.000 description 4
239000013543 active substance Substances 0.000 description 4
150000008055 alkyl aryl sulfonates Chemical class 0.000 description 4
239000003795 chemical substances by application Substances 0.000 description 4
238000010586 diagram Methods 0.000 description 4
150000002170 ethers Chemical class 0.000 description 4
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 4
229920001451 polypropylene glycol Polymers 0.000 description 4
238000002360 preparation method Methods 0.000 description 4
239000000047 product Substances 0.000 description 4
150000003839 salts Chemical class 0.000 description 4
125000001424 substituent group Chemical group 0.000 description 4
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
229920003171 Poly (ethylene oxide) Polymers 0.000 description 3
239000002202 Polyethylene glycol Substances 0.000 description 3
150000007513 acids Chemical class 0.000 description 3
239000004480 active ingredient Substances 0.000 description 3
239000003905 agrochemical Substances 0.000 description 3
239000003240 coconut oil Substances 0.000 description 3
235000019864 coconut oil Nutrition 0.000 description 3
239000012141 concentrate Substances 0.000 description 3
239000007788 liquid Substances 0.000 description 3
238000002156 mixing Methods 0.000 description 3
150000003013 phosphoric acid derivatives Chemical class 0.000 description 3
229920001223 polyethylene glycol Polymers 0.000 description 3
229920000151 polyglycol Polymers 0.000 description 3
239000010695 polyglycol Substances 0.000 description 3
229910052708 sodium Inorganic materials 0.000 description 3
239000011734 sodium Substances 0.000 description 3
QFMDFTQOJHFVNR-UHFFFAOYSA-N 1-[2,2-dichloro-1-(4-ethylphenyl)ethyl]-4-ethylbenzene Chemical compound C1=CC(CC)=CC=C1C(C(Cl)Cl)C1=CC=C(CC)C=C1 QFMDFTQOJHFVNR-UHFFFAOYSA-N 0.000 description 2
YZTJKOLMWJNVFH-UHFFFAOYSA-N 2-sulfobenzene-1,3-dicarboxylic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1S(O)(=O)=O YZTJKOLMWJNVFH-UHFFFAOYSA-N 0.000 description 2
CAAMSDWKXXPUJR-UHFFFAOYSA-N 3,5-dihydro-4H-imidazol-4-one Chemical class O=C1CNC=N1 CAAMSDWKXXPUJR-UHFFFAOYSA-N 0.000 description 2
244000182067 Fraxinus ornus Species 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
241001465754 Metazoa Species 0.000 description 2
241000209504 Poaceae Species 0.000 description 2
239000004721 Polyphenylene oxide Substances 0.000 description 2
239000004743 Polypropylene Substances 0.000 description 2
239000005601 Propoxycarbazone Substances 0.000 description 2
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical group CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 2
235000019484 Rapeseed oil Nutrition 0.000 description 2
239000004147 Sorbitan trioleate Substances 0.000 description 2
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
244000062793 Sorghum vulgare Species 0.000 description 2
VBIIFPGSPJYLRR-UHFFFAOYSA-M Stearyltrimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)C VBIIFPGSPJYLRR-UHFFFAOYSA-M 0.000 description 2
229940100389 Sulfonylurea Drugs 0.000 description 2
150000001298 alcohols Chemical class 0.000 description 2
125000001931 aliphatic group Chemical group 0.000 description 2
229910052783 alkali metal Inorganic materials 0.000 description 2
229910052784 alkaline earth metal Inorganic materials 0.000 description 2
150000008051 alkyl sulfates Chemical class 0.000 description 2
150000003863 ammonium salts Chemical class 0.000 description 2
239000010775 animal oil Substances 0.000 description 2
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
BCOZLGOHQFNXBI-UHFFFAOYSA-M benzyl-bis(2-chloroethyl)-ethylazanium;bromide Chemical compound [Br-].ClCC[N+](CC)(CCCl)CC1=CC=CC=C1 BCOZLGOHQFNXBI-UHFFFAOYSA-M 0.000 description 2
239000004359 castor oil Substances 0.000 description 2
235000019438 castor oil Nutrition 0.000 description 2
244000038559 crop plants Species 0.000 description 2
OILAIQUEIWYQPH-UHFFFAOYSA-N cyclohexane-1,2-dione Chemical class O=C1CCCCC1=O OILAIQUEIWYQPH-UHFFFAOYSA-N 0.000 description 2
239000003599 detergent Substances 0.000 description 2
239000003995 emulsifying agent Substances 0.000 description 2
235000019441 ethanol Nutrition 0.000 description 2
150000005452 ethyl sulfates Chemical class 0.000 description 2
150000002191 fatty alcohols Chemical class 0.000 description 2
239000003337 fertilizer Substances 0.000 description 2
229940013317 fish oils Drugs 0.000 description 2
ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 2
150000004820 halides Chemical class 0.000 description 2
125000001183 hydrocarbyl group Chemical group 0.000 description 2
125000002768 hydroxyalkyl group Chemical group 0.000 description 2
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
150000005451 methyl sulfates Chemical class 0.000 description 2
239000002480 mineral oil Substances 0.000 description 2
125000004433 nitrogen atom Chemical group N* 0.000 description 2
UYDLBVPAAFVANX-UHFFFAOYSA-N octylphenoxy polyethoxyethanol Chemical compound CC(C)(C)CC(C)(C)C1=CC=C(OCCOCCOCCOCCO)C=C1 UYDLBVPAAFVANX-UHFFFAOYSA-N 0.000 description 2
238000005554 pickling Methods 0.000 description 2
229920000570 polyether Polymers 0.000 description 2
150000003242 quaternary ammonium salts Chemical class 0.000 description 2
229920006395 saturated elastomer Polymers 0.000 description 2
150000004671 saturated fatty acids Chemical class 0.000 description 2
235000003441 saturated fatty acids Nutrition 0.000 description 2
229920002545 silicone oil Polymers 0.000 description 2
239000002689 soil Substances 0.000 description 2
229960000391 sorbitan trioleate Drugs 0.000 description 2
235000019337 sorbitan trioleate Nutrition 0.000 description 2
238000009331 sowing Methods 0.000 description 2
239000007921 spray Substances 0.000 description 2
238000003756 stirring Methods 0.000 description 2
239000003760 tallow Substances 0.000 description 2
150000004670 unsaturated fatty acids Chemical class 0.000 description 2
235000021122 unsaturated fatty acids Nutrition 0.000 description 2
235000013311 vegetables Nutrition 0.000 description 2
WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
RBSXHDIPCIWOMG-UHFFFAOYSA-N 1-(4,6-dimethoxypyrimidin-2-yl)-3-(2-ethylsulfonylimidazo[1,2-a]pyridin-3-yl)sulfonylurea Chemical compound CCS(=O)(=O)C=1N=C2C=CC=CN2C=1S(=O)(=O)NC(=O)NC1=NC(OC)=CC(OC)=N1 RBSXHDIPCIWOMG-UHFFFAOYSA-N 0.000 description 1
239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 description 1
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
WNTGYJSOUMFZEP-UHFFFAOYSA-N 2-(4-chloro-2-methylphenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C=C1C WNTGYJSOUMFZEP-UHFFFAOYSA-N 0.000 description 1
NUPJIGQFXCQJBK-UHFFFAOYSA-N 2-(4-isopropyl-4-methyl-5-oxo-4,5-dihydro-1H-imidazol-2-yl)-5-(methoxymethyl)nicotinic acid Chemical compound OC(=O)C1=CC(COC)=CN=C1C1=NC(C)(C(C)C)C(=O)N1 NUPJIGQFXCQJBK-UHFFFAOYSA-N 0.000 description 1
GOCUAJYOYBLQRH-UHFFFAOYSA-N 2-(4-{[3-chloro-5-(trifluoromethyl)pyridin-2-yl]oxy}phenoxy)propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=NC=C(C(F)(F)F)C=C1Cl GOCUAJYOYBLQRH-UHFFFAOYSA-N 0.000 description 1
YUVKUEAFAVKILW-UHFFFAOYSA-N 2-(4-{[5-(trifluoromethyl)pyridin-2-yl]oxy}phenoxy)propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=CC=C(C(F)(F)F)C=N1 YUVKUEAFAVKILW-UHFFFAOYSA-N 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
HCNBYBFTNHEQQJ-UHFFFAOYSA-N 2-[(4,6-dimethoxypyrimidin-2-yl)carbamoylsulfamoyl]-6-(trifluoromethyl)pyridine-3-carboxylic acid Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=C(N=2)C(F)(F)F)C(O)=O)=N1 HCNBYBFTNHEQQJ-UHFFFAOYSA-N 0.000 description 1
UWHURBUBIHUHSU-UHFFFAOYSA-N 2-[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamoylsulfamoyl]benzoic acid Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 UWHURBUBIHUHSU-UHFFFAOYSA-N 0.000 description 1
JDSQBDGCMUXRBM-UHFFFAOYSA-N 2-[2-(2-butoxypropoxy)propoxy]propan-1-ol Chemical group CCCCOC(C)COC(C)COC(C)CO JDSQBDGCMUXRBM-UHFFFAOYSA-N 0.000 description 1
IOYNQIMAUDJVEI-ZFNPBRLTSA-N 2-[N-[(E)-3-chloroprop-2-enoxy]-C-ethylcarbonimidoyl]-3-hydroxy-5-(oxan-4-yl)cyclohex-2-en-1-one Chemical compound C1C(=O)C(C(=NOC\C=C\Cl)CC)=C(O)CC1C1CCOCC1 IOYNQIMAUDJVEI-ZFNPBRLTSA-N 0.000 description 1
WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical class CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 description 1
LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
FOGYNLXERPKEGN-UHFFFAOYSA-N 3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfopropyl)phenoxy]propane-1-sulfonic acid Chemical compound COC1=CC=CC(CC(CS(O)(=O)=O)OC=2C(=CC(CCCS(O)(=O)=O)=CC=2)OC)=C1O FOGYNLXERPKEGN-UHFFFAOYSA-N 0.000 description 1
MBFHUWCOCCICOK-UHFFFAOYSA-N 4-iodo-2-[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamoylsulfamoyl]benzoic acid Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=C(I)C=2)C(O)=O)=N1 MBFHUWCOCCICOK-UHFFFAOYSA-N 0.000 description 1
QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
241000219144 Abutilon Species 0.000 description 1
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
241000743339 Agrostis Species 0.000 description 1
241000743985 Alopecurus Species 0.000 description 1
241000219318 Amaranthus Species 0.000 description 1
ITPDYQOUSLNIHG-UHFFFAOYSA-N Amiodarone hydrochloride Chemical compound [Cl-].CCCCC=1OC2=CC=CC=C2C=1C(=O)C1=CC(I)=C(OCC[NH+](CC)CC)C(I)=C1 ITPDYQOUSLNIHG-UHFFFAOYSA-N 0.000 description 1
235000005781 Avena Nutrition 0.000 description 1
244000075850 Avena orientalis Species 0.000 description 1
241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 1
241000339490 Brachyachne Species 0.000 description 1
241000209200 Bromus Species 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
241000219312 Chenopodium Species 0.000 description 1
235000007516 Chrysanthemum Nutrition 0.000 description 1
240000005250 Chrysanthemum indicum Species 0.000 description 1
WMLPCIHUFDKWJU-UHFFFAOYSA-N Cinosulfuron Chemical compound COCCOC1=CC=CC=C1S(=O)(=O)NC(=O)NC1=NC(OC)=NC(OC)=N1 WMLPCIHUFDKWJU-UHFFFAOYSA-N 0.000 description 1
229920000742 Cotton Polymers 0.000 description 1
241000234653 Cyperus Species 0.000 description 1
239000005504 Dicamba Substances 0.000 description 1
QNXAVFXEJCPCJO-UHFFFAOYSA-N Diclosulam Chemical compound N=1N2C(OCC)=NC(F)=CC2=NC=1S(=O)(=O)NC1=C(Cl)C=CC=C1Cl QNXAVFXEJCPCJO-UHFFFAOYSA-N 0.000 description 1
235000017896 Digitaria Nutrition 0.000 description 1
241001303487 Digitaria <clam> Species 0.000 description 1
241000192043 Echinochloa Species 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
LLQPHQFNMLZJMP-UHFFFAOYSA-N Fentrazamide Chemical compound N1=NN(C=2C(=CC=CC=2)Cl)C(=O)N1C(=O)N(CC)C1CCCCC1 LLQPHQFNMLZJMP-UHFFFAOYSA-N 0.000 description 1
239000005529 Florasulam Substances 0.000 description 1
QZXATCCPQKOEIH-UHFFFAOYSA-N Florasulam Chemical compound N=1N2C(OC)=NC=C(F)C2=NC=1S(=O)(=O)NC1=C(F)C=CC=C1F QZXATCCPQKOEIH-UHFFFAOYSA-N 0.000 description 1
239000005531 Flufenacet Substances 0.000 description 1
239000005558 Fluroxypyr Substances 0.000 description 1
239000005560 Foramsulfuron Substances 0.000 description 1
GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 description 1
244000068988 Glycine max Species 0.000 description 1
235000010469 Glycine max Nutrition 0.000 description 1
241000219146 Gossypium Species 0.000 description 1
239000005566 Imazamox Substances 0.000 description 1
PMAAYIYCDXGUAP-UHFFFAOYSA-N Indanofan Chemical compound O=C1C2=CC=CC=C2C(=O)C1(CC)CC1(C=2C=C(Cl)C=CC=2)CO1 PMAAYIYCDXGUAP-UHFFFAOYSA-N 0.000 description 1
239000005568 Iodosulfuron Substances 0.000 description 1
235000021506 Ipomoea Nutrition 0.000 description 1
241000207783 Ipomoea Species 0.000 description 1
241000520028 Lamium Species 0.000 description 1
241000209082 Lolium Species 0.000 description 1
235000003990 Monochoria hastata Nutrition 0.000 description 1
240000000178 Monochoria vaginalis Species 0.000 description 1
239000005586 Nicosulfuron Substances 0.000 description 1
239000005642 Oleic acid Substances 0.000 description 1
ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
240000007594 Oryza sativa Species 0.000 description 1
235000007164 Oryza sativa Nutrition 0.000 description 1
240000007930 Oxalis acetosella Species 0.000 description 1
235000008098 Oxalis acetosella Nutrition 0.000 description 1
229910019142 PO4 Inorganic materials 0.000 description 1
241000745991 Phalaris Species 0.000 description 1
241000209048 Poa Species 0.000 description 1
239000004698 Polyethylene Substances 0.000 description 1
XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Chemical compound CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 1
239000005616 Rimsulfuron Substances 0.000 description 1
241000857233 Rottboellia Species 0.000 description 1
240000000111 Saccharum officinarum Species 0.000 description 1
235000007201 Saccharum officinarum Nutrition 0.000 description 1
240000009132 Sagittaria sagittifolia Species 0.000 description 1
241001125046 Sardina pilchardus Species 0.000 description 1
241000202758 Scirpus Species 0.000 description 1
235000005775 Setaria Nutrition 0.000 description 1
241000232088 Setaria <nematode> Species 0.000 description 1
241000220261 Sinapis Species 0.000 description 1
241000207763 Solanum Species 0.000 description 1
235000002634 Solanum Nutrition 0.000 description 1
240000002439 Sorghum halepense Species 0.000 description 1
235000011684 Sorghum saccharatum Nutrition 0.000 description 1
235000021355 Stearic acid Nutrition 0.000 description 1
240000006694 Stellaria media Species 0.000 description 1
235000021536 Sugar beet Nutrition 0.000 description 1
239000005619 Sulfosulfuron Substances 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical class OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
235000019486 Sunflower oil Nutrition 0.000 description 1
229920002359 Tetronic® Polymers 0.000 description 1
239000005624 Tralkoxydim Substances 0.000 description 1
239000005626 Tribenuron Substances 0.000 description 1
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical class OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
235000021307 Triticum Nutrition 0.000 description 1
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

Life Sciences & Earth Sciences (AREA)
Organic Chemistry (AREA)
Chemical & Material Sciences (AREA)
Dentistry (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Plant Pathology (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)
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"
BR112012027301B1 (pt)	2010-04-26	2018-07-03	Dow Agrosciences Llc	Composição de dispersão de óleo estável com estabilidade aperfeiçoada
NZ613876A (en) *	2011-02-11	2015-03-27	Dow Agrosciences Llc	Stable agrochemical oil dispersions
MX368746B (es) *	2012-12-21	2019-10-14	Dow Agrosciences Llc	Composiciones acuosas de cloquintocet-mexilo de temperatura estable.
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
US20220361484A1 (en) *	2019-09-16	2022-11-17	Eastman Chemical Company	Rapid dispersal formulation containing a sulfopolymer
EP4030908A4 (en) *	2019-09-16	2023-10-04	Eastman Chemical Company	ESSENTIALLY NON-PHYTOTOXIC FORMULATION CONTAINING A SULFOPOLYMER
EP4030905A4 (en) *	2019-09-16	2023-10-04	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
DE59209933D1 (de) *	1991-12-31	2001-12-20	Aventis Cropscience 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
WO1999057983A1 (en) *	1998-05-14	1999-11-18	E.I. Du Pont De Nemours And Company	Crop-safened herbicidal mixtures

2001
- 2001-10-29 US US10/415,565 patent/US20040038824A1/en not_active Abandoned
- 2001-10-29 SK SK520-2003A patent/SK5202003A3/sk unknown
- 2001-10-29 PL PL01362967A patent/PL362967A1/pl not_active Application Discontinuation
- 2001-10-29 BR BR0115026-0A patent/BR0115026A/pt not_active Application Discontinuation
- 2001-10-29 EA EA200300505A patent/EA200300505A1/ru unknown
- 2001-10-29 CA CA002425023A patent/CA2425023A1/en not_active Abandoned
- 2001-10-29 TR TR2003/00551T patent/TR200300551T2/xx unknown
- 2001-10-29 MX MXPA03003747A patent/MXPA03003747A/es not_active Application Discontinuation
- 2001-10-29 HU HU0301593A patent/HUP0301593A3/hu unknown
- 2001-10-29 JP JP2002539326A patent/JP2004513115A/ja active Pending
- 2001-10-29 WO PCT/EP2001/012482 patent/WO2002036566A1/en not_active Ceased
- 2001-10-29 EP EP01992701A patent/EP1330438A1/en not_active Withdrawn
- 2001-10-29 AU AU2002221774A patent/AU2002221774A1/en not_active Abandoned
- 2001-10-29 CN CNA018181988A patent/CN1471513A/zh active Pending
- 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
TR200300551T2 (tr)	2003-09-22
ZA200302583B (en)	2004-04-28
WO2002036566A1 (en)	2002-05-10
PL362967A1 (pl)	2004-11-02
CN1471513A (zh)	2004-01-28
EA200300505A1 (ru)	2003-10-30
AU2002221774A1 (en)	2002-05-15
BR0115026A (pt)	2003-12-23
JP2004513115A (ja)	2004-04-30
US20040038824A1 (en)	2004-02-26
GT200100218A (es)	2002-06-13
HUP0301593A3 (en)	2004-11-29
CA2425023A1 (en)	2002-05-10
AR034419A1 (es)	2004-02-25
MXPA03003747A (es)	2003-07-28
HUP0301593A2 (hu)	2003-10-28
EP1330438A1 (en)	2003-07-30

Publication	Publication Date	Title
SK4722003A3 (en)	2003-09-11	Agrochemical compositions with quinoline safeners and use thereof
ES2259425T3 (es)	2006-10-01	Nuevos herbicidas.
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
SK5202003A3 (en)	2004-03-02	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
KR20050021461A (ko)	2005-03-07	액체 애주번트
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