OA12836A - Synergistic herbicidal compositions comprising mesotrione. - Google Patents

Synergistic herbicidal compositions comprising mesotrione. Download PDF

Info

Publication number: OA12836A
Authority: OA; OAPI
Prior art keywords: component; locus; mesotrione; herbicidal composition; végétation
Prior art date: 2001-06-11

Application number

OA1200300313A

Other languages

English (en)

Inventor

Derek Cornes

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.)

2001-06-11

Filing date

2002-06-06

Publication date

2006-09-15

2002-06-06 Application filed by Syngenta Participations Ag filed Critical Syngenta Participations Ag

2006-09-15 Publication of OA12836A publication Critical patent/OA12836A/en

Links

239000000203 mixture Substances 0.000 title claims abstract description 60
230000002363 herbicidal effect Effects 0.000 title claims abstract description 25
230000002195 synergetic effect Effects 0.000 title claims abstract description 15
239000005578 Mesotrione Substances 0.000 title claims abstract description 11
KPUREKXXPHOJQT-UHFFFAOYSA-N mesotrione Chemical compound [O-][N+](=O)C1=CC(S(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O KPUREKXXPHOJQT-UHFFFAOYSA-N 0.000 title claims abstract description 11
239000004009 herbicide Substances 0.000 claims abstract description 12
238000000034 method Methods 0.000 claims abstract description 10
IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 claims abstract description 9
AIMMSOZBPYFASU-UHFFFAOYSA-N n-(4,6-dimethoxypyrimidin-2-yl)-n'-[3-(2,2,2-trifluoroethoxy)pyridin-1-ium-2-yl]sulfonylcarbamimidate Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CN=2)OCC(F)(F)F)=N1 AIMMSOZBPYFASU-UHFFFAOYSA-N 0.000 claims abstract description 9
RXCPQSJAVKGONC-UHFFFAOYSA-N Flumetsulam Chemical compound N1=C2N=C(C)C=CN2N=C1S(=O)(=O)NC1=C(F)C=CC=C1F RXCPQSJAVKGONC-UHFFFAOYSA-N 0.000 claims abstract description 8
CAAMSDWKXXPUJR-UHFFFAOYSA-N 3,5-dihydro-4H-imidazol-4-one Chemical class O=C1CNC=N1 CAAMSDWKXXPUJR-UHFFFAOYSA-N 0.000 claims abstract description 7
RRKHIAYNPVQKEF-UHFFFAOYSA-N Pyriftalid Chemical compound COC1=CC(OC)=NC(SC=2C=3C(=O)OC(C)C=3C=CC=2)=N1 RRKHIAYNPVQKEF-UHFFFAOYSA-N 0.000 claims abstract description 7
150000003918 triazines Chemical class 0.000 claims abstract description 7
239000005504 Dicamba Substances 0.000 claims abstract description 6
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 claims abstract description 6
YLPGTOIOYRQOHV-UHFFFAOYSA-N Pretilachlor Chemical compound CCCOCCN(C(=O)CCl)C1=C(CC)C=CC=C1CC YLPGTOIOYRQOHV-UHFFFAOYSA-N 0.000 claims abstract description 5
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 claims abstract description 5
NQLVQOSNDJXLKG-UHFFFAOYSA-N prosulfocarb Chemical compound CCCN(CCC)C(=O)SCC1=CC=CC=C1 NQLVQOSNDJXLKG-UHFFFAOYSA-N 0.000 claims abstract description 4
150000003839 salts Chemical class 0.000 claims abstract description 4
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 claims abstract description 3
239000005603 Prosulfocarb Substances 0.000 claims abstract description 3
239000005629 Tritosulfuron Substances 0.000 claims abstract description 3
239000005621 Terbuthylazine Substances 0.000 claims description 4
ODCWYMIRDDJXKW-UHFFFAOYSA-N simazine Chemical compound CCNC1=NC(Cl)=NC(NCC)=N1 ODCWYMIRDDJXKW-UHFFFAOYSA-N 0.000 claims description 4
FZXISNSWEXTPMF-UHFFFAOYSA-N terbutylazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)(C)C)=N1 FZXISNSWEXTPMF-UHFFFAOYSA-N 0.000 claims description 4
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 claims description 3
CLQMBPJKHLGMQK-UHFFFAOYSA-N 2-(4-isopropyl-4-methyl-5-oxo-4,5-dihydro-1H-imidazol-2-yl)nicotinic acid Chemical compound N1C(=O)C(C(C)C)(C)N=C1C1=NC=CC=C1C(O)=O CLQMBPJKHLGMQK-UHFFFAOYSA-N 0.000 claims description 3
239000005566 Imazamox Substances 0.000 claims description 3
XVOKUMIPKHGGTN-UHFFFAOYSA-N Imazethapyr Chemical compound OC(=O)C1=CC(CC)=CN=C1C1=NC(C)(C(C)C)C(=O)N1 XVOKUMIPKHGGTN-UHFFFAOYSA-N 0.000 claims description 3
239000005583 Metribuzin Substances 0.000 claims description 3
FOXFZRUHNHCZPX-UHFFFAOYSA-N metribuzin Chemical compound CSC1=NN=C(C(C)(C)C)C(=O)N1N FOXFZRUHNHCZPX-UHFFFAOYSA-N 0.000 claims description 3
230000012010 growth Effects 0.000 abstract description 6
150000001875 compounds Chemical class 0.000 description 19
238000009472 formulation Methods 0.000 description 18
241000196324 Embryophyta Species 0.000 description 12
239000007788 liquid Substances 0.000 description 9
125000000217 alkyl group Chemical group 0.000 description 8
239000008187 granular material Substances 0.000 description 8
239000002689 soil Substances 0.000 description 8
230000000694 effects Effects 0.000 description 6
-1 chloro,methylmercapto Chemical group 0.000 description 5
230000001276 controlling effect Effects 0.000 description 5
240000008042 Zea mays Species 0.000 description 4
235000002017 Zea mays subsp mays Nutrition 0.000 description 4
125000003545 alkoxy group Chemical group 0.000 description 4
239000000729 antidote Substances 0.000 description 4
125000003118 aryl group Chemical group 0.000 description 4
239000000969 carrier Substances 0.000 description 4
239000000428 dust Substances 0.000 description 4
239000000463 material Substances 0.000 description 4
239000000843 powder Substances 0.000 description 4
125000004414 alkyl thio group Chemical group 0.000 description 3
239000013522 chelant Substances 0.000 description 3
239000003995 emulsifying agent Substances 0.000 description 3
230000008635 plant growth Effects 0.000 description 3
239000002904 solvent Substances 0.000 description 3
238000001228 spectrum Methods 0.000 description 3
239000007921 spray Substances 0.000 description 3
238000012360 testing method Methods 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
239000005995 Aluminium silicate Substances 0.000 description 2
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 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
240000007594 Oryza sativa Species 0.000 description 2
235000007164 Oryza sativa Nutrition 0.000 description 2
235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 2
235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 2
235000012211 aluminium silicate Nutrition 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
239000004927 clay Substances 0.000 description 2
229910052802 copper Inorganic materials 0.000 description 2
239000010949 copper Substances 0.000 description 2
235000005822 corn Nutrition 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
239000003112 inhibitor Substances 0.000 description 2
229910003480 inorganic solid Inorganic materials 0.000 description 2
239000003621 irrigation water Substances 0.000 description 2
HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 2
239000012669 liquid formulation Substances 0.000 description 2
235000009973 maize Nutrition 0.000 description 2
239000012528 membrane Substances 0.000 description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
230000000051 modifying effect Effects 0.000 description 2
239000003960 organic solvent Substances 0.000 description 2
239000002245 particle Substances 0.000 description 2
239000011148 porous material Substances 0.000 description 2
235000009566 rice Nutrition 0.000 description 2
229910052708 sodium Inorganic materials 0.000 description 2
239000011734 sodium Substances 0.000 description 2
241000894007 species Species 0.000 description 2
239000004094 surface-active agent Substances 0.000 description 2
239000010455 vermiculite Substances 0.000 description 2
229910052902 vermiculite Inorganic materials 0.000 description 2
235000019354 vermiculite Nutrition 0.000 description 2
238000009736 wetting Methods 0.000 description 2
239000008096 xylene Substances 0.000 description 2
125000006705 (C5-C7) cycloalkyl group Chemical group 0.000 description 1
CABMTIJINOIHOD-UHFFFAOYSA-N 2-[4-methyl-5-oxo-4-(propan-2-yl)-4,5-dihydro-1H-imidazol-2-yl]quinoline-3-carboxylic acid Chemical compound N1C(=O)C(C(C)C)(C)N=C1C1=NC2=CC=CC=C2C=C1C(O)=O CABMTIJINOIHOD-UHFFFAOYSA-N 0.000 description 1
108010020183 3-phosphoshikimate 1-carboxyvinyltransferase Proteins 0.000 description 1
PVSGXWMWNRGTKE-UHFFFAOYSA-N 5-methyl-2-[4-methyl-5-oxo-4-(propan-2-yl)-4,5-dihydro-1H-imidazol-2-yl]pyridine-3-carboxylic acid Chemical compound N1C(=O)C(C(C)C)(C)N=C1C1=NC=C(C)C=C1C(O)=O PVSGXWMWNRGTKE-UHFFFAOYSA-N 0.000 description 1
206010001557 Albinism Diseases 0.000 description 1
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
PFJJMJDEVDLPNE-UHFFFAOYSA-N Benoxacor Chemical compound C1=CC=C2N(C(=O)C(Cl)Cl)C(C)COC2=C1 PFJJMJDEVDLPNE-UHFFFAOYSA-N 0.000 description 1
241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
HCRWJJJUKUVORR-UHFFFAOYSA-N Desmetryn Chemical compound CNC1=NC(NC(C)C)=NC(SC)=N1 HCRWJJJUKUVORR-UHFFFAOYSA-N 0.000 description 1
229920001353 Dextrin Polymers 0.000 description 1
239000004375 Dextrin Substances 0.000 description 1
IKYICRRUVNIHPP-UHFFFAOYSA-N Dimethametryn Chemical compound CCNC1=NC(NC(C)C(C)C)=NC(SC)=N1 IKYICRRUVNIHPP-UHFFFAOYSA-N 0.000 description 1
239000005562 Glyphosate Substances 0.000 description 1
CAWXEEYDBZRFPE-UHFFFAOYSA-N Hexazinone Chemical compound O=C1N(C)C(N(C)C)=NC(=O)N1C1CCCCC1 CAWXEEYDBZRFPE-UHFFFAOYSA-N 0.000 description 1
239000005981 Imazaquin Substances 0.000 description 1
239000005579 Metamitron Substances 0.000 description 1
239000005586 Nicosulfuron Substances 0.000 description 1
239000004952 Polyamide Substances 0.000 description 1
229920002396 Polyurea Polymers 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
239000005604 Prosulfuron Substances 0.000 description 1
LTUNNEGNEKBSEH-UHFFFAOYSA-N Prosulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)CCC(F)(F)F)=N1 LTUNNEGNEKBSEH-UHFFFAOYSA-N 0.000 description 1
244000007853 Sarothamnus scoparius Species 0.000 description 1
244000061456 Solanum tuberosum Species 0.000 description 1
235000002595 Solanum tuberosum Nutrition 0.000 description 1
229920002472 Starch Polymers 0.000 description 1
235000021536 Sugar beet Nutrition 0.000 description 1
HFBWPRKWDIRYNX-UHFFFAOYSA-N Trietazine Chemical compound CCNC1=NC(Cl)=NC(N(CC)CC)=N1 HFBWPRKWDIRYNX-UHFFFAOYSA-N 0.000 description 1
241000209140 Triticum Species 0.000 description 1
235000021307 Triticum Nutrition 0.000 description 1
241001148683 Zostera marina Species 0.000 description 1
230000009471 action Effects 0.000 description 1
239000011149 active material Substances 0.000 description 1
230000006978 adaptation Effects 0.000 description 1
239000002671 adjuvant Substances 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
125000003282 alkyl amino group Chemical group 0.000 description 1
150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
RQVYBGPQFYCBGX-UHFFFAOYSA-N ametryn Chemical compound CCNC1=NC(NC(C)C)=NC(SC)=N1 RQVYBGPQFYCBGX-UHFFFAOYSA-N 0.000 description 1
ORFPWVRKFLOQHK-UHFFFAOYSA-N amicarbazone Chemical compound CC(C)C1=NN(C(=O)NC(C)(C)C)C(=O)N1N ORFPWVRKFLOQHK-UHFFFAOYSA-N 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
229940075522 antidotes Drugs 0.000 description 1
229960000892 attapulgite Drugs 0.000 description 1
239000000440 bentonite Substances 0.000 description 1
229910000278 bentonite Inorganic materials 0.000 description 1
SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
238000009835 boiling Methods 0.000 description 1
238000009395 breeding Methods 0.000 description 1
230000001488 breeding effect Effects 0.000 description 1
239000002775 capsule Substances 0.000 description 1
235000013877 carbamide Nutrition 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
239000011362 coarse particle Substances 0.000 description 1
230000000295 complement effect Effects 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
238000013270 controlled release Methods 0.000 description 1
150000001879 copper Chemical class 0.000 description 1
125000000753 cycloalkyl group Chemical group 0.000 description 1
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
235000019425 dextrin Nutrition 0.000 description 1
125000004663 dialkyl amino group Chemical group 0.000 description 1
GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
239000012895 dilution Substances 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
235000013399 edible fruits Nutrition 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
125000000031 ethylamino group Chemical group [H]C([H])([H])C([H])([H])N([H])[*] 0.000 description 1
238000001125 extrusion Methods 0.000 description 1
235000013312 flour Nutrition 0.000 description 1
230000009969 flowable effect Effects 0.000 description 1
238000012239 gene modification Methods 0.000 description 1
230000005017 genetic modification Effects 0.000 description 1
235000013617 genetically modified food Nutrition 0.000 description 1
239000003292 glue Substances 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
125000001475 halogen functional group Chemical group 0.000 description 1
COYBRKAVBMYYSF-UHFFFAOYSA-N heptan-2-yl [(5-chloroquinolin-8-yl)oxy]acetate Chemical group C1=CN=C2C(OCC(=O)OC(C)CCCCC)=CC=C(Cl)C2=C1 COYBRKAVBMYYSF-UHFFFAOYSA-N 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
230000003993 interaction Effects 0.000 description 1
239000003350 kerosene Substances 0.000 description 1
239000011159 matrix material Substances 0.000 description 1
VHCNQEUWZYOAEV-UHFFFAOYSA-N metamitron Chemical compound O=C1N(N)C(C)=NN=C1C1=CC=CC=C1 VHCNQEUWZYOAEV-UHFFFAOYSA-N 0.000 description 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
239000003094 microcapsule Substances 0.000 description 1
230000004048 modification Effects 0.000 description 1
238000012986 modification Methods 0.000 description 1
150000002790 naphthalenes Chemical class 0.000 description 1
229920003052 natural elastomer Polymers 0.000 description 1
229920001194 natural rubber Polymers 0.000 description 1
239000005645 nematicide Substances 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
229910052625 palygorskite Inorganic materials 0.000 description 1
239000010451 perlite Substances 0.000 description 1
235000019362 perlite Nutrition 0.000 description 1
239000000575 pesticide Substances 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
229920000058 polyacrylate Polymers 0.000 description 1
229920002239 polyacrylonitrile Polymers 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000011591 potassium Substances 0.000 description 1
WJNRPILHGGKWCK-UHFFFAOYSA-N propazine Chemical compound CC(C)NC1=NC(Cl)=NC(NC(C)C)=N1 WJNRPILHGGKWCK-UHFFFAOYSA-N 0.000 description 1
230000004044 response Effects 0.000 description 1
230000000717 retained effect Effects 0.000 description 1
239000004576 sand Substances 0.000 description 1
238000007789 sealing Methods 0.000 description 1
MGLWZSOBALDPEK-UHFFFAOYSA-N simetryn Chemical compound CCNC1=NC(NCC)=NC(SC)=N1 MGLWZSOBALDPEK-UHFFFAOYSA-N 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000000243 solution Substances 0.000 description 1
238000005507 spraying Methods 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
239000008107 starch Substances 0.000 description 1
229920003048 styrene butadiene rubber Polymers 0.000 description 1
239000000126 substance Substances 0.000 description 1
150000005846 sugar alcohols Polymers 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
230000001629 suppression Effects 0.000 description 1
239000000725 suspension Substances 0.000 description 1
229920003051 synthetic elastomer Polymers 0.000 description 1
229920003002 synthetic resin Polymers 0.000 description 1
239000000057 synthetic resin Substances 0.000 description 1
239000005061 synthetic rubber Substances 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
BCQMBFHBDZVHKU-UHFFFAOYSA-N terbumeton Chemical compound CCNC1=NC(NC(C)(C)C)=NC(OC)=N1 BCQMBFHBDZVHKU-UHFFFAOYSA-N 0.000 description 1
IROINLKCQGIITA-UHFFFAOYSA-N terbutryn Chemical compound CCNC1=NC(NC(C)(C)C)=NC(SC)=N1 IROINLKCQGIITA-UHFFFAOYSA-N 0.000 description 1
238000009834 vaporization Methods 0.000 description 1
230000008016 vaporization Effects 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
239000008158 vegetable oil Substances 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
239000012991 xanthate Substances 0.000 description 1

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
- A01N41/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom
- A01N41/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom containing a sulfur-to-oxygen double bond
- A01N41/10—Sulfones; Sulfoxides

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)

OA1200300313A 2001-06-11 2002-06-06 Synergistic herbicidal compositions comprising mesotrione. OA12836A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
GBGB0114198.5A GB0114198D0 (en)	2001-06-11	2001-06-11	Herbicidal composition

Publications (1)

Publication Number	Publication Date
OA12836A true OA12836A (en)	2006-09-15

Family

ID=9916351

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
OA1200300313A OA12836A (en)	2001-06-11	2002-06-06	Synergistic herbicidal compositions comprising mesotrione.

Country Status (26)

Country	Link
US (2)	US20040180790A1 (pl)
EP (1)	EP1399020A1 (pl)
JP (1)	JP2004528392A (pl)
KR (1)	KR20040007561A (pl)
CN (2)	CN1525817A (pl)
AP (2)	AP1788A (pl)
AU (1)	AU2002311427B2 (pl)
BG (1)	BG108307A (pl)
BR (1)	BR0209511B1 (pl)
CA (1)	CA2442316C (pl)
CZ (1)	CZ296227B6 (pl)
EC (1)	ECSP034887A (pl)
GB (1)	GB0114198D0 (pl)
HR (1)	HRP20031025A2 (pl)
HU (1)	HUP0303483A3 (pl)
MX (1)	MXPA03010782A (pl)
NZ (1)	NZ548148A (pl)
OA (1)	OA12836A (pl)
PL (1)	PL212955B1 (pl)
RS (1)	RS52390B (pl)
RU (1)	RU2286059C2 (pl)
SI (1)	SI21294A (pl)
SK (1)	SK287708B6 (pl)
UA (1)	UA77184C2 (pl)
WO (1)	WO2002100173A1 (pl)
ZA (1)	ZA200308397B (pl)

Families Citing this family (34)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB0116956D0 (en) *	2001-07-11	2001-09-05	Syngenta Ltd	Weed control process
GT200200189A (es)	2001-10-05	2003-05-21		Composiciones herbicidas
DE10212887A1 (de) *	2002-03-22	2003-10-02	Bayer Cropscience Ag	Selektive Herbizide auf Basis von substituierten Aminotriazinonen und substituierten Benzoylcyclohexandionen
GB0215544D0 (en)	2002-07-04	2002-08-14	Syngenta Ltd	Weed control process
US7973083B2 (en) *	2003-12-01	2011-07-05	Syngenta Crop Protection Llc	Pesticidally active compounds
BRPI0417347B1 (pt) *	2003-12-05	2014-11-25	Syngenta Participations Ag	Concentrado pesticida compreendendo inibidores de corrosão
AU2004296743B2 (en) *	2003-12-05	2010-08-05	Syngenta Participations Ag	Submicron mesotrione compositions
JP4965438B2 (ja) *	2004-06-18	2012-07-04	シンジェンタパーティシペーションズアクチェンゲゼルシャフト	除草組成物
KR101317660B1 (ko) *	2004-12-17	2013-10-16	신젠타 파티서페이션즈 아게	제초제 조성물
AU2013201392B2 (en) *	2006-03-06	2014-04-24	Syngenta Crop Protection Ag	Stabilized pesticidal granules
WO2007101620A1 (en) *	2006-03-06	2007-09-13	Syngenta Participations Ag	Stabilized pesticidal granules
TWI444137B (zh) *	2006-07-19	2014-07-11	Syngenta Participations Ag	除草組成物及其使用方法
TWI413634B (zh) *	2006-07-19	2013-11-01	Syngenta Participations Ag	除草組成物及其使用方法
TWI473566B (zh) *	2006-07-19	2015-02-21	Syngenta Participations Ag	除草組成物及其使用方法
JP5204104B2 (ja) *	2006-07-19	2013-06-05	シンジェンタパーティシペーションズアクチェンゲゼルシャフト	除草用組成物及びその使用方法
WO2009027034A2 (en) *	2007-08-27	2009-03-05	Syngenta Participations Ag	Herbicidal composition and method of use thereof
CN101790312B (zh) *	2007-08-27	2013-08-21	先正达参股股份有限公司	除草组合物及其使用方法
CA2696118A1 (en) *	2007-08-27	2009-03-05	Syngenta Participations Ag	Herbicidal composition and method of use thereof
CN101790307A (zh)	2007-08-27	2010-07-28	先正达参股股份有限公司	除草组合物及其使用方法
US8288320B2 (en)	2007-10-04	2012-10-16	Oms Investments, Inc.	Methods for preparing granular weed control products having improved distribution of agriculturally active ingredients coated thereon
WO2009089165A2 (en) *	2008-01-07	2009-07-16	Auburn University	Combinations of herbicides and safeners
CN102265872A (zh) *	2010-06-07	2011-12-07	南京华洲药业有限公司	一种含灭草松、麦草畏与硝磺草酮的除草组合物及其应用
WO2013029005A1 (en) *	2011-08-25	2013-02-28	Dow Agrosciences Llc	Pesticidal compositions with enhanced active ingredient retention in pest control zones
EP2708124B1 (en)	2011-11-10	2018-03-21	Rotam Agrochem International Co., Ltd	Herbicidal composition and method of using the same
WO2013067706A1 (en) *	2011-11-11	2013-05-16	Rotam Agrochem International Co., Ltd	Herbicidal composition and method of using the same
EP2832223A4 (en) *	2012-03-30	2015-12-30	Ishihara Sangyo Kaisha	HERBICIDE COMPOSITION
PT2959776T (pt) *	2013-02-22	2018-11-21	Ishihara Sangyo Kaisha	Utilização de uma composição herbicida compreendendo flazassulfurão e mesotriona
CN104026129A (zh) *	2013-08-21	2014-09-10	辽宁海佳农化有限公司	一种含硝磺草酮的水稻除草剂组合物及制法
HUE062815T2 (hu) *	2014-04-02	2023-12-28	Adama Agan Ltd	Karotinoid-bioszintézist gátló vegyület és ALS/AHAS mûködését gátló vegyület gyomirtó keveréke és alkalmazásai
CN104115835A (zh) *	2014-06-24	2014-10-29	江苏省激素研究所股份有限公司	一种除草剂组合物
UY38256A (es) *	2018-06-05	2020-01-31	Monsanto Technology Llc	Diferentes composiciones herbicidas de dispersión continua no acuosa y composiciones de dispersión continua acuosa
CN111213660A (zh) *	2020-03-23	2020-06-02	安徽美程化工有限公司	一种含二氯喹啉酸、硝磺草酮和特丁津的除草组合物
CA3194213A1 (en)	2020-09-10	2022-03-17	Monsanto Technology Llc	Herbicidal combinations comprising diflufenican and mesotrione
CN112970755B (zh) *	2021-03-15	2022-03-15	淄博新农基作物科学有限公司	一种包含三氟甲磺隆和硝磺草酮的除草组合物

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH0219355A (ja) *	1988-07-07	1990-01-23	Nippon Soda Co Ltd	４，４，５−トリメチル−２−（２−ニトロ−４−メチルスルホニルベンゾイル）シクロヘキサン−１，３−ジオン、その製造方法及び除草剤
JPH0832612B2 (ja) *	1989-10-18	1996-03-29	ヘキスト・アクチェンゲゼルシャフト	除草性有効物質組合せ剤
IL113138A (en) *	1994-04-22	1999-05-09	Zeneca Ltd	Herbicidal composition comprising a substituted 1, 3-cyclohexanedione compound and a 2-chloro-4- ethylamino-6- isopropylamino-s- triazine and a method of use thereof
US6008959A (en) *	1995-07-05	1999-12-28	U.S. Philips Corporation	Recording/reproducing apparatus for storing a digital information signal in a storage medium using packet a method and a record carrier, which further allows for editing the stored digital information signal by including references to additional packets
US5741756A (en) *	1995-07-19	1998-04-21	Zeneca Limited	Synergistic herbicidal composition comprising triketones and chloroacetanilides, and method of use thereof
US5840756A (en) *	1995-07-21	1998-11-24	Teva Pharmaceutical Industries Ltd.	Pharmaceutical composition of L-DOPA ester
DE69714742T2 (de) *	1996-06-21	2003-05-15	E.I. Du Pont De Nemours And Co., Wilmington	Herbizide mischungen
JP4154760B2 (ja) *	1998-08-05	2008-09-24	住友化学株式会社	除草剤組成物
KR100682203B1 (ko) *	1998-08-13	2007-02-12	바이엘 크롭사이언스 게엠베하	아실화된 아미노페닐술포닐 우레아를 갖는 제초제
US6339138B1 (en) *	1998-11-04	2002-01-15	General Electric Company	Method of manufacturing polycarbonates
BR0014670A (pt) *	1999-09-30	2002-06-18	Bayer Ag	Herbicidas seletivos na base de n-aril-triazolin(ti)onas
EP1351571A2 (de) *	1999-11-17	2003-10-15	Bayer CropScience AG	Selektive herbizide auf basis von 2,6-disubstituierten pyridin-derivaten
DE19955662B4 (de) *	1999-11-19	2011-03-31	Arysta LifeScience North America,	Herbizide auf Basis von Carbamoyltriazolinon
US6228973B1 (en) *	2000-06-02	2001-05-08	General Electric Company	Method for preparing high molecular weight polycarbonate
PL218885B1 (pl) *	2000-08-31	2015-02-27	Basf Se	Mieszanina chwastobójcza zawierająca tritosulfuron lub jego użyteczną w rolnictwie sól oraz sulfosulfuron lub jego użyteczną w rolnictwie sól, sposób zwalczania niepożądanej roślinności i zastosowanie mieszaniny chwastobójczej
GB0022932D0 (en) *	2000-09-18	2000-11-01	Aventis Cropscience Sa	New herbicidal composition

2001
- 2001-06-11 GB GBGB0114198.5A patent/GB0114198D0/en not_active Ceased
2002
- 2002-06-06 SK SK1624-2003A patent/SK287708B6/sk not_active IP Right Cessation
- 2002-06-06 AP APAP/P/2004/002956A patent/AP1788A/en active
- 2002-06-06 JP JP2003503005A patent/JP2004528392A/ja active Pending
- 2002-06-06 US US10/479,479 patent/US20040180790A1/en not_active Abandoned
- 2002-06-06 PL PL367249A patent/PL212955B1/pl not_active IP Right Cessation
- 2002-06-06 RU RU2004100312/04A patent/RU2286059C2/ru not_active IP Right Cessation
- 2002-06-06 MX MXPA03010782A patent/MXPA03010782A/es active IP Right Grant
- 2002-06-06 RS YU84803A patent/RS52390B/sr unknown
- 2002-06-06 CN CNA028116682A patent/CN1525817A/zh active Pending
- 2002-06-06 CZ CZ20033312A patent/CZ296227B6/cs not_active IP Right Cessation
- 2002-06-06 UA UA2004010205A patent/UA77184C2/uk unknown
- 2002-06-06 NZ NZ548148A patent/NZ548148A/en not_active IP Right Cessation
- 2002-06-06 EP EP02738344A patent/EP1399020A1/en not_active Withdrawn
- 2002-06-06 KR KR10-2003-7014799A patent/KR20040007561A/ko not_active Ceased
- 2002-06-06 BR BRPI0209511-4A patent/BR0209511B1/pt not_active IP Right Cessation
- 2002-06-06 WO PCT/GB2002/002534 patent/WO2002100173A1/en not_active Ceased
- 2002-06-06 CA CA2442316A patent/CA2442316C/en not_active Expired - Fee Related
- 2002-06-06 SI SI200220018A patent/SI21294A/sl not_active IP Right Cessation
- 2002-06-06 CN CNA2006100594715A patent/CN1820599A/zh active Pending
- 2002-06-06 HU HU0303483A patent/HUP0303483A3/hu unknown
- 2002-06-06 HR HR20031025A patent/HRP20031025A2/hr not_active Application Discontinuation
- 2002-06-06 OA OA1200300313A patent/OA12836A/en unknown
- 2002-06-06 AP AP2007003881A patent/AP2007003881A0/xx unknown
- 2002-06-06 AU AU2002311427A patent/AU2002311427B2/en not_active Ceased
2003
- 2003-09-09 US US10/658,697 patent/US6924250B2/en not_active Expired - Fee Related
- 2003-10-28 ZA ZA200308397A patent/ZA200308397B/en unknown
- 2003-11-03 BG BG108307A patent/BG108307A/bg unknown
- 2003-12-11 EC EC2003004887A patent/ECSP034887A/es unknown

Also Published As

Publication number	Publication date
ECSP034887A (es)	2004-02-26
GB0114198D0 (en)	2001-08-01
BR0209511A (pt)	2004-07-13
UA77184C2 (en)	2006-11-15
US20040048746A1 (en)	2004-03-11
SI21294A (sl)	2004-04-30
CZ20033312A3 (en)	2004-03-17
RU2286059C2 (ru)	2006-10-27
CZ296227B6 (cs)	2006-02-15
AP1788A (en)	2007-10-05
PL367249A1 (pl)	2005-02-21
CA2442316C (en)	2011-08-09
AP2004002956A0 (en)	2004-03-31
NZ548148A (en)	2007-11-30
CN1820599A (zh)	2006-08-23
KR20040007561A (ko)	2004-01-24
MXPA03010782A (es)	2004-03-02
US20040180790A1 (en)	2004-09-16
JP2004528392A (ja)	2004-09-16
AU2002311427B2 (en)	2007-11-22
HUP0303483A2 (hu)	2004-03-01
PL212955B1 (pl)	2012-12-31
HRP20031025A2 (en)	2004-08-31
SK287708B6 (en)	2011-07-06
ZA200308397B (en)	2004-09-03
AP2007003881A0 (en)	2007-02-28
US6924250B2 (en)	2005-08-02
CN1525817A (zh)	2004-09-01
BR0209511B1 (pt)	2013-02-19
SK16242003A3 (sk)	2004-05-04
WO2002100173A1 (en)	2002-12-19
BG108307A (bg)	2004-11-30
EP1399020A1 (en)	2004-03-24
HUP0303483A3 (en)	2005-11-28
CA2442316A1 (en)	2002-12-19
RS52390B (sr)	2013-02-28
RU2004100312A (ru)	2005-06-10
YU84803A (sh)	2006-08-17

Publication	Publication Date	Title
CA2442316C (en)	2011-08-09	Synergistic herbicidal compositions comprising mesotrione
AU2002311427A1 (en)	2003-05-15	Synergistic herbicidal compostions comprising mesotrione
CA2447760C (en)	2010-08-24	Weed control process
EP0756452B1 (en)	1999-05-12	Synergistic herbicidal composition and method of use thereof
CA2227180C (en)	2006-08-29	Synergistic herbicidal composition and method of use thereof
KR100296804B1 (ko)	2006-03-17	벼의잡초방제용제초제조성물