ZA200401406B - Herbicide and safening combinations - Google Patents

Info

Publication number

ZA200401406B

ZA200401406B ZA200401406A ZA200401406A ZA200401406B ZA 200401406 B ZA200401406 B ZA 200401406B ZA 200401406 A ZA200401406 A ZA 200401406A ZA 200401406 A ZA200401406 A ZA 200401406A ZA 200401406 B ZA200401406 B ZA 200401406B

Authority

ZA

South Africa

Prior art keywords

alkyl

group

formula

active composition

alkoxy

Prior art date

2001-09-13

Links

• Espacenet
• Global Dossier
• Discuss

• 239000004009 herbicide Substances 0.000 title claims description 50
• 230000002363 herbicidal effect Effects 0.000 title claims description 28
• 239000000203 mixture Substances 0.000 claims description 54
• -1 (Cs- Cs)-alkoxy Chemical group 0.000 claims description 41
• 241000196324 Embryophyta Species 0.000 claims description 31
• 150000001875 compounds Chemical class 0.000 claims description 26
• 244000038559 crop plants Species 0.000 claims description 21
• 229910052736 halogen Inorganic materials 0.000 claims description 20
• 150000002367 halogens Chemical class 0.000 claims description 20
• 239000001257 hydrogen Substances 0.000 claims description 16
• 229910052739 hydrogen Inorganic materials 0.000 claims description 16
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 16
• 229910052757 nitrogen Inorganic materials 0.000 claims description 13
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 12
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 10
• 239000000460 chlorine Substances 0.000 claims description 10
• 125000000623 heterocyclic group Chemical group 0.000 claims description 10
• 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 10
• 125000005842 heteroatom Chemical group 0.000 claims description 9
• 238000000034 method Methods 0.000 claims description 9
• 229910052760 oxygen Inorganic materials 0.000 claims description 9
• 229910052717 sulfur Chemical group 0.000 claims description 9
• 229910052801 chlorine Inorganic materials 0.000 claims description 8
• 125000004093 cyano group Chemical group *C#N 0.000 claims description 8
• 229910052731 fluorine Inorganic materials 0.000 claims description 8
• 125000001424 substituent group Chemical group 0.000 claims description 8
• 240000008042 Zea mays Species 0.000 claims description 7
• 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 claims description 7
• 235000002017 Zea mays subsp mays Nutrition 0.000 claims description 7
• 235000005822 corn Nutrition 0.000 claims description 7
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 7
• 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 7
• ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 6
• PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 6
• 240000007594 Oryza sativa Species 0.000 claims description 6
• 235000007164 Oryza sativa Nutrition 0.000 claims description 6
• 239000011737 fluorine Substances 0.000 claims description 6
• 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
• 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 6
• 235000009566 rice Nutrition 0.000 claims description 6
• 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims description 5
• 150000003839 salts Chemical class 0.000 claims description 5
• WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 4
• 240000005979 Hordeum vulgare Species 0.000 claims description 4
• 235000007340 Hordeum vulgare Nutrition 0.000 claims description 4
• 235000021307 Triticum Nutrition 0.000 claims description 4
• GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 4
• 229910052794 bromium Inorganic materials 0.000 claims description 4
• 125000006125 ethylsulfonyl group Chemical group 0.000 claims description 4
• 125000004433 nitrogen atom Chemical group N* 0.000 claims description 4
• 125000000719 pyrrolidinyl group Chemical group 0.000 claims description 4
• 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 3
• 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims description 3
• 235000007319 Avena orientalis Nutrition 0.000 claims description 3
• 244000075850 Avena orientalis Species 0.000 claims description 3
• 229910014585 C2-Ce Inorganic materials 0.000 claims description 3
• 229920000742 Cotton Polymers 0.000 claims description 3
• 244000068988 Glycine max Species 0.000 claims description 3
• 235000010469 Glycine max Nutrition 0.000 claims description 3
• 235000007238 Secale cereale Nutrition 0.000 claims description 3
• 244000082988 Secale cereale Species 0.000 claims description 3
• 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 3
• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
• 244000299507 Gossypium hirsutum Species 0.000 claims description 2
• 235000011684 Sorghum saccharatum Nutrition 0.000 claims description 2
• NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
• QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
• 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 2
• 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims description 2
• IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 2
• QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 2
• 239000001301 oxygen Chemical group 0.000 claims description 2
• 230000008569 process Effects 0.000 claims description 2
• 239000011593 sulfur Chemical group 0.000 claims description 2
• 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 claims 1
• 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 claims 1
• 240000006394 Sorghum bicolor Species 0.000 claims 1
• 229940100389 Sulfonylurea Drugs 0.000 claims 1
• 244000098338 Triticum aestivum Species 0.000 claims 1
• 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 claims 1
• YROXIXLRRCOBKF-UHFFFAOYSA-N sulfonylurea Chemical class OC(=N)N=S(=O)=O YROXIXLRRCOBKF-UHFFFAOYSA-N 0.000 claims 1
• 239000013543 active substance Substances 0.000 description 36
• 150000003254 radicals Chemical class 0.000 description 24
• 150000002148 esters Chemical class 0.000 description 15
• 238000009472 formulation Methods 0.000 description 15
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
• 239000008187 granular material Substances 0.000 description 12
• 239000000126 substance Substances 0.000 description 11
• 125000004432 carbon atom Chemical group C* 0.000 description 10
• 239000004495 emulsifiable concentrate Substances 0.000 description 10
• 239000002689 soil Substances 0.000 description 9
• 239000000839 emulsion Substances 0.000 description 8
• 230000009261 transgenic effect Effects 0.000 description 8
• 239000004562 water dispersible granule Substances 0.000 description 8
• 230000000885 phytotoxic effect Effects 0.000 description 7
• 239000000843 powder Substances 0.000 description 7
• 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 6
• 239000006185 dispersion Substances 0.000 description 6
• 239000000463 material Substances 0.000 description 6
• 125000006413 ring segment Chemical group 0.000 description 6
• 239000011734 sodium Substances 0.000 description 6
• 229910052708 sodium Inorganic materials 0.000 description 6
• 125000003342 alkenyl group Chemical group 0.000 description 5
• 125000003545 alkoxy group Chemical group 0.000 description 5
• 125000000217 alkyl group Chemical group 0.000 description 5
• 230000000694 effects Effects 0.000 description 5
• 239000003995 emulsifying agent Substances 0.000 description 5
• RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
• 238000000227 grinding Methods 0.000 description 5
• 238000002156 mixing Methods 0.000 description 5
• 238000002360 preparation method Methods 0.000 description 5
• 239000000725 suspension Substances 0.000 description 5
• YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 4
• 244000062793 Sorghum vulgare Species 0.000 description 4
• 239000002253 acid Substances 0.000 description 4
• 125000000304 alkynyl group Chemical group 0.000 description 4
• 239000011575 calcium Substances 0.000 description 4
• 235000013339 cereals Nutrition 0.000 description 4
• JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
• 235000014113 dietary fatty acids Nutrition 0.000 description 4
• 239000000194 fatty acid Substances 0.000 description 4
• 229930195729 fatty acid Natural products 0.000 description 4
• 125000001188 haloalkyl group Chemical group 0.000 description 4
• 150000004702 methyl esters Chemical class 0.000 description 4
• 229920000151 polyglycol Polymers 0.000 description 4
• 239000010695 polyglycol Substances 0.000 description 4
• 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 4
• 230000009467 reduction Effects 0.000 description 4
• 230000000007 visual effect Effects 0.000 description 4
• XBYZOHTXPQOOJM-UHFFFAOYSA-N 1,2-oxazol-3-yl(phenyl)methanone Chemical class C=1C=CC=CC=1C(=O)C=1C=CON=1 XBYZOHTXPQOOJM-UHFFFAOYSA-N 0.000 description 3
• 239000005995 Aluminium silicate Substances 0.000 description 3
• 239000004372 Polyvinyl alcohol Substances 0.000 description 3
• 240000000111 Saccharum officinarum Species 0.000 description 3
• 235000007201 Saccharum officinarum Nutrition 0.000 description 3
• VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
• 241000209140 Triticum Species 0.000 description 3
• 150000007513 acids Chemical class 0.000 description 3
• 125000002252 acyl group Chemical group 0.000 description 3
• 235000012211 aluminium silicate Nutrition 0.000 description 3
• 125000003118 aryl group Chemical group 0.000 description 3
• 239000000969 carrier Substances 0.000 description 3
• 239000002270 dispersing agent Substances 0.000 description 3
• 150000002191 fatty alcohols Chemical class 0.000 description 3
• 239000003337 fertilizer Substances 0.000 description 3
• FOUWCSDKDDHKQP-UHFFFAOYSA-N flumioxazin Chemical compound FC1=CC=2OCC(=O)N(CC#C)C=2C=C1N(C1=O)C(=O)C2=C1CCCC2 FOUWCSDKDDHKQP-UHFFFAOYSA-N 0.000 description 3
• 238000005469 granulation Methods 0.000 description 3
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• 125000004438 haloalkoxy group Chemical group 0.000 description 3
• 239000003112 inhibitor Substances 0.000 description 3
• 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 3
• 235000019713 millet Nutrition 0.000 description 3
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• OORLZFUTLGXMEF-UHFFFAOYSA-N sulfentrazone Chemical compound O=C1N(C(F)F)C(C)=NN1C1=CC(NS(C)(=O)=O)=C(Cl)C=C1Cl OORLZFUTLGXMEF-UHFFFAOYSA-N 0.000 description 3
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• 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 2
• 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 2
• JLYFCTQDENRSOL-UHFFFAOYSA-N 2-chloro-N-(2,4-dimethylthiophen-3-yl)-N-(1-methoxypropan-2-yl)acetamide Chemical compound COCC(C)N(C(=O)CCl)C=1C(C)=CSC=1C JLYFCTQDENRSOL-UHFFFAOYSA-N 0.000 description 2
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