ZA200401406B - Herbicide and safening combinations - Google Patents
Herbicide and safening combinations Download PDFInfo
- 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
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- 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
- 230000003179 granulation Effects 0.000 description 3
- 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
- 239000003960 organic solvent Substances 0.000 description 3
- 229920002451 polyvinyl alcohol Polymers 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- 238000001694 spray drying Methods 0.000 description 3
- 238000005507 spraying Methods 0.000 description 3
- 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
- 239000004094 surface-active agent Substances 0.000 description 3
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
- 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
- MDBGGTQNNUOQRC-UHFFFAOYSA-N Allidochlor Chemical compound ClCC(=O)N(CC=C)CC=C MDBGGTQNNUOQRC-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 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 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical class C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- FDNBWBAHQKZDSN-UHFFFAOYSA-N F5231 Chemical compound C1=C(Cl)C(NS(=O)(=O)CC)=CC(N2C(N(CCCF)N=N2)=O)=C1F FDNBWBAHQKZDSN-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 239000005562 Glyphosate Substances 0.000 description 2
- VGHPMIFEKOFHHQ-UHFFFAOYSA-N Metosulam Chemical compound N1=C2N=C(OC)C=C(OC)N2N=C1S(=O)(=O)NC1=C(Cl)C=CC(C)=C1Cl VGHPMIFEKOFHHQ-UHFFFAOYSA-N 0.000 description 2
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
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- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 description 2
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- 239000005616 Rimsulfuron Substances 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- XJCLWVXTCRQIDI-UHFFFAOYSA-N Sulfallate Chemical compound CCN(CC)C(=S)SCC(Cl)=C XJCLWVXTCRQIDI-UHFFFAOYSA-N 0.000 description 2
- PNRAZZZISDRWMV-UHFFFAOYSA-N Terbucarb Chemical compound CNC(=O)OC1=C(C(C)(C)C)C=C(C)C=C1C(C)(C)C PNRAZZZISDRWMV-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
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- 125000004442 acylamino group Chemical group 0.000 description 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 2
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- 125000004390 alkyl sulfonyl group Chemical group 0.000 description 2
- 125000004414 alkyl thio group Chemical group 0.000 description 2
- 239000000729 antidote Substances 0.000 description 2
- XOEMATDHVZOBSG-UHFFFAOYSA-N azafenidin Chemical compound C1=C(OCC#C)C(Cl)=CC(Cl)=C1N1C(=O)N2CCCCC2=N1 XOEMATDHVZOBSG-UHFFFAOYSA-N 0.000 description 2
- MAHPNPYYQAIOJN-UHFFFAOYSA-N azimsulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2N(N=CC=2C2=NN(C)N=N2)C)=N1 MAHPNPYYQAIOJN-UHFFFAOYSA-N 0.000 description 2
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- FUHMZYWBSHTEDZ-UHFFFAOYSA-M bispyribac-sodium Chemical compound [Na+].COC1=CC(OC)=NC(OC=2C(=C(OC=3N=C(OC)C=C(OC)N=3)C=CC=2)C([O-])=O)=N1 FUHMZYWBSHTEDZ-UHFFFAOYSA-M 0.000 description 2
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- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 2
- MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical compound C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 description 2
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- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 description 1
- ZSDSQXJSNMTJDA-UHFFFAOYSA-N trifluralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-N 0.000 description 1
- AKTQJCBOGPBERP-UHFFFAOYSA-N triflusulfuron Chemical compound FC(F)(F)COC1=NC(N(C)C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2C)C(O)=O)=N1 AKTQJCBOGPBERP-UHFFFAOYSA-N 0.000 description 1
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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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/80—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
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)
- Hydrogenated Pyridines (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10145019A DE10145019A1 (de) | 2001-09-13 | 2001-09-13 | Kombinationen aus Herbiziden und Safenern |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ZA200401406B true ZA200401406B (en) | 2007-03-28 |
Family
ID=7698831
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ZA200401406A ZA200401406B (en) | 2001-09-13 | 2004-02-20 | Herbicide and safening combinations |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US6914035B2 (fr) |
| EP (1) | EP1427281B1 (fr) |
| JP (1) | JP4384910B2 (fr) |
| CN (1) | CN1309302C (fr) |
| AR (2) | AR036480A1 (fr) |
| BR (1) | BR0212488B1 (fr) |
| CA (1) | CA2460481C (fr) |
| DE (2) | DE10145019A1 (fr) |
| DK (1) | DK1427281T3 (fr) |
| ES (1) | ES2294161T3 (fr) |
| FR (1) | FR12C0012I2 (fr) |
| HR (1) | HRP20040246B1 (fr) |
| HU (1) | HU229517B1 (fr) |
| MX (1) | MXPA04002382A (fr) |
| PL (1) | PL205316B1 (fr) |
| PT (1) | PT1427281E (fr) |
| RS (1) | RS50865B (fr) |
| RU (2) | RU2420065C2 (fr) |
| SI (1) | SI1427281T1 (fr) |
| UA (1) | UA76206C2 (fr) |
| WO (1) | WO2003022050A1 (fr) |
| ZA (1) | ZA200401406B (fr) |
Families Citing this family (46)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| UA78071C2 (en) * | 2002-08-07 | 2007-02-15 | Kumiai Chemical Industry Co | Herbicidal composition |
| DE10237461A1 (de) * | 2002-08-16 | 2004-02-26 | Bayer Cropscience Gmbh | Herbizide Mittel enthaltend Benzoylpyrazole und Safener |
| DE102005031787A1 (de) * | 2005-07-07 | 2007-01-18 | Bayer Cropscience Gmbh | Kulturpflanzenverträgliche herbizide Mittel enthaltend Herbizide Safener |
| US7560416B2 (en) * | 2005-09-21 | 2009-07-14 | Riceco, Llc | Synergistic composition and method of use |
| ES2635275T3 (es) * | 2005-11-17 | 2017-10-03 | Bayer Intellectual Property Gmbh | Agente herbicida acuoso a base de un concentrado de suspensión que contiene herbicidas y protectores selectivos |
| US7951995B2 (en) | 2006-06-28 | 2011-05-31 | Pioneer Hi-Bred International, Inc. | Soybean event 3560.4.3.5 and compositions and methods for the identification and detection thereof |
| EP3067425A1 (fr) | 2006-10-31 | 2016-09-14 | E. I. du Pont de Nemours and Company | Événement 305423-1 de soja et constructions pour la génération dudit soja |
| WO2009089165A2 (fr) * | 2008-01-07 | 2009-07-16 | Auburn University | Combinaisons d'herbicides et de phytoprotecteurs |
| EP2092825A1 (fr) | 2008-02-21 | 2009-08-26 | Bayer CropScience Aktiengesellschaft | Combinaison herbicide contenant un herbicide de la classe des diamino-s-triazines |
| CA2730388A1 (fr) * | 2008-07-11 | 2010-01-14 | Floratine Biosciences, Inc. | Compositions nutritives de silicium applicables de facon foliaire et procedes |
| RU2389184C1 (ru) * | 2009-03-23 | 2010-05-20 | Государственное учреждение "Научно-исследовательский технологический институт гербицидов и регуляторов роста растений с опытно-экспериментальным производством Академии наук Республики Башкортостан" | Способ определения синергистического эффекта поверхностно-активных веществ в гербицидных дисперсных системах |
| BR112012004979A8 (pt) | 2009-09-03 | 2017-03-21 | Fbsciences Holdings Inc | Composições para o tratamento de semente e métodos |
| EP2483221A4 (fr) * | 2009-09-28 | 2015-05-13 | Fbsciences Holdings Inc | Compositions pour engrais et procédés |
| AU2010297937B2 (en) * | 2009-09-28 | 2016-03-17 | Fbsciences, Holdings, Inc. | Methods of reducing plant stress |
| JP2011157334A (ja) * | 2010-02-04 | 2011-08-18 | Sumitomo Chemical Co Ltd | 雑草の防除方法 |
| JP5982367B2 (ja) | 2010-07-15 | 2016-08-31 | エフビーサイエンシズ・ホールディングス，インコーポレイテッド | 微生物組成物及び方法 |
| CA2805941A1 (fr) | 2010-08-13 | 2012-02-16 | Pioneer Hi-Bred International, Inc. | Procedes et compositions pour cibler des sequences d'interet pour le chloroplaste |
| PL2643464T3 (pl) | 2010-11-24 | 2019-08-30 | Pioneer Hi-Bred International, Inc. | Zdarzenie GAT DP-073496-4 w Brassica oraz kompozycje i sposoby jego identyfikacji i/lub wykrywania |
| WO2012071039A1 (fr) | 2010-11-24 | 2012-05-31 | Pioner Hi-Bred International, Inc. | Événement dp-061061-7 de brassica gat et compositions et procédés pour l'identifier et/ou le détecter |
| TWI667347B (zh) | 2010-12-15 | 2019-08-01 | 瑞士商先正達合夥公司 | 大豆品種ｓｙｈｔ０ｈ２及偵測其之組合物及方法 |
| EP2802204B1 (fr) | 2012-01-12 | 2020-09-09 | FBSciences Holdings, Inc. | Modulation de la biologie végétale |
| JP2013184912A (ja) * | 2012-03-07 | 2013-09-19 | Sumitomo Chemical Co Ltd | 除草用組成物 |
| HUE032666T2 (en) | 2012-05-24 | 2017-10-30 | Bayer Cropscience Ag | Herbicidal compositions containing N- (tetrazol-5-yl) arylcarboxylic acids |
| BR112014031260A2 (pt) | 2012-06-15 | 2019-08-20 | Du Pont | métodos e composições que envolvem variantes de als com preferência de substrato nativo |
| EP2935593A2 (fr) | 2012-12-21 | 2015-10-28 | Pioneer Hi-Bred International, Inc. | Compositions et procédés pour la conjugaison d'analogues d'auxine |
| US9713332B2 (en) | 2013-03-13 | 2017-07-25 | Pioneer Hi-Bred International, Inc. | Glyphosate application for weed control in Brassica |
| AU2014236154A1 (en) | 2013-03-14 | 2015-09-17 | Pioneer Hi-Bred International, Inc. | Compositions having dicamba decarboxylase activity and methods of use |
| US20160040149A1 (en) | 2013-03-14 | 2016-02-11 | Pioneer Hi-Bred International Inc. | Compositions Having Dicamba Decarboxylase Activity and Methods of Use |
| WO2014172551A1 (fr) | 2013-04-17 | 2014-10-23 | Sepro Corporation | Compositions et procédés herbicides |
| US11026423B2 (en) | 2013-04-17 | 2021-06-08 | Sepro Corporation | Herbicidal compositions and methods |
| UA118765C2 (uk) | 2013-08-09 | 2019-03-11 | Байєр Кропсайєнс Акцієнгезелльшафт | Третинні гербіцидні комбінації, що містять дві сульфонілсечовини |
| BR112016008489A2 (pt) | 2013-10-18 | 2017-10-03 | Pioneer Hi Bred Int | Sequências de glifosato-n-acetiltransferase (glyat) e métodos de uso |
| JP6452687B2 (ja) | 2013-10-25 | 2019-01-16 | バイエル・クロップサイエンス・アクチェンゲゼルシャフト | Ｎ−（１，３，４−オキサジアゾール−２−イル）−アリールカルボン酸アミド類を含んでいる除草剤組成物 |
| KR102336926B1 (ko) | 2014-10-06 | 2021-12-08 | 버텍스 파마슈티칼스 인코포레이티드 | 낭성 섬유증 막횡단 전도도 조절자의 조정제 |
| WO2017050635A1 (fr) | 2015-09-22 | 2017-03-30 | Bayer Cropscience Aktiengesellschaft | Utilisation de certaines combinaisons de principes actifs dans des plantes de culture à racine tubéreuse |
| EP3436446B1 (fr) | 2016-03-31 | 2023-06-07 | Vertex Pharmaceuticals Incorporated | Modulateurs du régulateur de la conductance transmembranaire de la fibrose kystique |
| UA124708C2 (uk) | 2016-09-30 | 2021-11-03 | Вертекс Фармасьютікалз Інкорпорейтед | Модулятор муковісцидозного регулятора трансмембранної провідності, фармацевтичні композиції, способи лікування та спосіб отримання модулятора |
| AU2017371200B2 (en) | 2016-12-09 | 2021-05-06 | Vertex Pharmaceuticals Incorporated | Modulator of cystic fibrosis transmembrane conductance regulator, pharmaceutical compositions, methods of treatment, and process for making the modulator |
| MA54105A (fr) | 2017-06-08 | 2021-09-15 | Vertex Pharma | Méthodes de traitement de la fibrose kystique |
| MA49631A (fr) | 2017-07-17 | 2020-05-27 | Vertex Pharma | Méthodes de traitement de la fibrose kystique |
| KR102606188B1 (ko) | 2017-08-02 | 2023-11-23 | 버텍스 파마슈티칼스 인코포레이티드 | 피롤리딘 화합물을 제조하기 위한 공정 |
| US10654829B2 (en) | 2017-10-19 | 2020-05-19 | Vertex Pharmaceuticals Incorporated | Crystalline forms and compositions of CFTR modulators |
| US11465985B2 (en) | 2017-12-08 | 2022-10-11 | Vertex Pharmaceuticals Incorporated | Processes for making modulators of cystic fibrosis transmembrane conductance regulator |
| TWI810243B (zh) | 2018-02-05 | 2023-08-01 | 美商維泰克斯製藥公司 | 用於治療囊腫纖化症之醫藥組合物 |
| US11414439B2 (en) | 2018-04-13 | 2022-08-16 | Vertex Pharmaceuticals Incorporated | Modulators of cystic fibrosis transmembrane conductance regulator, pharmaceutical compositions, methods of treatment, and process for making the modulator |
| EP3708936B1 (fr) | 2019-03-15 | 2024-04-17 | Polymetrix AG | Procédé de recyclage de polyoléfines |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TR27434A (tr) * | 1992-03-12 | 1995-05-23 | Rhone Poulenc Agrochimie | Yeni 4-benzoilisoksazol türevleri, bunlari ihtiva eden terkipler ve bunlarin herbisidler olarak kullanilmalari. |
| PL186631B1 (pl) * | 1996-03-15 | 2004-02-27 | Syngenta Participations Ag | Synergistyczna kompozycja herbicydowa oraz sposóbzwalczania niepożądanych roślin |
| DE19621522A1 (de) * | 1996-05-29 | 1997-12-04 | Hoechst Schering Agrevo Gmbh | Neue N-Acylsulfonamide, neue Mischungen aus Herbiziden und Antidots und deren Verwendung |
| DE19742951A1 (de) | 1997-09-29 | 1999-04-15 | Hoechst Schering Agrevo Gmbh | Acylsulfamoylbenzoesäureamide, diese enthaltende nutzpflanzenschützende Mittel und Verfahren zu ihrer Herstellung |
| DE19827855A1 (de) | 1998-06-23 | 1999-12-30 | Hoechst Schering Agrevo Gmbh | Kombinationen aus Herbiziden und Safenern |
| EP1089628A1 (fr) | 1998-06-26 | 2001-04-11 | Novartis Pharma AG. | Herbicide |
| DE19853827A1 (de) * | 1998-11-21 | 2000-05-25 | Aventis Cropscience Gmbh | Kombinationen aus Herbiziden und Safenern |
| PL201229B1 (pl) | 1999-09-08 | 2009-03-31 | Aventis Cropscience Uk Ltd | Sposób zmniejszania fitotoksyczności |
-
2001
- 2001-09-13 DE DE10145019A patent/DE10145019A1/de not_active Withdrawn
-
2002
- 2002-06-09 UA UA20040402921A patent/UA76206C2/uk unknown
- 2002-09-06 MX MXPA04002382A patent/MXPA04002382A/es active IP Right Grant
- 2002-09-06 ES ES02764874T patent/ES2294161T3/es not_active Expired - Lifetime
- 2002-09-06 JP JP2003526192A patent/JP4384910B2/ja not_active Expired - Lifetime
- 2002-09-06 DE DE50211255T patent/DE50211255D1/de not_active Expired - Lifetime
- 2002-09-06 PT PT02764874T patent/PT1427281E/pt unknown
- 2002-09-06 BR BRPI0212488-2A patent/BR0212488B1/pt active IP Right Grant
- 2002-09-06 HU HU0402105A patent/HU229517B1/hu active Protection Beyond IP Right Term
- 2002-09-06 EP EP02764874A patent/EP1427281B1/fr not_active Expired - Lifetime
- 2002-09-06 WO PCT/EP2002/009973 patent/WO2003022050A1/fr not_active Ceased
- 2002-09-06 RU RU2006131048/04A patent/RU2420065C2/ru active
- 2002-09-06 HR HRP20040246AA patent/HRP20040246B1/xx not_active IP Right Cessation
- 2002-09-06 RU RU2004111283/15A patent/RU2291616C2/ru active Protection Beyond IP Right Term
- 2002-09-06 CA CA2460481A patent/CA2460481C/fr not_active Expired - Lifetime
- 2002-09-06 CN CNB028178998A patent/CN1309302C/zh not_active Expired - Lifetime
- 2002-09-06 RS YUP-221/04A patent/RS50865B/sr unknown
- 2002-09-06 PL PL368759A patent/PL205316B1/pl unknown
- 2002-09-06 DK DK02764874T patent/DK1427281T3/da active
- 2002-09-06 SI SI200230662T patent/SI1427281T1/sl unknown
- 2002-09-11 AR ARP020103442A patent/AR036480A1/es not_active Application Discontinuation
- 2002-09-11 US US10/241,136 patent/US6914035B2/en not_active Expired - Lifetime
-
2004
- 2004-02-20 ZA ZA200401406A patent/ZA200401406B/en unknown
-
2012
- 2012-03-02 FR FR12C0012C patent/FR12C0012I2/fr active Active
-
2014
- 2014-01-09 AR ARP140100083A patent/AR094405A2/es unknown
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