RU2291616C2 - Комбинация из гербицидов и защитных средств - Google Patents
Комбинация из гербицидов и защитных средств Download PDFInfo
- Publication number
- RU2291616C2 RU2291616C2 RU2004111283/15A RU2004111283A RU2291616C2 RU 2291616 C2 RU2291616 C2 RU 2291616C2 RU 2004111283/15 A RU2004111283/15 A RU 2004111283/15A RU 2004111283 A RU2004111283 A RU 2004111283A RU 2291616 C2 RU2291616 C2 RU 2291616C2
- Authority
- RU
- Russia
- Prior art keywords
- formula
- alkyl
- agent according
- herbicidal
- plants
- Prior art date
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- 239000004009 herbicide Substances 0.000 title claims abstract description 58
- 239000003795 chemical substances by application Substances 0.000 title abstract description 12
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims abstract description 16
- 239000001257 hydrogen Substances 0.000 claims abstract description 16
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 16
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 14
- 150000002367 halogens Chemical class 0.000 claims abstract description 11
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims abstract description 9
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims abstract description 9
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 9
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims abstract description 8
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims abstract description 8
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims abstract description 7
- 239000000729 antidote Substances 0.000 claims abstract description 7
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 7
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 claims abstract description 6
- 125000004433 nitrogen atom Chemical group N* 0.000 claims abstract description 6
- 125000003386 piperidinyl group Chemical group 0.000 claims abstract description 5
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims abstract description 5
- 150000003839 salts Chemical class 0.000 claims abstract description 5
- 230000002363 herbicidal effect Effects 0.000 claims description 48
- 239000003223 protective agent Substances 0.000 claims description 48
- 241000196324 Embryophyta Species 0.000 claims description 43
- 239000000203 mixture Substances 0.000 claims description 39
- 150000001875 compounds Chemical class 0.000 claims description 22
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 14
- 240000008042 Zea mays Species 0.000 claims description 12
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 claims description 12
- 235000002017 Zea mays subsp mays Nutrition 0.000 claims description 12
- 235000005822 corn Nutrition 0.000 claims description 12
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 11
- 239000000460 chlorine Substances 0.000 claims description 10
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 9
- 239000002253 acid Substances 0.000 claims description 8
- 229910052801 chlorine Inorganic materials 0.000 claims description 8
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 8
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 7
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 5
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 4
- 150000007513 acids Chemical class 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 3
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims description 3
- 150000001408 amides Chemical class 0.000 claims description 2
- 238000010353 genetic engineering Methods 0.000 claims description 2
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 claims 2
- YROXIXLRRCOBKF-UHFFFAOYSA-N sulfonylurea Chemical group OC(=N)N=S(=O)=O YROXIXLRRCOBKF-UHFFFAOYSA-N 0.000 claims 1
- -1 C1-C4-flkyl Chemical group 0.000 abstract description 28
- 239000000126 substance Substances 0.000 abstract description 13
- 125000005843 halogen group Chemical group 0.000 abstract description 9
- 230000000694 effects Effects 0.000 abstract description 5
- 231100000674 Phytotoxicity Toxicity 0.000 abstract 1
- 230000003247 decreasing effect Effects 0.000 abstract 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 abstract 1
- 239000013543 active substance Substances 0.000 description 27
- 150000002148 esters Chemical class 0.000 description 19
- 238000009472 formulation Methods 0.000 description 19
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- 238000005507 spraying Methods 0.000 description 14
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- 229940088623 biologically active substance Drugs 0.000 description 13
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- 125000000623 heterocyclic group Chemical group 0.000 description 10
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- 125000004432 carbon atom Chemical group C* 0.000 description 9
- 239000000839 emulsion Substances 0.000 description 9
- 229910052731 fluorine Inorganic materials 0.000 description 9
- 239000011734 sodium Substances 0.000 description 9
- 229910052708 sodium Inorganic materials 0.000 description 9
- 125000000217 alkyl group Chemical group 0.000 description 8
- 238000000227 grinding Methods 0.000 description 8
- 125000005842 heteroatom Chemical group 0.000 description 8
- 229910052760 oxygen Inorganic materials 0.000 description 8
- 239000000843 powder Substances 0.000 description 8
- 239000007921 spray Substances 0.000 description 8
- 229910052717 sulfur Inorganic materials 0.000 description 8
- 239000004094 surface-active agent Substances 0.000 description 8
- 230000009261 transgenic effect Effects 0.000 description 8
- 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 7
- 125000004429 atom Chemical group 0.000 description 7
- 125000001309 chloro group Chemical group Cl* 0.000 description 7
- 239000003995 emulsifying agent Substances 0.000 description 7
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- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 6
- 230000009286 beneficial effect Effects 0.000 description 6
- 239000006185 dispersion Substances 0.000 description 6
- 239000011737 fluorine Substances 0.000 description 6
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 6
- 239000010695 polyglycol Substances 0.000 description 6
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- 239000002904 solvent Substances 0.000 description 6
- 125000001424 substituent group Chemical group 0.000 description 6
- 240000007594 Oryza sativa Species 0.000 description 5
- 235000007164 Oryza sativa Nutrition 0.000 description 5
- 125000003342 alkenyl group Chemical group 0.000 description 5
- 125000000304 alkynyl group Chemical group 0.000 description 5
- 125000004093 cyano group Chemical group *C#N 0.000 description 5
- 238000005516 engineering process Methods 0.000 description 5
- 238000002474 experimental method Methods 0.000 description 5
- 235000009566 rice Nutrition 0.000 description 5
- 239000002689 soil Substances 0.000 description 5
- 238000001694 spray drying Methods 0.000 description 5
- 239000000725 suspension Substances 0.000 description 5
- 244000045561 useful plants Species 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 4
- 240000000111 Saccharum officinarum Species 0.000 description 4
- 235000007201 Saccharum officinarum Nutrition 0.000 description 4
- 244000062793 Sorghum vulgare Species 0.000 description 4
- 125000002252 acyl group Chemical group 0.000 description 4
- 125000003545 alkoxy group Chemical group 0.000 description 4
- 238000007796 conventional method Methods 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
- 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 4
- 239000000463 material Substances 0.000 description 4
- 239000004476 plant protection product Substances 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 230000000007 visual effect Effects 0.000 description 4
- 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 description 3
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 description 3
- LAYXHUOYWYRVDY-UHFFFAOYSA-N 1,3-oxazol-2-yl(phenyl)methanone Chemical compound C=1C=CC=CC=1C(=O)C1=NC=CO1 LAYXHUOYWYRVDY-UHFFFAOYSA-N 0.000 description 3
- 239000005995 Aluminium silicate Substances 0.000 description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 3
- 125000004399 C1-C4 alkenyl group Chemical group 0.000 description 3
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 description 3
- 240000005979 Hordeum vulgare Species 0.000 description 3
- 235000007340 Hordeum vulgare Nutrition 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 239000004372 Polyvinyl alcohol Substances 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 3
- 235000012211 aluminium silicate Nutrition 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 3
- 229910052794 bromium Inorganic materials 0.000 description 3
- 239000000969 carrier Substances 0.000 description 3
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- 239000002270 dispersing agent Substances 0.000 description 3
- 150000004665 fatty acids Chemical group 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
- 239000003112 inhibitor Substances 0.000 description 3
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- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 3
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- 235000019713 millet Nutrition 0.000 description 3
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- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 3
- 238000009331 sowing Methods 0.000 description 3
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
- 239000000080 wetting agent Substances 0.000 description 3
- 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
- MDBGGTQNNUOQRC-UHFFFAOYSA-N Allidochlor Chemical compound ClCC(=O)N(CC=C)CC=C MDBGGTQNNUOQRC-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
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- 244000075850 Avena orientalis Species 0.000 description 2
- QNNQOOKFUPNAEY-UHFFFAOYSA-N C1=CC(S(=O)(=O)NC(N)=O)=C2S(=O)(=O)C(C)CC2=C1 Chemical compound C1=CC(S(=O)(=O)NC(N)=O)=C2S(=O)(=O)C(C)CC2=C1 QNNQOOKFUPNAEY-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
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
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- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical class OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 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
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- REEQLXCGVXDJSQ-UHFFFAOYSA-N trichlopyr Chemical compound OC(=O)COC1=NC(Cl)=C(Cl)C=C1Cl REEQLXCGVXDJSQ-UHFFFAOYSA-N 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
- IMEVJVISCHQJRM-UHFFFAOYSA-N triflusulfuron-methyl Chemical compound COC(=O)C1=CC=CC(C)=C1S(=O)(=O)NC(=O)NC1=NC(OCC(F)(F)F)=NC(N(C)C)=N1 IMEVJVISCHQJRM-UHFFFAOYSA-N 0.000 description 1
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-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 (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10145019.2 | 2001-09-13 | ||
| DE10145019A DE10145019A1 (de) | 2001-09-13 | 2001-09-13 | Kombinationen aus Herbiziden und Safenern |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2006131048/04A Division RU2420065C2 (ru) | 2001-09-13 | 2002-09-06 | Способ борьбы с вредными растениями в культурах полезных растений |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| RU2004111283A RU2004111283A (ru) | 2005-04-10 |
| RU2291616C2 true RU2291616C2 (ru) | 2007-01-20 |
Family
ID=7698831
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2004111283/15A RU2291616C2 (ru) | 2001-09-13 | 2002-09-06 | Комбинация из гербицидов и защитных средств |
| RU2006131048/04A RU2420065C2 (ru) | 2001-09-13 | 2002-09-06 | Способ борьбы с вредными растениями в культурах полезных растений |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2006131048/04A RU2420065C2 (ru) | 2001-09-13 | 2002-09-06 | Способ борьбы с вредными растениями в культурах полезных растений |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US6914035B2 (enExample) |
| EP (1) | EP1427281B1 (enExample) |
| JP (1) | JP4384910B2 (enExample) |
| CN (1) | CN1309302C (enExample) |
| AR (2) | AR036480A1 (enExample) |
| BR (1) | BR0212488B1 (enExample) |
| CA (1) | CA2460481C (enExample) |
| DE (2) | DE10145019A1 (enExample) |
| DK (1) | DK1427281T3 (enExample) |
| ES (1) | ES2294161T3 (enExample) |
| FR (1) | FR12C0012I2 (enExample) |
| HR (1) | HRP20040246B1 (enExample) |
| HU (1) | HU229517B1 (enExample) |
| MX (1) | MXPA04002382A (enExample) |
| PL (1) | PL205316B1 (enExample) |
| PT (1) | PT1427281E (enExample) |
| RS (1) | RS50865B (enExample) |
| RU (2) | RU2291616C2 (enExample) |
| SI (1) | SI1427281T1 (enExample) |
| UA (1) | UA76206C2 (enExample) |
| WO (1) | WO2003022050A1 (enExample) |
| ZA (1) | ZA200401406B (enExample) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| 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 |
| RU2802004C1 (ru) * | 2023-02-28 | 2023-08-22 | Акционерное общество "Щелково Агрохим" | Способ получения тифенсульфурон-метила |
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| 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 |
| DK1951052T3 (en) * | 2005-11-17 | 2017-08-14 | Bayer Ip Gmbh | AFFICIENT HERBICIDE AGENT ON A SUSPENSION CONCENTRATE CONTAINING HERBICIDES AND SAFENES |
| 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 |
| EP2078089B1 (en) | 2006-10-31 | 2016-05-04 | E. I. du Pont de Nemours and Company | Soybean event dp-305423-1 and compositions and methods for the identification and/or detection thereof |
| US20090215625A1 (en) * | 2008-01-07 | 2009-08-27 | Auburn University | Combinations of Herbicides and Safeners |
| EP2092825A1 (de) | 2008-02-21 | 2009-08-26 | Bayer CropScience Aktiengesellschaft | Herbizid-Kombinationen enthaltend ein Herbizid der Klasse der Diamino-s-triazine |
| CA2730388A1 (en) * | 2008-07-11 | 2010-01-14 | Floratine Biosciences, Inc. | Foliarly applicable silicon nutrition compositions & methods |
| CN102740689B (zh) | 2009-09-03 | 2015-09-23 | Fb科技控股公司 | 种子处理组合物及方法 |
| JP2013505892A (ja) * | 2009-09-28 | 2013-02-21 | 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 | 肥料組成物および方法 |
| AR081604A1 (es) * | 2009-09-28 | 2012-10-10 | Fbsciences Holdings Inc | Metodos para reducir el estres en las plantas y para regular al menos un gen de una especie vegetal |
| JP2011157334A (ja) * | 2010-02-04 | 2011-08-18 | Sumitomo Chemical Co Ltd | 雑草の防除方法 |
| EP2592920A4 (en) | 2010-07-15 | 2017-08-02 | FBSciences Holdings, Inc. | Microorganism compositions and methods |
| BR112013003224A2 (pt) | 2010-08-13 | 2016-06-07 | Pioneer Hi Bred Int | "construto de promotor quimérico, cassete de expressão, vetor de expressão, método de obtenção de uma planta, método para regular a expressão de um polinucleotídeo de interesse, polinucleotídeo, método para expressar um polinucleotídeo de interesse" |
| CA2818918A1 (en) | 2010-11-24 | 2012-05-31 | Pioneer Hi-Bred International, Inc. | Brassica gat event dp-061061-7 and compositions and methods for the identification and/or detection thereof |
| CN107815462A (zh) | 2010-11-24 | 2018-03-20 | 先锋国际良种公司 | 芸苔gat事件dp‑073496‑4及其鉴定和/或检测组合物和方法 |
| 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 |
| US10448635B2 (en) | 2012-01-12 | 2019-10-22 | Fbsciences Holdings, Inc. | Modulation of plant biology |
| JP2013184912A (ja) * | 2012-03-07 | 2013-09-19 | Sumitomo Chemical Co Ltd | 除草用組成物 |
| UA117810C2 (uk) | 2012-05-24 | 2018-10-10 | Байєр Кропсайєнс Акцієнгезелльшафт | Гербіцидні композиції, які містять n-(тетразол-5-іл)арилкарбоксаміди |
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| WO2014172551A1 (en) | 2013-04-17 | 2014-10-23 | Sepro Corporation | Herbicidal compositions and methods |
| 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 |
| UA120916C2 (uk) | 2013-10-25 | 2020-03-10 | Байєр Кропсайєнс Акцієнгезелльшафт | Гербіцидні композиції, що містять аміди n-(1,3,4-оксадіазол-2-іл)-арилкарбонової кислоти |
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| AU2018279646B2 (en) | 2017-06-08 | 2023-04-06 | Vertex Pharmaceuticals Incorporated | Methods of treatment for cystic fibrosis |
| CA3069226A1 (en) | 2017-07-17 | 2019-01-24 | Vertex Pharmaceuticals Incorporated | Methods of treatment for cystic fibrosis |
| ES2912657T3 (es) | 2017-08-02 | 2022-05-26 | Vertex Pharma | Procesos para preparar compuestos de pirrolidina |
| AU2018351533B2 (en) | 2017-10-19 | 2023-02-02 | Vertex Pharmaceuticals Incorporated | Crystalline forms and compositions of CFTR modulators |
| JP7245834B2 (ja) | 2017-12-08 | 2023-03-24 | バーテックス ファーマシューティカルズ インコーポレイテッド | 嚢胞性線維症膜コンダクタンス制御因子のモジュレーターを作成するためのプロセス |
| 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 (de) | 2019-03-15 | 2024-04-17 | Polymetrix AG | Verfahren zum recycling von polyolefinen |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| TR27434A (tr) * | 1992-03-12 | 1995-05-23 | Rhone Poulenc Agrochimie | Yeni 4-benzoilisoksazol türevleri, bunlari ihtiva eden terkipler ve bunlarin herbisidler olarak kullanilmalari. |
| EA001470B1 (ru) * | 1996-03-15 | 2001-04-23 | Новартис Аг | Синергетическая гербицидная композиция и способ борьбы с сорняками |
| 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 (de) * | 1998-06-26 | 2001-04-11 | Novartis Pharma AG. | Herbizides mittel |
| DE19853827A1 (de) | 1998-11-21 | 2000-05-25 | Aventis Cropscience Gmbh | Kombinationen aus Herbiziden und Safenern |
| HU230234B1 (hu) | 1999-09-08 | 2015-10-28 | Aventis Cropscience Uk Ltd. | Új herbicid készítmények |
-
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 EP EP02764874A patent/EP1427281B1/de not_active Expired - Lifetime
- 2002-09-06 RS YUP-221/04A patent/RS50865B/sr unknown
- 2002-09-06 RU RU2004111283/15A patent/RU2291616C2/ru active Protection Beyond IP Right Term
- 2002-09-06 BR BRPI0212488-2A patent/BR0212488B1/pt active IP Right Grant
- 2002-09-06 MX MXPA04002382A patent/MXPA04002382A/es active IP Right Grant
- 2002-09-06 DK DK02764874T patent/DK1427281T3/da active
- 2002-09-06 HR HRP20040246AA patent/HRP20040246B1/xx not_active IP Right Cessation
- 2002-09-06 JP JP2003526192A patent/JP4384910B2/ja not_active Expired - Lifetime
- 2002-09-06 HU HU0402105A patent/HU229517B1/hu active Protection Beyond IP Right Term
- 2002-09-06 CN CNB028178998A patent/CN1309302C/zh not_active Expired - Lifetime
- 2002-09-06 RU RU2006131048/04A patent/RU2420065C2/ru active
- 2002-09-06 SI SI200230662T patent/SI1427281T1/sl unknown
- 2002-09-06 CA CA2460481A patent/CA2460481C/en not_active Expired - Lifetime
- 2002-09-06 WO PCT/EP2002/009973 patent/WO2003022050A1/de not_active Ceased
- 2002-09-06 PL PL368759A patent/PL205316B1/pl unknown
- 2002-09-06 ES ES02764874T patent/ES2294161T3/es 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
- 2002-09-11 US US10/241,136 patent/US6914035B2/en not_active Expired - Lifetime
- 2002-09-11 AR ARP020103442A patent/AR036480A1/es not_active Application Discontinuation
-
2004
- 2004-02-20 ZA ZA200401406A patent/ZA200401406B/en unknown
-
2012
- 2012-03-02 FR FR12C0012C patent/FR12C0012I2/fr active Active
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2014
- 2014-01-09 AR ARP140100083A patent/AR094405A2/es unknown
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| 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 |
| RU2802004C1 (ru) * | 2023-02-28 | 2023-08-22 | Акционерное общество "Щелково Агрохим" | Способ получения тифенсульфурон-метила |
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