NO322756B1 - Herbicide blandinger med synergistisk virkning, samt fremgangsmate for bekjempelse av uonsket plantevekst ved bruk av disse. - Google Patents
Herbicide blandinger med synergistisk virkning, samt fremgangsmate for bekjempelse av uonsket plantevekst ved bruk av disse. Download PDFInfo
- Publication number
- NO322756B1 NO322756B1 NO19981240A NO981240A NO322756B1 NO 322756 B1 NO322756 B1 NO 322756B1 NO 19981240 A NO19981240 A NO 19981240A NO 981240 A NO981240 A NO 981240A NO 322756 B1 NO322756 B1 NO 322756B1
- Authority
- NO
- Norway
- Prior art keywords
- herbicidal
- alkoxy
- formula
- sulfonylurea
- alkyl
- Prior art date
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- 230000002363 herbicidal effect Effects 0.000 title claims description 41
- 239000000203 mixture Substances 0.000 title claims description 26
- 238000000034 method Methods 0.000 title claims description 10
- 230000008635 plant growth Effects 0.000 title claims description 4
- 230000002195 synergetic effect Effects 0.000 title description 7
- 150000001875 compounds Chemical class 0.000 claims description 25
- 239000004009 herbicide Substances 0.000 claims description 24
- 229940100389 Sulfonylurea Drugs 0.000 claims description 20
- -1 methoxy, ethoxy Chemical group 0.000 claims description 19
- 229910052739 hydrogen Inorganic materials 0.000 claims description 16
- 239000001257 hydrogen Substances 0.000 claims description 16
- YROXIXLRRCOBKF-UHFFFAOYSA-N sulfonylurea Chemical class OC(=N)N=S(=O)=O YROXIXLRRCOBKF-UHFFFAOYSA-N 0.000 claims description 16
- 229910052736 halogen Inorganic materials 0.000 claims description 15
- 150000002367 halogens Chemical class 0.000 claims description 15
- 150000002431 hydrogen Chemical class 0.000 claims description 13
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 9
- 150000003839 salts Chemical class 0.000 claims description 9
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 8
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 8
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 7
- ZOMSMJKLGFBRBS-UHFFFAOYSA-N bentazone Chemical compound C1=CC=C2NS(=O)(=O)N(C(C)C)C(=O)C2=C1 ZOMSMJKLGFBRBS-UHFFFAOYSA-N 0.000 claims description 7
- 239000011737 fluorine Substances 0.000 claims description 7
- 229910052731 fluorine Inorganic materials 0.000 claims description 7
- 239000005476 Bentazone Substances 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- CNBGNNVCVSKAQZ-UHFFFAOYSA-N benzidamine Natural products C12=CC=CC=C2C(OCCCN(C)C)=NN1CC1=CC=CC=C1 CNBGNNVCVSKAQZ-UHFFFAOYSA-N 0.000 claims description 6
- 239000000460 chlorine Substances 0.000 claims description 6
- 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 claims description 6
- 239000007787 solid Substances 0.000 claims description 6
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims description 6
- 125000004206 2,2,2-trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 claims description 5
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims description 4
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims description 4
- MZHCENGPTKEIGP-RXMQYKEDSA-N (R)-dichlorprop Chemical compound OC(=O)[C@@H](C)OC1=CC=C(Cl)C=C1Cl MZHCENGPTKEIGP-RXMQYKEDSA-N 0.000 claims description 4
- WNTGYJSOUMFZEP-SSDOTTSWSA-N (R)-mecoprop Chemical compound OC(=O)[C@@H](C)OC1=CC=C(Cl)C=C1C WNTGYJSOUMFZEP-SSDOTTSWSA-N 0.000 claims description 4
- 239000005505 Dichlorprop-P Substances 0.000 claims description 4
- 239000005507 Diflufenican Substances 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- 239000005576 Mecoprop-P Substances 0.000 claims description 4
- 239000005586 Nicosulfuron Substances 0.000 claims description 4
- 239000005616 Rimsulfuron Substances 0.000 claims description 4
- CSPPKDPQLUUTND-NBVRZTHBSA-N Sethoxydim Chemical compound CCO\N=C(/CCC)C1=C(O)CC(CC(C)SCC)CC1=O CSPPKDPQLUUTND-NBVRZTHBSA-N 0.000 claims description 4
- 239000005621 Terbuthylazine Substances 0.000 claims description 4
- MXWJVTOOROXGIU-UHFFFAOYSA-N atrazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)C)=N1 MXWJVTOOROXGIU-UHFFFAOYSA-N 0.000 claims description 4
- NNKKTZOEKDFTBU-YBEGLDIGSA-N cinidon ethyl Chemical compound C1=C(Cl)C(/C=C(\Cl)C(=O)OCC)=CC(N2C(C3=C(CCCC3)C2=O)=O)=C1 NNKKTZOEKDFTBU-YBEGLDIGSA-N 0.000 claims description 4
- WYEHFWKAOXOVJD-UHFFFAOYSA-N diflufenican Chemical compound FC1=CC(F)=CC=C1NC(=O)C1=CC=CN=C1OC1=CC=CC(C(F)(F)F)=C1 WYEHFWKAOXOVJD-UHFFFAOYSA-N 0.000 claims description 4
- 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 claims description 4
- 229910052760 oxygen Inorganic materials 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- FFSSWMQPCJRCRV-UHFFFAOYSA-N quinclorac Chemical compound ClC1=CN=C2C(C(=O)O)=C(Cl)C=CC2=C1 FFSSWMQPCJRCRV-UHFFFAOYSA-N 0.000 claims description 4
- MEFOUWRMVYJCQC-UHFFFAOYSA-N rimsulfuron Chemical compound CCS(=O)(=O)C1=CC=CN=C1S(=O)(=O)NC(=O)NC1=NC(OC)=CC(OC)=N1 MEFOUWRMVYJCQC-UHFFFAOYSA-N 0.000 claims description 4
- 229910052717 sulfur Inorganic materials 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
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 3
- 239000005501 Cycloxydim Substances 0.000 claims description 3
- 125000003545 alkoxy group Chemical group 0.000 claims description 3
- 125000004414 alkyl thio group Chemical group 0.000 claims description 3
- GGWHBJGBERXSLL-NBVRZTHBSA-N chembl113137 Chemical compound C1C(=O)C(C(=N/OCC)/CCC)=C(O)CC1C1CSCCC1 GGWHBJGBERXSLL-NBVRZTHBSA-N 0.000 claims description 3
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims description 2
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims description 2
- 125000006012 2-chloroethoxy group Chemical group 0.000 claims description 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 2
- 239000002671 adjuvant Substances 0.000 claims description 2
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 2
- 125000004789 chlorodifluoromethoxy group Chemical group ClC(O*)(F)F 0.000 claims description 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 2
- QPJDMGCKMHUXFD-UHFFFAOYSA-N cyanogen chloride Chemical compound ClC#N QPJDMGCKMHUXFD-UHFFFAOYSA-N 0.000 claims description 2
- 125000004786 difluoromethoxy group Chemical group [H]C(F)(F)O* 0.000 claims description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000006125 ethylsulfonyl group Chemical group 0.000 claims description 2
- 230000035784 germination Effects 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims description 2
- 239000007788 liquid Substances 0.000 claims description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 2
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims description 2
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 2
- 125000001424 substituent group Chemical group 0.000 claims description 2
- 125000001889 triflyl group Chemical group FC(F)(F)S(*)(=O)=O 0.000 claims description 2
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 2
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 2
- 101100054666 Streptomyces halstedii sch3 gene Proteins 0.000 claims 1
- 125000004438 haloalkoxy group Chemical group 0.000 claims 1
- 241000196324 Embryophyta Species 0.000 description 17
- 230000000694 effects Effects 0.000 description 9
- 239000003921 oil Substances 0.000 description 7
- 239000013543 active substance Substances 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 238000009472 formulation Methods 0.000 description 5
- 239000008187 granular material Substances 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 4
- 239000000839 emulsion Substances 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- BGNQYGRXEXDAIQ-UHFFFAOYSA-N Pyrazosulfuron-ethyl Chemical group C1=NN(C)C(S(=O)(=O)NC(=O)NC=2N=C(OC)C=C(OC)N=2)=C1C(=O)OCC BGNQYGRXEXDAIQ-UHFFFAOYSA-N 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 239000004480 active ingredient Substances 0.000 description 3
- 239000000969 carrier Substances 0.000 description 3
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- 235000021533 Beta vulgaris Nutrition 0.000 description 2
- 241000335053 Beta vulgaris Species 0.000 description 2
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- 239000005562 Glyphosate Substances 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 240000007594 Oryza sativa Species 0.000 description 2
- 235000007164 Oryza sativa Nutrition 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 240000006394 Sorghum bicolor Species 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
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- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- 150000001342 alkaline earth metals Chemical class 0.000 description 2
- 150000005215 alkyl ethers Chemical class 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
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- 239000011230 binding agent Substances 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
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- MZZBPDKVEFVLFF-UHFFFAOYSA-N cyanazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)(C)C#N)=N1 MZZBPDKVEFVLFF-UHFFFAOYSA-N 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
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- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 2
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- KGMBZDZHRAFLBY-UHFFFAOYSA-N n-(butoxymethyl)-n-(2-tert-butyl-6-methylphenyl)-2-chloroacetamide Chemical compound CCCCOCN(C(=O)CCl)C1=C(C)C=CC=C1C(C)(C)C KGMBZDZHRAFLBY-UHFFFAOYSA-N 0.000 description 2
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- 239000000377 silicon dioxide Substances 0.000 description 1
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- ODCWYMIRDDJXKW-UHFFFAOYSA-N simazine Chemical compound CCNC1=NC(Cl)=NC(NCC)=N1 ODCWYMIRDDJXKW-UHFFFAOYSA-N 0.000 description 1
- MGLWZSOBALDPEK-UHFFFAOYSA-N simetryn Chemical compound CCNC1=NC(NCC)=NC(SC)=N1 MGLWZSOBALDPEK-UHFFFAOYSA-N 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000004071 soot Substances 0.000 description 1
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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 1
- ZDXMLEQEMNLCQG-UHFFFAOYSA-N sulfometuron methyl Chemical group COC(=O)C1=CC=CC=C1S(=O)(=O)NC(=O)NC1=NC(C)=CC(C)=N1 ZDXMLEQEMNLCQG-UHFFFAOYSA-N 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
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- 229910052623 talc Inorganic materials 0.000 description 1
- 239000002641 tar oil Substances 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
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- AHTPATJNIAFOLR-UHFFFAOYSA-N thifensulfuron-methyl Chemical group S1C=CC(S(=O)(=O)NC(=O)NC=2N=C(OC)N=C(C)N=2)=C1C(=O)OC AHTPATJNIAFOLR-UHFFFAOYSA-N 0.000 description 1
- SRVJKTDHMYAMHA-WUXMJOGZSA-N thioacetazone Chemical compound CC(=O)NC1=CC=C(\C=N\NC(N)=S)C=C1 SRVJKTDHMYAMHA-WUXMJOGZSA-N 0.000 description 1
- 229960003231 thioacetazone Drugs 0.000 description 1
- 239000011573 trace mineral Substances 0.000 description 1
- 235000013619 trace mineral Nutrition 0.000 description 1
- DQFPEYARZIQXRM-LTGZKZEYSA-N tralkoxydim Chemical compound C1C(=O)C(C(/CC)=N/OCC)=C(O)CC1C1=C(C)C=C(C)C=C1C DQFPEYARZIQXRM-LTGZKZEYSA-N 0.000 description 1
- XOPFESVZMSQIKC-UHFFFAOYSA-N triasulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)OCCCl)=N1 XOPFESVZMSQIKC-UHFFFAOYSA-N 0.000 description 1
- 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
- IMEVJVISCHQJRM-UHFFFAOYSA-N triflusulfuron-methyl Chemical group 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
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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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/36—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< directly attached to at least one heterocyclic ring; Thio analogues thereof
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)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19534910A DE19534910A1 (de) | 1995-09-20 | 1995-09-20 | Herbizide Mischungen mit synergistischer Wirkung |
| PCT/EP1996/003996 WO1997010714A1 (de) | 1995-09-20 | 1996-09-12 | Herbizide mischungen mit synergistischer wirkung |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO981240L NO981240L (no) | 1998-03-19 |
| NO981240D0 NO981240D0 (no) | 1998-03-19 |
| NO322756B1 true NO322756B1 (no) | 2006-12-04 |
Family
ID=7772673
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO19981240A NO322756B1 (no) | 1995-09-20 | 1998-03-19 | Herbicide blandinger med synergistisk virkning, samt fremgangsmate for bekjempelse av uonsket plantevekst ved bruk av disse. |
Country Status (31)
| Country | Link |
|---|---|
| US (3) | US6054410A (ro) |
| EP (3) | EP0859548B1 (ro) |
| JP (1) | JP2000501377A (ro) |
| KR (1) | KR100428279B1 (ro) |
| CN (4) | CN1200652A (ro) |
| AR (1) | AR003640A1 (ro) |
| AT (3) | ATE442043T1 (ro) |
| AU (1) | AU710367B2 (ro) |
| BG (1) | BG64139B1 (ro) |
| BR (1) | BR9610586A (ro) |
| CA (1) | CA2230113A1 (ro) |
| CZ (3) | CZ297236B6 (ro) |
| DE (4) | DE19534910A1 (ro) |
| DK (3) | DK0859548T3 (ro) |
| EA (1) | EA001310B1 (ro) |
| ES (3) | ES2235197T3 (ro) |
| GE (1) | GEP20012544B (ro) |
| HU (2) | HU229791B1 (ro) |
| IL (1) | IL123609A (ro) |
| NL (1) | NL350067I2 (ro) |
| NO (1) | NO322756B1 (ro) |
| NZ (1) | NZ319131A (ro) |
| PL (1) | PL191615B1 (ro) |
| PT (3) | PT1477063E (ro) |
| RO (1) | RO118618B1 (ro) |
| SI (3) | SI1477063T1 (ro) |
| SK (1) | SK284100B6 (ro) |
| TR (8) | TR199802609T2 (ro) |
| UA (1) | UA53629C2 (ro) |
| WO (1) | WO1997010714A1 (ro) |
| ZA (1) | ZA967911B (ro) |
Families Citing this family (64)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6586367B2 (en) | 1996-09-05 | 2003-07-01 | Syngenta Crop Protection, Inc. | Process for the control of weeds |
| IT1292088B1 (it) * | 1997-06-05 | 1999-01-25 | Isagro Ricerca Srl | Composizioni erbicide |
| GB9814846D0 (en) | 1998-07-08 | 1998-09-09 | Rhone Poulenc Agriculture | New herbicidal compositions |
| DE19832017A1 (de) * | 1998-07-16 | 2000-01-27 | Hoechst Schering Agrevo Gmbh | Herbizide Mittel mit substituierten Phenylsulfonylharnstoffen zur Unkrautbekämpfung in Reis |
| WO2000003592A2 (de) * | 1998-07-16 | 2000-01-27 | Aventis Cropscience Gnbh | Herbizide mittel mit substituierten phenoxysulfonylharnstoffen |
| ATE294501T1 (de) | 1998-07-16 | 2005-05-15 | Bayer Cropscience Gmbh | Herbizide mittel |
| DE19836684A1 (de) | 1998-08-13 | 2000-02-17 | Hoechst Schering Agrevo Gmbh | Herbizide Mittel für tolerante oder resistente Reiskulturen |
| WO2000008932A1 (de) * | 1998-08-13 | 2000-02-24 | Aventis Cropscience Gmbh | Herbizide mittel mit acylierten aminophenylsulfonylharnstoffen |
| DE19836700A1 (de) † | 1998-08-13 | 2000-02-17 | Hoechst Schering Agrevo Gmbh | Herbizide Mittel für tolerante oder resistente Getreidekulturen |
| JP2000351703A (ja) * | 1999-06-07 | 2000-12-19 | Sumitomo Chem Co Ltd | 除草剤組成物 |
| CZ20021728A3 (cs) * | 1999-11-18 | 2002-10-16 | Bayer Aktiengesellschaft | Synergické herbicidní kombinace účinných látek a jejich pouľití |
| JP2003528117A (ja) * | 2000-03-27 | 2003-09-24 | ビーエーエスエフ アクチェンゲゼルシャフト | 相乗作用による除草方法及び除草剤組成物 |
| US6396408B2 (en) * | 2000-03-31 | 2002-05-28 | Donnelly Corporation | Digital electrochromic circuit with a vehicle network |
| PL204904B1 (pl) | 2000-04-04 | 2010-02-26 | Basf Ag | Kompozycja chwastobójcza, sposób zwalczania niepożądanych roślin i zastosowanie kompozycji chwastobójczej |
| AR030580A1 (es) * | 2000-08-31 | 2003-08-27 | Basf Ag | Mezclas herbicidas |
| TWI243019B (en) | 2000-08-31 | 2005-11-11 | Basf Ag | Process for the preparation of a solid herbicidal formulation |
| NZ517784A (en) * | 2002-03-14 | 2004-10-29 | Peter James Hayward | Synergistic mixture of triclopyr and sulfonylurea such as metsulfuron-methyl to make a herbicide composition |
| EP1917857A1 (en) | 2002-07-24 | 2008-05-07 | Basf Se | Synergistically acting herbicidal mixtures |
| ATE412337T1 (de) * | 2002-08-08 | 2008-11-15 | Syngenta Participations Ag | Herbizide zusammensetzungen |
| CN1305377C (zh) * | 2002-11-15 | 2007-03-21 | 王正权 | 嗪草酸与磺酰脲类的除草剂组合物 |
| BRPI0417671B1 (pt) * | 2003-12-19 | 2015-07-28 | Basf Ag | Método para controle de plantas coníferas |
| US7288462B2 (en) * | 2004-10-27 | 2007-10-30 | Carleton Life Support Systems, Inc. | Buffer zone for the prevention of metal migration |
| EP1856266A4 (en) * | 2005-03-02 | 2015-04-22 | Inst Nac De Tecnologia Agropecuaria | HERBICIDE-RESISTANT RICE PLANTS, POLYNUCLEOTIDES ENCODING HIGH HERBICIDE-RESISTANT ACETHYDROXYACID SYNTHASE SUBUNIT PROTEINS, AND METHODS OF USE |
| US20190032029A1 (en) * | 2005-03-02 | 2019-01-31 | Instituto Nacional De Technologia Agropecuaria | Herbicide-resistant rice plants, polynucleotides encoding herbicide-resistant acetohydroxyacid synthase large subunit proteins, and methods of use |
| CN103484531B (zh) * | 2005-07-01 | 2015-10-21 | 巴斯福股份公司 | 抗除草剂的向日葵植物、编码抗除草剂的乙酰羟酸合酶大亚基蛋白的多核苷酸和使用方法 |
| CN101262770A (zh) * | 2005-09-08 | 2008-09-10 | 拜尔作物科学股份公司 | 新型的含磺酰胺的固体配制剂 |
| EP1836894A1 (de) | 2006-03-25 | 2007-09-26 | Bayer CropScience GmbH | Neue Sulfonamid-haltige feste Formulungen |
| PT1928245E (pt) * | 2005-09-28 | 2010-12-23 | Ishihara Sangyo Kaisha | Composição herbicida |
| EP2052606A1 (de) * | 2007-10-24 | 2009-04-29 | Bayer CropScience AG | Herbizid-Kombination |
| EP2052608A1 (de) * | 2007-10-24 | 2009-04-29 | Bayer CropScience AG | Herbizid-Kombination |
| EP2052614A1 (de) * | 2007-10-24 | 2009-04-29 | Bayer CropScience AG | Herbizid-Kombination |
| EP2052615A1 (de) * | 2007-10-24 | 2009-04-29 | Bayer CropScience AG | Herbizid-Kombination |
| EP2052607A1 (de) * | 2007-10-24 | 2009-04-29 | Bayer CropScience AG | Herbizid-Kombination |
| EP2052609A1 (de) * | 2007-10-24 | 2009-04-29 | Bayer CropScience AG | Herbizid-Kombination |
| EP2052613A1 (de) * | 2007-10-24 | 2009-04-29 | Bayer CropScience AG | Herbizid-Kombination |
| EP2052612A1 (de) * | 2007-10-24 | 2009-04-29 | Bayer CropScience AG | Herbizid-Kombination |
| EP2052610A1 (de) * | 2007-10-24 | 2009-04-29 | Bayer CropScience AG | Herbizid-Kombination |
| EP2052611A1 (de) * | 2007-10-24 | 2009-04-29 | Bayer CropScience AG | Herbizid-Kombination |
| AU2009212525B2 (en) * | 2008-02-05 | 2012-06-21 | Arysta Lifescience North America, Llc | Solid formulation of low melting active compound |
| DE102008037631A1 (de) | 2008-08-14 | 2010-02-18 | Bayer Cropscience Ag | Herbizid-Kombination mit Dimethoxytriazinyl-substituierten Difluormethansulfonylaniliden |
| DE102008037629A1 (de) * | 2008-08-14 | 2010-02-18 | Bayer Cropscience Ag | Herbizid-Kombination mit Dimethoxytriazinyl-substituierten Difluormethansulfonylaniliden |
| CA2786612C (en) | 2010-01-11 | 2018-02-27 | The Lubrizol Corporation | Overbased alkylated arylalkyl sulfonates |
| AR081621A1 (es) * | 2010-02-04 | 2012-10-10 | Bayer Cropscience Ag | Procedimiento para la produccion de formulaciones estables de materiales solidos de sulfonamidas |
| US8324132B2 (en) | 2010-03-31 | 2012-12-04 | E. I. Du Pont De Nemours And Company | Mixture and method for controlling undesired vegetation |
| JP5829044B2 (ja) * | 2010-05-06 | 2015-12-09 | 石原産業株式会社 | 除草組成物 |
| CN101911948B (zh) * | 2010-08-20 | 2013-07-31 | 陕西上格之路生物科学有限公司 | 一种含醚磺隆的除草剂组合物 |
| EA017932B1 (ru) * | 2010-10-14 | 2013-04-30 | Юрий Аглямович ГАРИПОВ | Водно-гликолевый раствор гербицидной композиции |
| CN103039485A (zh) * | 2011-10-17 | 2013-04-17 | 南京华洲药业有限公司 | 一种含醚磺隆与二甲戊乐灵的混合除草剂及其应用 |
| CN102362597A (zh) * | 2011-11-08 | 2012-02-29 | 陕西美邦农药有限公司 | 一种含乙氧磺隆与唑草酮的除草组合物 |
| CN102550582A (zh) * | 2012-01-13 | 2012-07-11 | 河南金田地农化有限责任公司 | 一种除草组合物及其应用 |
| PT2823707T (pt) | 2012-03-09 | 2018-10-12 | Ishihara Sangyo Kaisha | Composição herbicida |
| US8979564B2 (en) * | 2013-03-15 | 2015-03-17 | Data I/O Corporation | Socket having a pin plate with a port aligned with a dimple in a pocket of a base plate |
| CN103250724A (zh) * | 2013-05-22 | 2013-08-21 | 吴江市德佐日用化学品有限公司 | 一种含噻吩磺隆与氯吡嘧磺隆的除草组合物 |
| CN105165866B (zh) * | 2013-07-03 | 2017-08-08 | 江苏龙灯化学有限公司 | 增效除草组合物 |
| US9072298B2 (en) * | 2013-11-01 | 2015-07-07 | Rotam Agrochem Intrnational Company Limited | Synergistic herbicidal composition |
| CN104805124A (zh) * | 2014-09-17 | 2015-07-29 | 德强生物股份有限公司 | 一种茵达霉素及其制备方法和用途 |
| CN104285997A (zh) * | 2014-10-09 | 2015-01-21 | 安徽丰乐农化有限责任公司 | 一种含氰氟草酯、氯吡嘧磺隆和氯氟吡氧乙酸的水稻茎叶除草剂 |
| CN104705331A (zh) * | 2015-03-23 | 2015-06-17 | 广东中迅农科股份有限公司 | 含有氯吡嘧磺隆和敌草隆以及莠灭净的除草组合物 |
| CN105557733A (zh) * | 2015-12-11 | 2016-05-11 | 汤云鹤 | 一种含氟唑磺隆和氟噻草胺的农药组合物及其在防治小麦田杂草中的应用 |
| CN105613536B (zh) * | 2016-03-31 | 2018-06-08 | 上海市农药研究所有限公司 | 农用除草剂及其应用 |
| CN107960421A (zh) * | 2016-10-20 | 2018-04-27 | 潍坊先达化工有限公司 | 一种除草组合物及其应用 |
| CN107197862A (zh) * | 2017-05-26 | 2017-09-26 | 浙江天丰生物科学有限公司 | 一种含仲丁灵、乙氧磺隆的可分散油悬浮剂及其制备方法 |
| CN108051511A (zh) * | 2017-11-25 | 2018-05-18 | 于世金 | 一种茶叶中酚类农药的检测方法 |
| US11576381B2 (en) | 2019-02-25 | 2023-02-14 | Albaugh, Llc | Composition and a method of using the composition to increase wheat yield |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3716657A1 (de) * | 1987-05-19 | 1988-12-01 | Basf Ag | Herbizide sulfonamide, verfahren zu ihrer herstellung und ihre verwendung zur beeinflussung des pflanzenwachstums |
| DE3909146A1 (de) * | 1989-03-21 | 1990-10-18 | Basf Ag | Herbizide ((1,3,5-triazin-2-yl) aminosulfonyl)benzoesaeureester, verfahren zu ihrer herstellung und ihre verwendung |
| DE4007683A1 (de) * | 1990-03-10 | 1991-09-12 | Basf Ag | Herbizide sulfonylharnstoffe, verfahren und zwischenprodukte zu ihrer herstellung |
| US5599769A (en) * | 1990-11-13 | 1997-02-04 | Hoechst Aktiengesellschaft | Synergistic herbicidal compositions comprising glyphosate or glufosinate in combination with a sulfonylurea herbicide |
| DE4038430A1 (de) * | 1990-12-01 | 1992-06-04 | Basf Ag | Herbizide n-((1,3,5-triazin-2-yl)-aminocarbonyl) benzolsulfonamide |
| RU94046249A (ru) * | 1992-06-16 | 1996-10-27 | Е.И.Дюпон де Немур энд Компани (US) | Сухие сыпучие композиции для сельского хозяйства на основе глифосата, изготовленные без сушки конечного продукта |
-
1995
- 1995-09-20 DE DE19534910A patent/DE19534910A1/de not_active Withdrawn
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