ZA200610566B - Herbicidal agents - Google Patents

Herbicidal agents Download PDF

Info

Publication number: ZA200610566B
Authority: ZA; South Africa
Prior art keywords: salts; alkyl; group; herbicides; alkoxy
Prior art date: 2004-07-17

Application number

ZA200610566A

Other languages

English (en)

Inventor

Hacker Erwin

Rose Eckhard

Dietrich Hansjorg

Original Assignee

Bayer Cropscience Gmbh

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

2004-07-17

Filing date

2006-12-15

Publication date

2008-06-25

2006-12-15 Application filed by Bayer Cropscience Gmbh filed Critical Bayer Cropscience Gmbh

2008-06-25 Publication of ZA200610566B publication Critical patent/ZA200610566B/en

Links

239000004009 herbicide Substances 0.000 title claims description 82
150000001875 compounds Chemical class 0.000 claims description 83
229910052799 carbon Inorganic materials 0.000 claims description 76
150000003839 salts Chemical class 0.000 claims description 75
-1 triclopyr-butotyl ester Chemical class 0.000 claims description 58
150000002148 esters Chemical class 0.000 claims description 33
230000002363 herbicidal effect Effects 0.000 claims description 28
229910052736 halogen Inorganic materials 0.000 claims description 22
150000002367 halogens Chemical class 0.000 claims description 22
239000000203 mixture Substances 0.000 claims description 17
239000002253 acid Substances 0.000 claims description 16
125000004432 carbon atom Chemical group C* 0.000 claims description 14
238000000034 method Methods 0.000 claims description 14
150000001721 carbon Chemical group 0.000 claims description 13
239000005562 Glyphosate Substances 0.000 claims description 8
238000009472 formulation Methods 0.000 claims description 7
XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 claims description 6
FIKAKWIAUPDISJ-UHFFFAOYSA-L paraquat dichloride Chemical class [Cl-].[Cl-].C1=C[N+](C)=CC=C1C1=CC=[N+](C)C=C1 FIKAKWIAUPDISJ-UHFFFAOYSA-L 0.000 claims description 5
REEQLXCGVXDJSQ-UHFFFAOYSA-N trichlopyr Chemical compound OC(=O)COC1=NC(Cl)=C(Cl)C=C1Cl REEQLXCGVXDJSQ-UHFFFAOYSA-N 0.000 claims description 5
CLQMBPJKHLGMQK-UHFFFAOYSA-N 2-(4-isopropyl-4-methyl-5-oxo-4,5-dihydro-1H-imidazol-2-yl)nicotinic acid Chemical compound N1C(=O)C(C(C)C)(C)N=C1C1=NC=CC=C1C(O)=O CLQMBPJKHLGMQK-UHFFFAOYSA-N 0.000 claims description 4
IAJOBQBIJHVGMQ-UHFFFAOYSA-N 2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid Chemical compound CP(O)(=O)CCC(N)C(O)=O IAJOBQBIJHVGMQ-UHFFFAOYSA-N 0.000 claims description 4
XMTQQYYKAHVGBJ-UHFFFAOYSA-N 3-(3,4-DICHLOROPHENYL)-1,1-DIMETHYLUREA Chemical compound CN(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 XMTQQYYKAHVGBJ-UHFFFAOYSA-N 0.000 claims description 4
CTSLUCNDVMMDHG-UHFFFAOYSA-N 5-bromo-3-(butan-2-yl)-6-methylpyrimidine-2,4(1H,3H)-dione Chemical compound CCC(C)N1C(=O)NC(C)=C(Br)C1=O CTSLUCNDVMMDHG-UHFFFAOYSA-N 0.000 claims description 4
KLSJWNVTNUYHDU-UHFFFAOYSA-N Amitrole Chemical compound NC1=NC=NN1 KLSJWNVTNUYHDU-UHFFFAOYSA-N 0.000 claims description 4
CHNUNORXWHYHNE-UHFFFAOYSA-N Oxadiazon Chemical compound C1=C(Cl)C(OC(C)C)=CC(N2C(OC(=N2)C(C)(C)C)=O)=C1Cl CHNUNORXWHYHNE-UHFFFAOYSA-N 0.000 claims description 4
239000005627 Triclopyr Substances 0.000 claims description 4
239000000654 additive Substances 0.000 claims description 4
ORFPWVRKFLOQHK-UHFFFAOYSA-N amicarbazone Chemical compound CC(C)C1=NN(C(=O)NC(C)(C)C)C(=O)N1N ORFPWVRKFLOQHK-UHFFFAOYSA-N 0.000 claims description 4
229940097068 glyphosate Drugs 0.000 claims description 4
RUCAXVJJQQJZGU-UHFFFAOYSA-M hydron;2-(phosphonatomethylamino)acetate;trimethylsulfanium Chemical compound C[S+](C)C.OP(O)(=O)CNCC([O-])=O RUCAXVJJQQJZGU-UHFFFAOYSA-M 0.000 claims description 4
PMHURSZHKKJGBM-UHFFFAOYSA-N isoxaben Chemical compound O1N=C(C(C)(CC)CC)C=C1NC(=O)C1=C(OC)C=CC=C1OC PMHURSZHKKJGBM-UHFFFAOYSA-N 0.000 claims description 4
QYPPRTNMGCREIM-UHFFFAOYSA-N methylarsonic acid Chemical compound C[As](O)(O)=O QYPPRTNMGCREIM-UHFFFAOYSA-N 0.000 claims description 4
FOXFZRUHNHCZPX-UHFFFAOYSA-N metribuzin Chemical compound CSC1=NN=C(C(C)(C)C)C(=O)N1N FOXFZRUHNHCZPX-UHFFFAOYSA-N 0.000 claims description 4
239000011814 protection agent Substances 0.000 claims description 4
239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 claims description 3
YOYAIZYFCNQIRF-UHFFFAOYSA-N 2,6-dichlorobenzonitrile Chemical compound ClC1=CC=CC(Cl)=C1C#N YOYAIZYFCNQIRF-UHFFFAOYSA-N 0.000 claims description 3
YHKBGVDUSSWOAB-UHFFFAOYSA-N 2-chloro-3-{2-chloro-5-[4-(difluoromethyl)-3-methyl-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl]-4-fluorophenyl}propanoic acid Chemical compound O=C1N(C(F)F)C(C)=NN1C1=CC(CC(Cl)C(O)=O)=C(Cl)C=C1F YHKBGVDUSSWOAB-UHFFFAOYSA-N 0.000 claims description 3
MBFHUWCOCCICOK-UHFFFAOYSA-N 4-iodo-2-[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamoylsulfamoyl]benzoic acid Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=C(I)C=2)C(O)=O)=N1 MBFHUWCOCCICOK-UHFFFAOYSA-N 0.000 claims description 3
239000003666 Amidosulfuron Substances 0.000 claims description 3
CTTHWASMBLQOFR-UHFFFAOYSA-N Amidosulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)N(C)S(C)(=O)=O)=N1 CTTHWASMBLQOFR-UHFFFAOYSA-N 0.000 claims description 3
239000005507 Diflufenican Substances 0.000 claims description 3
239000005510 Diuron Substances 0.000 claims description 3
HWATZEJQIXKWQS-UHFFFAOYSA-N Flazasulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CN=2)C(F)(F)F)=N1 HWATZEJQIXKWQS-UHFFFAOYSA-N 0.000 claims description 3
239000005560 Foramsulfuron Substances 0.000 claims description 3
239000005561 Glufosinate Substances 0.000 claims description 3
CAWXEEYDBZRFPE-UHFFFAOYSA-N Hexazinone Chemical compound O=C1N(C)C(N(C)C)=NC(=O)N1C1CCCCC1 CAWXEEYDBZRFPE-UHFFFAOYSA-N 0.000 claims description 3
239000005568 Iodosulfuron Substances 0.000 claims description 3
239000005570 Isoxaben Substances 0.000 claims description 3
239000005588 Oxadiazon Substances 0.000 claims description 3
239000005601 Propoxycarbazone Substances 0.000 claims description 3
HBPDKDSFLXWOAE-UHFFFAOYSA-N Tebuthiuron Chemical compound CNC(=O)N(C)C1=NN=C(C(C)(C)C)S1 HBPDKDSFLXWOAE-UHFFFAOYSA-N 0.000 claims description 3
NBQCNZYJJMBDKY-UHFFFAOYSA-N Terbacil Chemical compound CC=1NC(=O)N(C(C)(C)C)C(=O)C=1Cl NBQCNZYJJMBDKY-UHFFFAOYSA-N 0.000 claims description 3
VGPYEHKOIGNJKV-UHFFFAOYSA-N asulam Chemical compound COC(=O)NS(=O)(=O)C1=CC=C(N)C=C1 VGPYEHKOIGNJKV-UHFFFAOYSA-N 0.000 claims description 3
XOEMATDHVZOBSG-UHFFFAOYSA-N azafenidin Chemical compound C1=C(OCC#C)C(Cl)=CC(Cl)=C1N1C(=O)N2CCCCC2=N1 XOEMATDHVZOBSG-UHFFFAOYSA-N 0.000 claims description 3
HUBANNPOLNYSAD-UHFFFAOYSA-N clopyralid Chemical compound OC(=O)C1=NC(Cl)=CC=C1Cl HUBANNPOLNYSAD-UHFFFAOYSA-N 0.000 claims description 3
125000004093 cyano group Chemical group *C#N 0.000 claims description 3
IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 claims description 3
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 3
PXDNXJSDGQBLKS-UHFFFAOYSA-N foramsulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=C(NC=O)C=2)C(=O)N(C)C)=N1 PXDNXJSDGQBLKS-UHFFFAOYSA-N 0.000 claims description 3
JTHMVYBOQLDDIY-UHFFFAOYSA-N methyl 2-[(4-methyl-5-oxo-3-propoxy-1,2,4-triazole-1-carbonyl)sulfamoyl]benzoate Chemical compound O=C1N(C)C(OCCC)=NN1C(=O)NS(=O)(=O)C1=CC=CC=C1C(=O)OC JTHMVYBOQLDDIY-UHFFFAOYSA-N 0.000 claims description 3
UNAHYJYOSSSJHH-UHFFFAOYSA-N oryzalin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(S(N)(=O)=O)C=C1[N+]([O-])=O UNAHYJYOSSSJHH-UHFFFAOYSA-N 0.000 claims description 3
CHIFOSRWCNZCFN-UHFFFAOYSA-N pendimethalin Chemical compound CCC(CC)NC1=C([N+]([O-])=O)C=C(C)C(C)=C1[N+]([O-])=O CHIFOSRWCNZCFN-UHFFFAOYSA-N 0.000 claims description 3
NQQVFXUMIDALNH-UHFFFAOYSA-N picloram Chemical compound NC1=C(Cl)C(Cl)=NC(C(O)=O)=C1Cl NQQVFXUMIDALNH-UHFFFAOYSA-N 0.000 claims description 3
ISEUFVQQFVOBCY-UHFFFAOYSA-N prometon Chemical compound COC1=NC(NC(C)C)=NC(NC(C)C)=N1 ISEUFVQQFVOBCY-UHFFFAOYSA-N 0.000 claims description 3
PHNUZKMIPFFYSO-UHFFFAOYSA-N propyzamide Chemical compound C#CC(C)(C)NC(=O)C1=CC(Cl)=CC(Cl)=C1 PHNUZKMIPFFYSO-UHFFFAOYSA-N 0.000 claims description 3
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 3
ODCWYMIRDDJXKW-UHFFFAOYSA-N simazine Chemical compound CCNC1=NC(Cl)=NC(NCC)=N1 ODCWYMIRDDJXKW-UHFFFAOYSA-N 0.000 claims description 3
UWHURBUBIHUHSU-UHFFFAOYSA-N 2-[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamoylsulfamoyl]benzoic acid Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 UWHURBUBIHUHSU-UHFFFAOYSA-N 0.000 claims description 2
PVSGXWMWNRGTKE-UHFFFAOYSA-N 5-methyl-2-[4-methyl-5-oxo-4-(propan-2-yl)-4,5-dihydro-1H-imidazol-2-yl]pyridine-3-carboxylic acid Chemical compound N1C(=O)C(C(C)C)(C)N=C1C1=NC=C(C)C=C1C(O)=O PVSGXWMWNRGTKE-UHFFFAOYSA-N 0.000 claims description 2
DVOODWOZJVJKQR-UHFFFAOYSA-N 5-tert-butyl-3-(2,4-dichloro-5-prop-2-ynoxyphenyl)-1,3,4-oxadiazol-2-one Chemical group O=C1OC(C(C)(C)C)=NN1C1=CC(OCC#C)=C(Cl)C=C1Cl DVOODWOZJVJKQR-UHFFFAOYSA-N 0.000 claims description 2
239000005496 Chlorsulfuron Substances 0.000 claims description 2
239000005500 Clopyralid Substances 0.000 claims description 2
239000005504 Dicamba Substances 0.000 claims description 2
239000005514 Flazasulfuron Substances 0.000 claims description 2
239000005532 Flumioxazine Substances 0.000 claims description 2
JUJFQMPKBJPSFZ-UHFFFAOYSA-M Iodosulfuron-methyl-sodium Chemical compound [Na+].COC(=O)C1=CC=C(I)C=C1S(=O)(=O)[N-]C(=O)NC1=NC(C)=NC(OC)=N1 JUJFQMPKBJPSFZ-UHFFFAOYSA-M 0.000 claims description 2
239000005571 Isoxaflutole Substances 0.000 claims description 2
239000005583 Metribuzin Substances 0.000 claims description 2
239000005584 Metsulfuron-methyl Substances 0.000 claims description 2
LVKTWOXHRYGDMM-UHFFFAOYSA-N Naproanilide Chemical compound C=1C=C2C=CC=CC2=CC=1OC(C)C(=O)NC1=CC=CC=C1 LVKTWOXHRYGDMM-UHFFFAOYSA-N 0.000 claims description 2
239000005586 Nicosulfuron Substances 0.000 claims description 2
239000005587 Oryzalin Substances 0.000 claims description 2
239000005591 Pendimethalin Substances 0.000 claims description 2
239000005595 Picloram Substances 0.000 claims description 2
239000005602 Propyzamide Substances 0.000 claims description 2
239000005616 Rimsulfuron Substances 0.000 claims description 2
YIJZJEYQBAAWRJ-UHFFFAOYSA-N Thiazopyr Chemical compound N1=C(C(F)F)C(C(=O)OC)=C(CC(C)C)C(C=2SCCN=2)=C1C(F)(F)F YIJZJEYQBAAWRJ-UHFFFAOYSA-N 0.000 claims description 2
239000005626 Tribenuron Substances 0.000 claims description 2
RQVYBGPQFYCBGX-UHFFFAOYSA-N ametryn Chemical compound CCNC1=NC(NC(C)C)=NC(SC)=N1 RQVYBGPQFYCBGX-UHFFFAOYSA-N 0.000 claims description 2
GINJFDRNADDBIN-FXQIFTODSA-N bilanafos Chemical compound OC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@@H](N)CCP(C)(O)=O GINJFDRNADDBIN-FXQIFTODSA-N 0.000 claims description 2
JEDYYFXHPAIBGR-UHFFFAOYSA-N butafenacil Chemical compound O=C1N(C)C(C(F)(F)F)=CC(=O)N1C1=CC=C(Cl)C(C(=O)OC(C)(C)C(=O)OCC=C)=C1 JEDYYFXHPAIBGR-UHFFFAOYSA-N 0.000 claims description 2
VJYIFXVZLXQVHO-UHFFFAOYSA-N chlorsulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)Cl)=N1 VJYIFXVZLXQVHO-UHFFFAOYSA-N 0.000 claims description 2
SYJFEGQWDCRVNX-UHFFFAOYSA-N diquat Chemical class C1=CC=[N+]2CC[N+]3=CC=CC=C3C2=C1 SYJFEGQWDCRVNX-UHFFFAOYSA-N 0.000 claims description 2
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 claims description 2
OYIKARCXOQLFHF-UHFFFAOYSA-N isoxaflutole Chemical compound CS(=O)(=O)C1=CC(C(F)(F)F)=CC=C1C(=O)C1=C(C2CC2)ON=C1 OYIKARCXOQLFHF-UHFFFAOYSA-N 0.000 claims description 2
229940088649 isoxaflutole Drugs 0.000 claims description 2
AIMMSOZBPYFASU-UHFFFAOYSA-N n-(4,6-dimethoxypyrimidin-2-yl)-n'-[3-(2,2,2-trifluoroethoxy)pyridin-1-ium-2-yl]sulfonylcarbamimidate Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CN=2)OCC(F)(F)F)=N1 AIMMSOZBPYFASU-UHFFFAOYSA-N 0.000 claims description 2
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 2
FFSSWMQPCJRCRV-UHFFFAOYSA-N quinclorac Chemical compound ClC1=CN=C2C(C(=O)O)=C(Cl)C=CC2=C1 FFSSWMQPCJRCRV-UHFFFAOYSA-N 0.000 claims description 2
XOPFESVZMSQIKC-UHFFFAOYSA-N triasulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)OCCCl)=N1 XOPFESVZMSQIKC-UHFFFAOYSA-N 0.000 claims description 2
BQZXUHDXIARLEO-UHFFFAOYSA-N tribenuron Chemical compound COC1=NC(C)=NC(N(C)C(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 BQZXUHDXIARLEO-UHFFFAOYSA-N 0.000 claims description 2
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 claims description 2
229910014585 C2-Ce Inorganic materials 0.000 claims 2
239000005590 Oxyfluorfen Substances 0.000 claims 2
OQMBBFQZGJFLBU-UHFFFAOYSA-N Oxyfluorfen Chemical compound C1=C([N+]([O-])=O)C(OCC)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 OQMBBFQZGJFLBU-UHFFFAOYSA-N 0.000 claims 2
NVGOPFQZYCNLDU-UHFFFAOYSA-N norflurazon Chemical compound O=C1C(Cl)=C(NC)C=NN1C1=CC=CC(C(F)(F)F)=C1 NVGOPFQZYCNLDU-UHFFFAOYSA-N 0.000 claims 2
ROKVVMOXSZIDEG-UHFFFAOYSA-N 2-(3,5,6-trichloropyridin-2-yl)oxyacetate;triethylazanium Chemical compound CCN(CC)CC.OC(=O)COC1=NC(Cl)=C(Cl)C=C1Cl ROKVVMOXSZIDEG-UHFFFAOYSA-N 0.000 claims 1
KCTKQZUYHSKJLP-UHFFFAOYSA-N 2-(4-methyl-5-oxo-4-propan-2-yl-1h-imidazol-2-yl)pyridine-3-carboxylate;propan-2-ylazanium Chemical compound CC(C)[NH3+].N1C(=O)C(C(C)C)(C)N=C1C1=NC=CC=C1C([O-])=O KCTKQZUYHSKJLP-UHFFFAOYSA-N 0.000 claims 1
IRJQWZWMQCVOLA-ZBKNUEDVSA-N 2-[(z)-n-[(3,5-difluorophenyl)carbamoylamino]-c-methylcarbonimidoyl]pyridine-3-carboxylic acid Chemical compound N=1C=CC=C(C(O)=O)C=1C(/C)=N\NC(=O)NC1=CC(F)=CC(F)=C1 IRJQWZWMQCVOLA-ZBKNUEDVSA-N 0.000 claims 1
ZEKANFGSDXODPD-UHFFFAOYSA-N glyphosate-isopropylammonium Chemical compound CC(C)N.OC(=O)CNCP(O)(O)=O ZEKANFGSDXODPD-UHFFFAOYSA-N 0.000 claims 1
RSMUVYRMZCOLBH-UHFFFAOYSA-N metsulfuron methyl Chemical group COC(=O)C1=CC=CC=C1S(=O)(=O)NC(=O)NC1=NC(C)=NC(OC)=N1 RSMUVYRMZCOLBH-UHFFFAOYSA-N 0.000 claims 1
JRQGDDUXDKCWRF-UHFFFAOYSA-M sodium;n-(2-methoxycarbonylphenyl)sulfonyl-4-methyl-5-oxo-3-propoxy-1,2,4-triazole-1-carboximidate Chemical compound [Na+].O=C1N(C)C(OCCC)=NN1C(=O)[N-]S(=O)(=O)C1=CC=CC=C1C(=O)OC JRQGDDUXDKCWRF-UHFFFAOYSA-M 0.000 claims 1
239000000126 substance Substances 0.000 description 30
241000196324 Embryophyta Species 0.000 description 26
150000003254 radicals Chemical class 0.000 description 24
229910052739 hydrogen Inorganic materials 0.000 description 7
159000000000 sodium salts Chemical class 0.000 description 7
239000011575 calcium Substances 0.000 description 6
239000000460 chlorine Substances 0.000 description 6
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 6
125000001424 substituent group Chemical group 0.000 description 6
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 5
125000000217 alkyl group Chemical group 0.000 description 5
125000003277 amino group Chemical group 0.000 description 5
229910052801 chlorine Inorganic materials 0.000 description 5
150000007524 organic acids Chemical class 0.000 description 5
125000004178 (C1-C4) alkyl group Chemical group 0.000 description 4
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 4
239000000642 acaricide Substances 0.000 description 4
125000002252 acyl group Chemical group 0.000 description 4
125000003342 alkenyl group Chemical group 0.000 description 4
239000011737 fluorine Substances 0.000 description 4
229910052731 fluorine Inorganic materials 0.000 description 4
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
239000005648 plant growth regulator Substances 0.000 description 4
150000003460 sulfonic acids Chemical class 0.000 description 4
230000002195 synergetic effect Effects 0.000 description 4
KCZIUKYAJJEIQG-UHFFFAOYSA-N 1,3,5-triazin-2-amine Chemical class NC1=NC=NC=N1 KCZIUKYAJJEIQG-UHFFFAOYSA-N 0.000 description 3
HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 3
239000005711 Benzoic acid Substances 0.000 description 3
WPYMKLBDIGXBTP-UHFFFAOYSA-N Benzoic acid Natural products OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 3
MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
230000000895 acaricidal effect Effects 0.000 description 3
150000007513 acids Chemical class 0.000 description 3
150000003863 ammonium salts Chemical class 0.000 description 3
WXBLLCUINBKULX-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1.OC(=O)C1=CC=CC=C1 WXBLLCUINBKULX-UHFFFAOYSA-N 0.000 description 3
235000010233 benzoic acid Nutrition 0.000 description 3
125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 3
PKOMXLRKGNITKG-UHFFFAOYSA-L calcium;hydroxy(methyl)arsinate Chemical compound [Ca+2].C[As](O)([O-])=O.C[As](O)([O-])=O PKOMXLRKGNITKG-UHFFFAOYSA-L 0.000 description 3
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 3
239000000417 fungicide Substances 0.000 description 3
125000001188 haloalkyl group Chemical group 0.000 description 3
239000002917 insecticide Substances 0.000 description 3
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 3
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
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NZNNBZARHMXARB-UHFFFAOYSA-N 2-ethoxy-1-nitro-4-[4-(trifluoromethyl)phenoxy]benzene Chemical compound C1=C([N+]([O-])=O)C(OCC)=CC(OC=2C=CC(=CC=2)C(F)(F)F)=C1 NZNNBZARHMXARB-UHFFFAOYSA-N 0.000 description 1
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RBUPAHUNHATHNO-UHFFFAOYSA-N 7-fluoro-6-(1,3,4,5,6,7-hexahydroisoindol-2-yl)-4-prop-2-ynyl-1,4-benzoxazin-3-one Chemical compound FC1=CC2=C(N(C(CO2)=O)CC#C)C=C1N1CC=2CCCCC=2C1 RBUPAHUNHATHNO-UHFFFAOYSA-N 0.000 description 1
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239000005630 Diquat Substances 0.000 description 1
QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical class [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 1
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KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical class [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
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SLINHMUFWFWBMU-UHFFFAOYSA-N Triisopropanolamine Chemical class CC(O)CN(CC(C)O)CC(C)O SLINHMUFWFWBMU-UHFFFAOYSA-N 0.000 description 1
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
230000002730 additional effect Effects 0.000 description 1
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229910052783 alkali metal Inorganic materials 0.000 description 1
229910052784 alkaline earth metal Inorganic materials 0.000 description 1
125000004453 alkoxycarbonyl group Chemical group 0.000 description 1
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QWCKQJZIFLGMSD-UHFFFAOYSA-N alpha-aminobutyric acid Chemical compound CCC(N)C(O)=O QWCKQJZIFLGMSD-UHFFFAOYSA-N 0.000 description 1
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208000014347 autosomal dominant hyaline body myopathy Diseases 0.000 description 1
HYGWNUKOUCZBND-UHFFFAOYSA-N azanide Chemical compound [NH2-] HYGWNUKOUCZBND-UHFFFAOYSA-N 0.000 description 1
125000001584 benzyloxycarbonyl group Chemical group C(=O)(OCC1=CC=CC=C1)* 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
RXOVYXWVWDQDMC-UHFFFAOYSA-N carbamoyl 4-aminobenzenesulfonate Chemical compound NC(=O)OS(=O)(=O)C1=CC=C(N)C=C1 RXOVYXWVWDQDMC-UHFFFAOYSA-N 0.000 description 1
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MXZACTZQSGYANA-UHFFFAOYSA-N chembl545463 Chemical compound Cl.C1=CC(OC)=CC=C1C(N=C1)=CN2C1=NC(C)=C2O MXZACTZQSGYANA-UHFFFAOYSA-N 0.000 description 1
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125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
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125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000005842 heteroatom Chemical group 0.000 description 1
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229930195733 hydrocarbon Natural products 0.000 description 1
239000011630 iodine Substances 0.000 description 1
229910052740 iodine Inorganic materials 0.000 description 1
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
230000007774 longterm Effects 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
QYULRWVHFTYZFS-UHFFFAOYSA-N methyl 2-[carbamoyl-(4,6-dimethylpyrimidin-2-yl)sulfamoyl]benzoate Chemical compound COC(=O)C1=CC=CC=C1S(=O)(=O)N(C(N)=O)C1=NC(C)=CC(C)=N1 QYULRWVHFTYZFS-UHFFFAOYSA-N 0.000 description 1
XMSZANIMCDLNKA-UHFFFAOYSA-N methyl hypofluorite Chemical compound COF XMSZANIMCDLNKA-UHFFFAOYSA-N 0.000 description 1
150000007522 mineralic acids Chemical class 0.000 description 1
125000006682 monohaloalkyl group Chemical group 0.000 description 1
125000003136 n-heptyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
LBTPIFQNEKOAIM-UHFFFAOYSA-N n-phenylmethanesulfonamide Chemical compound CS(=O)(=O)NC1=CC=CC=C1 LBTPIFQNEKOAIM-UHFFFAOYSA-N 0.000 description 1
NYQXIOZBHWFCBU-UHFFFAOYSA-N n-phenylpyridine-3-carboxamide Chemical compound C=1C=CN=CC=1C(=O)NC1=CC=CC=C1 NYQXIOZBHWFCBU-UHFFFAOYSA-N 0.000 description 1
239000005645 nematicide Substances 0.000 description 1
229960003512 nicotinic acid Drugs 0.000 description 1
235000001968 nicotinic acid Nutrition 0.000 description 1
239000011664 nicotinic acid Substances 0.000 description 1
235000006408 oxalic acid Nutrition 0.000 description 1
125000002255 pentenyl group Chemical group C(=CCCC)* 0.000 description 1
125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
239000000575 pesticide Substances 0.000 description 1
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
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UYWQUFXKFGHYNT-UHFFFAOYSA-N phenylmethyl ester of formic acid Natural products O=COCC1=CC=CC=C1 UYWQUFXKFGHYNT-UHFFFAOYSA-N 0.000 description 1
125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 description 1
150000003009 phosphonic acids Chemical class 0.000 description 1
XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
159000000001 potassium salts Chemical class 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
230000002035 prolonged effect Effects 0.000 description 1
229940080818 propionamide Drugs 0.000 description 1
150000003242 quaternary ammonium salts Chemical class 0.000 description 1
230000035945 sensitivity Effects 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
239000002689 soil Substances 0.000 description 1
241000894007 species Species 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
239000007858 starting material Substances 0.000 description 1
230000000707 stereoselective effect Effects 0.000 description 1
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
150000003455 sulfinic acids Chemical class 0.000 description 1
FZMKKCQHDROFNI-UHFFFAOYSA-N sulfometuron Chemical compound CC1=CC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 FZMKKCQHDROFNI-UHFFFAOYSA-N 0.000 description 1
LOQQVLXUKHKNIA-UHFFFAOYSA-N thifensulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C2=C(SC=C2)C(O)=O)=N1 LOQQVLXUKHKNIA-UHFFFAOYSA-N 0.000 description 1
150000003566 thiocarboxylic acids Chemical class 0.000 description 1
125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- 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
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/66—1,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms
- A01N43/68—1,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms with two or three nitrogen atoms directly attached to ring carbon atoms

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)
Plural Heterocyclic Compounds (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

ZA200610566A 2004-07-17 2006-12-15 Herbicidal agents ZA200610566B (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE102004034571A DE102004034571A1 (de)	2004-07-17	2004-07-17	Herbizide Mittel

Publications (1)

Publication Number	Publication Date
ZA200610566B true ZA200610566B (en)	2008-06-25

Family

ID=34971606

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
ZA200610566A ZA200610566B (en)	2004-07-17	2006-12-15	Herbicidal agents

Country Status (32)

Country	Link
US (2)	US8236729B2 (ja)
EP (1)	EP1771071B1 (ja)
JP (1)	JP5530593B2 (ja)
KR (1)	KR101213793B1 (ja)
CN (1)	CN1997279B (ja)
AP (1)	AP2339A (ja)
AR (1)	AR049984A1 (ja)
AT (1)	ATE387090T1 (ja)
AU (1)	AU2005263406B2 (ja)
BR (1)	BRPI0513459B1 (ja)
CA (1)	CA2574137C (ja)
DE (2)	DE102004034571A1 (ja)
DK (1)	DK1771071T3 (ja)
EA (1)	EA010725B1 (ja)
EC (1)	ECSP077178A (ja)
EG (1)	EG25171A (ja)
ES (1)	ES2301024T3 (ja)
GT (1)	GT200500195A (ja)
IL (1)	IL180692A0 (ja)
MA (1)	MA28705B1 (ja)
MX (1)	MX2007000624A (ja)
MY (1)	MY137769A (ja)
NO (1)	NO20070942L (ja)
NZ (1)	NZ552622A (ja)
PL (1)	PL1771071T3 (ja)
PT (1)	PT1771071E (ja)
SG (1)	SG170118A1 (ja)
TN (1)	TNSN07011A1 (ja)
TW (1)	TWI365715B (ja)
UA (1)	UA85429C2 (ja)
WO (1)	WO2006007947A1 (ja)
ZA (1)	ZA200610566B (ja)

Families Citing this family (24)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
WO2009064830A1 (en) *	2007-11-16	2009-05-22	Sds Biotech K.K.	Selective weed control using karbutilate herbicidal compositions, and herbicidal composition comprising karbutilate and ametryn
CA2714065A1 (en) *	2008-02-05	2009-08-13	Arysta Lifescience North America, Llc	Solid formulation of low melting active compound
EP2092825A1 (de)	2008-02-21	2009-08-26	Bayer CropScience Aktiengesellschaft	Herbizid-Kombinationen enthaltend ein Herbizid der Klasse der Diamino-s-triazine
AU2014201131B2 (en) *	2008-02-21	2016-02-04	Bayer Cropscience Aktiengesellschaft	Herbicide combinations containing a herbicide from the class of diamino-s-triazines
US20110190132A1 (en) *	2008-03-02	2011-08-04	Syngenta Crop Protection, Inc.	Herbicidal method
EP2147600A1 (en)	2008-07-21	2010-01-27	Bayer CropScience AG	Method for weed control in lawn
CN101647452A (zh) *	2009-08-06	2010-02-17	陕西先农生物科技有限公司	45%己唑醇·多菌灵悬浮剂
US9723836B2 (en) *	2009-11-19	2017-08-08	Bayer Cropscience Ag	Synergistic pre-emergent and post-emergent weed control compositions and methods of use thereof
US20110218105A1 (en) *	2010-03-03	2011-09-08	Larry Walker	Pre-plant or pre-emergent herbicide compositions
ES2639198T5 (es) *	2011-06-24	2020-11-17	Dow Agrosciences Llc	Composición herbicida sinérgica que contiene penoxsulam y pendimetalina
UY35164A (es) *	2012-12-06	2014-06-30	Bayer Cropscience Ag	Procedimientos para combatir plantas dañinas resistentes
US9999222B2 (en) *	2014-04-23	2018-06-19	Basf Se	Herbicidal combination comprising azines
CN107105658A (zh) *	2014-11-18	2017-08-29	拜耳作物科学股份公司	某些除草剂结合物在块根作物植物中的用途
EA039479B1 (ru) *	2015-04-27	2022-01-31	Басф Се	Комбинации гербицидов, содержащие глюфосинат и индазифлам
AR105060A1 (es) *	2015-05-07	2017-09-06	Nufarm Australia Ltd	Concentrado emulsionable que comprende un herbicida de ácido fenoxi-alcanoico
EP3294064A1 (en) *	2015-05-11	2018-03-21	Bayer CropScience AG	Herbicide combinations comprising l-glufosinate and indaziflam
CA3046044A1 (en)	2016-12-07	2018-06-14	Bayer Cropscience Aktiengesellschaft	Herbicidal combination containing triafamone and indaziflam
US10757009B2 (en)	2018-11-20	2020-08-25	Amazon Technologies, Inc.	Global-scale connectivity using scalable virtual traffic hubs
CA3153003C (en)	2018-11-29	2023-10-17	Bayer Cropscience Lp	Herbicidal compositions for animal grazelands and methods for applying the same
HRP20230284T1 (hr) *	2018-12-07	2023-05-12	Bayer Aktiengesellschaft	Herbicidne kombinacije
US12160366B2 (en)	2021-03-30	2024-12-03	Amazon Technologies, Inc.	Multi-tenant offloaded protocol processing for virtual routers
US12483499B2 (en)	2023-03-27	2025-11-25	Amazon Technologies, Inc.	Custom configuration of cloud-based multi-network-segment gateways
US12021743B1 (en)	2023-03-27	2024-06-25	Amazon Technologies, Inc.	Software-defined multi-network-segment gateways for scalable routing of traffic between customer-premise network segments and cloud-based virtual networks
WO2025104120A1 (de)	2023-11-14	2025-05-22	Bayer Aktiengesellschaft	Herbizide zusammensetzungen enthaltend indaziflam und safener

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH04235105A (ja) *	1990-06-29	1992-08-24	Idemitsu Kosan Co Ltd	除草剤組成物
JP2908853B2 (ja) *	1990-08-15	1999-06-21	出光興産株式会社	除草剤組成物
AU6242896A (en) *	1995-11-27	1997-06-19	Idemitsu Kosan Co. Ltd	Triazine derivatives
DE19607450A1 (de) *	1996-02-28	1997-09-04	Hoechst Schering Agrevo Gmbh	2-Amino-4-bicycloamino-1,3,5-triazine, Verfahren zu deren Herstellung und deren Verwendung als Herbizide und Pflanzenwachstumsregulatoren
DE19641693A1 (de) *	1996-10-10	1998-04-16	Bayer Ag	Substituierte 2-Amino-4-alkylamino-1,3,5-triazine
DE19842894A1 (de) *	1998-09-18	2000-03-23	Hoechst Schering Agrevo Gmbh	Synergistische Wirkstoffkombinationen zur Bekämpfung von Schadpflanzen in Nutzpflanzenkulturen
DE10117508A1 (de) *	2001-04-07	2002-10-17	Bayer Cropscience Gmbh	Synergistische Wirkstoffkombinationen zur Bekämpfung von Schadpflanzen
DE10207037A1 (de) *	2002-02-20	2003-08-28	Bayer Cropscience Gmbh	2-Amino-4-bicyclyamino-6H-1,3.5-triazine, Verfahren zu deren Herstellung und deren Verwendung als Herbizide und Pflanzenwachstumsregulatoren
RS53108B (sr) *	2003-02-05	2014-06-30	Bayer Cropscience Ag.	Amino-1,3,5-triazini n-zamenjeni sa hiralnim bicikličnim radikalima, proces za njihovu pripremu, njihova jedinjenja i njihova primena kao herbicida i regulatora rasta biljaka

2004
- 2004-07-17 DE DE102004034571A patent/DE102004034571A1/de not_active Withdrawn
2005
- 2005-06-30 WO PCT/EP2005/007041 patent/WO2006007947A1/de not_active Ceased
- 2005-06-30 KR KR1020077001129A patent/KR101213793B1/ko not_active Expired - Lifetime
- 2005-06-30 SG SG201101843-9A patent/SG170118A1/en unknown
- 2005-06-30 CN CN2005800240678A patent/CN1997279B/zh not_active Expired - Lifetime
- 2005-06-30 JP JP2007520701A patent/JP5530593B2/ja not_active Expired - Lifetime
- 2005-06-30 PT PT05756429T patent/PT1771071E/pt unknown
- 2005-06-30 AT AT05756429T patent/ATE387090T1/de not_active IP Right Cessation
- 2005-06-30 UA UAA200701726A patent/UA85429C2/ru unknown
- 2005-06-30 MX MX2007000624A patent/MX2007000624A/es active IP Right Grant
- 2005-06-30 CA CA2574137A patent/CA2574137C/en not_active Expired - Lifetime
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- 2005-06-30 EA EA200700320A patent/EA010725B1/ru not_active IP Right Cessation
- 2005-06-30 DK DK05756429T patent/DK1771071T3/da active
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- 2005-06-30 PL PL05756429T patent/PL1771071T3/pl unknown
- 2005-07-14 US US11/181,402 patent/US8236729B2/en active Active
- 2005-07-14 AR ARP050102923A patent/AR049984A1/es active IP Right Grant
- 2005-07-14 TW TW094123928A patent/TWI365715B/zh not_active IP Right Cessation
- 2005-07-15 GT GT200500195A patent/GT200500195A/es unknown
- 2005-07-15 MY MYPI20053267A patent/MY137769A/en unknown
- 2005-08-15 US US11/203,953 patent/US20060014642A1/en not_active Abandoned
2006
- 2006-12-15 ZA ZA200610566A patent/ZA200610566B/en unknown
- 2006-12-29 MA MA29592A patent/MA28705B1/fr unknown
2007
- 2007-01-14 IL IL180692A patent/IL180692A0/en unknown
- 2007-01-16 TN TNP2007000011A patent/TNSN07011A1/fr unknown
- 2007-01-16 EC EC2007007178A patent/ECSP077178A/es unknown
- 2007-01-16 EG EGNA2007000042 patent/EG25171A/xx active
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Also Published As

Publication number	Publication date
CA2574137C (en)	2014-02-04
MY137769A (en)	2009-03-31
UA85429C2 (ru)	2009-01-26
AU2005263406A1 (en)	2006-01-26
JP2008506642A (ja)	2008-03-06
BRPI0513459A (pt)	2008-05-06
ES2301024T3 (es)	2008-06-16
WO2006007947A1 (de)	2006-01-26
EA010725B1 (ru)	2008-10-30
JP5530593B2 (ja)	2014-06-25
EA200700320A1 (ru)	2007-08-31
BRPI0513459B1 (pt)	2019-01-22
TW200612826A (en)	2006-05-01
TNSN07011A1 (fr)	2008-06-02
GT200500195A (es)	2006-04-04
DE102004034571A1 (de)	2006-02-23
SG170118A1 (en)	2011-04-29
KR20070035571A (ko)	2007-03-30
EP1771071A1 (de)	2007-04-11
ATE387090T1 (de)	2008-03-15
ECSP077178A (es)	2007-02-28
PT1771071E (pt)	2008-05-14
AR049984A1 (es)	2006-09-20
CN1997279B (zh)	2010-11-03
US8236729B2 (en)	2012-08-07
AU2005263406B2 (en)	2011-10-06
EP1771071B1 (de)	2008-02-27
IL180692A0 (en)	2007-06-03
DE502005003013D1 (de)	2008-04-10
US20060019829A1 (en)	2006-01-26
PL1771071T3 (pl)	2008-07-31
NO20070942L (no)	2007-03-30
MA28705B1 (fr)	2007-06-01
CA2574137A1 (en)	2006-01-26
AP2007003903A0 (en)	2007-02-28
KR101213793B1 (ko)	2012-12-18
EG25171A (en)	2011-10-04
TWI365715B (en)	2012-06-11
CN1997279A (zh)	2007-07-11
MX2007000624A (es)	2007-03-07
AP2339A (en)	2011-12-21
DK1771071T3 (da)	2008-06-23
US20060014642A1 (en)	2006-01-19
NZ552622A (en)	2010-08-27

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