ZA200401138B - Herbicidal compositions. - Google Patents
Herbicidal compositions. Download PDFInfo
- Publication number
- ZA200401138B ZA200401138B ZA200401138A ZA200401138A ZA200401138B ZA 200401138 B ZA200401138 B ZA 200401138B ZA 200401138 A ZA200401138 A ZA 200401138A ZA 200401138 A ZA200401138 A ZA 200401138A ZA 200401138 B ZA200401138 B ZA 200401138B
- Authority
- ZA
- South Africa
- Prior art keywords
- alkyl
- hydrogen
- halogen
- rss
- alkoxy
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 29
- 230000002363 herbicidal effect Effects 0.000 title claims description 15
- 244000038559 crop plants Species 0.000 claims description 14
- 239000004480 active ingredient Substances 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 7
- 239000005560 Foramsulfuron Substances 0.000 claims description 6
- 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 6
- WVQBLGZPHOPPFO-LBPRGKRZSA-N (S)-metolachlor Chemical compound CCC1=CC=CC(C)=C1N([C@@H](C)COC)C(=O)CCl WVQBLGZPHOPPFO-LBPRGKRZSA-N 0.000 claims description 5
- 239000005617 S-Metolachlor Substances 0.000 claims description 5
- 239000005629 Tritosulfuron Substances 0.000 claims description 5
- KVEQCVKVIFQSGC-UHFFFAOYSA-N tritosulfuron Chemical compound FC(F)(F)C1=NC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(F)(F)F)=N1 KVEQCVKVIFQSGC-UHFFFAOYSA-N 0.000 claims description 5
- 240000008042 Zea mays Species 0.000 claims description 4
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 claims description 4
- 235000002017 Zea mays subsp mays Nutrition 0.000 claims description 4
- 235000009973 maize Nutrition 0.000 claims description 4
- 239000002671 adjuvant Substances 0.000 claims description 3
- 238000009472 formulation Methods 0.000 claims description 3
- 230000008635 plant growth Effects 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 description 243
- 125000000217 alkyl group Chemical group 0.000 description 100
- 229910052739 hydrogen Inorganic materials 0.000 description 69
- 239000001257 hydrogen Substances 0.000 description 69
- 150000002431 hydrogen Chemical class 0.000 description 44
- 229910052736 halogen Inorganic materials 0.000 description 43
- 150000002367 halogens Chemical class 0.000 description 43
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 24
- 125000003545 alkoxy group Chemical group 0.000 description 24
- 150000001875 compounds Chemical class 0.000 description 24
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 19
- 125000001188 haloalkyl group Chemical group 0.000 description 18
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 18
- 125000004093 cyano group Chemical group *C#N 0.000 description 16
- 241000196324 Embryophyta Species 0.000 description 15
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 14
- 229910052760 oxygen Inorganic materials 0.000 description 14
- 239000001301 oxygen Substances 0.000 description 14
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 13
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 13
- 125000004414 alkyl thio group Chemical group 0.000 description 11
- 125000001072 heteroaryl group Chemical group 0.000 description 10
- -1 C(O)-phenyl Chemical group 0.000 description 9
- 239000000460 chlorine Substances 0.000 description 9
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- 125000004390 alkyl sulfonyl group Chemical group 0.000 description 8
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 8
- 125000003342 alkenyl group Chemical group 0.000 description 7
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 6
- 125000004644 alkyl sulfinyl group Chemical group 0.000 description 6
- 239000004009 herbicide Substances 0.000 description 6
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 5
- 125000000304 alkynyl group Chemical group 0.000 description 5
- 125000003118 aryl group Chemical group 0.000 description 5
- 125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 description 5
- 229910052717 sulfur Inorganic materials 0.000 description 5
- 239000011593 sulfur Substances 0.000 description 5
- 125000004001 thioalkyl group Chemical group 0.000 description 5
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 125000004438 haloalkoxy group Chemical group 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
- 150000001768 cations Chemical class 0.000 description 3
- 229910052801 chlorine Inorganic materials 0.000 description 3
- 125000000753 cycloalkyl group Chemical group 0.000 description 3
- 125000005036 alkoxyphenyl group Chemical group 0.000 description 2
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 description 2
- 125000004448 alkyl carbonyl group Chemical group 0.000 description 2
- 125000005037 alkyl phenyl group Chemical group 0.000 description 2
- 125000004103 aminoalkyl group Chemical group 0.000 description 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 2
- 230000002195 synergetic effect Effects 0.000 description 2
- 125000004214 1-pyrrolidinyl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- WVQBLGZPHOPPFO-UHFFFAOYSA-N 2-chloro-N-(2-ethyl-6-methylphenyl)-N-(1-methoxypropan-2-yl)acetamide Chemical compound CCC1=CC=CC(C)=C1N(C(C)COC)C(=O)CCl WVQBLGZPHOPPFO-UHFFFAOYSA-N 0.000 description 1
- 241000219144 Abutilon Species 0.000 description 1
- 241000219318 Amaranthus Species 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- 125000006415 CF Chemical group FC* 0.000 description 1
- 241000219312 Chenopodium Species 0.000 description 1
- 241000234653 Cyperus Species 0.000 description 1
- 235000017896 Digitaria Nutrition 0.000 description 1
- 241001303487 Digitaria <clam> Species 0.000 description 1
- 241000192043 Echinochloa Species 0.000 description 1
- 241001101998 Galium Species 0.000 description 1
- 235000021506 Ipomoea Nutrition 0.000 description 1
- 241000207783 Ipomoea Species 0.000 description 1
- 241000209504 Poaceae Species 0.000 description 1
- 241000857233 Rottboellia Species 0.000 description 1
- 235000005775 Setaria Nutrition 0.000 description 1
- 241000232088 Setaria <nematode> Species 0.000 description 1
- 241000220261 Sinapis Species 0.000 description 1
- 235000002634 Solanum Nutrition 0.000 description 1
- 241000207763 Solanum Species 0.000 description 1
- 240000002439 Sorghum halepense Species 0.000 description 1
- 240000005592 Veronica officinalis Species 0.000 description 1
- 241000405217 Viola <butterfly> Species 0.000 description 1
- 241001506766 Xanthium Species 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000009418 agronomic effect Effects 0.000 description 1
- 125000005138 alkoxysulfonyl group Chemical group 0.000 description 1
- 125000004691 alkyl thio carbonyl group Chemical group 0.000 description 1
- 230000008485 antagonism Effects 0.000 description 1
- 239000000729 antidote Substances 0.000 description 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 1
- 238000009395 breeding Methods 0.000 description 1
- 230000001488 breeding effect Effects 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- CURLHBZYTFVCRG-UHFFFAOYSA-N butan-2-yl n-(3-chlorophenyl)carbamate Chemical compound CCC(C)OC(=O)NC1=CC=CC(Cl)=C1 CURLHBZYTFVCRG-UHFFFAOYSA-N 0.000 description 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 125000006254 cycloalkyl carbonyl group Chemical group 0.000 description 1
- 125000004310 dioxan-2-yl group Chemical group [H]C1([H])OC([H])([H])C([H])(*)OC1([H])[H] 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 125000002541 furyl group Chemical group 0.000 description 1
- 238000010353 genetic engineering Methods 0.000 description 1
- 125000004440 haloalkylsulfinyl group Chemical group 0.000 description 1
- 125000004441 haloalkylsulfonyl group Chemical group 0.000 description 1
- 125000004995 haloalkylthio group Chemical group 0.000 description 1
- 125000005059 halophenyl group Chemical group 0.000 description 1
- 150000004677 hydrates Chemical class 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 125000005322 morpholin-1-yl group Chemical group 0.000 description 1
- 125000003566 oxetanyl group Chemical group 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 230000000885 phytotoxic effect Effects 0.000 description 1
- 125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 description 1
- ZFXYFBGIUFBOJW-UHFFFAOYSA-N theophylline Chemical compound O=C1N(C)C(=O)N(C)C2=C1NC=N2 ZFXYFBGIUFBOJW-UHFFFAOYSA-N 0.000 description 1
- 229960000278 theophylline Drugs 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- 238000003971 tillage Methods 0.000 description 1
- 239000000080 wetting agent Substances 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
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
- A01N43/42—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings condensed with carbocyclic rings
-
- 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 (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH17382001 | 2001-09-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
ZA200401138B true ZA200401138B (en) | 2004-10-25 |
Family
ID=4566088
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ZA200401138A ZA200401138B (en) | 2001-09-20 | 2004-02-12 | Herbicidal compositions. |
Country Status (23)
Country | Link |
---|---|
US (1) | US20040242421A1 (es) |
EP (1) | EP1429611A1 (es) |
JP (1) | JP2005502718A (es) |
KR (1) | KR20040035821A (es) |
CN (1) | CN1556672A (es) |
AP (1) | AP2004002979A0 (es) |
AR (1) | AR036546A1 (es) |
BG (1) | BG108633A (es) |
BR (1) | BR0212717A (es) |
CA (1) | CA2458203A1 (es) |
CO (1) | CO5560516A2 (es) |
EA (1) | EA200400415A1 (es) |
EC (1) | ECSP044980A (es) |
GT (1) | GT200200185A (es) |
HR (1) | HRP20040270A2 (es) |
HU (1) | HUP0402141A3 (es) |
MX (1) | MXPA04002120A (es) |
NZ (2) | NZ541924A (es) |
OA (1) | OA12662A (es) |
PL (1) | PL368037A1 (es) |
RS (1) | RS13904A (es) |
WO (1) | WO2003024226A1 (es) |
ZA (1) | ZA200401138B (es) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20070281859A1 (en) * | 2004-04-01 | 2007-12-06 | Basf Akiengesellschaft | Synergistically Acting Herbicidal Mixtures |
CN103749443B (zh) * | 2013-12-24 | 2016-01-27 | 江苏天容集团股份有限公司 | 提高甲基二磺隆安全性的除草组合物 |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5256630A (en) * | 1987-08-13 | 1993-10-26 | Monsanto Company | Safening mixtures of sulfonylurea and acetanilide herbicides |
DE4038430A1 (de) * | 1990-12-01 | 1992-06-04 | Basf Ag | Herbizide n-((1,3,5-triazin-2-yl)-aminocarbonyl) benzolsulfonamide |
UA63884C2 (en) * | 1995-04-12 | 2004-02-16 | Singenta Participations Ag | Herbicidal composition and a method of controlling the emergence of undesirable plants |
SI1104239T1 (en) * | 1998-08-13 | 2004-08-31 | Bayer Cropscience Gmbh | Herbicides with acylated aminophenylsulfonyl urea |
MXPA02004904A (es) * | 1999-11-18 | 2003-01-28 | Bayer Ag | Combinaciones sinergicas de productos activos herbicidas. |
-
2002
- 2002-09-18 AR ARP020103513A patent/AR036546A1/es not_active Application Discontinuation
- 2002-09-19 EP EP02779380A patent/EP1429611A1/en not_active Withdrawn
- 2002-09-19 NZ NZ541924A patent/NZ541924A/en unknown
- 2002-09-19 BR BR0212717-2A patent/BR0212717A/pt not_active IP Right Cessation
- 2002-09-19 NZ NZ531522A patent/NZ531522A/en unknown
- 2002-09-19 RS YU13904A patent/RS13904A/sr unknown
- 2002-09-19 WO PCT/EP2002/010540 patent/WO2003024226A1/en not_active Application Discontinuation
- 2002-09-19 AP APAP/P/2004/002979A patent/AP2004002979A0/en unknown
- 2002-09-19 CA CA002458203A patent/CA2458203A1/en not_active Abandoned
- 2002-09-19 OA OA1200400080A patent/OA12662A/en unknown
- 2002-09-19 HU HU0402141A patent/HUP0402141A3/hu unknown
- 2002-09-19 MX MXPA04002120A patent/MXPA04002120A/es unknown
- 2002-09-19 GT GT200200185A patent/GT200200185A/es unknown
- 2002-09-19 CN CNA028183630A patent/CN1556672A/zh active Pending
- 2002-09-19 JP JP2003528130A patent/JP2005502718A/ja active Pending
- 2002-09-19 US US10/490,141 patent/US20040242421A1/en not_active Abandoned
- 2002-09-19 EA EA200400415A patent/EA200400415A1/ru unknown
- 2002-09-19 PL PL02368037A patent/PL368037A1/xx not_active Application Discontinuation
- 2002-09-19 KR KR10-2004-7003996A patent/KR20040035821A/ko not_active Application Discontinuation
-
2004
- 2004-02-12 ZA ZA200401138A patent/ZA200401138B/en unknown
- 2004-02-17 EC EC2004004980A patent/ECSP044980A/es unknown
- 2004-02-18 CO CO04013830A patent/CO5560516A2/es not_active Application Discontinuation
- 2004-03-16 BG BG108633A patent/BG108633A/xx unknown
- 2004-03-19 HR HR20040270A patent/HRP20040270A2/hr not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
CN1556672A (zh) | 2004-12-22 |
US20040242421A1 (en) | 2004-12-02 |
CA2458203A1 (en) | 2003-03-27 |
BG108633A (en) | 2005-05-31 |
HUP0402141A3 (en) | 2007-02-28 |
ECSP044980A (es) | 2004-04-28 |
JP2005502718A (ja) | 2005-01-27 |
OA12662A (en) | 2006-06-19 |
NZ531522A (en) | 2005-10-28 |
NZ541924A (en) | 2006-02-24 |
BR0212717A (pt) | 2004-08-03 |
AR036546A1 (es) | 2004-09-15 |
HRP20040270A2 (en) | 2005-02-28 |
CO5560516A2 (es) | 2005-09-30 |
EP1429611A1 (en) | 2004-06-23 |
RS13904A (en) | 2006-10-27 |
GT200200185A (es) | 2003-05-12 |
MXPA04002120A (es) | 2004-06-07 |
KR20040035821A (ko) | 2004-04-29 |
WO2003024226A1 (en) | 2003-03-27 |
AP2004002979A0 (en) | 2004-03-31 |
PL368037A1 (en) | 2005-03-21 |
HUP0402141A2 (hu) | 2005-01-28 |
EA200400415A1 (ru) | 2004-08-26 |
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