ZA200609992B - Herbicidal suspension concentrate formulation - Google Patents
Herbicidal suspension concentrate formulation Download PDFInfo
- Publication number
- ZA200609992B ZA200609992B ZA200609992A ZA200609992A ZA200609992B ZA 200609992 B ZA200609992 B ZA 200609992B ZA 200609992 A ZA200609992 A ZA 200609992A ZA 200609992 A ZA200609992 A ZA 200609992A ZA 200609992 B ZA200609992 B ZA 200609992B
- Authority
- ZA
- South Africa
- Prior art keywords
- alkyl
- alkoxy
- halogen
- substituted
- cyano
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 32
- 238000009472 formulation Methods 0.000 title claims description 29
- 239000004546 suspension concentrate Substances 0.000 title claims description 3
- 230000002363 herbicidal effect Effects 0.000 title description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 205
- -1 triketones Chemical class 0.000 claims description 91
- 125000003545 alkoxy group Chemical group 0.000 claims description 84
- 229910052736 halogen Inorganic materials 0.000 claims description 67
- 150000002367 halogens Chemical class 0.000 claims description 61
- 125000004414 alkyl thio group Chemical group 0.000 claims description 54
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 54
- 125000004438 haloalkoxy group Chemical group 0.000 claims description 51
- 125000001188 haloalkyl group Chemical group 0.000 claims description 45
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 36
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 36
- 229910052739 hydrogen Inorganic materials 0.000 claims description 33
- 239000001257 hydrogen Substances 0.000 claims description 33
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 30
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 30
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 28
- 101100339555 Zymoseptoria tritici HPPD gene Proteins 0.000 claims description 25
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims description 24
- 150000001875 compounds Chemical class 0.000 claims description 24
- 125000004122 cyclic group Chemical group 0.000 claims description 24
- 125000004644 alkyl sulfinyl group Chemical group 0.000 claims description 23
- 125000002947 alkylene group Chemical group 0.000 claims description 23
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 23
- 239000003112 inhibitor Substances 0.000 claims description 23
- 229910052760 oxygen Inorganic materials 0.000 claims description 23
- 239000001301 oxygen Chemical group 0.000 claims description 23
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 21
- 125000003282 alkyl amino group Chemical group 0.000 claims description 21
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 21
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 20
- 125000000304 alkynyl group Chemical group 0.000 claims description 20
- 125000004432 carbon atom Chemical group C* 0.000 claims description 20
- 125000005843 halogen group Chemical group 0.000 claims description 20
- 125000003342 alkenyl group Chemical group 0.000 claims description 19
- 125000001424 substituent group Chemical group 0.000 claims description 19
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 18
- 125000004995 haloalkylthio group Chemical group 0.000 claims description 17
- 229910052717 sulfur Inorganic materials 0.000 claims description 17
- 125000003302 alkenyloxy group Chemical group 0.000 claims description 16
- 125000005133 alkynyloxy group Chemical group 0.000 claims description 16
- 125000000262 haloalkenyl group Chemical group 0.000 claims description 16
- 229910052757 nitrogen Inorganic materials 0.000 claims description 16
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 claims description 16
- 239000011593 sulfur Substances 0.000 claims description 16
- 239000003792 electrolyte Substances 0.000 claims description 14
- 125000004440 haloalkylsulfinyl group Chemical group 0.000 claims description 14
- 125000004441 haloalkylsulfonyl group Chemical group 0.000 claims description 14
- 229910020008 S(O) Inorganic materials 0.000 claims description 13
- 125000004471 alkyl aminosulfonyl group Chemical group 0.000 claims description 13
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims description 13
- 125000000232 haloalkynyl group Chemical group 0.000 claims description 13
- 239000012141 concentrate Substances 0.000 claims description 12
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims description 12
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
- 125000004450 alkenylene group Chemical group 0.000 claims description 11
- 125000005278 alkyl sulfonyloxy group Chemical group 0.000 claims description 10
- 125000000623 heterocyclic group Chemical group 0.000 claims description 10
- 229920006395 saturated elastomer Polymers 0.000 claims description 10
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 10
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 9
- 125000005108 alkenylthio group Chemical group 0.000 claims description 8
- 125000003118 aryl group Chemical group 0.000 claims description 8
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 8
- 125000005842 heteroatom Chemical group 0.000 claims description 8
- 125000002950 monocyclic group Chemical group 0.000 claims description 8
- 125000004434 sulfur atom Chemical group 0.000 claims description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 7
- 125000005109 alkynylthio group Chemical group 0.000 claims description 7
- 125000005291 haloalkenyloxy group Chemical group 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 7
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 7
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 claims description 7
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 claims description 6
- 125000004419 alkynylene group Chemical group 0.000 claims description 6
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 6
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 6
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims description 6
- VIXCLRUCUMWJFF-KGLIPLIRSA-N (1R,5S)-benzobicyclon Chemical compound CS(=O)(=O)c1ccc(C(=O)C2=C(Sc3ccccc3)[C@H]3CC[C@H](C3)C2=O)c(Cl)c1 VIXCLRUCUMWJFF-KGLIPLIRSA-N 0.000 claims description 5
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 claims description 4
- 125000004656 alkyl sulfonylamino group Chemical group 0.000 claims description 4
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims description 4
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- UHZZMRAGKVHANO-UHFFFAOYSA-M chlormequat chloride Chemical compound [Cl-].C[N+](C)(C)CCCl UHZZMRAGKVHANO-UHFFFAOYSA-M 0.000 claims description 4
- 239000005977 Ethylene Substances 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- 239000000725 suspension Substances 0.000 claims 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 claims description 2
- 239000005864 Sulphur Chemical group 0.000 claims description 2
- 239000004480 active ingredient Substances 0.000 claims description 2
- 125000004466 alkoxycarbonylamino group Chemical group 0.000 claims description 2
- 125000005194 alkoxycarbonyloxy group Chemical group 0.000 claims description 2
- 125000004949 alkyl amino carbonyl amino group Chemical group 0.000 claims description 2
- 125000005195 alkyl amino carbonyloxy group Chemical group 0.000 claims description 2
- 125000003806 alkyl carbonyl amino group Chemical group 0.000 claims description 2
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 claims description 2
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 2
- 125000002534 ethynyl group Chemical class [H]C#C* 0.000 claims description 2
- 125000005280 halo alkyl sulfonyloxy group Chemical group 0.000 claims description 2
- CTAPFRYPJLPFDF-UHFFFAOYSA-N isoxazole Chemical compound C=1C=NOC=1 CTAPFRYPJLPFDF-UHFFFAOYSA-N 0.000 claims description 2
- 150000002545 isoxazoles Chemical class 0.000 claims description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 2
- 125000000466 oxiranyl group Chemical group 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims description 2
- 150000003217 pyrazoles Chemical class 0.000 claims description 2
- PQTBTIFWAXVEPB-UHFFFAOYSA-N sulcotrione Chemical compound ClC1=CC(S(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O PQTBTIFWAXVEPB-UHFFFAOYSA-N 0.000 claims description 2
- 125000000446 sulfanediyl group Chemical group *S* 0.000 claims description 2
- 125000003396 thiol group Chemical class [H]S* 0.000 claims description 2
- 125000001425 triazolyl group Chemical group 0.000 claims description 2
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 2
- 239000013011 aqueous formulation Substances 0.000 claims 3
- 239000000243 solution Substances 0.000 claims 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- 102100033668 Cartilage matrix protein Human genes 0.000 claims 1
- 101001018382 Homo sapiens Cartilage matrix protein Proteins 0.000 claims 1
- 229920000180 alkyd Polymers 0.000 claims 1
- 125000005282 allenyl group Chemical group 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- 150000001721 carbon Chemical group 0.000 claims 1
- 239000012895 dilution Substances 0.000 claims 1
- 238000010790 dilution Methods 0.000 claims 1
- 239000008151 electrolyte solution Substances 0.000 claims 1
- 230000003019 stabilising effect Effects 0.000 claims 1
- KPUREKXXPHOJQT-UHFFFAOYSA-N mesotrione Chemical group [O-][N+](=O)C1=CC(S(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O KPUREKXXPHOJQT-UHFFFAOYSA-N 0.000 description 13
- 239000005578 Mesotrione Substances 0.000 description 11
- 239000004009 herbicide Substances 0.000 description 8
- 241000196324 Embryophyta Species 0.000 description 5
- 239000000126 substance Substances 0.000 description 4
- 239000005571 Isoxaflutole Substances 0.000 description 3
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 3
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 description 3
- 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 description 3
- 229940088649 isoxaflutole Drugs 0.000 description 3
- 239000011591 potassium Substances 0.000 description 3
- 229910052700 potassium Inorganic materials 0.000 description 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- JDWQITFHZOBBFE-UHFFFAOYSA-N Benzofenap Chemical compound C=1C=C(Cl)C(C)=C(Cl)C=1C(=O)C=1C(C)=NN(C)C=1OCC(=O)C1=CC=C(C)C=C1 JDWQITFHZOBBFE-UHFFFAOYSA-N 0.000 description 2
- 239000005562 Glyphosate Substances 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 2
- 239000002671 adjuvant Substances 0.000 description 2
- 125000001246 bromo group Chemical group Br* 0.000 description 2
- 229940097068 glyphosate Drugs 0.000 description 2
- 239000000575 pesticide Substances 0.000 description 2
- ASRAWSBMDXVNLX-UHFFFAOYSA-N pyrazolynate Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(=O)C=1C(C)=NN(C)C=1OS(=O)(=O)C1=CC=C(C)C=C1 ASRAWSBMDXVNLX-UHFFFAOYSA-N 0.000 description 2
- FKERUJTUOYLBKB-UHFFFAOYSA-N pyrazoxyfen Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(=O)C=1C(C)=NN(C)C=1OCC(=O)C1=CC=CC=C1 FKERUJTUOYLBKB-UHFFFAOYSA-N 0.000 description 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 2
- LNGRZPZKVUBWQV-UHFFFAOYSA-N (4-chloro-2-methylsulfonylphenyl)-(5-cyclopropyl-1,2-oxazol-4-yl)methanone Chemical compound CS(=O)(=O)C1=CC(Cl)=CC=C1C(=O)C1=C(C2CC2)ON=C1 LNGRZPZKVUBWQV-UHFFFAOYSA-N 0.000 description 1
- XBYZOHTXPQOOJM-UHFFFAOYSA-N 1,2-oxazol-3-yl(phenyl)methanone Chemical compound C=1C=CC=CC=1C(=O)C=1C=CON=1 XBYZOHTXPQOOJM-UHFFFAOYSA-N 0.000 description 1
- 125000004201 2,4-dichlorophenyl group Chemical group [H]C1=C([H])C(*)=C(Cl)C([H])=C1Cl 0.000 description 1
- JHNVAGCOUOBGJS-UHFFFAOYSA-N 2-(2-chloro-3-ethoxy-4-ethylsulfonylbenzoyl)-5-methylcyclohexane-1,3-dione Chemical compound C1=C(S(=O)(=O)CC)C(OCC)=C(Cl)C(C(=O)C2C(CC(C)CC2=O)=O)=C1 JHNVAGCOUOBGJS-UHFFFAOYSA-N 0.000 description 1
- 239000005630 Diquat Substances 0.000 description 1
- 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 1
- 150000001204 N-oxides Chemical class 0.000 description 1
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical class CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 239000001166 ammonium sulphate Substances 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 239000003139 biocide Substances 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 244000038559 crop plants Species 0.000 description 1
- 125000000000 cycloalkoxy group Chemical group 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- SYJFEGQWDCRVNX-UHFFFAOYSA-N diquat Chemical compound C1=CC=[N+]2CC[N+]3=CC=CC=C3C2=C1 SYJFEGQWDCRVNX-UHFFFAOYSA-N 0.000 description 1
- 150000002169 ethanolamines Chemical class 0.000 description 1
- 150000008040 ionic compounds Chemical class 0.000 description 1
- JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical compound CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
- FIKAKWIAUPDISJ-UHFFFAOYSA-L paraquat dichloride Chemical compound [Cl-].[Cl-].C1=C[N+](C)=CC=C1C1=CC=[N+](C)C=C1 FIKAKWIAUPDISJ-UHFFFAOYSA-L 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000375 suspending 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
- A01N25/04—Dispersions, emulsions, suspoemulsions, suspension concentrates or gels
-
- 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
- A01N61/00—Biocides, pest repellants or attractants, or plant growth regulators containing substances of unknown or undetermined composition, e.g. substances characterised only by the mode of action
Landscapes
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Zoology (AREA)
- Dentistry (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Wood Science & Technology (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- Toxicology (AREA)
- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Catching Or Destruction (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0414895.3A GB0414895D0 (en) | 2004-07-02 | 2004-07-02 | Herbicidal formulation |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ZA200609992B true ZA200609992B (en) | 2008-07-30 |
Family
ID=32843495
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ZA200609992A ZA200609992B (en) | 2004-07-02 | 2006-11-29 | Herbicidal suspension concentrate formulation |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US20080269060A1 (ja) |
| EP (1) | EP1796471B1 (ja) |
| JP (1) | JP4965441B2 (ja) |
| CN (1) | CN1976589B (ja) |
| AR (1) | AR052975A1 (ja) |
| AT (1) | ATE418867T1 (ja) |
| BR (1) | BRPI0512849B1 (ja) |
| CA (1) | CA2569897C (ja) |
| DE (1) | DE602005012129D1 (ja) |
| GB (1) | GB0414895D0 (ja) |
| GT (1) | GT200500181A (ja) |
| MX (1) | MXPA06014153A (ja) |
| UA (1) | UA87506C2 (ja) |
| WO (1) | WO2006003371A2 (ja) |
| ZA (1) | ZA200609992B (ja) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0601304D0 (en) * | 2006-01-23 | 2006-03-01 | Syngenta Ltd | Herbicide formulation |
| UA89599C2 (uk) * | 2006-08-04 | 2010-02-10 | Басф Се | Водний концентрат діючої речовини з гербіцидною дією та спосіб боротьби з небажаним ростом рослин |
| GB0708588D0 (en) * | 2007-05-03 | 2007-06-13 | Syngenta Participations Ag | Herbicidal formulation |
| PT2249642E (pt) * | 2008-02-20 | 2012-11-29 | Syngenta Participations Ag | Formulação herbicida |
| GB0810554D0 (en) | 2008-06-09 | 2008-07-16 | Syngenta Ltd | Herbicde composition |
| PL2723320T3 (pl) * | 2011-06-23 | 2016-06-30 | Swedish Orphan Biovitrum Int Ab | Ciekła kompozycja farmaceutyczna zawierająca nityzynon |
| EP2545774A1 (en) | 2011-07-12 | 2013-01-16 | Cheminova A/S | Aqueous HPPD inhibitor suspension concentrate compositions comprising smectite clay |
| GB201114332D0 (en) | 2011-08-19 | 2011-10-05 | Nufarm Uk Ltd | Novel inhibitor compositions and methods of use |
| BR112018067941B8 (pt) * | 2016-04-28 | 2023-01-31 | Kumiai Chemical Industry Co | Composição agroquímica herbicida e método herbicida usando a mesma |
| JP6871591B2 (ja) * | 2016-10-11 | 2021-05-12 | フマキラー株式会社 | 除草剤 |
| JP7079375B2 (ja) * | 2019-03-18 | 2022-06-01 | クミアイ化学工業株式会社 | 水性懸濁農薬組成物およびその散布方法 |
| US20210378241A1 (en) * | 2020-06-03 | 2021-12-09 | Generic Crop Science LLC | Combination comprising a benzamide herbicide and a pyridine carboxylic acid herbicide, and a method for making and using the combination |
| US20220167622A1 (en) * | 2020-12-02 | 2022-06-02 | Valent U.S.A. Llc | Aqueous composition of epyrifenacil, mesotrione and pyroxasulfone |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DK169734B1 (da) * | 1993-03-09 | 1995-01-30 | Kvk Agro As | Herbicidpræparat, fremgangsmåde til fremstilling heraf samt aktiverende additiv til opblanding med herbicidpræparater |
| DE19836684A1 (de) * | 1998-08-13 | 2000-02-17 | Hoechst Schering Agrevo Gmbh | Herbizide Mittel für tolerante oder resistente Reiskulturen |
| GB9904012D0 (en) * | 1999-02-22 | 1999-04-14 | Zeneca Ltd | Agrochemical formulation |
| EP1161868A1 (en) * | 2000-06-07 | 2001-12-12 | Aventis Cropscience S.A. | New herbicidal compositions |
| JP2002068903A (ja) * | 2000-08-29 | 2002-03-08 | Sds Biotech:Kk | 水面施用乳・懸濁状農薬組成物 |
| GB0103761D0 (en) * | 2001-02-15 | 2001-04-04 | Syngenta Ltd | Agrochemical formulation |
| US6423667B1 (en) * | 2001-05-15 | 2002-07-23 | Honeywell International Inc. | Ammonium sulfate suspensions in oils |
| GB0228326D0 (en) * | 2002-12-04 | 2003-01-08 | Syngenta Ltd | Method of controlling unwanted vegitation |
| GB0305679D0 (en) * | 2003-03-12 | 2003-04-16 | Syngenta Ltd | Agrochemical formulation |
| NZ547552A (en) * | 2003-12-05 | 2009-09-25 | Syngenta Participations Ag | Submicron suspension concentrate and suspoemulsion formulations comprising a herbicidally active amount of mesotrione |
| GB0405760D0 (en) * | 2004-03-15 | 2004-04-21 | Syngenta Participations Ag | Agrochemical formulation |
-
2004
- 2004-07-02 GB GBGB0414895.3A patent/GB0414895D0/en not_active Ceased
-
2005
- 2005-06-21 DE DE602005012129T patent/DE602005012129D1/de active Active
- 2005-06-21 CN CN2005800217633A patent/CN1976589B/zh active Active
- 2005-06-21 UA UAA200701039A patent/UA87506C2/ru unknown
- 2005-06-21 AT AT05753194T patent/ATE418867T1/de not_active IP Right Cessation
- 2005-06-21 EP EP05753194A patent/EP1796471B1/en active Active
- 2005-06-21 US US11/570,820 patent/US20080269060A1/en not_active Abandoned
- 2005-06-21 CA CA2569897A patent/CA2569897C/en active Active
- 2005-06-21 JP JP2007518675A patent/JP4965441B2/ja active Active
- 2005-06-21 BR BRPI0512849-8A patent/BRPI0512849B1/pt active IP Right Grant
- 2005-06-21 WO PCT/GB2005/002443 patent/WO2006003371A2/en active Application Filing
- 2005-06-21 MX MXPA06014153A patent/MXPA06014153A/es active IP Right Grant
- 2005-06-30 AR ARP050102735A patent/AR052975A1/es active IP Right Grant
- 2005-07-01 GT GT200500181A patent/GT200500181A/es unknown
-
2006
- 2006-11-29 ZA ZA200609992A patent/ZA200609992B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CN1976589B (zh) | 2012-12-12 |
| UA87506C2 (ru) | 2009-07-27 |
| US20080269060A1 (en) | 2008-10-30 |
| JP4965441B2 (ja) | 2012-07-04 |
| WO2006003371A3 (en) | 2006-04-27 |
| AR052975A1 (es) | 2007-04-18 |
| MXPA06014153A (es) | 2007-01-29 |
| WO2006003371A2 (en) | 2006-01-12 |
| ATE418867T1 (de) | 2009-01-15 |
| EP1796471B1 (en) | 2008-12-31 |
| CA2569897A1 (en) | 2006-01-12 |
| BRPI0512849A (pt) | 2008-04-08 |
| BRPI0512849B1 (pt) | 2019-10-01 |
| CA2569897C (en) | 2012-10-16 |
| DE602005012129D1 (de) | 2009-02-12 |
| CN1976589A (zh) | 2007-06-06 |
| GB0414895D0 (en) | 2004-08-04 |
| JP2008504354A (ja) | 2008-02-14 |
| GT200500181A (es) | 2006-03-02 |
| EP1796471A2 (en) | 2007-06-20 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ZA200609992B (en) | Herbicidal suspension concentrate formulation | |
| EP2249642B1 (en) | Herbicide formulation | |
| TWI603676B (zh) | 含有４－胺基－３－氯－５－氟－６－（４－氯－２－氟－３－甲氧基苯基）吡啶－２－羧酸或其衍生物及４－羥基苯基丙酮酸雙氧合酶（ｈｐｐｄ）抑制劑的除草組成物 | |
| ES2717283T3 (es) | Composiciones herbicidas que comprenden ácido 4-amino-3-cloro-5-fluoro-6-(4-cloro-2-fluoro-3-metoxfenil)piridina-2-carboxílico o un derivado de este y herbicidas inhibidores de la síntesis de VLCFA y síntesis de ácidos grasos/lípidos | |
| RU2632860C2 (ru) | Гербицидные композиции, содержащие 4-амино-3-хлор-5-фтор-6-(4-хлор-2-фтор-3-метоксифенил)пиридин-2-карбоновую кислоту или ее производное и ингибитор протопорфириногеноксидазы | |
| AU2009226874B2 (en) | Herbicidal compositions comprising pyroxasulfone IV | |
| BR102013018459A2 (pt) | Composições herbicidas compreendendo ácido 4-amino-3-cloro-5-fluoro-6-(4-cloro-2-fluoro-3-metox ifenil) piridina-2-carboxílico ou um derivado do mesmo e imidazolinonas | |
| BR102013018645A2 (pt) | Composições de herbicidas compreendendo ácido 4-amino-3-cloro-5-fluoro-6-(4-cloro-2-fluoro-3-metox ifenil)piridina-2-carboxílico ou um seu derivado do mesmo e glifosato ou glufosinato | |
| BR102013018660A2 (pt) | Composições herbicidas compreendendo ácido 4-amino-3-cloro-5-fluoro-6-(4-cloro-2-fluoro-3-metox ifenil) piridina-2-carboxílico, ou um derivado do mesmo, e halosulfuron, pirazosulfuron e esprocarb | |
| BR102013018526A2 (pt) | Composições herbicidas compreendendo ácido 4-amino-3-cloro-5-fluoro-6-(4-cloro-2-fluoro-3-metox ifenil) piridina-2-carboxílico ou seu derivado e uma dimetóxi-pirimidina e seus derivados | |
| BR102013018463A2 (pt) | Composições herbicidas compreendendo ácido 4-amino-3-cloro-5-fluoro-6-(4-cloro-2-fluoro-3-metox ifenil)piridina-2-carboxílico ou um derivado do mesmo e certas sul-fonilureias | |
| BR102013018460A2 (pt) | Composições herbicidas que compreendem ácido 4-amino-3-cloro-5-flúor-6-(4-cloro-2-flúor-3-metoxife nil) piridina-2-carboxílico ou um derivado do mesmo e clomazona | |
| BR102013018481A2 (pt) | Composições herbicidas compreendendo ácido 4-amino-3-cloro-5-fluoro-6-(4-cloro-2-fluoro-3-metox ifenil)piridina-2-carboxílico ou seu derivado e certos inibidores de ps ii | |
| BR102013018536A2 (pt) | Composições de herbicidas compreendendo ácido 4 -amino-3-cloro-5-fluoro-6-(4-cloro-2-fluoro-3- metoxifenil)piridina-2-carboxílico ou um derivado do mesmo e certos inibidores de ps ii | |
| BR102013018646A2 (pt) | Composições herbicidas compreendendo ácido 4-amino-3-cloro-5-flúor-6-(4-cloro-2-flúor-3-metoxife nil)piridina-2-carboxílico ou um derivado do mesmo e triazolopirimidina sulfonamidas | |
| BR102013018482A2 (pt) | Composições herbicidas compreendendo o ácido 4-amino-3-cloro-5-fluoro-6-(4-cloro-2-fluoro-3-metox ifenil) piridina-2-carboxílico ou um derivado do mesmo e inibidores de transporte da auxina | |
| BR112016013349B1 (pt) | controle de erva daninha herbicida sinergístico e aperfeiçoada tolerância de colheita a partir de combinações de 2,4-d-colina, glifosato, e glufosinato em áreas de colheita de soja, milho, algodão e outras tolerantes a 2,4-d-, glifosato e glufosinato | |
| BR112017012978B1 (pt) | composição adjuvante aquosa compreendendo sulfato de polialquileno glicol éter, composição compreendendo alquilglucamidas e os usos das mesmas | |
| BR102014001857A2 (pt) | Composições herbicidas compreendendo ácido 4-amino-3-cloro-6-(4-cloro-2-fluoro-3-metoxifenil)piri dina-2-carboxílico, ou um de seus derivados, e picloram ou um de seus derivados | |
| BR102014005580A2 (pt) | composições herbicidas compreendendo ácido 4-amino-3-cloro-5-fluoro-6-(4-cloro-2-fluoro-3-metoxifenil) piridina-2-carboxílico ou seu derivado e inseticidas | |
| TWI652990B (zh) | 包含４－胺基－３－氯－５－氟－６－（４－氯－２－氟－３－甲氧基苯基）吡啶－２－羧酸或其衍生物及殺真菌劑之除草組成物 | |
| JP6130494B2 (ja) | 殺菌剤組成物 | |
| JPWO2015093519A1 (ja) | 殺菌剤組成物 | |
| BR102013032903A2 (pt) | Composições herbicidas compreendendo ácido 4-amino-3-cloro-6-(4-cloro-2-fluoro-3-metoxifenil) piridino-2-carboxílico ou um derivado deste e flufenacet | |
| BR102014006264A2 (pt) | Composições herbicidas contendo ácido 4-amino-3-cloro-5-fluoro-6-(4-cloro-2-fluoro-3-metox ifenil)piridina-2-carboxílico ou um de seus deri-vados e protetores para uso em milho (milho graúdo) |