WO1993008689A1 - Compositions herbicides a activite synergique - Google Patents
Compositions herbicides a activite synergique Download PDFInfo
- Publication number
- WO1993008689A1 WO1993008689A1 PCT/EP1992/002535 EP9202535W WO9308689A1 WO 1993008689 A1 WO1993008689 A1 WO 1993008689A1 EP 9202535 W EP9202535 W EP 9202535W WO 9308689 A1 WO9308689 A1 WO 9308689A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- activity
- colby
- xxiii
- herbicidal
- mixtures
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 46
- 230000002363 herbicidal effect Effects 0.000 title claims abstract description 45
- 230000002195 synergetic effect Effects 0.000 title abstract description 7
- NUFNQYOELLVIPL-UHFFFAOYSA-N acifluorfen Chemical compound C1=C([N+]([O-])=O)C(C(=O)O)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 NUFNQYOELLVIPL-UHFFFAOYSA-N 0.000 claims abstract description 13
- BGZZWXTVIYUUEY-UHFFFAOYSA-N fomesafen Chemical compound C1=C([N+]([O-])=O)C(C(=O)NS(=O)(=O)C)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 BGZZWXTVIYUUEY-UHFFFAOYSA-N 0.000 claims abstract description 12
- 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 abstract description 12
- 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 abstract description 11
- 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 abstract description 11
- XKJMBINCVNINCA-UHFFFAOYSA-N Alfalone Chemical compound CON(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 XKJMBINCVNINCA-UHFFFAOYSA-N 0.000 claims abstract description 11
- XVOKUMIPKHGGTN-UHFFFAOYSA-N Imazethapyr Chemical compound OC(=O)C1=CC(CC)=CN=C1C1=NC(C)(C(C)C)C(=O)N1 XVOKUMIPKHGGTN-UHFFFAOYSA-N 0.000 claims abstract description 11
- 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 abstract description 11
- 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 abstract description 10
- 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 claims abstract description 10
- 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 abstract description 10
- XCSGPAVHZFQHGE-UHFFFAOYSA-N alachlor Chemical compound CCC1=CC=CC(CC)=C1N(COC)C(=O)CCl XCSGPAVHZFQHGE-UHFFFAOYSA-N 0.000 claims abstract description 10
- CONWAEURSVPLRM-UHFFFAOYSA-N lactofen Chemical compound C1=C([N+]([O-])=O)C(C(=O)OC(C)C(=O)OCC)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 CONWAEURSVPLRM-UHFFFAOYSA-N 0.000 claims abstract description 10
- 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 abstract description 9
- IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 claims abstract description 9
- FOXFZRUHNHCZPX-UHFFFAOYSA-N metribuzin Chemical compound CSC1=NN=C(C(C)(C)C)C(=O)N1N FOXFZRUHNHCZPX-UHFFFAOYSA-N 0.000 claims abstract description 9
- 239000004009 herbicide Substances 0.000 claims abstract description 7
- KLSJWNVTNUYHDU-UHFFFAOYSA-N Amitrole Chemical compound NC1=NC=NN1 KLSJWNVTNUYHDU-UHFFFAOYSA-N 0.000 claims abstract description 6
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 claims abstract description 6
- 239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 claims abstract description 5
- 239000005504 Dicamba Substances 0.000 claims abstract description 5
- 239000005510 Diuron Substances 0.000 claims abstract description 5
- 239000005562 Glyphosate Substances 0.000 claims abstract description 5
- 239000005573 Linuron Substances 0.000 claims abstract description 5
- 239000005583 Metribuzin Substances 0.000 claims abstract description 5
- 239000005590 Oxyfluorfen Substances 0.000 claims abstract description 5
- 239000005591 Pendimethalin Substances 0.000 claims abstract description 5
- NSWAMPCUPHPTTC-UHFFFAOYSA-N chlorimuron-ethyl Chemical group CCOC(=O)C1=CC=CC=C1S(=O)(=O)NC(=O)NC1=NC(Cl)=CC(OC)=N1 NSWAMPCUPHPTTC-UHFFFAOYSA-N 0.000 claims abstract description 5
- 229940097068 glyphosate Drugs 0.000 claims abstract description 5
- 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 claims abstract description 5
- CABMTIJINOIHOD-UHFFFAOYSA-N 2-[4-methyl-5-oxo-4-(propan-2-yl)-4,5-dihydro-1H-imidazol-2-yl]quinoline-3-carboxylic acid Chemical compound N1C(=O)C(C(C)C)(C)N=C1C1=NC2=CC=CC=C2C=C1C(O)=O CABMTIJINOIHOD-UHFFFAOYSA-N 0.000 claims abstract 4
- 239000005981 Imazaquin Substances 0.000 claims abstract 2
- 241000196324 Embryophyta Species 0.000 claims description 15
- 238000000034 method Methods 0.000 claims description 5
- 230000000694 effects Effects 0.000 description 27
- 244000237956 Amaranthus retroflexus Species 0.000 description 12
- 235000013479 Amaranthus retroflexus Nutrition 0.000 description 12
- 244000068988 Glycine max Species 0.000 description 11
- 240000003461 Setaria viridis Species 0.000 description 9
- 235000002248 Setaria viridis Nutrition 0.000 description 9
- 241000533293 Sesbania emerus Species 0.000 description 6
- 240000006928 Persicaria lapathifolia Species 0.000 description 5
- 241000205407 Polygonum Species 0.000 description 5
- 241000207890 Ipomoea purpurea Species 0.000 description 4
- 240000002439 Sorghum halepense Species 0.000 description 4
- 239000004480 active ingredient Substances 0.000 description 4
- 239000000969 carrier Substances 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 244000104272 Bidens pilosa Species 0.000 description 3
- 235000010662 Bidens pilosa Nutrition 0.000 description 3
- 241000209200 Bromus Species 0.000 description 3
- 244000285774 Cyperus esculentus Species 0.000 description 3
- 235000005853 Cyperus esculentus Nutrition 0.000 description 3
- 235000013603 Digitaria ischaemum Nutrition 0.000 description 3
- 241001426056 Eleusine coracana subsp. coracana Species 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 241000219144 Abutilon Species 0.000 description 2
- 241000143476 Bidens Species 0.000 description 2
- 241000611157 Brachiaria Species 0.000 description 2
- 235000017896 Digitaria Nutrition 0.000 description 2
- 241001303487 Digitaria <clam> Species 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- 241000207783 Ipomoea Species 0.000 description 2
- 235000021506 Ipomoea Nutrition 0.000 description 2
- 241001327265 Ischaemum Species 0.000 description 2
- FZERHIULMFGESH-UHFFFAOYSA-N N-phenylacetamide Chemical compound CC(=O)NC1=CC=CC=C1 FZERHIULMFGESH-UHFFFAOYSA-N 0.000 description 2
- 241000219782 Sesbania Species 0.000 description 2
- 240000005046 Urochloa mutica Species 0.000 description 2
- 239000002671 adjuvant Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
- 239000000575 pesticide Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- DADIXGBMXACICU-UHFFFAOYSA-N (1-ethoxy-1-oxobutan-2-yl) 5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrobenzoate Chemical compound C1=C([N+]([O-])=O)C(C(=O)OC(CC)C(=O)OCC)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 DADIXGBMXACICU-UHFFFAOYSA-N 0.000 description 1
- RNSYUVITKRQWMM-UHFFFAOYSA-N 2-[(4,6-dimethylpyridin-2-yl)carbamoylsulfamoyl]benzoic acid Chemical compound CC1=CC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=C1 RNSYUVITKRQWMM-UHFFFAOYSA-N 0.000 description 1
- 241000209136 Agropyron Species 0.000 description 1
- 241000743985 Alopecurus Species 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 241000219318 Amaranthus Species 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 241000404028 Anthemis Species 0.000 description 1
- 241001666377 Apera Species 0.000 description 1
- 244000075850 Avena orientalis Species 0.000 description 1
- 241000219198 Brassica Species 0.000 description 1
- 235000011331 Brassica Nutrition 0.000 description 1
- 241000320316 Carduus Species 0.000 description 1
- 241000132570 Centaurea Species 0.000 description 1
- 241000219312 Chenopodium Species 0.000 description 1
- 235000000509 Chenopodium ambrosioides Nutrition 0.000 description 1
- 244000098897 Chenopodium botrys Species 0.000 description 1
- 235000005490 Chenopodium botrys Nutrition 0.000 description 1
- 235000007516 Chrysanthemum Nutrition 0.000 description 1
- 240000005250 Chrysanthemum indicum Species 0.000 description 1
- 244000192528 Chrysanthemum parthenium Species 0.000 description 1
- 241000132536 Cirsium Species 0.000 description 1
- 241000207199 Citrus Species 0.000 description 1
- 241000207892 Convolvulus Species 0.000 description 1
- 241000234653 Cyperus Species 0.000 description 1
- 241000208296 Datura Species 0.000 description 1
- 241000192043 Echinochloa Species 0.000 description 1
- 241000202829 Eleocharis Species 0.000 description 1
- 235000007351 Eleusine Nutrition 0.000 description 1
- 241000209215 Eleusine Species 0.000 description 1
- 241000744304 Elymus Species 0.000 description 1
- 241000508725 Elymus repens Species 0.000 description 1
- 241001290564 Fimbristylis Species 0.000 description 1
- 241000816457 Galeopsis Species 0.000 description 1
- 241000748465 Galinsoga Species 0.000 description 1
- 241001101998 Galium Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 241001657712 Itata Species 0.000 description 1
- 241000347881 Kadua laxiflora Species 0.000 description 1
- 241000520028 Lamium Species 0.000 description 1
- 241000801118 Lepidium Species 0.000 description 1
- 235000019738 Limestone Nutrition 0.000 description 1
- 241000209082 Lolium Species 0.000 description 1
- 235000017945 Matricaria Nutrition 0.000 description 1
- 235000007232 Matricaria chamomilla Nutrition 0.000 description 1
- 240000007298 Megathyrsus maximus Species 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 241000209117 Panicum Species 0.000 description 1
- 235000006443 Panicum miliaceum subsp. miliaceum Nutrition 0.000 description 1
- 235000009037 Panicum miliaceum subsp. ruderale Nutrition 0.000 description 1
- 235000011096 Papaver Nutrition 0.000 description 1
- 240000001090 Papaver somniferum Species 0.000 description 1
- 241000209048 Poa Species 0.000 description 1
- 241000219295 Portulaca Species 0.000 description 1
- 241000490453 Rorippa Species 0.000 description 1
- 240000009132 Sagittaria sagittifolia Species 0.000 description 1
- 241000780602 Senecio Species 0.000 description 1
- 235000005775 Setaria Nutrition 0.000 description 1
- 241000232088 Setaria <nematode> Species 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 241000220261 Sinapis Species 0.000 description 1
- 241000207763 Solanum Species 0.000 description 1
- 235000002634 Solanum Nutrition 0.000 description 1
- 241000488874 Sonchus Species 0.000 description 1
- 240000006694 Stellaria media Species 0.000 description 1
- WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 description 1
- 241000219422 Urtica 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
- OMOVVBIIQSXZSZ-UHFFFAOYSA-N [6-(4-acetyloxy-5,9a-dimethyl-2,7-dioxo-4,5a,6,9-tetrahydro-3h-pyrano[3,4-b]oxepin-5-yl)-5-formyloxy-3-(furan-3-yl)-3a-methyl-7-methylidene-1a,2,3,4,5,6-hexahydroindeno[1,7a-b]oxiren-4-yl] 2-hydroxy-3-methylpentanoate Chemical compound CC12C(OC(=O)C(O)C(C)CC)C(OC=O)C(C3(C)C(CC(=O)OC4(C)COC(=O)CC43)OC(C)=O)C(=C)C32OC3CC1C=1C=COC=1 OMOVVBIIQSXZSZ-UHFFFAOYSA-N 0.000 description 1
- 229960001413 acetanilide Drugs 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 230000003042 antagnostic effect Effects 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 229960000892 attapulgite Drugs 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 150000008107 benzenesulfonic acids Chemical class 0.000 description 1
- 229920005551 calcium lignosulfonate Polymers 0.000 description 1
- RYAGRZNBULDMBW-UHFFFAOYSA-L calcium;3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Ca+2].COC1=CC=CC(CC(CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O RYAGRZNBULDMBW-UHFFFAOYSA-L 0.000 description 1
- CSPPKDPQLUUTND-UHFFFAOYSA-N chembl3186232 Chemical compound CCON=C(CCC)C1=C(O)CC(CC(C)SCC)CC1=O CSPPKDPQLUUTND-UHFFFAOYSA-N 0.000 description 1
- RIUXZHMCCFLRBI-UHFFFAOYSA-N chlorimuron Chemical compound COC1=CC(Cl)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 RIUXZHMCCFLRBI-UHFFFAOYSA-N 0.000 description 1
- 235000020971 citrus fruits Nutrition 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- -1 fatty alcohol sulfates Chemical class 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
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- 239000002480 mineral oil Substances 0.000 description 1
- 229940042472 mineral oil Drugs 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 239000010773 plant oil Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000011814 protection agent Substances 0.000 description 1
- 230000023798 response to herbicide Effects 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
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Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
Definitions
- This invention relates to a new herbicidal composition having synergistic activity comprising a mixture of
- herbicidal compositions which comprise, as active components, a mixture of
- XIII acifluorfen (XIV), lactofen (XV), fomesafen (XVI), pendimethalin (XVII), alachlor (XVIII), metolachlor (XIX), trifluralin (XX), chlorimuron-ethyl (XXI), imazaguin (XXII) and imazethapyr (XXIII), broaden the spectrum of weeds that can be controlled and show an increase in herbicidal activity in comparison with the individual components without losing the selectivity properties in agricultural crops.
- Glyphosate is the common name for N-(phosphonomethyl)- glycine
- sulfometuron-methyl is the common name for methyl
- 2,4-D is the common name for 2-(4-chloro-2-methylphenoxy)acetic acid
- dicamba is the common name for 3,6 dichloro-2-methoxybenzoic acid
- oxyfluorfen is the common name for 2-chloro- ⁇ , ⁇ , ⁇ -trifluoro-p-tolyl 3-ethoxy-4-nitrophenyl ether;
- glufosinate ammonium is the common name for ammonium
- amitrole is the common name for 1H-1,2,4-triazol-3-ylamine
- sethoxydim is the common name for ( ⁇ )-(EZ)-2-(1-ethoxyiminobutyl)-5-[2-(ethylthio)propyl]-3-hydroxycyclohex-2-enone;
- metribuzin is the common name for 4-amino-6-tert.-butyl-4,5-dihydro-3-methylthio-1,2,4-triazin-5-one;
- acifluorfen is the common name for 5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrobenzoic acid;
- lactofen is the common name for ( ⁇ ) -2-ethoxy-1-ethyl-2-oxoethyl 5-[chloro-4-(trifluoromethyl)phenoxy]- 2-nitrobenzoate;
- fomesafen is the common name for 5-[2-chloro- 4-(trifluoromethyl)phenoxy]-N-(methylsulfonyl)-2-nitrobenzamide;
- pendimethalin is the common name for N-(1-ethylpropyl)- 3,4-dimethyl-2,6-dinitroaniline;
- alachlor is the common name for 2-chloro-2',6'-diethyl- N-methoxymethylacetanilide
- metolachlor is the common name for 2-chloro-6'-ethyl- 2'-methy1-N-(2-methoxy-1-methylethyl)acetanilide;
- trifluralin is the common name for 2,6-dinitro- N,N-dipropyl-4-(trifluoromethyl)aniline;
- chlorimuron-ethyl is the common name for ethyl
- imazaguin is the common name for ( ⁇ )-2-[4,5-dihydro- 4-methyl-4-(1-methylethyl)-5-oxo-1H-imidazole-2-yl]- 5-ethyl-3-pyridinecarboxylic acid;
- imazethapyr is the common name for ( ⁇ )-2-[4,5-dihydro- 4-methyl-4-(1-methylethyl)-5-oxo-1H-2-yl]-3-quinoline carboxylic acid.
- the combinations of the invention are suitable for the control of important annual and perennial weeds
- Monocotyledonous weeds of the species Avena, Alopecurus, Echinochloa, Setaria, Panicum, Digitaria, Poa, Eleusine, Brachiaria, Lolium, Bromus, Cyperus, Agropyron ( Elymus), Sagittaria, Monocharia, Fimbristylis, Eleocharis,
- the combinations of I with II-XI can be applied pre- emergently, and the combinations of I with XII-XXIII can be applied post-emergently.
- the rate of use lies between
- the weight ratio of component I) to the other component is generally between 50:1 and 1:100.
- compositions of the invention can also be used in admixture with other active agents for example other plant-protection agents or pesticides, depending on the particular need.
- An improvement in the intensity and speed of action can be obtained, for example, by addition of suitable adjuvants, such as organic solvents, wetting agents and oils.
- suitable adjuvants such as organic solvents, wetting agents and oils.
- Such additives may allow a decrease in the dose.
- the designated active ingredients or their mixtures can suitably be used, for example, as powders, dusts,
- liquid carriers are, for example aliphatic and aromatic hydrocarbons, such as benzene, toluene, xylene, cyclohexanone, isophorone, dimethyl sulfoxide,
- Suitable solid carriers include mineral earths, e.g.
- limestone silicic acid and plant products, e.g. flours.
- surface-active agents there can be used for example calcium lignosulfonate, polyoxyethylenealkylphenyl ethers, naphthalenesulfonic acids and their salts, phenolsulfonic acids and their salts, formaldehyde condensates, fatty alcohol sulfates, as well as substituted benzenesulfonic acids and their salts.
- compositions can contain about 10 to 90 percent by weight active ingredients, and about 90 to 10 percent by weight liquid or solid carriers, as well as, optionally up to 20 percent by weight of surfactant.
- the agents can be applied in customary fashion, for example with water as the carrier in spray mixture volumes of approximately 100 to 1,000 1/ha.
- the agents can be applied using low-volume or ultra-low-volume techniques or in the form of so-called microgranules.
- compositions can be carried out in known manner, for example by milling or mixing
- individual components can be mixed just before use for example by the so-called commonly used tank-mixing method.
- X the herbicidal activity (%) of substance A at a rate of p g/ha.
- Y the herbicidal activity (%) of substance B at a rate of q g/ha.
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)
Abstract
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5508170A JPH07502498A (ja) | 1991-11-05 | 1992-10-30 | 共力作用除草剤組成物 |
CA002122898A CA2122898A1 (fr) | 1991-11-05 | 1992-10-30 | Compositions herbicides synergiques |
BR9206712A BR9206712A (pt) | 1991-11-05 | 1992-10-30 | Composições herbicidas sinergísticas |
EP92923266A EP0612213A1 (fr) | 1991-11-05 | 1992-10-30 | Compositions herbicides a activite synergique |
FI942050A FI942050A0 (fi) | 1991-11-05 | 1994-05-04 | Synergistisiä herbisidikoostumuksia |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEP4136740.5 | 1991-11-05 | ||
DE4136740A DE4136740A1 (de) | 1991-11-05 | 1991-11-05 | Herbizide mittel mit synergistischer wirkung |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1993008689A1 true WO1993008689A1 (fr) | 1993-05-13 |
Family
ID=6444326
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP1992/002535 WO1993008689A1 (fr) | 1991-11-05 | 1992-10-30 | Compositions herbicides a activite synergique |
Country Status (14)
Country | Link |
---|---|
EP (1) | EP0612213A1 (fr) |
JP (1) | JPH07502498A (fr) |
CN (1) | CN1073071A (fr) |
AU (1) | AU2920492A (fr) |
BR (1) | BR9206712A (fr) |
CA (1) | CA2122898A1 (fr) |
DE (1) | DE4136740A1 (fr) |
FI (1) | FI942050A0 (fr) |
HU (1) | HUT66872A (fr) |
IL (1) | IL103626A0 (fr) |
RU (1) | RU94021656A (fr) |
TW (1) | TW224932B (fr) |
WO (1) | WO1993008689A1 (fr) |
ZA (1) | ZA928540B (fr) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1995023509A1 (fr) * | 1994-03-01 | 1995-09-08 | E.I. Du Pont De Nemours And Company | Hydantoïnes bicycliques herbicides |
EP2710894A1 (fr) * | 2011-05-20 | 2014-03-26 | Nihon Nohyaku Co., Ltd. | Composition pour l'élimination du feuillage pourri de plantes cultivées |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE10209478A1 (de) * | 2002-03-05 | 2003-09-18 | Bayer Cropscience Gmbh | Herbizid-Kombinationen mit speziellen Sulfonylharnstoffen |
KR100703303B1 (ko) | 2005-04-28 | 2007-04-03 | 삼성전자주식회사 | 무선 통신 시스템에서 확장 실시간 폴링 서비스의 상향링크 자원 할당 요청 방법 |
UY32345A (es) * | 2008-12-19 | 2010-06-30 | Basf Se | Composiciones acuosas fluidas de concentrados de un herbicida de dinitoranilina microencapsulado |
EA019754B1 (ru) * | 2011-07-13 | 2014-06-30 | Юрий Аглямович ГАРИПОВ | Синергетическая гербицидная композиция |
CN103120180A (zh) * | 2011-11-17 | 2013-05-29 | 浙江新安化工集团股份有限公司 | 一种草甘膦与敌草隆的除草剂组合物及其制备方法 |
JP2016027002A (ja) * | 2012-11-16 | 2016-02-18 | 日本農薬株式会社 | 除草剤組成物 |
CN108782597B (zh) * | 2017-04-26 | 2021-08-06 | 四川利尔作物科学有限公司 | 一种含草甘膦和丙炔氟草胺的悬浮剂 |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0311135A2 (fr) * | 1987-10-09 | 1989-04-12 | Schering Aktiengesellschaft | Azoles et azines hétérocycliques substituées, procédé pour leur préparation et leur utilisation comme agents à activité herbicide |
-
1991
- 1991-11-05 DE DE4136740A patent/DE4136740A1/de not_active Withdrawn
-
1992
- 1992-10-30 JP JP5508170A patent/JPH07502498A/ja active Pending
- 1992-10-30 WO PCT/EP1992/002535 patent/WO1993008689A1/fr not_active Application Discontinuation
- 1992-10-30 HU HU9401307A patent/HUT66872A/hu unknown
- 1992-10-30 AU AU29204/92A patent/AU2920492A/en not_active Abandoned
- 1992-10-30 BR BR9206712A patent/BR9206712A/pt not_active Application Discontinuation
- 1992-10-30 RU RU94021656/04A patent/RU94021656A/ru unknown
- 1992-10-30 EP EP92923266A patent/EP0612213A1/fr not_active Withdrawn
- 1992-10-30 CA CA002122898A patent/CA2122898A1/fr not_active Abandoned
- 1992-11-03 IL IL103626A patent/IL103626A0/xx unknown
- 1992-11-05 CN CN92113786A patent/CN1073071A/zh active Pending
- 1992-11-05 ZA ZA928540A patent/ZA928540B/xx unknown
- 1992-12-04 TW TW081109737A patent/TW224932B/zh active
-
1994
- 1994-05-04 FI FI942050A patent/FI942050A0/fi unknown
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0311135A2 (fr) * | 1987-10-09 | 1989-04-12 | Schering Aktiengesellschaft | Azoles et azines hétérocycliques substituées, procédé pour leur préparation et leur utilisation comme agents à activité herbicide |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1995023509A1 (fr) * | 1994-03-01 | 1995-09-08 | E.I. Du Pont De Nemours And Company | Hydantoïnes bicycliques herbicides |
EP2710894A1 (fr) * | 2011-05-20 | 2014-03-26 | Nihon Nohyaku Co., Ltd. | Composition pour l'élimination du feuillage pourri de plantes cultivées |
EP2710894A4 (fr) * | 2011-05-20 | 2014-10-22 | Nihon Nohyaku Co Ltd | Composition pour l'élimination du feuillage pourri de plantes cultivées |
Also Published As
Publication number | Publication date |
---|---|
FI942050L (fi) | 1994-05-04 |
DE4136740A1 (de) | 1993-05-06 |
TW224932B (fr) | 1994-06-11 |
AU2920492A (en) | 1993-06-07 |
ZA928540B (en) | 1993-05-05 |
CN1073071A (zh) | 1993-06-16 |
JPH07502498A (ja) | 1995-03-16 |
RU94021656A (ru) | 1996-04-10 |
HU9401307D0 (en) | 1994-08-29 |
CA2122898A1 (fr) | 1993-05-13 |
IL103626A0 (en) | 1993-04-04 |
EP0612213A1 (fr) | 1994-08-31 |
BR9206712A (pt) | 1995-10-24 |
HUT66872A (en) | 1995-01-30 |
FI942050A0 (fi) | 1994-05-04 |
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