DE4216880A1 - Herbizide Mittel zur Unkrautbekämpfung in Reiskulturen - Google Patents
Herbizide Mittel zur Unkrautbekämpfung in ReiskulturenInfo
- Publication number
- DE4216880A1 DE4216880A1 DE4216880A DE4216880A DE4216880A1 DE 4216880 A1 DE4216880 A1 DE 4216880A1 DE 4216880 A DE4216880 A DE 4216880A DE 4216880 A DE4216880 A DE 4216880A DE 4216880 A1 DE4216880 A1 DE 4216880A1
- Authority
- DE
- Germany
- Prior art keywords
- alkyl
- methyl
- haloalkyl
- hydrogen
- chloro
- Prior art date
- Legal status (The legal status 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 status listed.)
- Withdrawn
Links
- 230000002363 herbicidal effect Effects 0.000 title claims abstract description 30
- 239000004009 herbicide Substances 0.000 title claims description 15
- 230000002195 synergetic effect Effects 0.000 title description 5
- 241000196324 Embryophyta Species 0.000 claims abstract description 41
- 235000007164 Oryza sativa Nutrition 0.000 claims abstract description 17
- 235000009566 rice Nutrition 0.000 claims abstract description 17
- HKPHPIREJKHECO-UHFFFAOYSA-N butachlor Chemical compound CCCCOCN(C(=O)CCl)C1=C(CC)C=CC=C1CC HKPHPIREJKHECO-UHFFFAOYSA-N 0.000 claims abstract description 9
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 8
- XIGAUIHYSDTJHW-UHFFFAOYSA-N mefenacet Chemical compound N=1C2=CC=CC=C2SC=1OCC(=O)N(C)C1=CC=CC=C1 XIGAUIHYSDTJHW-UHFFFAOYSA-N 0.000 claims abstract description 8
- 150000003839 salts Chemical group 0.000 claims abstract description 8
- BXEHUCNTIZGSOJ-UHFFFAOYSA-N Esprocarb Chemical compound CC(C)C(C)N(CC)C(=O)SCC1=CC=CC=C1 BXEHUCNTIZGSOJ-UHFFFAOYSA-N 0.000 claims abstract description 7
- 150000002367 halogens Chemical class 0.000 claims abstract description 7
- HZDIJTXDRLNTIS-DAXSKMNVSA-N n-[[(z)-but-2-enoxy]methyl]-2-chloro-n-(2,6-diethylphenyl)acetamide Chemical compound CCC1=CC=CC(CC)=C1N(COC\C=C/C)C(=O)CCl HZDIJTXDRLNTIS-DAXSKMNVSA-N 0.000 claims abstract description 7
- YLPGTOIOYRQOHV-UHFFFAOYSA-N Pretilachlor Chemical compound CCCOCCN(C(=O)CCl)C1=C(CC)C=CC=C1CC YLPGTOIOYRQOHV-UHFFFAOYSA-N 0.000 claims abstract description 6
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims abstract description 3
- 240000007594 Oryza sativa Species 0.000 claims abstract 2
- 239000004480 active ingredient Substances 0.000 claims description 43
- 239000000203 mixture Substances 0.000 claims description 40
- 239000005472 Bensulfuron methyl Substances 0.000 claims description 33
- XMQFTWRPUQYINF-UHFFFAOYSA-N bensulfuron-methyl Chemical group COC(=O)C1=CC=CC=C1CS(=O)(=O)NC(=O)NC1=NC(OC)=CC(OC)=N1 XMQFTWRPUQYINF-UHFFFAOYSA-N 0.000 claims description 33
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 26
- 150000001875 compounds Chemical class 0.000 claims description 25
- 229910052739 hydrogen Inorganic materials 0.000 claims description 20
- 239000001257 hydrogen Substances 0.000 claims description 20
- -1 2-propoxyethyl Chemical group 0.000 claims description 17
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 17
- 238000009472 formulation Methods 0.000 claims description 16
- 239000008187 granular material Substances 0.000 claims description 11
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims description 10
- 239000003795 chemical substances by application Substances 0.000 claims description 10
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 10
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 8
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 8
- 239000000839 emulsion Substances 0.000 claims description 8
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 7
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 7
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 7
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 7
- 229910052794 bromium Inorganic materials 0.000 claims description 7
- 239000000460 chlorine Substances 0.000 claims description 7
- 229910052801 chlorine Inorganic materials 0.000 claims description 7
- 239000004495 emulsifiable concentrate Substances 0.000 claims description 7
- 229910052731 fluorine Inorganic materials 0.000 claims description 7
- 239000011737 fluorine Substances 0.000 claims description 7
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 7
- 239000002689 soil Substances 0.000 claims description 7
- NXQDBZGWYSEGFL-UHFFFAOYSA-N Anilofos Chemical compound COP(=S)(OC)SCC(=O)N(C(C)C)C1=CC=C(Cl)C=C1 NXQDBZGWYSEGFL-UHFFFAOYSA-N 0.000 claims description 6
- NAGRVUXEKKZNHT-UHFFFAOYSA-N Imazosulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2N3C=CC=CC3=NC=2Cl)=N1 NAGRVUXEKKZNHT-UHFFFAOYSA-N 0.000 claims description 6
- QHTQREMOGMZHJV-UHFFFAOYSA-N Thiobencarb Chemical compound CCN(CC)C(=O)SCC1=CC=C(Cl)C=C1 QHTQREMOGMZHJV-UHFFFAOYSA-N 0.000 claims description 6
- BWUPSGJXXPATLU-UHFFFAOYSA-N dimepiperate Chemical compound C=1C=CC=CC=1C(C)(C)SC(=O)N1CCCCC1 BWUPSGJXXPATLU-UHFFFAOYSA-N 0.000 claims description 6
- 150000002431 hydrogen Chemical class 0.000 claims description 6
- 239000000243 solution Substances 0.000 claims description 6
- 239000004562 water dispersible granule Substances 0.000 claims description 6
- 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 5
- 238000002360 preparation method Methods 0.000 claims description 5
- 239000004563 wettable powder Substances 0.000 claims description 5
- 239000006185 dispersion Substances 0.000 claims description 4
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 4
- DEDOPGXGGQYYMW-UHFFFAOYSA-N molinate Chemical compound CCSC(=O)N1CCCCCC1 DEDOPGXGGQYYMW-UHFFFAOYSA-N 0.000 claims description 4
- 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 claims description 4
- VTRWMTJQBQJKQH-UHFFFAOYSA-N pyributicarb Chemical compound COC1=CC=CC(N(C)C(=S)OC=2C=C(C=CC=2)C(C)(C)C)=N1 VTRWMTJQBQJKQH-UHFFFAOYSA-N 0.000 claims description 4
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 4
- KOPFEFZSAMLEHK-UHFFFAOYSA-N 1h-pyrazole-5-carboxylic acid Chemical class OC(=O)C=1C=CNN=1 KOPFEFZSAMLEHK-UHFFFAOYSA-N 0.000 claims description 3
- 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 claims description 3
- WMLPCIHUFDKWJU-UHFFFAOYSA-N Cinosulfuron Chemical compound COCCOC1=CC=CC=C1S(=O)(=O)NC(=O)NC1=NC(OC)=NC(OC)=N1 WMLPCIHUFDKWJU-UHFFFAOYSA-N 0.000 claims description 3
- 229940126062 Compound A Drugs 0.000 claims description 3
- YUBJPYNSGLJZPQ-UHFFFAOYSA-N Dithiopyr Chemical compound CSC(=O)C1=C(C(F)F)N=C(C(F)(F)F)C(C(=O)SC)=C1CC(C)C YUBJPYNSGLJZPQ-UHFFFAOYSA-N 0.000 claims description 3
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 claims description 3
- 239000005567 Imazosulfuron Substances 0.000 claims description 3
- BGNQYGRXEXDAIQ-UHFFFAOYSA-N Pyrazosulfuron-ethyl Chemical group C1=NN(C)C(S(=O)(=O)NC(=O)NC=2N=C(OC)C=C(OC)N=2)=C1C(=O)OCC BGNQYGRXEXDAIQ-UHFFFAOYSA-N 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- XQMKFXNULSWWSY-UHFFFAOYSA-N (4-chlorophenyl)methylsulfanyl n,n-diethylcarbamate Chemical compound CCN(CC)C(=O)OSCC1=CC=C(Cl)C=C1 XQMKFXNULSWWSY-UHFFFAOYSA-N 0.000 claims description 2
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims description 2
- KMHCHZLTOITEAG-UHFFFAOYSA-N 1-(4,6-dimethoxy-1,3,5-triazin-2-yl)-1-[2-(2-methoxyethoxy)phenyl]sulfonylurea Chemical compound COCCOC1=CC=CC=C1S(=O)(=O)N(C(N)=O)C1=NC(OC)=NC(OC)=N1 KMHCHZLTOITEAG-UHFFFAOYSA-N 0.000 claims description 2
- YOZIAYORPGZVGO-UHFFFAOYSA-N 1-(azepan-1-yl)propane-1-thione Chemical compound CCC(=S)N1CCCCCC1 YOZIAYORPGZVGO-UHFFFAOYSA-N 0.000 claims description 2
- ZGPQEGJPFLCWRQ-UHFFFAOYSA-N 2-[4-(2,6-dichloro-3-methylbenzoyl)-2,5-dimethylpyrazol-3-yl]oxy-1-(4-methylphenyl)ethanone Chemical compound ClC=1C=CC(C)=C(Cl)C=1C(=O)C=1C(C)=NN(C)C=1OCC(=O)C1=CC=C(C)C=C1 ZGPQEGJPFLCWRQ-UHFFFAOYSA-N 0.000 claims description 2
- WUGGSSHDQTUOFT-UHFFFAOYSA-N 2-[[carbamoyl-(4,6-dimethoxypyrimidin-2-yl)sulfamoyl]oxymethyl]benzoic acid Chemical compound COC1=NC(=NC(=C1)OC)N(S(=O)(=O)OCC=1C(=CC=CC=1)C(=O)O)C(N)=O WUGGSSHDQTUOFT-UHFFFAOYSA-N 0.000 claims description 2
- DDPPGGGOLPAZPX-UHFFFAOYSA-N 2-methyl-2-phenyl-1-piperidin-1-ylpropane-1-thione Chemical compound C=1C=CC=CC=1C(C)(C)C(=S)N1CCCCC1 DDPPGGGOLPAZPX-UHFFFAOYSA-N 0.000 claims description 2
- NNYRZQHKCHEXSD-UHFFFAOYSA-N Daimuron Chemical compound C1=CC(C)=CC=C1NC(=O)NC(C)(C)C1=CC=CC=C1 NNYRZQHKCHEXSD-UHFFFAOYSA-N 0.000 claims description 2
- KDWQYMVPYJGPHS-UHFFFAOYSA-N Thenylchlor Chemical compound C1=CSC(CN(C(=O)CCl)C=2C(=CC=CC=2C)C)=C1OC KDWQYMVPYJGPHS-UHFFFAOYSA-N 0.000 claims description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 2
- 239000007864 aqueous solution Substances 0.000 claims description 2
- 239000004202 carbamide Substances 0.000 claims description 2
- 239000003094 microcapsule Substances 0.000 claims description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
- 229910052717 sulfur Chemical group 0.000 claims description 2
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims description 2
- 239000001993 wax Substances 0.000 claims description 2
- XIIAUQZZAXXOAS-UHFFFAOYSA-N CN1C(=C(C(=N1)S(=O)(=O)NC(=O)N)C(=O)O)C2=NC(=CC(=N2)OC)OC Chemical compound CN1C(=C(C(=N1)S(=O)(=O)NC(=O)N)C(=O)O)C2=NC(=CC(=N2)OC)OC XIIAUQZZAXXOAS-UHFFFAOYSA-N 0.000 claims 1
- ICWUMLXQKFTJMH-UHFFFAOYSA-N Etobenzanid Chemical compound C1=CC(OCOCC)=CC=C1C(=O)NC1=CC=CC(Cl)=C1Cl ICWUMLXQKFTJMH-UHFFFAOYSA-N 0.000 claims 1
- 239000004476 plant protection product Substances 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 abstract description 11
- 230000000694 effects Effects 0.000 abstract description 9
- 241000234653 Cyperus Species 0.000 abstract description 5
- 240000009132 Sagittaria sagittifolia Species 0.000 abstract description 3
- 241000748223 Alisma Species 0.000 abstract description 2
- 241000202829 Eleocharis Species 0.000 abstract description 2
- 241000169139 Monochoria Species 0.000 abstract description 2
- 235000003990 Monochoria hastata Nutrition 0.000 abstract description 2
- 241000341978 Rotala Species 0.000 abstract description 2
- 241000202758 Scirpus Species 0.000 abstract description 2
- 125000001188 haloalkyl group Chemical group 0.000 abstract 5
- 125000003545 alkoxy group Chemical group 0.000 abstract 4
- QMNFICMPAXFAPC-UHFFFAOYSA-N 2-benzoylcyclohexane-1,3-dione Chemical compound C=1C=CC=CC=1C(=O)C1C(=O)CCCC1=O QMNFICMPAXFAPC-UHFFFAOYSA-N 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 230000005923 long-lasting effect Effects 0.000 abstract 1
- 231100000053 low toxicity Toxicity 0.000 abstract 1
- 241000209094 Oryza Species 0.000 description 15
- 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 8
- 229910052708 sodium Inorganic materials 0.000 description 8
- 239000011734 sodium Substances 0.000 description 8
- 239000003995 emulsifying agent Substances 0.000 description 6
- 239000000843 powder Substances 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 239000002253 acid Substances 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
- 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 4
- 239000000463 material Substances 0.000 description 4
- 229920000151 polyglycol Polymers 0.000 description 4
- 239000010695 polyglycol Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 239000005995 Aluminium silicate Substances 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 239000004372 Polyvinyl alcohol Substances 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 239000003513 alkali Substances 0.000 description 3
- 235000012211 aluminium silicate Nutrition 0.000 description 3
- 239000000969 carrier Substances 0.000 description 3
- 239000012141 concentrate Substances 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 239000002270 dispersing agent Substances 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 239000003337 fertilizer Substances 0.000 description 3
- 230000012010 growth Effects 0.000 description 3
- 239000003621 irrigation water Substances 0.000 description 3
- 229920002451 polyvinyl alcohol Polymers 0.000 description 3
- PQTBTIFWAXVEPB-UHFFFAOYSA-N sulcotrione Chemical compound ClC1=CC(S(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O PQTBTIFWAXVEPB-UHFFFAOYSA-N 0.000 description 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- GBCCAVJIOHCZPZ-UHFFFAOYSA-N 4,4-dimethyl-2-(2-nitrobenzoyl)cyclohexane-1,3-dione Chemical compound O=C1C(C)(C)CCC(=O)C1C(=O)C1=CC=CC=C1[N+]([O-])=O GBCCAVJIOHCZPZ-UHFFFAOYSA-N 0.000 description 2
- GDRAVGVZLRCTDB-UHFFFAOYSA-N 5,5-dimethyl-2-(2-nitrobenzoyl)cyclohexane-1,3-dione Chemical compound O=C1CC(C)(C)CC(=O)C1C(=O)C1=CC=CC=C1[N+]([O-])=O GDRAVGVZLRCTDB-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 241000209510 Liliopsida Species 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 241000209504 Poaceae Species 0.000 description 2
- 229940100389 Sulfonylurea Drugs 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
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- 238000009835 boiling Methods 0.000 description 2
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- 239000003085 diluting agent Substances 0.000 description 2
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- 150000002170 ethers Chemical class 0.000 description 2
- 150000002191 fatty alcohols Chemical class 0.000 description 2
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- 239000002917 insecticide Substances 0.000 description 2
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- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
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- VSCOTPSNHSUTSM-UHFFFAOYSA-N (2-ethoxyphenyl) N-[(4,6-dimethoxypyridin-2-yl)carbamoyl]sulfamate Chemical compound COC1=CC(=NC(=C1)OC)NC(NS(=O)(=O)OC1=C(C=CC=C1)OCC)=O VSCOTPSNHSUTSM-UHFFFAOYSA-N 0.000 description 1
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- CMJUNAQINNWKAU-KTKRTIGZSA-N 2-[[(z)-2-oxononadec-10-enyl]amino]ethanesulfonic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)CNCCS(O)(=O)=O CMJUNAQINNWKAU-KTKRTIGZSA-N 0.000 description 1
- QTIRSGSXXNJVIQ-UHFFFAOYSA-N 2-chloro-n-(2,6-dimethylphenyl)-n-(3-methoxythiophen-2-yl)propanamide Chemical compound C1=CSC(N(C(=O)C(C)Cl)C=2C(=CC=CC=2C)C)=C1OC QTIRSGSXXNJVIQ-UHFFFAOYSA-N 0.000 description 1
- FOGYNLXERPKEGN-UHFFFAOYSA-N 3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfopropyl)phenoxy]propane-1-sulfonic acid Chemical compound COC1=CC=CC(CC(CS(O)(=O)=O)OC=2C(=CC(CCCS(O)(=O)=O)=CC=2)OC)=C1O FOGYNLXERPKEGN-UHFFFAOYSA-N 0.000 description 1
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- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- 241000192043 Echinochloa Species 0.000 description 1
- 241000759118 Eleocharis kuroguwai Species 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical class C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- RVGRUAULSDPKGF-UHFFFAOYSA-N Poloxamer Chemical compound C1CO1.CC1CO1 RVGRUAULSDPKGF-UHFFFAOYSA-N 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 229920001214 Polysorbate 60 Polymers 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 241001620634 Roger Species 0.000 description 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 241001464837 Viridiplantae Species 0.000 description 1
- 241001148683 Zostera marina Species 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000003905 agrochemical Substances 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 230000003042 antagnostic effect Effects 0.000 description 1
- 239000000729 antidote Substances 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 239000011324 bead Substances 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
- 239000011575 calcium Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 229920005551 calcium lignosulfonate Polymers 0.000 description 1
- 159000000007 calcium salts Chemical class 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
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- YRIUSKIDOIARQF-UHFFFAOYSA-N dodecyl benzenesulfonate Chemical compound CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 YRIUSKIDOIARQF-UHFFFAOYSA-N 0.000 description 1
- 229940071161 dodecylbenzenesulfonate Drugs 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 241001233957 eudicotyledons Species 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 230000035784 germination Effects 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- 239000003630 growth substance Substances 0.000 description 1
- 238000003306 harvesting Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 150000004679 hydroxides Chemical class 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
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 229910052622 kaolinite Inorganic materials 0.000 description 1
- 230000002045 lasting effect Effects 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical class CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 229920002113 octoxynol Polymers 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 230000002085 persistent effect Effects 0.000 description 1
- 230000000361 pesticidal effect Effects 0.000 description 1
- 150000004714 phosphonium salts Chemical class 0.000 description 1
- 231100000208 phytotoxic Toxicity 0.000 description 1
- 230000000885 phytotoxic effect Effects 0.000 description 1
- 230000008654 plant damage Effects 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001522 polyglycol ester Polymers 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- ASRAWSBMDXVNLX-UHFFFAOYSA-N pyrazolynate Chemical class 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 1
- 229910052903 pyrophyllite Inorganic materials 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000011885 synergistic combination Substances 0.000 description 1
- 238000003419 tautomerization reaction Methods 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000008096 xylene 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
- A01N35/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical
- A01N35/06—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical containing keto or thioketo groups as part of a ring, e.g. cyclohexanone, quinone; Derivatives thereof, e.g. ketals
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01C—PLANTING; SOWING; FERTILISING
- A01C1/00—Apparatus, or methods of use thereof, for testing or treating seed, roots, or the like, prior to sowing or planting
- A01C1/08—Immunising seed
-
- 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
- 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
- A01N25/12—Powders or granules
-
- 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
- A01N25/26—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 in coated particulate form
-
- 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
- A01N41/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom
- A01N41/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom containing a sulfur-to-oxygen double bond
- A01N41/10—Sulfones; Sulfoxides
Landscapes
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Environmental Sciences (AREA)
- Zoology (AREA)
- Dentistry (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Plant Pathology (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Toxicology (AREA)
- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Soil Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE4216880A DE4216880A1 (de) | 1992-05-21 | 1992-05-21 | Herbizide Mittel zur Unkrautbekämpfung in Reiskulturen |
| IT93MI001025A IT1265082B1 (it) | 1992-05-21 | 1993-05-19 | Erbicidi per la lotta contro piante infestanti in coltivazioni di riso |
| CN 93105937 CN1078852A (zh) | 1992-05-21 | 1993-05-20 | 防治稻田杂草的除草剂 |
| KR1019930008678A KR940005220A (ko) | 1992-05-21 | 1993-05-20 | 벼의 잡초 방제용 제초제 조성물 |
| JP5118316A JPH06128106A (ja) | 1992-05-21 | 1993-05-20 | 除草剤組成物 |
| TW082105277A TW278026B (enrdf_load_stackoverflow) | 1992-05-21 | 1993-07-02 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE4216880A DE4216880A1 (de) | 1992-05-21 | 1992-05-21 | Herbizide Mittel zur Unkrautbekämpfung in Reiskulturen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE4216880A1 true DE4216880A1 (de) | 1993-11-25 |
Family
ID=6459454
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE4216880A Withdrawn DE4216880A1 (de) | 1992-05-21 | 1992-05-21 | Herbizide Mittel zur Unkrautbekämpfung in Reiskulturen |
Country Status (6)
| Country | Link |
|---|---|
| JP (1) | JPH06128106A (enrdf_load_stackoverflow) |
| KR (1) | KR940005220A (enrdf_load_stackoverflow) |
| CN (1) | CN1078852A (enrdf_load_stackoverflow) |
| DE (1) | DE4216880A1 (enrdf_load_stackoverflow) |
| IT (1) | IT1265082B1 (enrdf_load_stackoverflow) |
| TW (1) | TW278026B (enrdf_load_stackoverflow) |
Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2720600A1 (fr) * | 1994-06-03 | 1995-12-08 | Basf Ag | Agents herbicides contenant de la 3-(2-chlorophénylméthyll)-1-(1-méthyl-1-phényléthyl)- et/ou 1-(1-méthyl-1-phényléthyl)-3-(4-tolyl)-urée, ainsi qu'au moins un éther-oxime de cyclohexénone. |
| WO1997003562A1 (en) * | 1995-07-19 | 1997-02-06 | Zeneca Limited | Synergistic herbicidal composition and method of use thereof |
| WO1997048276A1 (en) * | 1996-06-21 | 1997-12-24 | E.I. Du Pont De Nemours And Company | Herbicidal mixtures |
| WO2000003592A3 (de) * | 1998-07-16 | 2000-11-09 | Aventis Cropscience Gnbh | Herbizide mittel mit substituierten phenoxysulfonylharnstoffen |
| WO2001017350A1 (en) * | 1999-09-08 | 2001-03-15 | Aventis Cropscience Uk Limited | New herbicidal compositions |
| WO2002021919A1 (en) * | 2000-09-18 | 2002-03-21 | Bayer Cropscience S.A. | New herbicidial compositions |
| WO2002089582A1 (de) * | 2001-04-21 | 2002-11-14 | Bayer Cropscience Gmbh | Benzoylcyclohexandione enthaltende synergistische herbizide für den einsatz in reis-kulturen |
| WO2002085118A3 (de) * | 2001-04-21 | 2003-02-20 | Bayer Cropscience Gmbh | Synergistische benzoylcyclohexandione enthaltende herbizide fur den einsatz in reis-kulturen |
| WO2003047340A3 (de) * | 2001-12-07 | 2004-06-24 | Bayer Cropscience Gmbh | Synergistische herbizide mittel |
| US6878675B2 (en) | 2000-09-18 | 2005-04-12 | Bayer Cropscience S.A. | Herbicidal compositions |
| US6887829B2 (en) | 2000-09-18 | 2005-05-03 | Bayer Cropscience S.A. | Herbicidal compositions |
| WO2008155027A3 (de) * | 2007-06-19 | 2009-10-22 | Bayer Cropscience Ag | Synergistische kulturpflanzenverträgliche kombinationen enthaltend herbizide aus der gruppe der benzoylcyclohexandione für den einsatz in reis-kulturen |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1827106A2 (en) * | 2004-12-17 | 2007-09-05 | Syngeta Participations AG | Herbicidal compositions comprising prosulfocars |
| TWI334123B (en) | 2007-02-26 | 2010-12-01 | Au Optronics Corp | Lightting apparatus with current feedback |
| EP2532233A1 (en) * | 2011-06-07 | 2012-12-12 | Bayer CropScience AG | Active compound combinations |
| TWI574622B (zh) * | 2012-05-22 | 2017-03-21 | Ishihara Sangyo Kaisha | Herbicidal composition |
-
1992
- 1992-05-21 DE DE4216880A patent/DE4216880A1/de not_active Withdrawn
-
1993
- 1993-05-19 IT IT93MI001025A patent/IT1265082B1/it active IP Right Grant
- 1993-05-20 KR KR1019930008678A patent/KR940005220A/ko not_active Ceased
- 1993-05-20 CN CN 93105937 patent/CN1078852A/zh active Pending
- 1993-05-20 JP JP5118316A patent/JPH06128106A/ja not_active Withdrawn
- 1993-07-02 TW TW082105277A patent/TW278026B/zh active
Cited By (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2720600A1 (fr) * | 1994-06-03 | 1995-12-08 | Basf Ag | Agents herbicides contenant de la 3-(2-chlorophénylméthyll)-1-(1-méthyl-1-phényléthyl)- et/ou 1-(1-méthyl-1-phényléthyl)-3-(4-tolyl)-urée, ainsi qu'au moins un éther-oxime de cyclohexénone. |
| WO1997003562A1 (en) * | 1995-07-19 | 1997-02-06 | Zeneca Limited | Synergistic herbicidal composition and method of use thereof |
| US5741756A (en) * | 1995-07-19 | 1998-04-21 | Zeneca Limited | Synergistic herbicidal composition comprising triketones and chloroacetanilides, and method of use thereof |
| AU702902B2 (en) * | 1995-07-19 | 1999-03-11 | Syngenta Limited | Synergistic herbicidal composition and method of use thereof |
| CN1073798C (zh) * | 1995-07-19 | 2001-10-31 | 泽尼卡有限公司 | 除草组合物及其控制杂草的方法 |
| WO1997048276A1 (en) * | 1996-06-21 | 1997-12-24 | E.I. Du Pont De Nemours And Company | Herbicidal mixtures |
| US6046134A (en) * | 1996-06-21 | 2000-04-04 | E. I. Du Pont De Nemours And Company | Herbicidal mixtures |
| WO2000003592A3 (de) * | 1998-07-16 | 2000-11-09 | Aventis Cropscience Gnbh | Herbizide mittel mit substituierten phenoxysulfonylharnstoffen |
| WO2001017350A1 (en) * | 1999-09-08 | 2001-03-15 | Aventis Cropscience Uk Limited | New herbicidal compositions |
| US6878675B2 (en) | 2000-09-18 | 2005-04-12 | Bayer Cropscience S.A. | Herbicidal compositions |
| US6835694B2 (en) | 2000-09-18 | 2004-12-28 | Bayer Cropscience S.A. | Herbicidal compositions |
| WO2002021919A1 (en) * | 2000-09-18 | 2002-03-21 | Bayer Cropscience S.A. | New herbicidial compositions |
| US6887829B2 (en) | 2000-09-18 | 2005-05-03 | Bayer Cropscience S.A. | Herbicidal compositions |
| AU2002213920B2 (en) * | 2000-09-18 | 2006-12-21 | Bayer Cropscience S.A. | New herbicidial compositions |
| CN100360017C (zh) * | 2001-04-21 | 2008-01-09 | 拜尔作物科学有限公司 | 用于稻米作物的包含苯酰环己烷二酮类的协同性除草组合物 |
| WO2002085118A3 (de) * | 2001-04-21 | 2003-02-20 | Bayer Cropscience Gmbh | Synergistische benzoylcyclohexandione enthaltende herbizide fur den einsatz in reis-kulturen |
| KR100827155B1 (ko) * | 2001-04-21 | 2008-05-02 | 바이엘 크롭사이언스 게엠베하 | 쌀 경작에 살포하기 위한 벤조일사이클로헥산디온을포함하는 상승효과적 제초제 |
| US6809064B2 (en) | 2001-04-21 | 2004-10-26 | Aventis Cropscience Gmbh | Synergistic herbicidal compositions comprising herbicides from the benzoylcyclohexanedione group for use in rice crops |
| US6844294B2 (en) | 2001-04-21 | 2005-01-18 | Aventis Cropscience Gmbh | Synergistic herbicidal compositions comprising herbicides from the benzoylcyclohexanedione group for use in rice crops |
| KR100827154B1 (ko) * | 2001-04-21 | 2008-05-02 | 바이엘 크롭사이언스 게엠베하 | 쌀 경작에 살포하기 위한 벤조일사이클로헥산디온을포함하는 상승효과적 제초제 |
| WO2002089582A1 (de) * | 2001-04-21 | 2002-11-14 | Bayer Cropscience Gmbh | Benzoylcyclohexandione enthaltende synergistische herbizide für den einsatz in reis-kulturen |
| EA008437B1 (ru) * | 2001-12-07 | 2007-06-29 | Байер Кропсайенс Гмбх | Синергические гербицидные средства |
| US6919299B2 (en) | 2001-12-07 | 2005-07-19 | Bayer Cropscience Gmbh | Synergistic herbicidal compositions |
| WO2003047340A3 (de) * | 2001-12-07 | 2004-06-24 | Bayer Cropscience Gmbh | Synergistische herbizide mittel |
| EA013073B1 (ru) * | 2001-12-07 | 2010-02-26 | Байер Кропсайенс Аг | Гербицидное средство, способ борьбы с нежелательным ростом растений и применение |
| EP2140762A3 (de) * | 2001-12-07 | 2010-04-07 | Bayer CropScience AG | Synergische herbizide Mittel |
| EP2140761A3 (de) * | 2001-12-07 | 2010-07-21 | Bayer CropScience Aktiengesellschaft | Synergische herbizide Mittel |
| EA016146B1 (ru) * | 2001-12-07 | 2012-02-28 | Байер Кропсайенс Аг | Гербицидное средство, способ борьбы с нежелательным ростом растений и применение |
| WO2008155027A3 (de) * | 2007-06-19 | 2009-10-22 | Bayer Cropscience Ag | Synergistische kulturpflanzenverträgliche kombinationen enthaltend herbizide aus der gruppe der benzoylcyclohexandione für den einsatz in reis-kulturen |
| EP2232993A1 (de) * | 2007-06-19 | 2010-09-29 | Bayer CropScience AG | Synergistische kulturpflanzenverträgliche Kombination enthaltend Tembotrione, Sulcotrione und Isoxadifen-Ethyl für den Einsatz in Reis-Kulturen |
| EP2232992A1 (de) * | 2007-06-19 | 2010-09-29 | Bayer CropScience AG | Synergistische kulturpflanzenverträgliche herbizide Kombinationen enthaltend Tembotrione und Pyrazolynate für den Einsatz in Reis-Kulturen |
| US8673814B2 (en) | 2007-06-19 | 2014-03-18 | Bayer Cropscience Ag | Synergistic combinations which are compatible with cultivated plants and which comprise herbicides selected from the group consisting of benzoylcyclohexanediones for use in rice crops |
Also Published As
| Publication number | Publication date |
|---|---|
| IT1265082B1 (it) | 1996-10-30 |
| ITMI931025A0 (it) | 1993-05-19 |
| TW278026B (enrdf_load_stackoverflow) | 1996-06-11 |
| ITMI931025A1 (it) | 1994-11-19 |
| JPH06128106A (ja) | 1994-05-10 |
| CN1078852A (zh) | 1993-12-01 |
| KR940005220A (ko) | 1994-03-21 |
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