NL8301883A - Middel voor het ontbladeren van planten met synergistische activiteit. - Google Patents
Middel voor het ontbladeren van planten met synergistische activiteit. Download PDFInfo
- Publication number
- NL8301883A NL8301883A NL8301883A NL8301883A NL8301883A NL 8301883 A NL8301883 A NL 8301883A NL 8301883 A NL8301883 A NL 8301883A NL 8301883 A NL8301883 A NL 8301883A NL 8301883 A NL8301883 A NL 8301883A
- Authority
- NL
- Netherlands
- Prior art keywords
- urea
- methyl
- hydrogen
- alkyl
- phenyl
- Prior art date
Links
- 230000002195 synergetic effect Effects 0.000 title claims description 11
- 239000003795 chemical substances by application Substances 0.000 claims description 31
- -1 methyl mercapto Chemical class 0.000 claims description 26
- 239000001257 hydrogen Substances 0.000 claims description 20
- 229910052739 hydrogen Inorganic materials 0.000 claims description 20
- 240000002024 Gossypium herbaceum Species 0.000 claims description 19
- 235000004341 Gossypium herbaceum Nutrition 0.000 claims description 19
- 241000196324 Embryophyta Species 0.000 claims description 16
- 150000002431 hydrogen Chemical class 0.000 claims description 13
- 229910052717 sulfur Inorganic materials 0.000 claims description 13
- 239000004202 carbamide Substances 0.000 claims description 10
- 150000001875 compounds Chemical class 0.000 claims description 8
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
- HFCYZXMHUIHAQI-UHFFFAOYSA-N Thidiazuron Chemical compound C=1C=CC=CC=1NC(=O)NC1=CN=NS1 HFCYZXMHUIHAQI-UHFFFAOYSA-N 0.000 claims description 6
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 6
- 229910052760 oxygen Inorganic materials 0.000 claims description 6
- 239000001301 oxygen Substances 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 4
- 125000003545 alkoxy group Chemical group 0.000 claims description 4
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 4
- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 4
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 4
- 125000002112 pyrrolidino group Chemical group [*]N1C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims description 4
- 125000004434 sulfur atom Chemical group 0.000 claims description 4
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 4
- FXFCLNJIQWLFEL-UHFFFAOYSA-N 1-(3,4-dichlorophenyl)-1,3-dimethylurea Chemical compound CNC(=O)N(C)C1=CC=C(Cl)C(Cl)=C1 FXFCLNJIQWLFEL-UHFFFAOYSA-N 0.000 claims description 3
- VJXKPMICAFCWKC-UHFFFAOYSA-N 1-pyridin-2-yl-3-(thiadiazol-5-yl)urea Chemical compound C=1C=CC=NC=1NC(=O)NC1=CN=NS1 VJXKPMICAFCWKC-UHFFFAOYSA-N 0.000 claims description 3
- BZSXEZOLBIJVQK-UHFFFAOYSA-N 2-methylsulfonylbenzoic acid Chemical compound CS(=O)(=O)C1=CC=CC=C1C(O)=O BZSXEZOLBIJVQK-UHFFFAOYSA-N 0.000 claims description 3
- CCGPUGMWYLICGL-UHFFFAOYSA-N Neburon Chemical compound CCCCN(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 CCGPUGMWYLICGL-UHFFFAOYSA-N 0.000 claims description 3
- 125000004414 alkyl thio group Chemical group 0.000 claims description 3
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 3
- DSRNRYQBBJQVCW-UHFFFAOYSA-N metoxuron Chemical compound COC1=CC=C(NC(=O)N(C)C)C=C1Cl DSRNRYQBBJQVCW-UHFFFAOYSA-N 0.000 claims description 3
- WYXYBEOWQBGFQB-UHFFFAOYSA-N n-benzyl-7h-purin-2-amine Chemical class N=1C=C2NC=NC2=NC=1NCC1=CC=CC=C1 WYXYBEOWQBGFQB-UHFFFAOYSA-N 0.000 claims description 3
- HQYZTGGAEAFKIO-UHFFFAOYSA-N thiadiazol-5-ylurea Chemical class NC(=O)NC1=CN=NS1 HQYZTGGAEAFKIO-UHFFFAOYSA-N 0.000 claims description 3
- RPOZCTAHYSTBLD-UHFFFAOYSA-N 1-(2-methylphenyl)-3-(thiadiazol-5-yl)urea Chemical compound CC1=CC=CC=C1NC(=O)NC1=CN=NS1 RPOZCTAHYSTBLD-UHFFFAOYSA-N 0.000 claims description 2
- XKJMBINCVNINCA-UHFFFAOYSA-N Alfalone Chemical compound CON(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 XKJMBINCVNINCA-UHFFFAOYSA-N 0.000 claims description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
- 229910052794 bromium Inorganic materials 0.000 claims description 2
- 239000000460 chlorine Substances 0.000 claims description 2
- 229910052801 chlorine Inorganic materials 0.000 claims description 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 2
- AVKNGPAMCBSNSO-UHFFFAOYSA-N cyclohexylmethanamine Chemical compound NCC1CCCCC1 AVKNGPAMCBSNSO-UHFFFAOYSA-N 0.000 claims description 2
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 2
- XXOYNJXVWVNOOJ-UHFFFAOYSA-N fenuron Chemical compound CN(C)C(=O)NC1=CC=CC=C1 XXOYNJXVWVNOOJ-UHFFFAOYSA-N 0.000 claims description 2
- 229910052731 fluorine Inorganic materials 0.000 claims description 2
- 239000011737 fluorine Substances 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical class 0.000 claims description 2
- 125000005059 halophenyl group Chemical group 0.000 claims description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 2
- 125000006501 nitrophenyl group Chemical group 0.000 claims description 2
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 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
- 125000004076 pyridyl group Chemical group 0.000 claims description 2
- 239000011593 sulfur Substances 0.000 claims description 2
- BXCZJWHJYRELHY-UHFFFAOYSA-N thiadiazole-5-carboxylic acid Chemical class OC(=O)C1=CN=NS1 BXCZJWHJYRELHY-UHFFFAOYSA-N 0.000 claims description 2
- 125000003944 tolyl group Chemical group 0.000 claims description 2
- LOGWLCBCJBAONF-UHFFFAOYSA-N 1-(4-chlorophenyl)-1-methoxy-3-methylurea Chemical compound ClC1=CC=C(C=C1)N(C(=O)NC)OC LOGWLCBCJBAONF-UHFFFAOYSA-N 0.000 claims 1
- NHHQOYLPBUYHQU-UHFFFAOYSA-N 4-methylthiadiazole-5-carboxylic acid Chemical compound CC=1N=NSC=1C(O)=O NHHQOYLPBUYHQU-UHFFFAOYSA-N 0.000 claims 1
- UWOIIDFGNOJECK-UHFFFAOYSA-N BrC1=CC=C(C=C1)N(C(=O)NOC)C Chemical compound BrC1=CC=C(C=C1)N(C(=O)NOC)C UWOIIDFGNOJECK-UHFFFAOYSA-N 0.000 claims 1
- 239000000203 mixture Substances 0.000 description 21
- 230000035613 defoliation Effects 0.000 description 20
- 230000000694 effects Effects 0.000 description 12
- 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 description 11
- 239000013543 active substance Substances 0.000 description 7
- 125000004189 3,4-dichlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(Cl)C([H])=C1* 0.000 description 6
- KDCGOANMDULRCW-UHFFFAOYSA-N 7H-purine Chemical compound N1=CNC2=NC=NC2=C1 KDCGOANMDULRCW-UHFFFAOYSA-N 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 6
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 239000002837 defoliant Substances 0.000 description 4
- BMLIZLVNXIYGCK-UHFFFAOYSA-N monuron Chemical compound CN(C)C(=O)NC1=CC=C(Cl)C=C1 BMLIZLVNXIYGCK-UHFFFAOYSA-N 0.000 description 4
- LUBJCRLGQSPQNN-UHFFFAOYSA-N 1-Phenylurea Chemical compound NC(=O)NC1=CC=CC=C1 LUBJCRLGQSPQNN-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 3
- PHVNLLCAQHGNKU-UHFFFAOYSA-N Dimethipin Chemical compound CC1=C(C)S(=O)(=O)CCS1(=O)=O PHVNLLCAQHGNKU-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 241001300479 Macroptilium Species 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
- 159000000007 calcium salts Chemical class 0.000 description 3
- 239000000969 carrier Substances 0.000 description 3
- 229920005610 lignin Polymers 0.000 description 3
- 210000002741 palatine tonsil Anatomy 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- 125000004861 4-isopropyl phenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- 239000005995 Aluminium silicate Substances 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- MGJKQDOBUOMPEZ-UHFFFAOYSA-N N,N'-dimethylurea Chemical compound CNC(=O)NC MGJKQDOBUOMPEZ-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 235000012211 aluminium silicate Nutrition 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000007859 condensation product Substances 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 239000003906 humectant Substances 0.000 description 2
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 238000000034 method Methods 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- MVNXOMHBQUTVKY-UHFFFAOYSA-N 1-(3-chloro-4-fluorophenyl)-3-cyclopropylurea Chemical compound C1=C(Cl)C(F)=CC=C1NC(=O)NC1CC1 MVNXOMHBQUTVKY-UHFFFAOYSA-N 0.000 description 1
- KSOMURNRMIMLCA-UHFFFAOYSA-N 1-(4-bromophenyl)-1-methoxy-3-methylurea Chemical compound CNC(=O)N(OC)C1=CC=C(Br)C=C1 KSOMURNRMIMLCA-UHFFFAOYSA-N 0.000 description 1
- GAVZUXBKQVMADB-UHFFFAOYSA-N 1-cyclopropyl-3-phenylurea Chemical compound C=1C=CC=CC=1NC(=O)NC1CC1 GAVZUXBKQVMADB-UHFFFAOYSA-N 0.000 description 1
- OBGFMRSXJROQDT-UHFFFAOYSA-N 1-methoxy-1-methylurea Chemical compound CON(C)C(N)=O OBGFMRSXJROQDT-UHFFFAOYSA-N 0.000 description 1
- GIQXLBILFSQJRG-UHFFFAOYSA-N 1-methyl-1-phenyl-3-(thiadiazol-5-yl)urea Chemical compound C=1C=CC=CC=1N(C)C(=O)NC1=CN=NS1 GIQXLBILFSQJRG-UHFFFAOYSA-N 0.000 description 1
- HOUDZYFLQFMNQQ-UHFFFAOYSA-N 2-[2-[2-(2-nonoxyethoxy)ethoxy]ethoxy]ethoxybenzene Chemical compound CCCCCCCCCOCCOCCOCCOCCOC1=CC=CC=C1 HOUDZYFLQFMNQQ-UHFFFAOYSA-N 0.000 description 1
- JACPTQMMZGZAOL-KHPPLWFESA-N 2-[methyl-[(z)-octadec-9-enyl]amino]ethanesulfonic acid Chemical compound CCCCCCCC\C=C/CCCCCCCCN(C)CCS(O)(=O)=O JACPTQMMZGZAOL-KHPPLWFESA-N 0.000 description 1
- 125000004180 3-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(F)=C1[H] 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 241000219146 Gossypium Species 0.000 description 1
- 235000005206 Hibiscus Nutrition 0.000 description 1
- 235000007185 Hibiscus lunariifolius Nutrition 0.000 description 1
- 244000284380 Hibiscus rosa sinensis Species 0.000 description 1
- 235000019738 Limestone Nutrition 0.000 description 1
- WLFDQEVORAMCIM-UHFFFAOYSA-N Metobromuron Chemical compound CON(C)C(=O)NC1=CC=C(Br)C=C1 WLFDQEVORAMCIM-UHFFFAOYSA-N 0.000 description 1
- LKJPSUCKSLORMF-UHFFFAOYSA-N Monolinuron Chemical compound CON(C)C(=O)NC1=CC=C(Cl)C=C1 LKJPSUCKSLORMF-UHFFFAOYSA-N 0.000 description 1
- XGEGHDBEHXKFPX-UHFFFAOYSA-N N-methylthiourea Natural products CNC(N)=O XGEGHDBEHXKFPX-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 244000274883 Urtica dioica 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
- 230000009471 action Effects 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
- 150000003863 ammonium salts Chemical class 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
- 150000008107 benzenesulfonic acids Chemical class 0.000 description 1
- 230000004071 biological effect Effects 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
- 239000012876 carrier material Substances 0.000 description 1
- JXCGFZXSOMJFOA-UHFFFAOYSA-N chlorotoluron Chemical compound CN(C)C(=O)NC1=CC=C(C)C(Cl)=C1 JXCGFZXSOMJFOA-UHFFFAOYSA-N 0.000 description 1
- 239000008119 colloidal silica Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 238000003306 harvesting Methods 0.000 description 1
- 230000002363 herbicidal effect Effects 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- XGEGHDBEHXKFPX-NJFSPNSNSA-N methylurea Chemical compound [14CH3]NC(N)=O XGEGHDBEHXKFPX-NJFSPNSNSA-N 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 description 1
- CPPCRKJNHYHEQT-UHFFFAOYSA-N n-(cyclohexylmethyl)-4-methylthiadiazole-5-carboxamide Chemical compound N1=NSC(C(=O)NCC2CCCCC2)=C1C CPPCRKJNHYHEQT-UHFFFAOYSA-N 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- 125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 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
- 239000000575 pesticide Substances 0.000 description 1
- 125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000035945 sensitivity 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
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 230000007480 spreading Effects 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000000080 wetting agent 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/36—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< directly attached to at least one heterocyclic ring; Thio analogues thereof
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/30—Derivatives containing the group >N—CO—N aryl or >N—CS—N—aryl
-
- 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
- A01N57/12—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing acyclic or cycloaliphatic radicals
-
- 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
- A01N59/00—Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds
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)
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE3222622 | 1982-06-11 | ||
| DE19823222622 DE3222622A1 (de) | 1982-06-11 | 1982-06-11 | Mittel zur entblaetterung von pflanzen mit synergistischer wirkung |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NL8301883A true NL8301883A (nl) | 1984-01-02 |
Family
ID=6166199
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NL8301883A NL8301883A (nl) | 1982-06-11 | 1983-05-26 | Middel voor het ontbladeren van planten met synergistische activiteit. |
Country Status (20)
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4846872A (en) * | 1986-08-11 | 1989-07-11 | Fujisawa Pharmaceutical Co., Ltd. | Herbicide |
| IL84804A0 (en) * | 1986-12-18 | 1988-06-30 | Schering Ag | Plant defoliant compositions containing thiadiazole urea derivative and azacylcloheptane derivative and process for the preparation thereof |
| IL84803A (en) * | 1986-12-18 | 1991-01-31 | Schering Ag | Plant defoliant compositions containing thiadiazole urea derivative,a carboxamide or tributyl phosphate and halophenyl dialkyl urea derivative and process for the preparation thereof |
| DE3919037A1 (de) * | 1989-06-10 | 1990-12-13 | Hoechst Ag | Fluessige herbizide mischformulierungen |
| US5238905A (en) * | 1991-10-28 | 1993-08-24 | Union Oil Company Of California | Plant control composition and methods of use with thidiazuron and monocarbamide dihydrogen sulfate |
| DE19911165B4 (de) * | 1999-03-12 | 2008-03-13 | Bayer Cropscience Ag | Entlaubungsmittel |
| AR022889A1 (es) | 1999-03-12 | 2002-09-04 | Bayer Cropscience Ag | Agente desfoliante |
| US6562758B1 (en) * | 1999-12-15 | 2003-05-13 | Basf Corporation | Methods and compositions to defoliate crop plants and minimize plant regrowth following defoliation |
| US20070203025A1 (en) * | 2006-02-24 | 2007-08-30 | Udo Bickers | Defoliant |
| DE102006009101A1 (de) * | 2006-02-24 | 2007-09-06 | Bayer Cropscience Gmbh | Defoliant |
| EP1985180A1 (de) * | 2007-04-25 | 2008-10-29 | Bayer CropScience AG | Defoliant |
| EP2238835B1 (de) | 2009-04-07 | 2016-04-06 | Bayer Intellectual Property GmbH | Defoliant auf Basis von Thidiazuron und Flufenacet |
| EP2238834A1 (de) * | 2009-04-07 | 2010-10-13 | Bayer CropScience Aktiengesellschaft | Defoliant auf Basis von Thidiazuron und 1,2,4-Triazinonen |
| MX362986B (es) * | 2012-05-25 | 2019-02-28 | Lanxess Distrib Gmbh | Agentes de aclareo que contienen diuron. |
| CN106070279A (zh) * | 2016-06-03 | 2016-11-09 | 华南农业大学 | 一种植物生长调节剂噻苯隆·敌草隆静电液剂及其制作、用途和使用方法 |
| US12004509B2 (en) * | 2016-11-18 | 2024-06-11 | Indorama Ventures Oxides Australia Pty Limited | Co-formulation comprising a plant growth regulator and an oil, and methods of preparing and using said co-formulation |
| EP3709811A4 (en) | 2017-11-17 | 2021-08-18 | UPL Ltd | NEW DEFOLIANT COMBINATIONS |
| CN112640910B (zh) * | 2020-12-22 | 2022-03-15 | 中国农业科学院棉花研究所 | 一种含噻苯隆和利谷隆的脱叶催熟组合物 |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE548038A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1955-05-23 | |||
| US2954467A (en) | 1958-01-30 | 1960-09-27 | Hughes Aircraft Co | Gating circuit |
| GB1088982A (en) * | 1963-04-29 | 1967-10-25 | Ici Ltd | Herbicidal compositions |
| IL36220A0 (en) * | 1970-02-27 | 1971-04-28 | Ciba Geigy Ag | Use of a phenylurea for combating weeds in wheat,oats,rye,barley,rice and cotton |
| DE2039041C2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1970-08-06 | 1991-08-01 | Hoechst Ag, 6230 Frankfurt, De | |
| SU472488A3 (ru) * | 1971-10-29 | 1975-05-30 | Лиценция Талалманиокат Эртекезито Валалат (Инопредприятие) | Дефолиант |
| FR2215898B1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1973-02-02 | 1977-04-22 | Philagro Sa | |
| DK581374A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1973-11-16 | 1975-07-21 | Ici Ltd | |
| GB1502259A (en) * | 1974-02-18 | 1978-03-01 | Ici Ltd | Herbicidal formulations |
| DE2506690A1 (de) | 1975-02-14 | 1976-09-02 | Schering Ag | Mittel zur entblaetterung von pflanzen |
| DE2619861C2 (de) | 1976-05-03 | 1985-05-09 | Schering AG, 1000 Berlin und 4709 Bergkamen | 1-(2-Pyridyl)-3-(1,2,3-thiadiazol-5-yl)-harnstoff sowie diesen enthaltende Mittel zur Wachstumsregulierung und zur Entlbätterung von Pflanzen |
| DE2646712A1 (de) | 1976-10-14 | 1978-04-20 | Schering Ag | Mittel zur pflanzenwachstumsregulierung |
| DE2745968A1 (de) | 1977-10-10 | 1979-04-19 | Schering Ag | Mittel zur entblaetterung von pflanzen |
| NL7901292A (nl) * | 1978-02-23 | 1979-08-27 | Sandoz Ag | Werkwijze voor het bereiden van een ontbladeringsprepa- raat en voor het ontbladeren van bladdragende gewassen daarmede. |
| GB2017495A (en) * | 1978-02-23 | 1979-10-10 | Sandoz Ltd | Defoliation compositions |
| GB2074448B (en) * | 1980-03-19 | 1983-06-08 | Murphy Chemical Ltd | Selective weed control and compostions therefor |
| GB2078519B (en) * | 1980-06-19 | 1983-08-03 | May & Baker Ltd | Weed control using 3-(4-isopropylphenyl)-1,1-dimethylurea in conjunction with s-2,3,3-trichloroallyl diisopropylthiocarbamate |
| CH645515A5 (de) * | 1981-02-19 | 1984-10-15 | Siegfried Ag | Mittel zum entblaettern von kulturpflanzen. |
-
1982
- 1982-06-11 DE DE19823222622 patent/DE3222622A1/de not_active Withdrawn
-
1983
- 1983-05-19 IN IN331/DEL/83A patent/IN159301B/en unknown
- 1983-05-26 NL NL8301883A patent/NL8301883A/nl not_active Application Discontinuation
- 1983-06-02 AU AU15295/83A patent/AU565869B2/en not_active Expired
- 1983-06-03 TR TR21718A patent/TR21718A/xx unknown
- 1983-06-06 GB GB08315462A patent/GB2121686B/en not_active Expired
- 1983-06-07 IT IT21487/83A patent/IT1165452B/it active
- 1983-06-08 LU LU84854A patent/LU84854A1/de unknown
- 1983-06-08 EG EG34883A patent/EG16471A/xx active
- 1983-06-08 IL IL68918A patent/IL68918A/xx not_active IP Right Cessation
- 1983-06-09 MA MA20032A patent/MA19810A1/fr unknown
- 1983-06-09 SU SU833600946A patent/SU1327781A3/ru active
- 1983-06-09 GR GR71605A patent/GR77538B/el unknown
- 1983-06-09 FR FR8309571A patent/FR2528280A1/fr not_active Withdrawn
- 1983-06-10 DK DK266883A patent/DK266883A/da not_active Application Discontinuation
- 1983-06-10 BR BR8303101A patent/BR8303101A/pt not_active IP Right Cessation
- 1983-06-10 BE BE0/210985A patent/BE897029A/fr not_active IP Right Cessation
- 1983-06-10 ZA ZA834282A patent/ZA834282B/xx unknown
- 1983-06-10 ZW ZW135/83A patent/ZW13583A1/xx unknown
- 1983-06-13 US US06/503,725 patent/US4613354A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| DE3222622A1 (de) | 1983-12-15 |
| DK266883D0 (da) | 1983-06-10 |
| BE897029A (fr) | 1983-12-12 |
| BR8303101A (pt) | 1984-01-31 |
| ZW13583A1 (en) | 1983-09-14 |
| GR77538B (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1984-09-24 |
| IN159301B (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1987-05-02 |
| SU1327781A3 (ru) | 1987-07-30 |
| IT8321487A0 (it) | 1983-06-07 |
| IT8321487A1 (it) | 1984-12-07 |
| DK266883A (da) | 1983-12-12 |
| AU565869B2 (en) | 1987-10-01 |
| EG16471A (en) | 1994-07-30 |
| GB2121686A (en) | 1984-01-04 |
| GB2121686B (en) | 1986-05-21 |
| MA19810A1 (fr) | 1983-12-31 |
| TR21718A (tr) | 1985-04-17 |
| LU84854A1 (de) | 1983-11-17 |
| ZA834282B (en) | 1984-03-28 |
| FR2528280A1 (fr) | 1983-12-16 |
| GB8315462D0 (en) | 1983-07-13 |
| AU1529583A (en) | 1984-12-13 |
| IT1165452B (it) | 1987-04-22 |
| US4613354A (en) | 1986-09-23 |
| IL68918A (en) | 1987-03-31 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A85 | Still pending on 85-01-01 | ||
| BV | The patent application has lapsed |