CH394705A - Verfahren und Mittel zur Hemmung des Pflanzenwachstums - Google Patents
Verfahren und Mittel zur Hemmung des PflanzenwachstumsInfo
- Publication number
- CH394705A CH394705A CH6581258A CH6581258A CH394705A CH 394705 A CH394705 A CH 394705A CH 6581258 A CH6581258 A CH 6581258A CH 6581258 A CH6581258 A CH 6581258A CH 394705 A CH394705 A CH 394705A
- Authority
- CH
- Switzerland
- Prior art keywords
- triazine
- formula
- ethylamino
- radicals
- bis
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 9
- 230000008635 plant growth Effects 0.000 title claims description 8
- 230000002401 inhibitory effect Effects 0.000 title claims description 5
- 241000196324 Embryophyta Species 0.000 claims description 9
- 239000004480 active ingredient Substances 0.000 claims description 8
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 3
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 3
- 229910052794 bromium Inorganic materials 0.000 claims description 3
- 239000000460 chlorine Substances 0.000 claims description 3
- 229910052801 chlorine Inorganic materials 0.000 claims description 3
- 230000002363 herbicidal effect Effects 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 150000003918 triazines Chemical class 0.000 claims description 3
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical group [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 2
- 125000001589 carboacyl group Chemical group 0.000 claims description 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 2
- 229910052731 fluorine Chemical group 0.000 claims description 2
- 239000011737 fluorine Chemical group 0.000 claims description 2
- 229910052740 iodine Inorganic materials 0.000 claims description 2
- 239000011630 iodine Chemical group 0.000 claims description 2
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 claims 1
- -1 alkoxyalkyl radicals Chemical class 0.000 description 24
- 150000001875 compounds Chemical class 0.000 description 18
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 239000002253 acid Substances 0.000 description 5
- 150000007513 acids Chemical class 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- 238000009835 boiling Methods 0.000 description 4
- 235000014113 dietary fatty acids Nutrition 0.000 description 4
- 239000003995 emulsifying agent Substances 0.000 description 4
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- 229930195729 fatty acid Natural products 0.000 description 4
- 150000004665 fatty acids Chemical class 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 239000000080 wetting agent Substances 0.000 description 4
- DKZUHLAOOSCGSG-UHFFFAOYSA-N 4-N-ethyl-2-N-propan-2-yl-6-(trifluoromethyl)-1,3,5-triazine-2,4-diamine Chemical compound FC(C1=NC(=NC(=N1)NCC)NC(C)C)(F)F DKZUHLAOOSCGSG-UHFFFAOYSA-N 0.000 description 3
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
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- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 229910000019 calcium carbonate Inorganic materials 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 238000000354 decomposition reaction Methods 0.000 description 3
- 239000002270 dispersing agent Substances 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 239000008096 xylene Substances 0.000 description 3
- QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 2
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 2
- VLKWQQFBFMQSNA-UHFFFAOYSA-N 2-n,4-n-diethyl-6-(trifluoromethyl)-1,3,5-triazine-2,4-diamine Chemical compound CCNC1=NC(NCC)=NC(C(F)(F)F)=N1 VLKWQQFBFMQSNA-UHFFFAOYSA-N 0.000 description 2
- JBVPWMRUTFJUOG-UHFFFAOYSA-N 4-n-methyl-2-n-propan-2-yl-6-(trichloromethyl)-1,3,5-triazine-2,4-diamine Chemical compound CNC1=NC(NC(C)C)=NC(C(Cl)(Cl)Cl)=N1 JBVPWMRUTFJUOG-UHFFFAOYSA-N 0.000 description 2
- GXHIQVOEQSMHPL-UHFFFAOYSA-N 6-(chloromethyl)-4-N-ethyl-2-N-propan-2-yl-1,3,5-triazine-2,4-diamine Chemical compound ClCC1=NC(=NC(=N1)NCC)NC(C)C GXHIQVOEQSMHPL-UHFFFAOYSA-N 0.000 description 2
- QHFYHZBGKSVKIC-UHFFFAOYSA-N 6-(trichloromethyl)-1,3,5-triazine-2,4-diamine Chemical class NC1=NC(N)=NC(C(Cl)(Cl)Cl)=N1 QHFYHZBGKSVKIC-UHFFFAOYSA-N 0.000 description 2
- 239000005995 Aluminium silicate Substances 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical group ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- 239000005909 Kieselgur Substances 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000013543 active substance Substances 0.000 description 2
- 125000003342 alkenyl group Chemical group 0.000 description 2
- 235000012211 aluminium silicate Nutrition 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 239000000440 bentonite Substances 0.000 description 2
- 229910000278 bentonite Inorganic materials 0.000 description 2
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 239000012876 carrier material Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000011280 coal tar Substances 0.000 description 2
- 239000000084 colloidal system Substances 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 230000035613 defoliation Effects 0.000 description 2
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000003337 fertilizer Substances 0.000 description 2
- 235000013312 flour Nutrition 0.000 description 2
- 150000004820 halides Chemical class 0.000 description 2
- 125000002768 hydroxyalkyl group Chemical group 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
- 239000000463 material Substances 0.000 description 2
- 239000002480 mineral oil Substances 0.000 description 2
- 235000010446 mineral oil Nutrition 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 230000002028 premature Effects 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
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- 150000003254 radicals Chemical class 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
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- 239000000243 solution Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- 235000013311 vegetables Nutrition 0.000 description 2
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- DXUMYHZTYVPBEZ-UHFFFAOYSA-N 2,4,6-tris(trichloromethyl)-1,3,5-triazine Chemical compound ClC(Cl)(Cl)C1=NC(C(Cl)(Cl)Cl)=NC(C(Cl)(Cl)Cl)=N1 DXUMYHZTYVPBEZ-UHFFFAOYSA-N 0.000 description 1
- DGRMQIQMEUHSSW-UHFFFAOYSA-N 2-n,4-n-diethyl-6-(iodomethyl)-1,3,5-triazine-2,4-diamine Chemical compound CCNC1=NC(CI)=NC(NCC)=N1 DGRMQIQMEUHSSW-UHFFFAOYSA-N 0.000 description 1
- LWVNTGBZUZCBDW-UHFFFAOYSA-N 2-n,4-n-diethyl-6-(trichloromethyl)-1,3,5-triazine-2,4-diamine Chemical compound CCNC1=NC(NCC)=NC(C(Cl)(Cl)Cl)=N1 LWVNTGBZUZCBDW-UHFFFAOYSA-N 0.000 description 1
- ZWZJYBCZPFBUBN-UHFFFAOYSA-N 2-n,4-n-dimethyl-6-(tribromomethyl)-1,3,5-triazine-2,4-diamine Chemical compound CNC1=NC(NC)=NC(C(Br)(Br)Br)=N1 ZWZJYBCZPFBUBN-UHFFFAOYSA-N 0.000 description 1
- GGUXAVZFRSXFAY-UHFFFAOYSA-N 2-n,4-n-dimethyl-6-(trichloromethyl)-1,3,5-triazine-2,4-diamine Chemical compound CNC1=NC(NC)=NC(C(Cl)(Cl)Cl)=N1 GGUXAVZFRSXFAY-UHFFFAOYSA-N 0.000 description 1
- KJRQBRZSEZYRES-UHFFFAOYSA-N 2-n-ethyl-4-n-methyl-6-(trichloromethyl)-1,3,5-triazine-2,4-diamine Chemical compound CCNC1=NC(NC)=NC(C(Cl)(Cl)Cl)=N1 KJRQBRZSEZYRES-UHFFFAOYSA-N 0.000 description 1
- XOFYPUQJNDXJRM-UHFFFAOYSA-N 2-n-methyl-6-(trichloromethyl)-1,3,5-triazine-2,4-diamine Chemical compound CNC1=NC(N)=NC(C(Cl)(Cl)Cl)=N1 XOFYPUQJNDXJRM-UHFFFAOYSA-N 0.000 description 1
- XBDKAPXKOWSTCE-UHFFFAOYSA-N 6-(bromomethyl)-2-n,4-n-diethyl-1,3,5-triazine-2,4-diamine Chemical compound CCNC1=NC(CBr)=NC(NCC)=N1 XBDKAPXKOWSTCE-UHFFFAOYSA-N 0.000 description 1
- PEHJTVMOGGJPJM-UHFFFAOYSA-N 6-(chloromethyl)-1,3,5-triazine-2,4-diamine Chemical compound NC1=NC(N)=NC(CCl)=N1 PEHJTVMOGGJPJM-UHFFFAOYSA-N 0.000 description 1
- NAJOROZGNBNLLE-UHFFFAOYSA-N 6-(chloromethyl)-2-n,4-n-diethyl-1,3,5-triazine-2,4-diamine Chemical compound CCNC1=NC(CCl)=NC(NCC)=N1 NAJOROZGNBNLLE-UHFFFAOYSA-N 0.000 description 1
- QRYHWLNLXDLOBD-UHFFFAOYSA-N 6-(dibromomethyl)-1,3,5-triazine-2,4-diamine Chemical compound NC1=NC(N)=NC(C(Br)Br)=N1 QRYHWLNLXDLOBD-UHFFFAOYSA-N 0.000 description 1
- SPGKMPBOEWUUGR-UHFFFAOYSA-N 6-(dibromomethyl)-2-n,4-n-diethyl-1,3,5-triazine-2,4-diamine Chemical compound CCNC1=NC(NCC)=NC(C(Br)Br)=N1 SPGKMPBOEWUUGR-UHFFFAOYSA-N 0.000 description 1
- LCZNOQVPVRCZNN-UHFFFAOYSA-N 6-(dichloromethyl)-2-N-ethyl-4-N-methyl-1,3,5-triazine-2,4-diamine Chemical compound ClC(C1=NC(=NC(=N1)NC)NCC)Cl LCZNOQVPVRCZNN-UHFFFAOYSA-N 0.000 description 1
- DCQIZFJBLQBGES-UHFFFAOYSA-N 6-(dichloromethyl)-2-n,4-n-diethyl-1,3,5-triazine-2,4-diamine Chemical compound CCNC1=NC(NCC)=NC(C(Cl)Cl)=N1 DCQIZFJBLQBGES-UHFFFAOYSA-N 0.000 description 1
- GZLXOPSVKQQRHE-UHFFFAOYSA-N 6-(dichloromethyl)-4-N-ethyl-2-N-propan-2-yl-1,3,5-triazine-2,4-diamine Chemical compound ClC(C1=NC(=NC(=N1)NCC)NC(C)C)Cl GZLXOPSVKQQRHE-UHFFFAOYSA-N 0.000 description 1
- VJDJBZVESKUFKB-UHFFFAOYSA-N 6-(tribromomethyl)-1,3,5-triazine-2,4-diamine Chemical compound NC1=NC(N)=NC(C(Br)(Br)Br)=N1 VJDJBZVESKUFKB-UHFFFAOYSA-N 0.000 description 1
- 229940123208 Biguanide Drugs 0.000 description 1
- HMCXJXSTEIZDRQ-UHFFFAOYSA-N BrCC1=NC(=NC(=N1)NC)NCC Chemical compound BrCC1=NC(=NC(=N1)NC)NCC HMCXJXSTEIZDRQ-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- IGHIKGFQOQBXCW-UHFFFAOYSA-N ClCC1=NC(=NC(=N1)NC)NCC Chemical compound ClCC1=NC(=NC(=N1)NC)NCC IGHIKGFQOQBXCW-UHFFFAOYSA-N 0.000 description 1
- QVMGSYSVECYOLO-UHFFFAOYSA-N ClCC1=NC(=NC(=N1)NCC)N(CC)CC Chemical compound ClCC1=NC(=NC(=N1)NCC)N(CC)CC QVMGSYSVECYOLO-UHFFFAOYSA-N 0.000 description 1
- NYOJVFUNGHNNFN-UHFFFAOYSA-N FC(C1=NC(=NC(=N1)NCC)N(CC)CC)(F)F Chemical compound FC(C1=NC(=NC(=N1)NCC)N(CC)CC)(F)F NYOJVFUNGHNNFN-UHFFFAOYSA-N 0.000 description 1
- 240000002024 Gossypium herbaceum Species 0.000 description 1
- 235000004341 Gossypium herbaceum Nutrition 0.000 description 1
- 239000012359 Methanesulfonyl chloride Substances 0.000 description 1
- 244000061456 Solanum tuberosum Species 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 239000010775 animal oil Substances 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 235000012216 bentonite Nutrition 0.000 description 1
- 150000004283 biguanides Chemical class 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 235000010338 boric acid Nutrition 0.000 description 1
- YHASWHZGWUONAO-UHFFFAOYSA-N butanoyl butanoate Chemical compound CCCC(=O)OC(=O)CCC YHASWHZGWUONAO-UHFFFAOYSA-N 0.000 description 1
- DVECBJCOGJRVPX-UHFFFAOYSA-N butyryl chloride Chemical compound CCCC(Cl)=O DVECBJCOGJRVPX-UHFFFAOYSA-N 0.000 description 1
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- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 125000004965 chloroalkyl group Chemical group 0.000 description 1
- KQDDQXNVESLJNO-UHFFFAOYSA-N chloromethanesulfonyl chloride Chemical compound ClCS(Cl)(=O)=O KQDDQXNVESLJNO-UHFFFAOYSA-N 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 239000007799 cork Substances 0.000 description 1
- 244000038559 crop plants Species 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
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- 238000004090 dissolution Methods 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 230000005094 fruit set Effects 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 230000009036 growth inhibition Effects 0.000 description 1
- 125000001188 haloalkyl group Chemical group 0.000 description 1
- 238000003306 harvesting Methods 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- LSACYLWPPQLVSM-UHFFFAOYSA-N isobutyric acid anhydride Chemical compound CC(C)C(=O)OC(=O)C(C)C LSACYLWPPQLVSM-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- QARBMVPHQWIHKH-UHFFFAOYSA-N methanesulfonyl chloride Chemical compound CS(Cl)(=O)=O QARBMVPHQWIHKH-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- UONHNINKEKFQGS-UHFFFAOYSA-N n-[4-[acetyl(ethyl)amino]-6-(trichloromethyl)-1,3,5-triazin-2-yl]-n-ethylacetamide Chemical compound CCN(C(C)=O)C1=NC(N(CC)C(C)=O)=NC(C(Cl)(Cl)Cl)=N1 UONHNINKEKFQGS-UHFFFAOYSA-N 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 231100000208 phytotoxic Toxicity 0.000 description 1
- 230000000885 phytotoxic effect Effects 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 230000005070 ripening Effects 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 150000003470 sulfuric acid monoesters Chemical class 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 229940078499 tricalcium phosphate Drugs 0.000 description 1
- 229910000391 tricalcium phosphate Inorganic materials 0.000 description 1
- 235000019731 tricalcium phosphate Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/66—1,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms
- A01N43/68—1,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms with two or three nitrogen atoms directly attached to ring carbon atoms
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)
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH6581258A CH394705A (de) | 1958-11-05 | 1958-11-05 | Verfahren und Mittel zur Hemmung des Pflanzenwachstums |
| NL244879A NL127553C (fr) | 1958-11-05 | 1959-10-30 | |
| BE593864A BE593864Q (fr) | 1958-11-05 | 1960-08-08 | Agents herbicides à base de derivés triaziniques. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH6581258A CH394705A (de) | 1958-11-05 | 1958-11-05 | Verfahren und Mittel zur Hemmung des Pflanzenwachstums |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH394705A true CH394705A (de) | 1965-06-30 |
Family
ID=4526659
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH6581258A CH394705A (de) | 1958-11-05 | 1958-11-05 | Verfahren und Mittel zur Hemmung des Pflanzenwachstums |
Country Status (3)
| Country | Link |
|---|---|
| BE (1) | BE593864Q (fr) |
| CH (1) | CH394705A (fr) |
| NL (1) | NL127553C (fr) |
-
1958
- 1958-11-05 CH CH6581258A patent/CH394705A/de unknown
-
1959
- 1959-10-30 NL NL244879A patent/NL127553C/xx active
-
1960
- 1960-08-08 BE BE593864A patent/BE593864Q/fr active
Also Published As
| Publication number | Publication date |
|---|---|
| NL127553C (fr) | 1969-10-17 |
| BE593864Q (fr) | 1960-12-01 |
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