DD144714A5 - Herbizides gemisch - Google Patents
Herbizides gemisch Download PDFInfo
- Publication number
- DD144714A5 DD144714A5 DD79214210A DD21421079A DD144714A5 DD 144714 A5 DD144714 A5 DD 144714A5 DD 79214210 A DD79214210 A DD 79214210A DD 21421079 A DD21421079 A DD 21421079A DD 144714 A5 DD144714 A5 DD 144714A5
- Authority
- DD
- German Democratic Republic
- Prior art keywords
- carbon atoms
- glycinate
- ethyl
- trifluoroacetyl
- bis
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 28
- -1 bis (2,2-dimethylhydrazino) phosphonomethyl Chemical group 0.000 claims abstract description 38
- DHMQDGOQFOQNFH-UHFFFAOYSA-M Aminoacetate Chemical compound NCC([O-])=O DHMQDGOQFOQNFH-UHFFFAOYSA-M 0.000 claims abstract description 27
- 230000002363 herbicidal effect Effects 0.000 claims abstract description 27
- 150000001875 compounds Chemical class 0.000 claims abstract description 22
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims abstract description 19
- 125000000217 alkyl group Chemical group 0.000 claims description 35
- 125000004432 carbon atom Chemical group C* 0.000 claims description 29
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 11
- 125000003342 alkenyl group Chemical group 0.000 claims description 8
- 125000000304 alkynyl group Chemical group 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims description 7
- 239000001257 hydrogen Substances 0.000 claims description 7
- 239000000654 additive Substances 0.000 claims description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 5
- 230000000996 additive effect Effects 0.000 claims description 4
- 125000000623 heterocyclic group Chemical group 0.000 claims description 4
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 3
- 229910052757 nitrogen Inorganic materials 0.000 claims description 3
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 3
- HKOOXMFOFWEVGF-UHFFFAOYSA-N phenylhydrazine Chemical compound NNC1=CC=CC=C1 HKOOXMFOFWEVGF-UHFFFAOYSA-N 0.000 claims description 2
- 229940067157 phenylhydrazine Drugs 0.000 claims description 2
- YZCKVEUIGOORGS-OUBTZVSYSA-N Deuterium Chemical group [2H] YZCKVEUIGOORGS-OUBTZVSYSA-N 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 125000000031 ethylamino group Chemical group [H]C([H])([H])C([H])([H])N([H])[*] 0.000 claims 1
- 239000001963 growth medium Substances 0.000 claims 1
- 150000002431 hydrogen Chemical class 0.000 claims 1
- 239000004009 herbicide Substances 0.000 abstract description 9
- IUFYSVJXIZCCLT-UHFFFAOYSA-N ethyl 2-[bis[(2-phenylhydrazinyl)oxy]phosphorylmethyl-(2,2,2-trifluoroacetyl)amino]acetate Chemical compound C=1C=CC=CC=1NNOP(=O)(CN(CC(=O)OCC)C(=O)C(F)(F)F)ONNC1=CC=CC=C1 IUFYSVJXIZCCLT-UHFFFAOYSA-N 0.000 abstract description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 111
- 239000000243 solution Substances 0.000 description 26
- 241000196324 Embryophyta Species 0.000 description 22
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 20
- 239000011541 reaction mixture Substances 0.000 description 19
- 239000000706 filtrate Substances 0.000 description 18
- 238000003756 stirring Methods 0.000 description 16
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 12
- 239000003208 petroleum Substances 0.000 description 11
- 239000003921 oil Substances 0.000 description 10
- 235000019198 oils Nutrition 0.000 description 10
- 239000007787 solid Substances 0.000 description 10
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 10
- LZSIVOHWMMSWFI-UHFFFAOYSA-N ethyl 2-[dichlorooxyphosphorylmethyl-(2,2,2-trifluoroacetyl)amino]acetate Chemical compound CCOC(=O)CN(C(=O)C(F)(F)F)CP(=O)(OCl)OCl LZSIVOHWMMSWFI-UHFFFAOYSA-N 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 8
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- 239000007788 liquid Substances 0.000 description 7
- 239000004480 active ingredient Substances 0.000 description 6
- 150000002148 esters Chemical class 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- 210000000056 organ Anatomy 0.000 description 6
- 238000003359 percent control normalization Methods 0.000 description 6
- 230000001850 reproductive effect Effects 0.000 description 6
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- 150000001412 amines Chemical class 0.000 description 5
- 239000003995 emulsifying agent Substances 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 239000002270 dispersing agent Substances 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
- 239000000376 reactant Substances 0.000 description 4
- 239000000725 suspension Substances 0.000 description 4
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 4
- 239000000080 wetting agent Substances 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 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 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 125000003545 alkoxy group Chemical group 0.000 description 3
- 150000001408 amides Chemical class 0.000 description 3
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 3
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 125000001309 chloro group Chemical group Cl* 0.000 description 3
- 239000003085 diluting agent Substances 0.000 description 3
- OAKJQQAXSVQMHS-UHFFFAOYSA-N hydrazine Substances NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 3
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 3
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 241000894007 species Species 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- MKJBZNABCZRVPC-UHFFFAOYSA-N 2-[phosphonomethyl-(2,2,2-trifluoroacetyl)amino]acetic acid Chemical class OC(=O)CN(CP(O)(O)=O)C(=O)C(F)(F)F MKJBZNABCZRVPC-UHFFFAOYSA-N 0.000 description 2
- VVJKKWFAADXIJK-UHFFFAOYSA-N Allylamine Chemical compound NCC=C VVJKKWFAADXIJK-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 235000010829 Prunus spinosa Nutrition 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 125000004183 alkoxy alkyl group Chemical group 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- 150000008064 anhydrides Chemical class 0.000 description 2
- 239000012736 aqueous medium Substances 0.000 description 2
- KAUOMRSFTDRXRJ-UHFFFAOYSA-N butyl 2-[dichlorooxyphosphorylmethyl-(2,2,2-trifluoroacetyl)amino]acetate Chemical compound CCCCOC(=O)CN(C(=O)C(F)(F)F)CP(=O)(OCl)OCl KAUOMRSFTDRXRJ-UHFFFAOYSA-N 0.000 description 2
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 235000021186 dishes Nutrition 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 230000002262 irrigation Effects 0.000 description 2
- 238000003973 irrigation Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 239000006199 nebulizer Substances 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 231100000208 phytotoxic Toxicity 0.000 description 2
- 230000000885 phytotoxic effect Effects 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 150000003871 sulfonates Chemical class 0.000 description 2
- 239000003784 tall oil Substances 0.000 description 2
- 150000003512 tertiary amines Chemical class 0.000 description 2
- 238000011282 treatment Methods 0.000 description 2
- QAEDZJGFFMLHHQ-UHFFFAOYSA-N trifluoroacetic anhydride Chemical compound FC(F)(F)C(=O)OC(=O)C(F)(F)F QAEDZJGFFMLHHQ-UHFFFAOYSA-N 0.000 description 2
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
- BYCUWCJUPSUFBX-UHFFFAOYSA-N (2,3,4,5,6-pentafluorophenyl)hydrazine Chemical compound NNC1=C(F)C(F)=C(F)C(F)=C1F BYCUWCJUPSUFBX-UHFFFAOYSA-N 0.000 description 1
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
- FQHCPFMTXFJZJS-UHFFFAOYSA-N (4-methoxyphenyl)hydrazine;hydrochloride Chemical compound Cl.COC1=CC=C(NN)C=C1 FQHCPFMTXFJZJS-UHFFFAOYSA-N 0.000 description 1
- DIIIISSCIXVANO-UHFFFAOYSA-N 1,2-Dimethylhydrazine Chemical compound CNNC DIIIISSCIXVANO-UHFFFAOYSA-N 0.000 description 1
- NFAOATPOYUWEHM-UHFFFAOYSA-N 2-(6-methylheptyl)phenol Chemical compound CC(C)CCCCCC1=CC=CC=C1O NFAOATPOYUWEHM-UHFFFAOYSA-N 0.000 description 1
- RUZXGCSYZJJGOC-UHFFFAOYSA-N 2-[dichlorooxyphosphorylmethyl-(2,2,2-trifluoroacetyl)amino]butanoic acid Chemical compound CCC(C(O)=O)N(C(=O)C(F)(F)F)CP(=O)(OCl)OCl RUZXGCSYZJJGOC-UHFFFAOYSA-N 0.000 description 1
- IRPLGVBUUDVOOR-UHFFFAOYSA-N 2-methoxyethyl 2-[bis(butylaminooxy)phosphorylmethyl-(2,2,2-trifluoroacetyl)amino]acetate Chemical compound CCCCNOP(=O)(ONCCCC)CN(C(=O)C(F)(F)F)CC(=O)OCCOC IRPLGVBUUDVOOR-UHFFFAOYSA-N 0.000 description 1
- TXFJNXUNTJSKDD-UHFFFAOYSA-N 2-methoxyethyl 2-[dichlorooxyphosphorylmethyl-(2,2,2-trifluoroacetyl)amino]acetate Chemical compound COCCOC(=O)CN(C(=O)C(F)(F)F)CP(=O)(OCl)OCl TXFJNXUNTJSKDD-UHFFFAOYSA-N 0.000 description 1
- 125000006325 2-propenyl amino group Chemical group [H]C([H])=C([H])C([H])([H])N([H])* 0.000 description 1
- 240000002245 Acer pensylvanicum Species 0.000 description 1
- 235000006760 Acer pensylvanicum Nutrition 0.000 description 1
- NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical compound C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 description 1
- 241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
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- 244000286695 Melinis minutiflora var. inermis Species 0.000 description 1
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
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- TVBJDPLVNQSWIK-UHFFFAOYSA-N [dichloro-[[2-(2-chloroethoxy)-2-oxoethyl]-(2,2,2-trifluoroacetyl)amino]methyl]phosphonic acid Chemical compound OP(O)(=O)C(Cl)(Cl)N(C(=O)C(F)(F)F)CC(=O)OCCCl TVBJDPLVNQSWIK-UHFFFAOYSA-N 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
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- 230000033228 biological regulation Effects 0.000 description 1
- 125000001246 bromo group Chemical group Br* 0.000 description 1
- RMBGSBIZBRZJPK-UHFFFAOYSA-N butan-1-amine;2-dodecylbenzenesulfonic acid Chemical compound CCCCN.CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O RMBGSBIZBRZJPK-UHFFFAOYSA-N 0.000 description 1
- 125000004106 butoxy group Chemical group [*]OC([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
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- BAWFCEDURYGLKR-UHFFFAOYSA-N decyl 2-[dichlorooxyphosphorylmethyl-(2,2,2-trifluoroacetyl)amino]acetate Chemical compound CCCCCCCCCCOC(=O)CN(C(=O)C(F)(F)F)CP(=O)(OCl)OCl BAWFCEDURYGLKR-UHFFFAOYSA-N 0.000 description 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- SPCNPOWOBZQWJK-UHFFFAOYSA-N dimethoxy-(2-propan-2-ylsulfanylethylsulfanyl)-sulfanylidene-$l^{5}-phosphane Chemical compound COP(=S)(OC)SCCSC(C)C SPCNPOWOBZQWJK-UHFFFAOYSA-N 0.000 description 1
- JMGZBMRVDHKMKB-UHFFFAOYSA-L disodium;2-sulfobutanedioate Chemical compound [Na+].[Na+].OS(=O)(=O)C(C([O-])=O)CC([O-])=O JMGZBMRVDHKMKB-UHFFFAOYSA-L 0.000 description 1
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- REWPTDOTRHJFPE-UHFFFAOYSA-N ethyl 2-[bis[(propan-2-ylamino)oxy]phosphorylmethyl-(2,2,2-trifluoroacetyl)amino]acetate Chemical compound CCOC(=O)CN(C(=O)C(F)(F)F)CP(=O)(ONC(C)C)ONC(C)C REWPTDOTRHJFPE-UHFFFAOYSA-N 0.000 description 1
- JPEGDEDEQOLSKS-UHFFFAOYSA-N ethyl 2-[bis[[2-(2,3,4,5,6-pentafluorophenyl)hydrazinyl]oxy]phosphorylmethyl-(2,2,2-trifluoroacetyl)amino]acetate Chemical compound FC=1C(F)=C(F)C(F)=C(F)C=1NNOP(=O)(CN(CC(=O)OCC)C(=O)C(F)(F)F)ONNC1=C(F)C(F)=C(F)C(F)=C1F JPEGDEDEQOLSKS-UHFFFAOYSA-N 0.000 description 1
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- DIAIBWNEUYXDNL-UHFFFAOYSA-N n,n-dihexylhexan-1-amine Chemical compound CCCCCCN(CCCCCC)CCCCCC DIAIBWNEUYXDNL-UHFFFAOYSA-N 0.000 description 1
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- RGSODMOUXWISAG-UHFFFAOYSA-N n-prop-2-ynylprop-2-yn-1-amine Chemical compound C#CCNCC#C RGSODMOUXWISAG-UHFFFAOYSA-N 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
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- 125000004437 phosphorous atom Chemical group 0.000 description 1
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- LWMPFIOTEAXAGV-UHFFFAOYSA-N piperidin-1-amine Chemical compound NN1CCCCC1 LWMPFIOTEAXAGV-UHFFFAOYSA-N 0.000 description 1
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- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
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- 125000006225 propoxyethyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])OC([H])([H])C([H])([H])* 0.000 description 1
- 125000006308 propyl amino group Chemical group 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- 125000000719 pyrrolidinyl group Chemical group 0.000 description 1
- 125000000168 pyrrolyl group Chemical group 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- HIEHAIZHJZLEPQ-UHFFFAOYSA-M sodium;naphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(S(=O)(=O)[O-])=CC=CC2=C1 HIEHAIZHJZLEPQ-UHFFFAOYSA-M 0.000 description 1
- 239000008247 solid mixture Substances 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- 239000002195 soluble material Substances 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 230000036561 sun exposure Effects 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- 238000001665 trituration Methods 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 230000009105 vegetative growth Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6527—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having nitrogen and oxygen atoms as the only ring hetero atoms
- C07F9/6533—Six-membered rings
-
- 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
- A01N57/26—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-nitrogen bonds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/44—Amides thereof
- C07F9/4403—Amides thereof the acid moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4407—Amides of acyclic saturated acids which can have further substituents on alkyl
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/44—Amides thereof
- C07F9/4461—Amides thereof the amide moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4484—Compounds containing the structure C-P(=X)(N-acyl)-X, C-P(=X)(N-heteroatom)-X or C-P(=X)(N-CN)-X (X = O, S, Se)
- C07F9/4496—Compounds containing the structure P(=X)(N-N-) (X = O, S, Se)
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/553—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having one nitrogen atom as the only ring hetero atom
- C07F9/572—Five-membered rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/553—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having one nitrogen atom as the only ring hetero atom
- C07F9/576—Six-membered rings
- C07F9/59—Hydrogenated pyridine rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Crystallography & Structural Chemistry (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/922,923 US4359332A (en) | 1978-07-10 | 1978-07-10 | Amide and hydrazide derivatives of N-trifluoroacetyl-N-phosphonomethylglycine as herbicides |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DD144714A5 true DD144714A5 (de) | 1980-11-05 |
Family
ID=25447798
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD79223643A DD152789A5 (de) | 1978-07-10 | 1979-07-09 | Verfahren zur herstellung von n-trifluoracetyl-n-phosphonomethylglycinamid-und-hydrazinderivaten |
| DD79214210A DD144714A5 (de) | 1978-07-10 | 1979-07-09 | Herbizides gemisch |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD79223643A DD152789A5 (de) | 1978-07-10 | 1979-07-09 | Verfahren zur herstellung von n-trifluoracetyl-n-phosphonomethylglycinamid-und-hydrazinderivaten |
Country Status (19)
| Country | Link |
|---|---|
| US (1) | US4359332A (cs) |
| EP (1) | EP0008852B1 (cs) |
| JP (1) | JPS5543068A (cs) |
| AR (1) | AR222659A1 (cs) |
| AU (1) | AU521111B2 (cs) |
| BG (1) | BG31479A3 (cs) |
| BR (1) | BR7904360A (cs) |
| CA (1) | CA1122995A (cs) |
| CS (1) | CS208121B2 (cs) |
| DD (2) | DD152789A5 (cs) |
| DE (1) | DE2961820D1 (cs) |
| DK (1) | DK147916C (cs) |
| HU (1) | HU185008B (cs) |
| IL (1) | IL57748A (cs) |
| PH (1) | PH17797A (cs) |
| PL (1) | PL116633B1 (cs) |
| RO (1) | RO77789A (cs) |
| SU (1) | SU1169518A3 (cs) |
| ZA (1) | ZA793415B (cs) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MX6645E (es) * | 1979-12-26 | 1985-09-18 | Monsanto Co | Procedimiento para la preparacion de una composicion herbicida |
| US4545804A (en) * | 1983-11-21 | 1985-10-08 | Monsanto Company | N(Aminophosphinylmethyl) glycine derivatives |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2965668A (en) * | 1959-10-28 | 1960-12-20 | Dow Chemical Co | Phosphorohydrazidothioates |
| US3166565A (en) * | 1961-06-14 | 1965-01-19 | Dow Chemical Co | O-(isoxazolyl) o-alkyl phosphoramidates and phosphoramidothioates |
| US3197496A (en) * | 1961-08-09 | 1965-07-27 | Lubrizol Corp | Polyphosphorus ester derivatives of o, o-dihydrocarbyl-s-hydroxylalkyl phosphorodithioates |
| US3321516A (en) * | 1963-12-06 | 1967-05-23 | Pennsalt Chemicals Corp | Dialkylthiocarbamylphosphonic diamides |
| US3683026A (en) * | 1968-02-28 | 1972-08-08 | Basf Ag | Trisubstituted hydrazines |
| US3853530A (en) * | 1971-03-10 | 1974-12-10 | Monsanto Co | Regulating plants with n-phosphonomethylglycine and derivatives thereof |
| PH16509A (en) * | 1971-03-10 | 1983-11-08 | Monsanto Co | N-phosphonomethylglycine phytotoxicant composition |
| US3799758A (en) * | 1971-08-09 | 1974-03-26 | Monsanto Co | N-phosphonomethyl-glycine phytotoxicant compositions |
| US4050918A (en) * | 1974-05-20 | 1977-09-27 | Shell Oil Company | Herbicidal semicarbazides |
| US3972915A (en) * | 1974-08-14 | 1976-08-03 | Monsanto Company | N-phosphonomethylglycine phenyl hydrazides |
| US3970695A (en) * | 1975-05-23 | 1976-07-20 | Monsanto Company | N-(perfluoroacyl)-N-phosphonomethyl glycine compounds, method of preparing same |
| US4035176A (en) * | 1975-05-23 | 1977-07-12 | Monsanto Company | N-(perfluoroacyl)-N-phosphonomethyl glycine compounds, method of preparing same |
-
1978
- 1978-07-10 US US05/922,923 patent/US4359332A/en not_active Expired - Lifetime
-
1979
- 1979-07-06 AR AR277212A patent/AR222659A1/es active
- 1979-07-06 DE DE7979301307T patent/DE2961820D1/de not_active Expired
- 1979-07-06 EP EP79301307A patent/EP0008852B1/en not_active Expired
- 1979-07-09 CA CA331,414A patent/CA1122995A/en not_active Expired
- 1979-07-09 SU SU792788702A patent/SU1169518A3/ru active
- 1979-07-09 HU HU79MO1057A patent/HU185008B/hu unknown
- 1979-07-09 DD DD79223643A patent/DD152789A5/de unknown
- 1979-07-09 PH PH22750A patent/PH17797A/en unknown
- 1979-07-09 BR BR7904360A patent/BR7904360A/pt unknown
- 1979-07-09 IL IL57748A patent/IL57748A/xx unknown
- 1979-07-09 BG BG7944253A patent/BG31479A3/xx unknown
- 1979-07-09 DK DK287479A patent/DK147916C/da not_active IP Right Cessation
- 1979-07-09 AU AU48774/79A patent/AU521111B2/en not_active Ceased
- 1979-07-09 CS CS794813A patent/CS208121B2/cs unknown
- 1979-07-09 ZA ZA793415A patent/ZA793415B/xx unknown
- 1979-07-09 RO RO7998092A patent/RO77789A/ro unknown
- 1979-07-09 DD DD79214210A patent/DD144714A5/de unknown
- 1979-07-09 JP JP8737879A patent/JPS5543068A/ja active Pending
- 1979-07-09 PL PL1979216976A patent/PL116633B1/pl unknown
Also Published As
| Publication number | Publication date |
|---|---|
| BR7904360A (pt) | 1980-04-08 |
| DK147916C (da) | 1985-06-17 |
| DE2961820D1 (en) | 1982-02-25 |
| HU185008B (en) | 1984-11-28 |
| SU1169518A3 (ru) | 1985-07-23 |
| CA1122995A (en) | 1982-05-04 |
| DK147916B (da) | 1985-01-07 |
| EP0008852B1 (en) | 1982-01-13 |
| PL216976A1 (cs) | 1980-05-05 |
| BG31479A3 (en) | 1982-01-15 |
| JPS5543068A (en) | 1980-03-26 |
| EP0008852A1 (en) | 1980-03-19 |
| RO77789A (ro) | 1982-04-12 |
| AU521111B2 (en) | 1982-03-18 |
| AU4877479A (en) | 1980-01-17 |
| DD152789A5 (de) | 1981-12-09 |
| IL57748A (en) | 1983-09-30 |
| IL57748A0 (en) | 1979-11-30 |
| CS208121B2 (en) | 1981-08-31 |
| ZA793415B (en) | 1980-07-30 |
| AR222659A1 (es) | 1981-06-15 |
| US4359332A (en) | 1982-11-16 |
| PL116633B1 (en) | 1981-06-30 |
| PH17797A (en) | 1984-12-13 |
| DK287479A (da) | 1980-01-11 |
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