HUT54273A - Concentrated liquid herbicidal compositions comprising n-phosphonomethylglycine - Google Patents
Concentrated liquid herbicidal compositions comprising n-phosphonomethylglycine Download PDFInfo
- Publication number
- HUT54273A HUT54273A HU902645A HU264590A HUT54273A HU T54273 A HUT54273 A HU T54273A HU 902645 A HU902645 A HU 902645A HU 264590 A HU264590 A HU 264590A HU T54273 A HUT54273 A HU T54273A
- Authority
- HU
- Hungary
- Prior art keywords
- phosphonomethylglycine
- derivative
- composition according
- present
- amount
- Prior art date
Links
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 title claims abstract description 74
- 239000000203 mixture Substances 0.000 title claims abstract description 60
- 239000007788 liquid Substances 0.000 title claims description 8
- 230000002363 herbicidal effect Effects 0.000 title abstract description 9
- 239000005562 Glyphosate Substances 0.000 claims abstract description 24
- 229940097068 glyphosate Drugs 0.000 claims abstract description 24
- 239000004094 surface-active agent Substances 0.000 claims abstract description 24
- 239000012190 activator Substances 0.000 claims abstract description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 11
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 4
- 125000002947 alkylene group Chemical group 0.000 claims abstract description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 4
- 125000002252 acyl group Chemical group 0.000 claims abstract description 3
- 238000002360 preparation method Methods 0.000 claims description 15
- 239000004480 active ingredient Substances 0.000 claims description 13
- 239000012141 concentrate Substances 0.000 claims description 9
- 239000000725 suspension Substances 0.000 claims description 9
- 150000001875 compounds Chemical class 0.000 claims description 7
- 150000003863 ammonium salts Chemical class 0.000 claims description 5
- 239000003795 chemical substances by application Substances 0.000 claims description 5
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 4
- 239000002245 particle Substances 0.000 claims description 4
- 239000007787 solid Substances 0.000 claims description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 3
- 239000005977 Ethylene Substances 0.000 claims description 3
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 3
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 3
- 238000005507 spraying Methods 0.000 claims description 3
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 claims description 2
- 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 claims description 2
- 229910002651 NO3 Inorganic materials 0.000 claims description 2
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 claims description 2
- 229910019142 PO4 Inorganic materials 0.000 claims description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 2
- ZMZDMBWJUHKJPS-UHFFFAOYSA-M Thiocyanate anion Chemical compound [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 claims description 2
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims description 2
- 125000003342 alkenyl group Chemical group 0.000 claims description 2
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 2
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims description 2
- KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical compound C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 claims description 2
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Natural products SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 claims description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 2
- 239000010452 phosphate Substances 0.000 claims description 2
- 229910052700 potassium Inorganic materials 0.000 claims description 2
- 239000011591 potassium Substances 0.000 claims description 2
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 229910052708 sodium Inorganic materials 0.000 claims description 2
- 239000011734 sodium Substances 0.000 claims description 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 239000003125 aqueous solvent Substances 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 239000003960 organic solvent Substances 0.000 abstract description 3
- 239000006194 liquid suspension Substances 0.000 abstract 1
- 238000009472 formulation Methods 0.000 description 12
- 239000002904 solvent Substances 0.000 description 10
- 239000004009 herbicide Substances 0.000 description 9
- 239000000047 product Substances 0.000 description 9
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 8
- -1 N-phosphonomethylglycyl Chemical group 0.000 description 8
- 239000002270 dispersing agent Substances 0.000 description 7
- 238000006068 polycondensation reaction Methods 0.000 description 7
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- 239000002253 acid Substances 0.000 description 6
- 239000004615 ingredient Substances 0.000 description 6
- 239000000080 wetting agent Substances 0.000 description 6
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 5
- 235000011130 ammonium sulphate Nutrition 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 241000196324 Embryophyta Species 0.000 description 4
- 239000001166 ammonium sulphate Substances 0.000 description 4
- 239000002518 antifoaming agent Substances 0.000 description 4
- 239000000084 colloidal system Substances 0.000 description 4
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 4
- 230000001681 protective effect Effects 0.000 description 4
- 239000007921 spray Substances 0.000 description 4
- 239000004372 Polyvinyl alcohol Substances 0.000 description 3
- BLHHIPJSZPNBAA-UHFFFAOYSA-N [2,3,4-tris(2-phenylethyl)phenyl] dihydrogen phosphate Chemical compound C=1C=CC=CC=1CCC1=C(CCC=2C=CC=CC=2)C(OP(O)(=O)O)=CC=C1CCC1=CC=CC=C1 BLHHIPJSZPNBAA-UHFFFAOYSA-N 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 3
- 239000000440 bentonite Substances 0.000 description 3
- 229910000278 bentonite Inorganic materials 0.000 description 3
- 238000010790 dilution Methods 0.000 description 3
- 239000012895 dilution Substances 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 229920001296 polysiloxane Polymers 0.000 description 3
- 229920002451 polyvinyl alcohol Polymers 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 239000013008 thixotropic agent Substances 0.000 description 3
- XLLIQLLCWZCATF-UHFFFAOYSA-N 2-methoxyethyl acetate Chemical compound COCCOC(C)=O XLLIQLLCWZCATF-UHFFFAOYSA-N 0.000 description 2
- CAAMSDWKXXPUJR-UHFFFAOYSA-N 3,5-dihydro-4H-imidazol-4-one Chemical class O=C1CNC=N1 CAAMSDWKXXPUJR-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 239000005484 Bifenox Substances 0.000 description 2
- 241001354404 Cyanus Species 0.000 description 2
- 239000005507 Diflufenican Substances 0.000 description 2
- 239000005510 Diuron Substances 0.000 description 2
- SUSRORUBZHMPCO-UHFFFAOYSA-N MC-4379 Chemical compound C1=C([N+]([O-])=O)C(C(=O)OC)=CC(OC=2C(=CC(Cl)=CC=2)Cl)=C1 SUSRORUBZHMPCO-UHFFFAOYSA-N 0.000 description 2
- NUFNQYOELLVIPL-UHFFFAOYSA-N acifluorfen Chemical compound C1=C([N+]([O-])=O)C(C(=O)O)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 NUFNQYOELLVIPL-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- PLUHAVSIMCXBEX-UHFFFAOYSA-N azane;dodecyl benzenesulfonate Chemical compound N.CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 PLUHAVSIMCXBEX-UHFFFAOYSA-N 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
- MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- WYEHFWKAOXOVJD-UHFFFAOYSA-N diflufenican Chemical compound FC1=CC(F)=CC=C1NC(=O)C1=CC=CN=C1OC1=CC=CC(C(F)(F)F)=C1 WYEHFWKAOXOVJD-UHFFFAOYSA-N 0.000 description 2
- 239000003995 emulsifying agent Substances 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
- 238000000227 grinding Methods 0.000 description 2
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
- JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical class CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 2
- 239000007791 liquid phase Substances 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 235000019198 oils Nutrition 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 210000000225 synapse Anatomy 0.000 description 2
- 230000009974 thixotropic effect Effects 0.000 description 2
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 1
- 239000002794 2,4-DB Substances 0.000 description 1
- CABMTIJINOIHOD-UHFFFAOYSA-N 2-[4-methyl-5-oxo-4-(propan-2-yl)-4,5-dihydro-1H-imidazol-2-yl]quinoline-3-carboxylic acid Chemical compound N1C(=O)C(C(C)C)(C)N=C1C1=NC2=CC=CC=C2C=C1C(O)=O CABMTIJINOIHOD-UHFFFAOYSA-N 0.000 description 1
- UYXQLQUXXCIFQM-UHFFFAOYSA-N 2-hydroxy-1,3,2$l^{5}-dioxaphospholane 2-oxide Chemical compound OP1(=O)OCCO1 UYXQLQUXXCIFQM-UHFFFAOYSA-N 0.000 description 1
- CHZCERSEMVWNHL-UHFFFAOYSA-N 2-hydroxybenzonitrile Chemical compound OC1=CC=CC=C1C#N CHZCERSEMVWNHL-UHFFFAOYSA-N 0.000 description 1
- NLFTUWJSSFPBCB-UHFFFAOYSA-N 2-methyl-2-(phosphonoamino)propanoic acid Chemical compound CC(C)(C(=O)O)NP(=O)(O)O NLFTUWJSSFPBCB-UHFFFAOYSA-N 0.000 description 1
- UPMXNNIRAGDFEH-UHFFFAOYSA-N 3,5-dibromo-4-hydroxybenzonitrile Chemical compound OC1=C(Br)C=C(C#N)C=C1Br UPMXNNIRAGDFEH-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 class 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
- 240000006995 Abutilon theophrasti Species 0.000 description 1
- 239000002890 Aclonifen Substances 0.000 description 1
- 241000218473 Agrotis Species 0.000 description 1
- 241001621841 Alopecurus myosuroides Species 0.000 description 1
- 235000007320 Avena fatua Nutrition 0.000 description 1
- 241000209764 Avena fatua Species 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- 101000742062 Bos taurus Protein phosphatase 1G Proteins 0.000 description 1
- 235000008427 Brassica arvensis Nutrition 0.000 description 1
- 244000024671 Brassica kaber Species 0.000 description 1
- 235000004977 Brassica sinapistrum Nutrition 0.000 description 1
- 239000005489 Bromoxynil Substances 0.000 description 1
- 235000007516 Chrysanthemum Nutrition 0.000 description 1
- 244000189548 Chrysanthemum x morifolium Species 0.000 description 1
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 1
- 240000005702 Galium aparine Species 0.000 description 1
- 235000014820 Galium aparine Nutrition 0.000 description 1
- 239000005981 Imazaquin Substances 0.000 description 1
- 244000100545 Lolium multiflorum Species 0.000 description 1
- 239000005588 Oxadiazon Substances 0.000 description 1
- CHNUNORXWHYHNE-UHFFFAOYSA-N Oxadiazon Chemical compound C1=C(Cl)C(OC(C)C)=CC(N2C(OC(=N2)C(C)(C)C)=O)=C1Cl CHNUNORXWHYHNE-UHFFFAOYSA-N 0.000 description 1
- 244000106605 Panicum trichoides Species 0.000 description 1
- 241000170793 Phalaris canariensis Species 0.000 description 1
- 235000005632 Phalaris canariensis Nutrition 0.000 description 1
- 244000292693 Poa annua Species 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 244000234609 Portulaca oleracea Species 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- DDBMQDADIHOWIC-UHFFFAOYSA-N aclonifen Chemical compound C1=C([N+]([O-])=O)C(N)=C(Cl)C(OC=2C=CC=CC=2)=C1 DDBMQDADIHOWIC-UHFFFAOYSA-N 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- MXWJVTOOROXGIU-UHFFFAOYSA-N atrazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)C)=N1 MXWJVTOOROXGIU-UHFFFAOYSA-N 0.000 description 1
- KKBKMPQHDSDUJI-UHFFFAOYSA-N azanium;4-dodecylbenzenesulfonate Chemical compound [NH4+].CCCCCCCCCCCCC1=CC=C(S([O-])(=O)=O)C=C1 KKBKMPQHDSDUJI-UHFFFAOYSA-N 0.000 description 1
- MCOQHIWZJUDQIC-UHFFFAOYSA-N barban Chemical compound ClCC#CCOC(=O)NC1=CC=CC(Cl)=C1 MCOQHIWZJUDQIC-UHFFFAOYSA-N 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
- 239000004202 carbamide Substances 0.000 description 1
- 235000013877 carbamide Nutrition 0.000 description 1
- 239000012876 carrier material Substances 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 150000008422 chlorobenzenes Chemical class 0.000 description 1
- VJYIFXVZLXQVHO-UHFFFAOYSA-N chlorsulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)Cl)=N1 VJYIFXVZLXQVHO-UHFFFAOYSA-N 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 230000012010 growth Effects 0.000 description 1
- 239000005556 hormone Substances 0.000 description 1
- 229940088597 hormone Drugs 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 229910017053 inorganic salt Inorganic materials 0.000 description 1
- NRXQIUSYPAHGNM-UHFFFAOYSA-N ioxynil Chemical compound OC1=C(I)C=C(C#N)C=C1I NRXQIUSYPAHGNM-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 description 1
- 230000003020 moisturizing effect Effects 0.000 description 1
- VYQNWZOUAUKGHI-UHFFFAOYSA-N monobenzone Chemical compound C1=CC(O)=CC=C1OCC1=CC=CC=C1 VYQNWZOUAUKGHI-UHFFFAOYSA-N 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- 239000005416 organic matter Substances 0.000 description 1
- 239000003961 penetration enhancing agent Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- CMPQUABWPXYYSH-UHFFFAOYSA-N phenyl phosphate Chemical compound OP(O)(=O)OC1=CC=CC=C1 CMPQUABWPXYYSH-UHFFFAOYSA-N 0.000 description 1
- 239000005648 plant growth regulator Substances 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- ODCWYMIRDDJXKW-UHFFFAOYSA-N simazine Chemical compound CCNC1=NC(Cl)=NC(NCC)=N1 ODCWYMIRDDJXKW-UHFFFAOYSA-N 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical class OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- 150000003456 sulfonamides Chemical class 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical class NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 150000003738 xylenes Chemical class 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
-
- 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
- A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
- A01N57/20—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing acyclic or cycloaliphatic radicals
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
- Medicinal Preparation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR8906075A FR2648317A1 (fr) | 1989-05-02 | 1989-05-02 | Compositions liquides concentrees a base de n-phosphonomethylglycine |
| FR8907041A FR2647306A1 (fr) | 1989-05-24 | 1989-05-24 | Compositions liquides concentrees a base de n-phosphonomethylglycine |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| HU902645D0 HU902645D0 (en) | 1990-09-28 |
| HUT54273A true HUT54273A (en) | 1991-02-28 |
Family
ID=26227317
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HU902645A HUT54273A (en) | 1989-05-02 | 1990-05-02 | Concentrated liquid herbicidal compositions comprising n-phosphonomethylglycine |
Country Status (15)
| Country | Link |
|---|---|
| JP (1) | JPH02295907A (sv) |
| KR (1) | KR900017479A (sv) |
| AT (1) | ATA100290A (sv) |
| AU (1) | AU5450290A (sv) |
| CA (1) | CA2015797A1 (sv) |
| DE (1) | DE4013930A1 (sv) |
| DK (1) | DK107890A (sv) |
| GB (1) | GB2230955A (sv) |
| GR (1) | GR1000368B (sv) |
| HU (1) | HUT54273A (sv) |
| IT (1) | IT1240693B (sv) |
| LU (1) | LU87728A1 (sv) |
| NL (1) | NL9001009A (sv) |
| PT (1) | PT93938A (sv) |
| SE (2) | SE9001446D0 (sv) |
Families Citing this family (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DK165156C (da) * | 1989-12-20 | 1993-03-01 | Cheminova Agro As | Herbicid formulering indeholdende glyphosatsyre |
| US5118444A (en) * | 1991-04-10 | 1992-06-02 | Witco Corporation | Aqueous agricultural compositions exhibiting reduced irritation and corrosion |
| JP3773547B2 (ja) * | 1991-04-17 | 2006-05-10 | モンサント テクノロジー エルエルシー | グリホセート除草剤配合物 |
| CA2074993A1 (en) * | 1991-08-02 | 1993-02-03 | Miguel Molina Dayawon | Glyphosate-containing herbicidal compositions having enhanced effectiveness |
| US5430005A (en) * | 1991-08-02 | 1995-07-04 | Monsanto Company | Herbicidal compositions |
| US5258359A (en) * | 1991-08-02 | 1993-11-02 | Monsanto Company | Glyphosant-containing herbicidal compositions comprising acetylenic diol rainfastness enhancing agents |
| JPH0680504A (ja) * | 1992-07-17 | 1994-03-22 | Takeda Engei Kk | 除草製剤および除草方法 |
| DE69429336T2 (de) * | 1993-02-26 | 2002-08-22 | Zeon Corp., Tokio | Zusammensetzung von Pflanzenwachstums-Beschleuniger |
| DK169734B1 (da) | 1993-03-09 | 1995-01-30 | Kvk Agro As | Herbicidpræparat, fremgangsmåde til fremstilling heraf samt aktiverende additiv til opblanding med herbicidpræparater |
| EP0617894B1 (en) * | 1993-04-02 | 1998-12-16 | Monsanto Europe S.A./N.V. | Liquid concentrated herbicidal glyphosate compositions |
| US5565409A (en) * | 1993-04-02 | 1996-10-15 | Monsanto Company | Liquid concentrated herbicidal microemulsion compositions comprising glyphosate and either oxyfluorfen or acifluorfen |
| AU674464B2 (en) * | 1993-12-14 | 1996-12-19 | Nufarm Limited | Herbicidal composition |
| BR9406470A (pt) | 1993-12-28 | 1996-01-23 | Kao Corp | Composição e processo para aperfeiçoar produtos quimicos aplicáveis na agricultura e composição quimica aplicável na agricultura |
| US5622911A (en) * | 1994-02-14 | 1997-04-22 | Kao Corporation | Method for enhancing the efficacy of agricultural chemical with alkoxylated fatty acid amides |
| MY114016A (en) * | 1995-06-27 | 2002-07-31 | Kao Corp | Liquid enhancer composition for amino acid series herbicides |
| MY113674A (en) * | 1995-06-27 | 2002-04-30 | Kao Corp | Liquid composition for stabilizing bipyridinium series herbicides |
| EP0824314B1 (en) * | 1996-03-01 | 2002-09-25 | Kao Corporation | Efficacy enhancer for agricultural chemicals and agricultural chemical compositions |
| AR012585A1 (es) * | 1997-04-30 | 2000-11-08 | Dow Agrosciences Llc | Dispersiones pesticidas estables y metodos para su formacion |
| BRPI9916237B1 (pt) * | 1998-12-15 | 2016-02-23 | Basf Ag | composição de agentes de proteção de plantações, substancialmente isenta de água, processo para preparação de licor de aspersão para controle de plantas indesejáveis, e, composição |
| US6908882B1 (en) * | 1999-09-09 | 2005-06-21 | Monsanto Company | Enhanced method of killing weeds with glyphosate herbicide |
| US8232230B2 (en) | 2000-12-01 | 2012-07-31 | Helena Holding Company | Manufacture and use of a herbicide formulation |
| AU2002255869B2 (en) | 2001-09-26 | 2008-06-05 | Platte Chemical Co. | Herbicide compound in acid form and acidifying agent |
| AU2003266968A1 (en) * | 2002-09-04 | 2004-03-29 | Basf Aktiengesellschaft | In-situ production of suspension concentrate of diphenyl ether and n-(phosphono-methyl)glycine or homoalaninylmethyl-phosphinate herbicidal compositions and methods of use |
| DE10250551A1 (de) * | 2002-10-30 | 2004-05-19 | Clariant Gmbh | Pestizidformulierungen enthaltend alkoxylierte Amine |
| DE10250552A1 (de) * | 2002-10-30 | 2004-05-19 | Clariant Gmbh | Pestizidformulierungen enthaltend alkoxylierte Amine |
| KR100561598B1 (ko) * | 2004-05-18 | 2006-03-20 | 주식회사 대우일렉트로닉스 | 김치용기 지지장치를 갖는 김치 냉장고 |
| US8426341B2 (en) | 2005-05-27 | 2013-04-23 | Helena Holding Company | Herbicide formulation |
| JP5704297B2 (ja) * | 2009-12-15 | 2015-04-22 | 日産化学工業株式会社 | 水面拡散性および水中分散性が向上する水性懸濁状農薬組成物 |
| JP6800210B2 (ja) * | 2015-08-13 | 2020-12-16 | ビーエイエスエフ・ソシエタス・エウロパエアＢａｓｆ Ｓｅ | 水溶性溶媒、無機増粘剤及びアルコキシレートを含む非水性殺有害生物剤懸濁液 |
| JP7189658B2 (ja) * | 2017-05-23 | 2022-12-14 | 日本曹達株式会社 | 農薬組成物 |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4528023A (en) * | 1983-07-25 | 1985-07-09 | Stauffer Chemical Company | Enhancement of herbicidal activity of tetraaluminum salts of N-phosphonomethylglycine |
| ATE90835T1 (de) * | 1987-04-29 | 1993-07-15 | Monsanto Europe Sa | Formulierungen von glyphosat. |
-
1990
- 1990-04-23 SE SE9001446A patent/SE9001446D0/sv unknown
- 1990-04-24 GR GR900100309A patent/GR1000368B/el unknown
- 1990-04-26 NL NL9001009A patent/NL9001009A/nl not_active Application Discontinuation
- 1990-04-26 LU LU87728A patent/LU87728A1/fr unknown
- 1990-04-30 SE SE9001558A patent/SE9001558L/sv not_active Application Discontinuation
- 1990-04-30 DE DE4013930A patent/DE4013930A1/de not_active Withdrawn
- 1990-05-01 GB GB9009827A patent/GB2230955A/en not_active Withdrawn
- 1990-05-01 AU AU54502/90A patent/AU5450290A/en not_active Abandoned
- 1990-05-01 DK DK107890A patent/DK107890A/da not_active Application Discontinuation
- 1990-05-01 CA CA002015797A patent/CA2015797A1/en not_active Abandoned
- 1990-05-01 KR KR1019900006213A patent/KR900017479A/ko not_active Application Discontinuation
- 1990-05-02 PT PT93938A patent/PT93938A/pt not_active Application Discontinuation
- 1990-05-02 HU HU902645A patent/HUT54273A/hu unknown
- 1990-05-02 IT IT20184A patent/IT1240693B/it active IP Right Grant
- 1990-05-02 JP JP2116676A patent/JPH02295907A/ja active Pending
- 1990-05-02 AT AT0100290A patent/ATA100290A/de not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| AU5450290A (en) | 1990-11-08 |
| NL9001009A (nl) | 1990-12-03 |
| IT9020184A1 (it) | 1991-11-02 |
| LU87728A1 (fr) | 1991-11-15 |
| GR1000368B (el) | 1992-06-30 |
| CA2015797A1 (en) | 1990-11-02 |
| GB2230955A (en) | 1990-11-07 |
| PT93938A (pt) | 1991-01-08 |
| GR900100309A (en) | 1991-10-10 |
| SE9001558L (sv) | 1990-11-03 |
| KR900017479A (ko) | 1990-12-19 |
| DK107890A (da) | 1990-11-03 |
| HU902645D0 (en) | 1990-09-28 |
| GB9009827D0 (en) | 1990-06-20 |
| ATA100290A (de) | 1993-02-15 |
| SE9001558D0 (sv) | 1990-04-30 |
| IT1240693B (it) | 1993-12-17 |
| DK107890D0 (da) | 1990-05-01 |
| DE4013930A1 (de) | 1990-11-08 |
| IT9020184A0 (it) | 1990-05-02 |
| JPH02295907A (ja) | 1990-12-06 |
| SE9001446D0 (sv) | 1990-04-23 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| DFA9 | Temporary protection cancelled due to abandonment |