HUT54273A - Concentrated liquid herbicidal compositions comprising n-phosphonomethylglycine - Google Patents

Concentrated liquid herbicidal compositions comprising n-phosphonomethylglycine Download PDF

Info

Publication number: HUT54273A
Authority: HU; Hungary
Prior art keywords: phosphonomethylglycine; derivative; composition according; present; amount
Prior art date: 1989-05-02

Application number

HU902645A

Other languages

English (en)

Hungarian (hu)

Other versions

HU902645D0 (en

Inventor

Mohammad Dookhith

Hubert Linares

Original Assignee

Rhone Poulenc Agrochimie

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1989-05-02

Filing date

1990-05-02

Publication date

1991-02-28

1989-05-02 Priority claimed from FR8906075A external-priority patent/FR2648317A1/fr

1989-05-24 Priority claimed from FR8907041A external-priority patent/FR2647306A1/fr

1990-05-02 Application filed by Rhone Poulenc Agrochimie filed Critical Rhone Poulenc Agrochimie

1990-09-28 Publication of HU902645D0 publication Critical patent/HU902645D0/hu

1991-02-28 Publication of HUT54273A publication Critical patent/HUT54273A/hu

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)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Medicinal Preparation (AREA)

HU902645A 1989-05-02 1990-05-02 Concentrated liquid herbicidal compositions comprising n-phosphonomethylglycine HUT54273A (en)

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 (fr)
KR (1)	KR900017479A (fr)
AT (1)	ATA100290A (fr)
AU (1)	AU5450290A (fr)
CA (1)	CA2015797A1 (fr)
DE (1)	DE4013930A1 (fr)
DK (1)	DK107890A (fr)
GB (1)	GB2230955A (fr)
GR (1)	GR1000368B (fr)
HU (1)	HUT54273A (fr)
IT (1)	IT1240693B (fr)
LU (1)	LU87728A1 (fr)
NL (1)	NL9001009A (fr)
PT (1)	PT93938A (fr)
SE (2)	SE9001446D0 (fr)

Families Citing this family (31)

* Cited by examiner, † Cited by third party
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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
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
NZ243779A (en) *	1991-08-02	1993-10-26	Monsanto Co	Herbicidal composition comprising glyphosate and an acetylenic diol
JPH0680504A (ja) *	1992-07-17	1994-03-22	Takeda Engei Kk	除草製剤および除草方法
WO1994018833A1 (fr) *	1993-02-26	1994-09-01	Nippon Zeon Co., Ltd.	Promoteur de croissance de plantes
DK169734B1 (da) *	1993-03-09	1995-01-30	Kvk Agro As	Herbicidpræparat, fremgangsmåde til fremstilling heraf samt aktiverende additiv til opblanding med herbicidpræparater
EP0617894B1 (fr) *	1993-04-02	1998-12-16	Monsanto Europe S.A./N.V.	Compositions herbicides de glyphosate sous forme de concentrés liquides
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 (fr) *	1996-03-01	2002-09-25	Kao Corporation	Renfor ateur d'efficacite destine aux produits chimiques et aux compositions chimiques utilises en agriculture
IL124124A (en) *	1997-04-30	2003-06-24	Rohm & Haas	Stable pesticide dispersions
PL201888B1 (pl) *	1998-12-15	2009-05-29	Basf Ag	Preparat chwastobójczy
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
WO2003026429A1 (fr)	2001-09-26	2003-04-03	Platte Chemical Co.	Compositions herbicides comprenant une suspension concentree renfermant du glyphosate acide
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
EP3334277B2 (fr) *	2015-08-13	2024-02-28	Basf Se	Suspension de pesticide non aqueux comprenant un solvant soluble dans l'eau, un épaississant inorganique et un alcoxylate
JP7189658B2 (ja) *	2017-05-23	2022-12-14	日本曹達株式会社	農薬組成物
BE1031987B1 (nl) *	2023-09-18	2025-04-15	Globachem	Herbicidesamenstellingen

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* Cited by examiner, † Cited by third party
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US4528023A (en) *	1983-07-25	1985-07-09	Stauffer Chemical Company	Enhancement of herbicidal activity of tetraaluminum salts of N-phosphonomethylglycine
EP0290416B2 (fr) *	1987-04-29	2005-03-16	Monsanto Europe S.A.	Formulations de glyphosate

1990
- 1990-04-23 SE SE9001446A patent/SE9001446D0/xx 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 DE DE4013930A patent/DE4013930A1/de not_active Withdrawn
- 1990-04-30 SE SE9001558A patent/SE9001558L/xx not_active Application Discontinuation
- 1990-05-01 DK DK107890A patent/DK107890A/da not_active Application Discontinuation
- 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 CA CA002015797A patent/CA2015797A1/fr not_active Abandoned
- 1990-05-01 KR KR1019900006213A patent/KR900017479A/ko not_active Withdrawn
- 1990-05-02 IT IT20184A patent/IT1240693B/it active IP Right Grant
- 1990-05-02 PT PT93938A patent/PT93938A/pt not_active Application Discontinuation
- 1990-05-02 HU HU902645A patent/HUT54273A/hu unknown
- 1990-05-02 AT AT0100290A patent/ATA100290A/de not_active Application Discontinuation
- 1990-05-02 JP JP2116676A patent/JPH02295907A/ja active Pending

Also Published As

Publication number	Publication date
ATA100290A (de)	1993-02-15
IT9020184A0 (it)	1990-05-02
CA2015797A1 (fr)	1990-11-02
GR900100309A (en)	1991-10-10
NL9001009A (nl)	1990-12-03
SE9001446D0 (sv)	1990-04-23
AU5450290A (en)	1990-11-08
GB2230955A (en)	1990-11-07
DE4013930A1 (de)	1990-11-08
IT1240693B (it)	1993-12-17
PT93938A (pt)	1991-01-08
GR1000368B (el)	1992-06-30
LU87728A1 (fr)	1991-11-15
IT9020184A1 (it)	1991-11-02
JPH02295907A (ja)	1990-12-06
SE9001558D0 (sv)	1990-04-30
DK107890A (da)	1990-11-03
KR900017479A (ko)	1990-12-19
DK107890D0 (da)	1990-05-01
SE9001558L (sv)	1990-11-03
HU902645D0 (en)	1990-09-28
GB9009827D0 (en)	1990-06-20

Legal Events

Date	Code	Title	Description
1992-06-29	DFA9	Temporary protection cancelled due to abandonment

Publication	Publication Date	Title
GB2230955A (en)	1990-11-07	Concentrated liquid compositions based on N-phosphonomethylglycine
JP3152991B2 (ja)	2001-04-03	液状除草剤組成物
RU2190329C2 (ru)	2002-10-10	Гербицидные композиции, способ уничтожения или подавления сорняков или нежелательных растений
AU632900B2 (en)	1993-01-14	Glyphosate compositions and their use
RU2571051C2 (ru)	2015-12-20	Смеси поверхностно-активных веществ для гербицидов, основанных на действии ауксина
GB2267825A (en)	1993-12-22	Herbicide microemulsion concentrate
CA2379468C (fr)	2009-05-19	Formulations pesticides contenant un tensioactif phosphate ester et un lignosulfonate alcoxyle
CZ416991A3 (en)	1993-01-13	Liquid pesticidal agent based on an aqueous mixed dispersion
HUT54023A (en)	1991-01-28	Process for producing liquide plant protecting composition
EA022368B1 (ru)	2015-12-30	Сельскохозяйственные препараты с ацилморфолинами и полярными апротонными сорастворителями
CZ20021309A3 (cs)	2003-01-15	Herbicidní glyfosátová kompozice a adjuvans
US20020016264A1 (en)	2002-02-07	Pesticide formulations containing alkoxylated amine neutralized aromaticsulfonic acid surfactants
HU200886B (en)	1990-09-28	Composition for diminishing evaporation of plant protecting spray solutions
WO1996008150A1 (fr)	1996-03-21	Compositions de micro-emulsions pesticides aqueuses
JP2002522400A (ja)	2002-07-23	アルコキシル化アミンで中和された芳香族スルホン酸界面活性剤を含有する農薬製剤
AU2010268083B2 (en)	2014-11-27	Aqueous herbicide concentrate
EP1022942A1 (fr)	2000-08-02	Compositions agrochimiques
SI9400304A (en)	1995-04-30	Herbicide composition,activity-promoting agent for improving the efficacy of the herbicide, and a method for treating cultivated plants.
WO2021007683A1 (fr)	2021-01-21	Compositions herbicides stables comprenant de l'oxyde d'amine et de la bétaïne
SK22597A3 (en)	1997-09-10	A herbicidal composition and a method of killing weeds
WO2026072062A1 (fr)	2026-04-02	Formulations herbicides et procédés pour le traitement d'espèces de mauvaises herbes difficiles à éradiquer
CN116322323A (zh)	2023-06-23	水溶性浓缩组合物
MXPA01005970A (en)	2002-06-05	Pesticide formulations containing alkoxylated tristyrylphenol hemi-sulfate ester neutralized alkoxylated amine surfactants
EP0186966A1 (fr)	1986-07-09	Herbicides