LU87728A1 - Compositions liquides concentrees a base de n-phosphonomethylglycine - Google Patents

Compositions liquides concentrees a base de n-phosphonomethylglycine Download PDF

Info

Publication number: LU87728A1
Authority: LU; Luxembourg
Prior art keywords: phosphonomethylglycine; compositions according; derivative; compositions; derivatives
Prior art date: 1989-05-02

Application number

LU87728A

Other languages

English (en)

French (fr)

Inventor

Dookhith Mohammad

Linares Hubert

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

1990-04-26

Publication date

1991-11-15

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

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

1990-04-26 Application filed by Rhone Poulenc Agrochimie filed Critical Rhone Poulenc Agrochimie

1991-11-15 Publication of LU87728A1 publication Critical patent/LU87728A1/fr

Links

XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 title claims description 76
239000000203 mixture Substances 0.000 title claims description 60
239000007788 liquid Substances 0.000 title claims description 7
239000004094 surface-active agent Substances 0.000 claims description 25
239000005562 Glyphosate Substances 0.000 claims description 23
229940097068 glyphosate Drugs 0.000 claims description 23
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 15
150000003839 salts Chemical class 0.000 claims description 10
239000000725 suspension Substances 0.000 claims description 10
239000011149 active material Substances 0.000 claims description 9
239000002671 adjuvant Substances 0.000 claims description 6
150000003863 ammonium salts Chemical class 0.000 claims description 6
230000003213 activating effect Effects 0.000 claims description 5
229910052500 inorganic mineral Inorganic materials 0.000 claims description 5
239000011707 mineral Substances 0.000 claims description 5
239000003960 organic solvent 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
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 3
239000002245 particle Substances 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
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
125000000217 alkyl group Chemical group 0.000 claims description 2
125000002947 alkylene 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
125000004432 carbon atom Chemical group C* 0.000 claims description 2
125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims description 2
150000002430 hydrocarbons Chemical group 0.000 claims description 2
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Natural products SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 claims description 2
JJWLVOIRVHMVIS-UHFFFAOYSA-O isopropylaminium Chemical class CC(C)[NH3+] JJWLVOIRVHMVIS-UHFFFAOYSA-O 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
239000011591 potassium Substances 0.000 claims description 2
229910052700 potassium Inorganic materials 0.000 claims description 2
125000001325 propanoyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 claims description 2
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 2
239000011734 sodium Substances 0.000 claims description 2
229910052708 sodium Inorganic materials 0.000 claims description 2
IIACRCGMVDHOTQ-UHFFFAOYSA-M sulfamate Chemical compound NS([O-])(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-M 0.000 claims description 2
230000002363 herbicidal effect Effects 0.000 description 10
239000002904 solvent Substances 0.000 description 9
239000002253 acid Substances 0.000 description 7
239000012190 activator Substances 0.000 description 7
239000012141 concentrate Substances 0.000 description 7
238000009472 formulation Methods 0.000 description 7
239000004009 herbicide Substances 0.000 description 7
241000196324 Embryophyta Species 0.000 description 6
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
239000004480 active ingredient Substances 0.000 description 6
239000002270 dispersing agent Substances 0.000 description 6
150000002989 phenols Chemical class 0.000 description 6
239000000080 wetting agent Substances 0.000 description 6
-1 N-phosphonomethylglycyl group Chemical group 0.000 description 5
150000001875 compounds Chemical class 0.000 description 5
JLEXUIVKURIPFI-UHFFFAOYSA-N tris phosphate Chemical compound OP(O)(O)=O.OCC(N)(CO)CO JLEXUIVKURIPFI-UHFFFAOYSA-N 0.000 description 5
239000000084 colloidal system Substances 0.000 description 4
125000000286 phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 4
230000001681 protective effect Effects 0.000 description 4
239000013008 thixotropic agent Substances 0.000 description 4
239000002890 Aclonifen Substances 0.000 description 3
239000005588 Oxadiazon Substances 0.000 description 3
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 3
239000004372 Polyvinyl alcohol Substances 0.000 description 3
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 3
150000001412 amines Chemical class 0.000 description 3
OUGYROWSLPSPSY-UHFFFAOYSA-N azane;dodecylbenzene Chemical compound N.CCCCCCCCCCCCC1=CC=CC=C1 OUGYROWSLPSPSY-UHFFFAOYSA-N 0.000 description 3
239000000440 bentonite Substances 0.000 description 3
229910000278 bentonite Inorganic materials 0.000 description 3
SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 3
235000014113 dietary fatty acids Nutrition 0.000 description 3
230000001804 emulsifying effect Effects 0.000 description 3
150000002148 esters Chemical class 0.000 description 3
239000000194 fatty acid Substances 0.000 description 3
229930195729 fatty acid Natural products 0.000 description 3
230000002349 favourable effect Effects 0.000 description 3
239000003921 oil Substances 0.000 description 3
235000019198 oils Nutrition 0.000 description 3
229920001296 polysiloxane Polymers 0.000 description 3
229920002451 polyvinyl alcohol Polymers 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
239000005496 Chlorsulfuron 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
239000002202 Polyethylene glycol Substances 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
BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 2
229910052921 ammonium sulfate Inorganic materials 0.000 description 2
235000011130 ammonium sulphate Nutrition 0.000 description 2
239000002518 antifoaming agent Substances 0.000 description 2
150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
VGPYEHKOIGNJKV-UHFFFAOYSA-N asulam Chemical compound COC(=O)NS(=O)(=O)C1=CC=C(N)C=C1 VGPYEHKOIGNJKV-UHFFFAOYSA-N 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
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 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
230000006378 damage Effects 0.000 description 2
239000013530 defoamer Substances 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
150000002028 dodecanols Polymers 0.000 description 2
150000004665 fatty acids Chemical class 0.000 description 2
230000012010 growth Effects 0.000 description 2
HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
239000007791 liquid phase Substances 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 2
229920001223 polyethylene glycol Polymers 0.000 description 2
235000021395 porridge Nutrition 0.000 description 2
239000002002 slurry Substances 0.000 description 2
239000000243 solution Substances 0.000 description 2
238000009736 wetting Methods 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
239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 description 1
UWHURBUBIHUHSU-UHFFFAOYSA-N 2-[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamoylsulfamoyl]benzoic acid Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 UWHURBUBIHUHSU-UHFFFAOYSA-N 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
CHZCERSEMVWNHL-UHFFFAOYSA-N 2-hydroxybenzonitrile Chemical compound OC1=CC=CC=C1C#N CHZCERSEMVWNHL-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
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
101000742062 Bos taurus Protein phosphatase 1G Proteins 0.000 description 1
235000006463 Brassica alba Nutrition 0.000 description 1
235000008427 Brassica arvensis Nutrition 0.000 description 1
244000140786 Brassica hirta Species 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
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-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
244000278243 Limnocharis flava Species 0.000 description 1
235000003403 Limnocharis flava Nutrition 0.000 description 1
244000100545 Lolium multiflorum Species 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
244000234609 Portulaca oleracea Species 0.000 description 1
241000220261 Sinapis Species 0.000 description 1
229920002125 Sokalan® Polymers 0.000 description 1
240000006694 Stellaria media Species 0.000 description 1
ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
229940100389 Sulfonylurea Drugs 0.000 description 1
150000007513 acids Chemical class 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
125000001931 aliphatic group Chemical group 0.000 description 1
125000003545 alkoxy group Chemical group 0.000 description 1
AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
238000004458 analytical method Methods 0.000 description 1
230000002528 anti-freeze Effects 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
229960000892 attapulgite Drugs 0.000 description 1
230000004071 biological effect Effects 0.000 description 1
238000004364 calculation method Methods 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
238000005119 centrifugation Methods 0.000 description 1
150000008422 chlorobenzenes Chemical class 0.000 description 1
230000007797 corrosion Effects 0.000 description 1
238000005260 corrosion Methods 0.000 description 1
239000013078 crystal Substances 0.000 description 1
MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical class CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
239000012530 fluid Substances 0.000 description 1
239000006260 foam Substances 0.000 description 1
150000002334 glycols Chemical class 0.000 description 1
239000005556 hormone Substances 0.000 description 1
229940088597 hormone Drugs 0.000 description 1
239000003112 inhibitor Substances 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
JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical class CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
239000000463 material Substances 0.000 description 1
238000000034 method Methods 0.000 description 1
125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 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
229910052625 palygorskite Inorganic materials 0.000 description 1
230000000149 penetrating effect Effects 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
238000004525 petroleum distillation Methods 0.000 description 1
239000012071 phase Substances 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
230000008635 plant growth Effects 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
230000001737 promoting effect Effects 0.000 description 1
230000001105 regulatory 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
238000007711 solidification Methods 0.000 description 1
230000008023 solidification Effects 0.000 description 1
239000007921 spray Substances 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
YROXIXLRRCOBKF-UHFFFAOYSA-N sulfonylurea Chemical class OC(=N)N=S(=O)=O YROXIXLRRCOBKF-UHFFFAOYSA-N 0.000 description 1
229920002994 synthetic fiber Polymers 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
230000009974 thixotropic effect Effects 0.000 description 1
150000003918 triazines Chemical class 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
239000008158 vegetable oil Substances 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
- 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
- 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

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)
Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
Medicinal Preparation (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

LU87728A 1989-05-02 1990-04-26 Compositions liquides concentrees a base de n-phosphonomethylglycine LU87728A1 (fr)

Applications Claiming Priority (4)

Application Number	Priority Date	Filing Date	Title
FR8906075		1989-05-02
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
FR8907041		1989-05-24

Publications (1)

Publication Number	Publication Date
LU87728A1 true LU87728A1 (fr)	1991-11-15

Family

ID=26227317

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
LU87728A LU87728A1 (fr)	1989-05-02	1990-04-26	Compositions liquides concentrees a base de n-phosphonomethylglycine

Country Status (15)

Country	Link
JP (1)	JPH02295907A (de)
KR (1)	KR900017479A (de)
AT (1)	ATA100290A (de)
AU (1)	AU5450290A (de)
CA (1)	CA2015797A1 (de)
DE (1)	DE4013930A1 (de)
DK (1)	DK107890A (de)
GB (1)	GB2230955A (de)
GR (1)	GR1000368B (de)
HU (1)	HUT54273A (de)
IT (1)	IT1240693B (de)
LU (1)	LU87728A1 (de)
NL (1)	NL9001009A (de)
PT (1)	PT93938A (de)
SE (2)	SE9001446D0 (de)

Families Citing this family (31)

* Cited by examiner, † Cited by third party
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
US5430005A (en) *	1991-08-02	1995-07-04	Monsanto Company	Herbicidal compositions
CA2074993A1 (en) *	1991-08-02	1993-02-03	Miguel Molina Dayawon	Glyphosate-containing herbicidal compositions having enhanced effectiveness
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
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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 SE SE9001558A patent/SE9001558L/xx not_active Application Discontinuation
- 1990-04-30 DE DE4013930A patent/DE4013930A1/de not_active Withdrawn
- 1990-05-01 DK DK107890A patent/DK107890A/da not_active Application Discontinuation
- 1990-05-01 AU AU54502/90A patent/AU5450290A/en not_active Abandoned
- 1990-05-01 GB GB9009827A patent/GB2230955A/en not_active Withdrawn
- 1990-05-01 KR KR1019900006213A patent/KR900017479A/ko not_active Withdrawn
- 1990-05-01 CA CA002015797A patent/CA2015797A1/en not_active Abandoned
- 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 JP JP2116676A patent/JPH02295907A/ja active Pending
- 1990-05-02 HU HU902645A patent/HUT54273A/hu unknown
- 1990-05-02 AT AT0100290A patent/ATA100290A/de not_active Application Discontinuation

Also Published As

Publication number	Publication date
NL9001009A (nl)	1990-12-03
GB9009827D0 (en)	1990-06-20
SE9001558L (sv)	1990-11-03
SE9001446D0 (sv)	1990-04-23
GB2230955A (en)	1990-11-07
KR900017479A (ko)	1990-12-19
CA2015797A1 (en)	1990-11-02
PT93938A (pt)	1991-01-08
ATA100290A (de)	1993-02-15
GR1000368B (el)	1992-06-30
IT9020184A1 (it)	1991-11-02
IT1240693B (it)	1993-12-17
HUT54273A (en)	1991-02-28
HU902645D0 (en)	1990-09-28
DK107890D0 (da)	1990-05-01
JPH02295907A (ja)	1990-12-06
DK107890A (da)	1990-11-03
IT9020184A0 (it)	1990-05-02
SE9001558D0 (sv)	1990-04-30
GR900100309A (en)	1991-10-10
DE4013930A1 (de)	1990-11-08
AU5450290A (en)	1990-11-08

Publication	Publication Date	Title
LU87728A1 (fr)	1991-11-15	Compositions liquides concentrees a base de n-phosphonomethylglycine
LU87747A1 (fr)	1991-02-18	Compositions herbicides a base de n-phosphonomethylglycine et leur utilisation
EP0869713B1 (de)	2001-10-24	Pflanzenschutzmittel enthaltend mindestens ein wasserlöslichen wirkstoff und mindestens ein polyalkoxyliertes amidoamin
EP0192583B1 (de)	1989-05-24	Auf einer Verbindung der N-(Phosphonomethylglycyl)-sulfonylamin-Art basierende herbizide Mischungen
LU87936A1 (fr)	1992-12-15	Solutions herbicides a base de n-phosphonomethylglycine
FR2611437A1 (fr)	1988-09-09	Produit herbicide resultant de l'association de l'aclonifen avec l'oxadiazon ou le diflufenican
FR2656769A1 (fr)	1991-07-12	Melanges herbicides a base d'aclonifen.
FR2661315A2 (fr)	1991-10-31	Compositions liquides concentrees a base de n-phosphonomethylglycine.
EP0569264B1 (de)	1996-11-06	Sulfobernsteinsäurehalbestern enthaltende wasserlösliche Pflanzenschutzmittel
EP0290354A2 (de)	1988-11-09	Herbizide Mischung
FR2588724A1 (fr)	1987-04-24	Compositions fongicides a base de derive du triazole et leur utilisation
FR2647306A1 (fr)	1990-11-30	Compositions liquides concentrees a base de n-phosphonomethylglycine
FR2648317A1 (fr)	1990-12-21	Compositions liquides concentrees a base de n-phosphonomethylglycine
BE898428A (fr)	1984-06-12	Compositions fongicides et leur utilisation.
WO2000008927A1 (fr)	2000-02-24	Formulations phytosanitaires a forte teneur en matiere active
EP1191848B1 (de)	2004-05-06	Phytosanitäre zusammensetzung die einen wasserlöslichen wirkstoff und ein modifiziertes öl enthält
FR2671457A1 (fr)	1992-07-17	Melanges herbicides a base d'aclonifen.
FR2597720A1 (fr)	1987-10-30	Compositions herbicides liquides stabilisees a base de m-bis-carbamates et leur utilisation.
FR2491295A1 (fr)	1982-04-09	Composition herbicide a base d'une phenyluree et de cyanazine
FR2656985A1 (fr)	1991-07-19	Melanges herbicides a base d'aclonifen.
FR2590119A1 (fr)	1987-05-22	Compositions herbicides liquides stabilisees, a base de biscarbamate
FR2718980A1 (fr)	1995-10-27	Nouveau système émulsifiant pour la préparation de concentrés émulsionnables d'huiles végétales.
FR2656983A1 (fr)	1991-07-19	Melanges herbicides a base d'aclonifen.
FR2701194A1 (fr)	1994-08-12	Compositions phytosanitaires incorporant des sucroglycérides éthoxyles.
FR3010863A1 (fr)	2015-03-27	Formulation herbicide comprenant nicosulfuron et sulcotrione et procede de preparation de celle ci