NO860188L - Herbicide preparater. - Google Patents
Herbicide preparater. Download PDFInfo
- Publication number
- NO860188L NO860188L NO860188A NO860188A NO860188L NO 860188 L NO860188 L NO 860188L NO 860188 A NO860188 A NO 860188A NO 860188 A NO860188 A NO 860188A NO 860188 L NO860188 L NO 860188L
- Authority
- NO
- Norway
- Prior art keywords
- compounds
- group
- compound
- preparation
- herbicidal
- Prior art date
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- 230000002363 herbicidal effect Effects 0.000 title claims abstract description 35
- 238000002360 preparation method Methods 0.000 title claims description 61
- 239000004009 herbicide Substances 0.000 title claims description 10
- 150000003839 salts Chemical class 0.000 claims abstract description 16
- LUBJCRLGQSPQNN-UHFFFAOYSA-N 1-Phenylurea Chemical compound NC(=O)NC1=CC=CC=C1 LUBJCRLGQSPQNN-UHFFFAOYSA-N 0.000 claims abstract description 14
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 10
- KLSJWNVTNUYHDU-UHFFFAOYSA-N Amitrole Chemical compound NC1=NC=NN1 KLSJWNVTNUYHDU-UHFFFAOYSA-N 0.000 claims abstract description 8
- SIOXPEMLGUPBBT-UHFFFAOYSA-N picolinic acid Chemical compound OC(=O)C1=CC=CC=N1 SIOXPEMLGUPBBT-UHFFFAOYSA-N 0.000 claims abstract description 8
- PKRSYEPBQPFNRB-UHFFFAOYSA-N 2-phenoxybenzoic acid Chemical class OC(=O)C1=CC=CC=C1OC1=CC=CC=C1 PKRSYEPBQPFNRB-UHFFFAOYSA-N 0.000 claims abstract description 7
- CAAMSDWKXXPUJR-UHFFFAOYSA-N 3,5-dihydro-4H-imidazol-4-one Chemical compound O=C1CNC=N1 CAAMSDWKXXPUJR-UHFFFAOYSA-N 0.000 claims abstract description 7
- 150000001408 amides Chemical class 0.000 claims abstract description 6
- 235000010233 benzoic acid Nutrition 0.000 claims abstract description 6
- VHXDHGALQPVNKI-UHFFFAOYSA-N thiadiazol-4-ylurea Chemical compound NC(=O)NC1=CSN=N1 VHXDHGALQPVNKI-UHFFFAOYSA-N 0.000 claims abstract description 6
- AYQVYEBEWIDXRO-UHFFFAOYSA-N 1,3-benzothiazol-2-ylurea Chemical compound C1=CC=C2SC(NC(=O)N)=NC2=C1 AYQVYEBEWIDXRO-UHFFFAOYSA-N 0.000 claims abstract description 4
- SXERGJJQSKIUIC-UHFFFAOYSA-N 2-Phenoxypropionic acid Chemical class OC(=O)C(C)OC1=CC=CC=C1 SXERGJJQSKIUIC-UHFFFAOYSA-N 0.000 claims abstract description 4
- VXIVSQZSERGHQP-UHFFFAOYSA-N chloroacetamide Chemical compound NC(=O)CCl VXIVSQZSERGHQP-UHFFFAOYSA-N 0.000 claims abstract description 4
- 229930195733 hydrocarbon Natural products 0.000 claims abstract description 4
- VBEGHXKAFSLLGE-UHFFFAOYSA-N n-phenylnitramide Chemical compound [O-][N+](=O)NC1=CC=CC=C1 VBEGHXKAFSLLGE-UHFFFAOYSA-N 0.000 claims abstract description 4
- 229940081066 picolinic acid Drugs 0.000 claims abstract description 4
- 235000019260 propionic acid Nutrition 0.000 claims abstract description 4
- AAILEWXSEQLMNI-UHFFFAOYSA-N 1h-pyridazin-6-one Chemical compound OC1=CC=CN=N1 AAILEWXSEQLMNI-UHFFFAOYSA-N 0.000 claims abstract description 3
- 239000004215 Carbon black (E152) Substances 0.000 claims abstract description 3
- QJJFTJAQFNGRCK-UHFFFAOYSA-N 2-phenoxy-n-phenylpyridine-3-carboxamide Chemical compound C=1C=CN=C(OC=2C=CC=CC=2)C=1C(=O)NC1=CC=CC=C1 QJJFTJAQFNGRCK-UHFFFAOYSA-N 0.000 claims abstract 3
- 125000004104 aryloxy group Chemical group 0.000 claims abstract 3
- YROXIXLRRCOBKF-UHFFFAOYSA-N sulfonylurea Chemical compound OC(=N)N=S(=O)=O YROXIXLRRCOBKF-UHFFFAOYSA-N 0.000 claims abstract 3
- 150000001875 compounds Chemical class 0.000 claims description 133
- -1 triazinones Chemical class 0.000 claims description 41
- 241000196324 Embryophyta Species 0.000 claims description 40
- 239000000843 powder Substances 0.000 claims description 22
- 125000000217 alkyl group Chemical group 0.000 claims description 15
- 125000004432 carbon atom Chemical group C* 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 11
- 239000002689 soil Substances 0.000 claims description 9
- 239000004094 surface-active agent Substances 0.000 claims description 9
- 150000002148 esters Chemical class 0.000 claims description 7
- UPMXNNIRAGDFEH-UHFFFAOYSA-N 3,5-dibromo-4-hydroxybenzonitrile Chemical compound OC1=C(Br)C=C(C#N)C=C1Br UPMXNNIRAGDFEH-UHFFFAOYSA-N 0.000 claims description 6
- 239000005489 Bromoxynil Substances 0.000 claims description 6
- 239000005507 Diflufenican Substances 0.000 claims description 6
- 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 claims description 6
- VGPYEHKOIGNJKV-UHFFFAOYSA-N asulam Chemical compound COC(=O)NS(=O)(=O)C1=CC=C(N)C=C1 VGPYEHKOIGNJKV-UHFFFAOYSA-N 0.000 claims description 6
- MXWJVTOOROXGIU-UHFFFAOYSA-N atrazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)C)=N1 MXWJVTOOROXGIU-UHFFFAOYSA-N 0.000 claims description 6
- 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 claims description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 6
- LFULEKSKNZEWOE-UHFFFAOYSA-N propanil Chemical compound CCC(=O)NC1=CC=C(Cl)C(Cl)=C1 LFULEKSKNZEWOE-UHFFFAOYSA-N 0.000 claims description 6
- 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 claims description 5
- 239000005504 Dicamba Substances 0.000 claims description 5
- DHWRNDJOGMTCPB-UHFFFAOYSA-N Dimefuron Chemical compound ClC1=CC(NC(=O)N(C)C)=CC=C1N1C(=O)OC(C(C)(C)C)=N1 DHWRNDJOGMTCPB-UHFFFAOYSA-N 0.000 claims description 5
- 239000005510 Diuron Substances 0.000 claims description 5
- 239000005595 Picloram Substances 0.000 claims description 5
- 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 claims description 5
- IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 claims description 5
- PUIYMUZLKQOUOZ-UHFFFAOYSA-N isoproturon Chemical compound CC(C)C1=CC=C(NC(=O)N(C)C)C=C1 PUIYMUZLKQOUOZ-UHFFFAOYSA-N 0.000 claims description 5
- NQQVFXUMIDALNH-UHFFFAOYSA-N picloram Chemical compound NC1=C(Cl)C(Cl)=NC(C(O)=O)=C1Cl NQQVFXUMIDALNH-UHFFFAOYSA-N 0.000 claims description 5
- ODCWYMIRDDJXKW-UHFFFAOYSA-N simazine Chemical compound CCNC1=NC(Cl)=NC(NCC)=N1 ODCWYMIRDDJXKW-UHFFFAOYSA-N 0.000 claims description 5
- 239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 claims description 4
- 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 claims description 4
- CTSLUCNDVMMDHG-UHFFFAOYSA-N 5-bromo-3-(butan-2-yl)-6-methylpyrimidine-2,4(1H,3H)-dione Chemical compound CCC(C)N1C(=O)NC(C)=C(Br)C1=O CTSLUCNDVMMDHG-UHFFFAOYSA-N 0.000 claims description 4
- XKJMBINCVNINCA-UHFFFAOYSA-N Alfalone Chemical compound CON(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 XKJMBINCVNINCA-UHFFFAOYSA-N 0.000 claims description 4
- 239000005484 Bifenox Substances 0.000 claims description 4
- 239000005490 Carbetamide Substances 0.000 claims description 4
- 239000005981 Imazaquin Substances 0.000 claims description 4
- 239000005573 Linuron Substances 0.000 claims description 4
- 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 claims description 4
- WXZVAROIGSFCFJ-UHFFFAOYSA-N N,N-diethyl-2-(naphthalen-1-yloxy)propanamide Chemical compound C1=CC=C2C(OC(C)C(=O)N(CC)CC)=CC=CC2=C1 WXZVAROIGSFCFJ-UHFFFAOYSA-N 0.000 claims description 4
- 239000005585 Napropamide Substances 0.000 claims description 4
- AMRQXHFXNZFDCH-SECBINFHSA-N [(2r)-1-(ethylamino)-1-oxopropan-2-yl] n-phenylcarbamate Chemical compound CCNC(=O)[C@@H](C)OC(=O)NC1=CC=CC=C1 AMRQXHFXNZFDCH-SECBINFHSA-N 0.000 claims description 4
- NRXQIUSYPAHGNM-UHFFFAOYSA-N ioxynil Chemical compound OC1=C(I)C=C(C#N)C=C1I NRXQIUSYPAHGNM-UHFFFAOYSA-N 0.000 claims description 4
- FIKAKWIAUPDISJ-UHFFFAOYSA-L paraquat dichloride Chemical compound [Cl-].[Cl-].C1=C[N+](C)=CC=C1C1=CC=[N+](C)C=C1 FIKAKWIAUPDISJ-UHFFFAOYSA-L 0.000 claims description 4
- 150000003856 quaternary ammonium compounds Chemical class 0.000 claims description 4
- ZSDSQXJSNMTJDA-UHFFFAOYSA-N trifluralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-N 0.000 claims description 4
- 101000742062 Bos taurus Protein phosphatase 1G Proteins 0.000 claims description 3
- NDUPDOJHUQKPAG-UHFFFAOYSA-N Dalapon Chemical compound CC(Cl)(Cl)C(O)=O NDUPDOJHUQKPAG-UHFFFAOYSA-N 0.000 claims description 3
- KCOCSOWTADCKOL-UHFFFAOYSA-N Ethidimuron Chemical compound CCS(=O)(=O)C1=NN=C(N(C)C(=O)NC)S1 KCOCSOWTADCKOL-UHFFFAOYSA-N 0.000 claims description 3
- 239000005574 MCPA Substances 0.000 claims description 3
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- WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 claims description 3
- 125000003118 aryl group Chemical group 0.000 claims description 3
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- 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 claims description 3
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- UNAHYJYOSSSJHH-UHFFFAOYSA-N oryzalin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(S(N)(=O)=O)C=C1[N+]([O-])=O UNAHYJYOSSSJHH-UHFFFAOYSA-N 0.000 claims description 3
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- UBQKCCHYAOITMY-UHFFFAOYSA-N pyridin-2-ol Chemical class OC1=CC=CC=N1 UBQKCCHYAOITMY-UHFFFAOYSA-N 0.000 claims description 3
- 125000001424 substituent group Chemical group 0.000 claims description 3
- 150000003918 triazines Chemical class 0.000 claims description 3
- 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 claims description 2
- WVQBLGZPHOPPFO-UHFFFAOYSA-N 2-chloro-N-(2-ethyl-6-methylphenyl)-N-(1-methoxypropan-2-yl)acetamide Chemical compound CCC1=CC=CC(C)=C1N(C(C)COC)C(=O)CCl WVQBLGZPHOPPFO-UHFFFAOYSA-N 0.000 claims description 2
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- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical class OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 claims description 2
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- 239000000047 product Substances 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 150000003865 secondary ammonium salts Chemical class 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 229950006451 sorbitan laurate Drugs 0.000 description 1
- 235000011067 sorbitan monolaureate Nutrition 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 230000009885 systemic effect Effects 0.000 description 1
- XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical class NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 description 1
- 150000003866 tertiary ammonium salts Chemical class 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 239000003021 water soluble solvent Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 229920001285 xanthan gum Polymers 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
- A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
- A01N57/22—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing aromatic radicals
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)
- Cosmetics (AREA)
- Compounds Of Unknown Constitution (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR8501150A FR2576181B1 (fr) | 1985-01-23 | 1985-01-23 | Melanges herbicides a base de compose de type n-(phosphonomethylglycyl) |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO860188L true NO860188L (no) | 1986-07-24 |
Family
ID=9315673
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO860188A NO860188L (no) | 1985-01-23 | 1986-01-21 | Herbicide preparater. |
Country Status (23)
| Country | Link |
|---|---|
| EP (1) | EP0192583B1 (de) |
| JP (1) | JPS61172805A (de) |
| KR (1) | KR920007584B1 (de) |
| CN (1) | CN86100691A (de) |
| AT (1) | ATE43222T1 (de) |
| AU (1) | AU577658B2 (de) |
| BR (1) | BR8600228A (de) |
| CA (1) | CA1272890A (de) |
| DD (1) | DD251701A5 (de) |
| DE (1) | DE3663436D1 (de) |
| DK (1) | DK32986A (de) |
| FI (1) | FI82877C (de) |
| FR (1) | FR2576181B1 (de) |
| GB (1) | GB2169806B (de) |
| GR (1) | GR860116B (de) |
| HU (1) | HU200897B (de) |
| MA (1) | MA20611A1 (de) |
| NO (1) | NO860188L (de) |
| NZ (1) | NZ214880A (de) |
| OA (1) | OA08194A (de) |
| PH (1) | PH21453A (de) |
| PT (1) | PT81890B (de) |
| ZA (1) | ZA86443B (de) |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2589328A1 (fr) * | 1985-10-31 | 1987-05-07 | Stauffer Chemical Co | Methode et composition d'amelioration de l'activite herbicide de sels de n-phosphomethylglycine |
| US5147444A (en) * | 1986-06-27 | 1992-09-15 | Rhone Poulenc Agrochimie | Herbicidal compositions based on a glyphosate herbicide and acifluorfen |
| GB8626246D0 (en) * | 1986-11-03 | 1986-12-03 | Monsanto Europe Sa | Compositions containing glyphosate &c |
| JPH02501922A (ja) * | 1987-10-28 | 1990-06-28 | ローヌ‐プーラン・アグロシミ | グリホゼート型除草剤とフェノキシ安息香酸型除草剤とに基づく除草組成物、およびこれら組成物を用いる不用植物の処理方法 |
| HU202062B (en) * | 1987-11-18 | 1991-02-28 | Noevenyvedelmi Kutato Intezet | Herbicide composition containing more active components |
| GB8811763D0 (en) * | 1988-05-18 | 1988-06-22 | Monsanto Europe Sa | Compositions containing glyphosate simazine & diuron |
| US6930075B1 (en) | 1990-11-02 | 2005-08-16 | Monsanto Technology, Llc | Fatty acid-based herbicidal composition |
| US5599769A (en) * | 1990-11-13 | 1997-02-04 | Hoechst Aktiengesellschaft | Synergistic herbicidal compositions comprising glyphosate or glufosinate in combination with a sulfonylurea herbicide |
| CA2097913C (en) | 1991-01-08 | 2002-08-20 | Kristin Anne Arnold | Improved herbicidal formulation |
| ES2046132B1 (es) * | 1992-06-22 | 1994-08-01 | Aragonesas Energ & Ind | Procedimiento para obtener composiciones herbicidas estables, binarias o ternarias, conteniendo glifosato en forma acida junto con ureas sustituidas y/o triazinas. |
| GB9304294D0 (en) * | 1993-03-03 | 1993-04-21 | Zeneca Ltd | Herbicidal compositions |
| EP0617894B1 (de) * | 1993-04-02 | 1998-12-16 | Monsanto Europe S.A./N.V. | Flüssige konzentrierte herbizide Glyphosatzusammensetzungen |
| US5525577A (en) * | 1994-11-17 | 1996-06-11 | Basf Corporation | Safening effect of combinations of glyphosate and acifluorfen |
| US5928995A (en) * | 1995-05-05 | 1999-07-27 | E. I. Du Pont De Nemours And Company | Herbicidal mixtures |
| FR2733668A1 (fr) * | 1995-05-05 | 1996-11-08 | Du Pont | Compositions herbicides a base de n-phosphonomethylglycine ou de ses sels |
| DE19607633A1 (de) * | 1996-02-29 | 1997-09-04 | Bayer Ag | Herbizide Mittel auf Basis von N-Phosphonomethyl-glycinestern |
| US7008904B2 (en) | 2000-09-13 | 2006-03-07 | Monsanto Technology, Llc | Herbicidal compositions containing glyphosate and bipyridilium |
| EP1791431B1 (de) | 2004-09-17 | 2012-01-25 | Monsanto Technology, LLC | Glyphosate-formulierungen mit früh auftretenden verbrennungssymptomen |
| TW201433263A (zh) | 2005-07-04 | 2014-09-01 | Sumitomo Chemical Co | 製備殺蟲劑組成物之方法及抑制雜草之方法 |
| TWI395882B (zh) * | 2009-06-24 | 2013-05-11 | Pegatron Corp | 輔助固定組件 |
| KR20210038629A (ko) * | 2018-07-31 | 2021-04-07 | 바이엘 악티엔게젤샤프트 | 고염 함량을 갖는 농약 (작물 보호) 제형을 위한 증점제 조합물 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4405531A (en) * | 1975-11-10 | 1983-09-20 | Monsanto Company | Salts of N-phosphonomethylglycine |
| ES8603901A1 (es) * | 1983-07-27 | 1986-01-01 | Rhone Poulenc Agrochimie | Procedimiento de preparacion de sulfonamidas con grupo ansinometilfosfonico |
| FR2549839B1 (fr) * | 1983-07-27 | 1985-09-20 | Rhone Poulenc Agrochimie | Nouveaux herbicides a groupe sulfonamide derives de la n-phosphonomethyl glycine |
-
1985
- 1985-01-23 FR FR8501150A patent/FR2576181B1/fr not_active Expired
-
1986
- 1986-01-17 GR GR860116A patent/GR860116B/el unknown
- 1986-01-17 MA MA20836A patent/MA20611A1/fr unknown
- 1986-01-21 NO NO860188A patent/NO860188L/no unknown
- 1986-01-21 DE DE8686420019T patent/DE3663436D1/de not_active Expired
- 1986-01-21 BR BR8600228A patent/BR8600228A/pt unknown
- 1986-01-21 AT AT86420019T patent/ATE43222T1/de not_active IP Right Cessation
- 1986-01-21 CA CA000499991A patent/CA1272890A/en not_active Expired - Lifetime
- 1986-01-21 DD DD86286360A patent/DD251701A5/de not_active IP Right Cessation
- 1986-01-21 NZ NZ214880A patent/NZ214880A/en unknown
- 1986-01-21 AU AU52595/86A patent/AU577658B2/en not_active Ceased
- 1986-01-21 EP EP86420019A patent/EP0192583B1/de not_active Expired
- 1986-01-21 ZA ZA86443A patent/ZA86443B/xx unknown
- 1986-01-22 PT PT81890A patent/PT81890B/pt not_active IP Right Cessation
- 1986-01-22 GB GB08601468A patent/GB2169806B/en not_active Expired
- 1986-01-22 FI FI860312A patent/FI82877C/fi not_active IP Right Cessation
- 1986-01-22 DK DK32986A patent/DK32986A/da not_active Application Discontinuation
- 1986-01-22 JP JP61011813A patent/JPS61172805A/ja active Pending
- 1986-01-22 HU HU86311A patent/HU200897B/hu not_active IP Right Cessation
- 1986-01-22 PH PH33313A patent/PH21453A/en unknown
- 1986-01-22 CN CN198686100691A patent/CN86100691A/zh active Pending
- 1986-01-23 OA OA58773A patent/OA08194A/xx unknown
- 1986-01-23 KR KR1019860000417A patent/KR920007584B1/ko active IP Right Grant
Also Published As
| Publication number | Publication date |
|---|---|
| ZA86443B (en) | 1986-09-24 |
| BR8600228A (pt) | 1986-09-30 |
| GB2169806A (en) | 1986-07-23 |
| DK32986D0 (da) | 1986-01-22 |
| DK32986A (da) | 1986-07-24 |
| OA08194A (fr) | 1987-10-30 |
| JPS61172805A (ja) | 1986-08-04 |
| GR860116B (en) | 1986-04-09 |
| AU5259586A (en) | 1986-07-31 |
| FR2576181A1 (fr) | 1986-07-25 |
| FI860312A0 (fi) | 1986-01-22 |
| CN86100691A (zh) | 1986-12-03 |
| DD251701A5 (de) | 1987-11-25 |
| NZ214880A (en) | 1990-12-21 |
| PT81890B (pt) | 1988-05-27 |
| EP0192583B1 (de) | 1989-05-24 |
| CA1272890A (en) | 1990-08-21 |
| FI82877C (fi) | 1991-05-10 |
| PH21453A (en) | 1987-10-28 |
| PT81890A (fr) | 1986-02-01 |
| FI860312A (fi) | 1986-07-24 |
| FR2576181B1 (fr) | 1987-04-03 |
| MA20611A1 (fr) | 1986-10-01 |
| DE3663436D1 (en) | 1989-06-29 |
| EP0192583A1 (de) | 1986-08-27 |
| KR860005586A (ko) | 1986-08-11 |
| AU577658B2 (en) | 1988-09-29 |
| GB8601468D0 (en) | 1986-02-26 |
| ATE43222T1 (de) | 1989-06-15 |
| GB2169806B (en) | 1987-12-09 |
| FI82877B (fi) | 1991-01-31 |
| HUT40307A (en) | 1986-12-28 |
| KR920007584B1 (ko) | 1992-09-08 |
| HU200897B (en) | 1990-09-28 |
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