HU228374B1 - Novel surfactants and aqueous pesticide formulations - Google Patents
Novel surfactants and aqueous pesticide formulations Download PDFInfo
- Publication number
- HU228374B1 HU228374B1 HU0302482A HUP0302482A HU228374B1 HU 228374 B1 HU228374 B1 HU 228374B1 HU 0302482 A HU0302482 A HU 0302482A HU P0302482 A HUP0302482 A HU P0302482A HU 228374 B1 HU228374 B1 HU 228374B1
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- independently
- carbon atoms
- hydrocarbon
- substituted
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- 239000004094 surface-active agent Substances 0.000 title claims abstract description 366
- 239000003090 pesticide formulation Substances 0.000 title description 3
- 239000000203 mixture Substances 0.000 claims abstract description 387
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 claims abstract description 316
- 239000005562 Glyphosate Substances 0.000 claims abstract description 292
- 229940097068 glyphosate Drugs 0.000 claims abstract description 292
- 230000002363 herbicidal effect Effects 0.000 claims abstract description 100
- 239000012141 concentrate Substances 0.000 claims abstract description 98
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 62
- 239000004009 herbicide Substances 0.000 claims abstract description 38
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims abstract description 34
- 229910052700 potassium Inorganic materials 0.000 claims abstract description 34
- 239000011591 potassium Substances 0.000 claims abstract description 34
- 239000002253 acid Substances 0.000 claims abstract description 28
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 claims abstract description 23
- 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 abstract description 19
- 229910052708 sodium Inorganic materials 0.000 claims abstract description 19
- 239000011734 sodium Substances 0.000 claims abstract description 19
- 238000003860 storage Methods 0.000 claims abstract description 17
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 claims abstract description 14
- 230000000361 pesticidal effect Effects 0.000 claims abstract description 7
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 claims abstract description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 335
- 125000004432 carbon atom Chemical group C* 0.000 claims description 288
- 229910052739 hydrogen Inorganic materials 0.000 claims description 270
- 239000001257 hydrogen Substances 0.000 claims description 270
- 229930195733 hydrocarbon Natural products 0.000 claims description 249
- 239000004215 Carbon black (E152) Substances 0.000 claims description 221
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 213
- 150000002430 hydrocarbons Chemical class 0.000 claims description 210
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 195
- -1 alkylene carbonate Chemical compound 0.000 claims description 158
- 239000004973 liquid crystal related substance Substances 0.000 claims description 102
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 92
- 125000002947 alkylene group Chemical group 0.000 claims description 90
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- 125000003118 aryl group Chemical group 0.000 claims description 71
- 150000001875 compounds Chemical class 0.000 claims description 71
- LIOPHZNMBKHGAV-UHFFFAOYSA-M potassium;2-(phosphonomethylamino)acetate Chemical compound [K+].OC(=O)CNCP(O)([O-])=O LIOPHZNMBKHGAV-UHFFFAOYSA-M 0.000 claims description 56
- 150000001412 amines Chemical class 0.000 claims description 50
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 47
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 37
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 claims description 29
- 150000002148 esters Chemical class 0.000 claims description 25
- 150000001450 anions Chemical class 0.000 claims description 23
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 20
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 claims description 19
- 229910052757 nitrogen Inorganic materials 0.000 claims description 16
- 125000004122 cyclic group Chemical group 0.000 claims description 14
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 13
- 125000000623 heterocyclic group Chemical group 0.000 claims description 13
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 13
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- 239000000575 pesticide Substances 0.000 claims description 11
- 150000004985 diamines Chemical class 0.000 claims description 10
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- 238000002425 crystallisation Methods 0.000 claims description 9
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- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 7
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- 230000008020 evaporation Effects 0.000 claims description 5
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims description 4
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- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 claims description 4
- 239000000843 powder Substances 0.000 claims description 4
- PDYXIVPKOMYDOK-UHFFFAOYSA-N Glyphosate-monoammonium Chemical compound [NH4+].OC(=O)CNCP(O)([O-])=O PDYXIVPKOMYDOK-UHFFFAOYSA-N 0.000 claims description 3
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 3
- RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 claims description 2
- PIGFYZPCRLYGLF-UHFFFAOYSA-N Aluminum nitride Chemical compound [Al]#N PIGFYZPCRLYGLF-UHFFFAOYSA-N 0.000 claims description 2
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 claims description 2
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 claims description 2
- 230000003111 delayed effect Effects 0.000 claims description 2
- 238000011161 development Methods 0.000 claims description 2
- 150000002431 hydrogen Chemical class 0.000 claims 14
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 claims 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims 2
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 claims 2
- 239000001630 malic acid Substances 0.000 claims 2
- 235000011090 malic acid Nutrition 0.000 claims 2
- UBMQQOYKUSJILW-UHFFFAOYSA-N 2-aminoethanol;azane Chemical compound N.N.NCCO UBMQQOYKUSJILW-UHFFFAOYSA-N 0.000 claims 1
- OUCNSFUASBNULY-UHFFFAOYSA-O [NH4+].[K].[O-][N+]([O-])=O Chemical compound [NH4+].[K].[O-][N+]([O-])=O OUCNSFUASBNULY-UHFFFAOYSA-O 0.000 claims 1
- 239000001361 adipic acid Substances 0.000 claims 1
- 235000011037 adipic acid Nutrition 0.000 claims 1
- 230000001580 bacterial effect Effects 0.000 claims 1
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 claims 1
- 230000002427 irreversible effect Effects 0.000 claims 1
- 101150035468 phi gene Proteins 0.000 claims 1
- YWICANUUQPYHOW-UHFFFAOYSA-M sodium;2-(phosphonomethylamino)acetate Chemical compound [Na+].OP(O)(=O)CNCC([O-])=O YWICANUUQPYHOW-UHFFFAOYSA-M 0.000 claims 1
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 abstract description 30
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 abstract description 28
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 abstract description 7
- NRZWQKGABZFFKE-UHFFFAOYSA-N trimethylsulfonium Chemical class C[S+](C)C NRZWQKGABZFFKE-UHFFFAOYSA-N 0.000 abstract description 5
- 125000005537 sulfoxonium group Chemical group 0.000 abstract 1
- 238000009472 formulation Methods 0.000 description 118
- 125000003342 alkenyl group Chemical group 0.000 description 116
- 241000196324 Embryophyta Species 0.000 description 97
- 235000002639 sodium chloride Nutrition 0.000 description 80
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 71
- 239000005977 Ethylene Substances 0.000 description 71
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 69
- 235000008504 concentrate Nutrition 0.000 description 65
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 60
- 125000000304 alkynyl group Chemical group 0.000 description 47
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- 208000000785 Invasive Pulmonary Aspergillosis Diseases 0.000 description 37
- 239000000243 solution Substances 0.000 description 37
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical group N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 34
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- 238000002360 preparation method Methods 0.000 description 29
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- 238000000034 method Methods 0.000 description 24
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- 235000013162 Cocos nucifera Nutrition 0.000 description 17
- 244000060011 Cocos nucifera Species 0.000 description 17
- 229910021529 ammonia Inorganic materials 0.000 description 17
- 239000003093 cationic surfactant Substances 0.000 description 17
- 125000006353 oxyethylene group Chemical group 0.000 description 16
- 239000002904 solvent Substances 0.000 description 16
- 229910019142 PO4 Inorganic materials 0.000 description 15
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Natural products CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 14
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- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 13
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- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 12
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- 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 description 1
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- 125000005010 perfluoroalkyl group Chemical group 0.000 description 1
- HTYIXCKSEQQCJO-UHFFFAOYSA-N phenaglycodol Chemical compound CC(C)(O)C(C)(O)C1=CC=C(Cl)C=C1 HTYIXCKSEQQCJO-UHFFFAOYSA-N 0.000 description 1
- IDOWTHOLJBTAFI-UHFFFAOYSA-N phenmedipham Chemical compound COC(=O)NC1=CC=CC(OC(=O)NC=2C=C(C)C=CC=2)=C1 IDOWTHOLJBTAFI-UHFFFAOYSA-N 0.000 description 1
- IZRPKIZLIFYYKR-UHFFFAOYSA-N phenyltoloxamine Chemical compound CN(C)CCOC1=CC=CC=C1CC1=CC=CC=C1 IZRPKIZLIFYYKR-UHFFFAOYSA-N 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- SIOXPEMLGUPBBT-UHFFFAOYSA-N picolinic acid Chemical compound OC(=O)C1=CC=CC=N1 SIOXPEMLGUPBBT-UHFFFAOYSA-N 0.000 description 1
- 125000003386 piperidinyl group Chemical group 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
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- 239000005017 polysaccharide Substances 0.000 description 1
- ZDHURYWHEBEGHO-UHFFFAOYSA-N potassiopotassium Chemical compound [K].[K] ZDHURYWHEBEGHO-UHFFFAOYSA-N 0.000 description 1
- 229940114930 potassium stearate Drugs 0.000 description 1
- ANBFRLKBEIFNQU-UHFFFAOYSA-M potassium;octadecanoate Chemical compound [K+].CCCCCCCCCCCCCCCCCC([O-])=O ANBFRLKBEIFNQU-UHFFFAOYSA-M 0.000 description 1
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- FROBCXTULYFHEJ-OAHLLOKOSA-N propaquizafop Chemical compound C1=CC(O[C@H](C)C(=O)OCCON=C(C)C)=CC=C1OC1=CN=C(C=C(Cl)C=C2)C2=N1 FROBCXTULYFHEJ-OAHLLOKOSA-N 0.000 description 1
- WJNRPILHGGKWCK-UHFFFAOYSA-N propazine Chemical compound CC(C)NC1=NC(Cl)=NC(NC(C)C)=N1 WJNRPILHGGKWCK-UHFFFAOYSA-N 0.000 description 1
- 125000004368 propenyl group Chemical group C(=CC)* 0.000 description 1
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- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
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- 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 description 1
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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
- A01N61/00—Biocides, pest repellants or attractants, or plant growth regulators containing substances of unknown or undetermined composition, e.g. substances characterised only by the mode of action
-
- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/30—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests characterised by the surfactants
-
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/02—Saturated carboxylic acids or thio analogues thereof; Derivatives thereof
- A01N37/04—Saturated carboxylic acids or thio analogues thereof; Derivatives thereof polybasic
-
- 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)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Agronomy & Crop Science (AREA)
- Toxicology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US20552400P | 2000-05-19 | 2000-05-19 | |
| US20662800P | 2000-05-24 | 2000-05-24 | |
| US27323401P | 2001-03-02 | 2001-03-02 | |
| US27436801P | 2001-03-08 | 2001-03-08 | |
| PCT/US2001/016550 WO2001089302A2 (en) | 2000-05-19 | 2001-05-21 | Aqueous pesticide formulations and novel surfactants |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| HUP0302482A2 HUP0302482A2 (hu) | 2003-11-28 |
| HUP0302482A3 HUP0302482A3 (en) | 2009-01-28 |
| HU228374B1 true HU228374B1 (en) | 2013-03-28 |
Family
ID=27498575
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HU0302482A HU228374B1 (en) | 2000-05-19 | 2001-05-21 | Novel surfactants and aqueous pesticide formulations |
Country Status (20)
| Country | Link |
|---|---|
| US (3) | US7049270B2 (https=) |
| EP (2) | EP1721523A3 (https=) |
| JP (1) | JP5318313B2 (https=) |
| CN (1) | CN1444451A (https=) |
| AR (1) | AR028106A1 (https=) |
| AT (1) | ATE334591T1 (https=) |
| AU (2) | AU2001263361B2 (https=) |
| BR (1) | BR0110978B1 (https=) |
| CA (2) | CA2510398C (https=) |
| DE (1) | DE60121995T2 (https=) |
| ES (1) | ES2269409T3 (https=) |
| HN (1) | HN2001000105A (https=) |
| HU (1) | HU228374B1 (https=) |
| MX (1) | MX265024B (https=) |
| MY (1) | MY158895A (https=) |
| NZ (1) | NZ522396A (https=) |
| PH (1) | PH12001001235B1 (https=) |
| PL (2) | PL223350B1 (https=) |
| UY (1) | UY26722A1 (https=) |
| WO (1) | WO2001089302A2 (https=) |
Families Citing this family (94)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9819693D0 (en) | 1998-09-10 | 1998-11-04 | Zeneca Ltd | Glyphosate formulation |
| MY158895A (en) * | 2000-05-19 | 2016-11-30 | Monsanto Technology Llc | Potassium glyphosate formulations |
| US6992045B2 (en) | 2000-05-19 | 2006-01-31 | Monsanto Technology Llc | Pesticide compositions containing oxalic acid |
| US7008904B2 (en) | 2000-09-13 | 2006-03-07 | Monsanto Technology, Llc | Herbicidal compositions containing glyphosate and bipyridilium |
| US20030096708A1 (en) * | 2001-03-02 | 2003-05-22 | Monsanto Technology Llc | Pesticide concentrates containing etheramine surfactants |
| AUPR682201A0 (en) | 2001-08-03 | 2001-08-30 | Nufarm Limited | Glyphosate composition |
| EP2172107A2 (en) * | 2002-08-31 | 2010-04-07 | Monsanto Technology LLC | Process for the preparation of a dry pesticidal composition containing a dicarboxylate component |
| WO2004019681A2 (en) * | 2002-08-31 | 2004-03-11 | Monsanto Technology Llc | Pesticide compositions containing dicarboxylic acids |
| US7645543B2 (en) | 2002-10-15 | 2010-01-12 | Polyplus Battery Company | Active metal/aqueous electrochemical cells and systems |
| 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 |
| US20050026781A1 (en) * | 2003-04-22 | 2005-02-03 | Monsanto Technology Llc | Herbicidal compositions containing glyphosate and a pyridine analog |
| US9668471B2 (en) * | 2003-05-28 | 2017-06-06 | AgQuam LLC | Manufacture and use of agricultural spray adjuvants for hard water conditions |
| BRPI0413266B8 (pt) | 2003-08-04 | 2022-06-28 | Dow Agrosciences Llc | Composição de concentrado herbicida de alta potência, e método para controle de vegetação indesejável |
| GB0328530D0 (en) * | 2003-12-09 | 2004-01-14 | Syngenta Ltd | Agrochemical composition |
| WO2005087007A1 (en) * | 2004-03-10 | 2005-09-22 | Monsanto Technology Llc | Herbicidal compositions containing n-phosphonomethyl glycine and an auxin herbicide |
| US20050223425A1 (en) | 2004-03-30 | 2005-10-06 | Clinton William P | Methods for controlling plant pathogens using N-phosphonomethylglycine |
| US20060013780A1 (en) * | 2004-07-19 | 2006-01-19 | Ford Michael E | N,N'-dialkyl derivatives of polyhydroxyalkyl alkylenediamines |
| WO2006023431A2 (en) | 2004-08-19 | 2006-03-02 | Monsanto Technology Llc | Glyphosate salt herbicidal composition |
| MX2007003193A (es) * | 2004-09-17 | 2007-05-16 | Monsanto Technology Llc | Formulaciones de glifosato con sintomas de quemado temprano. |
| WO2006034459A1 (en) * | 2004-09-23 | 2006-03-30 | Akzo Nobel N.V. | Alkoxylated alkylamines / alkyl ether amines with peaked distribution |
| CA2848165C (en) * | 2004-09-23 | 2017-03-28 | Monsanto Technology Llc | Alkoxylated alkylamine quaternary surfactants for glyphosate |
| MX2007008012A (es) | 2004-12-30 | 2007-08-23 | Rhone Poulenc Chimie | Composicion herbicida que comprende una sal de aminofosfato o de aminofosfonato y una betaina. |
| AU2012200010B2 (en) * | 2005-03-04 | 2014-01-09 | Monsanto Technology Llc | Mitigating necrosis in transgenic glyphosate-tolerant cotton plants treated with herbicidal glyphosate formulations |
| US8129564B2 (en) | 2005-03-04 | 2012-03-06 | Monsanto Technology Llc | Mitigating necrosis in transgenic glyphosate-tolerant cotton plants treated with herbicidal glyphosate formulations |
| US8236731B2 (en) | 2005-05-24 | 2012-08-07 | Monsanto Technology Llc | Herbicide compatibility improvement |
| WO2007054540A2 (en) * | 2005-11-10 | 2007-05-18 | Rhodia Operations | Herbicidal composition comprising aminophosphate or aminophosphonate potassium salt |
| RU2411726C2 (ru) | 2005-11-14 | 2011-02-20 | Родиа Инк. | Сельскохозяйственная вспомогательная композиция, пестицидная композиция и способ для применения таких композиций |
| US8182943B2 (en) | 2005-12-19 | 2012-05-22 | Polyplus Battery Company | Composite solid electrolyte for protection of active metal anodes |
| CN101511175A (zh) * | 2006-03-23 | 2009-08-19 | 阿克佐诺贝尔股份有限公司 | 具有峰值分布的烷氧基化烷基胺或烷氧基化烷基醚胺 |
| BRPI0715012A2 (pt) * | 2006-09-22 | 2013-05-28 | Huntsman Spec Chem Corp | formulaÇço de pesticida com birrefrigÊncia de fluxo |
| US8288317B2 (en) * | 2006-10-09 | 2012-10-16 | Huntsman Petrochemical Llc | Liquid crystal agrochemical formulations |
| CN101186622B (zh) * | 2006-11-17 | 2013-03-20 | 浙江新安化工集团股份有限公司 | 一种制备固体草甘膦钾盐的方法 |
| US9012365B2 (en) | 2006-12-06 | 2015-04-21 | Akzo Nobel N.V. | Compatibility agents for herbicidal formulations comprising 2,4-(Dichlorophenoxy) acetic acid salts |
| EP2094083B1 (en) | 2006-12-06 | 2014-07-23 | Akzo Nobel N.V. | Alkylamidopropyl dialkylamine surfactants as adjuvants |
| FR2914647B1 (fr) | 2007-04-05 | 2011-10-21 | Rhodia Recherches Et Tech | Copolymere comprenant des unites betainiques et des unites hydrophobes et/ou amphiphiles,procede de preparation,et utilisations. |
| CN101784194B (zh) * | 2007-06-29 | 2016-03-30 | 陶氏益农公司 | 含有经取代的苯氧基链烷酸衍生物和草甘膦衍生物的协同性除草组合物 |
| US8133848B2 (en) | 2007-09-04 | 2012-03-13 | Nufarm Americas Inc. | Glyphosate composition and method of controlling weeds |
| EP2211622A2 (en) * | 2007-11-30 | 2010-08-04 | Cognis IP Management GmbH | Herbicidal compositions of lithium glyphosate and adjuvants |
| WO2009075591A1 (en) * | 2007-12-13 | 2009-06-18 | Donaghys Industries Limited | Herbicidal formulations for combinations of dimethylamine and potassium salts of glyphosate |
| WO2009075588A1 (en) * | 2007-12-13 | 2009-06-18 | Donaghys Industries Limited | Herbicidal formulations for triethanolamine salts of glyphosate |
| HRP20160477T1 (hr) * | 2008-06-18 | 2016-06-17 | Stepan Company | Koncentrat glifosata ultra-visokog udjela |
| EP2425716B1 (en) | 2008-08-19 | 2016-05-04 | Akzo Nobel N.V. | Thickening glyphosate formulations |
| CN102170781B (zh) * | 2008-09-04 | 2015-04-08 | 阿克佐诺贝尔股份有限公司 | 用于降低漂移的粘弹性体系 |
| CN102215695B (zh) * | 2008-09-29 | 2014-10-08 | 孟山都技术公司 | 包含酰胺基烷基胺表面活性剂的草甘膦制剂 |
| US9192158B2 (en) * | 2008-12-11 | 2015-11-24 | Monsanto Technology Llc | Herbicide formulations containing an etheramine and alkylamine alkoxylate surfactant system |
| BRPI1013462B1 (pt) | 2009-03-06 | 2018-02-27 | Syngenta Limited | Formulação herbicida aquosa, sistema de armazenagem e expedição e método de inibir o crescimento de uma planta indesejada |
| AU2010221301B2 (en) * | 2009-03-06 | 2015-03-19 | Jones Iii, Charles A. | Compatibilized electrolyte formulations |
| AR075817A1 (es) * | 2009-03-11 | 2011-04-27 | Monsanto Technology Llc | Formulaciones herbicidas que comprenden glifosato y gliceridos alcoxilados |
| MX2011013249A (es) * | 2009-06-16 | 2012-04-02 | Huntsman Int Llc | Composiciones de liberacion para compuestos lignocelulosicos. |
| WO2011008453A2 (en) | 2009-06-30 | 2011-01-20 | Monsanto Technology Llc | N-phosphonomethylglycine guanidine derivative salts |
| AR077768A1 (es) * | 2009-07-22 | 2011-09-21 | Huntsman Corp Australia Pty Ltd | Alcoxilatos de cocoalquilpoliamina como agentes para composiciones herbicidas de alto poder |
| US20120142532A1 (en) * | 2009-08-10 | 2012-06-07 | Monsanto Technology Llc | Low volatility auxin herbicide formulations |
| WO2011025860A1 (en) | 2009-08-28 | 2011-03-03 | E. I. Du Pont De Nemours And Company | Compositions and methods to control insect pests |
| BR112012011625B1 (pt) | 2009-11-16 | 2018-10-02 | Imtrade Australia Pty Ltd | formulações de glifosato de carga elevada e processo de preparação das mesmas |
| BR112013003347B1 (pt) * | 2010-08-10 | 2018-03-20 | Rhodia Operations | Composições de pesticidas agrícolas e método para controlar uma praga-alvo |
| CN104886049B (zh) * | 2010-09-15 | 2017-01-11 | 陶氏益农公司 | 用于控制除草剂喷雾漂移的胺和胺氧化物表面活性剂 |
| ES2702807T3 (es) | 2010-10-25 | 2019-03-05 | Stepan Co | Formulaciones de glifosato basadas en composiciones derivadas de metátesis de aceites naturales |
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- 2001-05-21 HU HU0302482A patent/HU228374B1/hu unknown
- 2001-05-21 JP JP2001585556A patent/JP5318313B2/ja not_active Expired - Lifetime
- 2001-05-21 MX MXPA02011487 patent/MX265024B/es active IP Right Grant
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- 2001-05-21 EP EP06013030A patent/EP1721523A3/en not_active Ceased
- 2001-05-21 AU AU6336101A patent/AU6336101A/xx active Pending
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