AR108835A2 - Tensioactivos de alquilamina cuaternaria alcoxilada para glifosato - Google Patents
Tensioactivos de alquilamina cuaternaria alcoxilada para glifosatoInfo
- Publication number
- AR108835A2 AR108835A2 ARP170101695A ARP170101695A AR108835A2 AR 108835 A2 AR108835 A2 AR 108835A2 AR P170101695 A ARP170101695 A AR P170101695A AR P170101695 A ARP170101695 A AR P170101695A AR 108835 A2 AR108835 A2 AR 108835A2
- Authority
- AR
- Argentina
- Prior art keywords
- imazaquinir
- glyphosate
- surfactants
- concentrate
- herbicidal concentrate
- Prior art date
Links
- 239000005562 Glyphosate Substances 0.000 title abstract 3
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 title abstract 3
- 229940097068 glyphosate Drugs 0.000 title abstract 3
- 150000003973 alkyl amines Chemical class 0.000 title 1
- 239000012141 concentrate Substances 0.000 abstract 4
- 239000004094 surface-active agent Substances 0.000 abstract 4
- 230000002363 herbicidal effect Effects 0.000 abstract 3
- 239000007788 liquid Substances 0.000 abstract 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 abstract 2
- PDYXIVPKOMYDOK-UHFFFAOYSA-N Glyphosate-monoammonium Chemical class [NH4+].OC(=O)CNCP(O)([O-])=O PDYXIVPKOMYDOK-UHFFFAOYSA-N 0.000 abstract 2
- 125000005210 alkyl ammonium group Chemical group 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- QZXCCPZJCKEPSA-UHFFFAOYSA-N chlorfenac Chemical compound OC(=O)CC1=C(Cl)C=CC(Cl)=C1Cl QZXCCPZJCKEPSA-UHFFFAOYSA-N 0.000 abstract 2
- 239000004009 herbicide Substances 0.000 abstract 2
- QYPPRTNMGCREIM-UHFFFAOYSA-N methylarsonic acid Chemical compound C[As](O)(O)=O QYPPRTNMGCREIM-UHFFFAOYSA-N 0.000 abstract 2
- FBUKVWPVBMHYJY-UHFFFAOYSA-N nonanoic acid Chemical compound CCCCCCCCC(O)=O FBUKVWPVBMHYJY-UHFFFAOYSA-N 0.000 abstract 2
- 229920006395 saturated elastomer Polymers 0.000 abstract 2
- XZIDTOHMJBOSOX-UHFFFAOYSA-N 2,3,6-TBA Chemical compound OC(=O)C1=C(Cl)C=CC(Cl)=C1Cl XZIDTOHMJBOSOX-UHFFFAOYSA-N 0.000 abstract 1
- 239000002794 2,4-DB Substances 0.000 abstract 1
- YIVXMZJTEQBPQO-UHFFFAOYSA-N 2,4-DB Chemical compound OC(=O)CCCOC1=CC=C(Cl)C=C1Cl YIVXMZJTEQBPQO-UHFFFAOYSA-N 0.000 abstract 1
- MZHCENGPTKEIGP-UHFFFAOYSA-N 2-(2,4-dichlorophenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C=C1Cl MZHCENGPTKEIGP-UHFFFAOYSA-N 0.000 abstract 1
- WNTGYJSOUMFZEP-UHFFFAOYSA-N 2-(4-chloro-2-methylphenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C=C1C WNTGYJSOUMFZEP-UHFFFAOYSA-N 0.000 abstract 1
- NUPJIGQFXCQJBK-UHFFFAOYSA-N 2-(4-isopropyl-4-methyl-5-oxo-4,5-dihydro-1H-imidazol-2-yl)-5-(methoxymethyl)nicotinic acid Chemical compound OC(=O)C1=CC(COC)=CN=C1C1=NC(C)(C(C)C)C(=O)N1 NUPJIGQFXCQJBK-UHFFFAOYSA-N 0.000 abstract 1
- YUVKUEAFAVKILW-UHFFFAOYSA-N 2-(4-{[5-(trifluoromethyl)pyridin-2-yl]oxy}phenoxy)propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=CC=C(C(F)(F)F)C=N1 YUVKUEAFAVKILW-UHFFFAOYSA-N 0.000 abstract 1
- OOLBCHYXZDXLDS-UHFFFAOYSA-N 2-[4-(2,4-dichlorophenoxy)phenoxy]propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=CC=C(Cl)C=C1Cl OOLBCHYXZDXLDS-UHFFFAOYSA-N 0.000 abstract 1
- MPPOHAUSNPTFAJ-UHFFFAOYSA-N 2-[4-[(6-chloro-1,3-benzoxazol-2-yl)oxy]phenoxy]propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=NC2=CC=C(Cl)C=C2O1 MPPOHAUSNPTFAJ-UHFFFAOYSA-N 0.000 abstract 1
- IAJOBQBIJHVGMQ-UHFFFAOYSA-N 2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid Chemical compound CP(O)(=O)CCC(N)C(O)=O IAJOBQBIJHVGMQ-UHFFFAOYSA-N 0.000 abstract 1
- LLWADFLAOKUBDR-UHFFFAOYSA-N 2-methyl-4-chlorophenoxybutyric acid Chemical compound CC1=CC(Cl)=CC=C1OCCCC(O)=O LLWADFLAOKUBDR-UHFFFAOYSA-N 0.000 abstract 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 abstract 1
- 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 abstract 1
- 239000005489 Bromoxynil Substances 0.000 abstract 1
- HSSBORCLYSCBJR-UHFFFAOYSA-N Chloramben Chemical compound NC1=CC(Cl)=CC(C(O)=O)=C1Cl HSSBORCLYSCBJR-UHFFFAOYSA-N 0.000 abstract 1
- QDHHCQZDFGDHMP-UHFFFAOYSA-N Chloramine Chemical compound ClN QDHHCQZDFGDHMP-UHFFFAOYSA-N 0.000 abstract 1
- NDUPDOJHUQKPAG-UHFFFAOYSA-N Dalapon Chemical compound CC(Cl)(Cl)C(O)=O NDUPDOJHUQKPAG-UHFFFAOYSA-N 0.000 abstract 1
- 239000005504 Dicamba Substances 0.000 abstract 1
- 239000005506 Diclofop Substances 0.000 abstract 1
- 239000005630 Diquat Substances 0.000 abstract 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical group C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 1
- 239000005977 Ethylene Substances 0.000 abstract 1
- YQVMVCCFZCMYQB-UHFFFAOYSA-N Flamprop Chemical compound C=1C=C(F)C(Cl)=CC=1N(C(C)C(O)=O)C(=O)C1=CC=CC=C1 YQVMVCCFZCMYQB-UHFFFAOYSA-N 0.000 abstract 1
- DHAHEVIQIYRFRG-UHFFFAOYSA-N Fluoroglycofen Chemical compound C1=C([N+]([O-])=O)C(C(=O)OCC(=O)O)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 DHAHEVIQIYRFRG-UHFFFAOYSA-N 0.000 abstract 1
- 239000005561 Glufosinate Substances 0.000 abstract 1
- 239000005566 Imazamox Substances 0.000 abstract 1
- 239000005574 MCPA Substances 0.000 abstract 1
- 239000005575 MCPB Substances 0.000 abstract 1
- 101150039283 MCPB gene Proteins 0.000 abstract 1
- 239000005595 Picloram Substances 0.000 abstract 1
- 229940100389 Sulfonylurea Drugs 0.000 abstract 1
- WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 abstract 1
- 239000005627 Triclopyr Substances 0.000 abstract 1
- 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 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- VGPYEHKOIGNJKV-UHFFFAOYSA-N asulam Chemical compound COC(=O)NS(=O)(=O)C1=CC=C(N)C=C1 VGPYEHKOIGNJKV-UHFFFAOYSA-N 0.000 abstract 1
- OTSAMNSACVKIOJ-UHFFFAOYSA-N azane;carbamoyl(ethoxy)phosphinic acid Chemical compound [NH4+].CCOP([O-])(=O)C(N)=O OTSAMNSACVKIOJ-UHFFFAOYSA-N 0.000 abstract 1
- ZOMSMJKLGFBRBS-UHFFFAOYSA-N bentazone Chemical compound C1=CC=C2NS(=O)(=O)N(C(C)C)C(=O)C2=C1 ZOMSMJKLGFBRBS-UHFFFAOYSA-N 0.000 abstract 1
- GINJFDRNADDBIN-FXQIFTODSA-N bilanafos Chemical compound OC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@@H](N)CCP(C)(O)=O GINJFDRNADDBIN-FXQIFTODSA-N 0.000 abstract 1
- IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 abstract 1
- SYJFEGQWDCRVNX-UHFFFAOYSA-N diquat Chemical compound C1=CC=[N+]2CC[N+]3=CC=CC=C3C2=C1 SYJFEGQWDCRVNX-UHFFFAOYSA-N 0.000 abstract 1
- -1 endotal Chemical compound 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- BGZZWXTVIYUUEY-UHFFFAOYSA-N fomesafen Chemical compound C1=C([N+]([O-])=O)C(C(=O)NS(=O)(=O)C)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 BGZZWXTVIYUUEY-UHFFFAOYSA-N 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 1
- NRXQIUSYPAHGNM-UHFFFAOYSA-N ioxynil Chemical compound OC1=C(I)C=C(C#N)C=C1I NRXQIUSYPAHGNM-UHFFFAOYSA-N 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- NDNKHWUXXOFHTD-UHFFFAOYSA-N metizoline Chemical compound CC=1SC2=CC=CC=C2C=1CC1=NCCN1 NDNKHWUXXOFHTD-UHFFFAOYSA-N 0.000 abstract 1
- 229960002939 metizoline Drugs 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- LNOPIUAQISRISI-UHFFFAOYSA-N n'-hydroxy-2-propan-2-ylsulfonylethanimidamide Chemical compound CC(C)S(=O)(=O)CC(N)=NO LNOPIUAQISRISI-UHFFFAOYSA-N 0.000 abstract 1
- JXTHEWSKYLZVJC-UHFFFAOYSA-N naptalam Chemical compound OC(=O)C1=CC=CC=C1C(=O)NC1=CC=CC2=CC=CC=C12 JXTHEWSKYLZVJC-UHFFFAOYSA-N 0.000 abstract 1
- 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 abstract 1
- NQQVFXUMIDALNH-UHFFFAOYSA-N picloram Chemical compound NC1=C(Cl)C(Cl)=NC(C(O)=O)=C1Cl NQQVFXUMIDALNH-UHFFFAOYSA-N 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- YROXIXLRRCOBKF-UHFFFAOYSA-N sulfonylurea Chemical class OC(=N)N=S(=O)=O YROXIXLRRCOBKF-UHFFFAOYSA-N 0.000 abstract 1
- REEQLXCGVXDJSQ-UHFFFAOYSA-N trichlopyr Chemical compound OC(=O)COC1=NC(Cl)=C(Cl)C=C1Cl REEQLXCGVXDJSQ-UHFFFAOYSA-N 0.000 abstract 1
- 125000004417 unsaturated alkyl group Chemical group 0.000 abstract 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
- 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
- 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)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Agronomy & Crop Science (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Toxicology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Reivindicación 1: Un concentrado herbicida líquido, acuoso y estable caracterizado porque comprende una sal glifosato de amonio y contiene al menos 120 g/l de e.a. glifosato, una relación molar ión amonio a glifosato entre 0,75 y 2,5, y dos tensioactivos de alquilamonio cuaternario alcoxilado correspondientes a la fórmula: RR’N⁽⁺⁾AB donde R es un grupo alquilo de cadena lineal o ramificada, saturado o insaturado que contiene entre 8 y 22 átomos de carbono, R’ es un grupo alquilo de cadena lineal o ramificada, saturado o insaturado que contiene entre 1 y 4 átomos de carbono, A es (R²O)ₚ(R³O)q(R⁴O)ᶻR⁸ y B es (R⁵O)ₚ’(R⁶O)q’(R⁷O)ᶻ’R⁹ donde cada R², R³, R⁴, R⁵, R⁶, y R⁷ es etileno, cada uno de R⁸, y R⁹ se selecciona independientemente del grupo formado por hidrógeno, metilo, y etilo, y p, q, p’, q’, z y z’ es cada uno independientemente entre sí un número entero entre 0 y 30 y la suma de (p + p’ + q + q’ + z + z’) es igual a al menos 2; donde la relación ponderal entre todos dichos uno o más agentes tensioactivos de alquilamonio cuaternario alcoxilado y e.a. de glifosato de amonio en dicho concentrado se encuentra entre 0,1:1 y 0,2:1 y la suma promedio de (p + p’ + q + q’ + z + z’) para uno de dichos dos tensioactivos se encuentra entre 2 y 5, y la suma promedio de (p + p’ + q + q’ + z + z’) para otro de dichos dos tensioactivos es de entre 5 y 15. Reivindicación 14: El concentrado herbicida líquido acuoso de la cláusula 1, caracterizado porque además comprende un co-herbicida. Reivindicación 15: El concentrado herbicida líquido acuoso de la cláusula 14, caracterizado porque dicho co-herbicida se selecciona del grupo que consiste en sulfonilurea, acifluorfen, asulam, benazolin, bentazon, bialafos, bromacilo, bromoxinil, cloramben, clopiralida, 2,4-D, 2,4-DB, dalapon, dicamba, diclorprop, diclofop, diquat, endotal, fenac, fenoxaprop, flamprop, fluazifop, fluoroglicofen, fomesafen, fosamina, glufosinato, haloxifop, imazamet, imazametabenz, imazamox, imazapir, imazaquin, imazetapir, ioxinil, MCPA, MCPB, mecoprop, ácido metilarsónico, naptalam, ácido nonanoico, paraquat, picloram, ácido sulfámico, 2,3,6-TBA, TCA y triclopir, sales de los mismos, y mezclas de los mismos.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US61259804P | 2004-09-23 | 2004-09-23 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR108835A2 true AR108835A2 (es) | 2018-10-03 |
Family
ID=35613907
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP050104010A AR053766A1 (es) | 2004-09-23 | 2005-09-26 | Tensioactivos de alquilamina cuarternaria alcoxilada para glifosato |
| ARP170101695A AR108835A2 (es) | 2004-09-23 | 2017-06-19 | Tensioactivos de alquilamina cuaternaria alcoxilada para glifosato |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP050104010A AR053766A1 (es) | 2004-09-23 | 2005-09-26 | Tensioactivos de alquilamina cuarternaria alcoxilada para glifosato |
Country Status (9)
| Country | Link |
|---|---|
| US (2) | US8722581B2 (es) |
| EP (2) | EP3036996A1 (es) |
| AR (2) | AR053766A1 (es) |
| AU (1) | AU2005286633B2 (es) |
| BR (2) | BRPI0515882A (es) |
| CA (2) | CA2848165C (es) |
| CR (1) | CR9075A (es) |
| MX (1) | MX2007003480A (es) |
| WO (1) | WO2006034426A1 (es) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2006023431A2 (en) | 2004-08-19 | 2006-03-02 | Monsanto Technology Llc | Glyphosate salt herbicidal composition |
| WO2006034426A1 (en) * | 2004-09-23 | 2006-03-30 | Akzo Nobel N.V. | Alkoxylated alkylamine quaternary surfactants for glyphosate |
| WO2006127501A2 (en) | 2005-05-24 | 2006-11-30 | Monsanto Technology Llc | Herbicide compatibility improvement |
| US8530385B2 (en) * | 2007-12-13 | 2013-09-10 | Donaghys Industries Limited | Herbicidal formulations for combinations of dimethylamine and potassium salts of glyphosate |
| CN105394079A (zh) * | 2007-12-13 | 2016-03-16 | 孟山都科技有限责任公司 | 一种高浓度的除草剂组合物和抑制植物生长的方法 |
| BRPI0914226B1 (pt) * | 2008-06-18 | 2021-01-19 | Stepan Company | concentrado contendo sal de glifosato de carga ultra alta, método para fabricação do mesmo e método para controlar vegetação indesejada |
| CA2989075C (en) | 2008-08-19 | 2018-07-24 | Akzo Nobel Chemicals International B.V. | Thickening glyphosate formulations with nitrogen containing surfactants |
| AR074976A1 (es) | 2008-09-29 | 2011-03-02 | Monsanto Technology Llc | Formulaciones de glifosfato que contienen agentes tensioactivos de amidoalquilaminas |
| RU2543281C2 (ru) | 2009-03-11 | 2015-02-27 | Акцо Нобель Н.В. | Состав гербицида, содержащий глифосат и алкоксилированные глицериды (варианты) и способ борьбы с нежелательной растительностью |
| EP2384625A1 (en) * | 2010-05-06 | 2011-11-09 | Akzo Nobel Chemicals International B.V. | Surfactant blends for auxin activity herbicides |
| US8324132B2 (en) | 2010-03-31 | 2012-12-04 | E. I. Du Pont De Nemours And Company | Mixture and method for controlling undesired vegetation |
| EP2520166A1 (en) | 2011-05-04 | 2012-11-07 | Taminco | New bisaminopropylamides and uses thereof in agricultural and detergent compositions |
| CN105025711A (zh) * | 2013-03-26 | 2015-11-04 | 阿克佐诺贝尔化学国际公司 | 浓缩的农业组合物 |
| CN109310095A (zh) | 2016-05-11 | 2019-02-05 | 孟山都技术公司 | 含酰胺基烷基胺表面活性剂的草甘膦制剂 |
| EP3996504A1 (en) * | 2019-07-11 | 2022-05-18 | Basf Se | Shear stable composition for spray drift control |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH072608B2 (ja) | 1986-12-04 | 1995-01-18 | モンサント コンパニ− | 水性濃厚除草剤配合物 |
| US5430005A (en) | 1991-08-02 | 1995-07-04 | Monsanto Company | Herbicidal compositions |
| US5462912A (en) * | 1991-10-09 | 1995-10-31 | Kao Corporation | Agricultural chemical composition enhancer comprising quaternary di(polyoxyalkylene) ammonium alkyl sulfates |
| US5317003A (en) | 1992-07-16 | 1994-05-31 | Monsanto Company | Herbicidal compositions comprising glyphosate salts and alkoxylated quaternary amine surfactants |
| MY111437A (en) * | 1992-07-31 | 2000-05-31 | Monsanto Co | Improved glyphosate herbicide formulation. |
| MY129957A (en) * | 1996-03-06 | 2007-05-31 | Kao Corp | Aqueous liquid agricultural composition |
| US5916863A (en) * | 1996-05-03 | 1999-06-29 | Akzo Nobel Nv | High di(alkyl fatty ester) quaternary ammonium compound from triethanol amine |
| NZ502397A (en) | 1997-07-22 | 2002-04-26 | Monsanto Co | Storage stable high-loaded ammonium glyphosate and surfactant formulations |
| US6992045B2 (en) * | 2000-05-19 | 2006-01-31 | Monsanto Technology Llc | Pesticide compositions containing oxalic acid |
| MY158895A (en) * | 2000-05-19 | 2016-11-30 | Monsanto Technology Llc | Potassium glyphosate formulations |
| PL221513B1 (pl) * | 2003-08-04 | 2016-04-29 | Dow Agrosciences Llc | Kompozycja chwastobójczego koncentratu o wysokiej mocy oraz sposób zwalczania niepożądanej roślinności |
| WO2006023431A2 (en) * | 2004-08-19 | 2006-03-02 | Monsanto Technology Llc | Glyphosate salt herbicidal composition |
| WO2006034426A1 (en) * | 2004-09-23 | 2006-03-30 | Akzo Nobel N.V. | Alkoxylated alkylamine quaternary surfactants for glyphosate |
-
2005
- 2005-09-23 WO PCT/US2005/034076 patent/WO2006034426A1/en active Application Filing
- 2005-09-23 CA CA2848165A patent/CA2848165C/en active Active
- 2005-09-23 US US11/575,800 patent/US8722581B2/en active Active
- 2005-09-23 BR BRPI0515882-6A patent/BRPI0515882A/pt active IP Right Grant
- 2005-09-23 EP EP15190163.4A patent/EP3036996A1/en not_active Withdrawn
- 2005-09-23 CA CA2581340A patent/CA2581340C/en active Active
- 2005-09-23 BR BR122015013990A patent/BR122015013990B1/pt active IP Right Grant
- 2005-09-23 MX MX2007003480A patent/MX2007003480A/es active IP Right Grant
- 2005-09-23 AU AU2005286633A patent/AU2005286633B2/en active Active
- 2005-09-23 EP EP05809918A patent/EP1809108A1/en not_active Ceased
- 2005-09-26 AR ARP050104010A patent/AR053766A1/es active IP Right Grant
-
2007
- 2007-04-20 CR CR9075A patent/CR9075A/es unknown
-
2014
- 2014-04-01 US US14/242,280 patent/US9596847B2/en active Active
-
2017
- 2017-06-19 AR ARP170101695A patent/AR108835A2/es active IP Right Grant
Also Published As
| Publication number | Publication date |
|---|---|
| BRPI0515882A (pt) | 2008-08-12 |
| US9596847B2 (en) | 2017-03-21 |
| CA2848165A1 (en) | 2006-03-30 |
| CA2848165C (en) | 2017-03-28 |
| CR9075A (es) | 2008-07-31 |
| EP3036996A1 (en) | 2016-06-29 |
| AR053766A1 (es) | 2007-05-23 |
| WO2006034426A1 (en) | 2006-03-30 |
| BR122015013990B1 (pt) | 2016-05-17 |
| AU2005286633B2 (en) | 2011-03-10 |
| CA2581340C (en) | 2014-05-27 |
| AU2005286633A1 (en) | 2006-03-30 |
| CA2581340A1 (en) | 2006-03-30 |
| EP1809108A1 (en) | 2007-07-25 |
| US20140213451A1 (en) | 2014-07-31 |
| US8722581B2 (en) | 2014-05-13 |
| MX2007003480A (es) | 2007-11-21 |
| US20090209425A1 (en) | 2009-08-20 |
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