AR123785A1 - Composición de concentrado hidrosoluble - Google Patents
Composición de concentrado hidrosolubleInfo
- Publication number
- AR123785A1 AR123785A1 ARP210102835A ARP210102835A AR123785A1 AR 123785 A1 AR123785 A1 AR 123785A1 AR P210102835 A ARP210102835 A AR P210102835A AR P210102835 A ARP210102835 A AR P210102835A AR 123785 A1 AR123785 A1 AR 123785A1
- Authority
- AR
- Argentina
- Prior art keywords
- formula
- water
- compound
- soluble concentrate
- acid
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title abstract 9
- 239000004550 soluble concentrate Substances 0.000 title abstract 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 7
- 239000002253 acid Substances 0.000 abstract 4
- 229910052784 alkaline earth metal Inorganic materials 0.000 abstract 3
- -1 alkaline earth metal salts Chemical class 0.000 abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 abstract 3
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 2
- YIVXMZJTEQBPQO-UHFFFAOYSA-N 2,4-DB Chemical compound OC(=O)CCCOC1=CC=C(Cl)C=C1Cl YIVXMZJTEQBPQO-UHFFFAOYSA-N 0.000 abstract 2
- 239000002794 2,4-DB Substances 0.000 abstract 2
- 239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 abstract 2
- FNQXFLGLLXHONX-UHFFFAOYSA-N 2-chloro-2-phenoxybutanoic acid Chemical compound CCC(Cl)(C(O)=O)OC1=CC=CC=C1 FNQXFLGLLXHONX-UHFFFAOYSA-N 0.000 abstract 2
- LLWADFLAOKUBDR-UHFFFAOYSA-N 2-methyl-4-chlorophenoxybutyric acid Chemical compound CC1=CC(Cl)=CC=C1OCCCC(O)=O LLWADFLAOKUBDR-UHFFFAOYSA-N 0.000 abstract 2
- 239000005574 MCPA Substances 0.000 abstract 2
- 239000005575 MCPB Substances 0.000 abstract 2
- WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 abstract 2
- 239000002671 adjuvant Substances 0.000 abstract 2
- 238000010790 dilution Methods 0.000 abstract 2
- 239000012895 dilution Substances 0.000 abstract 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 1
- HXKWSTRRCHTUEC-UHFFFAOYSA-N 2,4-Dichlorophenoxyaceticacid Chemical compound OC(=O)C(Cl)OC1=CC=C(Cl)C=C1 HXKWSTRRCHTUEC-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
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 abstract 1
- ZLSWBLPERHFHIS-UHFFFAOYSA-N Fenoprop Chemical compound OC(=O)C(C)OC1=CC(Cl)=C(Cl)C=C1Cl ZLSWBLPERHFHIS-UHFFFAOYSA-N 0.000 abstract 1
- 229910019142 PO4 Inorganic materials 0.000 abstract 1
- 239000004480 active ingredient Substances 0.000 abstract 1
- 239000003513 alkali Substances 0.000 abstract 1
- 229910052783 alkali metal Inorganic materials 0.000 abstract 1
- 150000003863 ammonium salts Chemical group 0.000 abstract 1
- 239000006184 cosolvent Substances 0.000 abstract 1
- 150000005690 diesters Chemical class 0.000 abstract 1
- 238000007865 diluting Methods 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 abstract 1
- 239000010452 phosphate Substances 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
- A01N39/00—Biocides, pest repellants or attractants, or plant growth regulators containing aryloxy- or arylthio-aliphatic or cycloaliphatic compounds, containing the group or, e.g. phenoxyethylamine, phenylthio-acetonitrile, phenoxyacetone
- A01N39/02—Aryloxy-carboxylic acids; Derivatives thereof
- A01N39/04—Aryloxy-acetic acids; Derivatives thereof
-
- 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
- A01N25/02—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 containing liquids as carriers, diluents or solvents
- A01N25/04—Dispersions, emulsions, suspoemulsions, suspension concentrates or gels
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01P—BIOCIDAL, PEST REPELLANT, PEST ATTRACTANT OR PLANT GROWTH REGULATORY ACTIVITY OF CHEMICAL COMPOUNDS OR PREPARATIONS
- A01P13/00—Herbicides; Algicides
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Plant Pathology (AREA)
- Environmental Sciences (AREA)
- Zoology (AREA)
- Engineering & Computer Science (AREA)
- Pest Control & Pesticides (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Dentistry (AREA)
- Agronomy & Crop Science (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Toxicology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Jellies, Jams, And Syrups (AREA)
Abstract
Reivindicación 1: Una composición de concentrado hidrosoluble que comprende: a) un principio activo agrícola seleccionado entre sales de ácidos fenoxi, donde la sal del ácido fenoxi se selecciona entre sales de amonio, sales de metales alcalinos o alcalinotérreos o una combinación de estas; b) un codisolvente seleccionado a partir del compuesto de fórmula (1): R¹OOC-R²-CONR³R⁴ (1) donde R¹ es un alquilo C₁₋₃; R² es un alquilo C₁₋₆ divalente lineal o ramificado; R³ y R⁴ son cada uno independientemente grupos metilo o etilo; y c) un adyuvante seleccionado entre los mono- o diésteres de tipo fosfato de fórmula (2): (R⁵O)ₘ-P(=O)(OM)ₙ (2) donde R⁵ es un grupo alquilo opcionalmente polialcoxilado, m y n son igual a 1 ó 2 siempre que la suma de m y n sea igual a 3, y M es un átomo de hidrógeno, un catión de un metal alcalino, un catión de un metal alcalinotérreo o un ión de amonio. Reivindicación 2: La composición de concentrado hidrosoluble de acuerdo con la reivindicación 1, donde el ácido fenoxi es uno o más que se seleccionan del grupo constituido por el ácido 2-metil-4-clorofenoxiacético (MCPA), ácido 4-(4-cloro-o-toliloxi)butírico (MCPB), ácido metilclorofenoxipropiónico (MCPP), ácido 2,4-diclorofenoxiacético (2,4-D), ácido 4-(2,4-diclorofenoxi)butírico (2,4-DB), ácido 2,4,5-triclorofenoxiacético (2,4,5-T), Diclorprop y Fenoprop. Reivindicación 5: La composición de concentrado hidrosoluble de acuerdo con cualquiera de las reivindicaciones 1 a 4, donde el compuesto de fórmula (1) es una mezcla que comprende: un compuesto de fórmula (1) donde R² es -CH(CH₂-CH₃)-CH₂-, un compuesto de fórmula (1) donde R² es -CH₂-CH(CH₂-CH₃)-, un compuesto de fórmula (1) donde R² es -CH(CH₃)-CH₂-CH₂- y un compuesto de fórmula (1) donde R² es -CH₂-CH₂-CH(CH₃)-. Reivindicación 6: La composición de concentrado hidrosoluble de acuerdo con las reivindicaciones 1, donde R⁵ es un alquilo C₄₋₁₂ opcionalmente etoxilado. Reivindicación 9: La composición de concentrado hidrosoluble de acuerdo con cualquiera de las reivindicaciones 1 a 8, donde la composición de concentrado hidrosoluble comprende además otro adyuvante seleccionado entre d) un compuesto de tipo betaína de fórmula (3): R⁶CONH-R⁷-N⁺-(R⁸R⁹)-CH₂COO⁻ (3) donde R⁶ es un alquilo C₃₋₃₀ lineal o ramificado; R⁷ es un alquilo C₁₋₄ divalente lineal o ramificado; R⁸ y R⁹ son cada uno independientemente un alquilo C₁₋₃. Reivindicación 11: Una dilución preparada diluyendo la composición de concentrado hidrosoluble de acuerdo con cualquiera de las reivindicaciones 1 a 10 con agua de 10 a 2000 veces. Reivindicación 12: Un método para controlar el crecimiento de plantas no deseadas, que comprende un paso de aplicar a las plantas o al emplazamiento de la planta no deseada una cantidad eficaz de la dilución de acuerdo con la reivindicación 11.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/EP2020/079256 WO2022078615A1 (en) | 2020-10-16 | 2020-10-16 | Water-soluble concentrate composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR123785A1 true AR123785A1 (es) | 2023-01-11 |
Family
ID=72944158
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP210102835A AR123785A1 (es) | 2020-10-16 | 2021-10-14 | Composición de concentrado hidrosoluble |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US20230397606A1 (es) |
| EP (1) | EP4228409A1 (es) |
| CN (1) | CN116322323A (es) |
| AR (1) | AR123785A1 (es) |
| AU (1) | AU2020472085A1 (es) |
| BR (1) | BR112023005407A2 (es) |
| CA (1) | CA3193327A1 (es) |
| WO (1) | WO2022078615A1 (es) |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5877112A (en) * | 1997-08-27 | 1999-03-02 | Helena Chemical Company | Agricultural formulation |
| WO2007030887A1 (en) * | 2005-09-16 | 2007-03-22 | Nufarm Australia Limited | Herbicide composition |
| BRPI0905784A2 (pt) * | 2008-01-25 | 2015-07-14 | Rhodia Operations | Uso de um composto esteramida, processos de preparação de um composto esteramida e composto esteramida |
| WO2013053834A1 (fr) * | 2011-10-13 | 2013-04-18 | Rhodia Operations | Composition, procédé d'obtention de la composition et formulation phytosanitaire la comprenant |
| MX2016013567A (es) * | 2014-04-17 | 2017-03-10 | Dow Agrosciences Llc | Concentrados pesticidas acuosos que contienen aceites parafinicos y metodos de uso. |
-
2020
- 2020-10-16 CN CN202080106199.XA patent/CN116322323A/zh active Pending
- 2020-10-16 BR BR112023005407A patent/BR112023005407A2/pt unknown
- 2020-10-16 AU AU2020472085A patent/AU2020472085A1/en active Pending
- 2020-10-16 US US18/249,355 patent/US20230397606A1/en active Pending
- 2020-10-16 EP EP20793348.2A patent/EP4228409A1/en active Pending
- 2020-10-16 WO PCT/EP2020/079256 patent/WO2022078615A1/en active Application Filing
- 2020-10-16 CA CA3193327A patent/CA3193327A1/en active Pending
-
2021
- 2021-10-14 AR ARP210102835A patent/AR123785A1/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CA3193327A1 (en) | 2022-04-21 |
| AU2020472085A1 (en) | 2023-05-04 |
| WO2022078615A1 (en) | 2022-04-21 |
| EP4228409A1 (en) | 2023-08-23 |
| BR112023005407A2 (pt) | 2023-04-25 |
| US20230397606A1 (en) | 2023-12-14 |
| CN116322323A (zh) | 2023-06-23 |
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