Identification | Back Directory | [Name]
3,4-D | [CAS]
588-22-7 | [Synonyms]
3,4-D 3,4-da 3,4-d (iso) 3,4-D solution LABOTEST-BB LT00233086 Adrenaline Impurity 70 3,4-DICHLOROPHENOXYACETIC ACID (3,4-dichlorophenoxy)-aceticaci 2-(3,4-dichlorophenoxy)acetic acid 2-(3,4-dichlorophenoxy)ethanoic acid Acetic acid, 2-(3,4-dichlorophenoxy)- 3,4-Dichlorophenoxyacetic acid solution | [EINECS(EC#)]
209-612-4 | [Molecular Formula]
C8H6Cl2O3 | [MDL Number]
MFCD00004303 | [MOL File]
588-22-7.mol | [Molecular Weight]
221.04 |
Chemical Properties | Back Directory | [Melting point ]
138-140 °C(lit.)
| [Boiling point ]
316.96°C (rough estimate) | [density ]
1.4564 (rough estimate) | [refractive index ]
1.5000 (estimate) | [Fp ]
2 °C | [storage temp. ]
APPROX 4°C
| [solubility ]
DMSO (Slightly), Methanol (Slightly) | [form ]
Crystalline Powder | [pka]
2.99±0.10(Predicted) | [color ]
White | [Water Solubility ]
457.6mg/L(25 ºC) |
Hazard Information | Back Directory | [Uses]
3,4-Dichlorophenoxyacetic acid was used in the synthesis of layered organic-inorganic nanohybrid material, zinc-aluminum-3,4-dicholorophenoxyacetate. | [Definition]
ChEBI: A chlorophenoxyacetic acid that is phenoxyacetic acid in which the hydrogens at positions 3 and 4 of the phenyl group are replaced by chlorines. | [General Description]
3,4-Dichlorophenoxyacetic acid is a phenoxyacetic herbicide. | [Synthesis]
GENERAL PROCEDURE: To a stirred solution of 4j (2.5 g, 9.8 mmol) in methanol (30 mL) was added 3N sodium hydroxide solution (13.1 mL, 39.3 mmol). After stirring for 1 h at room temperature, the reaction mixture was diluted with water (100 mL), acidified with 3N hydrochloric acid to pH < 7, and subsequently extracted with dichloromethane (100 mL x 2). The organic layers were combined, washed with saturated sodium chloride solution, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to afford 3,4-dichlorophenoxyacetic acid (2.12 g, 97% yield) as a white solid. The product was characterized by 1H NMR (300 MHz, DMSO-d6): δ 7.49 (d, J=8.8 Hz, 1H), 7.21 (s, 1H), 6.92 (d, J=8.8 Hz, 1H), 4.73 (s, 2H). | [References]
[1] Bulletin of the Korean Chemical Society, 2015, vol. 36, # 10, p. 2549 - 2552 [2] Patent: WO2017/212423, 2017, A1. Location in patent: Page/Page column 97; 98 |
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Energy Chemical
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