54050
4-Methoxyphenol
purum, ≥98.0% (HPLC)
Sinónimos:
4-Hydroxyanisole, 4-MP, HQMME, Hydroquinone monomethyl ether, MEHQ, p-Guaiacol
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Fórmula lineal:
CH3OC6H4OH
Número CAS:
Peso molecular:
124.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
205-769-8
Beilstein/REAXYS Number:
507924
MDL number:
Assay:
≥98.0% (HPLC)
Servicio técnico
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Permítanos ayudarlevapor density
4.3 (vs air)
Quality Level
vapor pressure
<0.01 mmHg ( 20 °C)
grade
purum
assay
≥98.0% (HPLC)
autoignition temp.
789 °F
impurities
≤2% hydroquinone dimethyl ether
bp
243 °C (lit.)
mp
54-56 °C, 55-57 °C (lit.)
SMILES string
COc1ccc(O)cc1
InChI
1S/C7H8O2/c1-9-7-4-2-6(8)3-5-7/h2-5,8H,1H3
InChI key
NWVVVBRKAWDGAB-UHFFFAOYSA-N
Gene Information
human ... TYR(7299)
General description
4-Methoxyphenol, a 4-alkoxyphenol, can be synthesized from hydroquinone. It undergoes polymerization in the presence of horseradish peroxidase (enzymatic catalyst) and sodium dodecyl sulfate (surfactant) to afford poly(4-methoxyphenol).
Application
4-Methoxyphenol may be used in to synthesize chiral building blocks such as 1,2-diols. It also has various industrial applications, such as an antioxidant, an inhibitor for the polymerization reactions and a stabilizing agent.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Skin Sens. 1
Clase de almacenamiento
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
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Enantioselective ring opening of epoxides with 4-methoxyphenol catalyzed by gallium heterobimetallic complexes: An efficient method for the synthesis of optically active 1, 2-diol monoethers.
Iida T, et al.
Angewandte Chemie (International Edition in English), 37(16), 2223-2226 (1998)
Simple synthesis of non-symmetric 1, 4-dialkoxybenzenes via 4-alkoxyphenols.
Radoslaw M, et al.
Organic Communications, 9(1) (2016)
Synthesis of poly (4-methoxyphenol) by enzyme-catalyzed polymerization and evaluation of its antioxidant activity.
Zheng K, et al.
New. J. Chem., 37(12), 4185-4191 (2013)