54050
4-甲氧基苯酚
purum, ≥98.0% (HPLC)
别名:
4-MP, HQMME, MEHQ, 对愈创木酚, 对羟基苯甲醚, 氢醌单甲醚
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线性分子式:
CH3OC6H4OH
化学文摘社编号:
分子量:
124.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
205-769-8
Beilstein/REAXYS Number:
507924
MDL number:
产品名称
4-甲氧基苯酚, purum, ≥98.0% (HPLC)
InChI key
NWVVVBRKAWDGAB-UHFFFAOYSA-N
InChI
1S/C7H8O2/c1-9-7-4-2-6(8)3-5-7/h2-5,8H,1H3
SMILES string
COc1ccc(O)cc1
vapor density
4.3 (vs air)
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.)
Quality Level
Gene Information
human ... TYR(7299)
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Application
4-甲氧基苯酚可用于合成手性构件，如 1,2-二醇。它还具有多种工业应用，如抗氧化剂、聚合反应抑制剂和稳定剂。
General description
4-甲氧基苯酚，4-烷氧基苯酚，可由氢醌合成。在辣根过氧化物酶（酶催化剂）和十二烷基硫酸钠（表面活性剂）存在下进行聚合，得到聚（4-甲氧基苯酚）。
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Skin Sens. 1
存储类别
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
Paolo Ruzza et al.
Journal of medicinal chemistry, 52(15), 4973-4976 (2009-07-16)
We report the synthesis and preliminary in vitro biological evaluations of 4-[(4-hydroxyphenyl)sulfanyl]but-3-en-2-one, a compound designed as a potential bifunctional antimelanoma agent, bearing both a tyrosinase-activatable phenolic moiety and a GSH-reactive alpha,beta-unsaturated carbonyl group. Both the E (1) and Z (2)
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)
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)
Majid Y Moridani
Cancer letters, 243(2), 235-245 (2006-01-24)
In the current work we investigated for the first time the biochemical basis of 4-hydroxyanisole (4-HA) induced toxicity in B16-F0 melanoma cells. It was found that dicoumarol, a diaphorase inhibitor, and 1-bromoheptane, a GSH depleting agent, increased 4-HA induced toxicity
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