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Merck
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13-1980

Sigma-Aldrich

4-Methoxyphenol

SAJ first grade, ≥97.0%

Sinónimos:

4-Hydroxyanisole, 4-MP, HQMME, Hydroquinone monomethyl ether, MEHQ, p-Guaiacol

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About This Item

Fórmula lineal:
CH3OC6H4OH
Número de CAS:
150-76-5
Peso molecular:
124.14
Beilstein/REAXYS Number:
507924
EC Number:
205-769-8
MDL number:
MFCD00002332
UNSPSC Code:
12352104
PubChem Substance ID:
329750097
grade:
SAJ first grade
assay:
≥97.0%
bp:
243 °C (lit.)
vapor pressure:
<0.01 mmHg ( 20 °C)

grade

SAJ first grade

vapor density

4.3 (vs air)

vapor pressure

<0.01 mmHg ( 20 °C)

assay

≥97.0%

autoignition temp.

789 °F

availability

available only in Japan

bp

243 °C (lit.)

mp

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)

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pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Skin Sens. 1

Storage Class

11 - Combustible Solids

wgk_germany

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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Certificados de análisis (COA)

Lot/Batch Number
U7845
U1464
A9161
A9145
A6244

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Byeoung-Soo Park et al.
Journal of agricultural and food chemistry, 51(1), 295-300 (2002-12-28)
Volatiles were isolated from the dried inner bark of Tabebuia impetiginosa using steam distillation under reduced pressure followed by continuous liquid-liquid extraction. The extract was analyzed by gas chromatography and gas chromatography-mass spectrometry. The major volatile constituents of T. impetiginosa
Lisa M Colosi et al.
Environmental science & technology, 41(3), 891-896 (2007-03-03)
Natural organic matter (NOM) of hydroxylated aromatic character can undergo catalyst-mediated self-coupling reactions to form larger molecular aggregates. Indeed, such reactions are central to natural humification processes. Nonhydroxylated persistent aromatic contaminants such as polychlorinated biphenyls (PCBs) are, conversely, inert with
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
Jean Paul Ortonne et al.
Cutis, 74(4), 261-264 (2004-11-24)
The objective of this open-label, noncontrolled study was to evaluate the safety of a combination solution containing 4-hydroxyanisole (mequinol) 2%/tretinoin 0.01% (Solagé) with a sunscreen in the treatment of solar lentigines. The study included a total of 406 subjects for
Ronald Vargas et al.
Water research, 44(3), 911-917 (2009-11-20)
Dearomatization levels during electrochemical oxidation of p-methoxyphenol (PMP) and p-nitrophenol (PNP) have been determined through UV-Vis spectroscopy using solid phase extraction (UV-Vis/SPE). The results show that the method is satisfactory to determine the ratio between aromatic compounds and aliphatic acids
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