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mequinol

Structure via PubChem · Public domain (PubChem)

EntityQ2862455· pop 15· linked from 82 articles

Also known as 4-hydroxyanisole, BMS-181158, Leucobasal®, Leucodine B, p-hydroxyanisole, p-Guaiacol, 4-Methoxyphenol

Mequinol, MeHQ or 4-methoxyphenol, is an organic compound with the formula . It is a phenol with a methoxy group in the para position. A colorless solid, it is used in dermatology and organic chemistry.

Chemical data

Formula
C7H8O2
Molecular weight
124.14 g/mol
IUPAC name
4-methoxyphenol
SMILES
COC1=CC=C(C=C1)O
InChIKey
NWVVVBRKAWDGAB-UHFFFAOYSA-N
XLogP
1.3
Polar surface area
29.5 Ų
H-bond donors
1
H-bond acceptors
2
Formal charge
0

via PubChem

Drug data · ChEMBL

Max clinical phase
Approved
Molecule type
Small molecule
First approval
1999
Admin. routes
topical

via ChEMBL · EBI

Wikidata facts

Mass
124.052
Has use
medication
Show 13 more facts
melting point
56
chemical formula
C₇H₈O₂
boiling point
469
canonical SMILES
COC1=CC=C(C=C1)O
NIOSH Pocket Guide ID
0390
density
1.55
flash point
270
solubility
4
ionization energy
7.5
vapor pressure
0.01
time-weighted average exposure limit
5
subject has role
antioxidant
Commons category
4-Methoxyphenol
Sources (3)

via Wikidata · CC0

~1 min read

Encyclopedic overview

6 sections
Contents
  • Use in dermatology
  • Organic chemistry
  • Safety
  • See also
  • References
  • External links

Mequinol, MeHQ or 4-methoxyphenol, is an organic compound with the formula . It is a phenol with a methoxy group in the para position. A colorless solid, it is used in dermatology and organic chemistry.

==Use in dermatology== Mequinol is a common active ingredient in topical drugs used for skin depigmentation. As a topical drug mequinol is often mixed with tretinoin, a topical retinoid. A common formulation for this drug is an ethanolic solution of 2% mequinol and 0.01% tretinoin by mass. Dermatologists commonly prescribe the drug to treat liver spots.

Excerpted from Wikipedia’s “mequinol” article, available under the CC BY-SA 4.0 licence.