Mequinol

Chemical compound From Wikipedia, the free encyclopedia

Mequinol, MeHQ or 4-methoxyphenol, is an organic compound with the formula CH3OC6H4OH. It is a phenol with a methoxy group in the para position. A colorless solid, it is used in dermatology[1] and organic chemistry.[2]

Quick facts Clinical data, Other names ...
Mequinol
Clinical data
Other names4-Hydroxyanisole; para-Guaiacol
AHFS/Drugs.comInternational Drug Names
MedlinePlusa682437
Routes of
administration
Topical
ATC code
Legal status
Legal status
  • CA: Unscheduled
  • US: ℞-only and Unscheduled
  • In general: unscheduled
Identifiers
  • 4-Methoxyphenol
CAS Number
PubChem CID
IUPHAR/BPS
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard100.005.246 Edit this at Wikidata
Chemical and physical data
FormulaC7H8O2
Molar mass124.139 g·mol−1
Density1.55 g/cm3
Melting point52.5 °C (126.5 °F)
Boiling point243 °C (469 °F)
  • InChI=1S/C7H8O2/c1-9-7-4-2-6(8)3-5-7/h2-5,8H,1H3 checkY
  • Key:NWVVVBRKAWDGAB-UHFFFAOYSA-N checkY
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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.[1] Dermatologists commonly prescribe the drug to treat liver spots.

Lower dosages of mequinol have been used in conjunction with a Q-switched laser to depigment skin in patients with disseminated idiopathic vitiligo.[3]

Organic chemistry

In organic chemistry 4-methoxyphenol is used as a polymerisation inhibitor (e.g. acrylates or styrene monomers).[2]

4-Methoxyphenol can be produced from p-benzoquinone and methanol via a free radical reaction.[4][5]

Safety

The U.S. National Institute for Occupational Safety and Health (NIOSH) has set a recommended exposure limit (REL) of 5 mg/m3 over an 8-hour workday.[6]

See also

References

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