Mequinol
100px | |
Systematic (IUPAC) name | |
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4-Methoxyphenol
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Clinical data | |
AHFS/Drugs.com | International Drug Names |
MedlinePlus | a682437 |
Legal status |
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Routes of administration |
Topical |
Identifiers | |
CAS Number | 150-76-5 ![]() |
ATC code | D11AX06 (WHO) |
PubChem | CID: 9015 |
IUPHAR/BPS | 6827 |
ChemSpider | 8665 ![]() |
UNII | 6HT8U7K3AM ![]() |
KEGG | D04926 ![]() |
ChEMBL | CHEMBL544 ![]() |
Synonyms | 4-Hydroxyanisole; para-Guaiacol |
Chemical data | |
Formula | C7H8O2 |
Molecular mass | 124.13722 g/mol |
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Physical data | |
Density | 1.55 g/cm3 |
Melting point | 52.5 °C (126.5 °F) |
Boiling point | 243 °C (469 °F) |
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Mequinol, MEHQ or 4-Methoxyphenol, is a phenol used in dermatology[1] and organic chemistry.[2]
Contents
Uses
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 solar lentigines, liver spots, or age 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 to inhibit the radical polymerization of monomers (e.g. acrylates or styrene monomers).[2]
Preparation
4-Methoxyphenol is produced from p-benzoquinone and methanol via a free radical reaction.[4][5]
Safety
People can be exposed to 4-methoxyphenol in the workplace by breathing it in, skin absorption, swallowing it, skin contact, and eye contact. The 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
- Monobenzone (benzyloxyphenol)
- Hydroquinone
- Guaiacol
- 2-Hydroxy-5-methoxybenzaldehyde
References
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