Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

Mequinol

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Mequinol
Clinical data
Other names4-Hydroxyanisole;para-Guaiacol
AHFS/Drugs.comInternational Drug Names
MedlinePlusa682437
Routes of
administration
Topical
ATC code
Legal status
Legal status
Identifiers
  • 4-Methoxyphenol
CAS Number
PubChemCID
IUPHAR/BPS
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard(EPA)
ECHA InfoCard100.005.246Edit 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
  (verify)

Mequinol,MeHQ or4-methoxyphenol, is anorganic compound with the formulaCH3OC6H4OH. It is aphenol with amethoxy group in the para position. A colorless solid, it is used indermatology[1] andorganic chemistry.[2]

Use in dermatology

[edit]

Mequinol is a commonactive ingredient intopical drugs used forskin depigmentation. As a topical drug mequinol is often mixed withtretinoin, a topicalretinoid. A commonformulation for this drug is anethanolic solution of 2% mequinol and 0.01% tretinoin by mass.[1]Dermatologists commonly prescribe the drug to treatliver spots.

Lower dosages of mequinol have been used in conjunction with aQ-switchedlaser to depigment skin in patients withdisseminatedidiopathicvitiligo.[3]

Organic chemistry

[edit]

In organic chemistry 4-methoxyphenol is used as apolymerisation inhibitor (e.g.acrylates orstyrene monomers).[2]

4-Methoxyphenol can be produced fromp-benzoquinone andmethanol via afree radical reaction.[4][5]

Safety

[edit]

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

See also

[edit]

References

[edit]
  1. ^abStiefel Laboratories, Inc."Full Prescribing Information"(PDF). US Food and Drug Administration. Retrieved2 January 2015.
  2. ^abHudnall PM (2000). "Hydroquinone".Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH.doi:10.1002/14356007.a13_499.ISBN 978-3-527-30673-2.
  3. ^Komen L, Zwertbroek L, Burger SJ, van der Veen JP, de Rie MA, Wolkerstorfer A (December 2013). "Q-switched laser depigmentation in vitiligo, most effective in active disease".The British Journal of Dermatology.169 (6):1246–51.doi:10.1111/bjd.12571.PMID 23909405.S2CID 43542975.
  4. ^Gambarotti C, Melone L, Punta C, Shisodia SU (2013). "Selective Monoetherification of 1,4-Hydroquinone Promoted by NaNO2".Current Organic Chemistry.17 (10):1108–1113.doi:10.2174/1385272811317100011.
  5. ^US 4933504, Correale M, Panseri P, Romano U, Minisci F, "Process for the preparation of mono-ethers of hydroquinones" 
  6. ^"4-Methoxyphenol".NIOSH Pocket Guide to Chemical Hazards. CDC. Retrieved2015-11-20.

External links

[edit]
  • "Mequinol".Drug Information Portal. U.S. National Library of Medicine.
Otherdermatological preparations (D11)
Anti-seborrheics
Skin lightening
Skin darkening
Anti-inflammatories
Alopecia treatments
Hair growth inhibitors
Others
Retrieved from "https://en.wikipedia.org/w/index.php?title=Mequinol&oldid=1252495047"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2025 Movatter.jp