Hydroquinone
|
WikiDoc Resources for Hydroquinone |
|
Articles |
|---|
|
Most recent articles on Hydroquinone Most cited articles on Hydroquinone |
|
Media |
|
Powerpoint slides on Hydroquinone |
|
Evidence Based Medicine |
|
Clinical Trials |
|
Ongoing Trials on Hydroquinone at Clinical Trials.gov Clinical Trials on Hydroquinone at Google
|
|
Guidelines / Policies / Govt |
|
US National Guidelines Clearinghouse on Hydroquinone
|
|
Books |
|
News |
|
Commentary |
|
Definitions |
|
Patient Resources / Community |
|
Patient resources on Hydroquinone Discussion groups on Hydroquinone Patient Handouts on Hydroquinone Directions to Hospitals Treating Hydroquinone Risk calculators and risk factors for Hydroquinone
|
|
Healthcare Provider Resources |
|
Causes & Risk Factors for Hydroquinone |
|
Continuing Medical Education (CME) |
|
International |
|
|
|
Business |
|
Experimental / Informatics |
Please Take Over This Page and Apply to be Editor-In-Chief for this topic: There can be one or more than one Editor-In-Chief. You may also apply to be an Associate Editor-In-Chief of one of the subtopics below. Please mail us [1] to indicate your interest in serving either as an Editor-In-Chief of the entire topic or as an Associate Editor-In-Chief for a subtopic. Please be sure to attach your CV and or biographical sketch.
Overview
Hydroquinone, also benzene-1,4-diol or quinol, is an aromatic organic compound which is a type of phenol, having the chemical formula C6H4(OH)2. Its chemical structure, shown in the table at right, has two hydroxyl groups bonded to a benzene ring in a para position. It is a white granular solid at room temperature and pressure.
Nomenclature
Hydroquinone is the name recommended by the International Union of Pure and Applied Chemistry (IUPAC) in its 1993 Recommendations for the Nomenclature of Organic Chemistry.[2]
Properties
Hydroquinone can undergo mild oxidation to convert to the compound parabenzoquinone, C6H4O2, often called p-quinone or simply quinone. Reduction of quinone reverses this reaction back to hydroquinone. Some biochemical compounds in nature have this sort of hydroquinone or quinone section in their structures, such as Coenzyme Q, and can undergo similar redox interconversions.
The hydroxyl groups of hydroquinone are quite weakly acidic. Hydroquinone can lose an H+ from one of the hydroxyls to form a monophenolate ion or lose an H+ from both to form a diphenolate ion.
Uses
Hydroquinone has a variety of uses principally associated with its action as a reducing agent which is soluble in water. It is a major component in most photographic developers where, with the compound Metol, it reduces silver halides to elemental silver.
In human medicine, hydroquinone is used as a topical application in skin whitening to reduce the color of skin as it does not have the same predisposition to cause dermatitis as Metol does. This use is banned in some countries (e.g. France) because of fears of a cancer risk.
The disodium diphenolate salt of hydroquinone is used as an alternating comonomer unit in the production of the polymer PEEK.
As a polymerization inhibitor, hydroquinone prevents polymerization of acrylic acid, methyl methacrylate, etc.
It is also used as a raw material of herbicides, rubber antioxidants and dye stuffs.
Natural occurrences
Hydroquinones are one of the two primary reagents in the defensive glands of bombardier beetles, along with hydrogen peroxide (and perhaps other chemicals, depending on the species), which collect in a reservoir. The reservoir opens through a muscle-controlled valve onto a thick-walled reaction chamber. This chamber is lined with cells that secrete catalases and peroxidases. When the contents of the reservoir are forced into the reaction chamber, the catalases and peroxidases rapidly break down the hydrogen peroxide and catalyze the oxidation of the hydroquinones into p-quinones. These reactions release free oxygen and generate enough heat to bring the mixture to the boiling point and vaporize about a fifth of it, producing a hot spray from the beetle's abdomen.
See also
References
- ^ Panico, R.; & Powell, W. H. (Eds.) (1994). A Guide to IUPAC Nomenclature of Organic Compounds 1993. Oxford: Blackwell Science. ISBN 0-632-03488-2.
External links
- International Chemical Safety Card 0166
- NIOSH Pocket Guide to Chemical Hazards
- IARC Monograph: "Hydroquinone"
- Template:Ecb
- IUPAC Nomenclature of Organic Chemistry (online version of the "Blue Book")