Hydroxyacetone
Hydroxyacetone
Chemical compound
Hydroxyacetone, also known as acetol, is the organic chemical with the formula CH3C(O)CH2OH. It consists of a primary alcohol substituent on acetone. It is an α-hydroxyketone, also called a ketol, and is the simplest hydroxy ketone structure. It is a colorless, distillable liquid.
Names | |
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Preferred IUPAC name
1-Hydroxypropan-2-one | |
Systematic IUPAC name
1-Hydroxyacetone | |
Other names
1-Hydroxy-2-propanone Acetomethyl alcohol Acetol | |
Identifiers | |
3D model (JSmol) |
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605368 | |
ChemSpider | |
ECHA InfoCard | 100.003.750 |
EC Number |
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PubChem CID |
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UNII | |
CompTox Dashboard (EPA) |
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Properties | |
C3H6O2 | |
Molar mass | 74.079 g·mol−1 |
Appearance | Colorless liquid |
Odor | Sweet |
Density | 1.059 g/cm3[1] |
Melting point | −17 °C (1 °F; 256 K) |
Boiling point | 145–146 °C (293–295 °F; 418–419 K) |
Vapor pressure | 7.5 hPa at 20 °C[2] |
Refractive index (nD) |
1.415[1] |
Hazards | |
GHS labelling: | |
H226[2] | |
Flash point | 56 °C (closed cup)[2] |
Explosive limits | Upper limit: 14.9%(V) Lower limit: 3%(V)[2] |
Lethal dose or concentration (LD, LC): | |
LD50 (median dose) |
2200 mg/kg (rat, oral)[3] |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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It is produced commercially by dehydration of glycerol.[4]
Hydroxyacetone is commercially available, but it also may be synthesized on a laboratory scale by a substitution reaction on bromoacetone.[5]
It undergoes rapid polymerization, including forming a hemiacetal cyclic dimer. Under alkaline conditions, it undergoes a rapid aldol condensation.
Hydroxyacetone can be produced by degradation of various sugars. In foods, it is formed by the Maillard reaction. It reacts further to form other compounds with various aromas.[6] As such it finds some use as a flavoring.
- Acyloin, the simplest secondary α-hydroxy ketone.
- Nodzu, Ryuzaburo (1935). "On the Action of Phosphate Upon Hexoses. I. The Formation of Acetol From Glucose in Acidic Solution of Potassium Phosphate". Bull. Chem. Soc. Jpn. 10 (3): 122–130. doi:10.1246/bcsj.10.122.
- Sigma-Aldrich Co., Hydroxyacetone. Retrieved on 2 July 2015.
- Carl J. Sullivan, Anja Kuenz, Klaus‐Dieter Vorlop (2018). "Propanediols". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a22_163.pub2. ISBN 978-3527306732.
{{cite encyclopedia}}
: CS1 maint: multiple names: authors list (link) - Levene, P. A.; Walti, A. (1930). "Acetol". Org. Synth. 10: 1. doi:10.15227/orgsyn.010.0001.
- Nursten, Harry E. (1998). "The Mechanism of Formation of 3-Methylcyclopent-2-en-2-olone". In O'Brien, J.; Nursten, H. E.; Crabbe, M. J.; Ames, J. M. (eds.). The Maillard Reaction in Foods and Medicine. Elsevier. pp. 65–68. ISBN 9781845698447.
- Media related to Hydroxyacetone at Wikimedia Commons