W446207
Hydroxyacetone
≥95%, FG
Synonym(s):
1-Hydroxy-2-propanone, Acetol
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About This Item
Linear Formula:
CH3COCH2OH
CAS Number:
Molecular Weight:
74.08
PubChem Substance ID:
UNSPSC Code:
12164502
Colour Index Number:
11101
FEMA Number:
4462
Flavis number:
7.169
EC Number:
204-124-8
MDL number:
Beilstein/REAXYS Number:
605368
Organoleptic:
sweet
Grade:
FG, Kosher
Biological source:
synthetic
InChI
1S/C3H6O2/c1-3(5)2-4/h4H,2H2,1H3
InChI key
XLSMFKSTNGKWQX-UHFFFAOYSA-N
SMILES string
CC(=O)CO
biological source
synthetic
grade
FG, Kosher
reg. compliance
EU Regulation 1334/2008 & 178/2002
assay
≥95%
Quality Level
bp
145-146 °C (lit.)
mp
−17 °C (lit.)
density
1.082 g/mL at 25 °C (lit.)
application(s)
flavors and fragrances
organoleptic
sweet
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Other Notes
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signalword
Warning
hcodes
Hazard Classifications
Flam. Liq. 3 - Muta. 2
Storage Class
3 - Flammable liquids
wgk
WGK 1
flash_point_f
133.7 °F - closed cup
flash_point_c
56.5 °C - closed cup
Regulatory Information
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Xianliang Zhou et al.
Environmental science & technology, 43(8), 2753-2759 (2009-05-30)
A method has been modified and optimized for the measurements of hydroxyacetone as well as formaldehyde and glycolaldehyde, based on aqueous scrubbing using a coil sampler followed by DNPH derivatization and HPLC analysis. Derivatization equilibrium and kinetics were studied to
Maciej Gasior et al.
Epilepsia, 48(4), 793-800 (2007-03-28)
Acetone, one of the principal ketone bodies elevated during treatment with the ketogenic diet, exhibits anticonvulsant properties that may contribute to the seizure protection conferred by the diet. The anticonvulsant mechanism of acetone is unknown, but it is metabolized to
Jieni Lian et al.
Bioresource technology, 118, 177-186 (2012-06-19)
The presence of very reactive C1-C4 molecules adversely affects the quality bio-oils produced from the pyrolysis of lignocellulosic materials. In this paper a scheme to produce lipids with Cryptococcus curvatus from the carboxylic acids in the pyrolytic aqueous phase collected
Akshay Kumar et al.
Organic & biomolecular chemistry, 9(8), 2731-2742 (2011-03-02)
A new series of water compatible primary-tertiary diamine catalysts derived from natural primary amino acids bearing a hydrophobic side chain have been synthesized. These new primary-tertiary diamine-Brønsted acid conjugates bifunctional organocatalysts efficiently catalyzes the asymmetric direct syn selective cross-aldol reaction
Jacek Mlynarski et al.
Chemical Society reviews, 41(2), 587-596 (2011-07-29)
The key role of carbohydrates in biological processes and their visible existence in our everyday life have stimulated the interest of leading research groups on the smart and simple synthesis of common and rare sugar molecules. Now, more than 120
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