All Photos(2)
About This Item
Linear Formula:
CH3COCH3
CAS Number:
Molecular Weight:
58.08
Beilstein:
635680
EC Number:
MDL number:
UNSPSC Code:
12352115
eCl@ss:
39021201
PubChem Substance ID:
NACRES:
NA.21
grade:
Laboratory Reagent
Assay:
≥99.5%
bp:
56 °C/760 mmHg (lit.)
vapor pressure:
184 mmHg ( 20 °C)
Recommended Products
grade
Laboratory Reagent
Quality Level
vapor density
2 (vs air)
vapor pressure
184 mmHg ( 20 °C)
Assay
≥99.5%
form
liquid
expl. lim.
13.2 %
impurities
≤0.5% water
evapn. residue
≤0.002%
refractive index
n20/D 1.359 (lit.)
pH
5-6 (20 °C, 395 g/L)
bp
56 °C/760 mmHg (lit.)
mp
−94 °C (lit.)
density
0.791 g/mL at 25 °C (lit.)
format
neat
SMILES string
CC(C)=O
InChI
1S/C3H6O/c1-3(2)4/h1-2H3
InChI key
CSCPPACGZOOCGX-UHFFFAOYSA-N
Looking for similar products? Visit Product Comparison Guide
Related Categories
General description
Acetone is a polar organic solvent. It can undergo photocatalytic oxidation in the presence of mixed TiO2-rare earth oxides.
Application
Acetone undergoes aldolization in the presence of Mg-Al layered double hydroxides (LDH) as catalysts and Cl- and/or CO32- as compensating anions to afford diacetone alcohol and mesityl oxide as the main products. Its enantioselective Aldol condensation with various isatins in the presence of a dipeptide catalyst forms 1-alkyl 3-(2-oxopropyl)-3-hydroxyindolin-2-ones. Aqueous solution of acetone may be used as a medium for the oxidation of alkynes to 1,2-diketones using potassium permanganate.
Acetone′s luminesence intensity is dependent upon the solution components . The absorption of UV light by acetone, results in its photolysis and the production of radials .
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3
Target Organs
Central nervous system
Supplementary Hazards
Storage Class Code
3 - Flammable liquids
WGK
WGK 1
Flash Point(F)
1.4 °F - closed cup
Flash Point(C)
-17.0 °C - closed cup
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
Preparation of 1,2-diketones: oxidation of alkynes by potassium permanganate in aqueous acetone
Srinivasan NS and Donald GL
The Journal of Organic Chemistry, 44(9), 1574-1574 (1979)
Aldol condensation of acetone over layered double hydroxides of the meixnerite type.
Tichit D, et al.
Applied Clay Science, 13(5), 401-415 (1998)
Gianluigi Luppi et al.
The Journal of organic chemistry, 70(18), 7418-7421 (2005-08-27)
[reaction: see text] The aldol condensation of acetone with several isatins is described. The desired compound was obtained in quantitative yield and with good enantioselectivities up to 77%. The best results were obtained with 10 mol % H-D-Pro-L-beta3-hPhg-OBn as a
An investigation on photocatalytic activities of mixed TiO2-rare earth oxides for the oxidation of acetone in air.
Lin J and Jimmy CY.
Journal of Photochemistry and Photobiology A: Chemistry, 116(1), 63-67 (1998)
Sinisa Bjelic et al.
Journal of molecular biology, 426(1), 256-271 (2013-10-29)
Designed retroaldolases have utilized a nucleophilic lysine to promote carbon-carbon bond cleavage of β-hydroxy-ketones via a covalent Schiff base intermediate. Previous computational designs have incorporated a water molecule to facilitate formation and breakdown of the carbinolamine intermediate to give the
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service