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00586

Sigma-Aldrich

Acetone

purum, ≥99.0% (GC)

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About This Item

Linear Formula:
CH3COCH3
CAS Number:
Molecular Weight:
58.08
Beilstein:
635680
EC Number:
MDL number:
UNSPSC Code:
12352115
PubChem Substance ID:

vapor density

2 (vs air)
2 (vs air)

vapor pressure

184 mmHg ( 20 °C)
184 mmHg

grade

purum

Assay

≥99.0% (GC)

form

liquid

expl. lim.

13.2 %
8 % (lit.)

impurities

≤1% water

refractive index

n20/D 1.359 (lit.)
n20/D 1.359

bp

56 °C/760 mmHg (lit.)
56 °C/760 mmHg (lit.)

mp

-94 °C (lit.)
−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

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General description

Photocatalytic activity of mixtures of TiO2 (P25) with rare earth oxides for the oxidation of acetone has been reported. The vapor-phase Aldol condensation of acetone over MgO promoted with alkali (Li, Na, K and Cs) or alkaline earth (Ca, Sr and Ba) metal ions has been studied. Acetone undergoes Aldol condensation in the presence of catalysts Mg-Al layered double hydroxides (LDH) and Cl- and/or CO32- as compensating anions to afford diacetone alcohol and mesityl oxide. Enantioselective Aldol condensation of acetone with several isatins has been described.

Application

Acetone may be employed in the following studies:
  • As organic solvent to investigate the zeta potential of TiO2 and Al2O3 powders.
  • Synthesis of poly(ortho esters) (POE), biodegradable carriers for drug delivery devices.
  • Spectrophotometric determination of ester groups in lipids.
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 .

Pictograms

FlameExclamation mark

Signal Word

Danger

Hazard 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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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A Merkli et al.
Journal of biomaterials science. Polymer edition, 4(5), 505-516 (1993-01-01)
Since the late 1970s, three families of poly(ortho esters) (POE) were synthesized to provide bioerodible carriers for drug delivery devices. The most recent POE is a semi-solid polymer with a viscous behavior at room temperature. Polymer synthesis by a transesterification
Location of the shear plane in the electric double layer in an organic medium.
Siffert B, et al.
Journal of Colloid and Interface Science, 163(2), 327-333 (1992)
Base catalysis for the synthesis of α,β-unsaturated ketones from the vapor-phase aldol condensation of acetone.
Di Cosimo JI, et al.
Applied Catalysis A: General, 137(1), 149-166 (1996)
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
A simplified spectrophotometric determination of ester groups in lipids.
F SNYDER et al.
Biochimica et biophysica acta, 34, 244-245 (1959-07-01)

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