00586
Acetone
purum, ≥99.0% (GC)
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
CH3COCH3
CAS Number:
Molecular Weight:
58.08
EC Number:
200-662-2
UNSPSC Code:
12352115
PubChem Substance ID:
Beilstein/REAXYS Number:
635680
MDL number:
NACRES:
NA.21
InChI key
CSCPPACGZOOCGX-UHFFFAOYSA-N
InChI
1S/C3H6O/c1-3(2)4/h1-2H3
SMILES string
CC(C)=O
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
mp
-94 °C (lit.), −94 °C (lit.)
density
0.791 g/mL at 25 °C (lit.)
format
neat
Looking for similar products? Visit Product Comparison Guide
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 .
signalword
Danger
hcodes
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3
target_organs
Central nervous system
supp_hazards
Storage Class
3 - Flammable liquids
wgk
WGK 1
flash_point_f
1.4 °F - closed cup
flash_point_c
-17.0 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves
Regulatory Information
新产品
This item has
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.
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)
A simplified spectrophotometric determination of ester groups in lipids.
F SNYDER et al.
Biochimica et biophysica acta, 34, 244-245 (1959-07-01)
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
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