179973
Acetone
Laboratory Reagent, ≥99.5%
Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Linear Formula:
CH3COCH3
CAS Number:
Molecular Weight:
58.08
NACRES:
NA.21
PubChem Substance ID:
eCl@ss:
39021201
UNSPSC Code:
12352115
EC Number:
200-662-2
MDL number:
Beilstein/REAXYS Number:
635680
Assay:
≥99.5%
Grade:
Laboratory Reagent
Bp:
56 °C/760 mmHg (lit.)
Vapor pressure:
184 mmHg ( 20 °C)
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 %
dilution
(for analytical testing)
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
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 .
Still not finding the right product?
Explore all of our products under Acetone
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
Regulatory Information
监管及禁止进口产品
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.
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)
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
Aldol condensation of acetone over layered double hydroxides of the meixnerite type.
Tichit D, et al.
Applied Clay Science, 13(5), 401-415 (1998)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 179973-4L | 04061838754622 |
| 179973-4X4L | 04061837224171 |
| 179973-18L-CS | 04061837713583 |
| 179973-1L | 04061838754608 |
| 179973-2.5L | 04061838754615 |
| 179973-4X4L-PB | 04061837224188 |
| 179973-6X1L | 04061838754639 |