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Merck
CN

534064

Acetone

histological grade, ≥99.5%

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About This Item

Linear Formula:
CH3COCH3
CAS Number:
Molecular Weight:
58.08
UNSPSC Code:
12352115
NACRES:
NA.21
PubChem Substance ID:
EC Number:
200-662-2
Beilstein/REAXYS Number:
635680
MDL number:
eCl@ss:
39021201
Assay:
≥99.5%
Bp:
56 °C/760 mmHg (lit.)
Vapor pressure:
184 mmHg ( 20 °C)
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vapor density

2 (vs air)

Quality Level

vapor pressure

184 mmHg ( 20 °C)

assay

≥99.5%

expl. lim.

13.2 %

impurities

<0.5% water

evapn. residue

<0.001%

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.)

solubility

water: miscible

density

0.791 g/mL at 25 °C (lit.)

application(s)

histology

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 an organic solvent widely used in the polymer and pharmaceutical industry. It is found in mammalian tissues as a by-product of metalbolism. It shows potent anticonvulsant property. Acetone in combination with tetraalkylammonium chloride forms an efficient solvent system for dissolving cellulose. The dehydration of acetone can be accomplised by pervaporation using P84 (polyimide membrane)/TAEA (tripodal amine (tris(2-aminoethyl)amine) cross-linked asymmetric flat sheet membranes. The acetone vapors can undergo photolysis in a titanium dioxide (TiO2) photocatalyst immobilized UV irradiated reactor.

Application

Acetone may be employed in the following studies:
  • As a precursor for the synthesis of methyl isobutyl ketone (MIBK) in the presence of sulfonated graphene oxide-Pd/cordierite catalyst.
  • Synthesis of (4-hydroxymethyl-2,2-dimethyl-1,3-dioxolane), a solketal from glycerol using supercritical fluids (SCF) technology.
  • As a starting material to synthesize methyl methacrylate.
It may be used in the synthesis of the following acetone hydrazones:
  • 1-isopropylidene-2-methylhydrazine
  • 1-isopropylidene-2-hydroxyethylhydrazine
  • 1-isopropylidene-2-formylhydrazine
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 .


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pictograms

FlameExclamation mark

signalword

Danger

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

易制毒化学品(3类)
危险化学品

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Johanson G.
Patty's Industrial Hygiene and Toxicology, 735-752 (2012)
Marc Kostag et al.
Macromolecular rapid communications, 35(16), 1419-1422 (2014-06-14)
Acetone containing tetraalkylammonium chloride is found to be an efficient solvent for cellulose. The addition of an amount of 10 mol% (based on acetone) of well-soluble salt triethyloctylammonium chloride (Et3 OctN Cl) adjusts the solvent's properties (increases the polarity) to
Acetone as an anticonvulsant.
Likhodii S, et al.
Epilepsia, 49(8), 83-86 (2008)



Global Trade Item Number

SKUGTIN
534064-18L-CS04061838161826
534064-4X4L04061832559773
534064-20L04061838254047
534064-4L04061832559674
534064-500ML04061832559780