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Merck
CN

534064

Acetone

histological grade, ≥99.5%

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About This Item

Linear Formula:
CH3COCH3
CAS Number:
67-64-1
Molecular Weight:
58.08
UNSPSC Code:
12352115
NACRES:
NA.21
PubChem Substance ID:
329757881
EC Number:
200-662-2
Beilstein/REAXYS Number:
635680
MDL number:
MFCD00008765
Assay:
≥99.5%
Application(s):
histology
Bp:
56 °C/760 mmHg (lit.)
Vapor pressure:
184 mmHg ( 20 °C)

Key Documents

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Product Name

Acetone, histological grade, ≥99.5%

InChI key

CSCPPACGZOOCGX-UHFFFAOYSA-N

InChI

1S/C3H6O/c1-3(2)4/h1-2H3

SMILES string

CC(C)=O

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

<0.001%

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

Quality Level

100

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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 .

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.

wgk

WGK 1

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Danger

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3

target_organs

Central nervous system

supp_hazards

EUH066

Storage Class

3 - Flammable liquids

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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Certificates of Analysis (COA)

Lot/Batch Number
SHBT3972
SHBT1277
SHBS7410
SHBR9590
SHBR7728

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Johanson G.
Patty's Industrial Hygiene and Toxicology, 735-752 (2012)
Acetone as an anticonvulsant.
Likhodii S, et al.
Epilepsia, 49(8), 83-86 (2008)
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
Photocatalytic degradation of acetone and methanol in a flow-through photoreactor with immobilized TiO2.
Moulis F and Krysa J.
Research on Chemical Intermediates, 41(12), 9233-9242 (2015)
Synthesis and characterization of acetone hydrazones.
Miro SC and Delalu H.
Zeitschrift fur Anorganische und Allgemeine Chemie, 638(1), 57-63 (2012)
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