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Merck

673781

Sigma-Aldrich

Acetona

ACS reagent, ≥99.5%

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About This Item

Fórmula lineal:
CH3COCH3
Número de CAS:
Peso molecular:
58.08
Beilstein/REAXYS Number:
635680
EC Number:
MDL number:
UNSPSC Code:
12352115
PubChem Substance ID:
NACRES:
NA.21

grade

ACS reagent

Quality Level

vapor density

2 (vs air)

vapor pressure

184 mmHg ( 20 °C)

assay

≥99.5%

form

liquid

expl. lim.

13.2 %

impurities

≤0.0003 meq/g Titr. acid
≤0.0006 meq/g Titr. base
≤0.002% aldehyde as formaldehyde
≤0.05% isopropanol
≤0.05% methanol
≤0.5% water

evapn. residue

≤0.001%

color

APHA: ≤10

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.)

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

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.1 Its anticonvulsant property has been studied. Acetone in combination with tetraalkylammonium chloride forms an efficient solvent system for dissolving cellulose. P84 (polyimide membrane)/TAEA (tripodal amine (tris(2-aminoethyl)amine) cross-linked asymmetric flat sheet membranes based pervaporation for the dehydration of acetone has been reported. A recent study reports the photolysis of acetone vapors in a titanium dioxide (TiO2) photocatalyst immobilized, UV irradiated reactor.

Application

La intensidad de luminiscencia de la acetona depende de los componentes de la disolución . La absorción de luz ultravioleta por la acetona tiene como consecuencia su fotólisis y la producción de radiales .
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.1
It may be used in the synthesis of the following acetone hydrazones:
  • 1-isopropylidene-2-methylhydrazine
  • 1-isopropylidene-2-hydroxyethylhydrazine
  • 1-isopropylidene-2-formylhydrazine

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Referencia del producto
Descripción
Precios

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_germany

WGK 1

flash_point_f

1.4 °F - closed cup

flash_point_c

-17.0 °C - closed cup


Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Slide 1 of 4

1 of 4

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
Sulfonated graphene oxide supported Pd bifunctional catalyst for one-pot synthesis of methyl isobutyl ketone from acetone with high conversion and selectivity.
Liu M, et al.
J. Mol. Catal. A: Chem., 408, 85-90 (2015)
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)
P84 polyimide membranes modified by a tripodal amine for enhanced pervaporation dehydration of acetone.
Mangindaan DW, et al.
Chemical Engineering Science, 122, 14-23 (2015)

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