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Merck
CN

439126

Acetone

suitable for HPLC, ≥99.9%

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About This Item

Linear Formula:
CH3COCH3
CAS Number:
Molecular Weight:
58.08
UNSPSC Code:
12190000
NACRES:
NA.02
PubChem Substance ID:
EC Number:
200-662-2
Beilstein/REAXYS Number:
635680
MDL number:
Assay:
≥99.9%
Grade:
HPLC grade
Technique(s):
HPLC: suitable
Bp:
56 °C/760 mmHg (lit.)
Vapor pressure:
184 mmHg ( 20 °C)
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grade

HPLC grade

Quality Level

vapor density

2 (vs air)

vapor pressure

184 mmHg ( 20 °C)

assay

≥99.9%

form

liquid

expl. lim.

13.2 %

technique(s)

HPLC: suitable

impurities

≤0.5% (water)

evapn. residue

<0.0002%

color

clear colorless

refractive index

n20/D 1.359 (lit.)

bp

56 °C/760 mmHg (lit.)

mp

−94 °C (lit.)

solubility

water: miscible

density

0.791 g/mL at 25 °C (lit.)

λ

H2O reference

UV absorption

λ: 330 nm Amax: 1.00, λ: 340 nm Amax: 0.10, λ: 350 nm Amax: 0.02, λ: 400 nm Amax: 0.01

suitability

suitable (pesticide analysis)

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 ketone. Mixtures of TiO2 (P25) with rare earth oxides (La2O3 or Y2O3) calcined at 700°C or 650°C has been reported to efficiently photocatalyze the oxidation of acetone. Its aldol condensation in vapor-phase has been investigated over MgO promoted with alkali (Li, Na, K and Cs) or alkaline earth (Ca, Sr and Ba) metal ions. It undergoes Aldol condensation 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. Enantioselective Aldol condensation of acetone with various isatins in the presence of dipeptides (catalyst) has been described.

Application

Acetone was used in the affinity purification of modified proteins using streptavidin beads for the mass spectrometric (MS) identification of poly(ADP-ribose) polymerases (PARP) substrate proteins.
It may be used in the following studies:
  • NMR spectroscopic evaluation of glucose metabolism in biological samples (blood).
  • Preparation of 13wt% amorphous poly (lactic acid) (PLA) solution, which was required for the preparation of electrospun PLA membranes.
  • 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.
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 .

Packaging

M-Bottle for Solvents
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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

ppe

Eyeshields, Faceshields, Gloves

Regulatory Information

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Hong Jiang et al.
Current protocols in chemical biology, 4(1), 19-34 (2012-11-29)
Poly(ADP-ribose) polymerases (PARPs) play important roles in various biological processes, including DNA repair, transcriptional regulation, mitosis, and RNA processing. PARP inhibitors are in clinical trials for treating human cancers. Understanding the biological function of PARPs will be important to fully
Ketalization of glycerol to solketal in supercritical acetone.
Royon D, et al.
Journal of Supercritical Fluids, 58(1), 88-92 (2011)
Synthesis and characterization of acetone hydrazones.
Miro SC and Delalu H.
Zeitschrift fur Anorganische und Allgemeine Chemie, 638(1), 57-63 (2012)



Global Trade Item Number

SKUGTIN
439126-18L04061837478987
439126-20L-P2-3C04061837289880
439126-20L04061832245928
439126-4L04061832245935
439126-4X4L04061837478994
439126-50L-P2-3C04061838511843