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439126

Sigma-Aldrich

Acétone

suitable for HPLC, ≥99.9%

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About This Item

Formule linéaire :
CH3COCH3
Numéro CAS:
Poids moléculaire :
58.08
Numéro Beilstein :
635680
Numéro CE :
Numéro MDL:
Code UNSPSC :
12190000
ID de substance PubChem :
Nomenclature NACRES :
NA.02

Densité de vapeur

2 (vs air)

Niveau de qualité

Pression de vapeur

184 mmHg ( 20 °C)

Pureté

≥99.9%

Forme

liquid

Limite d'explosivité

13.2 %

Technique(s)

HPLC: suitable

Impuretés

≤0.5% (water)

Résidus d'évap.

<0.0002%

Couleur

clear colorless

Indice de réfraction

n20/D 1.359 (lit.)

Point d'ébullition

56 °C/760 mmHg (lit.)

Pf

−94 °C (lit.)

Solubilité

water: miscible

Densité

0.791 g/mL at 25 °C (lit.)

λ

H2O reference

Absorption UV

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

Adéquation

suitable (pesticide analysis)

Format

neat

Chaîne SMILES 

CC(C)=O

InChI

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

Clé InChI

CSCPPACGZOOCGX-UHFFFAOYSA-N

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Catégories apparentées

Description générale

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

L′intensité de la luminescence de l′acétone dépend des constituants de la solution . L′absorption des rayonnements UV par l′acétone entraîne sa photolyse et la production de radicaux .
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

Pictogrammes

FlameExclamation mark

Mention d'avertissement

Danger

Mentions de danger

Classification des risques

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

Organes cibles

Central nervous system

Risques supp

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

1.4 °F - closed cup

Point d'éclair (°C)

-17.0 °C - closed cup

Équipement de protection individuelle

Eyeshields, Faceshields, Gloves


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Consulter la Bibliothèque de documents

Development of eco-efficient micro-porous membranes via electrospinning and annealing of poly (lactic acid).
Li L, et al.
Journal of Membrane Science, 436, 57-67 (2013)
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)
Saskia Kley et al.
American journal of physiology. Regulatory, integrative and comparative physiology, 296(4), R936-R943 (2009-02-06)
Obesity is a risk factor for type 2 diabetes in cats. The risk of developing diabetes is severalfold greater for male cats than for females, even after having been neutered early in life. The purpose of this study was to
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
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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