439126
Acetona
suitable for HPLC, ≥99.9%
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Fórmula lineal:
CH3COCH3
Número CAS:
Peso molecular:
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)
Servicio técnico
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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
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 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:
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.
- 1-isopropylidene-2-methylhydrazine
- 1-isopropylidene-2-hydroxyethylhydrazine
- 1-isopropylidene-2-formylhydrazine
Packaging
M-Bottle for Solvents
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As a global leader in lab reagents, we are constantly looking for new ways to optimize the safety of our products. The newly developed 4L solvent bottle design features advanced sealing technology that eliminates leaks to make the handling of solvents safer and more convenient than ever before.
See all the new features here!
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signalword
Danger
hcodes
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3
target_organs
Central nervous system
supp_hazards
Clase de almacenamiento
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
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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
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
Synthesis and characterization of acetone hydrazones.
Miro SC and Delalu H.
Zeitschrift fur Anorganische und Allgemeine Chemie, 638(1), 57-63 (2012)