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A propos de cet article
Formule linéaire :
CH3CN
Numéro CAS:
Poids moléculaire :
41.05
EC Number:
200-835-2
UNSPSC Code:
12191502
PubChem Substance ID:
Beilstein/REAXYS Number:
741857
MDL number:
Assay:
≥99.9% (GC)
Technique(s):
HPLC-GC: suitable
Bp:
81-82 °C (lit.)
Vapor pressure:
72.8 mmHg ( 20 °C)
Service technique
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Laissez-nous vous aidervapor density
1.41 (vs air)
vapor pressure
72.8 mmHg ( 20 °C)
assay
≥99.9% (GC)
form
liquid
autoignition temp.
973 °F
expl. lim.
16 %
technique(s)
HPLC-GC: suitable
impurities
≤0.005% free acid (as CH3COOH), ≤0.02% water (Karl Fischer), ≤1 mg/L non-volatile matter
color
colorless
transmittance
200 nm, >50%, 220 nm, >90%
refractive index
n20/D 1.344 (lit.)
bp
81-82 °C (lit.)
mp
−45 °C (lit.)
density
0.786 g/mL at 25 °C (lit.)
application(s)
general analytical
format
neat
SMILES string
CC#N
InChI
1S/C2H3N/c1-2-3/h1H3
InChI key
WEVYAHXRMPXWCK-UHFFFAOYSA-N
General description
Acetonitrile (MeCN), an aliphatic nitrile, is a colorless liquid with a characteristic odor. MeCN has low viscosity, high elution strength and is highly miscible in water. It is widely used as a solvent and intermediate in organic syntheses and is transparent to UV-visible light, making it highly applicable in spectrophotometric and fluorimetric techniques. It also plays a major role as an extractant medium in liquid-liquid extraction, solid-phase extraction or microextraction.
Application
Acetonitrile may be used as solvent in the following processes:
- Organic synthesis
- Liquid-liquid extraction, solid-phase extraction or microextraction.
- Spectrophotometric and fluorimetric techniques.
- Electrolytes in lithium-ion batteries
- Determination of pKa values of organic superbases using the isodensity polarization continuum model (IPCM).
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signalword
Danger
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2
Classe de stockage
3 - Flammable liquids
flash_point_f
35.6 °F - closed cup
flash_point_c
2.0 °C - closed cup
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Palladium-Catalyzed Oxidative Arylalkylation of Activated Alkenes: Dual C-H Bond Cleavage of an Arene and Acetonitrile.
Wu T, et al.
Angewandte Chemie (International Edition in English), 50(52), 12578-12581 (2011)
Liquid phase hydrogenation of acetonitrile to ethylamine over the Co-B amorphous alloy catalyst.
Li H, et al.
J. Catal., 214(1), 15-25 (2003)
Hydrogen peroxide oxygenation of alkanes including methane and ethane catalyzed by iron complexes in acetonitrile.
Shul'pin GB, et al.
Advanced Synthesis & Catalysis, 346(2-3), 317-332 (2004)

