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CN34892

Acetonitrilo

Preparateur, ≥99.9% (GC), Customized plastic drum

Sinónimos:

ACN, Cianometano, Cianuro de metilo, Nitrilo de etilo

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Fórmula lineal:
CH3CN
Número CAS:
75-05-8
Peso molecular:
41.05
EC Number:
200-835-2
UNSPSC Code:
12191502
PubChem Substance ID:
329798433
Beilstein/REAXYS Number:
741857
MDL number:
MFCD00001878
Assay:
≥99.9% (GC)
Technique(s):
HPLC-GC: suitable
Bp:
81-82 °C (lit.)
Vapor pressure:
72.8 mmHg ( 20 °C)
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vapor 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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pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2

Clase de almacenamiento

3 - Flammable liquids

flash_point_f

35.6 °F - closed cup

flash_point_c

2.0 °C - closed cup

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Basicity of some organic superbases in acetonitrile.
Kovacevic B and Maksic ZB.
Organic Letters, 3(10), 1523-1526 (2001)
Dynamics of ultrafast intramolecular charge transfer with 4-(dimethylamino) benzonitrile in acetonitrile.
Druzhinin SI, et al.
The Journal of Physical Chemistry A, 110(9), 2955-2969 (2006)
Cerium (III) chloride promoted highly regioselective ring opening of epoxides and aziridines using NaN3 in acetonitrile: a facile synthesis of 1,2-azidoalcohols and 1,2-azidoamines.
Sabitha G, et al.
Organic Letters, 4(3), 343-345 (2002)
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