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线性分子式:
CH3CN
化学文摘社编号:
分子量:
41.05
UNSPSC Code:
12191502
PubChem Substance ID:
eCl@ss:
39031501
EC Number:
200-835-2
Beilstein/REAXYS Number:
741857
MDL number:
InChI key
WEVYAHXRMPXWCK-UHFFFAOYSA-N
InChI
1S/C2H3N/c1-2-3/h1H3
SMILES string
CC#N
vapor density
1.41 (vs air)
vapor pressure
72.8 mmHg ( 20 °C)
assay
≥99.5%
form
liquid
autoignition temp.
973 °F
expl. lim.
16 %
technique(s)
solid phase extraction (SPE): suitable
color
colorless
refractive index
n20/D 1.344 (lit.)
bp
81-82 °C (lit.)
mp
−45 °C (lit.)
solubility
water: miscible
density
0.786 g/mL at 25 °C (lit.)
suitability
suitable (Maldi-TOF mass spectroscopy)
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General description
Acetonitrile (MeCN), an aliphatic nitrile, is a colorless liquid with a pleasant odor. It is widely used as a solvent and intermediate in organic syntheses. It is transparent to UV-visible light, making it highly applicable in spectrophotometric and fluorimetric techniques. As MeCN has low viscosity, high elution strength and is highly miscible in water, it is utilized as a mobile phase component in many chromatographic techniques. It also plays a major role as an extractant medium in liquid-liquid extraction, solid-phase extraction or microextraction. Its infrared spectrum has been recorded. Synthesis of alkyl hydroperoxides in MeCN by alkane oxidation with hydrogen peroxide in the presence of iron complexes has been studied. The hydrogenation of MeCN to form ethylamine using Co-B amorphous alloy catalyst has been investigated.
Application
Acetonitrile (MeCN) was used to constitute mobile phase A, which is employed in the UPLC (ultra-performance liquid chromatography) based separation of underivatized amino acids derived from monoclonal antibody producing Chinese hamster ovary (CHO) cells.
It may be used as solvent in the following processes:
It may be used as solvent in the following processes:
- Determination of pKa values of organic superbases using isodensity polarization continuum model (IPCM).
- Preparation of 1,2-azidoalcohols and 1,2-azidoamines via cerium(III) chloride assisted ring opening of epoxides and aziridines by sodium azide.
- Synthesis of cyano-bearing indolinones by oxidative arylalkylation of olefins in the presence of palladium catalyst.
signalword
Danger
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2
存储类别
3 - Flammable liquids
wgk
WGK 2
flash_point_f
35.6 °F - closed cup
flash_point_c
2.0 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
Atefeh Ghorbaniaghdam et al.
PloS one, 9(3), e90832-e90832 (2014-03-19)
Monoclonal antibody producing Chinese hamster ovary (CHO) cells have been shown to undergo metabolic changes when engineered to produce high titers of recombinant proteins. In this work, we have studied the distinct metabolism of CHO cell clones harboring an efficient
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)
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)
Basicity of some organic superbases in acetonitrile.
Kovacevic B and Maksic ZB.
Organic Letters, 3(10), 1523-1526 (2001)
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)
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