A3396
乙腈
≥99.5%
别名:
ACN, 乙腈, 氰甲烷, 甲基氰
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关于此项目
线性分子式:
CH3CN
化学文摘社编号:
分子量:
41.05
Beilstein:
741857
EC 号:
MDL编号:
UNSPSC代码:
12191502
eCl@ss:
39031501
PubChem化学物质编号:
蒸汽密度
1.41 (vs air)
蒸汽压
72.8 mmHg ( 20 °C)
方案
≥99.5%
表单
liquid
自燃温度
973 °F
expl. lim.
16 %
技术
solid phase extraction (SPE): suitable
颜色
colorless
折射率
n20/D 1.344 (lit.)
沸点
81-82 °C (lit.)
mp
−45 °C (lit.)
溶解性
water: miscible
密度
0.786 g/mL at 25 °C (lit.)
适用性
suitable (Maldi-TOF mass spectroscopy)
SMILES字符串
CC#N
InChI
1S/C2H3N/c1-2-3/h1H3
InChI key
WEVYAHXRMPXWCK-UHFFFAOYSA-N
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一般描述
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.
应用
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.
警示用语:
Danger
危险分类
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2
储存分类代码
3 - Flammable liquids
WGK
WGK 2
闪点(°F)
35.6 °F - closed cup
闪点(°C)
2.0 °C - closed cup
个人防护装备
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
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)
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)
Infrared spectra of acetonitrile and acetonitrile-d3.
Pace EL and Noe LJ.
J. Chem. Phys. , 49, 5317-5325 (1968)
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