CN34892
Acetonitrile
Preparateur, ≥99.9% (GC), Customized plastic drum
동의어(들):
ACN, Cyanomethane, Ethyl nitrile, Methyl cyanide
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모든 사진(1)
About This Item
Linear Formula:
CH3CN
CAS Number:
Molecular Weight:
41.05
Beilstein:
741857
EC Number:
MDL number:
UNSPSC 코드:
12191502
PubChem Substance ID:
분석:
≥99.9% (GC)
bp:
81-82 °C (lit.)
vapor pressure:
72.8 mmHg ( 20 °C)
추천 제품
vapor density
1.41 (vs air)
vapor pressure
72.8 mmHg ( 20 °C)
분석
≥99.9% (GC)
양식
liquid
autoignition temp.
973 °F
expl. lim.
16 %
불순물
≤0.005% free acid (as CH3COOH)
≤0.02% water (Karl Fischer)
≤1 mg/L non-volatile matter
색상
colorless
투과
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.)
형식
neat
SMILES string
CC#N
InChI
1S/C2H3N/c1-2-3/h1H3
InChI key
WEVYAHXRMPXWCK-UHFFFAOYSA-N
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일반 설명
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.
애플리케이션
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).
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2
Storage Class Code
3 - Flammable liquids
WGK
WGK 2
Flash Point (°F)
35.6 °F - closed cup
Flash Point (°C)
2.0 °C - closed cup
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)
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)
Infrared spectra of acetonitrile and acetonitrile-d3.
Pace EL and Noe LJ.
J. Chem. Phys. , 49, 5317-5325 (1968)
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)
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