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CN34891

Sigma-Aldrich

Acetonitrile

≥99.9% (GC), suitable for solid phase extraction (SPE)

Sinonimo/i:

ACN, Cianometano, Cianuro di metile, Etilnitrile

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About This Item

Formula condensata:
CH3CN
Numero CAS:
Peso molecolare:
41.05
Beilstein:
741857
Numero CE:
Numero MDL:
Codice UNSPSC:
12352001
ID PubChem:

product name

Acetonitrile, Preparateur, ≥99.9% (GC), One-time steel-plastic (SP) drum

Densità del vapore

1.41 (vs air)

Tensione di vapore

72.8 mmHg ( 20 °C)

Saggio

≥99.9% (GC)

Forma fisica

liquid

Temp. autoaccensione

973 °F

Limite di esplosione

16 %

tecniche

solid phase extraction (SPE): suitable

Impurezze

≤0.005% free acid (as CH3COOH)
≤0.02% water (Karl Fischer)
≤1 mg/L non-volatile matter

Colore

colorless

Trasmittanza

200 nm, >50%
220 nm, >90%

Indice di rifrazione

n20/D 1.344 (lit.)

P. eboll.

81-82 °C (lit.)

Punto di fusione

−45 °C (lit.)

Densità

0.786 g/mL at 25 °C (lit.)

Formato

neat

Stringa SMILE

CC#N

InChI

1S/C2H3N/c1-2-3/h1H3
WEVYAHXRMPXWCK-UHFFFAOYSA-N

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Descrizione generale

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.

Applicazioni

Acetonitrile may be used as solvent in the following processes:
  • Determination of pKa values of organic superbases using the 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.
  • To study the dynamics of the intramolecular charge-transfer (ICT) reaction of 4-(dimethylamino)benzonitrile.

Pittogrammi

FlameExclamation mark

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

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

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

35.6 °F - closed cup

Punto d’infiammabilità (°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)
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)

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