CN34891

Acetonitrilo

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

• Sinônimo(s): ACN, Cianeto de metila, Cianometano, Etil-nitrilo
• Fórmula linear: CH₃CN
• Número CAS: 75-05-8
• Peso molecular: 41.05
• Beilstein: 741857
• Número CE: 200-835-2
• Número MDL: MFCD00001878
• Código UNSPSC: 12352001
• ID de substância PubChem: 329798432
• Ensaio: ≥99.9% (GC)
• técnica(s): solid phase extraction (SPE): suitable
• p.e.: 81-82 °C (lit.)
• pressão de vapor: 72.8 mmHg ( 20 °C)

Propriedades

• Nome do produto: Acetonitrilo, Preparateur, ≥99.9% (GC), One-time steel-plastic (SP) drum
• densidade de vapor: 1.41 (vs air)
• pressão de vapor: 72.8 mmHg ( 20 °C)
• Ensaio: ≥99.9% (GC)
• Formulário: liquid
• temperatura de autoignição: 973 °F
• Lim. expl.: 16 %
• técnica(s): solid phase extraction (SPE): suitable
• Impurezas: ≤0.005% free acid (as CH₃COOH); ≤0.02% water (Karl Fischer); ≤1 mg/L non-volatile matter
• cor: colorless
• transmitância: 200 nm, >50%; 220 nm, >90%
• índice de refração: n20/D 1.344 (lit.)
• p.e.: 81-82 °C (lit.)
• pf: −45 °C (lit.)
• densidade: 0.786 g/mL at 25 °C (lit.)
• Formato: neat
• cadeia de caracteres SMILES: CC#N
• InChI: 1S/C2H3N/c1-2-3/h1H3
• chave InChI: WEVYAHXRMPXWCK-UHFFFAOYSA-N

Descrição

Descrição geral

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.[1] 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.[2] Its infrared spectrum has been recorded.[3] Synthesis of alkyl hydroperoxides in MeCN by alkane oxidation with hydrogen peroxide in the presence of iron complexes has been studied.[4] The hydrogenation of MeCN to form ethylamine using Co-B amorphous alloy catalyst has been investigated.[5]

Aplicação

Acetonitrile may be used as solvent in the following processes:

• Determination of pKa values of organic superbases using the isodensity polarization continuum model (IPCM).[6]
• Preparation of 1,2-azidoalcohols and 1,2-azidoamines via cerium(III) chloride assisted ring opening of epoxides and aziridines by sodium azide.[7]
• Synthesis of cyano-bearing indolinones by oxidative arylalkylation of olefins in the presence of palladium catalyst.[8]
• To study the dynamics of the intramolecular charge-transfer (ICT) reaction of 4-(dimethylamino)benzonitrile.[9]

Informações de segurança

• Pictogramas: GHS02,GHS07
• Palavra indicadora: Danger
• Frases de perigo: H225,H302 + H312 + H332,H319
• Declarações de precaução: P210 - P280 - P301 + P312 - P303 + P361 + P353 - P304 + P340 + P312 - P305 + P351 + P338
• Classificações de perigo: Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2
• Código de classe de armazenamento: 3 - Flammable liquids
• Classe de risco de água (WGK): WGK 2
• Ponto de fulgor (°F): 35.6 °F - closed cup
• Ponto de fulgor (°C): 2.0 °C - closed cup