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Merck

675415

Sigma-Aldrich

Acetonitril

≥99.9%, HPLC Plus, suitable for HPLC, poly-coated bottles

Synonym(e):

ACN, Cyanomethan, Ethylnitril, Methylcyanid

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About This Item

Lineare Formel:
CH3CN
CAS-Nummer:
Molekulargewicht:
41.05
Beilstein:
741857
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12190000
PubChem Substanz-ID:

product name

Acetonitril, HPLC Plus, ≥99.9%, poly-coated bottles

Qualität

HPLC Plus

Qualitätsniveau

Dampfdichte

1.41 (vs air)

Dampfdruck

72.8 mmHg ( 20 °C)

Assay

≥99.9%

Form

liquid

Selbstzündungstemp.

525 °F
973 °F

Expl.-Gr.

16 %

Methode(n)

HPLC: suitable

Verunreinigungen

≤0.01% water

Abdampfrückstand

≤0.0002%

Farbe

colorless

Brechungsindex

n20/D 1.344 (lit.)

bp

81-82 °C (lit.)

mp (Schmelzpunkt)

−45 °C (lit.)

Löslichkeit

water: soluble

Dichte

0.786 g/mL at 25 °C (lit.)

Absorption

≤1 mAU at 210 nm

UV-Absorption

λ: 195 nm Amax: ≤0.10
λ: 200 nm Amax: ≤0.02
λ: 228 nm Amax: ≤0.005

Anwendung(en)

food and beverages

Format

neat

SMILES String

CC#N

InChI

1S/C2H3N/c1-2-3/h1H3

InChIKey

WEVYAHXRMPXWCK-UHFFFAOYSA-N

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Verwandte Kategorien

Allgemeine Beschreibung

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. 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.

Anwendung


  • Anthocyanin Separation: Acetonitrile is employed in high-performance liquid chromatography (HPLC) for the selective separation of anthocyanins. Studies have demonstrated the benefits of replacing acetonitrile with methanol in the mobile phase to control the selectivity and improve the resolution of anthocyanin separation, providing a more sustainable approach to chromatographic analysis (Deineka et al., Journal of Analytical Chemistry, 2021).

  • Detection of α-Amino Acids: Acetonitrile is used in the development of chemiluminescence methods for detecting α-amino acids. A mixed solution of water, acetonitrile, and ethyl acetate has been shown to enhance the sensitivity and accuracy of amino acid detection, making it a valuable tool for biochemical and clinical analyses (Kan et al., American Journal of Analytical Chemistry, 2020).

  • Electrochemical Detection of Biomarkers: Acetonitrile is utilized in the electrochemical detection of biomarkers such as 5-formyluracil. Labeling with (2-benzimidazolyl) acetonitrile enhances the selectivity and sensitivity of the detection, making it an important method for biomedical research and diagnostics (Tang et al., Analytical Chemistry, 2021).

  • Ligand-Assisted Excitation of Europium Complexes: Acetonitrile is used in studying the ligand-assisted excitation of Eu(III) complexes. The interaction of europium complexes with xenon difluoride in acetonitrile solution provides insights into their photophysical properties, which are essential for developing luminescent materials for various applications, including lighting and display technologies (Masyagutova et al., Journal of Fluorine Chemistry, 2024).


Piktogramme

FlameExclamation mark

Signalwort

Danger

Gefahreneinstufungen

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

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 2

Flammpunkt (°F)

35.6 °F - closed cup

Flammpunkt (°C)

2.0 °C - closed cup

Persönliche Schutzausrüstung

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Die Dokumentenbibliothek aufrufen

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)
Eagleson M.
Concise Encyclopedia Chemistry, 6-6 (1994)
Acetonitrile, the polarity chameleon.
Zarzycki PK, et al.
Analytical and Bioanalytical Chemistry, 397(3), 905-908 (2010)

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