1.15500
Acetonitrilo
≥90% (HPLC), for preparative purposes, synthesis, cleaning, extraction and analytical purposes, EMPLURA®
Sinónimos:
ACN, Cianometano, Cianuro de metilo, Nitrilo de etilo
About This Item
Productos recomendados
product name
Acetonitrilo, EMPLURA®
grado
for analytical purposes
for cleaning
for extraction
for preparative purposes
for synthesis
Nivel de calidad
100
200
densidad de vapor
1.41 (vs air)
presión de vapor
72.8 mmHg ( 20 °C)
97 hPa ( 20 °C)
Línea del producto
EMPLURA®
Análisis
≥90% (HPLC)
formulario
liquid
temp. de autoignición
524 °C
973 °F
lim. expl.
16 %
fabricante / nombre comercial
Calbiochem®
impurezas
≤0.00016 meq/g Acidity
≤0.5% Water
residuo de evap.
≤0.005%
índice de refracción
n20/D 1.344 (lit.)
bp
81-82 °C (lit.)
mp
−45 °C (lit.)
temperatura de transición
flash point 2 °C
densidad
0.786 g/mL at 25 °C (lit.)
aplicaciones
environmental
food and beverages
industrial qc
pharmaceutical
formato
neat
Condiciones de envío
ambient
temp. de almacenamiento
−20°C
cadena SMILES
CC#N
InChI
1S/C2H3N/c1-2-3/h1H3
Clave InChI
WEVYAHXRMPXWCK-UHFFFAOYSA-N
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Descripción general
Aplicación
- Electroanalysis and Spectroelectrochemistry: Acetonitrile is widely used in electroanalysis and spectroelectrochemistry due to its excellent solvent properties and compatibility with a variety of electrodes. Recent research has demonstrated its use in the electroanalysis of nonaromatic explosives in the presence of dissolved oxygen. This application enhances the sensitivity and accuracy of detecting explosive compounds, which is critical for environmental monitoring and safety assessments (Holubowitch et al., Analytical Chemistry, 2020).
- Chromatographic Separation of Anthocyanins: Acetonitrile is a preferred solvent in high-performance liquid chromatography (HPLC) for the separation of anthocyanins and other phenolic compounds. Studies have explored the selectivity control of anthocyanin separation by replacing acetonitrile with methanol in the mobile phase, highlighting the solvent′s role in optimizing chromatographic conditions for improved resolution and detection sensitivity (Deineka et al., Journal of Analytical Chemistry, 2021).
- Peroxyoxalate Chemiluminescence Detection: Acetonitrile is used in peroxyoxalate chemiluminescence for the detection of α-amino acids. The solvent′s ability to form stable mixed solutions with water and ethyl acetate enhances the chemiluminescence reaction, allowing for sensitive and selective detection of amino acids in various samples. This application is essential for biochemical and clinical analyses (Kan et al., American Journal of Analytical Chemistry, 2020).
- Electrochemical Detection of DNA Modifications: Acetonitrile is utilized in electrochemical methods for detecting DNA modifications, such as 5-formyluracil. The solvent′s role in stabilizing the (2-benzimidazolyl) acetonitrile labeling reaction enhances the selectivity and sensitivity of detecting DNA modifications, which is crucial for genomic and biomedical research (Tang et al., Analytical Chemistry, 2021).
- Alternative Solvent in Chromatography: Research has investigated replacing acetonitrile with ethanol in reversed-phase HPLC for determining anthocyanins. This substitution aims to maintain chromatographic performance while reducing the environmental impact and costs associated with acetonitrile use. The findings demonstrate the feasibility of using ethanol as a greener alternative without compromising analytical quality (Deineka et al., Journal of Analytical Chemistry, 2023).
Advertencia
Nota de análisis
Identity (IR): conforms
Acidity: ≤ 0.00016 meq/g
Density (d 20 °C/ 4 °C): 0.782 - 0.783
Evaporation residue: ≤ 0.005 %
Water: ≤ 0.5 %
Información legal
Palabra de señalización
Danger
Frases de peligro
Clasificaciones de peligro
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2
Código de clase de almacenamiento
3 - Flammable liquids
Clase de riesgo para el agua (WGK)
WGK 2
Punto de inflamabilidad (°C)
2.0 °C - closed cup
Certificados de análisis (COA)
Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»
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