Acetonitrile(ACN) - suitable for mass spectrometry (MS), UltraPureChrom™, for UHPLC , CAS No.75-05-8

CAS: 75-05-8 Cat. No.: A433531 Formula: C₂H₃N Peso molecolare: 41.05 Beilstein Registry Number: 741857 Numero EC: 200-835-2

GRADE & PURITY Suitable for mass spectrometry (MS), UltraPureChrom™, for UHPLC

Synonyms

Acetonitril (GERMAN, DUTCH) | ACETONITRILE | ace-tonitrile | aceto-nitrile | acetonitrile- | DTXCID909 | acetonitnle | Acetonitrile 1000 microg/mL in Methanol | Acetonitrile, puriss., 95% | Acetonitrile, Environmental Grade | Acetonitrile, for DNA synthes

Storage

Room temperature

Shipped In

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Panoramica

Acetonitrile, an aliphatic nitrile, is a highly volatile, aprotic polar organic solvent that finds wide use in analytical determinations. It is UV-transparent − a property that facilitates its utilization in spectrophotometric and fluorimetric analyses. Its low viscosity, high elution strength and miscibility in water makes it viable in many chromatography systems. Its other applications include its use as a mobile phase additive and as an extraction solvent in liquid-liquid extraction (LLC), solid-phase extraction (SPE) and microextraction for chromatographic applications, etc.

Application

Acetonitrile, an organic solvent, is used as a mobile phase/extraction solvent in the ultra-high performance liquid chromatorgraphy − tandem mass spectrometry (UHPLC-MS) analysis of pesticides in tobacco samples. It can be potentially used with a reverse-phase column to determine the concentration of diclofenac (DCF). Acetonitrile may be used: As an extraction solvent for the quantification of pesticide analytes in foodstuffs and tea, industrial dyes in juice and wine by ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS). As an organic modifier in the determination of bisphenol A-diglycidyl ether, bisphenol F-diglycidyl ether and their derivatives in canned food and beverages by fast LC–MS/MS.

Specifications

Sinonimi

Acetonitril (GERMAN, DUTCH) | ACETONITRILE | ace-tonitrile | aceto-nitrile | acetonitrile- | DTXCID909 | acetonitnle | Acetonitrile 1000 microg/mL in Methanol | Acetonitrile, puriss., 95% | Acetonitrile, Environmental Grade | Acetonitrile, for DNA synthes

Specifiche e purezza

suitable for mass spectrometry (MS), UltraPureChrom™, for UHPLC

Condizioni di conservazione di stoccaggio

Room temperature

Spedito in

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Grado

Adatto alla spettrometria di massa (MS), for UHPLC, UltraPureChrom™

Nomi e identificatori

• Pubchem Sid: 508811849
• Sorrisi canonici: CC#N
• IUPAC Name: acetonitrile
• InChIKey: WEVYAHXRMPXWCK-UHFFFAOYSA-N
• INCHI: 1S/C2H3N/c1-2-3/h1H3
• Isomeri SMILES: CC#N
• WGK Germania: 2
• Numero UN: 1648
• Gruppo di imballaggio: II
• Peso molecolare: 41.05
• Beilstein: 741857

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Classe Organonitrogen compounds
      • Subclass Organic cyanides

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Classe: Organonitrogen compounds
• Subclass: Organic cyanides
• Intermediate Tree Nodes: Not available
• Direct Parent: Nitriles
• Alternative Parents: Organopnictogen compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Nitrile - Carbonitrile - Organopnictogen compound - Hydrocarbon derivative - Aliphatic acyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as nitriles. These are compounds having the structure RC#N; thus C-substituted derivatives of hydrocyanic acid, HC#N.
• External Descriptors: aliphatic nitrile

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Obiettivi associati (non umani)

Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)

Discover Target: Nfe2l2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Meccanismi d'azione

Proprietà chimiche e fisiche

• Indice di rifrazione: 1.343-1.345
• Punto di infiammabilità (°C): 2 °C
• Punto di ebollizione (°C): 81-82°C
• Punto di fusione (°C): -46°C
• Peso molecolare: 41.050 g/mol
• XLogP3: 0.000
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 41.0265 Da
• Monoisotopic Mass: 41.0265 Da
• Topological Polar Surface Area: 23.800 Ų
• Heavy Atom Count: 3
• Formal Charge: 0
• Complexity: 29.300
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1