1-N-(2-Phenylethyl)benzene-1,4-diamine CAS 39563-55-8

Purity 97%+In StockPharmaceutical Standards
CAS No.39563-55-8
Molecular FormulaC14H16N2
Molecular Weight212.29 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-N-(2-Phenylethyl)benzene-1,4-diamine CAS 39563-55-8 chemical structure

Description

CATO manufactures 1-N-(2-Phenylethyl)benzene-1,4-diamine under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

CATO supplies 1-N-(2-Phenylethyl)benzene-1,4-diamine (CAS 39563-55-8), a certified reference material (molecular formula C14H16N2, MW 212.29 g/mol) for analytical method development and quality control.

1-N-(2-Phenylethyl)benzene-1,4-diamine (C14H16N2) contains a nitrogen-containing heterocyclic scaffold, a nitrile group. Its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

Physical & Chemical Properties

Molecular FormulaC14H16N2
Molecular Weight212.29 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1968
Nitrogen Atoms2

Related N Standards

Recommended Standards

Why CATO?