N-(4-Chlorobenzyl)-3,5-dimethylaniline CAS 356532-17-7

Purity 97%+In StockPharmaceutical Standards
CAS No.356532-17-7
Molecular FormulaC15H16ClN
Molecular Weight245.75 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(4-Chlorobenzyl)-3,5-dimethylaniline CAS 356532-17-7 chemical structure

Description

The occurrence of N-(4-Chlorobenzyl)-3,5-dimethylaniline is closely related to a nitrogen-containing heterocyclic scaffold, a nitrile group, chlorine substitution in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies N-(4-Chlorobenzyl)-3,5-dimethylaniline (CAS 356532-17-7), a certified reference material (molecular formula C15H16ClN, MW 245.75 g/mol) for analytical method development and quality control.

Based on its molecular formula C15H16ClN, N-(4-Chlorobenzyl)-3,5-dimethylaniline contains a nitrogen-containing heterocyclic scaffold, a nitrile group, chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 245.75 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC15H16ClN
Molecular Weight245.75 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentCl-containing
Nitrogen Atoms1

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