(4-Chlorobenzyl)(3,4-dimethoxybenzyl)amine hydrobromide CAS 1609400-57-8

Purity 97%+In StockPharmaceutical Standards
CAS No.1609400-57-8
Molecular FormulaC16H18ClNO2
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(4-Chlorobenzyl)(3,4-dimethoxybenzyl)amine hydrobromide CAS 1609400-57-8 chemical structure

Description

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.

(4-Chlorobenzyl)(3,4-dimethoxybenzyl)amine hydrobromide (CAS 1609400-57-8) is a high-purity analytical reference standard with the molecular formula C16H18ClNO2HBr and a molecular weight of 372.69 g/mol.

The molecular framework of (4-Chlorobenzyl)(3,4-dimethoxybenzyl)amine hydrobromide (C16H18ClNO2HBr) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine/bromine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

CATO manufactures (4-Chlorobenzyl)(3,4-dimethoxybenzyl)amine hydrobromide 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.

Physical & Chemical Properties

Molecular FormulaC16H18ClNO2 HBr
Molecular Weight372.69 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1993
Halogen ContentCl/Br-containing
Nitrogen Atoms1

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