(3,4-dimethoxyphenyl)(phenyl)methanamine hydrochloride CAS 23731-51-3

Purity 97%+In StockPharmaceutical Standards
CAS No.23731-51-3
Molecular FormulaC15H18NO2
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(3,4-dimethoxyphenyl)(phenyl)methanamine hydrochloride CAS 23731-51-3 chemical structure

Description

As a certified reference material (CRM), (3,4-dimethoxyphenyl)(phenyl)methanamine hydrochloride meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

CATO supplies (3,4-dimethoxyphenyl)(phenyl)methanamine hydrochloride (CAS 23731-51-3), a certified reference material (molecular formula C15H18NO2Cl, MW 279.76 g/mol) for analytical method development and quality control.

The molecular framework of (3,4-dimethoxyphenyl)(phenyl)methanamine hydrochloride (C15H18NO2Cl) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine 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 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).

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

Physical & Chemical Properties

Molecular FormulaC15H18NO2 Cl
Molecular Weight279.76 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
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.)1963
Halogen ContentCl-containing
Nitrogen Atoms1

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