N-Benzylidene-(2-hydroxy-1-naphthyl)benzylamine CAS 53983-76-9

Purity 97%+In StockPharmaceutical Standards
CAS No.53983-76-9
Molecular FormulaC24H19NO
Molecular Weight337.41 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-Benzylidene-(2-hydroxy-1-naphthyl)benzylamine CAS 53983-76-9 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 337.41 g/mol gives N-Benzylidene-(2-hydroxy-1-naphthyl)benzylamine distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies N-Benzylidene-(2-hydroxy-1-naphthyl)benzylamine (CAS 53983-76-9), a certified reference material (molecular formula C24H19NO, MW 337.41 g/mol) for analytical method development and quality control.

Owing to a steroid core, an amide group, a hydroxyl group, an ether linkage, N-Benzylidene-(2-hydroxy-1-naphthyl)benzylamine is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 337.41 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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.

CATO manufactures N-Benzylidene-(2-hydroxy-1-naphthyl)benzylamine 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 FormulaC24H19NO
Molecular Weight337.41 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)16.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1972
Nitrogen Atoms1

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