2-((2-((2-Hydroxybenzyl)amino)phenyl)thio)-N-(p-tolyl)acetamide CAS 763124-66-9

Purity 97%+In StockPharmaceutical Standards
CAS No.763124-66-9
Molecular FormulaC22H22N2O2S
Molecular Weight378.49 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-((2-((2-Hydroxybenzyl)amino)phenyl)thio)-N-(p-tolyl)acetamide CAS 763124-66-9 chemical structure

Description

CATO manufactures 2-((2-((2-Hydroxybenzyl)amino)phenyl)thio)-N-(p-tolyl)acetamide 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 2-((2-((2-Hydroxybenzyl)amino)phenyl)thio)-N-(p-tolyl)acetamide (CAS 763124-66-9), a certified reference material (molecular formula C22H22N2O2S, MW 378.49 g/mol) for analytical method development and quality control.

The molecular framework of 2-((2-((2-Hydroxybenzyl)amino)phenyl)thio)-N-(p-tolyl)acetamide (C22H22N2O2S) is characterized by a steroid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage. 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.

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 FormulaC22H22N2O2S
Molecular Weight378.49 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)13.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1986
Nitrogen Atoms2
Sulfur Atoms1

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