N-(5-(Phenoxymethyl)-3-phenyloxazolidin-2-ylidene)aniline CAS 34028-37-0

Purity 97%+In StockPharmaceutical Standards
CAS No.34028-37-0
Molecular FormulaC22H20N2O2
Molecular Weight344.41 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(5-(Phenoxymethyl)-3-phenyloxazolidin-2-ylidene)aniline CAS 34028-37-0 chemical structure

Description

The molecular framework of N-(5-(Phenoxymethyl)-3-phenyloxazolidin-2-ylidene)aniline (C22H20N2O2) is characterized by a steroid core, an amide 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.

N-(5-(Phenoxymethyl)-3-phenyloxazolidin-2-ylidene)aniline (CAS 34028-37-0), molecular formula C22H20N2O2 and molecular weight 344.41 g/mol, is a CATO reference standard with documented purity and traceability.

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.

As a certified reference material (CRM), N-(5-(Phenoxymethyl)-3-phenyloxazolidin-2-ylidene)aniline 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.

Physical & Chemical Properties

Molecular FormulaC22H20N2O2
Molecular Weight344.41 g/mol
AppearancePale yellow to yellow crystalline powder
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)14.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1966
Nitrogen Atoms2

Related N Standards

Recommended Standards

Why CATO?