N-Phenethyl-4-(2-phenoxyethoxy)aniline CAS 1040691-13-1

Purity 97%+In StockPharmaceutical Standards
CAS No.1040691-13-1
Molecular FormulaC22H23NO2
Molecular Weight333.42 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-Phenethyl-4-(2-phenoxyethoxy)aniline CAS 1040691-13-1 chemical structure

Description

The occurrence of N-Phenethyl-4-(2-phenoxyethoxy)aniline is closely related to a steroid core, an amide group, a hydroxyl group, an ether linkage in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies N-Phenethyl-4-(2-phenoxyethoxy)aniline (CAS 1040691-13-1), a certified reference material (molecular formula C22H23NO2, MW 333.42 g/mol) for analytical method development and quality control.

The molecular framework of N-Phenethyl-4-(2-phenoxyethoxy)aniline (C22H23NO2) 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.

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-Phenethyl-4-(2-phenoxyethoxy)aniline 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 FormulaC22H23NO2
Molecular Weight333.42 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
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Nitrogen Atoms1

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