4-(4-Benzylphenoxy)-3-methylaniline CAS 946663-76-9

Purity 97%+In StockPharmaceutical Standards
CAS No.946663-76-9
Molecular FormulaC20H19NO
Molecular Weight289.37 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(4-Benzylphenoxy)-3-methylaniline CAS 946663-76-9 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 289.37 g/mol gives 4-(4-Benzylphenoxy)-3-methylaniline distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

4-(4-Benzylphenoxy)-3-methylaniline (CAS 946663-76-9), molecular formula C20H19NO and molecular weight 289.37 g/mol, is a CATO reference standard with documented purity and traceability.

4-(4-Benzylphenoxy)-3-methylaniline (C20H19NO) contains a steroid core, an amide group, a hydroxyl group, an ether linkage. Its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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).

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 4-(4-Benzylphenoxy)-3-methylaniline 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 FormulaC20H19NO
Molecular Weight289.37 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)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Nitrogen Atoms1

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