n-(4-Methoxyphenyl)-3-phenylprop-2-en-1-imine CAS 88315-63-3

Purity 97%+In StockPharmaceutical Standards
CAS No.88315-63-3
Molecular FormulaC16H15NO
Molecular Weight237.30 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

n-(4-Methoxyphenyl)-3-phenylprop-2-en-1-imine CAS 88315-63-3 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including n-(4-Methoxyphenyl)-3-phenylprop-2-en-1-imine.

CATO supplies n-(4-Methoxyphenyl)-3-phenylprop-2-en-1-imine (CAS 88315-63-3), a certified reference material (molecular formula C16H15NO, MW 237.30 g/mol) for analytical method development and quality control.

The molecular framework of n-(4-Methoxyphenyl)-3-phenylprop-2-en-1-imine (C16H15NO) is characterized by a nitrogen-containing heterocyclic scaffold, 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 aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

As a certified reference material (CRM), n-(4-Methoxyphenyl)-3-phenylprop-2-en-1-imine 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 FormulaC16H15NO
Molecular Weight237.30 g/mol
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)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1982
Nitrogen Atoms1

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