3-(Diphenylmethoxy)-1,2-propanediol CAS 19574-66-4

Purity >95%In StockPharmacopoeial Impurity Standards
CAS No.19574-66-4
Molecular FormulaC16H18O3
Molecular Weight258.31 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

3-(Diphenylmethoxy)-1,2-propanediol CAS 19574-66-4 chemical structure

Description

The molecular framework of 3-(Diphenylmethoxy)-1,2-propanediol (C16H18O3) is characterized by a carboxylic acid group, a hydroxyl group, an ether linkage, a polycyclic aromatic system. 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 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).

3-(Diphenylmethoxy)-1,2-propanediol (CAS 19574-66-4) is a certified pharmaceutical impurity reference standard with the molecular formula C16H18O3 and a molecular weight of 258.31 g/mol.

This reference standard supports related-substances testing and method development in line with ICH Q3A/Q3B guidance on impurity control, and is suitable for system suitability testing and forced-degradation studies.

As a certified reference material (CRM), 3-(Diphenylmethoxy)-1,2-propanediol 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 FormulaC16H18O3
Molecular Weight258.31 g/mol
AppearancePale yellow to yellow crystalline powder
Purity>95%
StorageStore at 2-8°C, protect from light, keep sealed and dry
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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1962

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