Desogestrel EP Impurity C/Desogestrel USP RC D CAS 54024-21-4

Purity >95%In StockPharmacopoeial Impurity Standards
CAS No.54024-21-4
Molecular FormulaC20H28O
Molecular Weight284.44 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Desogestrel EP Impurity C/Desogestrel USP RC D CAS 54024-21-4 chemical structure

Description

The molecular framework of Desogestrel EP Impurity C/Desogestrel USP RC D (C20H28O) is characterized by a steroid core, 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.

Desogestrel EP Impurity C/Desogestrel USP RC D (CAS 54024-21-4) is a certified pharmaceutical impurity reference standard with the molecular formula C20H28O and a molecular weight of 284.44 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.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC20H28O
Molecular Weight284.44 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity>95%
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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1972

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