Ledipasvir Impurity 32 CAS CATO-C4X-331332

Purity 97%+In StockPharmacopoeial Impurity Standards
CAS No.CATO-C4X-331332
Molecular FormulaC17H21NO2
Molecular Weight271.35 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Ledipasvir Impurity 32 CAS CATO-C4X-331332 chemical structure

Description

Ledipasvir Impurity 32 (CAS CATO-C4X-331332) is a certified pharmaceutical impurity reference standard with the molecular formula C17H21NO2 and a molecular weight of 271.35 g/mol.

Owing to a steroid core, an amide group, a hydroxyl group, an ether linkage, Ledipasvir Impurity 32 is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 271.35 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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.

CATO manufactures Ledipasvir Impurity 32 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 FormulaC17H21NO2
Molecular Weight271.35 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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
Nitrogen Atoms1

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