Lovastatin Impurity 20 CAS CATO-C4X-168420

Purity 95%In StockPharmacopoeial Impurity Standards
CAS No.CATO-C4X-168420
Molecular Formula-
Molecular WeightN/A
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Lovastatin Impurity 20 CAS CATO-C4X-168420 chemical structure

Description

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 process- or degradation-related impurity, Lovastatin Impurity 20 (CAS CATO-C4X-168420, N/A) is essential for impurity profiling, related-substances testing, and forced-degradation studies in pharmaceutical development.

Lovastatin Impurity 20 is supplied as a fully characterized reference material; its structural identity, assigned purity, and stability data are documented in the batch-specific Certificate of Analysis (COA).

CATO manufactures Lovastatin Impurity 20 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 FormulaC15H31A C8H16 C6H10 3*C2H6 CH4
Molecular Weight451.89 g/mol
Purity95%
StorageStore at room temperature
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate
StabilityStable under recommended storage conditions
Degree of Unsaturation (DBE)-0.5

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