Relebactam Impurity 29 CAS CATO-C4X-214429

Purity 95%In StockPharmacopoeial Impurity Standards
CAS No.CATO-C4X-214429
Molecular FormulaHRbS
Molecular WeightN/A
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Relebactam Impurity 29 CAS CATO-C4X-214429 chemical structure

Description

The occurrence of Relebactam Impurity 29 is closely related to a structurally diverse molecular composition in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

As a process- or degradation-related impurity, Relebactam Impurity 29 (CAS CATO-C4X-214429, N/A) is essential for impurity profiling, related-substances testing, and forced-degradation studies in pharmaceutical development.

Relebactam Impurity 29 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).

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 Relebactam Impurity 29 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 FormulaHRbS C4H9NS C7H16 C7H15A2 C2H6
Molecular Weight451.19 g/mol
Purity95%
StorageStore at room temperature, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)-2.0
Nitrogen Atoms1
Sulfur Atoms2

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