Lefamulinum Impurity 15 CAS CATO-C4X-304715

Purity 90%In StockPharmacopoeial Impurity Standards
CAS No.CATO-C4X-304715
Molecular FormulaC29H47NO5S
Molecular Weight521.75 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Lefamulinum Impurity 15 CAS CATO-C4X-304715 chemical structure

Description

As a process- or degradation-related impurity, Lefamulinum Impurity 15 (CAS CATO-C4X-304715, C29H47NO5S) is essential for impurity profiling, related-substances testing, and forced-degradation studies in pharmaceutical development.

Lefamulinum Impurity 15 (C29H47NO5S) contains a steroid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage. The carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

Recommended for quantitative analysis by HPLC, GC, LC-MS/MS, or GC-MS as an external calibration standard; it can also be used for spiked-recovery experiments, LOD/LOQ determination, and LC-MS/MS multiple-reaction-monitoring (MRM) calibration.

CATO manufactures Lefamulinum Impurity 15 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 FormulaC29H47NO5S
Molecular Weight521.75 g/mol
Purity90%
StorageStore at room temperature, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
Nitrogen Atoms1
Sulfur Atoms1

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