Lenalidomide

Lenalidomide Impurities

Lenalidomide impurities include process-related compounds, degradation products, and structurally related analogs that may arise during synthesis, formulation, or storage. As a thalidomide derivative used in the treatment of multiple myeloma, myelodysplastic syndromes, and other hematologic malignancies, impurity profiling is essential to ensure product safety, therapeutic efficacy, and regulatory compliance. All impurity compounds are structurally characterized and qualified under ICH guidelines for toxicological evaluation and analytical validation.

Lenalidomide EP Impurities

We offer pharmacopeial and non-pharmacopeial Lenalidomide impurity compounds that conform to European Pharmacopoeia (EP) specifications. These standards support method development, impurity profiling, and stability studies. EP traceable compounds are available upon request and are supplied with validated analytical data including HPLC purity, NMR, and MS characterization.

Lenalidomide Related Compounds

Our catalog includes structurally related compounds and synthetic intermediates associated with Lenalidomide. These compounds are used in forced degradation studies, impurity identification, and toxicological qualification. All entries are supported by comprehensive analytical documentation and meet international regulatory expectations.

Lenalidomide Impurity Reference Standards

Lenalidomide impurity reference standards are supplied with validated analytical data including NMR, MS, and HPLC purity. These compounds are used in pharmaceutical R&D, method validation, and GMP-compliant quality control. EP/USP traceable entries are available upon request. All products are re-tested at regular intervals to ensure consistency and reliability.