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Clearsynth is a leading innovator in pharmaceutical reference standards, offering high-quality Reference Standards for Retapamulin, including both pharmacopeial and non-pharmacopeial impurities, metabolites, stable isotope products, and nitrosamines (N-NO products). Our Retapamulin impurity reference standards are invaluable for pharmaceutical research, supporting product development, ANDA and DMF submissions, quality control (QC), method validation, and stability studies. They also aid in identifying unknown impurities and assessing genotoxic potential.
Our Retapamulin-related products undergo thorough characterization and are supplied with detailed Certificates of Analysis (COA) and analytical data that meet regulatory requirements. All supplied products are re-tested at regular intervals to ensure ongoing quality and compliance.

Retapamulin Related Compounds

API Standards

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Retapamulin API Standards CS-O-02231 224452-66-8 In Stock


Impurities

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-4,7,9,12-tetramethyl-3... Impurities CS-O-57216 Not Available Enquire
RETAPAMULIN DIMER Impurities CS-O-57222 Not Available Enquire
Retapamulin Impurity 3 Impurities CS-O-57219 Not Available Enquire
Retapamulin Impurity 4 Impurities CS-O-57215 Not Available Enquire
Retapamulin Impurity 5 Impurities CS-O-57221 Not Available Enquire