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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

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


Impurity

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-4,7,9,12-tetramethyl-3... Impurity CS-O-57216 ---- Enquire
RETAPAMULIN DIMER Impurity CS-O-57222 ---- Enquire
Retapamulin Impurity 3 Impurity CS-O-57219 ---- Enquire
Retapamulin Impurity 4 Impurity CS-O-57215 ---- Enquire
Retapamulin Impurity 5 Impurity CS-O-57221 ---- Enquire
Retapamulin Impurity 2 Impurity CS-O-57220 Not Available Enquire