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Clearsynth is a leading innovator in pharmaceutical reference standards, offering high-quality Reference Standards for Diflucortolone Valerate, including both pharmacopeial and non-pharmacopeial impurities, metabolites, stable isotope products, and nitrosamines (N-NO products). Our Diflucortolone Valerate 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 Diflucortolone Valerate-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.

Diflucortolone Valerate Related Compounds

API Standards

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Diflucortolone 21-Valerate API Standards CS-P-07906 59198-70-8 In Stock


Impurities

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
6β-fluoro diflucortolone valerate Impurities CS-O-49360 Not Available Enquire
Diflucortolone Valerate Impurity 14 Impurities CS-EO-03213 Not Available Enquire
Diflucortolone Valerate Impurity 6 Impurities CS-EO-01151 Not Available Enquire