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

Ufenamate Related Compounds

Impurities

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
N-Nitroso Ufenamate Impurities CS-O-46405 Not Available In Stock


Intermediates

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Ufenamate Intermediates CS-T-87391 67330-25-0 In Stock