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

Suplatast Related Compounds

Impurities

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Suplatast Acrylamide D5 Impurities CS-O-45786 Not Available Enquire
Suplatast Acrylamide impurity Impurities CS-O-45785 Not Available Enquire
Suplatast Tosilate D5 Impurities CS-O-45784 Not Available Enquire
Suplatast Tosylate Impurities CS-O-05284 94055-76-2 Enquire


Intermediates

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Suplatast Acrylamide impurity D4 Intermediates CS-T-96060 Not Available Enquire
Suplatast-d4 Tosylate Intermediates CS-T-96059 94055-76-2 (Unlabelled) Enquire