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

Cetilistat Related Compounds

API Standards

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Cetilistat API Standards CS-O-01199 282526-98-1 In Stock


Impurities

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Cetilistat Impurity 1 Impurities CS-P-01248 Not Available Enquire
Cetilistat Impurity 2 Impurities CS-P-00879 228176-16-0 Enquire
Cetilistat Impurity 3 Impurities CS-P-00880 135498-43-0 Enquire
Cetilistat Impurity 4 Impurities CS-P-00881 2835-98-5 Enquire
Cetilistat Impurity B Impurities CS-P-01245 890655-08-0 Enquire
Cetilistat Impurity C Impurities CS-P-01246 282526-87-8 Enquire
Cetilistat Impurity D Impurities CS-P-01247 282526-78-7 Enquire