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

Fimasartan Related Compounds

Stable Isotopes

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Fimasartan D4 Stable Isotopes CS-O-34067 247257-48-3 (Unlabeled) Enquire


API

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Fimasartan API CS-P-00994 247257-48-3 In Stock
Fimasartan Potassium Trihydrate API CS-ED-02423 1020110-23-9 Enquire


Impurity

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Fimasartan Impurity 2 Impurity CS-P-00996 1361024-52-3 In Stock
Fimasartan Potassium Trihydrate Impurity A Impurity CS-O-32434 1315478-13-7 Enquire