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

Umifenovir Related Compounds

API Standards

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Arbidol API Standards CS-ZH-08074 131707-25-0 Enquire


Metabolites

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Arbidol Sulfone Metabolites CS-P-07044 151455-32-2 Enquire
Arbidol Sulfoxide Metabolites CS-P-07043 151455-33-3 Enquire


Impurities

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Arbidol Impurity I Impurities CS-P-07045 153633-10-4 Enquire
ethyl 6-bromo-5-hydroxy-1-methyl-2-((phenylthio)methyl)-4-(p... Impurities CS-O-35980 924838-15-3 Enquire
Umifenovir Sulfate Impurities CS-O-35792 1443454-70-3 Enquire


Glucuronides

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Umifenovir Glucuronide Glucuronides CS-O-35793 Not Available Enquire