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

Epinastine Related Compounds

API

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Epinastine Hydrochloride API CS-O-30902 108929-04-0 In Stock


Impurity

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
9,13β-Dehydro Epinastine Hydrochloride Impurity CS-T-51759 141342-70-3 In Stock
Epinastine Impurity 1 Hydrochloride Impurity CS-P-07870 141342-71-4 (free base) Enquire
7-Bromo Epinastine (Impurity B) Hydrobromide Impurity CS-P-07874 1217052-16-8 (free base) Enquire
9-Oxo Epinastine Hydrobromide Impurity CS-P-07871 745761-19-7 Enquire
Epinastine EP Impurity A (Dehydro Epinastine) Impurity CS-P-07873 706753-75-5 Enquire
Epinastine Related Compound A Impurity CS-P-07872 41218-84-2 Enquire


Therapeutic

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Epinastine Therapeutic CS-O-15503 80012-43-7 In Stock