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

Endoxifen Related Compounds

API Standards

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Endoxifen API Standards CS-EK-02697 110025-28-0 Enquire
Endoxifen citrate API Standards CS-O-47341 1372937-28-4 Enquire
Norendoxifen API Standards CS-ED-42202 1308808-22-1 Enquire
Pipendoxifene API Standards CS-T-40042 198480-55-6 Enquire


Impurities

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
4'-hydroxy Endoxifen Impurities CS-O-52320 1277171-34-2 Enquire
Endoxifen O-glucuronide Impurities CS-ED-41832 Not Available Enquire
Endoxifen Z-isomer hydrochloride Impurities CS-O-33935 1032008-74-4 Enquire