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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

Stable Isotopes

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Pipendoxifene (Piperidine-D10) Stable Isotopes CS-T-103090 198480-55-6(Unlabelled) Enquire
Endoxifen-D5 Stable Isotopes CS-CX-00685 Not Available Enquire


API

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


Impurity

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
4'-hydroxy Endoxifen Impurity CS-O-52320 1277171-34-2 Enquire
E)-Endoxifen Impurity CS-T-79533 114828-90-9 Enquire
Endoxifen E-isomer Hydrochloride Impurity CS-O-60285 1197194-61-8 Enquire
Endoxifen O-glucuronide Impurity CS-ED-41832 Not Available Enquire
Endoxifen Z-Isomer Hydrochloride Impurity CS-O-33935 1032008-74-4 Enquire