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

Ubrogepant Related Compounds

API

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Ubrogepant API CS-T-62623 1374248-77-7 Enquire


Impurity

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
(3R,5S,6R)-Ubrogepant Diastereiomer impurity Impurity CS-O-45056 Not Available Enquire
N-Destrifluoroethyl Ubrogepant Impurity CS-O-45054 Not Available Enquire
Ubrogepant Benzamide impurity Impurity CS-O-45055 Not Available Enquire
Ubrogepant-R-isomer Impurity CS-O-46820 Not Available Enquire


Intermediate

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
3-amino-6-methyl-5-phenyl-1-(2,2,2-trifluoroethyl)piperidin-... Intermediate CS-O-53489 ---- Enquire