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

Udenafil Related Compounds

Stable Isotopes

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Udenafil-D7 Stable Isotopes CS-P-01189 1175992-76-3 Enquire


API

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Udenafil API CS-T-46099 268203-93-6 In Stock


Impurity

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Udenafil Impurity 3 Impurity CS-P-01738 319491-68-4 In Stock
S-des[2-(1-Methyl-2-pyrrolidinyl)ethyl]amine S-Hydroxy Udena... Impurity CS-O-33279 Not Available Enquire
Udenafil Impurity 2 Impurity CS-P-01737 268204-07-5 Enquire