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

Atrasentan Related Compounds

Stable Isotopes

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Atrasentan mandelate salt D3 Stable Isotopes CS-O-35169 Not Available Enquire
Atrasentan-D3 Stable Isotopes CS-O-53692 1129545-21-6 Enquire


API Standards

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Atrasentan API Standards CS-ED-00035 173937-91-2 Enquire
Atrasentan Hydrochloride API Standards CS-T-04368 195733-43-8 Enquire