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

Auristatin Related Compounds

Stable Isotopes

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Auristatin F-D3 Stable Isotopes CS-T-103344 163768-50-1(unlabelled) Enquire
Monomethyl auristatin E-d8 Stable Isotopes CS-O-32867 2070009-72-0 Enquire
Monomethyl Auristatin F-d8 (MMAF-d8) Stable Isotopes CS-O-58976 2983160-12-7 Enquire


API Standards

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Auristatin F API Standards CS-T-95836 163768-50-1 Enquire
Auristatin F-HPA API Standards CS-O-43825 1415659-09-4 Enquire


Intermediates

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Auristatin F Intermediates CS-ED-11772 163768-50-1 Enquire
Monomethyl Auristatin D (MMAD) Intermediates CS-T-82891 203849-91-6 Enquire


Glucuronides

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
MonoMethyl Auristatin E-Beta-D-glucuronide Glucuronides CS-O-38716 Not Available Enquire