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

Ophiobolin Related Compounds

API

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Ophiobolin A API CS-ED-41603 4611-05-6 Enquire


Metabolite

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Anhydro ophiobolin A Metabolite CS-CM-00008 6026-65-9 Enquire


Impurity

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Ophiobolin H Impurity CS-O-57807 90108-64-8 Enquire
Ophiobolin U Impurity CS-O-57628 ---- Enquire