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

Bufotenine Related Compounds

API Standards

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Bufotenine API Standards CS-T-09093 487-93-4 Enquire


Impurities

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Bufotenine Sulfate Impurities CS-O-46654 16369-08-7 Enquire


Intermediates

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
5-Methoxy-N,N-dimethyltryptamine Intermediates CS-EK-00083 1019-45-0 Enquire