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

Hexoprenaline Related Compounds

API Standards

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Hexoprenaline API Standards CS-T-55631 3215-70-1 Enquire
Hexoprenaline Sulphate API Standards CS-P-01040 32266-10-7 Enquire


Impurities

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Hexoprenaline diol impurity Impurities CS-O-57956 Not Available Enquire
Hexoprenaline Impurity 1 Impurities CS-O-57955 Not Available Enquire