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

Isoxsuprine Related Compounds

Stable Isotopes

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Isoxsuprine-13C6 hydrochloride (mixture of diastereomers) Stable Isotopes CS-W-00532 Not Available Enquire


API Standards

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Isoxsuprine Hydrochloride API Standards CS-O-01667 579-56-6 Enquire


Impurities

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Isoxsuprine EP impurity A Impurities CS-EO-00717 1518-97-4 Enquire
Isoxsuprine EP impurity B Impurities CS-O-13828 395-28-8 Enquire