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

Oxfendazole Related Compounds

Stable Isotopes

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Oxfendazole D3 Stable Isotopes CS-W-00188 1228182-54-4 Enquire


API

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Oxfendazole API CS-W-00072 53716-50-0 In Stock


Impurity

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Fenbendazole Sulfone Impurity CS-W-00073 54029-20-8 In Stock
Fenbendazole-Amine Sulfoxide Impurity CS-T-75006 69489-26-5 In Stock
Oxfendazole EP Impurity D Impurity CS-O-38219 2197014-92-7 Enquire