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

Febantel Related Compounds

API Standards

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Febantel API Standards CS-T-54665 58306-30-2 In Stock
Fenbendazole API Standards CS-O-11650 43210-67-9 In Stock


Impurities

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
1-Nitro Febantel Impurities CS-T-32617 63470-85-9 Enquire
2-(Methoxymethyl)-5-(phenylthio)-1H-benzimidazole Impurities CS-T-32569 92114-71-1 In Stock
Febantel EP Impurity A Impurities CS-T-16101 92088-58-9 In Stock