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

Clenbuterol Hydrochloride Related Compounds

API Standards

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Clenbuterol Hydrochloride API Standards CS-T-72356 21898-19-1 In Stock


Impurities

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Clenbuterol EP Impurity A Impurities CS-O-14281 62909-66-4 In Stock
Clenbuterol EP Impurity B Impurities CS-O-14282 69708-36-7 Enquire
Clenbuterol EP Impurity C Impurities CS-T-02385 37148-48-4 In Stock


Intermediates

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Hydroxymethyl clenbuterol Hydrochloride Intermediates CS-W-00036 37162-89-3 Enquire