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

Cefazolin Sodium Related Compounds

API

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Cefazolin Sodium API CS-O-04000 27164-46-1 In Stock
Cefazolin sodium pentahydrate API CS-O-54305 115850-11-8 Enquire


Impurity

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Cefazolin EP Impurity J Impurity CS-O-13463 1675245-00-7 In Stock
Cefazolin Open-Ring Delta-3 Impurity CS-O-37322 ---- Enquire