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

Cefminox Related Compounds

API

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
cefminox sodium API CS-O-01068 75498-96-3 In Stock
Cefminox Sodium Heptahydrate API CS-T-50434 1351813-81-4 In Stock


Impurity

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Cefminox Sodium Impurity 1 Impurity CS-P-00848 Not Available Enquire
Cefminox Sodium Impurity 2 Impurity CS-P-00849 51138-06-8 Enquire
Cefminox Sodium Impurity 3 Impurity CS-P-00850 Not Available Enquire
Cefminox Sodium Impurity 4 Impurity CS-P-00851 Not Available Enquire
Cefminox Sodium Impurity 5 Impurity CS-P-00852 Not Available Enquire
Cefminox Sodium Impurity 6 HCL Impurity CS-P-00853 Not Available Enquire