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

Imrecoxib Related Compounds

API Standards

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Imrecoxib API Standards CS-AP-00026 395683-14-4 Enquire


Metabolites

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Imrecoxib Metabolite (M2) Metabolites CS-AP-00025 896729-08-1 Enquire
Imrecoxib Metabolite (M4) Metabolites CS-AP-00024 896729-07-0 Enquire


Impurities

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Imrecoxib related compound Impurities CS-AP-00027 Not Available Enquire