Candesartan Pharmaceutical Reference Standards

Aligns Pharma science supply high-quality impurities reference standards of Candesartan, pharmacopeial and non-pharmacopeial Candesartan impurities, metabolites, stable isotope products, and nitrosamines (N-NO products). Candesartan impurities reference standards are useful in pharmaceutical research. They are useful in product development, ANDA and DMF filing, quality control (QC), method validation, and stability studies. It is also useful in the identification of unknown impurities and the assessment of genotoxic potential.

Candesartan Cilexetil is an angiotensin-receptor blocker that may be used alone or with other agents to treat hypertension. It is administered orally as the prodrug, candesartan cilexetil, which is rapidly converted to its active metabolite, candesartan, during absorption in the gastrointestinal tract.

 

Our Candesartan impurities reference standard offering includes

  • Candesartan related products are thoroughly characterized with NMR, MASS, IR and HPLC/ GC purity.
  • Candesartan products are supplied with detailed COA & analytical data meeting regulatory compliance.
  • We can also provide Candesartan EP/USP traceable standards based on your requirements.
  • The supplied Candesartan related products are re-tested at regular intervals.

 

CAT No: APS-C00101
CAS No: 145040-37-5
Mol.F.: C33H34N6O6
Mol.Wt.: 610.7
Inv. Status: Inquire