Mesalazine EP Impurity F

Mesalazine EP Impurity F, also known as Mesalazine Impurity F (CAS No. 570-23-0), is a high-purity pharmaceutical impurity reference standard with the molecular formula C₇H₇NO₃ and a molecular weight of 153.14 g/mol. It is widely used for pharmaceutical impurity profiling, related substance analysis, HPLC method development, analytical method validation, stability studies, and Quality Control (QC) applications. Characterized using advanced analytical techniques such as HPLC, LC-MS/MS, MS, NMR, and IR spectroscopy, it ensures accurate impurity identification, structural confirmation, and quantitative analysis of Mesalazine API-related impurities. Manasa Life Sciences, a trusted pharmaceutical reference material manufacturer in India, supplies high-quality EP impurity standards, certified reference materials (CRM), and analytical reference standards with excellent purity, consistency, and reliable analytical performance. Our reference standards support pharmaceutical research, API testing, QC laboratories, CROs, and CDMOs while helping meet the requirements of European Pharmacopoeia (EP), United States Pharmacopeia (USP), ICH, US FDA, and EMA regulatory guidelines.