Cefaclor impurities include process-related compounds, degradation products, and structurally related analogs formed during synthesis or storage. These impurities are monitored to ensure the safety and efficacy of this second-generation cephalosporin antibiotic used to treat respiratory, urinary, and skin infections. All materials are structurally confirmed and qualified under ICH guidelines for pharmaceutical analysis and toxicological evaluation.
We offer pharmacopeial and non-pharmacopeial Cefaclor impurities that comply with European Pharmacopoeia (EP) specifications. These impurity standards are essential for method development, impurity profiling, and stability testing. Analytical techniques such as HPLC, LC-MS, and NMR are used for their identification and quantification. EP traceable standards are available upon request.
Our catalog includes Cefaclor-related compounds such as synthetic intermediates, stereoisomers, and stable isotope-labeled analogs. These compounds are essential for forced degradation studies, impurity identification, and genotoxicity screening. All materials are thoroughly characterized and supported by detailed analytical documentation.
Cefaclor impurity reference standards are supplied with validated analytical data including NMR, MS, and HPLC purity. These standards are used in pharmaceutical R&D, ANDA and DMF filings, method validation, and GMP-compliant quality control. EP/USP traceable materials are available upon request, and all products meet international regulatory expectations. Supplied materials are re-tested at regular intervals to ensure consistency.
Address
Plot No. CP-135, Pimpri-Chinhwad MIDC, Pune-411019, Maharashtra, India.
© 2014-2024 SynThink Research Chemicals. All Rights Reserved.
Register to add the product to RFQ list
Already have an account? Log in here
Don’t have an account? Register here
