|Product Name||Candesartan EP Impurity E|
|Synonyms||1H-N1-Ethyl Candesartan; (1RS)-1-[[(cyclohexyloxy)carbonyl]oxy]ethyl 2-ethoxy-1-[[2′-(1-ethyl-1H-tetrazol-5-yl)biphenyl-4-yl]methyl]-1H-benzimidazole-7-carboxylate|
Order Candesartan EP Impurity E product with CAS: 914613-35-7 and speed up your Candesartan project. This product is also known as 1H-N1-Ethyl Candesartan; (1RS)-1-[[(cyclohexyloxy)carbonyl]oxy]ethyl 2-ethoxy-1-[[2′-(1-ethyl-1H-tetrazol-5-yl)biphenyl-4-yl]methyl]-1H-benzimidazole-7-carboxylate and can be used as working standard or secondary reference standard. Additional internal validation as per respective FDA regulations/guidelines may require. This compound is generally used for Quality Control (QC), Quality Assurance (QA) during commercial production of Candesartan and its related formulations. Moreover, 1H-N1-Ethyl Candesartan is also used in process of Abbreviated New Drug Application (ANDA) filing to FDA and toxicity study of respective drug formulation. Please also find out other Candesartan related compounds developed in our R&D.
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All products / Impurities / standards are provided with certificate of analysis (CoA) along with the characterization data like 1H-NMR, MASS, HPLC Purity, MSDS (whatever relevant and possible). Moreover, additional data like 13C-NMR, 13C-DEPT NMR, GC, GC-MS, IC, Potency, TGA, Structure Elucidation etc. will be provided on request (extra charges may apply). Products provide by SynThink are for research and development (R&D) use only.
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