|Product Name||Atorvastatin EP Impurity E|
|CAS Number||501121-34-2, 1105067-88-6 (Ca Salt)|
|Synonyms||Atorvastatin USP RC E; ent-Atorvastatin; (3S, 5S)-Atorvastatin; (3S,5S)-7-[3-(Phenylcarbamoyl)-5-(4-fluorophenyl)-2-isopropyl-4-phenyl-1H-pyrrol-1-yl]-3,5-dihydroxyheptanoic acid; (βS,δS)-2-(4-Fluorophenyl)-β,δ-dihydroxy-5-(1-methylethyl)-3-phenyl-4-[(phenylamino)carbonyl]-1H-pyrrole-1-heptanoic Acid|
Atorvastatin EP Impurity E product with CAS number 501121-34-2, 1105067-88-6 (Ca Salt) and catalog number SA17813 is related to Atorvastatin. This product is used for Abbreviated New Drug Application (ANDA) filing to FDA as well as for Quality Control (QC), toxicity studies and other analytical studies during commercial production of Atorvastatin.
Atorvastatin (lipid-lowering agent) is used to treat high cholesterol, and to lower the risk of stroke, heart attack. Atorvastatin is in a group of drugs called HMG CoA reductase inhibitors, or “statins.”
All products / Impurities / standards are provided with certificate of analysis (CoA) along with the characterization data like 1H-NMR, MASS, HPLC Purity etc. (whatever relevant and possible). Moreover, additional data like 13C-NMR, 13C-DEPT NMR, GC, GC-MS, IC, Potency, TGA, etc. will be provided on request (extra charges may apply).
This product is for research and development (R&D) use only.
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