Rosuvastatin EP Impurity L, also known as Rosuvastatin 6,7-Dihydro Impurity ;Dihydro Rosuvastatin Calcium is a highly characterized reference material. It fully complies with stringent regulatory standards, including those set by USP, EMA, JP, and BP. This product is essential for use in Abbreviated New Drug Applications (ANDA), New Drug Applications (NDA), and the commercial production of Rosuvastatin . Moreover, it comes with a detailed Structure Elucidation Report (SER), ensuring its accuracy and reliability for a wide range of analytical applications.“ Rosuvastatin EP Impurity L ( CAS No: 1024064-70-7 ) or (3R,5S)-7-[4-(4-Fluorophenyl)-6-(1-methylethyl)-2-[methyl (methyl sulfonyl)amino]-5-pyrimidinyl]-3,5-dihydroxy-heptanoic acid calcium salt is an impurity of Rosuvastatin. Rosuvastatin works by reducing the amount of cholesterol made by the liver. Lowering
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To provide the best experiences, we use technologies like cookies to store and/or access device information. Consenting to these technologies will allow us to process data such as browsing behavior or unique IDs on this site. Not consenting or withdrawing consent, may adversely affect certain features and functions.
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The technical storage or access is strictly necessary for the legitimate purpose of enabling the use of a specific service explicitly requested by the subscriber or user, or for the sole purpose of carrying out the transmission of a communication over an electronic communications network.
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