Atorvastatin EP Impurity C Sodium salt

Atorvastatin EP Impurity C Sodium salt

VS CAT No VS-A037086
CAS No 1807481-00-0
Mol.F. C33H34F2N2O5 : Na
Mol.Wt. 576.6 : 23.0
Inv. Status Custom Synthesis
Rel. CAS No 693793-53-2 (Ca salt) ; 693794-20-6 (free base)

Chemical Name: (3R,5R)-7-[2,3-bis(4-fluorophenyl)-4-(phenylcarbamoyl)-5-(propan-2-yl)-1H-pyrrol-1-yl]-3,5-dihydroxyheptanoic acid Sodium salt (as per EP);Sodium (3R,5R)-7-[2,3-Bis(4-fluorophenyl)-5-isopropyl-4-(phenylcarbamoyl)-1H-pyrrol-1-yl]-3,5-dihydroxyheptanoate (as per USP)

Synonym: Atorvastatin USP Related Compound C ; fluoroatorvastatin (EP)

Shipping Temperature: Ambient

Country of Origin: India

Smiles: O=C(C(C(C1=CC=C(F)C=C1)=C(C2=CC=C(F)C=C2)N3CC[C@@H](O)C[C@@H](O)CC(O)=O)=C3C(C)C)NC4=CC=CC=C4.[Na]

Atorvastatin EP Impurity C Sodium salt is chemically (3R,5R)-7-[2,3-bis(4-fluorophenyl)-4-(phenylcarbamoyl)-5-(propan-2-yl)-1H-pyrrol-1-yl]-3,5-dihydroxyheptanoic acid Sodium salt (as per EP);Sodium (3R,5R)-7-[2,3-Bis(4-fluorophenyl)-5-isopropyl-4-(phenylcarbamoyl)-1H-pyrrol-1-yl]-3,5-dihydroxyheptanoate (as per USP). It is also known as Atorvastatin USP Related Compound C ; fluoroatorvastatin (EP). Atorvastatin EP Impurity C Sodium salt is supplied with detailed characterization data compliant with regulatory guideline. Atorvastatin EP Impurity C Sodium salt can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Atorvastatin.

The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. Vsquare products are for analytical purpose only and not for human use.