Atorvastatin EP Impurity F Sodium sal

Atorvastatin EP Impurity F Sodium sal

VS CAT No VS-A037112
CAS No 1371615-56-3
Mol.F. C40H47FN3O8 : Na
Mol.Wt. 716.8 : 23.0
Inv. Status Custom Synthesis
Rel. CAS No 887196-24-9 (free base) ; 2093520-34-2 (K salt) ; 1105067-87-5 (Ca salt)

Chemical Name: (3R,5R)-7-[(3R,5R)-7-[2-(4-fluorophenyl)-3-phenyl-4-(phenylcarbamoyl)-5-(propan-2-yl)-1H-pyrrol-1-yl]-3,5-dihydroxyheptanamido]-3,5-dihydroxyheptanoic acid Sodium salt (as per EP)

Synonym: Diamino Atorvastatin Sodium

Shipping Temperature: Ambient

Country of Origin: India

Smiles: O=C([O-])C[C@H](O)C[C@H](O)CCNC(C[C@H](O)C[C@H](O)CCN1C(C2=CC=C(F)C=C2)=C(C3=CC=CC=C3)C(C(NC4=CC=CC=C4)=O)=C1C(C)C)=O.[Na+]

Atorvastatin EP Impurity F Sodium salt is chemically (3R,5R)-7-[(3R,5R)-7-[2-(4-fluorophenyl)-3-phenyl-4-(phenylcarbamoyl)-5-(propan-2-yl)-1H-pyrrol-1-yl]-3,5-dihydroxyheptanamido]-3,5-dihydroxyheptanoic acid Sodium salt (as per EP). It is also known as Diamino Atorvastatin Sodium. Atorvastatin EP Impurity F Sodium salt is supplied with detailed characterization data compliant with regulatory guideline. Atorvastatin EP Impurity F 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.