Atorvastatin Epoxy Pyrrolooxazin 6-Hydroxy Analog (USP)
| VS CAT No | VS-A037057 |
| CAS No | 1316291-19-6 |
| Mol.F. | C33H34FN2O7 : Na |
| Mol.Wt. | 589.6 : 23.0 |
| Inv. Status | Custom Synthesis |
| Rel. CAS No | 873950-17-5 (free base) |
Chemical Name: Sodium, 4-{6-(4-Fluorophenyl)-7,8-epoxy-6-hydroxy-8a-isopropyl-7-phenyl-8-(phenylcarbamoyl)hexahydro-2H-pyrrolo[2,1-b][1,3]oxazin-2-yl}-3-hydroxybutanoate(as per USP)
Synonym: Atorvastatin Cyclic Isopropyl Impurity ; Atorvastatin FXA Impurity
Shipping Temperature: Ambient
Country of Origin: India
Smiles: O=C(NC1=CC=CC=C1)C2(O3)C(C(C)C)(OC(CC(CC([O-])=O)O)CC4)N4C(C5=CC=C(F)C=C5)(O)C23C6=CC=CC=C6.[Na+]
Atorvastatin Epoxy Pyrrolooxazin 6-Hydroxy Analog (USP) is chemically Sodium, 4-{6-(4-Fluorophenyl)-7,8-epoxy-6-hydroxy-8a-isopropyl-7-phenyl-8-(phenylcarbamoyl)hexahydro-2H-pyrrolo[2,1-b][1,3]oxazin-2-yl}-3-hydroxybutanoate(as per USP). It is also known as Atorvastatin Cyclic Isopropyl Impurity ; Atorvastatin FXA Impurity. Atorvastatin Epoxy Pyrrolooxazin 6-Hydroxy Analog (USP) is supplied with detailed characterization data compliant with regulatory guideline. Atorvastatin Epoxy Pyrrolooxazin 6-Hydroxy Analog (USP) 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.