Atenolol EP Impurity G
| VS CAT No | VS-A035008 |
| CAS No | 56392-14-4 |
| Mol.F. | C14H21NO4 |
| Mol.Wt. | 267.3 |
| Inv. Status | Custom Synthesis |
| Rel. CAS No | 207287-28-3 (HCl salt) ; 162936-16-5 (potassium salt) |
Chemical Name: [4-[(2RS)-2-Hydroxy-3-[(propan-2-yl)amino]propoxy]phenyl]acetic acid (as per EP) ; 2-{4-[2-Hydroxy-3-(isopropylamino)propoxy]phenyl}acetic acid (as per USP)
Synonym: Atenolol USP Related Compound G
Shipping Temperature: Ambient
Country of Origin: India
Smiles: CC(NCC(O)COC1=CC=C(CC(O)=O)C=C1)C
Atenolol EP Impurity G is chemically [4-[(2RS)-2-Hydroxy-3-[(propan-2-yl)amino]propoxy]phenyl]acetic acid (as per EP) ; 2-{4-[2-Hydroxy-3-(isopropylamino)propoxy]phenyl}acetic acid (as per USP). It is also known as Atenolol USP Related Compound G. Atenolol EP Impurity G is supplied with detailed characterization data compliant with regulatory guideline. Atenolol EP Impurity G 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 Atenolol.
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.