Sumatriptan EP Impurity E
| CAT No | VV-S002008 |
| CAS No | 88919-22-6 |
| Mol.F. | C12H17N3O2S |
| Mol.Wt. | 267.4 |
Chemical Name: 1-[3-(2-aminoethyl)-1H-indol-5-yl]-N-methylmethanesulfonamide,(as per EP) ; N-Methyl-1-{3-[2-(methylamino)ethyl]-1H-indol-5-yl}methanesulfonamide (as per USP)
Synonym: Sumatriptan amino (USP)
Shipping Temperature: Ambient
Country of Origin: India
Smiles: O=S(CC1=CC=C2C(C(CCN)=CN2)=C1)(NC)=O
Sumatriptan EP Impurity E is chemically 1-[3-(2-aminoethyl)-1H-indol-5-yl]-N-methylmethanesulfonamide,(as per EP) ; N-Methyl-1-{3-[2-(methylamino)ethyl]-1H-indol-5-yl}methanesulfonamide (as per USP). It is also known as Sumatriptan amino (USP). Sumatriptan EP Impurity E is supplied with detailed characterization data compliant with regulatory guideline. Sumatriptan EP Impurity E 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 Sumatriptan.
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.