Sumatriptan EP Impurity B (HCl salt)
| CAT No | VV-S002005 |
| CAS No | NA |
| Mol.F. | C13H19N3O2S : HCl |
| Mol.Wt. | 281.4 : 36.5 |
Chemical Name: N-Methyl-1-{3-[2-(methylamino)ethyl]-1H-indol-5-yl}methanesulfonamide hydrochloride (as per EP) ; N-Methyl-1-{3-[2-(methylamino)ethyl]-1H-indol-5-yl}methanesulfonamide Hydrochloride (as per USP)
Synonym: N-Desmethyl Sumatriptan ; Sumatriptan monomethyl (USP) ;
Shipping Temperature: Ambient
Country of Origin: India
Smiles: O=S(CC1=CC=C2C(C(CCNC)=CN2)=C1)(NC)=O.Cl
Sumatriptan EP Impurity B (HCl salt) is chemically N-Methyl-1-{3-[2-(methylamino)ethyl]-1H-indol-5-yl}methanesulfonamide hydrochloride (as per EP) ; N-Methyl-1-{3-[2-(methylamino)ethyl]-1H-indol-5-yl}methanesulfonamide Hydrochloride (as per USP). It is also known as N-Desmethyl Sumatriptan ; Sumatriptan monomethyl (USP) ; . Sumatriptan EP Impurity B (HCl salt) is supplied with detailed characterization data compliant with regulatory guideline. Sumatriptan EP Impurity B (HCl 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 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.