Sumatriptan EP Impurity A

Sumatriptan EP Impurity A

CAT No VV-S002003
CAS No 545338-89-4
Mol.F. C27H37N5O2S
Mol.Wt. 495.7

Chemical Name: 1-[3-[2-(Dimethylamino)ethyl]-2-[[3-[2-(dimethylamino)ethyl]-1H-indol-5-yl]methyl]-1H-indol-5-yl]-N-methylmethanesulfonamide (as per EP)

Synonym: Sumatriptan USP Related Compound A

Shipping Temperature: Ambient

Country of Origin: India

Smiles: O=S(CC1=CC=C2C(C(CCN(C)C)=C(CC3=CC(C(CCN(C)C)=CN4)=C4C=C3)N2)=C1)(NC)=O

Sumatriptan EP Impurity A is chemically 1-[3-[2-(Dimethylamino)ethyl]-2-[[3-[2-(dimethylamino)ethyl]-1H-indol-5-yl]methyl]-1H-indol-5-yl]-N-methylmethanesulfonamide (as per EP). It is also known as Sumatriptan USP Related Compound A. Sumatriptan EP Impurity A is supplied with detailed characterization data compliant with regulatory guideline. Sumatriptan EP Impurity A 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.