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Sumatriptan EP Impurity A

N° de SZ CAT:SZ-S015002
Número CAS545338-89-4
Mol.F.C27H37N5O2S
Peso Molecular495.7
Status de FaturaLimited Stock

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

Sinônimo: Sumatriptan USP Related Compound A

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

Sorrisos: 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. SynZeal products are for analytical purpose only and not for human use.

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