Tramadol EP Impurity A (HCl salt)

Tramadol EP Impurity A (HCl salt) is chemically (1RS,2SR)-2-[(dimethylamino)methyl]-1-(3-methoxyphenyl)cyclohexan-1-ol hydrochloride (as per EP) ; (RS,SR)-1-(3-Methoxyphenyl)-2-(dimethylaminomethyl)cyclohexanol hydrochloride(USP). It is also known as Tramadol USP Related Compound A. Tramadol EP Impurity A (HCl salt) is supplied with detailed characterization data compliant with regulatory guideline. Tramadol EP Impurity A (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 Tramadol.

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.