Maprotiline Hydrochloride EP Ipurity D is chemically 3-(9,10-Ethanoanthracen-9(10H)-yl)-N-methylprop-2-en-1-amine (as per EP) ; (3-(9,10-dihydro-9,10-ethanoanthracen-9-yl)-N-methylprop-2-en-1-amine (as per USP). It is also known as Dehydromaprotiline ; USP Related Compound D. Maprotiline Hydrochloride EP Ipurity D is supplied with detailed characterization data compliant with regulatory guideline. Maprotiline Hydrochloride EP Ipurity D 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 Maprotiline Hydrochloride.

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.