Dutasteride EP Impurity D

Rapid and Sensitive LC–MS–MS Method for the Simultaneous Estimation of Alfuzosin and Dutasteride in Human Plasma
Noel A. Gomes1,2,&, Ashutosh Pudage2 , Santosh S. Joshi2 , Vikas V. Vaidya1 , Sagar A. Parekh2 , Amod V. Tamhankar
Chromatographia 69(1):9-18
 
Development and validation of stability indicating RP-HPLC with UV detection method: Analysis of Dutasteride in pharmaceutical dosage forms
Atkuru Veera Venkata Naga Krishna Sunil Kumar1*, Chandra Bala Sekaran2 and Tamanampudi Varahala Reddy3
Journal of Chemical and Pharmaceutical Research, 2015, 7(6):60-70

Dutasteride EP Impurity D is chemically N-[2,5-Bis(trifluoromethyl)phenyl]-3-oxo-4-azaandrost-1,5-diene-17α-carboxamide ;. It is also known as 5,6-Dehydro-17α-Dutasteride ; Dutasteride 17α-5-ene. Dutasteride EP Impurity D is supplied with detailed characterization data compliant with regulatory guideline. Dutasteride EP Impurity 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 Dutasteride.

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.