Chlorambucil EP Impurity E

Method development and validation for the estimation of chlorambucil in bulk and pharmaceutical dosage forms using UV-​VIS spectrophotometric method
By Dey, Suddhasattya; Samal, Himansu Bhusan; Monica, P.; Reddy, Sandeep; Karthik, G.; Gujrati, Rohit; Geeta, B.
From Journal of Pharmacy Research (2011), 4(9), 3244-3246
 
High-​performance liquid chromatography of chlorambucil analogs
By Workman, P.; Oppitz, M.; Donaldson, J.; Lee, F. Y. F.
From Journal of Chromatography, Biomedical Applications (1987), 422, 315-21
 

 

Chlorambucil EP Impurity E is chemically 4-[4-[[2-[[4-[4-[bis(2-chloroethyl)amino]phenyl]butanoyl]oxy]ethyl](2-chloroethyl)amino]phenyl]butanoic acid (as per EP). It is also known as Chlorambucil Dimer Impurity. Chlorambucil EP Impurity E is supplied with detailed characterization data compliant with regulatory guideline. Chlorambucil EP Impurity E 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 Chlorambucil.

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.