Regadenoson Impurity B

A Validated RP-HPLC Method for the Determination of 2-Chloroadenosine as Process Related Impurity in Regadenosen Parenteral Dosage Form
Y Rajesh Babu , VVSS Appala Raju and N Appala Raju
J. Chem. Pharm. Res., 2017, 9(7):55-61

Regadenoson Impurity B is chemically 1-(6-Amino-9-β-D-ribofuranosyl-9H-purin-2-yl)-1H-pyrazole-4-carboxylic acid. Regadenoson Impurity B is supplied with detailed characterization data compliant with regulatory guideline. Regadenoson Impurity B 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 Regadenoson.

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.