Valsartan Desvaleryl Nitroso Impurity

Valsartan Desvaleryl Nitroso Impurity is chemically ((2'-(2-Nitroso-2H-tetrazol-5-yl)-[1,1'-biphenyl]-4-yl)methyl)-L-valine. Valsartan Desvaleryl Nitroso Impurity is supplied with detailed characterization data compliant with regulatory guideline. Valsartan Desvaleryl Nitroso Impurity 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 Valsartan .

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.

Identification and characterization of potential impurities of valsartan, AT1 receptor antagonist
A.Sampath, A. Raghupathi Reddy, B.Yakambaram, A.Thirupathi, M.Prabhakar, P. Pratap Reddy, V. Prabhakar Reddy
Journal of Pharmaceutical and Biomedical Analysis Volume 50, Issue 3, 15 October 2009, Pages 405-412
 
Monitoring of Impurity Level of Valsartan and Hydrochlorothiazide Employing an RP–HPLC Gradient Mode
Darko Ivanović,Anđelija Malenović,Biljana Jančić,Prof. Dr. Mirjana Medenica  &Marija Mašković
Journal of Liquid Chromatography & Related Technologies  Volume 30, 2007 - Issue 19 Pages 2879-2890
 
A liquid chromatographic method for separation of sacubitril–valsartan and their stereoisomeric impurities
Lu Zhou, Liang Zou, Lili Sun, Hui Zhang, Wenkai Hui and  Qiaogen Zou
Anal. Methods, 2018,10, 1046-1053

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• In Stock product will dispatch in 24 h after receipt of purchase order. It usually take 2-3 days to receive products in India and 5-6 working days for export customer depending on destination.
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• Controlled substance charges need to follow as per quotation. The specific inputs are required for controlled substance because regulatory status will differ based on destination.
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• For ice pack there are no additional charges.

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