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Suvorexant Impurity 25 is chemically (R)-4-Benzyl-7-methyl-1,4-diazepane-2,5-dione.
Suvorexant Impurity 25 is supplied with detailed characterization data compliant with regulatory guideline. Suvorexant Impurity 25 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 Suvorexant.

The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. ISP Standards products are for analytical purpose only and not for human use.

N-Nitroso Palonosetron Impurity is chemically N-((R)-1-Phenylethyl)-N-((S)-quinuclidin-3-yl)nitrous amide.
N-Nitroso Palonosetron Impurity is supplied with detailed characterization data compliant with regulatory guideline. N-Nitroso Palonosetron 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 Palonosetron.

The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. ISP Standards products are for analytical purpose only and not for human use.