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Azilsartan Impurity 32
Vardenafil Impurity 9
Title Azilsartan Impurity 32 Vardenafil Impurity 9
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Description

Azilsartan Impurity 32 is chemically 5,5′-(((2-Oxobutane-1,1-diyl)bis(oxy))bis(methylene))bis(4-methyl-1,3-dioxol-2-one).
Azilsartan Impurity 32 is supplied with detailed characterization data compliant with regulatory guideline. Azilsartan Impurity 32 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 Azilsartan.

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.

Vardenafil Impurity 9 is chemically Methyl 2-(2-ethoxyphenyl)-5-methyl-4-oxo-3,4-dihydroimidazo[5,1-f][1,2,4]triazine-7-carboxylate.
Vardenafil Impurity 9 is supplied with detailed characterization data compliant with regulatory guideline. Vardenafil Impurity 9 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 Vardenafil.

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.

Availability In stock In stock
CAS No    
Inv. Status Custom Synthesis Custom Synthesis
Mol.F. C14H16O9 C16H16N4O4
ISP CAT No ISP-A004057 ISP-V006030
Mol.Wt. 328.3 328.3