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Zolpidem EP Impurity E is chemically (2E)-N,N-dimethyl-4-(4-methylphenyl)-4-oxobut-2-enamide (as per EP) ; N,N-Dimethyl-4-oxo-4-(p-tolyl)but-2-enamide (as per USP).
It is also known as Tolyloyl Acrylamide (USP).
Zolpidem EP Impurity E is supplied with detailed characterization data compliant with regulatory guideline. Zolpidem 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 Zolpidem.

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.

Carfilzomib (2S,4R)-1,2-Hydroxy-O-Acetate is chemically (4S,7S,10S,13R,15S)-10-benzyl-15-hydroxy-7,13-diisobutyl-15-methyl-1-morpholino-2,5,8,11,14-pentaoxo-4-phenethyl-3,6,9,12-tetraazahexadecan-16-yl acetate.
Carfilzomib (2S,4R)-1,2-Hydroxy-O-Acetate is supplied with detailed characterization data compliant with regulatory guideline. Carfilzomib (2S,4R)-1,2-Hydroxy-O-Acetate 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 Carfilzomib.

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.

Vilanterol Impurity 12 is chemically Tert-butyl (2-(2,2-dimethyl-4H-benzo[d][1,3]dioxin-6-yl)-2-oxoethyl)carbamate.
Vilanterol Impurity 12 is supplied with detailed characterization data compliant with regulatory guideline. Vilanterol Impurity 12 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 Vilanterol.

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.

Chlordiazepoxide Impurity 2 is chemically (7-Chloro-5-phenyl-2,3-dihydro-1H-benzo[e][1,4]diazepin-2-yl)methanamine.
Chlordiazepoxide Impurity 2 is supplied with detailed characterization data compliant with regulatory guideline. Chlordiazepoxide Impurity 2 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 Chlordiazepoxide.

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.