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Acalabrutinib Impurity 14 is chemically 4-(8-Amino-3-((1R)-2-((S)-2-(8-amino-1-(4-(phenylcarbamoyl)phenyl)imidazo[1,5-a]pyrazin-3-yl)pyrrolidine-1-carbonyl)cyclopentyl)imidazo[1,5-a]pyrazin-1-yl)-N-(pyridin-2-yl)benzamide.
Acalabrutinib Impurity 14 is supplied with detailed characterization data compliant with regulatory guideline. Acalabrutinib Impurity 14 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 Acalabrutinib.

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.

Droxidopa Nitroso Impurity 1 is chemically 2,3,8,9-Tetrahydroxy-13-nitroso-11,12-dihydro-5,11-epiminodibenzo[a,e][8]annulene-5(6H)-carboxylic acid.
Droxidopa Nitroso Impurity 1 is supplied with detailed characterization data compliant with regulatory guideline. Droxidopa Nitroso Impurity 1 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 Droxidopa.

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.

Posaconazole Impurity 24 is chemically ((3S,5R)-5-((1H-1,2,4-triazol-1-yl)methyl)-5-(2,6-difluorophenyl)tetrahydrofuran-3-yl)methyl 4-methylbenzenesulfonate.
Posaconazole Impurity 24 is supplied with detailed characterization data compliant with regulatory guideline. Posaconazole Impurity 24 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 Posaconazole.

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.