Compare products Close window [X]

Ceftriaxone Impurity 1 is chemically S-(Benzo[d]thiazol-2-yl) (E)-2-(2-aminothiazol-4-yl)-2-(methoxyimino)ethanethioate.
Ceftriaxone Impurity 1 is supplied with detailed characterization data compliant with regulatory guideline. Ceftriaxone 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 Ceftriaxone.

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.

2′,7-Bis(triethylsilyl)taxol is chemically (2aR,4S,4aS,6R,9S,11S,12S,12aR,12bS)-9-(((2R,3S)-3-benzamido-3-phenyl-2-((triethylsilyl)oxy)propanoyl)oxy)-12-(benzoyloxy)-11-hydroxy-4a,8,13,13-tetramethyl-5-oxo-4-((triethylsilyl)oxy)-3,4,4a,5,6,9,10,11,12,12a-decahydro-1H-7,11-methanocyclodeca[3,4]benzo[1,2-b]oxete-6,12b(2aH)-diyl diacetate.
2′,7-Bis(triethylsilyl)taxol is supplied with detailed characterization data compliant with regulatory guideline. 2′,7-Bis(triethylsilyl)taxol 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 Paclitaxel.

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.

Sofosbuvir Impurity 80 is chemically 1-((2S,3S,4S,5S)-3-Fluoro-4-hydroxy-5-(hydroxymethyl)-3-methyltetrahydrofuran-2-yl)pyrimidine-2,4(1H,3H)-dione.
Sofosbuvir Impurity 80 is supplied with detailed characterization data compliant with regulatory guideline. Sofosbuvir Impurity 80 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 Sofosbuvir.

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.