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Ruxolitinib N-Oxide Impurity 1 is chemically (R)-4-(1-(2-cyano-1-cyclopentylethyl)-1H-pyrazol-4-yl)-7H-pyrrolo[2,3-d]pyrimidine 1-oxide.
Ruxolitinib N-Oxide Impurity 1 is supplied with detailed characterization data compliant with regulatory guideline. Ruxolitinib N-Oxide 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 Ruxolitinib.

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.

Fluvastatin Impurity 11 is chemically (3R,5S,E)-7-(3-(3-Fluorophenyl)-1-isopropyl-1H-indol-2-yl)-3,5-dihydroxyhept-6-enoic acid.
Fluvastatin Impurity 11 is supplied with detailed characterization data compliant with regulatory guideline. Fluvastatin Impurity 11 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 Fluvastatin.

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.

Adenosine EP Impurity H is chemically 2-Amino-9-β-D-ribofuranosyl-1,9-dihydro-6H-purin-6-one (as per EP);
2-Amino-9-β-d-ribofuranosylpurine-6(1H)-one (as per USP).
It is also known as Guanosine (EP) ; DL-Guanosine ; Guanine ribonucleoside.
Adenosine EP Impurity H is supplied with detailed characterization data compliant with regulatory guideline. Adenosine EP Impurity H 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 Adenosine.

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.