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Metoprolol Methoxy Epoxide Impurity is chemically 1-[2-(2-Methoxyethyl)phenyoxy]-2,3-epoxypropane.
It is also known as Metoprolol Methoxy Epoxide Impurity.
Metoprolol Methoxy Epoxide Impurity is supplied with detailed characterization data compliant with regulatory guideline. Metoprolol Methoxy Epoxide Impurity 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 Metoprolol.

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.

Budesonide EP Impurity C (R-Isomer) is chemically (4aR,4bS,5S,6aS,7aR,9R,10aR,11aS,11bS)-5-hydroxy-7a-(hydroxymethyl)-4a,6a-dimethyl-9-propyl-4b,6,6a,7a,10a,11,11a,11b,12,13-decahydrochryseno[2,3-d][1,3]dioxole-2,7(4aH,5H)-dione.
Budesonide EP Impurity C (R-Isomer) is supplied with detailed characterization data compliant with regulatory guideline. Budesonide EP Impurity C (R-Isomer) 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 Budesonide.

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.

Amrubicin Impurity 1 is chemically (7S,9S)-9-acetyl-9-amino-6,7,11-trihydroxy-7,8,9,10-tetrahydrotetracene-5,12-dione.
Amrubicin Impurity 1 is supplied with detailed characterization data compliant with regulatory guideline. Amrubicin 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 Amrubicin.

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 Impurity 41 is chemically Tert-Butyl ((S)-2,6-Dimethyl-3-oxohept-1-en-4-yl)carbamate.
Carfilzomib Impurity 41 is supplied with detailed characterization data compliant with regulatory guideline. Carfilzomib Impurity 41 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.