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Cefepime EP Impurity D is chemically (2Z)-(2-Aminothiazol-4-yl)(methoxyimino)acetic acid (as per EP);
(Z)-2-(2-Aminothiazol-4-yl)-2-(methoxyimino)acetic acid (as per USP).
It is also known as Cefepime USP Related Compound D ; Thiazolylglyoxalic methyloxime.
Cefepime EP Impurity D is supplied with detailed characterization data compliant with regulatory guideline. Cefepime EP Impurity D 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 Cefepime.

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.

Beraprost is chemically 4-((1R,2R,3aS,8bS)-2-Hydroxy-1-((3S,E)-3-hydroxy-4-methyloct-1-en-6-yn-1-yl)-2,3,3a,8b-tetrahydro-1H-cyclopenta[b]benzofuran-5-yl)butanoic acid.
Beraprost is supplied with detailed characterization data compliant with regulatory guideline. Beraprost 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 Beraprost.

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.

Hydralazine Impurity 14 is chemically (1R,2R,3R,4R)-1-([1,2,4]Triazolo[3,4-a]phthalazin-3-yl)pentane-1,2,3,4,5-pentaol.
Hydralazine Impurity 14 is supplied with detailed characterization data compliant with regulatory guideline. Hydralazine 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 Hydralazine.

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.

Zidovudine EP Impurity G is chemically 1-[(2R,4S,5S)-4-azido-5-(hydroxymethyl)tetrahydrofuran-2-yl]-3-[(2S,3S,5R)-2-(hydroxymethyl)-5-(5-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)tetrahydrofuran-3-yl]-5-methylpyrimidine-2,4(1H,3H)-dione.
Zidovudine EP Impurity G is supplied with detailed characterization data compliant with regulatory guideline. Zidovudine EP Impurity G 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 Zidovudine.

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.