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N-Nitroso Ticagrelor EP Impurity D is chemically N-((1R,2S)-2-(3,4-difluorophenyl)cyclopropyl)-N-(3-((3aS,4R,6S,6aR)-6-(2-hydroxyethoxy)-2,2-dimethyltetrahydro-4H-cyclopenta[d][1,3]dioxol-4-yl)-5-(propylthio)-3H-[1,2,3]triazolo[4,5-d]pyrimidin-7-yl)nitrous amide hydrochloride. N-Nitroso Ticagrelor EP Impurity D is supplied with detailed characterization data compliant with regulatory guideline. N-Nitroso Ticagrelor 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 Ticagrelor.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.

Zanubrutinib Impurity 15 is chemically 3-((7S)-3-carbamoyl-2-(4-phenoxyphenyl)-7-(piperidin-4-yl)-5,6,7,7a-tetrahydro-4H-pyrrolo[3,2-b]pyridin-4-yl)propanoic acid.
Zanubrutinib Impurity 15 is supplied with detailed characterization data compliant with regulatory guideline. Zanubrutinib Impurity 15 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 Zanubrutinib.

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.

Cyclopropyl Urea Impurity is chemically 1-(2-Chloro-4-hydroxyphenyl)-3-cyclopropylurea.
It is also known as Desquinolinyl Lenvatinib.
Cyclopropyl Urea Impurity is supplied with detailed characterization data compliant with regulatory guideline. Cyclopropyl Urea 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 Lenvatinib.

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.

3-Hydroxy Azithromycinoic Acid Sodium Salt  is chemically (2R,3S,4S,5R,8R)-5-(((2S,3R,4S,6R)-4-(dimethylamino)-3-hydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)-3,6-dihydroxy-2,4,6,8-tetramethyl-9-(methyl((2R,3R,4R,5R)-3,4,5-trihydroxy-4-methylheptan-2-yl)amino)nonanoic acid, sodium salt.
3-Hydroxy Azithromycinoic Acid Sodium Salt  is supplied with detailed characterization data compliant with regulatory guideline. 3-Hydroxy Azithromycinoic Acid Sodium Salt  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 Azithromycin.

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.

Dydrogesterone bis(Ethylene Acetal) is chemically (9R,10S,13S,14R,17S)-10,13-Dimethyl-17-(2-methyl-1,3-dioxolan-2-yl)-1,2,4,9,10,11,12,13,14,15,16,17-dodecahydrospiro[cyclopenta[a]phenanthrene-3,2′-[1,3]dioxolane].
Dydrogesterone bis(Ethylene Acetal) is supplied with detailed characterization data compliant with regulatory guideline. Dydrogesterone bis(Ethylene Acetal) 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 Dydrogesterone .

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.