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Title | Oteracil Potassium | Indomethacin EP Impurity G | Pyrantel EP Impurity A | Posaconazole Impurity 44 | Cyantraniliprole Impurity 7 | Tiamulin EP Impurity M | Myristyl Stearate | Lusutrombopag Impurity 1 | Methylprednisolone EP Impurity C |
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Description |
Oteracil Potassiumis chemically Potassium 4,6-dioxo-1,4,5,6-tetrahydro-1,3,5-triazine-2-carboxylate. Oteracil Potassium is supplied with detailed characterization data compliant with regulatory guideline. Oteracil Potassium 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 Oteracil.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. |
Indomethacin EP Impurity G is chemically 2-(1-(3,4-Dichlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl)acetic acid. 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. |
Pyrantel EP Impurity A is chemically 1-methyl-2-[(Z)-2-(thiophen-2-yl)eth-1-en-1-yl]-1,4,5,6-tetrahydropyrimidine. 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. |
Posaconazole Impurity 44 is chemically 4-(4-((2-((4-(((3R,5R)-5-((1H-1,2,4-triazol-1-yl)methyl)-5-(2,4-difluorophenyl)tetrahydrofuran-3-yl)methoxy)phenyl)amino)ethyl)amino)phenyl)-2-((2S,3S)-2-hydroxypentan-3-yl)-2,4-dihydro-3H-1,2,4-triazol-3-one. 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. |
Cyantraniliprole Impurity 7 is chemically 3-Bromo-1-(3-chloropyridin-2-yl)-N-(4-formamido-2-methyl-6-(methylcarbamoyl)phenyl)-1H-pyrazole-5-carboxamide. 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. |
Tiamulin EP Impurity M is chemically (3aS,4R,5S,6S,8R,9R,9aR,10R)-6-ethenyl-4,6,9,10-tetramethyl-1-oxodecahydro-3a,9propano-3aH-cyclopentacycloocten-5,8-diyl diacetate. Tiamulin EP Impurity M is supplied with detailed characterization data compliant with regulatory guideline. Tiamulin EP Impurity M 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 Tiamulin .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. |
Myristyl Stearate is chemically Tetradecyl stearate. 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. |
Lusutrombopag Impurity 1is chemically (E)-3,5-dichloro-4-(3-ethoxy-2-methyl-3-oxoprop-1-en-1-yl)benzoic acid. Lusutrombopag Impurity 1 is supplied with detailed characterization data compliant with regulatory guideline. Lusutrombopag 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 Lusutrombopag.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. |
Methylprednisolone EP Impurity C is chemically 11β-hydroxy-6α-methylandrosta-1,4-diene-3,17-dione,. 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. |
Availability | In stock | In stock | In stock | In stock | In stock | In stock | In stock | In stock | In stock |
CAS No | 2207-75-2 | 402849-26-7 | 36700-38-6 | 1370190-94-5 | 2957882-50-5 | 14431-61-9 | 17661-50-6 | 1110767-89-9 | 61919-52-6 |
Inv. Status | Custom Synthesis | In Stock | Custom Synthesis | In Stock | Custom Synthesis | Custom Synthesis | Custom Synthesis | Custom Synthesis | In Stock |
Mol.F. | C4H2N3O4 : K | C19H15Cl2NO4 | C11H14N2S | C35H40F2N8O4 | C19H16BrClN6O3 | C24H36O5 | C32H64O2 | C13H12Cl2O4 | C20H26O3 |
ISP CAT No | ISP-O064001 | ISP-I017008 | ISP-P050002 | ISP-P022064 | ISP-T044014 | ISP-M039990 | ISP-L055002 | ISP-M037004 | |
Mol.Wt. | 156.1 : 39.1 | 392.2 | 206.3 | 674.8 | 491.7 | 404.6 | 480.9 | 303.1 | 314.4 |