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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
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.
It is also known as Indomethacin 3,4-DiChloro Analog.
Indomethacin EP Impurity G is supplied with detailed characterization data compliant with regulatory guideline. Indomethacin 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 Indomethacin.

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.
Pyrantel EP Impurity A is supplied with detailed characterization data compliant with regulatory guideline. Pyrantel EP Impurity A 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 Pyrantel.

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.
It is also known as Desethylene Posaconazole.
Posaconazole Impurity 44 is supplied with detailed characterization data compliant with regulatory guideline. Posaconazole Impurity 44 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 Posaconazole.

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.
Cyantraniliprole Impurity 7 is supplied with detailed characterization data compliant with regulatory guideline. Cyantraniliprole Impurity 7 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 Cyantraniliprole.

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.
Myristyl Stearate is supplied with detailed characterization data compliant with regulatory guideline. Myristyl Stearate 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 Miscellaneous.

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,.
It is also known as Methylprednisolone USP Related Compound C .
Methylprednisolone EP Impurity C is supplied with detailed characterization data compliant with regulatory guideline. Methylprednisolone EP Impurity C 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 Methylprednisolone.

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.

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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