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Sofosbuvir Impurity 81
Sitagliptin Acetone Enamine
Sofosbuvir Impurity 36
Linagliptin Dimer Impurity 2
Fosaprepitant Impurity 12
N-Nitroso Pantoprazole EP Impurity B
Mebeverine Impurity 2
Mebeverine Impurity 3
Fosaprepitant Impurity 8
Title Sofosbuvir Impurity 81 Sitagliptin Acetone Enamine Sofosbuvir Impurity 36 Linagliptin Dimer Impurity 2 Fosaprepitant Impurity 12 N-Nitroso Pantoprazole EP Impurity B Mebeverine Impurity 2 Mebeverine Impurity 3 Fosaprepitant Impurity 8
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Description

Sofosbuvir Impurity 81 is chemically 1-((2R,3R,4R,5R)-3,4-Dihydroxy-5-(hydroxymethyl)-3-methyltetrahydrofuran-2-yl)pyrimidine-2,4(1H,3H)-dione.
Sofosbuvir Impurity 81 is supplied with detailed characterization data compliant with regulatory guideline. Sofosbuvir Impurity 81 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 Sofosbuvir.

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.

Sitagliptin Acetone Enamine is chemically (E)-3-(Isopropylamino)-1-(3-(trifluoromethyl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)-4-(2,4,5-trifluorophenyl)but-2-en-1-one.
Sitagliptin Acetone Enamine is supplied with detailed characterization data compliant with regulatory guideline. Sitagliptin Acetone Enamine 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 Sitagliptin.

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.

Sofosbuvir Impurity 36 is chemically 1-((2S,3S,4R,5R)-3,4-Dihydroxy-5-(hydroxymethyl)-3-methyltetrahydrofuran-2-yl)pyrimidine-2,4(1H,3H)-dione.
Sofosbuvir Impurity 36 is supplied with detailed characterization data compliant with regulatory guideline. Sofosbuvir Impurity 36 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 Sofosbuvir.

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.

Linagliptin Dimer Impurity 2 is chemically 8-((R)-3-aminopiperidin-1-yl)-1-((4-((2-((8-((R)-3-aminopiperidin-1-yl)-7-(but-2-yn-1-yl)-3-methyl-2,6-dioxo-2,3,6,7-tetrahydro-1H-purin-1-yl)methyl)-4-methyl-1,4-dihydroquinazolin-4-yl)methyl)quinazolin-2-yl)methyl)-7-(but-2-yn-1-yl)-3-methyl-3,7-dihydro-1H-purine-2,6-dione.
Linagliptin Dimer Impurity 2 is supplied with detailed characterization data compliant with regulatory guideline. Linagliptin Dimer Impurity 2 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 Linagliptin.

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.

Fosaprepitant Impurity 12 is chemically (S)-4-Benzyl-2-((R)-1-(3,5-bis(trifluoromethyl)phenyl)ethoxy)morpholin-3-one.
Fosaprepitant Impurity 12 is supplied with detailed characterization data compliant with regulatory guideline. Fosaprepitant Impurity 12 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 Fosaprepitant.

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.

N-Nitroso Pantoprazole EP Impurity B is chemically 5-(Difluoromethoxy)-2-(((3,4-dimethoxypyridin-2-yl)methyl)thio)-1-nitroso-1H-benzo[d]imidazole.
It is also known as N-Nitroso Pantoprazole USP Related Compound B ; N-Nitroso Pantoprazole Sulfide.
N-Nitroso Pantoprazole EP Impurity B is supplied with detailed characterization data compliant with regulatory guideline. N-Nitroso Pantoprazole EP Impurity B 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 Pantoprazole.

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.

Mebeverine Impurity 2 is chemically 4-Bromobutyl 3-hydroxy-4-methoxybenzoate.
Mebeverine Impurity 2 is supplied with detailed characterization data compliant with regulatory guideline. Mebeverine Impurity 2 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 Mebeverine.

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.

Mebeverine Impurity 3 is chemically 4-Bromobutyl 4-hydroxy-3-methoxybenzoate.
Mebeverine Impurity 3 is supplied with detailed characterization data compliant with regulatory guideline. Mebeverine Impurity 3 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 Mebeverine.

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.

Fosaprepitant Impurity 8 is chemically 5-(((2R,3S)-3-((S)-1-(3,5-Bis(trifluoromethyl)phenyl)ethoxy)-2-(4-fluorophenyl)morpholino)methyl)-1,2-dihydro-3H-1,2,4-triazol-3-one.
Fosaprepitant Impurity 8 is supplied with detailed characterization data compliant with regulatory guideline. Fosaprepitant Impurity 8 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 Fosaprepitant.

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 31448-54-1     1418133-47-7 327623-36-9     943723-19-1  
Inv. Status Out of Stock Custom Synthesis Custom Synthesis In Stock Custom Synthesis Inquire In Stock In Stock Custom Synthesis
Mol.F. C10H14N2O6 C19H19F6N5O C10H14N2O6 C50H56N16O4 C21H19F6NO3 C16H14F2N4O4S C12H15BrO4 C12H15BrO4 C23H21F7N4O3
ISP CAT No ISP-S010104 ISP-S009176 ISP-S010059 ISP-L024014 ISP-F017033 ISP-P009080 ISP-M054017 ISP-M054018 ISP-F017027
Mol.Wt. 258.2 447.4 258.2 945.1 447.4 396.4 303.2 303.2 534.4