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Bendamustine Monohydroxy Isopropyl Ester Impurity
Linolenic Acid-13C18
Dihydroartemisinin D-Glucuronide
Quetiapine Nitroso Impurity 1
Pemetrexed Impurity 45
N-Nitroso Sumatriptan EP Impurity E
Siponimod Impurity 24
Linolenic Acid-13C18
Pentoxifylline Impurity 2
Title Bendamustine Monohydroxy Isopropyl Ester Impurity Linolenic Acid-13C18 Dihydroartemisinin D-Glucuronide Quetiapine Nitroso Impurity 1 Pemetrexed Impurity 45 N-Nitroso Sumatriptan EP Impurity E Siponimod Impurity 24 Linolenic Acid-13C18 Pentoxifylline Impurity 2
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Description

Bendamustine Monohydroxy Isopropyl Ester Impurity is chemically isopropyl 4-(5-((2-chloroethyl)(2-hydroxyethyl)amino)-1-methyl-1H-benzo[d]imidazol-2-yl)butanoate hydrochloride.
Bendamustine Monohydroxy Isopropyl Ester Impurity is supplied with detailed characterization data compliant with regulatory guideline. Bendamustine Monohydroxy Isopropyl Ester 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 Bendamustine.

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.

Linolenic Acid-13C18 is chemically (9Z,12Z,15Z)-Octadeca-9,12,15-trienoic-1,2,3,4,5,6,7,8,9,10,11,12,13,14,15,16,17,18-13C18 acid.
Linolenic Acid-13C18 is supplied with detailed characterization data compliant with regulatory guideline. Linolenic Acid-13C18 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.

Dihydroartemisinin D-Glucuronide is chemically (3R,5aS,6R,8aS,9S,12R,12aS)-Decahydro-3,6,9-trimethyl- 3,12-epoxy-12H-pyrano[4,3-j]-1,2-benzodioxepin-10-yl β-D-Glucopyranosiduronic Acid.
It is also known as Dihydroartemisinin glucuronide.
Dihydroartemisinin D-Glucuronide is supplied with detailed characterization data compliant with regulatory guideline. Dihydroartemisinin D-Glucuronide 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 Artemisinin.

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.

Quetiapine Nitroso Impurity 1is chemically 10-Nitroso-10,11-dihydrodibenzo[b,f][1,4]thiazepine. Quetiapine Nitroso Impurity 1 is supplied with detailed characterization data compliant with regulatory guideline. Quetiapine Nitroso 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 Quetiapine.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.

Pemetrexed Impurity 45 is chemically (E)-4-(2-(2-Amino-4-oxo-4,7-dihydro-1H-pyrrolo[2,3-d]pyrimidin-5-yl)vinyl)benzoic acid.
Pemetrexed Impurity 45 is supplied with detailed characterization data compliant with regulatory guideline. Pemetrexed Impurity 45 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 Pemetrexed.

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 Sumatriptan EP Impurity E is chemically 1-(3-(2-Aminoethyl)-1-nitroso-1H-indol-5-yl)-N-methylmethanesulfonamide.
N-Nitroso Sumatriptan EP Impurity E is supplied with detailed characterization data compliant with regulatory guideline. N-Nitroso Sumatriptan EP Impurity E 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 Sumatriptan.

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.

Siponimod Impurity 24 is chemically 1-Cyclohexyl-4-methyl-2-(trifluoromethyl)benzene.
Siponimod Impurity 24 is supplied with detailed characterization data compliant with regulatory guideline. Siponimod Impurity 24 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 Siponimod.

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.

Linolenic Acid-13C18 is chemically (9Z,12Z,15Z)-Octadeca-9,12,15-trienoic-1,2,3,4,5,6,7,8,9,10,11,12,13,14,15,16,17,18-13C18 acid.
Linolenic Acid-13C18 is supplied with detailed characterization data compliant with regulatory guideline. Linolenic Acid-13C18 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.

Pentoxifylline Impurity 2 is chemically Methyl 5-(3,7-dimethyl-2,6-dioxo-2,3,4,5,6,7-hexahydro-1H-purin-1-yl)pentanoate.
Pentoxifylline Impurity 2 is supplied with detailed characterization data compliant with regulatory guideline. Pentoxifylline 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 Pentoxifylline.

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   287111-28-8 198976-06-6 2101854-40-2 1839064-36-6   1449293-48-4 287111-28-8  
Inv. Status In Stock Custom Synthesis Custom Synthesis In Stock Custom Synthesis Custom Synthesis Custom Synthesis Custom Synthesis Custom Synthesis
Mol.F. C19H28ClN3O3 : HCl 13C18H30O2 C21H32O11 C13H10N2OS C15H12N4O3 C12H16N4O3S C14H17F3 13C18H30O2 C13H20N4O4
ISP CAT No ISP-B010016 ISP-M039D24 ISP-A055006 ISP-Q001078 ISP-P014060 ISP-S015046 ISP-S036029 ISP-M039D24 ISP-P063015
Mol.Wt. 381.9 : 36 .5 296.3 460.5 242.3 296.3 296.3 242.3 296.3 296.3