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Zolmitriptan EP Impurity A
Vildagliptin Deshydroxy Impurity
Etodolac EP Impurity L
Pitavastatin Impurity 3
Vibegron Impurity 25
Pitavastatin Impurity 4
Title Zolmitriptan EP Impurity A Vildagliptin Deshydroxy Impurity Etodolac EP Impurity L Pitavastatin Impurity 3 Vibegron Impurity 25 Pitavastatin Impurity 4
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Description

Zolmitriptan EP Impurity A is chemically (R)-4-({3-[2-(Dimethylamino)ethyl]indol-5-yl}methyl)oxazolidin-2-one ;.
It is also known as Zolmitriptan R-Isomer .
Zolmitriptan EP Impurity A is supplied with detailed characterization data compliant with regulatory guideline. Zolmitriptan 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 Zolmitriptan.

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.

Vildagliptin Deshydroxy Impurity is chemically (2S)-1-{2-[(1-Adamantyl)amino]acetyl} pyrrolidine-2-carbonitrile.
Vildagliptin Deshydroxy Impurity is supplied with detailed characterization data compliant with regulatory guideline. Vildagliptin Deshydroxy 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 Vildagliptin.

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.

Etodolac EP Impurity L  is chemically (EZ)-3-[7-ethyl-3-(2-hydroxyethyl)-1H-indol-2-yl]pent-3-enoic acid (as per EP).
Etodolac EP Impurity L  is supplied with detailed characterization data compliant with regulatory guideline. Etodolac EP Impurity L  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 Etodolac.

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.

Pitavastatin Impurity 3 is chemically 6-Cyclopropyl-10-fluoro-7,8-dihydrobenzo[k]phenanthridine.
Pitavastatin Impurity 3 is supplied with detailed characterization data compliant with regulatory guideline. Pitavastatin 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 Pitavastatin.

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.

Vibegron Impurity 25 is chemically 1-Oxo-1-phenylhex-5-yn-2-yl tert-butylcarbamate.
Vibegron Impurity 25 is supplied with detailed characterization data compliant with regulatory guideline. Vibegron Impurity 25 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 Vibegron.

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.

Pitavastatin Impurity 4 is chemically 6-Cyclopropyl-10-fluorobenzo[k]phenanthridine.
Pitavastatin Impurity 4 is supplied with detailed characterization data compliant with regulatory guideline. Pitavastatin Impurity 4 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 Pitavastatin.

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 139264-24-7 741657-02-3 2789629-50-9 1187966-94-4   1187966-95-5
Inv. Status Limited Stock In Stock In Stock Custom Synthesis Custom Synthesis Custom Synthesis
Mol.F. C16H21N3O2 C17H25N3O C17H21NO3 C20H16FN C17H21NO3 C20H14FN
ISP CAT No ISP-Z004012 ISP-V008035 ISP-E023013 ISP-P023037 ISP-V042027 ISP-P023038
Mol.Wt. 287.4 287.4 287.4 289.4 287.4 287.4