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N-Methyltetrafluorophthalimide
Imidacloprid EP impurity D
Lisdexamphetamine-D3
Medroxyprogesterone Acetate EP Impurity A
Apremilast Impurity 26
Agomelatine D6
Cinnarizine EP Impurity E
Title N-Methyltetrafluorophthalimide Imidacloprid EP impurity D Lisdexamphetamine-D3 Medroxyprogesterone Acetate EP Impurity A Apremilast Impurity 26 Agomelatine D6 Cinnarizine EP Impurity E
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Description

N-Methyltetrafluorophthalimide is chemically 4,5,6,7-Tetrafluoro-2-methylisoindoline-1,3-dione.
N-Methyltetrafluorophthalimide is supplied with detailed characterization data compliant with regulatory guideline. N-Methyltetrafluorophthalimide 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 Moxifloxacin.

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.

Imidacloprid EP impurity Dis chemically N-[1-[[6-[(2-Aminoethyl)amino]pyridin-3-yl]methyl]-4,5-dihydro-1H-imidazol-2-yl]nitramide (as per EP). Imidacloprid EP impurity D is supplied with detailed characterization data compliant with regulatory guideline. Imidacloprid EP impurity D 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 Imidacloprid.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.

Lisdexamphetamine-D3 is chemically (S)-2,6-diamino-N-((S)-1-phenylpropan-2-yl-3,3,3-d3)hexanamide.
Lisdexamphetamine-D3 is supplied with detailed characterization data compliant with regulatory guideline. Lisdexamphetamine-D3 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 Lisdexamfetamine.

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.

Medroxyprogesterone Acetate EP Impurity A is chemically Pregn-​4-​ene-​3,​20-​dione, 17-​(acetyloxy)​-​6-​hydroxy-​6-​methyl-​, (6β)​-; Pregn-4-ene-3,20-dione, 6β,17-dihydroxy-6-methyl-, 17-acetate (7CI,8CI); (6β)-17-(Acetyloxy)-6-hydroxy-6-methylpregn-4-ene-3,20-dione.
Medroxyprogesterone Acetate EP Impurity A is supplied with detailed characterization data compliant with regulatory guideline. Medroxyprogesterone Acetate 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 Progesterone.

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.

Apremilast Impurity 26 is chemically (S)-2-(1-(3-Ethoxy-4-methoxyphenyl)-2-(methylsulfonyl)ethyl)-5-nitroisoindoline-1,3-dione.
Apremilast Impurity 26 is supplied with detailed characterization data compliant with regulatory guideline. Apremilast Impurity 26 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 Apremilast.

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.

Agomelatine D6 is chemically N-(2-(7-(methoxy-d3)naphthalen-1-yl)ethyl)acetamide-2,2,2-d3.
Agomelatine D6 is supplied with detailed characterization data compliant with regulatory guideline. Agomelatine D6 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 Agomelatine.

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.

Cinnarizine EP Impurity E is chemically 1,4-Bis(diphenylmethyl)piperazine.
Cinnarizine EP Impurity E is supplied with detailed characterization data compliant with regulatory guideline. Cinnarizine 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 Cinnarizine.

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 33795-85-6     984-47-4   1079389-42-6 216581-01-0
Inv. Status Custom Synthesis Custom Synthesis Custom Synthesis In Stock In Stock In Stock Custom Synthesis
Mol.F. C9H3F4NO2 C11H17N7O2 C15H22D3N3O C24H34O5 C20H20N2O8S C15H11D6NO2 C30H30N2
ISP CAT No ISP-M033012 ISP-I070005 ISP-L092D01 ISP-P008021 ISP-A051045 ISP-A044D01  
Mol.Wt. 233.1 279.3 266.4 402.5 448.4 249.3 418.6