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Valsartan N-Oxide 1
Apremilast Impurity 16
Amoxapine 8-Hydroxy Impurity
Brexpiprazole Impurity 36
Title Valsartan N-Oxide 1 Apremilast Impurity 16 Amoxapine 8-Hydroxy Impurity Brexpiprazole Impurity 36
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Description

Valsartan N-Oxide 1 is chemically (S)-5-(4′-((N-(1-Carboxy-2-methylpropyl)pentanamido)methyl)-[1,1′-biphenyl]-2-yl)-1H-tetrazole 2-oxide.
Valsartan N-Oxide 1 is supplied with detailed characterization data compliant with regulatory guideline. Valsartan N-Oxide 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 Valsartan .

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 16 is chemically (S)-3-Acetamido-2-((1-(3-ethoxy-4-methoxyphenyl)-2-(methylsulfonyl)ethyl) carbamoyl)benzoic Acid.
It is also known as Apremilast 3-Acetamido Benzoic Acid Imurity.
Apremilast Impurity 16 is supplied with detailed characterization data compliant with regulatory guideline. Apremilast Impurity 16 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.

Amoxapine 8-Hydroxy Impurity is chemically 2-Chloro-11-(piperazin-1-yl)dibenzo[b,f][1,4]oxazepin-8-ol.
Amoxapine 8-Hydroxy Impurity is supplied with detailed characterization data compliant with regulatory guideline. Amoxapine 8-Hydroxy 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 Amoxapine.

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.

Brexpiprazole Impurity 36 is chemically 1-(4-Bromobutyl)-7-hydroxyquinolin-2(1H)-one.
Brexpiprazole Impurity 36 is supplied with detailed characterization data compliant with regulatory guideline. Brexpiprazole 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 Brexpiprazole.

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.

Availability In stock In stock In stock In stock
CAS No   2096492-41-8 61443-78-5  
Inv. Status Out of Stock, Custom Synthesis Out of Stock, Custom Synthesis Custom Synthesis Custom Synthesis
Mol.F. C24H29N5O4 C22H26N2O8S C17H16ClN3O2 C13H14BrNO2
ISP CAT No ISP-V001013 ISP-A051027 ISP-A048028 ISP-B011039
Mol.Wt. 451.5 478.5 329.8 296.2