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Vortioxetine D8 HBr Salt
Dimyristoyl Phosphatidylcholine-d9
Ketoconazole Impurity 1
Zidovudine EP Impurity K
Title Vortioxetine D8 HBr Salt Dimyristoyl Phosphatidylcholine-d9 Ketoconazole Impurity 1 Zidovudine EP Impurity K
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Description

Vortioxetine D8 HBr Salt is chemically 1-(2-((2,4-Dimethylphenyl)thio)phenyl)piperazine-2,2,3,3,5,5,6,6-d8 hydrobromide.
Vortioxetine D8 HBr Salt is supplied with detailed characterization data compliant with regulatory guideline. Vortioxetine D8 HBr Salt 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 Vortioxetine.

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.

Dimyristoyl Phosphatidylcholine-d9 is chemically (R)-2,3-bis(tetradecanoyloxy)propyl (2-(tris(methyl-d3)ammonio)ethyl) phosphate.
It is also known as DMPC-d9.
Dimyristoyl Phosphatidylcholine-d9 is supplied with detailed characterization data compliant with regulatory guideline. Dimyristoyl Phosphatidylcholine-d9 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 Colfosceril Palmitate.

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.

Ketoconazole Impurity 1 is chemically 1-(4-(4-Hydroxyphenyl)-3,4-dihydropyrazin-1(2H)-yl)ethan-1-one.
Ketoconazole Impurity 1 is supplied with detailed characterization data compliant with regulatory guideline. Ketoconazole 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 Ketoconazole.

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.

Zidovudine EP Impurity K is chemically 1,1′,1′′-(methoxymethanetriyl)tribenzene .
It is also known as Methyl trityl ether.
Zidovudine EP Impurity K is supplied with detailed characterization data compliant with regulatory guideline. Zidovudine EP Impurity K 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 Zidovudine.

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   71479-88-4 581806-59-9 596-31-6
Inv. Status Custom Synthesis Custom Synthesis Custom Synthesis In Stock
Mol.F. C18H14D8N2S : HBr C36H63D9NO8P C12H14N2O2 C20H18O
ISP CAT No ISP-V018D01   ISP-K001011 ISP-Z003010
Mol.Wt. 306.5 : 80.9 687.0 218.3 274.4