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Cefalotin Impurity 2
Des-AEEA-Tirzepatide
Linagliptin Dimer Impurity 5
Salbutamol EP Impurity B
Diclofenac Diethylamine Salt
Apixaban Impurity 50
Title Cefalotin Impurity 2 Des-AEEA-Tirzepatide Linagliptin Dimer Impurity 5 Salbutamol EP Impurity B Diclofenac Diethylamine Salt Apixaban Impurity 50
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Description

Cefalotin Impurity 2 is chemically (6R,7R)-3-(Acetoxymethyl)-8-oxo-7-(thiophene-2-carboxamido)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid.
Cefalotin Impurity 2 is supplied with detailed characterization data compliant with regulatory guideline. Cefalotin 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 Cefalotin.

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.

Des-AEEA-Tirzepatide is chemically . Des-AEEA-Tirzepatide is supplied with detailed characterization data compliant with regulatory guideline. Des-AEEA-Tirzepatide 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 Tirzepatide.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.

Linagliptin Dimer Impurity 5 is chemically 8-((R)-3-aminopiperidin-1-yl)-1-((4-(3-(2-((8-((S)-3-aminopiperidin-1-yl)-7-(but-2-yn-1-yl)-3-methyl-2,6-dioxo-2,3,6,7-tetrahydro-1H-purin-1-yl)methyl)quinazolin-4-yl)-2-(4-methylquinazolin-2-yl)propyl)quinazolin-2-yl)methyl)-7-(but-2-yn-1-yl)-3-methyl-3,7-dihydro-1H-purine-2,6-dione.
Linagliptin Dimer Impurity 5 is supplied with detailed characterization data compliant with regulatory guideline. Linagliptin Dimer Impurity 5 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 Linagliptin.

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.

Salbutamol EP Impurity B is chemically (1RS)-2-[(1,1-Dimethylethyl)amino]-1-(4-hydroxyphenyl)ethanol (as per EP)
.
It is also known as Salbutamol BP Impurity C ; Albuterol USP Related Compound I ; Levalbuterol USP Related Compound B ; Buctopamine ; t-Butylnorsynephrine.
Salbutamol EP Impurity B is supplied with detailed characterization data compliant with regulatory guideline. Salbutamol EP Impurity B 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 Salbutamol .

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.

Diclofenac Diethylamine Salt is chemically Diethylamine 2-(2-((2,6-dichlorophenyl)amino)phenyl)acetate.
Diclofenac Diethylamine Salt is supplied with detailed characterization data compliant with regulatory guideline. Diclofenac Diethylamine 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 Diclofenac.

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.

Apixaban Impurity 50 is chemically 1-(4-Methoxyphenyl)-7-oxo-6-(4-(2-oxopiperidin-1-yl)phenyl)-3a,4,5,6,7,7a-hexahydro-1H-pyrazolo[3,4-c]pyridine-3-carboxylic acid.
Apixaban Impurity 50 is supplied with detailed characterization data compliant with regulatory guideline. Apixaban Impurity 50 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 Apixaban.

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 104758-14-7 NA   96948-64-0 78213-16-8  
Inv. Status In Stock Custom Synthesis Custom Synthesis In Stock In Stock Custom Synthesis
Mol.F. C15H14N2O6S2 C213H326N46O62 C60H62N18O4 C12H19NO2 C14H11Cl2NO2 : C4H11N C25H26N4O5
ISP CAT No   ISP-T170005 ISP-L024017 ISP-S003003   ISP-A062070
Mol.Wt. 382.4 4523.2 1099.3 209.3 296.1 : 73.1 462.5