Compare products Close window [X]

Cefadroxil Impurity 3 is chemically 7-((2R)-2-(2-Amino-2-(4-hydroxyphenyl)acetamido)-2-(4-hydroxyphenyl)acetamido)-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-3-ene-2-carboxylic acid.
Cefadroxil Impurity 3 is supplied with detailed characterization data compliant with regulatory guideline. Cefadroxil 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 Cefadroxil.

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.

N-Nitroso Sotalol EP Impurity A is chemically N-(4-(2-(Isopropyl(nitroso)amino)ethyl)phenyl)methanesulfonamide.
N-Nitroso Sotalol EP Impurity A is supplied with detailed characterization data compliant with regulatory guideline. N-Nitroso Sotalol 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 Sotalol.

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.

Albendazole EP Impurity I is chemically Methyl N-(5-propoxy-1H-benzimidazol-2-yl)carbamate (as per EP).
It is also known as Oxibendazole ; Anthelcide EQ ; Loditac.
Albendazole EP Impurity I is supplied with detailed characterization data compliant with regulatory guideline. Albendazole EP Impurity I 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 Albendazole.

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.