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Ticagrelor Related Compound 95
Bilastine Impurity 19
Cytarabine EP Impurity D
Bilastine Impurity 18
Title Ticagrelor Related Compound 95 Bilastine Impurity 19 Cytarabine EP Impurity D Bilastine Impurity 18
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Description

Ticagrelor Related Compound 95 is chemically (1S,2S,3S)-3-(2-hydroxyethoxy)-5-((3-((3aS,4S,6S,6aR)-6-(2-hydroxyethoxy)-2,2-dimethyltetrahydro-4H-cyclopenta[d][1,3]dioxol-4-yl)-5-(propylthio)-3H-[1,2,3]triazolo[4,5-d]pyrimidin-7-yl)amino)cyclopentane-1,2-diol. Ticagrelor Related Compound 95 is supplied with detailed characterization data compliant with regulatory guideline. Ticagrelor Related Compound 95 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 Ticagrelor.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.

Bilastine Impurity 19 is chemically Ethyl 2-(piperidin-4-yl)-1H-benzo[d]imidazole-1-carboxylate.
Bilastine Impurity 19 is supplied with detailed characterization data compliant with regulatory guideline. Bilastine Impurity 19 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 Bilastine.

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.

Cytarabine EP Impurity D is chemically Pyrimidin-2,4(1H,3H)-dione (as per EP).
It is also known as Uracil.
Cytarabine EP Impurity D is supplied with detailed characterization data compliant with regulatory guideline. Cytarabine 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 Cytarabine.

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.

Bilastine Impurity 18 is chemically Ethyl 4-(1H-benzo[d]imidazol-2-yl)piperidine-1-carboxylate.
Bilastine Impurity 18 is supplied with detailed characterization data compliant with regulatory guideline. Bilastine Impurity 18 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 Bilastine.

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 NA   66-22-8 317595-60-1
Inv. Status Custom Synthesis Custom Synthesis Custom Synthesis In Stock
Mol.F. C24H38N6O8S C15H19N3O2 C4H4N2O2 C15H19N3O2
ISP CAT No ISP-T023105 ISP-B034029   ISP-B034028
Mol.Wt. 570.7 273.3 112.1 273.3