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Title	Rivastigmine Impurity 3	Cisatracurium Besylate EP Impurity R	Cyclophosphamide Impurity 16	Cyclophosphamide Impurity 13	Cyclophosphamide Impurity 15
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Description	Rivastigmine Impurity 3 is chemically 3-(1-(dimethylamino)ethyl)phenol hydrochloride. Rivastigmine Impurity 3 is supplied with detailed characterization data compliant with regulatory guideline. Rivastigmine 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 Rivastigmine. 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.	Cisatracurium Besylate EP Impurity Ris chemically Pentane-1,5-diyl bis[3-[(1R)-1-[(3,4-dimethoxyphenyl)methyl]-6,7-dimethoxy-3,4-dihydroisoquinolin-2(1H)-yl]propanoate] Dibenzenesulfonate (as per EP). Cisatracurium Besylate EP Impurity R is supplied with detailed characterization data compliant with regulatory guideline. Cisatracurium Besylate EP Impurity R 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 Cisatracurium.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.	Cyclophosphamide Impurity 16 is chemically 3-Aminopropyl ethyl hydrogen phosphate. Cyclophosphamide Impurity 16 is supplied with detailed characterization data compliant with regulatory guideline. Cyclophosphamide 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 Cyclophosphamide. 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.	Cyclophosphamide Impurity 13 is chemically Bis(2-chloroethyl)phosphoramidic dichloride. Cyclophosphamide Impurity 13 is supplied with detailed characterization data compliant with regulatory guideline. Cyclophosphamide Impurity 13 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 Cyclophosphamide. 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.	Cyclophosphamide Impurity 15 is chemically 3-(2-Chloroethyl)-2-oxo-2-ethoxyoxy-1, 3, 6, 2-oxadiazaphosphonane. Cyclophosphamide Impurity 15 is supplied with detailed characterization data compliant with regulatory guideline. Cyclophosphamide Impurity 15 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 Cyclophosphamide. 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	In stock
CAS No	5441-61-2	1253910-09-6	1361416-62-7	127-88-8
Inv. Status	In Stock	Custom Synthesis	Custom Synthesis	Custom Synthesis	Custom Synthesis
Mol.F.	C10H15NO : HCl	C51H66N2O12 : 2(C6H6O3S)	C5H14NO4P	C4H8Cl4NOP	C9H20ClN2O4P
ISP CAT No	ISP-R018022
Mol.Wt.	165.2 : 36.5	899.1 : 2(158.2)	183.1	258.9	286.7

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