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Title	Mitoxantrone Dihydrochloride	Sulpiride EP Impurity G	Daclatasvir Impurity B	Dehydroandrosterone Acetate
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Description	Mitoxantrone Dihydrochloride is chemically 1,4-Bis[(2-(2-hydroxyethylamino)ethyl)amino]-5,8-dihydroxyanthraquinone Dihydrochloride. Mitoxantrone Dihydrochloride is supplied with detailed characterization data compliant with regulatory guideline. Mitoxantrone Dihydrochloride 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 Mitoxantrone. 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.	Sulpiride EP Impurity G is chemically N-[[(2RS)-1-éthylpyrrolidin-2-yl]méthyl]-2-hydroxy-5-sulfamoylbenzamide (as per EP). Sulpiride EP Impurity G is supplied with detailed characterization data compliant with regulatory guideline. Sulpiride EP Impurity G 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 Sulpiride. 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.	Daclatasvir Impurity B is chemically Methyl ((S)-1-((S)-2-(5-(4′-(2-((S)-1-acetylpyrrolidin-2-yl)-1H-imidazol-5-yl)-[1,1′-biphenyl]-4-yl)-1H-imidazol-2-yl)pyrrolidin-1-yl)-3-methyl-1-oxobutan-2-yl)carbamate. Daclatasvir Impurity B is supplied with detailed characterization data compliant with regulatory guideline. Daclatasvir 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 Daclatasvir. 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.	Dehydroandrosterone Acetate is chemically (3R,8R,9S,10R,13S,14S)-10,13-dimethyl-17-oxo-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl acetate. It is also known as 3α-Acetoxyandrost-5-en-17-one. Dehydroandrosterone Acetate is supplied with detailed characterization data compliant with regulatory guideline. Dehydroandrosterone Acetate 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 Abiraterone Acetate. 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	70476-82-3	67381-52-6	2226541-13-3	5223-99-4
Inv. Status	Custom Synthesis	Limited Stock	In Stock	Custom Synthesis
Mol.F.	C22H28N4O6 : 2(HCl)	C14H21N3O4S	C35H41N7O4	C21H30O3
ISP CAT No	ISP-M047001	ISP-S018008		ISP-A006049
Mol.Wt.	444.5 : 2(36.5)	327.4	623.8	330.5

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