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Raloxifene Impurity 9 is chemically 6-Methoxy-2-(4-hydroxyphenyl)benzo[b]thiophene; 4-(6-Methoxybenzo[b]thien-2-yl)phenol;.
Raloxifene Impurity 9 is supplied with detailed characterization data compliant with regulatory guideline. Raloxifene Impurity 9 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 Raloxifene.

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.

Posaconazole Impurity 22 is chemically D-​threo-​Pentitol, 2,​5-​anhydro-​1,​3,​4-​trideoxy-​2-​C-​(2,​4-​difluorophenyl)​-​4-​[[[4-​[4-​[1-​[(1S,​2S)​-​1-​ethyl-​2-​hydroxypropyl]​-​1,​5-​dihydro-​5-​oxo-​4H-​1,​2,​4-​triazol-​4-​yl]​phenyl]​-​2,​3,​4,​5-​tetrahydro-​1H-​1,​4-​benzodiazepin-​7-​yl]​oxy]​methyl]​-​1-​(1H-​1,​2,​4-​triazol-​1-​yl)​-;.
Posaconazole Impurity 22 is supplied with detailed characterization data compliant with regulatory guideline. Posaconazole Impurity 22 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 Posaconazole.

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.

Lurasidone Impurity 22 is chemically ((1R,2R)-cyclohexane-1,2-diyl)bis(methylene) bis(4-(benzo[d]isothiazol-3-yl)piperazine-1-carboxylate).
Lurasidone Impurity 22 is supplied with detailed characterization data compliant with regulatory guideline. Lurasidone Impurity 22 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 Lurasidone.

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.

Rac-Tamsulosin EP Impurity H (HCl salt) is chemically N-(2-(2-Ethoxyphenoxy)ethyl)-1-(4-methoxyphenyl)propan-2-amine hydrochloride. Rac-Tamsulosin EP Impurity H (HCl salt) is supplied with detailed characterization data compliant with regulatory guideline. Rac-Tamsulosin EP Impurity H (HCl 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 Tamsulosin.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.