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Raloxifene Impurity 9
Bilastine Impurity 27
Posaconazole Impurity 22
Lurasidone Impurity 35
Lurasidone Impurity 22
Alpelisib Impurity 6
Title Raloxifene Impurity 9 Bilastine Impurity 27 Posaconazole Impurity 22 Lurasidone Impurity 35 Lurasidone Impurity 22 Alpelisib Impurity 6
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Description

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.

Bilastine Impurity 27 is chemically 1-(2-Ethoxyethyl)-2-(piperidin-4-yl)-1H-benzo[d]imidazole hydrochloride.
Bilastine Impurity 27 is supplied with detailed characterization data compliant with regulatory guideline. Bilastine Impurity 27 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.

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 35is chemically 2-(piperazin-1-yl)benzo[d]thiazole. Lurasidone Impurity 35 is supplied with detailed characterization data compliant with regulatory guideline. Lurasidone Impurity 35 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.

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.

Alpelisib Impurity 6 is chemically Methyl ((4-methyl-5-(2-(1,1,1-trifluoro-2-methylpropan-2-yl)pyridin-4-yl)thiazol-2-yl)carbamoyl)-L-prolinate.
Alpelisib Impurity 6 is supplied with detailed characterization data compliant with regulatory guideline. Alpelisib Impurity 6 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 Alpelisib.

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.

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CAS No 175460-94-3 1841081-72-8 1388148-30-8 55745-83-0 1807983-61-4 2667583-13-1
Inv. Status Out of Stock In Stock Custom Synthesis In Stock Custom Synthesis Custom Synthesis
Mol.F. C15H12O2S C16H23N3O : HCl C36H40F2N8O4 C11H13N3S C32H38N6O4S2 C20H23F3N4O3S
ISP CAT No ISP-R007017 ISP-B034040 ISP-P022042 ISP-L035049 ISP-L035041 ISP-A085009
Mol.Wt. 256.3 273.4 : 36.5 686.8 219.3 634.8 456.5