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Vortioxetine Impurity 21 is chemically 1,4-bis(2-((2,4-dimethylphenyl)thio)phenyl)piperazine.
Vortioxetine Impurity 21 is supplied with detailed characterization data compliant with regulatory guideline. Vortioxetine Impurity 21 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 Vortioxetine.

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.

N,O-Dibenzylated Formoterol is chemically N-(5-(2-(Benzyl(1-(4-methoxyphenyl)propan-2-yl)amino)-1-hydroxyethyl)-2-(benzyloxy)phenyl)formamide.
It is also known as rac-O-Benzyl N-Benzyl Formoterol.
N,O-Dibenzylated Formoterol is supplied with detailed characterization data compliant with regulatory guideline. N,O-Dibenzylated Formoterol 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 Formoterol.

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.

Albendazole EP Impurity J is chemically Methyl N-(4,6-dichloro-1H-benzimidazol-2-yl)carbamate (as per EP).
Albendazole EP Impurity J is supplied with detailed characterization data compliant with regulatory guideline. Albendazole EP Impurity J 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 Albendazole.

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.

L-Ascorbic Acid Monosodium Salt (Sodium Ascorbate) is chemically (R)-5-((S)-1,2-Dihydroxyethyl)-3,4-dihydroxyfuran-2(5H)-one, sodium salt.
L-Ascorbic Acid Monosodium Salt (Sodium Ascorbate) is supplied with detailed characterization data compliant with regulatory guideline. L-Ascorbic Acid Monosodium Salt (Sodium Ascorbate) 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 Ascorbic Acid.

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.

Avanafil Impurity 22 is chemically Ethyl (S)-4-((3,5-dichloro-4-methoxybenzyl)amino)-2-(2-(hydroxymethyl)pyrrolidin-1-yl)pyrimidine-5-carboxylate.
Avanafil Impurity 22 is supplied with detailed characterization data compliant with regulatory guideline. Avanafil 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 Avanafil.

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.

Valaciclovir EP Impurity P is chemically [Methylenebis[azanediyl(6-oxo-1,6-dihydro-9H-purine-2,9-diyl)methyleneoxyethan-2,1-diyl]] di-L-valinate (as per EP).
It is also known as Valaciclovir Dimer ; .
Valaciclovir EP Impurity P is supplied with detailed characterization data compliant with regulatory guideline. Valaciclovir EP Impurity P 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 Valaciclovir.

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.

Neurosporene is chemically (6E,8E,10E,12E,14E,16E,18E,20E,22E,26E)-2,6,10,14,19,23,27,31-octamethyldotriaconta-2,6,8,10,12,14,16,18,20,22,26,30-dodecaene.
Neurosporene is supplied with detailed characterization data compliant with regulatory guideline. Neurosporene 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 Miscellaneous.

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.

Avanafil Impurity 4 is chemically (S)-2-(2-(Hydroxymethyl)pyrrolidin-1-yl)-4-((4-methoxybenzyl)amino)-N-(pyrimidin-2-ylmethyl)pyrimidine-5-carboxamide.
Avanafil Impurity 4 is supplied with detailed characterization data compliant with regulatory guideline. Avanafil Impurity 4 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 Avanafil.

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.