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2-Debenzoyl Paclitaxel 2-Pentenoate is chemically (4S,4aS,6R,9S,11S,12S,12aR,12bS)-9-(((2R,3S)-3-benzamido-2-hydroxy-3-phenylpropanoyl)oxy)-4,11-dihydroxy-4a,8,13,13-tetramethyl-5-oxo-12-(((E)-pent-2-enoyl)oxy)-3,4,4a,5,6,9,10,11,12,12a-decahydro-1H-7,11-methanocyclodeca[3,4]benzo[1,2-b]oxete-6,12b(2aH)-diyl diacetate.
2-Debenzoyl Paclitaxel 2-Pentenoate is supplied with detailed characterization data compliant with regulatory guideline. 2-Debenzoyl Paclitaxel 2-Pentenoate 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 Paclitaxel.

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.

Etoricoxib Impurity 29 is chemically 2-(4-(Methylsulfonyl)phenyl)-1-(pyridin-3-yl)ethan-1-one.
Etoricoxib Impurity 29 is supplied with detailed characterization data compliant with regulatory guideline. Etoricoxib Impurity 29 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 Etoricoxib.

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.

Clobazam EP Impurity B is chemically 1-Methyl-5-phenyl-1,5-dihydro-3H-1,5-benzodiazepine-2,4-dione (as per EP) ; 1-Methyl-5-phenyl-1,5-dihydro-2H-benzo[b][1,4]diazepine-2,4(3H)-dione (as per USP).
It is also known as Deschloro Clobazam (USP).
Clobazam EP Impurity B is supplied with detailed characterization data compliant with regulatory guideline. Clobazam EP 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 Clobazam.

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.

Semaglutide Iso Aspartic acid-15 is chemically (3S,9S,12S,15S,18S,21S,25S,28S,31S,34S,37S,40S,46S,49S,52S,55S,82R)-55-(((6S,12S,15S,18S,21S,24S,27S,30S,33S)-21-((1H-indol-3-yl)methyl)-1-amino-30-benzyl-27-((S)-sec-butyl)-35-carboxy-6-((carboxymethyl)carbamoyl)-12-(3-guanidinopropyl)-1-imino-18-isobutyl-15-isopropyl-24-methyl-8,11,14,17,20,23,26,29,32-nonaoxo-2,7,10,13,16,19,22,25,28,31-decaazapentatriacontan-33-yl)carbamoyl)-3-(2-((S)-2-amino-3-(1H-imidazol-5-yl)propanamido)-2-methylpropanamido)-46-(3-amino-3-oxopropyl)-12-benzyl-40-(2-carboxyethyl)-34-(4-hydroxybenzyl)-9,15-bis((R)-1-hydroxyethyl)-18,28,31-tris(hydroxymethyl)-37-isobutyl-25-isopropyl-49,52-dimethyl-4,7,10,13,16,19,23,26,29,32,35,38,41,44,47,50,53,61,70,79,84-henicosaoxo-63,66,72,75-tetraoxa-5,8,11,14,17,20,24,27,30,33,36,39,42,45,48,51,54,60,69,78,83-henicosaazahectane-1,21,82,100-tetracarboxylic acid.
Semaglutide Iso Aspartic acid-15 is supplied with detailed characterization data compliant with regulatory guideline. Semaglutide Iso Aspartic acid-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 Semaglutide.

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.