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Demethyl Benzydamine Hydrochloride
Etoricoxib Impurity 3
Nintedanib Impurity 56
Clodronate Impurity 1
Title Demethyl Benzydamine Hydrochloride Etoricoxib Impurity 3 Nintedanib Impurity 56 Clodronate Impurity 1
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Description

Demethyl Benzydamine Hydrochloride is chemically 3-((1-Benzyl-1H-indazol-3-yl)oxy)-N-methylpropan-1-amine hydrochloride.
Demethyl Benzydamine Hydrochloride is supplied with detailed characterization data compliant with regulatory guideline. Demethyl Benzydamine Hydrochloride 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 Benzydamine.

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 3 is chemically (E)-5-(1,3-Bis(4-(methylsulfonyl)phenyl)prop-1-en-2-yl)-2-methylpyridine.
Etoricoxib Impurity 3 is supplied with detailed characterization data compliant with regulatory guideline. Etoricoxib Impurity 3 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.

Nintedanib Impurity 56 is chemically Methyl 4-chloro-3-nitrobenzoate. Nintedanib Impurity 56 is supplied with detailed characterization data compliant with regulatory guideline. Nintedanib Impurity 56 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 Nintedanib.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.

Clodronate Impurity 1 is chemically Tetraisopropyl (chloromethylene)bis(phosphonate).
Clodronate Impurity 1 is supplied with detailed characterization data compliant with regulatory guideline. Clodronate Impurity 1 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 Clodronate.

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 39860-97-4   14719-83-6 20107-67-9
Inv. Status Custom Synthesis Custom Synthesis Custom Synthesis Custom Synthesis
Mol.F. C18H21N3O : HCl C23H23NO4S2 C8H6ClNO4 C13H29ClO6P2
ISP CAT No ISP-B069006 ISP-E030008 ISP-N023079  
Mol.Wt. 295.4 : 36.5 441.6 215.6 378.8