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Dabigatran Impurity F | CAS 211915-07-0 - Request Quote

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Dabigatran Impurity F

SZ CAT No:SZ-D012056
CAS No
211915-07-0
Mol.F.
C36H45N7O5
Mol.Wt.
655.8
Inv. Status
Synthesis on demand

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Usage Note:

Dabigatran Impurity F is chemically Ethyl 3-(1-methyl-2-(((4-(N-((octyloxy)carbonyl)carbamimidoyl)phenyl)amino)methyl)-N-(pyridin-2-yl)-1H-benzo[d]imidazole-5-carboxamido)propanoate. Dabigatran Impurity F is supplied with detailed characterization data compliant with regulatory guideline. Dabigatran Impurity F 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 Dabigatran.

The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. SynZeal products are for analytical purpose only and not for human use.

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Dabigatran Reference Standard

Dabigatran Impurity F for ANDA Filing

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SynZeal will update these details as per new developments or findings in product specifications without further notice.

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