Dapagliflozin EP Impurity B

Dapagliflozin EP Impurity B

VS CAT No VS-D015049
CAS No NA
Mol.F. C23H29ClO6
Mol.Wt. 436.9
Inv. Status Custom Synthesis

Chemical Name: (1S)-1,5-Anhydro-1-C-[4-chloro-3-[(4-ethoxy-3-ethylphenyl)methyl]phenyl]-D-glucitol (as per EP) ; (2S,3R,4R,5S,6R)-2-[4-Chloro-3-(4-ethoxy-3-ethylbenzyl)phenyl]-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol (as per USP)

Synonym: Ethyl Dapagliflozin (USP)

Shipping Temperature: Ambient

Country of Origin: India

Smiles: O[C@H]1[C@H](C2=CC=C(Cl)C(CC3=CC=C(OCC)C(CC)=C3)=C2)O[C@H](CO)[C@@H](O)[C@@H]1O

Dapagliflozin EP Impurity B is chemically (1S)-1,5-Anhydro-1-C-[4-chloro-3-[(4-ethoxy-3-ethylphenyl)methyl]phenyl]-D-glucitol (as per EP) ; (2S,3R,4R,5S,6R)-2-[4-Chloro-3-(4-ethoxy-3-ethylbenzyl)phenyl]-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol (as per USP). It is also known as Ethyl Dapagliflozin (USP). Dapagliflozin EP Impurity B is supplied with detailed characterization data compliant with regulatory guideline. Dapagliflozin 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 Dapagliflozin.

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