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Dapagliflozin EP Impurity B | CAS 3093141-55-7 - Request Quote

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Dapagliflozin EP Impurity B

SZ CAT No:SZ-D015049
CAS No
3093141-55-7
Mol.F.
C23H29ClO6
Mol.Wt.
436.9
Inv. Status
In Stock
Shipping Condition Room Temperature

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Usage Note:

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. SynZeal products are for analytical purpose only and not for human use.

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Dapagliflozin EP Impurity B for Method Validation

Dapagliflozin Reference Standard

Dapagliflozin EP Impurity B for ANDA Filing

Dapagliflozin EP Impurity B for Forced Degradation Studies

Dapagliflozin EP Impurity B Identification Standards

Dapagliflozin EP Impurity B for DMF Filing

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SynZeal product information given on this website is as per the existing understanding while publishing the details on website. The customer is responsible for assessing the accuracy of the information at the time of actual purchase.

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

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