Therapeutic Uses
Anti-Diabetic
Storage Condition
Store at refrigerator (2-8°C) for long term storage
Synonyms
Dapagliflozin acetyl Furanose impurity
Application Notes
Useful research chemical for a range of applications
Purity by HPLC
Not less than 95 %
Hazard Compound
No -Refer MSDS for accurate information
Dapagliflozin Impurity 21 is a drug product that is used as an analytical standard for HPLC, as well as in research and development of drugs.
Refund Policy
We are committed to offering products of the highest quality in order to meet the needs of our customers, and have elaborate systems in
place to ensure that material specifications, their certification and all handling and storage conditions are communicated at the time of
material handover.
We have invested in the highest quality packaging materials and use international logistics partners to service our customers. While all
possible precautions have been taken to deliver the required product(s), there may be some rare situations when our product does not
meet your requirements. Should that arise, please contact us with your concerns and we will endeavour to address them on a priority
basis. If there is no other option, we will either replace your product(s) or issue a refund or account credit, whichever you prefer.
If there is an issue with one or more of our products, our policy is that it must be reported to us within 45 days of your receiving shipment.
While we will always address product issues after the 45 day return window has passed, we cannot issue a refund or account credit. As
always, we appreciate your support.
Dapagliflozin Impurity 21 usage and description
Dapagliflozin Impurity 21 is a chemical compound that is commonly used in the pharmaceutical industry as a reference standard and impurity marker for the development and quality control of dapagliflozin, a medication used to treat type 2 diabetes. The impurity is a byproduct of the manufacturing process of dapagliflozin and is considered to be a degradation product of the active pharmaceutical ingredient.
Chemically, Dapagliflozin Impurity 21 is identified as (2S,3R,4R,5S,6R)-2-(hydroxymethyl)-6-(trifluoromethyl)tetrahydro-2H-pyran-3,4,5-triol. It is a white to off-white powder with a molecular weight of 324.14 g/mol.
The usage of Dapagliflozin Impurity 21 is primarily for analytical purposes such as identification, quantification, and characterization of dapagliflozin in drug products. It is also used as a reference standard for developing and validating analytical methods for dapagliflozin and its related compounds.
In conclusion, Dapagliflozin Impurity 21 plays a crucial role in the development and quality control of dapagliflozin, ensuring that the medication is of high quality and safe for patient use. Its chemical properties and usage make it an important compound within the pharmaceutical industry.
