Therapeutic Uses
Antibiotics
Storage Condition
Store at refrigerator (2-8°C) for long term storage
Synonyms
(2E)-1-[5,6-Dihydro-3-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyrazin-7(8H)-yl]-4-(2,4,5-trifluorophenyl)-2-buten-1-one
Application Notes
Useful research chemical for a range of applications
Purity by HPLC
Not less than 90%
Hazard Compound
No -Refer MSDS for accurate information
Sitagliptin FP Impurity D 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.
Sitagliptin FP Impurity D usage and description
Sitagliptin FP Impurity D is a chemical compound that is commonly used in the pharmaceutical industry. It is an impurity of Sitagliptin, a medication used to treat type 2 diabetes. The impurity is formed during the manufacturing process of Sitagliptin and is usually found in small quantities in the final product.
The usage of Sitagliptin FP Impurity D is primarily for analytical purposes. It is used as a reference material for the identification and quantification of Sitagliptin in pharmaceutical formulations. It is also used in the development and validation of analytical methods for Sitagliptin analysis.
In terms of chemical information, Sitagliptin FP Impurity D is a heterocyclic compound with a molecular weight of 435.49 g/mol. Its chemical formula is C20H28N8O2S2. The impurity is usually identified and quantified using high-performance liquid chromatography (HPLC) coupled with mass spectrometry (MS).
It is important to note that the presence of Sitagliptin FP Impurity D in Sitagliptin formulations should be controlled and kept at low levels, as its presence may impact the efficacy and safety of the medication. Therefore, the analytical methods used for the detection and quantification of the impurity are crucial in ensuring the quality of Sitagliptin formulations.
