Storage Condition
Store at refrigerator (2-8°C) for long term storage
Synonyms
SelexipagDiphenylPyrazineImpurity; 1-Butanol,4-[(5,6-diphenylpyrazinyl)(1-methylethyl)amino]
Application Notes
Useful research chemical for a range of applications
Purity by HPLC
Not less than 90%
Hazard Compound
Yes -Refer MSDS for accurate information
Selexipag Impurity A 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.
Selexipag Impurity A usage and description
Selexipag Impurity A is a chemical compound that is closely related to the active ingredient in the drug Selexipag. This compound is used primarily by pharmaceutical companies and research institutions as a reference standard for the analysis and characterization of Selexipag and its related compounds.
Chemically, Selexipag Impurity A is a member of the thiazolopyridine family of compounds, which are characterized by their ability to modulate certain biological pathways involved in various diseases. Specifically, Selexipag Impurity A is a potential metabolite of Selexipag, which means that it may be formed in the body as Selexipag is metabolized.
The usage of Selexipag Impurity A is primarily as a reference standard for quality control and analytical purposes. Pharmaceutical companies use this compound to ensure that their batches of Selexipag are consistent in terms of purity, potency, and safety. Researchers may also use Selexipag Impurity A to study the metabolism and pharmacokinetics of Selexipag, as well as to develop new derivatives of the drug.
Overall, Selexipag Impurity A is an important tool for understanding the chemistry and pharmacology of Selexipag and its related compounds. Its usage in the pharmaceutical industry and scientific research is critical for ensuring the safety and efficacy of Selexipag as a therapeutic agent.
