Storage Condition
Store at refrigerator (2-8ยฐC) for long term storage
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
Selexipag DPB Desisopropyl Impurity is a drug product that is used as an analytical standard for HPLC, as well as in research and development of drugs.
Refund Policy
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Selexipag DPB Desisopropyl Impurity usage and description
Selexipag is a medication used to treat pulmonary arterial hypertension (PAH). It is a selective prostacyclin receptor agonist that works by increasing the production of cyclic AMP and relaxing the pulmonary arterial smooth muscles. Selexipag is available in tablet form for oral administration.
Selexipag DPB Desisopropyl Impurity is a chemical impurity that can be found in Selexipag. It is a byproduct of the manufacturing process and does not have any therapeutic value. The impurity is typically present in low concentrations and does not pose a significant risk to patients.
Chemically, Selexipag DPB Desisopropyl Impurity is a derivative of the parent compound Selexipag. It is a white to off-white powder that is soluble in organic solvents but insoluble in water. The impurity is characterized by its purity and structure, which can be determined through various analytical techniques including high-performance liquid chromatography (HPLC) and mass spectrometry.
When using Selexipag, it is important to ensure that the drug is free from any impurities, including Selexipag DPB Desisopropyl Impurity. Manufacturers and regulatory agencies monitor the impurity levels to ensure that the drug is safe and effective for patients. Overall, Selexipag DPB Desisopropyl Impurity is a minor impurity that does not affect the therapeutic value of Selexipag.