Therapeutic Uses
Antiretroviral / Anti-HIV
Storage Condition
Store at refrigerator (2-8°C) for long term storage
Synonyms
Darunavir Amine dimer impurity, Not available
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
Darunavir Amine dimer impurity is a drug product that is used as an analytical standard for HPLC, as well as in research and development of drugs.
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Darunavir Amine dimer impurity usage and description
Darunavir Amine dimer impurity is a chemical impurity that is commonly found in the production of the antiretroviral drug, Darunavir. This impurity is formed during the synthesis of Darunavir and can have an impact on the quality and efficacy of the final product. The impurity is a dimer form of the amine group present in Darunavir, and it is typically present in small amounts in the final product.
The presence of Darunavir Amine dimer impurity can affect the potency of the drug and can also lead to adverse reactions in patients. Therefore, it is important to monitor the levels of this impurity during the manufacturing process and to ensure that it is removed or reduced to an acceptable level.
Chemically, Darunavir Amine dimer impurity is a byproduct of the reaction between two molecules of Darunavir's amine group, which results in the formation of a dimeric compound. The impurity is typically identified and quantified using analytical techniques such as high-performance liquid chromatography (HPLC) or mass spectrometry (MS).
Overall, the monitoring and control of Darunavir Amine dimer impurity levels is essential for ensuring the safety and efficacy of Darunavir as a treatment for HIV/AIDS.
