Storage Condition
Store at refrigerator (2-8°C) for long term storage
Synonyms
5-(4'-((5-(Azidomethyl)-2-1-yl)methyl)-[1,1'-biphenyl]-2-yl)-1H-tetrazole
Application Notes
Useful research chemical for a range of applications
Hazard Compound
No -Refer MSDS for accurate information
Losartan Azide 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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Losartan Azide impurity usage and description
Losartan Azide is an impurity that is commonly found in Losartan potassium, a medication used to treat high blood pressure. The compound is a derivative of the parent compound Losartan and is formed as a result of the incomplete reaction between Losartan and sodium azide.
Losartan Azide impurity is a white or off-white crystalline powder that is slightly soluble in water and organic solvents such as methanol, ethanol, and acetone. It has a molecular weight of 452.5 g/mol and a chemical formula of C22H22ClKN6O.
While Losartan Azide impurity itself does not have any therapeutic benefits, it is important to monitor its levels in Losartan potassium as it can potentially cause toxicity and adverse effects. Therefore, it is essential to minimize the levels of this impurity during the manufacturing process of Losartan potassium to ensure its safety and efficacy.
In conclusion, Losartan Azide impurity is an unwanted by-product that can be formed during the synthesis of Losartan potassium. It is important to monitor and control its levels in Losartan potassium to ensure therapeutic efficacy and safety for patients with high blood pressure.