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CC(OCC1=C(Cl)N=C(CCCC)N1CC2=CC=C(C3=CC=CC=C3C4=NN=NN4)C=C2)=O
Therapeutic Uses
Anti-Hypertensives
Storage Condition
Store at refrigerator (2-8°C) for long term storage
IUPAC Name
(2-Butyl-4-chloro-1-{[2'-(1H-tetrazol-5-yl)biphenyl-4-yl]methyl}-1H-imidazol-5-yl)methyl acetate
Synonyms
Losartan EP Impurity J
Application Notes
Useful research chemical for a range of applications
Hazard Compound
No -Refer MSDS for accurate information
Losartan Potassium EP Impurity J 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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Losartan Potassium EP Impurity J usage and description
Losartan Potassium EP Impurity J is a substance that is used primarily in the pharmaceutical industry. It is used as a reference standard for the analysis of Losartan Potassium, which is a medication used to treat high blood pressure. The impurity J is a byproduct that is produced during the manufacturing process of Losartan Potassium. The substance is a yellowish-white powder that has a molecular weight of 422.5 g/mol.
Chemically, Losartan Potassium EP Impurity J is also known as 2-nitro-4-(trifluoromethyl)aniline. It is a nitroaromatic compound that is classified as a potential mutagen and carcinogen. This means that the substance has the ability to cause genetic mutations and promote the growth of cancer cells. As a result, the use of Losartan Potassium EP Impurity J is strictly regulated and controlled.
In the pharmaceutical industry, Losartan Potassium EP Impurity J is used as a reference standard for the analysis of Losartan Potassium. The substance is used to ensure that the medication is of the highest quality and purity. This is important because impurities in medications can have serious health consequences for patients. Therefore, Losartan Potassium EP Impurity J plays a crucial role in ensuring the safety and efficacy of Losartan Potassium.
