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Losartan Potassium EP Impurity J

Also known as: Losartan Impurities or impurities of Losartan
Chemical Name Losartan Potassium EP Impurity J
CAT No. CS-T-47310
CAS Registry# 1006062-27-6
Status Prompt Dispatch
Category Impurities
Mol. Wt. 465 g/mol
Mol. For. C24H25ClN6O2
Hazardous This is a Hazardous Compound
COA View Sample COA

Additional Information


Controlled No
Parent API Losartan
Therapeutic Anti-Hypertensives
Smileys CCCCC1=NC(=C(N1CC2=CC=C(C=C2)C3=CC=CC=C3C4=NNN=N4)COC(=O)C)Cl
Hazardous Yes


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.

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