Therapeutic Uses
Anti-Hypertensives
Storage Condition
Store at refrigerator (2-8°C) for long term storage
Synonyms
Trityl Losartan; [2-Butyl-5-chloro-3-[[2′-(1-trityl-1H-tetrazol-5-yl)biphenyl-4-yl]methyl]-3H-imidazol-4-yl]methanol
Application Notes
Useful research chemical for a range of applications
Hazard Compound
No -Refer MSDS for accurate information
Losartan N1-Trityl 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
We are committed to offering products of the highest quality in order to meet the needs of our customers, and have elaborate systems in
place to ensure that material specifications, their certification and all handling and storage conditions are communicated at the time of
material handover.
We have invested in the highest quality packaging materials and use international logistics partners to service our customers. While all
possible precautions have been taken to deliver the required product(s), there may be some rare situations when our product does not
meet your requirements. Should that arise, please contact us with your concerns and we will endeavour to address them on a priority
basis. If there is no other option, we will either replace your product(s) or issue a refund or account credit, whichever you prefer.
If there is an issue with one or more of our products, our policy is that it must be reported to us within 45 days of your receiving shipment.
While we will always address product issues after the 45 day return window has passed, we cannot issue a refund or account credit. As
always, we appreciate your support.
Losartan N1-Trityl Impurity usage and description
Losartan N1-Trityl Impurity is a chemical compound that is used in the synthesis of Losartan, a medication that is used to treat hypertension and other cardiovascular disorders. The impurity is a byproduct of the chemical reaction that is used to produce Losartan, and it is important to monitor the levels of the impurity in the drug product to ensure its safety and efficacy.
Chemically, Losartan N1-Trityl Impurity is a trityl-protected amino acid that is formed during the synthesis of Losartan. The trityl group is a benzyl protecting group that is used to protect the amino group during the synthesis. The impurity is typically removed during the purification process, but trace amounts may remain in the final drug product.
The presence of Losartan N1-Trityl Impurity in the final drug product can potentially affect its safety and efficacy. Therefore, regulatory agencies such as the FDA have set limits on the allowable levels of the impurity in Losartan products. Manufacturers of Losartan must ensure that the levels of this impurity are within acceptable limits before the drug is released to the market.
In conclusion, Losartan N1-Trityl Impurity is an important chemical compound that is closely monitored during the production of Losartan. Its presence in the final drug product can affect its safety and efficacy, and manufacturers must ensure that its levels are within acceptable limits before releasing the drug to the market.
