Therapeutic Uses
Antiretroviral / Anti-HIV
Storage Condition
Store at refrigerator (2-8°C) for long term storage
Synonyms
(2E)-3-[4-[[2-[(4-Cyanophenyl)amino]-4-pyrimidinyl]amino]-3,5-dimethylphenyl]-2-propenamide
Application Notes
Useful research chemical for a range of applications
Hazard Compound
No -Refer MSDS for accurate information
Rilpivirine Amide Impurity 1 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.
Rilpivirine Amide Impurity 1 usage and description
Rilpivirine amide 1 impurity is a synthetic organic compound that is used as a reference standard for analytical purposes in the pharmaceutical industry. It is a potential impurity that may be present in Rilpivirine, an antiviral medication used for the treatment of HIV-1 infection.
Chemically, Rilpivirine amide 1 impurity is an amide derivative of Rilpivirine that is formed during the synthesis of the drug. It has the molecular formula C22H18F3N5O2 and a molecular weight of 447.4 g/mol. The compound is a white to off-white powder that is soluble in organic solvents like methanol and DMSO.
Rilpivirine amide 1 impurity is used as a reference standard in the development and validation of analytical methods to detect and quantify impurities in Rilpivirine. It is also used in quality control to ensure the purity and potency of the drug substance and finished product.
The presence of impurities in pharmaceuticals can affect their safety and efficacy. Thus, it is essential to monitor and control impurities in Rilpivirine to ensure that it is safe for use. Rilpivirine amide 1 impurity is an important tool in this process, providing accurate and reliable analytical data for the pharmaceutical industry.
