Storage Condition
Store at refrigerator (2-8°C) for long term storage
Application Notes
Useful research chemical for a range of applications
Purity by HPLC
Not less than 90%
Hazard Compound
Yes -Refer MSDS for accurate information
Nebivolol Impurity A 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.
Nebivolol Impurity A usage and description
Nebivolol Impurity A is a chemical compound that is commonly used in the pharmaceutical industry as a reference standard for the analysis and testing of nebivolol, a beta-blocker medication used to treat high blood pressure and other cardiovascular conditions. This impurity is a minor component of nebivolol drug substance and is often present in trace amounts.
Chemically, Nebivolol Impurity A is known as (1RS,2RS)-1-(6-methoxyquinolin-4-yl)-2-(3-methylphenyl)ethanol. It has a molecular weight of 315.4 g/mol and a molecular formula of C20H21NO2. It is a white to off-white crystalline powder that is soluble in methanol, ethanol, and acetonitrile.
The usage of Nebivolol Impurity A in the pharmaceutical industry is primarily for analytical purposes. It is used as a reference standard in the development and validation of analytical methods for the quantification of nebivolol in drug products. Additionally, it is used to identify and characterize the impurities present in nebivolol drug substance and drug products.
In conclusion, Nebivolol Impurity A is an important reference standard in the pharmaceutical industry for the analysis and testing of nebivolol drug substance and drug products. Its usage in the development and validation of analytical methods ensures the quality and safety of nebivolol medications.
