Therapeutic Uses
Anti-Hypertensives
Storage Condition
Store at refrigerator (2-8°C) for long term storage
Synonyms
Bisoprolol EP Impurity M, 177034-57-0
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
Bisoprolol EP Impurity M 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.
Bisoprolol EP Impurity M usage and description
Bisoprolol EP Impurity M is a chemical compound that is commonly used in the pharmaceutical industry as a reference standard for the analysis of the active pharmaceutical ingredient (API) Bisoprolol. This impurity is typically used in quality control processes to ensure the purity and potency of Bisoprolol products.
Chemically, Bisoprolol EP Impurity M is known as 2-[4-[2-(1-methylethoxy)ethyl]phenoxy]-2-methylpropanoic acid. It is a white to off-white crystalline powder that is soluble in water and other polar solvents. This impurity is considered to be a minor component in Bisoprolol formulations, and its presence in the API can be detected using analytical techniques such as high-performance liquid chromatography (HPLC).
The usage of Bisoprolol EP Impurity M is strictly regulated by the pharmaceutical industry, as its presence in Bisoprolol formulations can affect the efficacy and safety of the drug. Therefore, it is important for pharmaceutical manufacturers to accurately measure and control the levels of this impurity in their products to maintain the quality and consistency of the drug.
Overall, Bisoprolol EP Impurity M plays a crucial role in ensuring the quality of Bisoprolol formulations and is an important component in the pharmaceutical industry.
