Therapeutic Uses
Anti-Hypertensives
Storage Condition
Store at refrigerator (2-8°C) for long term storage
Synonyms
(2RS)-2-[4-(2-isopropoxy-ethoxymethyl)phenoxy]-3-isopropylaminopropan-2-ol
Application Notes
Useful research chemical for a range of applications
Hazard Compound
No -Refer MSDS for accurate information
Bisoprolol EP Impurity F 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.
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possible precautions have been taken to deliver the required product(s), there may be some rare situations when our product does not
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basis. If there is no other option, we will either replace your product(s) or issue a refund or account credit, whichever you prefer.
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While we will always address product issues after the 45 day return window has passed, we cannot issue a refund or account credit. As
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Bisoprolol EP Impurity F usage and description
Bisoprolol EP Impurity F is a chemical compound that is used in the pharmaceutical industry as a reference standard for the quality control and analytical testing of bisoprolol, a beta-blocker medication used to treat high blood pressure, heart failure, and angina. This impurity is a degradation product of bisoprolol and is formed during the manufacturing process or storage of the drug. It is important to monitor and control the levels of impurities in pharmaceutical products to ensure their safety and efficacy.
Bisoprolol EP Impurity F is chemically known as 2-(4-{2-[(1-methylethyl)amino]ethoxy}phenyl)acetic acid. It is a white to off-white powder with a molecular weight of 303.4 g/mol. The compound has a melting point of 148-152°C and is soluble in methanol, ethanol, and water.
The chemical structure of Bisoprolol EP Impurity F contains a phenyl ring, an ethoxy group, and an amino group. The presence of these functional groups is important for the biological activity of bisoprolol and its metabolites. The impurity can be detected and quantified using analytical techniques such as high-performance liquid chromatography (HPLC) and gas chromatography-mass spectrometry (GC-MS).
In summary, Bisoprolol EP Impurity F is a degradation product of bisoprolol that is used as a reference standard for quality control and analytical testing in the pharmaceutical industry. Its chemical structure and properties are important for the safety and efficacy of bisoprolol and its metabolites.
