Bisoprolol Fumarate Final API
(+_)-1-(4[[2-(1-methylethoxy) ethoxy methyl]phenoxy]-3-[(1-methylethyl) amino]-2-propanol
| Chemical Name | (+_)-1-(4[[2-(1-methylethoxy) ethoxy methyl]phenoxy]-3-[(1-methylethyl) amino]-2-propanol |
|---|---|
| CAS No. | 66722-44-9 |
| Molecular Formula | |
| Molecular Weight | |
| Chemical Structure |
![(+_)-1-(4[[2-(1-methylethoxy) ethoxy methyl]phenoxy]-3-[(1-methylethyl) amino]-2-propanol Structure](https://bhavanishlifesciences.com/wp-content/uploads/2026/10/bisoprolol-fumarate-final-api-structure.png) |
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Bisoprolol Fumarate Final API
(+_)-1-(4[[2-(1-methylethoxy) ethoxy methyl]phenoxy]-3-[(1-methylethyl) amino]-2-propanol (CAS Number 66722-44-9) is the final active pharmaceutical ingredient (API) produced at the end of the synthetic route for Bisoprolol Fumarate. It is supplied as a high-purity reference material to support process development, route verification, and regulatory documentation for Bisoprolol Fumarate manufacturing.
Bisoprolol Fumarate intermediates reference standards are useful in pharmaceutical research. They are useful in product development, ANDA and DMF filing, Quality control (QC), method validation, and stability studies. It is also useful in the identification of unknown intermediates and the assessment of genotoxic potential.
We are the BHAVANISH LIFE SCIENCES specializes in manufacturing and supplying of Bisoprolol Fumarate intermediates that meet specific pharmacopeial standards (USP/EP/BP/IP) as well as process-related intermediates.
This related products or intermediates are thoroughly characterized. Supplied with detailed COA & analytical data Like NMR / MASS / HPLC / GC / IR / TGA / Potency / Structure elucidation data (SER Report) meeting regulatory compliance.
BHAVANISH LIFE SCIENCES provides this compound for research and development and Analytical testing use only, and is not meant for human consumption. With product information including CAS number, molecular formula, molecular weight details.
BHAVANISH LIFE SCIENCES in providing high-quality impurity standards to support pharmaceutical companies in maintaining drug safety and efficacy.
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