Bisoprolol EP Impurity G

Product Name Bisoprolol EP Impurity G
CAT No. CS-O-07382
CAS No. 1215342-36-1
Category Impurities
Stock IN-Stock
Mol. Wt. 355.47 g/mol
Mol. For. C₁₉H₃₃NO₅
Hazardous This is not a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Therapeutic Anti-Hypertensives
Canonical Smiles CC(C)NCC(COC1=CC=C(C=C1)COCOCCOC(C)C)O
InchIKey NGCBVUSSEGADND-UHFFFAOYSA-N
Inchl InChI=1S/C19H33NO5/c1-15(2)20-11-18(21)13-25-19-7-5-17(6-8-19)12-23-14-22-9-10-24-16(3)4/h5-8,15-16,18,20-21H,9-14H2,1-4H3
IUPAC 1-(propan-2-ylamino)-3-[4-(2-propan-2-yloxyethoxymethoxymethyl)phenoxy]propan-2-ol
Controlled No
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Bisoprolol is a beta-blocker medication that is commonly used to treat high blood pressure and heart failure. Bisoprolol EP Impurity G is a specific impurity that may be present in bisoprolol formulations. Chemically, Bisoprolol EP Impurity G is known as 2-[(4-tert-butylphenoxy)methyl]-1,4-dioxane. It is a white to off-white powder with a molecular weight of 308.43 g/mol. This impurity may form during the synthesis, purification, or storage of bisoprolol. While the exact effects of Bisoprolol EP Impurity G are not well understood, it is generally considered to be a potential impurity that should be monitored and controlled in bisoprolol formulations. The presence of impurities in drugs can affect their efficacy and safety, and may also impact the stability of the product. Therefore, it is important to carefully monitor the levels of Bisoprolol EP Impurity G in bisoprolol formulations, and to ensure that they are kept within acceptable limits. This can be achieved through careful manufacturing processes, quality control testing, and appropriate storage conditions. Overall, while the exact effects of Bisoprolol EP Impurity G are not well understood, it is important to monitor and control its presence in bisoprolol formulations to ensure the safety and efficacy of the medication.

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