Bisoprolol EP Impurity M
| Product Name | Bisoprolol EP Impurity M |
|---|---|
| Alternate Names | Bisoprolol Impurities, Impurities of Bisoprolol |
| CAT No. | CS-O-07384 |
| CAS No. | 177034-57-0 |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 210.27 g/mol |
| Mol. For. | C₁₂H₁₈O₃ |
| Hazardous | This is a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Parent API | Bisoprolol |
| Purity | 95% |
| Therapeutic | Anti-Hypertensives |
| Smileys | CC(C)OCCOCC1=CC=C(C=C1)O |
| Canonical Smiles | CC(C)OCCOCC1=CC=C(C=C1)O |
| InchIKey | ISQLWWCGQXEAJG-UHFFFAOYSA-N |
| Inchl | InChI=1S/C12H18O3/c1-10(2)15-8-7-14-9-11-3-5-12(13)6-4-11/h3-6,10,13H,7-9H2,1-2H3 |
| IUPAC | 4-(2-propan-2-yloxyethoxymethyl)phenol |
| Controlled | No |
| Shipping | Free for purchase above 1000$ |
| Delivery | In-Stock, products will be dispatched within 24 hours via FedEx for USA, Europe, and other countries. |
| Return | Returns/replacement accepted if you are not satisfied with the quality of the product, (please send us an email with the reason/issues which are facing, within 15 days, after receipt of the product). |
| Ordering | Place your order online or by email sales@clearsynth.com |
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.
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Related Compounds
Bisoprolol Alcohol Impurity | Bisoprolol EP Impurity F Butenedioic acid salt | Bisoprolol O-Phosphate | Bisoprolol EP Impurity A | Bisoprolol EP Impurity Q | Bisoprolol N-Methyl Impurity | N-Desisopropyl-N-formyl Bisoprolol | R-(+)-Bisoprolol Fumarate | N-Acetyl Bisoprolol | Bisoprolol EP Impurity L hydrochloride | Bisoprolol Impurity 4 | Bisoprolol EP Impurity T | Bisoprolol EP Impurity R | Bisoprolol Impurity 11 (mixture of isomers) | Dehydro Bisoprolol | Bisoprolol Diene Impurity | Bisoprolol EP Impurity B | Bisoprolol Phenol Impurity | Bisoprolol Related Compound D | Bisoprolol Carboxylic Acid Impurity | Des O-isopropyl Bisoprolol | Dehydro Bisoprolol Hemifumarate | Bisoprolol EP Impurity D | Bisoprolol EP Impurity C | Bisoprolol glycerol diether impurity | Bisoprolol EP Impurity B Hemifumarate (Bisoprolol n-Propyl Derivative Hemifumarate) | Bisoprolol benzyl alcohol fumarate | Bisoprolol Dimer | Bisoprolol Ester Impurity | Bisoprolol Benzylalcohol | N-Formylbisoprolol | Bisoprolol Epoxide Impurity | Bisoprolol Impurity | Bisoprolol EP Impurity J | Bisoprolol EP Impurity G fumarate salt | Bisoprolol EP Impurity D (TFA) | Bisoprolol EP Impurity N | Bisoprolol EP Impurity F | Bisoprolol Impurity 3 |