Atenolol Impurity H
| Product Name | Atenolol Impurity H |
|---|---|
| Alternate Names | Atenolol Impurities, Impurities of Atenolol |
| CAT No. | CS-O-07262 |
| CAS No. | 29277-73-4 |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 248.32 g/mol |
| Mol. For. | C₁₄H₂₀N₂O₂ |
| Hazardous | This is a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Parent API | Atenolol |
| Purity | 95% |
| Therapeutic | Anti-Migraines |
| Smileys | OC(CNC(C)C)COC1=CC=C(CC#N)C=C1 |
| Canonical Smiles | CC(C)NCC(COC1=CC=C(C=C1)CC#N)O |
| InchIKey | VGJIPAKCLDHBAL-UHFFFAOYSA-N |
| Inchl | InChI=1S/C14H20N2O2/c1-11(2)16-9-13(17)10-18-14-5-3-12(4-6-14)7-8-15/h3-6,11,13,16-17H,7,9-10H2,1-2H3 |
| IUPAC | 2-[4-[2-hydroxy-3-(propan-2-ylamino)propoxy]phenyl]acetonitrile |
| 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 |
Atenolol Impurity H is a chemical compound that is commonly used in the pharmaceutical industry as a reference standard for quality control purposes. It is an impurity of the drug Atenolol, which is a beta-blocker medication used to treat high blood pressure and other cardiovascular conditions. This impurity is often used in the analytical testing of Atenolol products to ensure their purity and potency.
Atenolol Impurity H is also known as 2-[(3-chlorophenyl)amino]-2-methylpropanenitrile. Its chemical formula is C10H11ClN2, and its molecular weight is 188.66 g/mol. This impurity is a white to off-white crystalline powder that is soluble in organic solvents such as methanol, ethanol, and acetonitrile.
The presence of Atenolol Impurity H in Atenolol products can affect the drug's efficacy and safety. Therefore, it is essential to monitor and control the levels of this impurity in pharmaceutical formulations. The International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) has established limits for the amount of Atenolol Impurity H that is acceptable in Atenolol products.
In conclusion, Atenolol Impurity H is a critical reference standard that is widely used in the pharmaceutical industry to ensure the quality and purity of Atenolol products. Its chemical properties and usage information are crucial for analytical testing and quality control purposes.
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Related Compounds
Atenolol EP Impurity C | Hydroxyatenolol | Atenolol EP Impurity G | Atenolol EP Impurity G (sodium salt) | Atenolol Blocker Acid Impurity | Atenolol EP Impurity D | R Atenolol | Atenolol EP Impurity F | Atenolol EP Impurity B | N-Nitroso-Atenolol EP Impurity G | Atenolol Impurity Standard BP | N-FORMYL ATENOLOL | N-Nitroso Atenolol-D7 | N-Nitroso-Atenolol EP Impurity H | Atenolol EP Impurity G | Atenolol EP impurity E | Atenolol EP Impurity I |