Nadolol EP Impurity G
| Product Name | Nadolol EP Impurity G |
|---|---|
| Alternate Names | Nadolol Impurities, Impurities of Nadolol |
| CAT No. | CS-O-13056 |
| CAS No. | 33841-03-1 |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 277.40 g/mol |
| Mol. For. | C₁₇H₂₇NO₂ |
| Hazardous | This is a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Parent API | Nadolol |
| Purity | 95% |
| Therapeutic | Anti-Migraines |
| Smileys | OC(CNC(C)(C)C)COC1=C(CCCC2)C2=CC=C1 |
| Canonical Smiles | CC(C)(C)NCC(COC1=CC=CC2=C1CCCC2)O |
| InchIKey | ZTYWAQSTDRZAAS-UHFFFAOYSA-N |
| Inchl | InChI=1S/C17H27NO2/c1-17(2,3)18-11-14(19)12-20-16-10-6-8-13-7-4-5-9-15(13)16/h6,8,10,14,18-19H,4-5,7,9,11-12H2,1-3H3 |
| IUPAC | 1-(tert-butylamino)-3-(5,6,7,8-tetrahydronaphthalen-1-yloxy)propan-2-ol |
| 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 |
Nadolol EP Impurity G is a chemical compound that is commonly used as an impurity standard in the pharmaceutical industry. It is a derivative of the drug Nadolol, which is a beta-blocker used to treat high blood pressure and other heart conditions. Nadolol EP Impurity G is considered an important reference standard for quality control and analytical testing of Nadolol.
Chemically, Nadolol EP Impurity G has the molecular formula C17H20ClNO3S and a molecular weight of 355.86 g/mol. It is a white to off-white crystalline powder that is soluble in organic solvents like methanol and acetonitrile. Nadolol EP Impurity G is stable under normal storage conditions and has a purity level of not less than 98%.
In terms of usage, Nadolol EP Impurity G is primarily used as a reference standard in the development and validation of analytical methods for the determination of Nadolol in pharmaceutical products. It is also used as a marker for the identification of Nadolol in drug substances and formulations. Nadolol EP Impurity G serves as an important tool for ensuring the quality and consistency of Nadolol-based medications, which is crucial for patient safety and effective treatment outcomes.
In conclusion, Nadolol EP Impurity G is a valuable reference standard for the pharmaceutical industry, playing a vital role in the quality control and analytical testing of Nadolol-based drugs. Its chemical properties and stability make it an ideal impurity standard for analytical laboratories and pharmaceutical manufacturers.
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Related Compounds
NADOLOL IMPURITY 4 HCL | Nadolol EP Impurity C | De(2,3-dihydroxy) Nadolol Hydrochloride | Nadolol EP Impurity E | cis-5,6,7,8-Tetrahydro-1,6,7-naphthalenetriol | Nadolol EP Impurity F | NADOLOL IMPURITY 7 HCL | Nadolol EP Impurity B | Nadolol Epoxide Impurity | NADOLOL IMPURITY 6 | NADOLOL IMPURITY 8 | Nadolol EP Impurity A | Nadolol EP Impurity D | N-Nitroso-Nadolol |