Sumatriptan EP Impurity E
| Product Name | Sumatriptan EP Impurity E |
|---|---|
| Alternate Names | Sumatriptan Impurities, Impurities of Sumatriptan |
| CAT No. | CS-O-08214 |
| CAS No. | 88919-22-6 |
| Category | Impurities |
| Stock | Enquire |
| Mol. Wt. | 267.35 g/mol |
| Mol. For. | C₁₂H₁₇N₃O₂S |
| Hazardous | This is a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Parent API | Sumatriptan |
| Purity | 95% |
| Therapeutic | Anti-Migraines |
| Smileys | O=S(CC1=CC2=C(NC=C2CCN)C=C1)(NC)=O |
| 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 |
Sumatriptan EP Impurity E is a synthetic organic compound that is often used as a reference standard or impurity in the development and validation of analytical methods for the detection and quantification of Sumatriptan in pharmaceutical formulations. Sumatriptan is a medication used for the treatment of migraines, and its EP Impurity E is one of its impurities that can be present in Sumatriptan formulations.
Chemically, Sumatriptan EP Impurity E is identified as 1-(2-phenyl-1,2,3,4-tetrahydronaphthalen-1-yl)ethanone. It has a molecular weight of 224.32 g/mol and a melting point of 68-70°C. The compound is soluble in organic solvents such as methanol, ethanol, and acetonitrile.
Sumatriptan EP Impurity E is typically used in analytical laboratories for the development and validation of analytical methods such as high-performance liquid chromatography (HPLC), gas chromatography (GC), and mass spectrometry (MS). These methods are used to determine the purity of Sumatriptan in pharmaceutical formulations or to identify any impurities that may be present.
Overall, Sumatriptan EP Impurity E is an important reference standard for quality control purposes in the pharmaceutical industry, and its usage in analytical laboratories is critical for ensuring the safety and efficacy of Sumatriptan-containing medications.
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Related Compounds
Sumatriptan Impurity 3 | Sumatriptan EP Impurity F | Sumatriptan Aminophenyl Impurity | Sumatriptan EP Impurity B | Sumatriptan impurity 1 | Sumatriptan EP Impurity D | Sumatriptan degradation impurity | N,N-Dinitroso Sumatriptan | Sumatriptan EP Impurity C | Sumatriptan Hydrazine Impurity | Methyl (4-Nitrophenyl)methanesulfonate | Sumatriptan EP Impurity H | Sumatriptan EP Impurity B HCl salt | Sumatriptan EP Impurity G | Sumatriptan Succinate Related Compound A | N-Nitroso Desmethyl Sumatriptan impurity | Sumatriptan 3-Hydroxy-2-Oxo Impurity | N-Nitroso sumatriptan | Sumatriptan EP Impurity A | Sumatriptan C Dimer | Sumatriptan Succinate Related Compound C | Sumatriptan Succinate impurity II | Sumatriptan EP Impurity B HCl Salt | Sumatriptan N-Nitroso impurity |