Sumatriptan EP Impurity B
| Product Name | Sumatriptan EP Impurity B |
|---|---|
| Alternate Names | Sumatriptan Impurities, Impurities of Sumatriptan |
| CAT No. | CS-O-08211 |
| CAS No. | 88919-51-1 |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 281.4 g/mol |
| Mol. For. | C13H19N3O2S |
| Hazardous | This is a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Parent API | Sumatriptan |
| Purity | 95% |
| Therapeutic | Anti-Migraines |
| Smileys | CNCCC1=CNC2=C1C=C(C[S](NC)(=O)=O)C=C2 |
| Canonical Smiles | CNCCC1=CNC2=C1C=C(C=C2)CS(=O)(=O)NC |
| InchIKey | YDTVAJYBEHCVJY-UHFFFAOYSA-N |
| Inchl | InChI=1S/C13H19N3O2S/c1-14-6-5-11-8-16-13-4-3-10(7-12(11)13)9-19(17,18)15-2/h3-4,7-8,14-16H,5-6,9H2,1-2H3 |
| IUPAC | N-methyl-1-[3-[2-(methylamino)ethyl]-1H-indol-5-yl]methanesulfonamide |
| 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 B is a chemical compound that belongs to the class of triptans, which are used in the treatment of migraines and cluster headaches. This impurity is an intermediate compound that is formed during the synthesis of Sumatriptan. Sumatriptan EP Impurity B is not intended for use as a medication, but it is used in the pharmaceutical industry as a reference standard or reference material for quality control purposes.
The chemical name of Sumatriptan EP Impurity B is (S)-N-[2-(1-methyl-2-pyrrolidinyl)ethyl]-5-[2-(phenylsulfonylamino)ethyl]-1H-indole-3-acetamide. Its molecular formula is C21H28N4O3S and the molecular weight is 424.54 g/mol.
Sumatriptan EP Impurity B is a white to off-white powder that is soluble in organic solvents like methanol, ethanol, and DMSO. It has a melting point range of 178-181°C. This impurity is used in the characterization and determination of purity of Sumatriptan by various analytical techniques such as HPLC, NMR, and Mass spectrometry.
In conclusion, Sumatriptan EP Impurity B is a crucial reference standard in the pharmaceutical industry for quality control of Sumatriptan. It is not intended for human consumption and should be handled with care by trained professionals.
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Related Compounds
Sumatriptan Impurity 3 | Sumatriptan impurity 1 | Sumatriptan EP Impurity B HCl salt | Sumatriptan N-Nitroso impurity | Sumatriptan Succinate Related Compound A | Sumatriptan Hydrazine Impurity | N-Nitroso sumatriptan | Sumatriptan EP Impurity B HCl Salt | Sumatriptan EP Impurity H | Sumatriptan C Dimer | Sumatriptan degradation impurity | N,N-Dinitroso Sumatriptan | Sumatriptan EP Impurity F | Methyl (4-Nitrophenyl)methanesulfonate | N-Nitroso Desmethyl Sumatriptan impurity | Sumatriptan Succinate impurity II | Sumatriptan Aminophenyl Impurity | Sumatriptan 3-Hydroxy-2-Oxo Impurity | Sumatriptan EP Impurity D | Sumatriptan Succinate Related Compound C | Sumatriptan EP Impurity E | Sumatriptan EP Impurity A | Sumatriptan EP Impurity G | Sumatriptan EP Impurity C |