Sumatriptan EP Impurity D
| Product Name | Sumatriptan EP Impurity D |
|---|---|
| Alternate Names | Sumatriptan Impurities, Impurities of Sumatriptan |
| CAT No. | CS-O-08213 |
| CAS No. | 212069-94-8 |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 311.40 g/mol |
| Mol. For. | C₁₄H₂₁N₃O₃S |
| Hazardous | This is a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Parent API | Sumatriptan |
| Purity | 95% |
| Therapeutic | Anti-Migraines |
| Smileys | C[N+](C)([O-])CCC1=CNC2=C1C=C(C[S](NC)(=O)=O)C=C2 |
| Canonical Smiles | CNS(=O)(=O)CC1=CC2=C(C=C1)NC=C2CC[N+](C)(C)[O-] |
| InchIKey | GRHYJEBKFWDYFD-UHFFFAOYSA-N |
| Inchl | InChI=1S/C14H21N3O3S/c1-15-21(19,20)10-11-4-5-14-13(8-11)12(9-16-14)6-7-17(2,3)18/h4-5,8-9,15-16H,6-7,10H2,1-3H3 |
| IUPAC | N,N-dimethyl-2-[5-(methylsulfamoylmethyl)-1H-indol-3-yl]ethanamine oxide |
| 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 D is a chemical compound that is used in pharmaceutical research and development as an impurity standard for the analysis of Sumatriptan, a medication used to treat migraine headaches. This impurity is a byproduct of the manufacturing process of Sumatriptan and is classified as a potential genotoxic impurity.
Sumatriptan EP Impurity D is a white powder with a molecular weight of 296.38 g/mol. Its chemical formula is C13H15N3O2S, and its structure contains a triptan core with a sulfonamide group and an amide group. The compound has a melting point of 206-209°C and is soluble in organic solvents such as methanol, ethanol, and acetonitrile.
In pharmaceutical analysis, Sumatriptan EP Impurity D is used as a reference standard for the detection and quantification of Sumatriptan impurities in drug products. The presence of this impurity can affect the safety and efficacy of the drug, making it essential to monitor and control its levels during the manufacturing process.
Overall, Sumatriptan EP Impurity D plays a crucial role in the quality control of Sumatriptan products, ensuring that they meet stringent regulatory standards for safety and efficacy.
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Related Compounds
Sumatriptan Hydrazine Impurity | Sumatriptan EP Impurity B | N-Nitroso sumatriptan | Sumatriptan Succinate impurity II | Sumatriptan EP Impurity G | Sumatriptan EP Impurity F | Methyl (4-Nitrophenyl)methanesulfonate | Sumatriptan C Dimer | Sumatriptan Aminophenyl Impurity | Sumatriptan Impurity 3 | Sumatriptan EP Impurity C | Sumatriptan EP Impurity E | Sumatriptan Succinate Related Compound A | Sumatriptan degradation impurity | N,N-Dinitroso Sumatriptan | Sumatriptan EP Impurity B HCl salt | Sumatriptan impurity 1 | Sumatriptan EP Impurity B HCl Salt | Sumatriptan EP Impurity H | Sumatriptan 3-Hydroxy-2-Oxo Impurity | Sumatriptan N-Nitroso impurity | Sumatriptan Succinate Related Compound C | Sumatriptan EP Impurity A | N-Nitroso Desmethyl Sumatriptan impurity |