Sumatriptan EP Impurity A
| Product Name | Sumatriptan EP Impurity A |
|---|---|
| Alternate Names | Sumatriptan Impurities, Impurities of Sumatriptan |
| CAT No. | CS-O-08210 |
| CAS No. | 545338-89-4 |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 495.68 g/mol |
| Mol. For. | C₂₇H₃₇N₅O₂S |
| Hazardous | This is a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Parent API | Sumatriptan |
| Purity | 95% |
| Therapeutic | Anti-Migraines |
| Smileys | CN(C)CCC(C1=CC(C[S](NC)(=O)=O)=CC=C1N2)=C2CC3=CC=C4C(C(CCN(C)C)=CN4)=C3 |
| Canonical Smiles | CNS(=O)(=O)CC1=CC2=C(C=C1)NC(=C2CCN(C)C)CC3=CC4=C(C=C3)NC=C4CCN(C)C |
| InchIKey | UVOHQDUMFGSNEJ-UHFFFAOYSA-N |
| Inchl | InChI=1S/C27H37N5O2S/c1-28-35(33,34)18-20-7-9-26-24(15-20)22(11-13-32(4)5)27(30-26)16-19-6-8-25-23(14-19)21(17-29-25)10-12-31(2)3/h6-9,14-15,17,28-30H,10-13,16,18H2,1-5H3 |
| IUPAC | 1-[3-[2-(dimethylamino)ethyl]-2-[[3-[2-(dimethylamino)ethyl]-1H-indol-5-yl]methyl]-1H-indol-5-yl]-N-methylmethanesulfonamide |
| 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 A is a chemical compound that is commonly used in the pharmaceutical industry as a reference standard for analytical purposes. It is a known impurity of Sumatriptan, a medication that is used to treat migraines and cluster headaches. The chemical structure of Sumatriptan EP Impurity A is closely related to that of Sumatriptan, with both compounds containing a similar chemical backbone.
Sumatriptan EP Impurity A is typically used as a reference standard in analytical methods such as high-performance liquid chromatography (HPLC), gas chromatography (GC), and mass spectrometry (MS). These techniques are used to determine the purity and identity of Sumatriptan and other related compounds in drug formulations.
The chemical formula of Sumatriptan EP Impurity A is C14H20N2O2S, with a molecular weight of 284.38 g/mol. It is a white to off-white crystalline powder that is sparingly soluble in water and soluble in organic solvents such as methanol and ethanol.
In conclusion, Sumatriptan EP Impurity A is a useful reference standard for analytical purposes in the pharmaceutical industry. Its chemical structure is closely related to Sumatriptan, and it is used to determine the purity and identity of Sumatriptan and related compounds in drug formulations.
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Related Compounds
Sumatriptan 3-Hydroxy-2-Oxo Impurity | Methyl (4-Nitrophenyl)methanesulfonate | Sumatriptan Hydrazine Impurity | Sumatriptan EP Impurity F | Sumatriptan EP Impurity B HCl Salt | Sumatriptan C Dimer | Sumatriptan EP Impurity E | Sumatriptan Succinate Related Compound A | Sumatriptan EP Impurity C | Sumatriptan EP Impurity B | Sumatriptan EP Impurity B HCl salt | Sumatriptan EP Impurity G | Sumatriptan EP Impurity H | Sumatriptan degradation impurity | Sumatriptan EP Impurity D | Sumatriptan impurity 1 | Sumatriptan Succinate impurity II | Sumatriptan Aminophenyl Impurity | N,N-Dinitroso Sumatriptan | N-Nitroso Desmethyl Sumatriptan impurity | Sumatriptan N-Nitroso impurity | Sumatriptan Succinate Related Compound C | Sumatriptan Impurity 3 | N-Nitroso sumatriptan |