Nimesulide EP Impurity A
| Product Name | Nimesulide EP Impurity A |
|---|---|
| CAT No. | CS-T-92564 |
| CAS No. | 51765-56-1 |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 353.31 g/mol |
| Mol. For. | C₁₃H₁₁N₃O₇S |
| Hazardous | This is a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Smileys | CS(=O)(=O)NC1=C(C=C(C=C1OC2=CC=CC=C2)[N+](=O)[O-])[N+](=O)[O-] |
| Canonical Smiles | CS(=O)(=O)NC1=C(C=C(C=C1OC2=CC=CC=C2)[N+](=O)[O-])[N+](=O)[O-] |
| InchIKey | REBQHYRUDRMDOA-UHFFFAOYSA-N |
| Inchl | InChI=1S/C13H11N3O7S/c1-24(21,22)14-13-11(16(19)20)7-9(15(17)18)8-12(13)23-10-5-3-2-4-6-10/h2-8,14H,1H3 |
| IUPAC | N-(2,4-dinitro-6-phenoxyphenyl)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 |
Nimesulide EP Impurity A is a chemical compound that is often used in research and development activities related to the non-steroidal anti-inflammatory drug (NSAID) nimesulide. This impurity is a by-product of the manufacturing process of nimesulide and is typically present in small amounts in the final product.
The chemical name of Nimesulide EP Impurity A is 4-Nitro-2-phenoxyaniline. It has a molecular weight of 238.24 g/mol and a chemical formula of C13H10N2O3. The compound is a yellowish-orange powder and is sparingly soluble in water.
In research and development, Nimesulide EP Impurity A is commonly used as a reference standard for the identification and quantification of impurities in nimesulide products. It is often used in analytical methods such as high-performance liquid chromatography (HPLC) and mass spectrometry (MS).
The presence of impurities in pharmaceutical products is of great concern, as they may affect the safety and efficacy of the drug. Therefore, the accurate identification and quantification of impurities in nimesulide products is essential to ensure the quality and safety of the drug. Nimesulide EP Impurity A is an important tool in this process.
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