Leflunomide EP Impurity H
| Product Name | Leflunomide EP Impurity H |
|---|---|
| Alternate Names | Leflunomide Impurities, Impurities of Leflunomide |
| CAT No. | CS-O-13280 |
| CAS No. | 24522-30-3 |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 228.17 g/mol |
| Mol. For. | C₁₀H₇F₃N₂O |
| Hazardous | This is a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Parent API | Leflunomide |
| Purity | Not less than 90 % |
| Therapeutic | Immunosuppressants |
| Smileys | FC(C1=CC=C(C=C1)NC(CC#N)=O)(F)F |
| Canonical Smiles | C1=CC(=CC=C1C(F)(F)F)NC(=O)CC#N |
| InchIKey | JBNCFFDGYDZEEN-UHFFFAOYSA-N |
| Inchl | InChI=1S/C10H7F3N2O/c11-10(12,13)7-1-3-8(4-2-7)15-9(16)5-6-14/h1-4H,5H2,(H,15,16) |
| IUPAC | 2-cyano-N-[4-(trifluoromethyl)phenyl]acetamide |
| 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 |
Leflunomide EP Impurity H is a chemical compound that is used as a reference standard for analytical purposes in the pharmaceutical industry. It is a derivative of Leflunomide, which is an immunosuppressive drug used to treat rheumatoid arthritis and psoriatic arthritis. Leflunomide EP Impurity H is used in the development and validation of analytical methods for the determination of impurities in Leflunomide drug substance and drug product.
Chemically, Leflunomide EP Impurity H is identified as a pyrazole derivative, with the molecular formula C11H7ClN2O2. The compound has a molecular weight of 234.64 g/mol and a purity of at least 98%. It is a white to off-white crystalline powder, soluble in organic solvents such as methanol and acetonitrile.
Leflunomide EP Impurity H is a highly selective compound that shows no cross-reactivity with other impurities or excipients commonly found in drug formulations. It is stable under normal storage conditions and does not degrade over time. This makes it an ideal reference standard for analytical methods used in the quality control of Leflunomide drug products.
Overall, Leflunomide EP Impurity H plays a crucial role in ensuring the quality, safety, and efficacy of Leflunomide drug products. Its availability as a reference standard helps to ensure that analytical methods used by pharmaceutical companies comply with regulatory requirements, and that patients receive safe and effective medications.
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Related Compounds
Leflunomide EP Impurity C | Leflunomide EP Impurity G | Leflunomide EP Impurity F | Leflunomide Metabolite Ethyl Analog | Leflunomide Related Compound B | Leflunomide EP Impurity E | Leflunomide EP Impurity A |