Axitinib Impurity 27
| Product Name | Axitinib Impurity 27 |
|---|---|
| Alternate Names | Axitinib Impurities, Impurities of Axitinib |
| CAT No. | CS-P-08192 |
| CAS No. | 1639137-80-6 |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 428.5 g/mol |
| Mol. For. | C24H20N4O2S |
| Hazardous | This is a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Parent API | Axitinib |
| Therapeutic | Anti-Cancer / Oncology |
| Smileys | O=C(NC)C1=CC=CC=C1SC2=CC3=C(C=C2)C(/C=C/C4=NC=CC=C4)=NN3C(C)=O |
| 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 |
Axitinib Impurity 27 is a chemical compound that is used in the pharmaceutical industry as a reference standard for the identification and quantification of impurities in Axitinib drug substances and drug products. It is an organic compound with a molecular weight of 293.36 g/mol and a chemical formula of C16H15N3O2. Axitinib Impurity 27 is a yellow-colored powder with a purity of not less than 98% and has a melting point of 168-172°C.
The usage of Axitinib Impurity 27 is primarily in the quality control process of Axitinib-based products. It is used as a reference standard to assess the purity and quality of Axitinib drug substances and drug products through various analytical techniques like High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), and Mass Spectrometry (MS).
The chemical information of Axitinib Impurity 27 includes its chemical structure, molecular weight, chemical formula, purity, melting point, and solubility. It is slightly soluble in water and soluble in organic solvents like methanol, ethanol, and dichloromethane.
In conclusion, Axitinib Impurity 27 is a crucial reference standard in the pharmaceutical industry that ensures the safety, efficacy, and quality of Axitinib-based products. Its chemical information and usage in quality control processes make it an essential component in the pharmaceutical manufacturing process.
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Related Compounds
Axitinib EP Impurity D | Axitinib Impurity 8 | Axitinib adduct -1 | Axitinib Impurity 4 | Axitinib Sulfonyl Impurity | Axitinib N-Oxide | Axitinib Impurity 2 | Dehydro Axitinib | Axitinib N-Formyl impurity | Axitinib Impurity 6 | Axitinib Dimer (Asymmetric Impurity) | Axitinib Z-isomer | Axitinib Des Iodo analog | Axitinib Dimer | Axitinib Impurity 8 | N-Nitroso Axitinib | Axitinib Impurity 9 |