Afatinib Impurity 5
| Chemical Name | Afatinib Impurity 5 |
|---|---|
| Alternate Names | Afatinib Impurities, Impurities of Afatinib |
| CAT No. | CS-O-13089 |
| CAS Registry# | 179552-74-0 |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 348.72 g/mol |
| Mol. For. | C₁₅H₁₀CIFN₄O₃ |
| Hazardous | This is not a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Parent API | Afatinib |
| Therapeutic | Anti-Cancer / Oncology |
| Smileys | ClC1=C(F)C=CC(NC2=NC=NC3=CC(OC)=C([N+]([O-])=O)C=C23)=C1 |
| Canonical Smiles | COC1=C(C=C2C(=C1)N=CN=C2NC3=CC(=C(C=C3)F)Cl)[N+](=O)[O-] |
| InchIKey | VKEKKVCWODTGAP-UHFFFAOYSA-N |
| Inchl | InChI=1S/C15H10ClFN4O3/c1-24-14-6-12-9(5-13(14)21(22)23)15(19-7-18-12)20-8-2-3-11(17)10(16)4-8/h2-7H,1H3,(H,18,19,20) |
| IUPAC | N-(3-chloro-4-fluorophenyl)-7-methoxy-6-nitroquinazolin-4-amine |
| 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 |
Afatinib Impurity 5 is a chemical compound that is used as a reference standard in the pharmaceutical industry. It is a potential impurity that is often found in samples of the drug Afatinib, which is used in the treatment of non-small cell lung cancer. As a reference standard, it is used for qualitative and quantitative analysis of Afatinib in drug samples.
The chemical structure of Afatinib Impurity 5 is closely related to that of Afatinib, but it has slight differences in its molecular structure. It is a yellowish-brown powder that is soluble in organic solvents such as methanol and acetonitrile. The molecular formula of Afatinib Impurity 5 is C24H27ClFN5O4.
The chemical information of Afatinib Impurity 5 is important in drug development and quality control. It is used to ensure that the final product is pure and free of impurities that may affect its efficacy or safety. The impurity level of Afatinib Impurity 5 is monitored during the manufacturing process to ensure that it is within acceptable limits.
In conclusion, Afatinib Impurity 5 is an important reference standard that is used in the pharmaceutical industry to ensure the quality and purity of the drug Afatinib. Its chemical information is essential in the development and production of safe and effective drugs.
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Related Compounds
Afatinib Impurity E | Afatinib Impurity D | Afatinib Impurity 9 | Afatinib Impurity 16 | Afatinib Impurity 4 | Afatinib Impurity 20 | Afatinib Butoxy Analog | Afatinib imp-VI | N-Nitroso Afatinib | Afatinib Impurity 7 | Afatinib Impurity 6 | Afatinib Impurity F | Afatinib Impurity 3 | Afatinib Impurity AFT-8 | Afatinib Impurity 23 | Afatinib N-Oxide | Afatinib Impurity 10 | Afatinib Impurity G | Afatinib Hydroxy impurity | Afatinib Impurity 4 | Afatinib Impurity K | Afatinib Impurity A | Afatinib Maleic Acid Adduct | Afatinib Impurity I | Afatinib Impurity 2 | Afatinib Impurity 8 | Afatinib 5-hydroxypyrrolidin-2-one Impurity | Afatinib Impurity J HCl | Afatinib Impurity 22 | Afatinib Dimer impurity | Afatinib Impurity C | ethyl (E)-4-(dimethylamino)but-2-enoate hydrochloride | Afatinib Impurity H | Afatinib Impurity 1 | Afatinib Sulfonic Acid Analog |