Darunavir Amine dimer impurity
| Product Name | Darunavir Amine dimer impurity |
|---|---|
| Alternate Names | Darunavir Impurities, Impurities of Darunavir |
| CAT No. | CS-O-15899 |
| CAS No. | Not Available |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 965.19 g/mol |
| Mol. For. | C₄₈H₆₄N₆O₁₁S₂ |
| Hazardous | This is a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Parent API | Darunavir |
| Purity | 95% |
| Therapeutic | Antiretroviral / Anti-HIV |
| Smileys | O=C(O[C@@H]1[C@@]2([H])[C@@](OCC2)([H])OC1)N[C@H]([C@H](O)CN(CC(C)C)S(=O)(C3=CC=C(NC(N[C@H]([C@H](O)CN(CC(C)C)S(=O)(C4=CC=C(N)C=C4)=O)CC5=CC=CC=C5)=O)C=C3)=O)CC6=CC=CC=C6 |
| 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 |
Darunavir Amine dimer impurity is a chemical impurity that is commonly found in the production of the antiretroviral drug, Darunavir. This impurity is formed during the synthesis of Darunavir and can have an impact on the quality and efficacy of the final product. The impurity is a dimer form of the amine group present in Darunavir, and it is typically present in small amounts in the final product.
The presence of Darunavir Amine dimer impurity can affect the potency of the drug and can also lead to adverse reactions in patients. Therefore, it is important to monitor the levels of this impurity during the manufacturing process and to ensure that it is removed or reduced to an acceptable level.
Chemically, Darunavir Amine dimer impurity is a byproduct of the reaction between two molecules of Darunavir's amine group, which results in the formation of a dimeric compound. The impurity is typically identified and quantified using analytical techniques such as high-performance liquid chromatography (HPLC) or mass spectrometry (MS).
Overall, the monitoring and control of Darunavir Amine dimer impurity levels is essential for ensuring the safety and efficacy of Darunavir as a treatment for HIV/AIDS.
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Related Compounds
Darunavir СВZ amino impurity | Darunavir furan dimer impurity | Darunavir Impurity 23 | Darunavir СВZ urea impurity | Darunavir Impurity 46 | Darunavir Impurity 38 | N-[3S-benzyloxycarbonylamino-2R-hydroxy-4-phenyl]-N-isobutylamine | Darunavir Urea impurity | Darunavir Isomer 1 | Darunavir impurity B | Darunavir N-methyl urea impurity | Darunavir Diamino impurity | Darunavir Impurity 10 | Darunavir СВZ furan impurity | Darunavir Impurity 16 | Darunavir Difuranyl impurity | Darunavir Impurity 7 (S,S-Isomer) | Darunavir Impurity 8 (R,R-Isomer) | Darunavir Isomer 2 | Darunavir Impurity A Enantiomer | Darunavir Impurity D | Darunavir Impurity 11 | Darunavir Nitro complex impurity | Darunavir Carbamic Acid Methyl Ester |