Ritonavir EP Impurity U
| Product Name | Ritonavir EP Impurity U |
|---|---|
| Alternate Names | Ritonavir Impurities, Impurities of Ritonavir |
| CAT No. | CS-EO-00166 |
| CAS No. | Not Available |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 1016.34 g/mol |
| Mol. For. | C51H69N9O7S3 |
| Hazardous | This is not a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Parent API | Ritonavir |
| Smileys | CC(C)[C@H](NC(N(C)CC1=CSC(C(C)C)=N1)=O)C(O[C@H]([C@@H](NC(OCC2=CN=CS2)=O)CC3=CC=CC=C3)C[C@@H](NC([C@@H](NC(N(C)CC4=CSC(C(C)C)=N4)=O)C(C)C)=O)CC5=CC=CC=C5)=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 |
Ritonavir EP Impurity U is a chemical compound that is used in the pharmaceutical industry as a reference standard for quality control purposes. It is a highly pure substance that is used to ensure the accuracy and consistency of the analytical methods used in the analysis of Ritonavir, a drug used to treat HIV infections.
The chemical formula of Ritonavir EP Impurity U is C20H28N2O5, and it has a molecular weight of 376.45 g/mol. The compound is a white to off-white powder that is soluble in organic solvents such as methanol, ethanol, and dimethyl sulfoxide (DMSO).
Ritonavir EP Impurity U is typically used in the analytical testing of Ritonavir to determine the purity, potency, and quality of the drug. It is also used to validate analytical methods and equipment used in the manufacturing of Ritonavir.
The compound is manufactured under strict quality control measures and is guaranteed to meet the highest standards of purity and quality. It is important to note that Ritonavir EP Impurity U is not intended for use in humans or animals and should only be used by trained professionals in a laboratory setting.
In conclusion, Ritonavir EP Impurity U is an important reference standard in the pharmaceutical industry that is used to ensure the quality and consistency of Ritonavir, a drug used to treat HIV infections. Its high purity and quality make it an essential tool in the analytical testing and manufacturing of Ritonavir.
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Related Compounds
S-(1-methyl-1H-imidazol-4-yl) 2-methylpropanethioate | Ritonavir EP Impurity R | O-Acetyl Ritonavir | Ritonavir Hydroxy impurity | Ritonavir Impurity S | Ritonavir Acid Impurity | Ritonavir Hydrogen Peroxide Impurity | Ritonavir Impurity T | Ritonavir EP Impurity E | Thiazol-5-ylmethyl ((2S, 3S, 5S)-3-hydroxy-5-(2-(3-((5-isopropylthiazol-2-yl) methyl)-3-methylureido | Ritonavir Impurity 30 | Ritonavir EP Impurity P | Ritonavir EP Impurity D | Ritonavir Impurity 22 | Ritonavir Hydroxypropyl carbamate | Ritonavir Impurity U | Ritonavir Geo-isomer Hcl | Ritonavir Impurity 23 | Ritonavir-Glycerol carbamate Analog | Ritonavir Impurity 27 | Ritonavir EP Impurity F | Ritonavir EP Impurity I | Ritonavir 2,5-Thiazoylmethyl-Dicarbamate | Des(isopropylthiazolyl)-N-methyl Ritonavir | Ritonavir EP Impurity N | Ritonavir EP Impurity I | Ritonavir Enantiomer | Ritonavir Impurity G | Ritonavir EP Impurity M | Ritonavir Geo-isomer | Ritonavir EP Impurity S | thiazol-5-ylmethyl ((2S,3S,5S)-3-hydroxy-5-((R)-2-(3-((5-(2-hydroxypropan-2-yl)thiazol-2-yl)methyl)- | thiazol-5-ylmethyl ((2S,3S,5S)-5-((S)-2-(3-((2-(2-hydroperoxypropan-2-yl)thiazol-4-yl)methyl)-3-methylureido)-3-methylbutanamido)-3-hydroxy-1,6-diphenylhexan-2-yl)carbamate | Ritonavir EP Impurity O | Ritonavir EP Impurity Q | Ritonavir EP Impurity K |