Oseltamivir Nitroso Impurity 1
Also known as: Oseltamivir Nitrosamine Impurities or nitrosamine impurities of Oseltamivir| Product Name | Oseltamivir Nitroso Impurity 1 |
|---|---|
| Alternate Names | Oseltamivir Impurities, Impurities of Oseltamivir |
| CAT No. | CS-EO-02085 |
| CAS No. | Not Available |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 356.46 g/mol |
| Mol. For. | C₁₈H₃₂N₂O₅ |
| Hazardous | This is not a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Parent API | Oseltamivir |
| 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 |
Oseltamivir Nitroso Impurity 1 is a chemical compound that is commonly used in the pharmaceutical industry. It is used as an impurity in the production of Oseltamivir, a drug that is used to treat influenza viruses. Oseltamivir Nitroso Impurity 1 is formed during the synthesis of Oseltamivir and hence it is important to have a good understanding of its chemical properties and usage.
Oseltamivir Nitroso Impurity 1 is a nitroso compound that has a molecular weight of 235.2 g/mol. It is a yellowish powder that is soluble in water and ethanol. The compound is highly reactive and has a short half-life, which makes it difficult to isolate and study. Despite this, it is an important impurity in the production of Oseltamivir, as it can affect the efficacy and safety of the final product.
The presence of Oseltamivir Nitroso Impurity 1 in the final product can lead to adverse effects on patients, including liver toxicity and allergic reactions. Therefore, it is important to monitor and control the levels of this impurity during the production of Oseltamivir. Various techniques such as high-performance liquid chromatography (HPLC) and mass spectrometry (MS) are used for the detection and quantification of Oseltamivir Nitroso Impurity 1.
In conclusion, Oseltamivir Nitroso Impurity 1 is a significant impurity in the production of Oseltamivir. It is important to monitor and control its levels during the manufacturing process to ensure the safety and efficacy of the final product.
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Related Compounds
Oseltamivir Impurity 32 | Oseltamivir Nitroso Impurity 2 | Oseltamivir RSS Isomer | Oseltamivir Impurity 24 | Oseltamivir Pyrrole analog | Oseltamivir glucose adduct-2 | Oseltamivir EP Imp R | Oseltamivir Impurity 15 | Oseltamivir Impurity 8 | Oseltamivir RSR Isomer | Oseltamivir Impurity 25 | Oseltamivir-Glucose Adduct 1 | OSELTAMIVIR CITRIC ACID ADDUCT | Oseltamivir Impurity 14 | Oseltamivir Related Compound B | Oseltamivir Acid Methyl Ester | Acetamido azidesulfonamide | Oseltamivir Impurity 6 | Oseltamivir Impurity 41 | Oseltamivir Impurity 15 | Oseltamivir Impurity 23 | Oseltamivir Phosphate Impurity B | Ethyl (3S, 4S, 5S)-4-acetamido-5-amino-3-(1- ethyl propoxy) cyclohex-1-ene-1-carboxylate | Oseltamivir Impurity 26 | Oseltamivir Related Compound A | N-Nitroso Oseltamivir impurity | Oseltamivir Impurity 28 | OSELTAMIVIR CITRIC ACID ADDUCT 2 | ethyl 4-(pentan-3-yloxy)benzoate | Oseltamivir Impurity 22 | Oseltamivir EP Impurity E HCl | Oseltamivir RRR Isomer | OSELTAMIVIR CITRIC ACID ADDUCT II | Oseltamivir Impurity 7 | Oseltamivir Impurity 31 | Oseltamivir Impurity 52 | Rel 4-N-Desacetyl-5-N-acetyl Oseltamivir Acid | Oseltamivir impurity A | Oseltamivir Acid Methyl Ester Phosphate Salt | Oseltamivir Impurity 4 | Oseltamivir Impurity 48 | Oseltamivir diallyl amine impurity | Oseltamivir EP Imp U | Rac- Oseltamivir hydroxymethyl furan | Oseltamivir 5-Desamino 5-(2-Formyl 5-Hydroxymethylpyrrol-1-yl) | Oseltamivir EP Impurity B | ent-Oseltamivir Phosphate | Oseltamivir Impurity 19 | Oseltamivir Impurity 27 |