Losartan Potassium EP Impurity C
| Product Name | Losartan Potassium EP Impurity C |
|---|---|
| Alternate Names | Losartan Impurities, Impurities of Losartan |
| CAT No. | CS-T-31272 |
| CAS No. | 860644-28-6 |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 462.01 g/mol |
| Mol. For. | C₂₂H₂₃ClKN₆O |
| Hazardous | This is a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Parent API | Losartan |
| Therapeutic | Anti-Hypertensives |
| 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 |
Losartan Potassium EP Impurity C is a chemical compound that is commonly used in the pharmaceutical industry as a reference standard for the quality control of losartan potassium. Losartan potassium is an angiotensin II receptor antagonist that is used in the treatment of hypertension and diabetic nephropathy. Impurity C is a degradation product of losartan potassium that is formed during the manufacturing process or storage of the drug.
The chemical formula for Losartan Potassium EP Impurity C is C22H23ClN6O2S and it has a molecular weight of 474.98 g/mol. It is a yellow to orange crystalline powder that is soluble in methanol, ethanol, and water.
The usage of Losartan Potassium EP Impurity C is crucial for the identification, quantification, and control of impurities in losartan potassium. It is used as a reference standard for chromatographic methods, such as high-performance liquid chromatography (HPLC) and gas chromatography-mass spectrometry (GC-MS), that are used to analyze the purity of losartan potassium.
In conclusion, Losartan Potassium EP Impurity C is a vital chemical compound that plays a significant role in the quality control of losartan potassium. Its usage ensures the safety and efficacy of losartan potassium as a pharmaceutical drug.
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Related Compounds
Losartan EP Impurity M | Losartan a-Butyl-losartan Aldehyde Adduct | Losartan Dimer Azide | Losartan EP Impurity C | Losartan Amine | N-Trityl Losartan Isomer | Losartan isocyano Impurity | Losartan Impurity 15 | Losartan Impurity 29 | Losartan Potassium EP Impurity K | Losartan EP Impurity F | Losartan Potassium EP Impurity A | Losartan N1-Trityl Impurity | Losartan EP Impurity B | Losartan Potassium EP Impurity E | Losartan Potassium EP Impurity J | Losartan Impurity 7 | Losartan Related Compound E | Losartan Impurity 5 | N-Trityl Losartan Carboxaldehyde | N-Trityl Losartan Carboxylic Acid | Losartan Impurity 1 | Losartan Acetyloxy Impurity | Losartan Impurity 8 | Losartan Imidazo[1,5-b]isoquinoline Impurity | Des[2-(1H-tetrazol-5-yl)] 2-Cyanolosartan Carboxaldehyde | Losartan Impurity 6 | Nitroso Losartan | Losartan Hydroxy N1-Trityl Impurity | Losartan Azide impurity | Losartan Potassium EP Impurity H | Des[2-(1H-tetrazol-5-yl)] 2-Cyanolosartan | Losartan EP Impurity L | Losartan Related Compound D | Losartan Acetyloxy N1-Trityl Impurity |