Fenofibrate EP Impurity A
| Product Name | Fenofibrate EP Impurity A |
|---|---|
| Alternate Names | Fenofibrate Impurities, Impurities of Fenofibrate |
| CAT No. | CS-O-30874 |
| CAS No. | 42019-78-3 |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 232.66 g/mol |
| Mol. For. | C₁₃H₉ClO₂ |
| Hazardous | This is a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Parent API | Fenofibrate |
| Purity | Not less than 90 % |
| Therapeutic | Anti-Hyperlipidemics |
| Smileys | C1=CC(=CC=C1C(=O)C2=CC=C(C=C2)Cl)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 |
Fenofibrate EP Impurity A is a chemical compound that is used as an impurity reference standard for the analysis and testing of Fenofibrate drugs. Fenofibrate is a medication used to treat high cholesterol and triglyceride levels in the blood, and impurities in the drug can affect its efficacy and safety.
Fenofibrate EP Impurity A has a molecular weight of 326.4 g/mol and a chemical formula of C18H16O4. It is a yellow to orange crystalline powder that is sparingly soluble in water and soluble in organic solvents such as methanol and ethanol.
The chemical structure of Fenofibrate EP Impurity A is similar to that of the active ingredient in Fenofibrate, but it contains an additional functional group in its chemical structure. This impurity can be formed during the manufacturing process of Fenofibrate or can be present in the raw materials used to make the drug.
To ensure the quality and safety of Fenofibrate drugs, regulatory agencies such as the United States Pharmacopeia (USP) and the European Pharmacopoeia (EP) require the testing and analysis of Fenofibrate EP Impurity A in the drug. This impurity reference standard is used in analytical methods such as high-performance liquid chromatography (HPLC) and gas chromatography (GC) to quantify the amount of impurities in Fenofibrate drugs.
In conclusion, Fenofibrate EP Impurity A is an important reference standard used in the analysis and testing of Fenofibrate drugs to ensure their quality and safety.
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Related Compounds
Fenofibrate EP Impurity G | Fenofibrate Related compound at RRT 0.50 | Fenofibrate Impurity 9 | Fenofibrate Impurity 1 |