Furosemide EP impurity E
| Product Name | Furosemide EP impurity E |
|---|---|
| Alternate Names | Furosemide Impurities, Impurities of Furosemide |
| CAT No. | CS-O-07846 |
| CAS No. | 50-84-0 |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 191.01 g/mol |
| Mol. For. | C₇H₄Cl₂O₂ |
| Hazardous | This is a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Parent API | Furosemide |
| Therapeutic | Anti-Hypertensives |
| Smileys | C1=CSC2=C1C=CS2 |
| Canonical Smiles | C1=CC(=C(C=C1Cl)Cl)C(=O)O |
| InchIKey | ATCRIUVQKHMXSH-UHFFFAOYSA-N |
| Inchl | InChI=1S/C7H4Cl2O2/c8-4-1-2-5(7(10)11)6(9)3-4/h1-3H,(H,10,11) |
| IUPAC | 2,4-dichlorobenzoic acid |
| 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 |
Furosemide EP impurity E, also known as 4-chloro-5-sulfamoylanthranilic acid, is a chemical compound that is commonly used as a reference standard in the pharmaceutical industry. It is primarily employed for analytical purposes, such as in the development of new drug formulations and the quality control of existing ones.
Furosemide EP impurity E is an impurity that can be found in small amounts in Furosemide, a diuretic drug that is used to treat conditions such as high blood pressure, edema, and congestive heart failure. It is important to monitor the levels of impurities in Furosemide to ensure its purity, safety, and efficacy.
With a chemical formula of C7H6ClNO4S, Furosemide EP impurity E is a crystalline solid that is slightly soluble in water and ethanol. It has a melting point of 220-225°C and a molecular weight of 241.64 g/mol. Its structure is characterized by a chlorobenzene ring, a sulfonamide group, and a carboxylic acid group.
In conclusion, Furosemide EP impurity E is a valuable reference standard that plays a crucial role in the pharmaceutical industry. Its analytical use helps ensure the purity and quality of Furosemide, a widely used diuretic drug.
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Related Compounds
Tetrahydro Furosemide | Furosemide Impurity 8 | Furosemide Impurity 1 | Furosemide Amide Impurity | Furosemide Impurity 1 Hydrochloride (Furfurylamine Hydrochloride) | Furosemide EP impurity B | Furosemide EP impurity A | Furosemide Dessulfamoyl impurity | Furosemide Deschloro impurity | Furosemide Dichloro impurity | Furosemide EP impurity D | Tetrahydro Furosemide | Furosemide Impurity 14 (N-Nitroso-Furosemide) Sodium salt | Furosemide Imine impurity | Furosemide oxo impurity |