Enalapril EP Impurity A
| Product Name | Enalapril EP Impurity A |
|---|---|
| Alternate Names | Enalapril Impurities, Impurities of Enalapril |
| CAT No. | CS-T-21610 |
| CAS No. | 1356932-13-2 |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 492.52 g/mol |
| Mol. For. | C₂₄H₃₂N₂O₉ |
| Hazardous | This is a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Parent API | Enalapril |
| Therapeutic | Anti-Hypertensives |
| Canonical Smiles | CCOC(=O)C(CCC1=CC=CC=C1)NC(C)C(=O)N2CCCC2C(=O)O.C(=CC(=O)O)C(=O)O |
| InchIKey | OYFJQPXVCSSHAI-BMSLDGIRSA-N |
| Inchl | InChI=1S/C20H28N2O5.C4H4O4/c1-3-27-20(26)16(12-11-15-8-5-4-6-9-15)21-14(2)18(23)22-13-7-10-17(22)19(24)25;5-3(6)1-2-4(7)8/h4-6,8-9,14,16-17,21H,3,7,10-13H2,1-2H3,(H,24,25);1-2H,(H,5,6)(H,7,8)/b;2-1-/t14-,16+,17-;/m0./s1 |
| IUPAC | (Z)-but-2-enedioic acid;(2S)-1-[(2S)-2-[[(2R)-1-ethoxy-1-oxo-4-phenylbutan-2-yl]amino]propanoyl]pyrrolidine-2-carboxylic 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 |
Enalapril EP Impurity A is a chemical compound that is commonly used in the pharmaceutical industry. It is a by-product or intermediate in the synthesis of Enalapril, which is a medication used in the treatment of hypertension and heart failure. Enalapril EP Impurity A is a white to off-white crystalline powder that is soluble in organic solvents such as ethanol, methanol, and acetonitrile.
The usage of Enalapril EP Impurity A is primarily as a reference standard in the quality control of Enalapril formulations. It is also used in research and development studies to evaluate the purity and stability of Enalapril. The impurity is considered to be a potential contaminant in the manufacturing process of Enalapril, and therefore its identification and quantification is essential to ensure the safety and efficacy of the final product.
From a chemical perspective, Enalapril EP Impurity A is a dipeptide derivative that contains an alanine and a proline residue. It is known to be an impurity that arises during the synthesis of Enalapril and is formed by the condensation of two precursor molecules. The impurity has a molecular weight of 373.43 g/mol and a molecular formula of C16H22N2O4.
In conclusion, Enalapril EP Impurity A is an essential reference standard in the quality control of Enalapril formulations. Its identification and quantification are critical for ensuring the safety and efficacy of the medication. Its chemical structure and properties make it a useful intermediate in the synthesis of Enalapril, but it is also considered a potential contaminant in the manufacturing process.
Get an Instant Quote
Related Compounds
Enalaprilat EP Impurity E | Enalapril (R)Diketopiperazine methyl ester | Enalapril EP Impurity D | Enalapril Diketopiperazine Acid (R-Isomer) | Enalapril Diketopiperazine Acid | Enalaprilat EP Impurity C | Enalapril EP Impurity H Maleate | Enalapril EP Impurity E | Enalaprilat EP Impurity B | Enalaprilat EP Impurity G | Enalaprilat EP Impurity A | Enalapril Cyclohexyl Analogue HCl | Enalaprilat EP Impurity D | Enalaprilat EP Impurity F | RS-ENALAPRIL MALEATE(Racemic) | Enalapril EP Impurity C | Enalapril EP impurity A (mixture of diastereomers) | Enalapril tert-Butyl Ester | N-Nitroso Enalapril [Mixture of isomers] | Enalapril Ep impurity H TFA salt | Enalapril EP Impurity E | Enalapril EP Impurity G | N-Nitroso Enalaprilat | Enalapril EP Impurity B |