Ramipril EP Impurity N
| Product Name | Ramipril EP Impurity N |
|---|---|
| CAT No. | CS-O-08077 |
| CAS No. | 129939-63-5 |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 416.51 g/mol |
| Mol. For. | C₂₃H₃₂N₂O₅ |
| Hazardous | This is a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Therapeutic | Anti-Hypertensives |
| Smileys | O=C([C@@H](N[C@@H](CCC1=CC=CC=C1)C(OCC)=O)C)N2[C@]3([H])CCC[C@@]3(C[C@@H]2C(O)=O)[H] |
| Canonical Smiles | CCOC(=O)C(CCC1=CC=CC=C1)NC(C)C(=O)N2C3CCCC3CC2C(=O)O |
| InchIKey | HDACQVRGBOVJII-ABHMUUKNSA-N |
| Inchl | InChI=1S/C23H32N2O5/c1-3-30-23(29)18(13-12-16-8-5-4-6-9-16)24-15(2)21(26)25-19-11-7-10-17(19)14-20(25)22(27)28/h4-6,8-9,15,17-20,24H,3,7,10-14H2,1-2H3,(H,27,28)/t15-,17+,18-,19+,20+/m0/s1 |
| IUPAC | (2R,3aR,6aR)-1-[(2S)-2-[[(2S)-1-ethoxy-1-oxo-4-phenylbutan-2-yl]amino]propanoyl]-3,3a,4,5,6,6a-hexahydro-2H-cyclopenta[b]pyrrole-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 |
Ramipril EP Impurity N, also known as (2S,3aR,7aS)-1-[(S)-N-[(S)-1-Carboxy-3-phenylpropyl]valyl]octahydro-1H-indole-2-carboxylic acid, is a synthetic organic compound that serves as a reference standard for quality control and analytical purposes in the pharmaceutical industry.
Ramipril EP Impurity N is a minor impurity that is usually present in small quantities in the synthesis of Ramipril, a popular drug that is used to treat hypertension, heart failure, and prevent strokes. The impurity is formed during the synthesis process and can affect the quality, purity, and stability of the final product. Therefore, it is essential to monitor and control the levels of Ramipril EP Impurity N during the manufacturing process.
Chemically, Ramipril EP Impurity N is a complex molecule that contains an octahydro-1H-indole ring system, a carboxylic acid group, and a valyl substituent. The compound is soluble in polar solvents such as water, methanol, and ethanol and has a molecular weight of 391.5 g/mol.
In conclusion, Ramipril EP Impurity N is a critical analytical tool that is used to ensure the quality and purity of Ramipril during the manufacturing process. Its chemical properties and usage make it an essential reference standard for pharmaceutical companies that produce Ramipril.
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