Ramipril EP Impurity A
| Product Name | Ramipril EP Impurity A |
|---|---|
| Alternate Names | Ramipril Impurities, Impurities of Ramipril |
| CAT No. | CS-O-08079 |
| CAS No. | 108313-11-7 |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 402.48 g/mol |
| Mol. For. | C₂₂H₃₀N₂O₅ |
| Hazardous | This is a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Parent API | Ramipril |
| Therapeutic | Anti-Hypertensives |
| Smileys | CC(C(=O)N1C2CCCC2CC1C(=O)O)NC(CCC3=CC=CC=C3)C(=O)OC |
| Canonical Smiles | CC(C(=O)N1C2CCCC2CC1C(=O)O)NC(CCC3=CC=CC=C3)C(=O)OC |
| InchIKey | DBAQBRAQKYAQEO-GBBGEASQSA-N |
| Inchl | InChI=1S/C22H30N2O5/c1-14(20(25)24-18-10-6-9-16(18)13-19(24)21(26)27)23-17(22(28)29-2)12-11-15-7-4-3-5-8-15/h3-5,7-8,14,16-19,23H,6,9-13H2,1-2H3,(H,26,27)/t14-,16-,17-,18-,19-/m0/s1 |
| IUPAC | (2S,3aS,6aS)-1-[(2S)-2-[[(2S)-1-methoxy-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 A, also known as (2S,3S)-3-amino-2-hydroxy-4-phenylbutanoic acid, is a chemical compound that is used as a reference standard for the identification and quantification of impurities in ramipril drug substance and its formulations. It is a chiral molecule with a molecular weight of 219.26 g/mol and a molecular formula of C11H13NO3.
Ramipril EP Impurity A is typically used in pharmaceutical analysis to ensure the purity and quality of ramipril drug products. It is considered a significant impurity due to its potential to affect the efficacy and safety of the drug. Therefore, its accurate identification and quantification are critical for ensuring the quality and safety of ramipril-containing drug products.
The chemical information of Ramipril EP Impurity A includes its chemical structure, molecular weight, and molecular formula. It is a white to off-white powder that is stable under normal conditions. Its solubility in water and organic solvents varies, depending on the type of solvent used.
In conclusion, Ramipril EP Impurity A is an important reference standard used in the pharmaceutical industry to ensure the purity and quality of ramipril drug products. Its accurate identification and quantification are critical to ensuring the safety and efficacy of ramipril-containing drug products.
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Related Compounds
N-Nitroso-Ramipril in 1mg/1ml in methanol | ent-Ramipril | Tris(hydroxymethyl) aminomethane salt of ramipril 2 | N-Nitroso Ramipril (Mixture of isomers) | ramipril keto impurity | Ramipril EP Impurity J | Cyclohexyl Ramipril Hydrochloride | Ramipril EP Impurity D | Ramipril EP Impurity C | Ramipril - Isomer Impurity 1 | Ramipril EP Impurity I | Ramipril EP Impurity K | Tris(hydroxymethyl) aminomethane salt of ramipril 1 | Ramipril EP Impurity G | Ramipril Benzyl Ester | Ramipril EP Impurity O | Ramipril EP Impurity H | RAMIPRIL IMPURITY K DIASTEREOMER I | Ramipril isopropyl ester | Ramipril EP Impurity M |