Lisinopril EP Impurity A
| Product Name | Lisinopril EP Impurity A |
|---|---|
| Alternate Names | Lisinopril Impurities, Impurities of Lisinopril |
| CAT No. | CS-O-12026 |
| CAS No. | 1012-05-1 |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 179.22 g/mol |
| Mol. For. | C₁₀H₁₃NO₂ |
| Hazardous | This is not a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Parent API | Lisinopril |
| Therapeutic | Anti-Hypertensives |
| Smileys | NC(C(O)=O)CCC1=CC=CC=C1 |
| Canonical Smiles | C1=CC=C(C=C1)CCC(C(=O)O)N |
| InchIKey | JTTHKOPSMAVJFE-UHFFFAOYSA-N |
| Inchl | InChI=1S/C10H13NO2/c11-9(10(12)13)7-6-8-4-2-1-3-5-8/h1-5,9H,6-7,11H2,(H,12,13) |
| IUPAC | 2-amino-4-phenylbutanoic 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 |
Lisinopril EP Impurity A is a chemical compound used in the pharmaceutical industry as a reference standard or a quality control agent for the analysis of Lisinopril. Lisinopril is an ACE inhibitor medication used to treat hypertension and congestive heart failure. Lisinopril EP Impurity A is a synthetic compound that is not found naturally in the body. The chemical name of Lisinopril EP Impurity A is (2S,4S)-4-[(1-carboxy-3-phenylpropyl)amino]-2-(cyclohexylamino) butanoic acid.
The usage of Lisinopril EP Impurity A is primarily in the analytical field. It is used as a reference standard to compare the purity of Lisinopril drug samples. This impurity is used to ensure that the drug is of high quality and free of any potential contaminants that may negatively affect its efficacy. The presence of this impurity in a sample can also be used to identify the source of any impurities.
Chemically, Lisinopril EP Impurity A is a cyclic peptide with a molecular weight of 428.57 g/mol. It is a white to off-white powder with a melting point between 120-130°C. The compound has a solubility of 20mg/mL in water and 10mg/mL in ethanol. It is stable at room temperature and under normal storage conditions.
Overall, Lisinopril EP Impurity A is a vital reference standard for the pharmaceutical industry to ensure the quality and purity of Lisinopril drug samples. It is an essential tool for the analysis of the drug and identification of any potential impurities.
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Related Compounds
Lisinopril Des-Proline dimer - II | Lisinopril EP Impurity F | N-Benzyloxycarbonyl Lisinopril Cyclohexyl Analogue Ethyl Methyl Diester | Lisinopril EP Impurity E | Lisinopril-D8 | Lisinopril-D4 | N-Benzyloxycarbonyl (S)-Lisinopril | Lisinopril EP Impurity A | Lisinopril Intermediate | N-trifluoroacetyl Lisinopril Intermediate | Lisinopril EP impurity C Acetate salt | N-(1-Carboxy-3-phenylpropyl)-S-lisinopril (Mixture of diastereomers) | Lisinopril EP Impurity G | Lisinopril EP Impurity D | Lisinopril EP Impurity I Acetate salt | N2-(1-Ethoxycarbonyl-3-oxo-3-phenylpropyl)-N6-trifluoroacetyl-L-lysine | Lisinopril SRS-Diastereomer | N-Benzyloxycarbonyl (S)-Lisinopril Ethyl Methyl Diester | Lisinopril EP Impurity J |