Captopril EP Impurity F
| Product Name | Captopril EP Impurity F |
|---|---|
| Alternate Names | Captopril Impurities, Impurities of Captopril |
| CAT No. | CS-O-07523 |
| CAS No. | 63250-36-2 |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 217.3 g/mol |
| Mol. For. | C9H15NO3S |
| Hazardous | This is a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Parent API | Captopril |
| Purity | 95% |
| Therapeutic | Anti-Hypertensives |
| Smileys | CC(CS)C(=O)N1CCCC1C(=O)O |
| Canonical Smiles | CC(CS)C(=O)N1CCCC1C(=O)O |
| InchIKey | FAKRSMQSSFJEIM-BQBZGAKWSA-N |
| Inchl | InChI=1S/C9H15NO3S/c1-6(5-14)8(11)10-4-2-3-7(10)9(12)13/h6-7,14H,2-5H2,1H3,(H,12,13)/t6-,7-/m0/s1 |
| IUPAC | (2S)-1-[(2R)-2-methyl-3-sulfanylpropanoyl]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 |
Captopril EP Impurity F is a chemical compound that is commonly used in the pharmaceutical industry as a reference standard for testing the purity and potency of captopril, a medication used to treat hypertension and heart failure. This impurity is a degradation product of captopril that is formed as a result of various chemical reactions or improper storage conditions.
The chemical structure of Captopril EP Impurity F consists of a thiol group attached to a proline amino acid. The presence of this impurity in captopril can affect its stability and efficacy, which is why it is important to monitor its levels in drug formulations.
To use Captopril EP Impurity F, it is typically dissolved in a suitable solvent and then analyzed using high-performance liquid chromatography (HPLC) or other analytical techniques. The data obtained from these tests can be used to ensure the quality and consistency of captopril products, as well as to identify any potential impurities that may be present.
Overall, Captopril EP Impurity F is an important tool for pharmaceutical companies and regulatory agencies in ensuring the safety and effectiveness of captopril and other related drugs.
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Related Compounds
Captopril EP Impurity B | Captopril EP Impurity O | Captopril EP Impurity M | Captopril EP Impurity L | Captopril RC 7 | Captopril Impurity 2 | Captopril Ethyl Ester | Captopril EP Impurity G | Captopril EP Impurity E | S-[3-(N-Ethylmaleimide)] Captopril | Captopril Impurity N | Captopril EP Impurity H | Captopril EP Impurity I | Captopril EP Impurity D | D-Captopril | S-Nitrosocaptopril | Captopril Acid Amine Salt |