Lamivudine EP Impurity A
| Product Name | Lamivudine EP Impurity A |
|---|---|
| Alternate Names | Lamivudine Impurities, Impurities of Lamivudine |
| CAT No. | CS-O-10183 |
| CAS No. | 173829-09-9 |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 476.54 g/mol |
| Mol. For. | C₂₅H₂₈N₆O₄ |
| Hazardous | This is a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Parent API | Lamivudine |
| Purity | 95% |
| Therapeutic | Antiretroviral / Anti-HIV |
| Smileys | C1C(OC(S1)C(=O)O)N2C=CC(=NC2=O)N |
| Canonical Smiles | C1C(OC(S1)C(=O)O)N2C=CC(=NC2=O)N |
| InchIKey | PIIRVEZNDVLYQA-CAHLUQPWSA-N |
| Inchl | InChI=1S/C8H9N3O4S/c9-4-1-2-11(8(14)10-4)5-3-16-7(15-5)6(12)13/h1-2,5,7H,3H2,(H,12,13)(H2,9,10,14)/t5-,7+/m0/s1 |
| IUPAC | (2R,5S)-5-(4-amino-2-oxopyrimidin-1-yl)-1,3-oxathiolane-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 |
Lamivudine EP Impurity A is a chemical compound that is commonly used in the pharmaceutical industry as a reference standard for the identification and quantification of impurities in Lamivudine drug substances. The chemical name of Lamivudine EP Impurity A is 2-Amino-1,6-dihydro-6-oxo-4-pyrimidinecarboxylic acid, and its molecular formula is C6H6N4O3.
The usage of Lamivudine EP Impurity A is primarily in the quality control process of the manufacturing of Lamivudine drug products. It is used as a reference standard in chromatographic analysis to identify and quantify unknown impurities in a sample of Lamivudine. This reference standard is essential to ensure the purity and quality of the final product, which is critical in pharmaceuticals.
The chemical information of Lamivudine EP Impurity A includes its molecular weight, melting point, boiling point, and solubility in different solvents. It is a white crystalline powder that is soluble in water and slightly soluble in methanol and ethanol. Its melting point is around 290°C, and the boiling point is around 520°C.
In conclusion, Lamivudine EP Impurity A is an important reference standard used in the quality control process of the manufacturing of Lamivudine drug products. Its chemical information and properties are crucial in the identification and quantification of impurities, which ensures the purity and quality of the final product.
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Related Compounds
Lamivudine Monophosphate Ammonium Salt | rel-(1R,2S,5R)-5-Methyl-2-(1-methylethyl)cyclohexyl 2,2-dihydroxyacetate | Lamivudine EP Impurity H | Lamivudine Methylene dimer impurity | Lamivudine Dimer | Lamivudine EP Impurity D | Rac-Lamivudine EP Impurity B | Mono POC Lamivudine | Lamivudine EP Impurity G | Lamivudine Impurity 6 | Lamivudine Resolution Mixture C | Lamivudine Impurity 2 | Lamivudine EP Impurity I | Lamivudine Impurity 5 | Lamivudine Diastereomer | Lamivudine Impurity 21 | Lamivudine Formaldehyde Adduct Impurity | Lamivudine EP Impurity J |