Ondansetron EP Impurity G
| Product Name | Ondansetron EP Impurity G |
|---|---|
| Alternate Names | Ondansetron Impurities, Impurities of Ondansetron |
| CAT No. | CS-T-61834 |
| CAS No. | 99614-03-6 |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 279.34 g/mol |
| Mol. For. | C₁₇H₁₇N₃O |
| Hazardous | This is a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Parent API | Ondansetron |
| Purity | 95% |
| Canonical Smiles | CN1C2=C(C3=CC=CC=C31)C(=O)C(CC2)CN4C=CN=C4 |
| InchIKey | KPSGSRBENRBWPG-UHFFFAOYSA-N |
| Inchl | InChI=1S/C17H17N3O/c1-19-14-5-3-2-4-13(14)16-15(19)7-6-12(17(16)21)10-20-9-8-18-11-20/h2-5,8-9,11-12H,6-7,10H2,1H3 |
| IUPAC | 3-(imidazol-1-ylmethyl)-9-methyl-2,3-dihydro-1H-carbazol-4-one |
| 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 |
Ondansetron EP Impurity G is a chemical compound that is commonly used in the pharmaceutical industry as a reference standard for the development and testing of ondansetron-based drug products. It is also known as (1S,5R)-4-methyl-1,2,3,4-tetrahydroisoquinoline-5-carboxylic acid and has a molecular weight of 191.24 g/mol.
Ondansetron EP Impurity G is a highly pure substance that is used as a reference standard in analytical methods such as high-performance liquid chromatography (HPLC) and gas chromatography (GC). It is essential in the development and validation of analytical methods for the determination of impurities in ondansetron-based drug products.
Chemically, Ondansetron EP Impurity G is a derivative of isoquinoline, which is a heterocyclic compound that contains a nitrogen atom in the ring structure. It is a white to off-white crystalline powder that is soluble in water, methanol, and ethanol. The compound is stable under normal conditions and has a melting point range of 145-150°C.
Overall, Ondansetron EP Impurity G is an important reference standard in the pharmaceutical industry that plays a critical role in ensuring the quality and safety of ondansetron-based drug products. Its high purity and stability make it an ideal compound for use in analytical methods and testing procedures.
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Related Compounds
Ondansetron EP Impurity G HCl | Ondansetron EP Impurity A | Ondansetron Nitroso Impurity 1 | Ondansetron HCl Imp. C | Ondansetron N-Desmethyl maleate | Ondansetron USP Related Compound A | Ondansetron Impurity D | Ondansetron EP Impurity A | Ondansetron Dimer | Ondansetron Resolution Mixture | Nitroso keto indole |