Ketorolac EP Impurity D
| Product Name | Ketorolac EP Impurity D |
|---|---|
| Alternate Names | Ketorolac Impurities, Impurities of Ketorolac |
| CAT No. | CS-O-14760 |
| CAS No. | 1391053-45-4 |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 285.29 g/mol |
| Mol. For. | C₁₆H₁₅NO₄ |
| Hazardous | This is a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Parent API | Ketorolac |
| Therapeutic | Anti-Migraines |
| Smileys | COC1(CCN2C1=CC=C2C(=O)C3=CC=CC=C3)C(=O)O |
| Canonical Smiles | COC1(CCN2C1=CC=C2C(=O)C3=CC=CC=C3)C(=O)O |
| InchIKey | GDFTXJNJRPKPJY-UHFFFAOYSA-N |
| Inchl | InChI=1S/C16H15NO4/c1-21-16(15(19)20)9-10-17-12(7-8-13(16)17)14(18)11-5-3-2-4-6-11/h2-8H,9-10H2,1H3,(H,19,20) |
| IUPAC | 5-benzoyl-1-methoxy-2,3-dihydropyrrolizine-1-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 |
Ketorolac EP Impurity D, also known as 5-Bromo-2-methyl-3-(2-oxo-1,3-dioxolan-4-yl) pyridine, is a chemical compound that is commonly used as an impurity reference standard in the pharmaceutical industry. It is a heterocyclic organic compound that consists of a pyridine ring with a bromine atom and a methyl group attached to it. The compound has a molecular weight of 297.1 g/mol and a melting point of 84-87°C.
Ketorolac EP Impurity D is primarily used in the quality control of Ketorolac Tromethamine, which is a nonsteroidal anti-inflammatory drug (NSAID) used to treat moderate to severe pain. It is used as a reference standard to ensure that the Ketorolac Tromethamine drug product meets the required purity standards. The impurity is also used in the development and validation of analytical methods for the identification and quantification of Ketorolac EP Impurity D in pharmaceutical products.
The chemical information of Ketorolac EP Impurity D is important for regulatory compliance and quality control purposes. It is essential to ensure that the impurity is within acceptable limits as per the guidelines set by regulatory authorities. The compound is typically analyzed using techniques such as high-performance liquid chromatography (HPLC) and gas chromatography-mass spectrometry (GC-MS) to determine its purity and identity.
In conclusion, Ketorolac EP Impurity D is an important reference standard in the pharmaceutical industry, which is used to ensure the quality and purity of Ketorolac Tromethamine drug products. Its chemical information is crucial for quality control and regulatory compliance purposes.
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Related Compounds
Bromo ketorolac | Ketorolac EP Impurity F | Ketorolac EP Impurity H | N-Nitroso Ketorolac 2-Benzoylpyrrole Impurity | Ketorolac EP Impurity A | N-Nitroso Ketorolac Triethylester Intermediate | Ketorolac 1-Keto Analog | Ketorolac EP Impurity G | Ketorolac EP Impurity I | Ketorolac tromethamine | Ketorolac EP Impurity E | N-(1,3-dihydroxy-2-(hydroxymethyl)propan-2-yl)-N-hydroxynitrous amide | N-(1,3-dihydroxy-2-(hydroxymethyl)propan-2-yl)-N-methylnitrous amide | Ketorolac EP Impurity C | Ketorolac EP Impurity J | Ketorolac EP Impurity B |