Ranitidine EP Impurity H
| Product Name | Ranitidine EP Impurity H |
|---|---|
| Alternate Names | Ranitidine Impurities, Impurities of Ranitidine |
| CAT No. | CS-T-34500 |
| CAS No. | 72078-82-1 |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 118.09 g/mol |
| Mol. For. | C₃H₆N₂O₃ |
| Hazardous | This is a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Parent API | Ranitidine |
| Purity | Not less than 90 % |
| Therapeutic | Anti ulcer |
| Smileys | O=C(NC)C[N](=O)=O |
| Canonical Smiles | CNC(=O)C[N+](=O)[O-] |
| InchIKey | RXGDLJRIJKYANC-UHFFFAOYSA-N |
| Inchl | InChI=1S/C3H6N2O3/c1-4-3(6)2-5(7)8/h2H2,1H3,(H,4,6) |
| IUPAC | N-methyl-2-nitroacetamide |
| 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 |
Ranitidine EP Impurity H is a chemical compound that is often used in the pharmaceutical industry for research and development purposes. It is a byproduct of the synthesis of Ranitidine hydrochloride, an H2 receptor antagonist that is commonly used for the treatment of gastric and duodenal ulcers, gastroesophageal reflux disease (GERD), and Zollinger-Ellison syndrome.
The chemical formula for Ranitidine EP Impurity H is C13H22N4O2S, and its molecular weight is 298.41 g/mol. It is a white to off-white crystalline powder that is soluble in water, methanol, and ethanol.
Although Ranitidine EP Impurity H is not intended for human consumption, it is an important compound for analytical and quality control purposes in the pharmaceutical industry. It is used as a reference standard for the identification and quantification of impurities in Ranitidine hydrochloride drug products.
The purity of Ranitidine EP Impurity H is typically measured using high-performance liquid chromatography (HPLC) or gas chromatography (GC). The maximum allowable limit of this impurity in Ranitidine hydrochloride drug products is generally set at 0.2% or lower.
In conclusion, Ranitidine EP Impurity H is an important chemical compound for the pharmaceutical industry, particularly for the analysis and quality control of Ranitidine hydrochloride drug products. Its chemical properties and purity levels are closely monitored to ensure the safety and efficacy of these medications.
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Related Compounds
Ranitidine EP Impurity G | Ranitidine N,S-Dioxide | Desmethyl Ranitidine | Ranitidine EP impurity A | Ranitidine EP Impurity E | Ranitidine EP Impurity D | Ranitidine Impurity F.HCl | Ranitidine EP Impurity F | Ranitidine Related Compound A | Ranitidine N-Nitroso Impurity | Ranitidine EP Impurity K | Ranitidine Impurity 2 | Ranitidine EP Impurity B | Ranitidine EP Impurity J | Ranitidine oxalic acid | Ranitidine EP Impurity I |