Ranitidine Impurity F.HCl
| Product Name | Ranitidine Impurity F.HCl |
|---|---|
| Alternate Names | Ranitidine Impurities, Impurities of Ranitidine |
| CAT No. | CS-T-19969 |
| CAS No. | 81074-81-9 |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 191.66 g/mol |
| Mol. For. | C₈H₁₄ClNO₂ |
| Hazardous | This is a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Parent API | Ranitidine |
| Therapeutic | Anti ulcer |
| Smileys | CN(C)CC1=CC=C(O1)CO.Cl |
| Canonical Smiles | CN(C)CC1=CC=C(O1)CO.Cl |
| InchIKey | UDLQUVLALYCAMJ-UHFFFAOYSA-N |
| Inchl | InChI=1S/C8H13NO2.ClH/c1-9(2)5-7-3-4-8(6-10)11-7;/h3-4,10H,5-6H2,1-2H3;1H |
| IUPAC | [5-[(dimethylamino)methyl]furan-2-yl]methanol;hydrochloride |
| 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 Impurity F.HCl is a chemical compound that is commonly used in the pharmaceutical industry as an impurity reference standard for the analysis and identification of ranitidine hydrochloride. Ranitidine is a histamine H2 receptor antagonist that is used as an anti-ulcer drug to treat gastrointestinal disorders such as peptic ulcers, gastroesophageal reflux disease (GERD), and Zollinger-Ellison syndrome. Ranitidine Impurity F.HCl is typically used as a reference standard in quality control testing to ensure that the ranitidine hydrochloride drug product is of consistent quality and purity.
Chemically, Ranitidine Impurity F.HCl is a hydrochloride salt of a compound that is structurally related to ranitidine. It is a white to off-white crystalline powder that has a molecular weight of 314.83 g/mol. Ranitidine Impurity F.HCl is typically synthesized through a combination of chemical reactions, which involves the use of various raw materials and reagents such as ranitidine, hydrochloric acid, and solvents like methanol and acetone.
Overall, Ranitidine Impurity F.HCl is an important reference standard that is used in the pharmaceutical industry to ensure the quality and purity of ranitidine hydrochloride drug products. It is a valuable tool for pharmaceutical manufacturers, quality control laboratories, and regulatory agencies in monitoring the safety and efficacy of ranitidine-based medications.
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Related Compounds
Ranitidine EP Impurity K | Ranitidine Related Compound A | Ranitidine oxalic acid | Ranitidine N,S-Dioxide | Ranitidine EP Impurity I | Ranitidine EP Impurity D | Desmethyl Ranitidine | Ranitidine EP Impurity G | Ranitidine EP Impurity B | Ranitidine EP impurity A | Ranitidine EP Impurity F | Ranitidine N-Nitroso Impurity | Ranitidine EP Impurity J | Ranitidine Impurity 2 | Ranitidine EP Impurity H | Ranitidine EP Impurity E |