Ranitidine EP Impurity D
| Product Name | Ranitidine EP Impurity D |
|---|---|
| Alternate Names | Ranitidine Impurities, Impurities of Ranitidine |
| CAT No. | CS-O-13642 |
| CAS No. | 117846-02-3 |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 301.36 g/mol |
| Mol. For. | C₁₂H₁₉N₃O₄S |
| Hazardous | This is a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Parent API | Ranitidine |
| Purity | Not less than 95 % |
| Therapeutic | Anti ulcer |
| Smileys | CN(C)CC1=CC=C(O1)CSCCNC(=O)C[N+](=O)[O-] |
| Canonical Smiles | CN(C)CC1=CC=C(O1)CSCCNC(=O)C[N+](=O)[O-] |
| InchIKey | PFYRWZJFERNHFP-UHFFFAOYSA-N |
| Inchl | InChI=1S/C12H19N3O4S/c1-14(2)7-10-3-4-11(19-10)9-20-6-5-13-12(16)8-15(17)18/h3-4H,5-9H2,1-2H3,(H,13,16) |
| IUPAC | N-[2-[[5-[(dimethylamino)methyl]furan-2-yl]methylsulfanyl]ethyl]-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 D is a chemical compound that is commonly used in the pharmaceutical industry for the manufacturing of Ranitidine, a medication used to treat stomach ulcers and acid reflux. Ranitidine EP Impurity D is a by-product or impurity that is formed during the synthesis of Ranitidine. It is a white to off-white powder that is soluble in water and organic solvents.
The chemical name of Ranitidine EP Impurity D is N-nitroso-N-methyl-4-amino-5-nitroso-2-methoxybenzamide. It is a derivative of benzamide and contains a nitroso group, which is responsible for its reactivity and potential toxicity. Studies have shown that N-nitroso compounds can cause DNA damage and increase the risk of cancer.
Due to its potential toxicity, Ranitidine EP Impurity D is strictly regulated by regulatory authorities such as the US Food and Drug Administration (FDA) and the European Medicines Agency (EMA). The maximum allowable limit of Ranitidine EP Impurity D in Ranitidine products is set at 0.1% by weight.
In conclusion, Ranitidine EP Impurity D is an important chemical compound in the pharmaceutical industry, but its potential toxicity highlights the importance of strict regulation and quality control in manufacturing processes.
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Related Compounds
Ranitidine EP Impurity H | Ranitidine EP Impurity K | Ranitidine Impurity 2 | Ranitidine Related Compound A | Ranitidine EP impurity A | Ranitidine EP Impurity G | Ranitidine EP Impurity F | Ranitidine EP Impurity E | Ranitidine Impurity F.HCl | Ranitidine N,S-Dioxide | Ranitidine EP Impurity J | Ranitidine EP Impurity B | Ranitidine oxalic acid | Ranitidine N-Nitroso Impurity | Ranitidine EP Impurity I | Desmethyl Ranitidine |