Rivaroxaban EP Impurity I
| Product Name | Rivaroxaban EP Impurity I |
|---|---|
| Alternate Names | Rivaroxaban Impurities, Impurities of Rivaroxaban |
| CAT No. | CS-T-85606 |
| CAS No. | 1151893-81-0 |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 598.48 g/mol |
| Mol. For. | C₂₄H₂₁Cl₂N₃O₇S₂ |
| Hazardous | This is a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Parent API | Rivaroxaban |
| Therapeutic | Anti-Thrombotics |
| Smileys | C1C(OC(=O)N1C2=CC=C(C=C2)N(CCOCC(=O)O)C(=O)C3=CC=C(S3)Cl)CNC(=O)C4=CC=C(S4)Cl |
| Canonical Smiles | C1C(OC(=O)N1C2=CC=C(C=C2)N(CCOCC(=O)O)C(=O)C3=CC=C(S3)Cl)CNC(=O)C4=CC=C(S4)Cl |
| InchIKey | XEOFNNZMYBBFPT-INIZCTEOSA-N |
| Inchl | InChI=1S/C24H21Cl2N3O7S2/c25-19-7-5-17(37-19)22(32)27-11-16-12-29(24(34)36-16)15-3-1-14(2-4-15)28(9-10-35-13-21(30)31)23(33)18-6-8-20(26)38-18/h1-8,16H,9-13H2,(H,27,32)(H,30,31)/t16-/m0/s1 |
| IUPAC | 2-[2-[N-(5-chlorothiophene-2-carbonyl)-4-[(5S)-5-[[(5-chlorothiophene-2-carbonyl)amino]methyl]-2-oxo-1,3-oxazolidin-3-yl]anilino]ethoxy]acetic 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 |
Rivaroxaban EP Impurity I is a chemical compound that is commonly used in the pharmaceutical industry as a reference standard for quality control and analytical testing purposes. The chemical formula for Rivaroxaban EP Impurity I is not publicly available, but it is known to be a byproduct or impurity of the synthesis of rivaroxaban, a popular anticoagulant medication used to prevent blood clots.
As an impurity, Rivaroxaban EP Impurity I can negatively affect the quality and efficacy of the final product. Therefore, it is important to monitor and control the levels of this impurity during the manufacturing process. This is where reference standards come in handy, as they provide a way to accurately measure the impurity levels and ensure the product meets the required quality standards.
Chemically, Rivaroxaban EP Impurity I is a complex organic compound that can be challenging to synthesize and purify. It is also known to have a high molecular weight and may exhibit different physical and chemical properties than the main drug molecule.
In summary, Rivaroxaban EP Impurity I is an important chemical compound used in the pharmaceutical industry for quality control and analytical testing purposes. Its chemical properties and potential impact on the final product make it an essential reference standard for the manufacturing of rivaroxaban and other related drugs.
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Related Compounds
Rivaroxaban Impurity 48 | Rivaroxaban Methyl ester impurity | Rivaroxaban Racemic Mixture | Rivaroxaban Impurity A | Rivaroxaban Methyl Oxalic Impurity | Rivaroxaban Impurity 17 | N-Nitroso Rivaroxaban Stage -1 Impurity | Rivaroxaban Impurity 1 | Rivaroxaban Impurity 50 | Rivaroxaban Impurity 14 | Rivaroxaban Impurity 2 | Rivaroxaban Impurity G | Rivaroxaban Impurity 3 | Rivaroxaban EP Impurity J | Rivaroxaban Impurity 8 | Rivaroxaban Impurity L | Rivaroxaban Impurity 53 | Rivaroxaban Impurity 42 | Rivaroxaban Morpholinone Open Ring Impurity | Rivaroxaban nitrosamine impurity II | Rivaroxaban Impurity 39 | Rivaroxaban Impurity 75 | Rivaroxaban amine dimer | Rivaroxaban Impurity 49 | Rivaroxaban Impurity H HCl salt | Rivaroxaban Impurity D | methyl 2-(2-(phenylamino)ethoxy)acetate | Rivaroxaban Amide Dimer | Rivaroxaban impurity 10 | Rivaroxaban EP Impurity D | Rivaroxaban EP Impurity B | Rivaroxaban Impurity 89 | Rivaroxaban Open-Ring Acid Impurity | Dechloro-Rivaroxaban | Rivaroxaban Dimer | N-Phenyldiethanolamine | N-Nitroso Decarbonyl Rac-Rivaroxaban | Rivaroxaban Nitroso Impurity 13 | Rivaroxaban Impurity 57 | Rivaroxaban Sulfoxide | N-((2-oxo-3-(4-(3-oxomorpholino)phenyl)oxazolidin-5-yl)methyl)acetamide | Rivaroxaban Impurity H | Rivaroxaban Impurity 47 | Rivaroxaban EP Impurity H | Rac-Rivaroxaban Diphthalimido Morpholinone Analog | Rivaroxaban Impurity 6 | Rivaroxaban EP Impurity G | Rivaroxaban Impurity 29 | Rivaroxaban Methyl Ester Impurity | Rivaroxaban RVXRC-11 hydrochloride | Rivaroxaban Amino Acid Phthalimide Nitroso Impurity |