Rivaroxaban EP Impurity G

Product Name Rivaroxaban EP Impurity G
Alternate Names Rivaroxaban Impurities, Impurities of Rivaroxaban
CAT No. CS-O-31251
CAS No. 446292-08-6
Category Impurities
Stock IN-Stock
Mol. Wt. 421.40 g/mol
Mol. For. C₂₂H₁₉N₃O₆
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Rivaroxaban
Purity 95%
Therapeutic Anti-Thrombotics
Smileys C1COCC(=O)N1C2=CC=C(C=C2)N3CC(OC3=O)CN4C(=O)C5=CC=CC=C5C4=O
Canonical Smiles C1COCC(=O)N1C2=CC=C(C=C2)N3CC(OC3=O)CN4C(=O)C5=CC=CC=C5C4=O
InchIKey KUQNYAUTIWQAKY-MRXNPFEDSA-N
Inchl InChI=1S/C22H19N3O6/c26-19-13-30-10-9-23(19)14-5-7-15(8-6-14)24-11-16(31-22(24)29)12-25-20(27)17-3-1-2-4-18(17)21(25)28/h1-8,16H,9-13H2/t16-/m1/s1
IUPAC 2-[[(5S)-2-oxo-3-[4-(3-oxomorpholin-4-yl)phenyl]-1,3-oxazolidin-5-yl]methyl]isoindole-1,3-dione
Controlled No
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Rivaroxaban EP Impurity G is a chemical compound that is commonly used as a reference standard in laboratory testing for the drug Rivaroxaban. Rivaroxaban is an anticoagulant medication that is used to prevent blood clots and reduce the risk of stroke in patients with certain medical conditions, such as atrial fibrillation, deep vein thrombosis, and pulmonary embolism. Rivaroxaban EP Impurity G is a synthetic derivative of Rivaroxaban that is used to establish the purity and quality of the active ingredient in the drug. The chemical formula for Rivaroxaban EP Impurity G is C19H18N4O4S, and its molecular weight is 402.43 g/mol. It is a white powder that is soluble in organic solvents like methanol, ethanol, and acetone. The compound is stable under normal storage conditions and does not degrade over time. Rivaroxaban EP Impurity G is typically used in analytical laboratories to develop and validate analytical methods for the quantitative determination of Rivaroxaban in drug products. It is also used as a reference standard for the characterization and identification of impurities and related compounds in Rivaroxaban formulations. The use of Rivaroxaban EP Impurity G ensures the accuracy, reliability, and reproducibility of laboratory testing results, which is critical for ensuring the safety and efficacy of the drug for patient use.

Related Compounds

Rivaroxaban Impurity 3 | Rivaroxaban impurity 10 | Rivaroxaban Dimer | Rivaroxaban EP Impurity D | Rivaroxaban EP Impurity I | Rivaroxaban RVXRC-11 hydrochloride | Rivaroxaban Impurity G | N-Nitroso Decarbonyl Rac-Rivaroxaban | Rivaroxaban Impurity 6 | N-((2-oxo-3-(4-(3-oxomorpholino)phenyl)oxazolidin-5-yl)methyl)acetamide | Rivaroxaban Methyl Ester Impurity | Rivaroxaban EP Impurity B | Rivaroxaban Impurity 53 | Rivaroxaban Impurity 14 | Rac-Rivaroxaban Diphthalimido Morpholinone Analog | Rivaroxaban Morpholinone Open Ring Impurity | Rivaroxaban EP Impurity J | Rivaroxaban Sulfoxide | Rivaroxaban Methyl ester impurity | N-Nitroso Rivaroxaban Stage -1 Impurity | Rivaroxaban Impurity 49 | Rivaroxaban Methyl Oxalic Impurity | Rivaroxaban Impurity 8 | Rivaroxaban Impurity 57 | Rivaroxaban amine dimer | Dechloro-Rivaroxaban | Rivaroxaban Impurity 42 | Rivaroxaban Impurity H | N-Phenyldiethanolamine | Rivaroxaban Impurity L | Rivaroxaban Impurity 2 | Rivaroxaban Impurity 29 | Rivaroxaban Impurity D | Rivaroxaban Impurity 89 | Rivaroxaban Open-Ring Acid Impurity | Rivaroxaban Impurity 39 | Rivaroxaban Amino Acid Phthalimide Nitroso Impurity | Rivaroxaban Impurity 48 | Rivaroxaban Nitroso Impurity 13 | Rivaroxaban nitrosamine impurity II | methyl 2-(2-(phenylamino)ethoxy)acetate | Rivaroxaban Impurity A | Rivaroxaban Impurity 1 | Rivaroxaban Impurity 50 | Rivaroxaban Impurity 47 | Rivaroxaban Amide Dimer | Rivaroxaban Impurity 75 | Rivaroxaban Impurity 17 | Rivaroxaban Racemic Mixture | Rivaroxaban EP Impurity H | Rivaroxaban Impurity H HCl salt |

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