Rivaroxaban EP Impurity H

Product Name Rivaroxaban EP Impurity H
Alternate Names Rivaroxaban Impurities, Impurities of Rivaroxaban
CAT No. CS-O-16749
CAS No. 1770812-37-7
Category Impurities
Stock IN-Stock
Mol. Wt. 470.33 g/mol
Mol. For. C₁₉H₁₇Cl₂N₃O₅S
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Rivaroxaban
Purity Not less than 95 %
Therapeutic Anti-Thrombotics
Smileys C1COCC(=O)N1C2=CC=C(C=C2)N3CC(OC3=O)CNC(=O)C4=CC(=C(S4)Cl)Cl
Canonical Smiles C1COCC(=O)N1C2=CC=C(C=C2)N3CC(OC3=O)CNC(=O)C4=CC(=C(S4)Cl)Cl
InchIKey CCLKYVZRBJQFLK-ZDUSSCGKSA-N
Inchl InChI=1S/C19H17Cl2N3O5S/c20-14-7-15(30-17(14)21)18(26)22-8-13-9-24(19(27)29-13)12-3-1-11(2-4-12)23-5-6-28-10-16(23)25/h1-4,7,13H,5-6,8-10H2,(H,22,26)/t13-/m0/s1
IUPAC 4,5-dichloro-N-[[(5S)-2-oxo-3-[4-(3-oxomorpholin-4-yl)phenyl]-1,3-oxazolidin-5-yl]methyl]thiophene-2-carboxamide
Controlled No
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Rivaroxaban EP Impurity H is a synthetic compound that is used for analytical and research purposes. It is a high-quality impurity standard that is used in the development and validation of analytical methods for the detection and quantification of Rivaroxaban, a widely prescribed anticoagulant medication. Rivaroxaban EP Impurity H is typically used as a reference standard in quality control laboratories to ensure the accuracy and precision of analytical methods used to detect Rivaroxaban in pharmaceutical formulations. It is also used in the research and development of new anticoagulant medications. The chemical information of Rivaroxaban EP Impurity H includes its molecular weight, chemical structure, and purity level. The molecular weight of the compound is 455.5 g/mol, and its chemical structure includes a benzothiazole ring and a carboxylic acid group. The purity level of the compound is typically above 98%, which ensures the reliability and accuracy of analytical methods that use the compound as a reference standard. Overall, Rivaroxaban EP Impurity H is an important tool for the development, validation, and quality control of analytical methods used in the detection and quantification of Rivaroxaban and other anticoagulant medications. Its high purity and chemical stability make it an ideal reference standard for use in pharmaceutical research and development.

Related Compounds

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

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