Rivaroxaban EP Impurity D

Product Name Rivaroxaban EP Impurity D
Alternate Names Rivaroxaban Impurities, Impurities of Rivaroxaban
CAT No. CS-T-67095
CAS No. 1365267-35-1
Category Impurities
Stock IN-Stock
Mol. Wt. 608.60 g/mol
Mol. For. C₂₉H₃₂N₆O₉
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Rivaroxaban
Therapeutic Anti-Thrombotics
Smileys C1COCC(=O)N1C2=CC=C(C=C2)N3CC(OC3=O)CNC(=O)NCC4CN(C(=O)O4)C5=CC=C(C=C5)N6CCOCC6=O
Canonical Smiles C1COCC(=O)N1C2=CC=C(C=C2)N3CC(OC3=O)CNC(=O)NCC4CN(C(=O)O4)C5=CC=C(C=C5)N6CCOCC6=O
InchIKey RMYVVSKNFAMRGJ-ZEQRLZLVSA-N
Inchl InChI=1S/C29H32N6O9/c36-25-17-41-11-9-32(25)19-1-5-21(6-2-19)34-15-23(43-28(34)39)13-30-27(38)31-14-24-16-35(29(40)44-24)22-7-3-20(4-8-22)33-10-12-42-18-26(33)37/h1-8,23-24H,9-18H2,(H2,30,31,38)/t23-,24-/m0/s1
IUPAC 1,3-bis[[(5S)-2-oxo-3-[4-(3-oxomorpholin-4-yl)phenyl]-1,3-oxazolidin-5-yl]methyl]urea
Controlled No
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Rivaroxaban EP Impurity D is a chemical compound that is used extensively in the pharmaceutical industry as a reference standard in the development and testing of the drug, Rivaroxaban. Rivaroxaban is an anticoagulant medication that is used to prevent the formation of blood clots that can lead to serious medical conditions such as stroke and pulmonary embolism. Rivaroxaban EP Impurity D, also known as (S)-4-(4-Amino-1-oxo-1,3-dihydroisoindol-2-yl)-N-((5-chloropyridin-2-yl)oxycarbonyl)proline, is a key intermediate in the synthesis of Rivaroxaban. It is a white to off-white powder that is soluble in water and organic solvents such as methanol, ethanol, and dimethyl sulfoxide. The chemical structure of Rivaroxaban EP Impurity D is characterized by a pyridine ring, an isoindole ring, and a proline residue. It is a chiral compound with a stereocenter at the proline residue, making it exist in two enantiomeric forms, (S)- and (R)-. The (S)-enantiomer is the active form of the compound and is responsible for the pharmacological activity of Rivaroxaban. In conclusion, Rivaroxaban EP Impurity D is a vital reference standard used in the development and quality control of Rivaroxaban, an essential anticoagulant medication. Its chemical properties and structure enable it to play a significant role in ensuring the safety and efficacy of Rivaroxaban in treating and preventing blood clots.

Related Compounds

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

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