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| Product | Description | |
|---|---|---|
| Rivaroxaban Dimer Impurity | A Rivaroxaban Metabolite.Rivaroxaban inhibits both free Factor Xa and Factor Xa bound in the prothrombinase complex. It is a highly selective direct Factor Xa inhibitor with oral bioavailability and rapid onset of action. Grades: > 95%. Molecular formula: C38H36Cl2N6O10S2. Mole weight: 871.78. |  |
| Rivaroxaban EP Impurity I | Rivaroxaban EP Impurity I (Imp I) is the impurity reference for Rivaroxaban EP [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1151893-81-0. Pack Sizes: 5 mg; 10 mg. Product ID: HY-I0454. |  |
| Rivaroxaban Impurity 1 | An impurity of Rivaroxaban.Metabolite.Rivaroxaban inhibits both free Factor Xa and Factor Xa bound in the prothrombinase complex. It is a highly selective direct Factor Xa inhibitor with oral bioavailability and rapid onset of action. Grades: > 95%. Molecular formula: C15H24N4O2. Mole weight: 292.38. | |
| Rivaroxaban Impurity 10 | An impurity of Rivaroxaban.Metabolite.Rivaroxaban inhibits both free Factor Xa and Factor Xa bound in the prothrombinase complex. It is a highly selective direct Factor Xa inhibitor with oral bioavailability and rapid onset of action. Synonyms: Rivaroxaban Impurity 10; BCP23648; Rivaroxaban Impurity H pound>>5-Chloro-N-[4-[(5S)-5-[[[(5-chloro-2-thienyl)carbonyl]amino]methyl]-2-oxo-3-oxazolidinyl]phenyl]-N-[2-[2-(methylamino)-2-oxoethoxy]ethyl]-2-thiophenecarboxamide. Grades: > 95%. Molecular formula: C25H24Cl2N4O6S2. Mole weight: 611.53. | |
| Rivaroxaban Impurity 11 | An impurity of Rivaroxaban.Metabolite.Rivaroxaban inhibits both free Factor Xa and Factor Xa bound in the prothrombinase complex. It is a highly selective direct Factor Xa inhibitor with oral bioavailability and rapid onset of action. Synonyms: Rivaroxaban Impurity 11; SCHEMBL455793; DTXSID90623242; DEXXSYVEWAYIGZ-UHFFFAOYSA-N; BCP14166; BCP34183; LS-14306; FT-0661929; 4-(4-(5-(Aminomethyl)-2-oxooxazolidin-3-yl)phenyl)morpholin-3-one; 4-{4-[5-(AMINOMETHYL)-2-OXO-1,3-OXAZOLIDIN-3-YL]PHENYL}MORPHOLIN-3-ONE; 4-{4-[5-(aminomethyl)-2-oxo-1,3-oxazolidine-3-yl]-phenyl}-morpholine-3-one; racemic 4-[4-[5-(aminomethyl)-2-oxo-1,3-oxazolidin-3-yl]phenyl]morpholine-3-one; 4-{4-[(5S)-5-aminomethyl)-2-oxo-1,3-oxazolidin-3-yl}morpholin-3-on; 4-[4-[(5S)-5-(AMinoMethyl)-2-oxo-3-oxazolidinyl]phenyl]-3-Morpholinone; Rivaroxaban Amine Impurity; (R)-4-(4-(5-(Aminomethyl)-2-oxooxazolidin-3-yl)phenyl)morpholin-3-one. Grades: > 95%. Molecular formula: C14H17N3O4. Mole weight: 291.31. | |
| Rivaroxaban Impurity 12 | An impurity of Rivaroxaban.Metabolite.Rivaroxaban inhibits both free Factor Xa and Factor Xa bound in the prothrombinase complex. It is a highly selective direct Factor Xa inhibitor with oral bioavailability and rapid onset of action. Grades: > 95%. Molecular formula: C17H18ClN3O4S. Mole weight: 395.87. | |
| Rivaroxaban Impurity 13 | An impurity of Rivaroxaban.Metabolite.Rivaroxaban inhibits both free Factor Xa and Factor Xa bound in the prothrombinase complex. It is a highly selective direct Factor Xa inhibitor with oral bioavailability and rapid onset of action. Grades: > 95%. Molecular formula: C19H18ClN3O7S. Mole weight: 467.89. | |
| Rivaroxaban Impurity 14 | An impurity of Rivaroxaban.Metabolite.Rivaroxaban inhibits both free Factor Xa and Factor Xa bound in the prothrombinase complex. It is a highly selective direct Factor Xa inhibitor with oral bioavailability and rapid onset of action. Grades: > 95%. Molecular formula: C19H20ClN3O6S. Mole weight: 453.9. | |
| Rivaroxaban Impurity 15 | An impurity of Rivaroxaban.Metabolite.Rivaroxaban inhibits both free Factor Xa and Factor Xa bound in the prothrombinase complex. It is a highly selective direct Factor Xa inhibitor with oral bioavailability and rapid onset of action. Grades: > 95%. Molecular formula: C19H18ClN3O6S. Mole weight: 451.89. | |
| Rivaroxaban Impurity 16 | An impurity of Rivaroxaban.Metabolite.Rivaroxaban inhibits both free Factor Xa and Factor Xa bound in the prothrombinase complex. It is a highly selective direct Factor Xa inhibitor with oral bioavailability and rapid onset of action. Grades: > 95%. Molecular formula: C19H18ClN3O6S. Mole weight: 451.89. | |
| Rivaroxaban Impurity 17 | An impurity of Rivaroxaban.Metabolite.Rivaroxaban inhibits both free Factor Xa and Factor Xa bound in the prothrombinase complex. It is a highly selective direct Factor Xa inhibitor with oral bioavailability and rapid onset of action. Grades: > 95%. Molecular formula: C5H4ClNOS. Mole weight: 161.61. | |
| Rivaroxaban Impurity 18 | An impurity of Rivaroxaban.Metabolite.Rivaroxaban inhibits both free Factor Xa and Factor Xa bound in the prothrombinase complex. It is a highly selective direct Factor Xa inhibitor with oral bioavailability and rapid onset of action. Grades: > 95%. Molecular formula: C7H6ClNO3S. Mole weight: 219.65. | |
| Rivaroxaban Impurity 19 | An impurity of Rivaroxaban.Metabolite.Rivaroxaban inhibits both free Factor Xa and Factor Xa bound in the prothrombinase complex. It is a highly selective direct Factor Xa inhibitor with oral bioavailability and rapid onset of action. Grades: > 95%. Molecular formula: C14H16N2O5. Mole weight: 292.29. | |
| Rivaroxaban Impurity 2 | An impurity of Rivaroxaban.Metabolite.Rivaroxaban inhibits both free Factor Xa and Factor Xa bound in the prothrombinase complex. It is a highly selective direct Factor Xa inhibitor with oral bioavailability and rapid onset of action. Grades: > 95%. Molecular formula: C14H21N3O3. Mole weight: 279.34. | |
| Rivaroxaban Impurity 20 | An impurity of Rivaroxaban.Metabolite.Rivaroxaban inhibits both free Factor Xa and Factor Xa bound in the prothrombinase complex. It is a highly selective direct Factor Xa inhibitor with oral bioavailability and rapid onset of action. Grades: > 95%. Molecular formula: C14H14N2O5. Mole weight: 290.28. | |
| Rivaroxaban Impurity 21 | An impurity of Rivaroxaban.Metabolite.Rivaroxaban inhibits both free Factor Xa and Factor Xa bound in the prothrombinase complex. It is a highly selective direct Factor Xa inhibitor with oral bioavailability and rapid onset of action. Grades: > 95%. Molecular formula: C14H16N2O6. Mole weight: 308.29. | |
| Rivaroxaban Impurity 22 | An impurity of Rivaroxaban.Metabolite.Rivaroxaban inhibits both free Factor Xa and Factor Xa bound in the prothrombinase complex. It is a highly selective direct Factor Xa inhibitor with oral bioavailability and rapid onset of action. Grades: > 95%. Molecular formula: C14H14N2O6. Mole weight: 306.28. | |
| Rivaroxaban Impurity 23 | An impurity of Rivaroxaban.Metabolite.Rivaroxaban inhibits both free Factor Xa and Factor Xa bound in the prothrombinase complex. It is a highly selective direct Factor Xa inhibitor with oral bioavailability and rapid onset of action. Grades: > 95%. Molecular formula: C16H19N3O6. Mole weight: 349.35. | |
| Rivaroxaban Impurity 24 | An impurity of Rivaroxaban.Metabolite.Rivaroxaban inhibits both free Factor Xa and Factor Xa bound in the prothrombinase complex. It is a highly selective direct Factor Xa inhibitor with oral bioavailability and rapid onset of action. Grades: > 95%. Molecular formula: C28H31N5O8. Mole weight: 565.59. | |
| Rivaroxaban Impurity 25 | An impurity of Rivaroxaban.Metabolite.Rivaroxaban inhibits both free Factor Xa and Factor Xa bound in the prothrombinase complex. It is a highly selective direct Factor Xa inhibitor with oral bioavailability and rapid onset of action. Grades: > 95%. Molecular formula: C19H18ClN3O5S. Mole weight: 435.89. | |
| Rivaroxaban Impurity 26 | An impurity of Rivaroxaban.Metabolite.Rivaroxaban inhibits both free Factor Xa and Factor Xa bound in the prothrombinase complex. It is a highly selective direct Factor Xa inhibitor with oral bioavailability and rapid onset of action. Grades: > 95%. Molecular formula: C23H21Cl2N3O5S2. Mole weight: 554.47. | |
| Rivaroxaban Impurity 27 | An impurity of Rivaroxaban.Metabolite.Rivaroxaban inhibits both free Factor Xa and Factor Xa bound in the prothrombinase complex. It is a highly selective direct Factor Xa inhibitor with oral bioavailability and rapid onset of action. Synonyms: 2- (2-HYDROXY-3- ( (4- (3-OXOMORPHOLINO) PHENYL) AMINO) PROPYL) ISOINDOLINE-1, 3-DIONE; 2- (2-hydroxy-3- (4- (3-oxomorpholino) phenylamino) propyl) isoindoline-1, 3-dione; 2-[2-hydroxy-3-[4-(3-oxomorpholin-4-yl)anilino]propyl]isoindole-1,3-dione; Rivaroxaban Impurity 27; SCHEMBL900690; DTXSID30623241; BCP33898; CS-M0562; AKOS024465124; SB64516; SB66138; CS-13656; FT-0669935; A889954; 2-{2-Hydroxy-3-[4-(3-oxomorpholin-4-yl)anilino]propyl}-1H-isoindole-1,3(2H)-dione. Grades: > 95%. Molecular formula: C21H21N3O5. Mole weight: 395.42. | |
| Rivaroxaban Impurity 28 | An impurity of Rivaroxaban.Metabolite.Rivaroxaban inhibits both free Factor Xa and Factor Xa bound in the prothrombinase complex. It is a highly selective direct Factor Xa inhibitor with oral bioavailability and rapid onset of action. Synonyms: Rivaroxaban Impurity 9; MFCD11977665; Rivaroxaban Impurity 28; SCHEMBL460444; DTXSID70623240; KUQNYAUTIWQAKY-UHFFFAOYSA-N; BCP26424; BCP34034; AKOS032947492; SB19801; SY046859; FT-0673880; (S)-2-[[2-Oxo-3-[4-(3-oxomorpholino)phenyl]-5-oxazolidinyl]methyl]isoindoline-1,3-dione; 2-((2-Oxo-3-(4-(3-oxomorpholino)phenyl)oxazolidin-5-yl)methyl)isoindoline-1,3-dione; 2-{2-Oxo-3-[4-(3-oxo-morpholin-4-yl)-phenyl]-oxazolidin-5-ylmethyl}-isoindole-1,3-dione; 2-({2-Oxo-3-[4-(3-oxomorpholin-4-yl)phenyl]-1,3-oxazolidin-5-yl}methyl)-1H-isoindole-1,3(2H)-dione; 2-{[(5R)-2-oxo-3-[4-(3-oxomorpholin-4-yl)phenyl]-1,3-oxazolidin-5-yl]methyl}-2,3-dihydro-1H-isoindole-1,3-dione. Grades: > 95%. Molecular formula: C22H19N3O6. Mole weight: 421.41. | |
| Rivaroxaban Impurity 29 | An impurity of Rivaroxaban.Metabolite.Rivaroxaban inhibits both free Factor Xa and Factor Xa bound in the prothrombinase complex. It is a highly selective direct Factor Xa inhibitor with oral bioavailability and rapid onset of action. Grades: > 95%. Molecular formula: C14H17N3O4. Mole weight: 291.31. | |
| Rivaroxaban Impurity 3 | An impurity of Rivaroxaban.Metabolite.Rivaroxaban inhibits both free Factor Xa and Factor Xa bound in the prothrombinase complex. It is a highly selective direct Factor Xa inhibitor with oral bioavailability and rapid onset of action. Grades: > 95%. Molecular formula: C19H20ClN3O6S. Mole weight: 453.9. | |
| Rivaroxaban Impurity 30 | An impurity of Rivaroxaban.Metabolite.Rivaroxaban inhibits both free Factor Xa and Factor Xa bound in the prothrombinase complex. It is a highly selective direct Factor Xa inhibitor with oral bioavailability and rapid onset of action. Grades: > 95%. Molecular formula: C18H18ClN3O3S. Mole weight: 391.88. | |
| Rivaroxaban Impurity 33 | Rivaroxaban Impurity 33. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1325210-62-5. Molecular formula: C18H20ClN3O4S. Mole weight: 409.89. Catalog: APB1325210625. |  |
| Rivaroxaban Impurity 34 | Rivaroxaban Impurity 34. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1411775-06-8. Molecular formula: C14H17N3O4. Mole weight: 291.31. Catalog: APB1411775068. | |
| Rivaroxaban Impurity 38 | Rivaroxaban Impurity 38. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1252018-10-2. Molecular formula: C13H17ClN2O3. Mole weight: 284.74. Catalog: APB1252018102. | |
| Rivaroxaban Impurity 4 | An impurity of Rivaroxaban.Metabolite.Rivaroxaban inhibits both free Factor Xa and Factor Xa bound in the prothrombinase complex. It is a highly selective direct Factor Xa inhibitor with oral bioavailability and rapid onset of action. Synonyms: N-[[(5S)-2-Oxo-3-[4-(3-oxo-4-morpholinyl)phenyl]-5-oxazolidinyl]methyl]-acetamide. Grades: > 95%. CAS No. 1429334-00-8. Molecular formula: C16H19N3O5. Mole weight: 333.35. | |
| Rivaroxaban Impurity 40 | Rivaroxaban Impurity 40. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1403383-56-1. Molecular formula: C13H19N3O3. Mole weight: 265.31. Catalog: APB1403383561. | |
| Rivaroxaban Impurity 5 | An impurity of Rivaroxaban.Metabolite.Rivaroxaban inhibits both free Factor Xa and Factor Xa bound in the prothrombinase complex. It is a highly selective direct Factor Xa inhibitor with oral bioavailability and rapid onset of action. Grades: > 95%. Molecular formula: C29H32N6O9. Mole weight: 608.61. | |
| Rivaroxaban Impurity 6 | An impurity of Rivaroxaban.Metabolite.Rivaroxaban inhibits both free Factor Xa and Factor Xa bound in the prothrombinase complex. It is a highly selective direct Factor Xa inhibitor with oral bioavailability and rapid onset of action. Synonyms: Rivaroxaban Impurity 6; SCHEMBL1160965; BCP34083; A900747. Grades: > 95%. Molecular formula: C19H19N3O5S. Mole weight: 401.44. | |
| Rivaroxaban Impurity 64 | Rivaroxaban Impurity 64. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1403383-55-0. Molecular formula: C13H20ClN3O3. Mole weight: 301.77. Catalog: APB1403383550. | |
| Rivaroxaban Impurity 68 | Rivaroxaban Impurity 68. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1132681-38-9. Molecular formula: C19H14D4ClN3O5S. Mole weight: 439.9. Catalog: APB1132681389. | |
| Rivaroxaban Impurity 7 | An impurity of Rivaroxaban.Metabolite.Rivaroxaban inhibits both free Factor Xa and Factor Xa bound in the prothrombinase complex. It is a highly selective direct Factor Xa inhibitor with oral bioavailability and rapid onset of action. Grades: > 95%. Molecular formula: C19H17Cl2N3O5S. Mole weight: 470.33. | |
| Rivaroxaban Impurity 76 | Rivaroxaban Impurity 76. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1327778-39-1. Molecular formula: C13H16N2O4. Mole weight: 264.28. Catalog: APB1327778391. | |
| Rivaroxaban Impurity 8 | An impurity of Rivaroxaban.Metabolite.Rivaroxaban inhibits both free Factor Xa and Factor Xa bound in the prothrombinase complex. It is a highly selective direct Factor Xa inhibitor with oral bioavailability and rapid onset of action. Synonyms: 1,2-Benzenedicarboxamide, N1,N2-bis[[(5S)-2-oxo-3-[4-(3-oxo-4-morpholinyl)phenyl]-5-oxazolidinyl]methyl]-; N1,N2-bis(((S)-2-oxo-3-(4-(3-oxomorpholino)phenyl)oxazolidin-5-yl)methyl)phthalamide; Bis-[Des(5-Chloro-2-carboxythienyl)] Rivaroxaban Phthalamide; 1-N,2-N-bis[[(5S)-2-oxo-3-[4-(3-oxomorpholin-4-yl)phenyl]-1,3-oxazolidin-5-yl]methyl]benzene-1,2-dicarboxamide; N1,N2-Bis[[(5S)-2-oxo-3-[4-(3-oxo-4-morpholinyl)phenyl]-5-oxazolidinyl]methyl]-1,2-benzenedicarboxamide; YIDJJGFGEMPGOA-NSOVKSMOSA-N; SCHEMBL806189; DTXSID901111714; CS-M2663; AKOS037650424; CS-14788; N,N'-bis[{(5S)-2-oxo-3-[4-(3-oxomorpholin-4-yl)phenyl]-1,3-oxazolidin-5-yl}methyl]benzene-1,2-diamide; F19453. Grades: > 95%. CAS No. 1365267-36-2. Molecular formula: C36H36N6O10. Mole weight: 712.72. | |
| Rivaroxaban Impurity 9 | An impurity of Rivaroxaban.Metabolite.Rivaroxaban inhibits both free Factor Xa and Factor Xa bound in the prothrombinase complex. It is a highly selective direct Factor Xa inhibitor with oral bioavailability and rapid onset of action. Synonyms: 2-[[(5S)-2-Oxo-3-[4-(3-oxo-4-morpholinyl)phenyl]-5-oxazolidinyl]methyl]-1H-isoindole-1,3(2H)-dione. Grades: > 95%. CAS No. 446292-08-6. Molecular formula: C22H19N3O6. Mole weight: 421.41. | |
| Rivaroxaban Impurity 90 | Rivaroxaban Impurity 90. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: 4-(3-aminophenyl)morpholin-3-one. CAS No. 1082495-22-4. Molecular formula: C10H12N2O2. Mole weight: 192.21. Catalog: APB1082495224. | |
| Rivaroxaban Impurity 97 | Rivaroxaban Impurity 97. Uses: For analytical and research use. Group: Impurity standards. CAS No. 122-98-5. Molecular formula: C8H11NO. Mole weight: 137.18. Catalog: APB122985. | |
| Rivaroxaban Impurity A hydrochloride | Rivaroxaban Impurity A hydrochloride is an impurity of Rivaroxaban, a factor Xa (FXa) inhibitor used for the prevention and treatment of thromboembolic disorders. Synonyms: 2- [2- [ [4- [ (5S) ?-5- [ [ [ (5-Chloro-2-thienyl) ?carbonyl] ?amino] ?methyl] ?-2-oxo-3-oxazolidinyl] ?phenyl] ?amino] ?ethoxy] ?-acetic Acid Hydrochloride. CAS No. 931117-61-2. Molecular formula: C19H21Cl2N3O6S. Mole weight: 490.36. | |
| Rivaroxaban Impurity C | Rivaroxaban Impurity C. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1415566-28-7. Molecular formula: C19H19N3O5S. Mole weight: 401.44. Catalog: APB1415566287. | |
| Rivaroxaban Impurity G | An impurity of Rivaroxaban.Metabolite.Rivaroxaban inhibits both free Factor Xa and Factor Xa bound in the prothrombinase complex. It is a highly selective direct Factor Xa inhibitor with oral bioavailability and rapid onset of action. Synonyms: 5-Chloro-N-[(2R)-2-hydroxy-3-[[4-(3-oxo-4-morpholinyl)phenyl]amino]propyl]-2-thiophencarboxamide; 5-Chloro-N-[(2R)-2-hydroxy-3-[[4-(3-oxo-4-morpholinyl)phenyl]amino]propyl]-2-thiophenecarboxamide. Grades: > 95%. CAS No. 721401-53-2. Molecular formula: C18H20ClN3O4S. Mole weight: 409.89. | |
| Rivaroxaban Impurity L | An impurity of Rivaroxaban.Metabolite.Rivaroxaban inhibits both free Factor Xa and Factor Xa bound in the prothrombinase complex. It is a highly selective direct Factor Xa inhibitor with oral bioavailability and rapid onset of action. Grades: > 95%. Molecular formula: C19H18ClN3O5S. Mole weight: 435.89. | |
| Rivaroxaban Impurity L | Rivaroxaban Impurity L. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1855920-54-5. Molecular formula: C19H18ClN3O5S. Mole weight: 435.88. Catalog: APB1855920545. | |
| Rivaroxaban Metabolite 5 | A deuterated Rivaroxaban. Grades: > 95%. Molecular formula: C19H20ClN3O6S. Mole weight: 453.9. | |
| Rivaroxaban Metabolite 8 | A Rivaroxaban Metabolite.Rivaroxaban inhibits both free Factor Xa and Factor Xa bound in the prothrombinase complex. It is a highly selective direct Factor Xa inhibitor with oral bioavailability and rapid onset of action. Grades: > 95%. Molecular formula: C19H18ClN3O6S. Mole weight: 451.89. | |
| Rivaroxaban Metabolite 9 | A Rivaroxaban Metabolite.Rivaroxaban inhibits both free Factor Xa and Factor Xa bound in the prothrombinase complex. It is a highly selective direct Factor Xa inhibitor with oral bioavailability and rapid onset of action. Grades: > 95%. Molecular formula: C19H18ClN3O6S. Mole weight: 451.89. | |
| Rivaroxaban O-Carboxy Benzamide Impurity | An impurity of Rivaroxaban.Metabolite.Rivaroxaban inhibits both free Factor Xa and Factor Xa bound in the prothrombinase complex. It is a highly selective direct Factor Xa inhibitor with oral bioavailability and rapid onset of action. Grades: > 95%. Molecular formula: C22H21N3O7. Mole weight: 439.43. | |
| Rivaroxaban Open-Ring N-Methyl Impurity | An impurity of Rivaroxaban. Rivaroxaban inhibits both free Factor Xa and Factor Xa bound in the prothrombinase complex. It is a highly selective direct Factor Xa inhibitor with oral bioavailability and rapid onset of action. Synonyms: 4'-Desmorpholino 4'-[N-(5-chloro-2-carboxy-thienyl)N-(5-Carboxy-3-oxa-pentyl)]amino Rivaroxaban; (S)-5-chloro-N-(4-(5-((5-chlorothiophene-2-carboxamido)methyl)-2-oxooxazolidin-3-yl)phenyl)-N-(2-(2-(methylamino)-2-oxoethoxy)ethyl)thiophene-2-carboxamide. CAS No. 1807455-76-0. Molecular formula: C25H24Cl2N4O6S2. Mole weight: 611.52. | |
| Rivaroxaban Pseudodimer | Rivaroxaban Pseudodimer is an impurity of Rivaroxaban, a factor Xa (FXa) inhibitor used for the prevention and treatment of thromboembolic disorders. Synonyms: 5-chloro-N- [ [ (5S) -3- [4- [ (5-chlorothiophene-2-carbonyl) - [2- [2-oxo-2- [ [ (5S) -2-oxo-3- [4- (3-oxomorpholin-4-yl) phenyl] -1, 3-oxazolidin-5-yl] methylamino] ethoxy] ethyl] amino] phenyl] -2-oxo-1, 3-oxazolidin-5-yl] methyl] thiophene-2-carboxamide. CAS No. 1632463-24-1. Molecular formula: C38H36Cl2N6O10S2. Mole weight: 871.8. | |
| Rivaroxaban Related Compound | Cas No. 24065-33-6. | |
| Rivaroxaban Related Compound (5-Chloro-2-Thiophenecarboxylic Acid N-Methylamide) | An impurity of Rivaroxaban.Metabolite.Rivaroxaban inhibits both free Factor Xa and Factor Xa bound in the prothrombinase complex. It is a highly selective direct Factor Xa inhibitor with oral bioavailability and rapid onset of action. Synonyms: 5-chloro-N-methyl-2-thiophenecarboxamide. Grades: > 95%. CAS No. 97799-98-9. Molecular formula: C6H6ClNOS. Mole weight: 175.64. | |
| Rivaroxaban Related Compound (Ethyl 4-(3-Oxomorpholino)-Phenylcarbamate) | An impurity of Rivaroxaban.Metabolite.Rivaroxaban inhibits both free Factor Xa and Factor Xa bound in the prothrombinase complex. It is a highly selective direct Factor Xa inhibitor with oral bioavailability and rapid onset of action. Synonyms: N-[4-(3-Oxo-4-morpholinyl)phenyl]carbamic acid ethyl ester. Grades: > 95%. CAS No. 1327778-39-1. Molecular formula: C13H16N2O4. Mole weight: 264.28. | |
| Rivaroxaban Related Compound (R-4-(4-(5-(Aminomethyl)-2-Oxooxazolidin-3-yl)phenyl-Morpholin-3-One HCl) | An impurity of Rivaroxaban.Metabolite.Rivaroxaban inhibits both free Factor Xa and Factor Xa bound in the prothrombinase complex. It is a highly selective direct Factor Xa inhibitor with oral bioavailability and rapid onset of action. Grades: > 95%. Molecular formula: C14H17N3O4 HCl. Mole weight: 327.77. | |
| Rivaroxaban Related Impurity 1 | An impurity of Rivaroxaban.Metabolite.Rivaroxaban inhibits both free Factor Xa and Factor Xa bound in the prothrombinase complex. It is a highly selective direct Factor Xa inhibitor with oral bioavailability and rapid onset of action. Synonyms: 4,5-Dichlorothiophene-2-carboxylic Acid. Grades: > 95%. CAS No. 31166-29-7. Molecular formula: C5H2Cl2O2S. Mole weight: 197.04. | |
| Rivaroxaban starting material impurity 1 | Rivaroxaban starting material impurity 1. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1082588-73-5. Molecular formula: C10H12N2O2. Mole weight: 192.22. Catalog: APB1082588735. | |
| Rivaroxaban Urea Dimer Impurity | An impurity of Rivaroxaban. Rivaroxaban inhibits both free Factor Xa and Factor Xa bound in the prothrombinase complex. It is a highly selective direct Factor Xa inhibitor with oral bioavailability and rapid onset of action. Synonyms: N,N'-Bis[Des(5-chloro-2-carvoxythienyl) Rivaroxaban] Urea; N,N'-Bis[[(5S)-2-oxo-3-[4-(3-oxo-4-morpholinyl)phenyl]-5-oxazolidinyl]methyl]urea; Urea, N,N'-bis[[(5S)-2-oxo-3-[4-(3-oxo-4-morpholinyl)phenyl]-5-oxazolidinyl]methyl]-. CAS No. 1365267-35-1. Molecular formula: C29H32N6O9. Mole weight: 608.60. | |
| Rivastigmine | Rivastigmine (ENA 713 free base) is an orally active and potent cholinesterase (ChE) inhibitor and inhibits butyrylcholinesterase (BChE) and acetylcholinesteras (AChE) with IC 50 s of 0.037 μM , 4.15 μM, respectively. Rivastigmine can pass the blood brain barrier (BBB). Rivastigmine is a parasympathomimetic or cholinergic agent used for the research of mild to moderate dementia of the Alzheimer's type and dementia due to Parkinson's disease [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ENA 713 free base; SDZ-ENA 713 free base. CAS No. 123441-03-2. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg; 200 mg; 500 mg. Product ID: HY-17368. | |
| Rivastigmine | 1g Pack Size. Group: Bioactive Small Molecules, Research Organics & Inorganics. Formula: C14H22N2O2. CAS No. 123441-03-2. Prepack ID 18740742-1g. Molecular Weight 250.34. See USA prepack pricing. |  |
| Rivastigmine | Harmful by inhalation and in contact with skin. CAS No. 123441-03-2. Product ID: 8-01829. Molecular formula: C14H22N2O2. Mole weight: 250.34. |  |
| Rivastigmine | Rivastigmine, a carbamate derivative, is a reversible cholinesterase inhibitor that is selective for the central nervous system to treat Alzheimer's Disease. Uses: Neuroprotective agents. Synonyms: [3-[(1S)-1-(dimethylamino)ethyl]phenyl] N-ethyl-N-methylcarbamate; (S)-N-ethyl-3-((1-dimethyl-amino)ethyl)-N-methylphenylcarbamate; 713, ENA; 713, SDZ ENA; ENA 713; ENA 713, SDZ; ENA-713; ENA713; Exelon; Hydrogen Tartrate, Rivastigmine; rivastigmine; Rivastigmine Hydrogen Tartrate; RivastigmineTartrate; SDZ ENA 713; Tartrate, Rivastigmine Hydrogen; 123441-03-2; ENA 713 free base; (S)-3-(1-(dimethylamino)ethyl)phenyl ethyl(methyl)carbamate; 3-((1S)-1-(Dimethylamino)ethyl)phenyl ethylmethylcarbamate; 3-[(1S)-1-(dimethylamino)ethyl]phenyl ethyl(methyl)carbamate; AB1004572; 3-[(1S)-1-(dimethylamino)ethyl]phenyl N-ethyl-N-methylcarbamate; Exelonreg; Nimvastid; 3-((1S)-1-(Dimethylamino)ethyl)phenyl N-ethyl-N-methylcarbamate; (S)-3-[1-(dimethylamino)ethyl]phenyl N-ethyl-N-methylcarbamate; [3-[(1S)-1-(dimethylamino)ethyl]phenyl] N-ethyl-N-methyl-carbamate; [3-[(1S)-1-dimethylaminoethyl]phenyl] N-ethyl-N-methylcarbamate; 3-((1S)-1-(Dimethylamino)ethyl)phenyl N-ethyl-N-methylcarbamate; 3-((1S)-1-(Dimethylamino)ethyl)phenyl N-ethyl N-methyl carbamate; Ethyl-methyl-carbamic acid 3-(1-dimethylamino-ethyl)-phenyl. CAS No. 123441-03-2. Molecular formula: C14H22N2O2. Mole weight: 250.34. | |
| Rivastigmine | Rivastigmine. Group: Biochemicals. Grades: Highly Purified. CAS No. 123441-03-2. Pack Sizes: 1g, 2g, 5g, 10g, 25g. Molecular Formula: C14H22N2O2. US Biological Life Sciences. |  Worldwide |
| Rivastigmine Carbamate Impurity | A impurity of Rivastigmine.Rivastigmine is a cholinesterase inhibitor. It works by increasing the amount of a certain substance (acetylcholine) in the brain, which may help reduce symptoms of dementia in patients with Alzheimer disease. Synonyms: 3-Nitrophenyl Ester N-Ethyl-N-methylcarbamic Acid. Grades: > 95%. CAS No. 1346242-31-6. Molecular formula: C10H12N2O4. Mole weight: 224.22. | |
| RivastigMine Diethyl Analog | RivastigMine Diethyl Analog. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1230021-34-7. Molecular formula: C15H24N2O2. Mole weight: 264.37. Catalog: APB1230021347. | |
| Rivastigmine EP Impurity A | Rivastigmine EP Impurity A. Uses: For analytical and research use. Group: Impurity standards. CAS No. 139306-10-8. Molecular formula: C10H15NO. Mole weight: 165.24. Catalog: APB139306108. | |
| Rivastigmine Ether Impurity HCl | A impurity of Rivastigmine.Rivastigmine is a cholinesterase inhibitor. It works by increasing the amount of a certain substance (acetylcholine) in the brain, which may help reduce symptoms of dementia in patients with Alzheimer disease. Grades: > 95%. Molecular formula: C16H18N2O3. HCl. Mole weight: 322.79. | |
| Rivastigmine Hydrogen Tartrate | A Hydrogen Tartrate salt of Rivastigmine.Rivastigmine is a cholinesterase inhibitor. It works by increasing the amount of a certain substance (acetylcholine) in the brain, which may help reduce symptoms of dementia in patients with Alzheimer disease. Uses: Cholinesterase inhibitors. Synonyms: Rivastigmine tartrate; 129101-54-8; Rivastigmine Hydrogen Tartrate; SDZ-ENA 713; Rivastigmine bitartrate; ENA 713; Rivastigmine hydrogentartrate; Rivastigmine (tartrate); (S)-3-(1-(Dimethylamino)ethyl)phenyl ethyl(methyl)carbamate (2R,3R)-2,3-dihydroxysuccinate; Rivastigmine Tartrate Salt; UNII-9IY2357JPE; Rivastigmine actavis; 9IY2357JPE; CHEBI:64358; Rivastigmine tartrate (Exelon); RIVASTIGMINE (AS HYDROGEN TARTRATE); Rivastigmine tartrate (USP); Rivastigmine tartrate [USP]; (2R,3R)-2,3-dihydroxybutanedioic acid 3-[(1S)-1-(dimethylamino)ethyl]phenyl N-ethyl-N-methylcarbamate; (2R,3R)-2,3-dihydroxybutanedioic acid; [3-[(1S)-1-(dimethylamino)ethyl]phenyl] N-ethyl-N-methylcarbamate; Carbamic acid, ethylmethyl-, 3-((1S)-1-(dimethylamino)ethyl)phenyl ester, (2R,3R)-2,3-dihydroxybutanedioate (1:1). Grades: > 95%. Molecular formula: C14H22N2O2. C4H6O6. Mole weight: 400.43. | |
| Rivastigmine Impurity 1 | A impurity of Rivastigmine.Rivastigmine is a cholinesterase inhibitor. It works by increasing the amount of a certain substance (acetylcholine) in the brain, which may help reduce symptoms of dementia in patients with Alzheimer disease. Grades: > 95%. Molecular formula: C10H15NO2. Mole weight: 181.24. | |
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