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| Product | Description | |
|---|---|---|
| Rivaroxaban | 1g Pack Size. Group: Bioactive Small Molecules, Research Organics & Inorganics. Formula: C19H18ClN3O5S. CAS No. 366789-02-8. Prepack ID 89987190-1g. Molecular Weight 435.8813. See USA prepack pricing. |  |
| Rivaroxaban | 5-Chloro-N-[[(5S)-2-oxo-3-[4-(3-oxo-4-morpholinyl)phenyl]-5-oxazolidinyl]methyl]-2-thiophenecarboxamide. antihypertensive, calcium channel protein inhibitor. Grades: USP. CAS No. 366789-02-8. Product ID: 8-04759. Molecular formula: C19H18ClN3O5S. Mole weight: 435.88. |  |
| Rivaroxaban | Rivaroxaban (BAY 59-7939) is a highly potent, selective and direct Factor Xa ( FXa ) inhibitor, achieving a strong gain in anti-FXa potency ( IC 50 0.7 nM; K i 0.4 nM) [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BAY 59-7939. CAS No. 366789-02-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg. Product ID: HY-50903. |  |
| Rivaroxaban | Rivaroxaban is a new oral anticoagulant for adult patients with nonvalvular atrial fibrillation (except atrial fibrillation due to rheumatic valvular heart disease, and atrial fibrillation following heart valve replacement) to reduce the risk of stroke and systemic embolism. CAS No. 366789-02-8. Product ID: PAP-0069. Molecular formula: C19H18ClN3O5S. Category: Cardiovascular. Product Keywords: Cardiovascular Series; Rivaroxaban; PAP-0069; Cardiovascular; C19H18ClN3O5S; 366789-02-8. Appearance: Solid. Standard: EP. Grade: CEP/ISO. Physical State: solid. Solubility: insoluble in H2O; insoluble in EtOH; ≥13.9 mg/mL in DMSO with gentle warming. Storage: Inert atmosphere,2-8°C. Applications: Rivaroxaban is used primarily to treat venous thrombosis in adults. Boiling Point: 732.6±60.0 °C(Predicted). Melting Point: 228-229°C. Density: 1.460±0.06 g/cm3(Predicted). |  |
| Rivaroxaban | Rivaroxaban is an orally active, direct inhibitor of Factor Xa (Ki = 0.4 nM), which is a crucial component of the intrinsic and extrinsic pathways of the blood coagulation cascade.1 It demonstrates >10,000-fold greater selectivity for Factor Xa compared to other related serine proteases.1 In various animal arterial and venous thrombosis models, rivaroxaban is reported to inhibit thrombin formation without prolonging bleeding time and has been approved for clinical use as an anticoagulant in the prevention of stroke and the treatment of venous thromboembolisms. Group: Biochemicals. Alternative Names: 5-Chloro-N-[[(5S)-2-oxo-3-[4-(3-oxo-4-morpholinyl)phenyl]-5-oxazolidinyl]methyl]-2-thiophenecarboxamide; BAY 59-7939. Grades: Highly Purified. CAS No. 366789-02-8. Pack Sizes: 100mg, 250mg, 500mg. Molecular Formula: C19H18ClN3O5S, Molecular Weight: 435.88. US Biological Life Sciences. |  Worldwide |
| Rivaroxaban | Rivaroxaban. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 5-Chloro-N-[[(5S)-2-oxo-3-[4-(3-oxo-4-morpholinyl)phenyl]-5-oxazolidinyl]methyl]-2-thiophenecarboxamide. Appearance: White to Off-White Solid. CAS No. 366789-02-8. Molecular formula: C19H18ClN3O5S. Mole weight: 435.88. Purity: ≥98%. Product ID: ACM366789028. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Rivaroxaban Amine Impurity | Rivaroxaban Amine Impurity is an impurity of Rivaroxaban, a factor Xa (FXa) inhibitor used for the prevention and treatment of thromboembolic disorders. Synonyms: 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. CAS No. 1151893-81-0. Molecular formula: C24H21Cl2N3O7S2. Mole weight: 598.48. |  |
| Rivaroxaban Aminomethyl Hydrochloride Impurity | Cas No. 898543-06-1. | |
| Rivaroxaban-d4 | A novel labeled antithrombotic agent. A highly potent and selective, direct FXa inhibitor. Group: Biochemicals. Alternative Names: 5-Chloro-N-[[(5S)-2-oxo-3-[4-(3-oxo-4-morpholinyl)phenyl-d4]-5-oxazolidinyl]methyl]-2-thiophenecarboxamide; BAY 59-7939-d4. Grades: Highly Purified. CAS No. 1132681-38-9. Pack Sizes: 1mg. Molecular Formula: C??H??D?ClN?O?S, Molecular Weight: 439.91. US Biological Life Sciences. | Worldwide |
| Rivaroxaban Dichloro 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: 2-Thiophenecarboxamide, 4,5-dichloro-N-[[(5S)-2-oxo-3-[4-(3-oxo-4-morpholinyl)phenyl]-5-oxazolidinyl]methyl]-; (S)-4,5-dichloro-N-((2-oxo-3-(4-(3-oxomorpholino)phenyl)oxazolidin-5-yl)methyl)thiophene-2-carboxamide. Grades: 95%. CAS No. 1770812-37-7. Molecular formula: C19H17Cl2N3O5S. Mole weight: 470.33. | |
| 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. | |
| 2-Hydroxy-3-oxo-Rivaroxaban | 2-Hydroxy Rivaroxaban is a metabolite of Rivaroxaban (R538000) which is an antithrombotic agent. Rivaroxaban is a highly potent and selective, direct FXa inhibitor. Group: Biochemicals. Grades: Highly Purified. CAS No. 1160169-99-2. Pack Sizes: 500ug, 5mg. Molecular Formula: C19H18ClN3O6S, Molecular Weight: 451.88. US Biological Life Sciences. | Worldwide |
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