A directory of where to buy chemicals in the USA, including: distributors, industrial manufacturers, bulk supplies and wholesalers of raw ingredients & finished goods.
Search for products or services, then visit the suppliers website for prices or more information.
| Product | Description | |
|---|---|---|
| Ritalinic acid hydrochloride solution | 1.0 mg/mL in methanol (as free base), ampule of 1 mL, certified reference material. Group: Certified reference materials (crms). |  |
| RITA (NSC 652287) | RITA is an inhibitor of p53-HDM-2 interaction, which binds to p53dN with a Kd of 1.5 nM, and also induces DNA-DNA cross-links. Synonyms: NSC-652287; NSC652287; NSC 652287; RITA. CAS No. 213261-59-7. Molecular formula: C14H12O3S2. Mole weight: 292.367. |  |
| Ritanserin | Ritanserin is a potent and long-acting 5-HT2 receptor antagonist (Ki = 0.39 nM) with high selectivity for 5-HT2A over 5-HT1 receptors (IC50s = 0.9 nM and >1000 nM, respectively). Synonyms: 6-[2-[4-[Bis(4-fluorophenyl)methylene]-1-piperidinyl]ethyl]-7-methyl-5H-thiazolo[3,2-a]pyrimidin-5-one; Ritanserin; R-55667; R 55667; R55667. Grades: ≥99% by HPLC. CAS No. 87051-43-2. Molecular formula: C27H25F2N3OS. Mole weight: 477.57. | |
| Ritanserin | Ritanserin (R 55667) is a highly potent, relatively selective, orally active, long acting antagonist of 5-HT 2 receptor , with an IC 50 of 0.9 nM, less active on Histamine H 1 , Dopamine D 2 , Adrenergic α 1 , Adrenergic α 2 receptors [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: R 55667. CAS No. 87051-43-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-10791. |  |
| Ritanserin | powder. Group: Fluorescence/luminescence spectroscopy. | |
| Ritanserin | Ritanserin. Group: Biochemicals. Grades: Purified. CAS No. 87051-43-2. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. |  Worldwide |
| RIT D-2214 | RIT D-2214 is a penicillin antibiotic produced by Acremonium chrysogenum. It is active against gram-positive and gram-negative bacteria. Molecular formula: C13H19N3O6S2. Mole weight: 377.4. | |
| Ritiometan | Ritiometan is an antibacterial that is used in nasal sprays. Group: Biochemicals. Grades: Highly Purified. CAS No. 34914-39-1. Pack Sizes: 100mg, 1g. Molecular Formula: C7H10O6S3. US Biological Life Sciences. | Worldwide |
| Ritlecitinib | Ritlecitinib (PF-06651600) is an orally active and selective JAK3 inhibitor with an IC 50 of 33.1 nM [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: PF-06651600. CAS No. 1792180-81-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 500 mg. Product ID: HY-100754. | |
| Ritlecitinib tosylate | Ritlecitinib tosylate is an orally active and selective JAK3 inhibitor with an IC 50 of 33.1 nM. Ritlecitinib tosylate is used for inflammatory and autoimmune diseases research [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: PF-06651600 tosylate. CAS No. 2192215-81-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-100754C. | |
| Ritobegron ethyl hydrochloride | Ritobegron is a potential Bladder selectivity of the novel β3-agonist. Uses: Beta 3 adrenergic receptor agonists. Synonyms: KUC 7483; KUC7483; KUC-7483;ethyl 2-(4-(2-(((1R,2S)-1-hydroxy-1-(4-hydroxyphenyl)propan-2-yl)amino)ethyl)-2,5-dimethylphenoxy)acetate hydrochloride. Grades: ≥98%. CAS No. 476333-91-2. Molecular formula: C23H32ClNO5. Mole weight: 437.96. | |
| Ritodrine hydrochloride | Ritodrine (DU21220) hydrochloride is a potent and orally active β-adrenergic agonist. Ritodrine hydrochloride decreases preterm delivery and uterine contraction. Ritodrine hydrochloride has the potential for the research of preterm labor [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: DU21220 hydrochloride. CAS No. 23239-51-2. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-B0452. | |
| Ritodrine hydrochloride | Ritodrine hydrochloride. Group: Biochemicals. Alternative Names: N-[2-(p-Hydroxyphenyl)ethyl]-N-[2-(p-hydroxyphenyl)-2-hydroxy-1-methylethyl]amine hydrochloride; N-(p-Hydroxyphenylethyl)-4-hydroxynorephedrine hydrochloride; Du-21220. Grades: Highly Purified. CAS No. 23239-51-2. Pack Sizes: 500mg, 1g, 2g, 5g, 10g. Molecular Formula: C17H22ClNO3. US Biological Life Sciences. | Worldwide |
| Ritodrine Hydrochloride | Ritodrine HCl is a hydrochloride salt of ritodrine which is a β-2 adrenergic receptor agonist.Ritodrine (discontinued preparation: Yutopar) is a tocolytic drug, used to stop premature labor. This drug has been removed from the US market, according to FDA Orange Book. It was available in oral tablets or as an injection and was typically used as the hydrochloride salt, ritodrine hydrochloride. Uses: Tocolytic agents. Synonyms: NSC 291565; NSC291565; NSC-291565. Grades: >98%. CAS No. 23239-51-2. Molecular formula: C17H21NO3.HCl. Mole weight: 323.81. | |
| Ritodrine Hydrochloride (N-[2-(p-Hydroxyphenyl)ethyl]-N-[2-(p-hydroxyphenyl)-2-hydroxy-1-methylethyl]amine Hydrochloride, N-(p-Hydroxyphenylethyl)-4-hydroxynorephedrine Hydrochloride, Du-21220, Miolene, Prempar, Pre-Par) | A b2-Adrenergic agonist. Group: Biochemicals. Alternative Names: N-[2-(p-Hydroxyphenyl)ethyl]-N-[2-(p-hydroxyphenyl)-2-hydroxy-1-methylethyl]amine Hydrochloride;N-(p-Hydroxyphenylethyl)-4-hydroxynorephedrine Hydrochloride; Du-21220; Miolene; Prempar; Pre-Par. Grades: Highly Purified. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| Ritolukast | Ritolukast (Wy-48252) is an orally active aerosol leukotriene ( LTD 4 /E 4 ) receptor antagonist. Ritolukast can be used to inhibit the bronchoconstriction caused by aerosol LTD 4 in guinea pigs, with an ID 50 of 0.5mg/kg [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Wy-48252. CAS No. 111974-60-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-156978. | |
| Ritonavir | Ritonavir (ABT 538) is an inhibitor of HIV protease used to treat HIV infection and AIDS. Ritonavir is also a SARS-CoV 3CLpro inhibitor with an IC50 of 1.61 μM. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Thiazol-5-ylmethyl ((2S,3S,5S)-3-hydroxy-5-((S)-2-(3-((2-isopropylthiazol-4-yl)methyl)-3-methylureido)-3-methylbutanamido)-1,6-diphenylhexan-2-yl)carbamate. Product Category: Inhibitors. Appearance: White to almost white powder to crystaline. CAS No. 155213-67-5. Molecular formula: C37H48N6O5S2. Mole weight: 720.94. Purity: 0.98. IUPACName: 1,3-thiazol-5-ylmethyl N-[(2S,3S,5S)-3-hydroxy-5-[[(2S)-3-methyl-2-[[methyl-[(2-propan-2-yl-1,3-thiazol-4-yl)methyl]carbamoyl]amino]butanoyl]amino]-1,6-diphenylhexan-2-yl]carbamate. Canonical SMILES: CC(C)C1=NC(=CS1)CN(C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC2=CC=CC=C2)C[C@@H]([C@H](CC3=CC=CC=C3)NC(=O)OCC4=CN=CS4)O. Product ID: ACM155213675. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Ritonavir | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopypharma & vet compounds & metabolitespharma & vet compounds & metabolitesapi standardsbritish pharmacopoeiacovid-19 research and reference materialsenzyme activators, inhibitors & substrateseuropean pharmacopoeia (ph. eur.)pharmaceutical toxicologypharmacopoeial standards. Alternative Names: ABT 538,2,7,10,12-Tetraazatridecanoic acid, 4-hydroxy-12-methyl-9-(1-methylethyl)-13-[2-(1-methylethyl)-4-thiazolyl]-8,11-dioxo-3,6-bis(phenylmethyl)-, 5-thiazolylmethyl ester, (3S,4S,6S,9S)-, 2,4,7,12-Tetraazatridecan-13-oic acid, 10-hydroxy-2-methyl-5-(1-methylethyl)-1-[2-(1-methylethyl)-4-thiazolyl]-3,6-dioxo-8,11-bis(phenylmethyl)-, 5-thiazolylmethyl ester, (5S,8S,10S,11S)- (9CI), 2,4,7,12-Tetraazatridecan-13-oic acid, 10-hydroxy-2-methyl-5-(1-methylethyl)-1-[2-(1-methylethyl)-4-thiazolyl]-3,6-dioxo-8,11-bis(phenylmethyl)-, 5-thiazolylmethyl ester, [5S-(5R*,8R*,10R*,11R*)]-, Ritonavir, NSC 693184, A 84538, RTV, Norvir, Abbott 84538. | |
| Ritonavir | 100mg Pack Size. Group: Bioactive Small Molecules, Research Organics & Inorganics. Formula: C37H48N6O5S2. CAS No. 155213-67-5. Prepack ID 74228920-100mg. Molecular Weight 720.94. See USA prepack pricing. |  |
| Ritonavir | A selective HIV protease inhibitor. Group: Biochemicals. Alternative Names: (3S,4S,6S,9S)-4-Hydroxy-12-methyl-9-(1-methylethyl)-13-[2-(1-methylethyl)-4-thiazolyl]-8,11-dioxo-3,6-bis(phenylmethyl)-2,7,10,12-tetraazatridecanoic acid 5-thiazolylmethyl ester; A 84538; ABT 538. Grades: Highly Purified. CAS No. 155213-67-5. Pack Sizes: 50mg, 100mg, 250mg, 500mg. Molecular Formula: C37H48N6O5S2, Molecular Weight: 720.95. US Biological Life Sciences. | Worldwide |
| Ritonavir | Ritonavir (ABT 538) is an inhibitor of HIV protease used to treat HIV infection and AIDS. Ritonavir is also a SARS-CoV 3CL pro inhibitor with an IC 50 of 1.61 μM. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ABT 538; RTV. CAS No. 155213-67-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 500 mg. Product ID: HY-90001. | |
| Ritonavir-13C3 | A stable labeled selective HIV protease inhibitor Ritonavir. Group: Biochemicals. Alternative Names: (3S,4S,6S,9S)-4-Hydroxy-12-methyl-9-(1-methylethyl)-13-[2-(1-methylethyl)-4-thiazolyl]-8,11-dioxo-3,6-bis(phenylmethyl)-2,7,10,12-tetraazatridecanoic Acid 5-Thiazolylmethyl-13C3 Ester; A 84538-13C3; ABT 538-13C3; Norvir-13C3. Grades: Highly Purified. Pack Sizes: 500ug. US Biological Life Sciences. | Worldwide |
| Ritonavir-d6 | A deuterated selective HIV protease inhibitor. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 500ug. US Biological Life Sciences. | Worldwide |
| Ritonavir EP Impurity A | Ritonavir EP Impurity A. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (S)-2-(3-((2-isopropylthiazol-4-yl)methyl)-3-methylureido)-3-methylbutanoic acid. CAS No. 154212-61-0. Molecular formula: C14H23N3O3S. Mole weight: 313.42. Catalog: APB154212610. | |
| Ritonavir EP Impurity C | Ritonavir EP Impurity C. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: thiazol-5-ylmethyl ((2S,3S,5S)-5-acetamido-3-hydroxy-1,6-diphenylhexan-2-yl)carbamate. CAS No. 1010808-43-1. Molecular formula: C25H29N3O4S. Mole weight: 467.58. Catalog: APB1010808431. | |
| Ritonavir EP Impurity F | Ritonavir EP Impurity F. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: thiazol-5-ylmethyl ((2S,3S,5S)-3-hydroxy-5-((S)-4-isopropyl-2,5-dioxoimidazolidin-1-yl)-1,6-diphenylhexan-2-yl)carbamate. CAS No. 1010809-61-6. Molecular formula: C29H34N4O5S. Mole weight: 550.67. Catalog: APB1010809616. | |
| Ritonavir EP Impurity F | An impurity of Ritonavir.Ritonavir is a selective HIV protease inhibitor. Synonyms: N-[(1S,2S,4S)-2-Hydroxy-4-[(4S)-4-(1-methylethyl)-2,5-dioxo-1-imidazolidinyl]-5-phenyl-1-(phenylmethyl)pentyl]carbamic Acid 5-Thiazolylmethyl Ester; 1,3-Thiazol-5-ylmethyl N-[(1S,2S,4S)-1-benzyl-2-hydroxy-4-((4S)-4-isopropyl-2,5- dioxoimidazolidin-1-yl)-5-phenylpentyl]carbamate; Thiazol-5-ylmethyl (2S,3S,5S)-3-hydroxy-5-[(S)-4-isorpopyl-2,5-dioxoimidazolidin-1-yl]-1,6-diphenylhexan-2-ylcarbamate. Grades: > 95%. CAS No. 1010809-61-6. Molecular formula: C29H34N4O5S. Mole weight: 550.68. | |
| Ritonavir EP Impurity H | Ritonavir EP Impurity H. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (4S,5S)-thiazol-5-ylmethyl 4-benzyl-5-((S)-2-((S)-4-isopropyl-2,5-dioxoimidazolidin-1-yl)-3-phenylpropyl)-2-oxooxazolidine-3-carboxylate. CAS No. 1010809-43-4. Molecular formula: C30H32N4O6S. Mole weight: 576.66. Catalog: APB1010809434. | |
| Ritonavir EP Impurity K | Ritonavir EP Impurity K. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: isobutyl (thiazol-5-ylmethyl) ((2S,3S,5S)-3-hydroxy-1,6-diphenylhexane-2,5-diyl)dicarbamate. CAS No. 1010809-39-8. Molecular formula: C28H35N3O5S. Mole weight: 525.66. Catalog: APB1010809398. | |
| Ritonavir EP Impurity O | Ritonavir EP Impurity O. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: thiazol-5-ylmethyl ((2S,3R,5S)-3-hydroxy-5-((S)-2-(3-((2-isopropylthiazol-4-yl)methyl)-3-methylureido)-3-methylbutanamido)-1,6-diphenylhexan-2-yl)carbamate. CAS No. 1414933-81-5. Molecular formula: C37H48N6O5S2. Mole weight: 720.94. Catalog: APB1414933815. | |
| Ritonavir EP Impurity Q | Ritonavir EP Impurity Q. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1414933-82-6. Molecular formula: C37H48N6O5S2. Mole weight: 720.95. Catalog: APB1414933826. | |
| Ritonavir EP Impurity R | Ritonavir EP Impurity R. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1414933-80-4. Molecular formula: C37H48N6O5S2. Mole weight: 720.95. Catalog: APB1414933804. | |
| Ritonavir Geo-isomer | An impurity of Ritonavir.Ritonavir is a selective HIV protease inhibitor. Synonyms: (S)-(2S,3S,5S)-5-amino-1,6-diphenyl-2-(((thiazol-5-ylmethoxy)carbonyl)amino)hexan-3-yl 2-(3-((2-isopropylthiazol-4-yl)methyl)-3-methylureido)-3-methylbutanoate. - See more at: https://www. clearsynth. com/en/CSO14873. html#sthash. XUZUHQfR. dpuf. Grades: > 95%. CAS No. 959315-21-0. Molecular formula: C37H48N6O5S2. Mole weight: 720.96. | |
| Ritonavir Impurity | An impurity of Ritonavir.Ritonavir is a selective HIV protease inhibitor. Grades: > 95%. Molecular formula: C31H41N5O5S. Mole weight: 595.77. | |
| Ritonavir Impurity 1 | Ritonavir Impurity 1. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1414933-89-3. Molecular formula: C23H32N2O3. Mole weight: 384.52. Catalog: APB1414933893. | |
| Ritonavir Impurity 2 | An impurity of Ritonavir.Ritonavir is a selective HIV protease inhibitor. Grades: > 95%. Molecular formula: C47H52N6O7S2. Mole weight: 877.1. | |
| Ritonavir Impurity (2S, 3S, 5S) -5-Amino-1, 6-diphenyl-2- ([[thiazol-5-ylmethoxy) carbonyl]amino]hexan-3-yl 2-(3-((2-isopropylthiazol-4-yl)methyl)-3-methylureido)-3-methylbutanoate | Ritonavir Impurity (2S, 3S, 5S) -5-Amino-1, 6-diphenyl-2- ([[thiazol-5-ylmethoxy) carbonyl]amino]hexan-3-yl 2-(3-((2-isopropylthiazol-4-yl)methyl)-3-methylureido)-3-methylbutanoate. Group: Biochemicals. Alternative Names: Ritonavir Impurity. Grades: Highly Purified. CAS No. 959315-21-0. Pack Sizes: 10mg, 50mg. Molecular Formula: C??H??N?O?S? xHCl, Molecular Weight: 720.94. US Biological Life Sciences. | Worldwide |
| Ritonavir Impurity 4 | Ritonavir Impurity 4. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1010809-54-7. Molecular formula: C32H42N4O8S. Mole weight: 642.77. Catalog: APB1010809547. | |
| Ritonavir impurity B (Monoacyl Valine) Hydrochloride | An impurity of Ritonavir.Ritonavir is a selective HIV protease inhibitor. Synonyms: 1,3-Thiazol-5-ylmethyl N-[5-[(2-amino-3-methylbutanoyl)amino]-3-hydroxy-1,6-diphenylhexan-2-yl]carbamate; hydrochloride; pentyl]-carbaMic Acid 5-ThiazolylMethyl Ester Monohydrochloride; [4-[(2-AMino-3-Methyl-1-oxobutyl)aMino]-2-hydroxy-5-phenyl-1-(phenylMethyl); A937311; [4-[(2-amino-3-methyl-1-oxobutyl)amino]-2-hydroxy-5-phenyl-1-(phenylmethyl) pentyl]-carbamic acid 5-thiazolylmethyl ester monohydrochloride; Thiazol-5-ylmethyl (5-(2-amino-3-methylbutanamido)-3-hydroxy-1,6-diphenylhexan-2-yl)carbamate hydrochloride. Grades: > 95%. CAS No. 165315-97-9. Molecular formula: C30H39N3O4S.HCl. Mole weight: 574.19. | |
| Ritonavir Impurity E (Hydroxy Ritonavir) | An impurity of Ritonavir.Ritonavir is a selective HIV protease inhibitor. Synonyms: [5S-(5R*,8R*,10R*,11R*)]-10-Hydroxy-1-[2-(1-hydroxy-1-methylethyl)-4-thiazolyl]-2-methyl-5-(1-methylethyl)-3,6-dioxo-8,11-bis(phenylmethyl)-2,4,7,12-tetraazatridecan-13-oic Acid 5-Thiazolylmethyl Ester. Grades: > 95%. CAS No. 176655-56-4. Molecular formula: C37H48N6O6S2. Mole weight: 736.96. | |
| Ritonavir Impurity G (Hydroperoxide Impurity) | An impurity of Ritonavir.Ritonavir is a selective HIV protease inhibitor. Synonyms: Thiazol-5-ylmethyl ((2S,3S,5S)-5-((S)-2-(3-((2-(2-hydroperoxypropan-2-yl)thiazol-4-yl)methyl)-3-methylureido)-3-methylbutanamido)-3-hydroxy-1,6-diphenylhexan-2-yl)carbamate ; (Hydroperoxide Impurity). Grades: > 95%. Molecular formula: C37H48N6O7S2. Mole weight: 752.96. | |
| Ritonavir Impurity H | An impurity of Ritonavir.Ritonavir is a selective HIV protease inhibitor. Synonyms: (4S,5S)-4-Benzyl-5-[(2S)-2-((4S)-4-isopropyl-2,5-dioxoimidazolidin-1-yl)-3-phenylpropyl]-2-oxo-1,3-oxazolidine-3-carboxylate thiazol-5-ylmethyl Ester; , (4S,5S)-5-[(2S)-2-[(4S)-4-(1-methylethyl)-2,5-dioxo-1-imidazolidinyl]-3-phenylpropyl]-2-oxo-4-(phenylmethyl)-3-oxazolidinecarboxylic Acid 5-Thiazolylmethyl Ester; (4S,5S)-Thiazol-5-ylmethyl 4-Benzyl-5-[(S)-2-[(s)-4-isopropyl-2,5-dioxoimidazolidin-1- yl]-3-phenylpropyl]-2-oxooxazolidne-3-carboxylate. Grades: > 95%. CAS No. 1010809-43-4. Molecular formula: C30H32N4O6S. Mole weight: 576.68. | |
| Ritonavir Impurity L | An impurity of Ritonavir.Ritonavir is a selective HIV protease inhibitor. Synonyms: (2S) -3-Methyl-2- [ [ [methyl [ [2- (1-methylethyl) -4-thiazolyl] methyl] amino] carbonyl] amino] -N- [ (1S) -1- [ [ (4S, 5S) -2-oxo-4- (phenylmethyl) -5-oxazolidinyl] methyl] -2-phenylethyl] -butanamide. Grades: > 95%. CAS No. 256328-82-2. Molecular formula: C33H43N5O4S. Mole weight: 605.81. | |
| Ritonavir Impurity O | An impurity of Ritonavir.Ritonavir is a selective HIV protease inhibitor. Synonyms: Thiazol-5-ylmethyl ((2S,3R,5S)-3-Hydroxy-5-((S)-2-(3-((2-isopropylthiazol-4-yl)methyl)-3-methylureido)-3-methylbutanamido)-1,6-diphenylhexan-2-yl)carbamate; (3S,4R,6S,9S)-4-Hydroxy-12-methyl-9-(1-methylethyl)-13-[2-(1-methylethyl)-4-thiazolyl]-8,11-dioxo-3,6-bis(phenylmethyl)-2,7,10,12-Tetraazatridecanoic acid 5-thiazolylmethyl Ester; Ritonavir Impurity O (EP). Grades: > 95%. CAS No. 1414933-81-5. Molecular formula: C37H48N6O5S2. Mole weight: 720.96. | |
| Ritonavir Impurity S | An impurity of Ritonavir.Ritonavir is a selective HIV protease inhibitor. Synonyms: N-De-4-ethyl-2-isopropylthiazole Ritonavir N-(Thiazol-5-ylmethyl ((2S,3S)-3-Hydroxy-1,6-diphenylhexan-2-yl)carbamate). Grades: > 95%. Molecular formula: C52H61N7O8S2. Mole weight: 976.24. | |
| Ritonavir Impurity T | An impurity of Ritonavir.Ritonavir is a selective HIV protease inhibitor. Synonyms: (2S,2'S)-N,N'-((2S,3S,5S)-3-Hydroxy-1,6-diphenylhexane-2,5-diyl)bis(2-(3-((2-isopropylthiazol-4-yl)m. Grades: > 95%. Molecular formula: C46H66N8O5S2. Mole weight: 875.22. | |
| Ritonavir Intermediate 33 | Ritonavir Intermediate 33. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1414933-83-7. Molecular formula: C23H32N2O3. Mole weight: 384.52. Catalog: APB1414933837. | |
| Ritonavir Intermediate 34 | Ritonavir Intermediate 34. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1414933-85-9. Molecular formula: C23H32N2O3. Mole weight: 384.52. Catalog: APB1414933859. | |
| Ritonavir metabolite | Ritonavir metabolite is a metabolite of Ritonavir, which is a HIV protease inhibitor. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Desthiazolylmethyloxycarbonyl Ritonavir. CAS No. 176655-55-3. Pack Sizes: 1 mg; 5 mg. Product ID: HY-G0009. | |
| Rituximab | Rituximab is an anti-CD20 monoclonal antibody used for the treatment of certain autoimmune diseases and hematological cancers such as non-Hodgkin's lymphoma, chronic lymphocytic leukemia, rheumatoid arthritis, etc. Its binding to CD20, which exists on the surface of immune system B cells, leads to death of cells. Uses: The treatment of non-hodgkin's lymphoma, chronic lymphocytic leukemia, rheumatoid arthritis, etc. Synonyms: Immunoglobulin G1; Hsdb 7455; Hsdb-7455; Hsdb7455; Immunoglobulin G 1 (human-mouse monoclonal idec-C2B8 gamma1-chain anti-human antigen cd 20), disulfide with human-mouse monoclonal idec-C2B8 kappa-chain, dimer; Mab thera; Mabthera; Rituxan; Unii-4F4X42syq6; Retuxin. CAS No. 174722-31-7. Molecular formula: C6416H9874N1688O1987S44. Mole weight: 143859.7. | |
| Rituximab | Rituximab is an anti-CD20 chimeric monoclonal antibody used for research of certain autoimmune diseases and cancer. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: Anti-Human CD20 type I, Chimeric Antibody. CAS No. 174722-31-7. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-P9913. | |
| Rituximab | Rituximab Inhibitor. Uses: Scientific use. Product Category: T9910. CAS No. 174722-31-7. |  |
| Rituximab (anti-CD20) | Rituximab (anti-CD20) is an anti-CD20 chimeric monoclonal antibody used to treat certain autoimmune diseases and types of cancer [1]. Uses: Scientific research. Group: Inhibitory antibodies. CAS No. 174722-31-7. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-P9913A. | |
| R-Ivabradine hydrochloride | R-Ivabradine hydrochloride |  Sarchem Laboratories New Jersey NJ |
| 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 | 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 (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. 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 | 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 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 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. | |
Our database is helping our users find suppliers everyday.
