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| Product | Description | |
|---|---|---|
| Levamisole Impurity A | Synonyms: 3-(2-Amino-2-phenyl-ethyl)-thiazolidin-2-one. Grades: > 95%. Molecular formula: C11H14N2OS. Mole weight: 222.31. |  |
| Levamisole Impurity B | Synonyms: 3-Styryl-thiazolidin-2-ylideneamine. Grades: > 95%. CAS No. 20406-02-4. Molecular formula: C11H12N2S. Mole weight: 204.30. | |
| Levamisole Impurity C | Synonyms: 1-(2-Mercapto-ethyl)-4-phenyl-imidazolidin-2-one. Grades: > 95%. Molecular formula: C11H14N2OS. Mole weight: 222.31. | |
| Levamisole Impurity D | impurity of Levamisole Hydrochloride. Synonyms: 6-Phenyl-2,3-dihydro1midazo[2,1-b][1,3]thiazole. Grades: > 95%. CAS No. 4335-28-8. Molecular formula: C11H10N2S. Mole weight: 202.28. | |
| Levamisole Impurity D (HCl salt form) | The hydrochloride of Levamisole Impurity D. Levamisole is a medication used for the treatment of parasitic worm infections. It was also indicated to be effective for colon cancer therapy in combination with fluorouracil. Synonyms: 6-phenyl-2,3-dihydroimidazo[2,1-b]thiazole hydrochloride; AC1MD4BJ; CTK8I7338; MolPort-000-653-456. Grades: 95%. CAS No. 4335-29-9. Molecular formula: C11H11ClN2S. Mole weight: 238.733. | |
| Levamisole Impurity E | Grades: > 95%. Molecular formula: C22H26N4O2S2. Mole weight: 442.61. | |
| Levamisole Phosphate | Levamisole Phosphate is the salt of Levamisole, which is an antibiotic used against parasitic worm infections and has potential activity in anticancer studies. Synonyms: Imidazo[2,1-b]thiazole, 2,3,5,6-tetrahydro-6-phenyl-, (6S)-, phosphate (1:1); Imidazo[2,1-b]thiazole, 2,3,5,6-tetrahydro-6-phenyl-, phosphate (1:1), (-)-; (S)-6-Phenyl-2,3,5,6-tetrahydroimidazo-[2,1-b]thiazole phosphate; L-Tetramisole dihydrogen phosphate; Ripercol. Grades: ≥95%. CAS No. 32093-35-9. Molecular formula: C11H15N2O4PS. Mole weight: 302.29. | |
| Levamisol HCl USP | Levamisol HCl USP. Grades: USP. CAS No. 16595-80-5. Product ID: 8-01705. Molecular formula: C11H12N3S HCl. Mole weight: 240.75. Properties: 99.0- 101.0%. Source : anitbiotic. |  |
| Levamisol hydrochloride | analytical standard. Group: Application areaspharma & vet compounds & metabolitesstandards for environmental regulatory methodspharma & vet compounds & metabolites. Alternative Names: Imidazo[2,1-b]thiazole, 2,3,5,6-tetrahydro-6-phenyl-, monohydrochloride, (-)- (8CI), Nilverm forte, Nemicide, Levacide, Spartakon L, l-Tetramisole hydrochloride, Meglum, Tramisole, Levomysol hydrochloride, Imidazo[2,1-b]thiazole, 2,3,5,6-tetrahydro-6-phenyl-, monohydrochloride, (6S)- (9CI), Solaskil, Levadin, R 12654, Imidazo[2,1-b]thiazole, 2,3,5,6-tetrahydro-6-phenyl-, monohydrochloride, (S)-, Ripercol L, Citarin L,Levamisole Hydrochloride, Tramisol, Dekaris, KW 2LE-T, NSC 177023, Century-Ace, L-Narpenol, Ergamisole, Imidazo[2,1-b]thiazole, 2,3,5,6-tetrahydro-6-phenyl-, hydrochloride (1:1), (6S)-, Ascaridil, Levasole, (-)-Levamisole hydrochloride, Ergamisol, Decaris. |  |
| Levamlodipine | Levamlodipine is an impurity of Amlodipine. Amlodipine is a long-acting dihydropyridine L-type calcium channel blocker. Amlodipine is used to lower blood pressure and prevent chest pain. Synonyms: (S)-Amlodipine; (4S)-2-[(2-Aminoethoxy)methyl]-4-(2-chlorophenyl)-1,4-dihydro-6-methyl-3,5-pyridinedicarboxylic Acid 3-Ethyl 5-Methyl Ester. Grades: >98%. CAS No. 103129-82-4. Molecular formula: C20H25ClN2O5. Mole weight: 408.87. | |
| Levamlodipine | Levamlodipine ((S)-Amlodipine) is a powerful dihydropyridine calcium channel blocker, possessing vasodilation properties and used in the treatment of hypertension and angina [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: (S)-Amlodipine; Levoamlodipine. CAS No. 103129-82-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-14744. |  |
| Levamlodipine besylate | Levamlodipine besylate ((S)-Amlodipine besylate) is an orally active calcium channel blocker with antioxidant and vasodilatory properties. Levamlodipine besylate can reduce serum malondialdehyde (MDA) levels, increase superoxide dismutase (SOD) activity, and improve oxidative stress. Levamlodipine besylate can be used for research on vascular dementia, hypertension, and cerebrovascular diseases [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: (S)-Amlodipine besylate; Levoamlodipine besylate. CAS No. 150566-71-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-14744A. | |
| Levamlodipine besylate | Levamlodipine besylate is an impurity of Amlodipine. Amlodipine is a long-acting dihydropyridine L-type calcium channel blocker. Amlodipine is used to lower blood pressure and prevent chest pain. Synonyms: (S)-Amlodipine Besylate; S-Amlodipine benzenesulfonate. Grades: >98%. CAS No. 150566-71-5. Molecular formula: C20H25ClN2O5.C6H6O3S. Mole weight: 567.05. | |
| Levan | Levan is a fructose derivative, it is moisturizing and anti-inflammatory, it is also used to help improve skin barrier function. Uses: Designed for use in research and industrial production. Product Category: Heterocyclic Organic Compound. CAS No. 9013-95-0. Molecular formula: C18H32O16. Density: 1.82 g/cm³. Product ID: ACM9013950. Alfa Chemistry ISO 9001:2015 Certified. |  |
| LEVAN | LEVAN. Synonyms: levan from erwinia herbicola;Levan from Zymomonas mobilis; FRUCTAN; fromzymomonasmobilis; (2R, 3S, 4R, 5R)-5-[[ (2R, 3S, 4R, 5R)-5-[[ (2R, 3S, 4R, 5R)-3, 4-dihydroxy-2, 5-bis (hydroxymethyl)oxolan-2-yl]oxymethyl]-3, 4-dihydroxy-2- (hydroxymethyl)oxolan-2-yl]oxymethyl]-2- (hydroxymethyl)oxolane-2, 3, 4-triol; LEVAN, FROM SERRATIA LEVANICUM;Gum levan. CAS No. 9013-95-0. Product ID: CDF4-0168. Molecular formula: C18H32O16. Category: Sweeteners. Product Keywords: Food Ingredients; Sweeteners; LEVAN; CDF4-0168; 9013-95-0; C18H32O16; 1308068-626-2; 9013-95-0. Purity: 0.99. EC Number: 1308068-626-2. Solubility: H2O: 10 mg/mL, hazy, faintly yellow. Storage: 2-8°C. Product Description: Levan is a polysaccharide produced by some microorganisms and plants. It is a non-typical biopolymer composed of fructose units linked by β-(2→6). Levan is an exopolysaccharide (synthesized outside the cell). |  |
| levanase | Levanase (EC 3.2.1.65) is an enzyme with systematic name (2->6)-beta-D-fructan fructanohydrolase. Group: Enzymes. Synonyms: levan hydrolase; 2,6-β-D-fructan fructanohydrolase. Enzyme Commission Number: EC 3.2.1.65. CAS No. 9041-11-6. Levanase. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3929; levanase; EC 3.2.1.65; 9041-11-6; levan hydrolase; 2,6-β-D-fructan fructanohydrolase. Cat No: EXWM-3929. |  |
| Levanase 32A from Bacillus subtilis, Recombinant | Levanase (EC 3.2.1.65, levan hydrolase, 2,6-beta-D-fructan fructanohydrolase) is an enzyme with systematic name (2->6)-beta-D-fructan fructanohydrolase. This enzyme catalyses the following chemical reaction: Random hydrolysis of (2->6)-beta-D-fructofuranosidic linkages in (2->6)-beta-D-fructans (levans) containing more than 3 fructose units. Group: Enzymes. Synonyms: Levanase; EC 3.2.1.65; levan hydrolase; 2,6-beta-D-fructan fructanohydrolase; (2->6)-beta-D-fructan fructanohydrolase. Enzyme Commission Number: EC 3.2.1.65. CAS No. 9041-11-6. Purity: >90% by SDS-PAGE. Levanase. Mole weight: 37.2 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Bacillus subtilis. Levanase; EC 3.2.1.65; levan hydrolase; 2,6-beta-D-fructan fructanohydrolase; (2->6)-beta-D-fructan fructanohydrolase; Levanase 32A. Cat No: NATE-1386. | |
| Levanase 32A from Bacteroides thetaiotaomicron, Recombinant | Levanase (EC 3.2.1.65, levan hydrolase, 2,6-beta-D-fructan fructanohydrolase) is an enzyme with systematic name (2->6)-beta-D-fructan fructanohydrolase. This enzyme catalyses the following chemical reaction: Random hydrolysis of (2->6)-beta-D-fructofuranosidic linkages in (2->6)-beta-D-fructans (levans) containing more than 3 fructose units. Group: Enzymes. Synonyms: Levanase; EC 3.2.1.65; levan hydrolase; 2,6-beta-D-fructan fructanohydrolase; (2->6)-beta-D-fructan fructanohydrolase. Enzyme Commission Number: EC 3.2.1.65. CAS No. 9041-11-6. Purity: >90% by SDS-PAGE. Levanase. Mole weight: 37.9 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Bacteroides thetaiotaomicron. Levanase; EC 3.2.1.65; levan hydrolase; 2,6-beta-D-fructan fructanohydrolase; (2->6)-beta-D-fructan fructanohydrolase; Levanase 32A. Cat No: NATE-1385. | |
| Levan - from Erwinia herbicola | Levan, extracted from Erwinia herbicola, is an all-natural biopolymer operating as a pivotal component within drug conveyance architectures and tissue regenerative constructs. The incredible potential of Levan extends to studying prevalent maladies encompassing cancer, diabetes and cardiovascular afflictions. Levan has commendable attributes of biocompatibility and biodegradability. Synonyms: Inulin - from chicory; Levan - from Erwinia herbicola; Inulin - from Jerusalem artichoke; YI01274; YL75175; YL76657. Molecular formula: (C6H10O5)n. Mole weight: 666.6. | |
| Levan from Erwinia herbicola | Levan from Erwinia herbicola. Group: Polysaccharide. CAS No. 9013-95-0. Product ID: (2R, 3S, 4S, 5R)-5-[[ (2R, 3S, 4S, 5R)-5-[[ (2R, 3S, 4S, 5R)-3, 4-dihydroxy-2, 5-bis (hydroxymethyl)oxolan-2-yl]oxymethyl]-3, 4-dihydroxy-2- (hydroxymethyl)oxolan-2-yl]oxymethyl]-2- (hydroxymethyl)oxolane-2, 3, 4-triol. Molecular formula: 504.4g/mol. Mole weight: C18H32O16. C (C1C (C (C (O1) (CO)OCC2C (C (C (O2) (CO)OCC3C (C (C (O3) (CO)O)O)O)O)O)O)O)O. InChI=1S/C18H32O16/c19-1-7-10 (23)14 (27)17 (5-21, 33-7)31-3-9-12 (25)15 (28)18 (6-22, 34-9)30-2-8-11 (24)13 (26)16 (29, 4-20)32-8/h7-15, 19-29H, 1-6H2/t7-, 8-, 9-, 10-, 11-, 12-, 13+, 14+, 15+, 16-, 17-, 18-/m1/s1. ZFTFOHBYVDOAMH-XNOIKFDKSA-N. |  |
| Levan - from Jerusalem artichoke | Levan is a fructose derivative, it is moisturizing and anti-inflammatory, it is also used to help improve skin barrier function. CAS No. 9013-95-0. Molecular formula: (C6H10O5)n. | |
| levan fructotransferase (DFA-IV-forming) | This enzyme, like EC 4.2.2.17 [inulin fructotransferase (DFA-I-forming)] and EC 4.2.2.18 [inulin fructotransferase (DFA-III-forming)] eliminates the fructan chain from the terminal disaccharide leaving a difructose dianhydride. These enzymes have long been known as fructotransferases, so this is retained in the accepted name. Since the transfer is intramolecular, the reaction is an elimination and, hence, the enzyme is a lyase, belonging in EC 4. Group: Enzymes. Synonyms: 2,6-β-D-fructan D-fructosyl-D-fructosyltransferase (forming di-β-D-fructofuranose 2,6':2',6-dianhydride); levan fructotransferase; 2,6-β-D-fructan lyase (di-β-D-fructofuranose-2,6':2',6-dianhydride-forming). Enzyme Commission Number: EC 4.2.2.16. CAS No. 88593-15-1. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-5091; levan fructotransferase (DFA-IV-forming); EC 4.2.2.16; 88593-15-1; 2,6-β-D-fructan D-fructosyl-D-fructosyltransferase (forming di-β-D-fructofuranose 2,6':2',6-dianhydride); levan fructotransferase; 2,6-β-D-fructan lyase (di-β-D-fructofuranose-2,6':2',6-dianhydride-forming). Cat No: EXWM-5091. | |
| levansucrase | Some other sugars can act as D-fructosyl acceptors. Group: Enzymes. Synonyms: sucrose 6-fructosyltransferase; β-2,6-fructosyltransferase; β-2,6-fructan:D-glucose 1-fructosyltransferase; sucrose:2,6-β-D-fructan 6-β-D-fructosyltransferase; sucrose:(2?6)-β-D-fructan 6-β-D-fructosyltransferase. Enzyme Commission Number: EC 2.4.1.10. CAS No. 9030-17-5. Levansucrase. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2327; levansucrase; EC 2.4.1.10; 9030-17-5; sucrose 6-fructosyltransferase; β-2,6-fructosyltransferase; β-2,6-fructan:D-glucose 1-fructosyltransferase; sucrose:2,6-β-D-fructan 6-β-D-fructosyltransferase; sucrose:(2?6)-β-D-fructan 6-β-D-fructosyltransferase. Cat No: EXWM-2327. | |
| Levcromakalim | LevCromakalim is an ATP-sensitive K+channel(KATP) activator used in the management of hypertension in diabetes mellitus. Synonyms: (3S,4R)-3-hydroxy-2,2-dimethyl-4-(2-oxopyrrolidin-1-yl)-3,4-dihydrochromene-6-carbonitrile; BRL 38226; BRL 38227; BRL-34915; BRL-38226; BRL-38227; BRL38226; BRL38227; Cromakalim; Cromakalim, (3R-cis)-Isomer; Cromakalim, (3R-trans)-Isomer; Cromakalim, (3S-cis)-Isomer; Cromakalim, (3S-trans)-Isomer; Cromakalim, (trans)-Isomer; Lemakalim; Levcromakalim. CAS No. 94535-50-9. Molecular formula: C16H18N2O3. Mole weight: 286.33. | |
| Levcromakalim | Levcromakalim ((-)-Cromakalim) is an ATP-sensitive K + channel (K ATP ) activator. Uses: Scientific research. Group: Signaling pathways. Alternative Names: (-)-Cromakalim; BRL 38227. CAS No. 94535-50-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg. Product ID: HY-14255. | |
| L-evernosamine nitrososynthase | Requires FAD. Isolated from the bacterium Micromonospora carbonacea var. africana. The nitroso group is probably spontaneously oxidized to a nitro group giving dTDP-β-L-evernitrose, which is involved in the biosynthesis of the antibiotic everninomycin. The reaction was studied using dTDP-β-L-4-epi-vancosamine (dTDP-4-O-desmethyl-β-L-evernitrosamine). Group: Enzymes. Enzyme Commission Number: EC 1.14.13.187. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0786; L-evernosamine nitrososynthase; EC 1.14.13.187. Cat No: EXWM-0786. | |
| Levetiracetam | Levetiracetam. CAS No. 102767-28-2. Product ID: 8-04663. Molecular formula: C8H14N2O2. Mole weight: 170.21. Purity: 0.95. Properties: from glycyrrhiza root (licorice). | |
| Levetiracetam | Levetiracetam is an anticonvulsant medication used to treat epilepsy. Synonyms: UCB-L059, SIB-S1; UCB L059, SIB S1; UCBL059, SIBS1. Grades: >98%. CAS No. 102767-28-2. Molecular formula: C8H14N2O2. Mole weight: 170.21. | |
| Levetiracetam | Levetiracetam, an antiepileptic agent, binds the synaptic vesicle protein SV2A. Levetiracetam enhances Temozolomide effect on glioblastoma stem cell proliferation and apoptosis. Levetiracetam modulates HDAC levels ultimately silencing MGMT , thus increasing Temozolomide effectiveness. A chemosensitizer agent [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: UCB L059. CAS No. 102767-28-2. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg; 500 mg. Product ID: HY-B0106. | |
| Levetiracetam | 25g Pack Size. Group: Bioactive Small Molecules, Research Organics & Inorganics. Formula: C8H14N2O2. CAS No. 102767-28-2. Prepack ID 89966312-25g. Molecular Weight 170.21. See USA prepack pricing. |  |
| Levetiracetam Carboxylic Acid | Levetiracetam intermediate. Synonyms: (αS)-α-Ethyl-2-oxo-1-pyrrolidineacetic Acid. Grades: > 95%. CAS No. 102849-49-0. Molecular formula: C8H13NO3. Mole weight: 171.20. | |
| Levetiracetam Carboxylic Acid | Levetiracetam intermediate. Group: Biochemicals. Alternative Names: (αS)-. Grades: Highly Purified. CAS No. 102849-49-0. Pack Sizes: 1mg. US Biological Life Sciences. |  Worldwide |
| Levetiracetam-d3 | Labeled Levetiracetam, which is used as an anticonvulsant. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Levetiracetam-d3 (contains d0) | The labelled (S)-enantiomer of Etiracetam (E932970) and the ethyl analog of Piracetam (P500800). Used as an anticonvulsant. Group: Biochemicals. Alternative Names: (αS)-α-(Ethyl-d3)-2-oxo-. Grades: Highly Purified. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Levetiracetam-d6 (ring-d6) | Levetiracetam-d6 (ring-d6) can be used as internal standard for the determination of Levetiracetam (HY-B0106) content in whole blood [1]. Uses: Scientific research. Group: Isotope-labeled compounds. Alternative Names: UCB L059-d6 (ring-d6). CAS No. 1133229-30-7. Pack Sizes: 1 mg; 5 mg. Product ID: HY-110225. | |
| Levetiracetam EP Impurity D | Levetiracetam EP Impurity D. Uses: For analytical and research use. Group: Impurity standards. CAS No. 103765-01-1. Molecular formula: C8H14N2O2. Mole weight: 170.21. Catalog: APB103765011. | |
| Levetiracetam Impurity 12 | Levetiracetam Impurity 12. Uses: For analytical and research use. Group: Impurity standards. CAS No. 10476-43-0. Molecular formula: C4H11ClN2O. Mole weight: 138.6. Catalog: APB10476430. | |
| Levetiracetam Impurity 13 | Levetiracetam Impurity 13. Uses: For analytical and research use. Group: Impurity standards. CAS No. 102767-31-7. Molecular formula: C8H15ClN2O2. Mole weight: 206.67. Catalog: APB102767317. | |
| Levetiracetam Impurity 3 | a related compound of Levetiracetam. Synonyms: (S)-N-(1-Amino-1-oxobutan-2-yl)-4-chlorobutanamide; N-[(1S)-1-(Aminocarbonyl)propyl]-4-chlorobutanamide; (S)-N-[1-(Aminocarbonyl)propyl]-4-chlorobutanamide; USP Levetiracetam Related Compound A. Grades: > 95%. CAS No. 102767-31-7. Molecular formula: C8H15ClN2O2. Mole weight: 206.67. | |
| Levetiracetam Impurity A | An impurity of Levetiracetam, a medication indicated for the treatment of epilepsy. Synonyms: alpha-Ethyl-2-oxo-1-pyrrolidineacetic acid; Levetiracetam Carboxylic Acid. Grades: > 95%. CAS No. 67118-31-4. Molecular formula: C8H13NO3. Mole weight: 171.20. | |
| Levetiracetam Impurity B | Levetiracetam Impurity B is an impurity of Levetiracetam, a medication indicated for the treatment of epilepsy. Synonyms: (Z)-2-(2-oxopyrrolidin-1-yl)but-2-enamide. Grades: >95%. CAS No. 358629-47-7. Molecular formula: C8H12N2O2. Mole weight: 168.19. | |
| Levetiracetam Impurity C | impurity of Levetiracetam. Synonyms: 2(1H)-Pyridone; 2-pyridone; 2-Pyridinol; Pyridin-2-ol; 2-Hydroxy Pyridine; pyridin-2(1H)-one. Grades: > 95%. CAS No. 72762-00-6. Molecular formula: C5H5NO. Mole weight: 95.10. | |
| Levetiracetam Impurity D | the enantiomer to Levetiracetam. Synonyms: (αR)-α-Ethyl-2-oxo-1-pyrrolidineacetamide; (R)-Levetiracetam. Grades: > 95%. CAS No. 103765-01-1. Molecular formula: C8H14N2O2. Mole weight: 170.21. | |
| Levetiracetam Racemic Mixture | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Levetiracetam Related Compound A | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Levetiracetam Related Compound B | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Levetiracetam (UCB-L059, SIB-S1, Keppra) | Used as an anticonvulsant. Group: Biochemicals. Alternative Names: UCB-L059; SIB-S1; Keppra; (αS)-α-Ethyl-2-oxo-1-pyrrolidineacetamide; 2(S)-(2-Oxopyrrolidin-1-yl)butyramide; (-)-Levetiracetam; Levesam 500; (S)-Levetiracetam. Grades: Highly Purified. CAS No. 102767-28-2. Pack Sizes: 100mg, 250mg, 500mg. Molecular Formula: C?H??N?O?, Molecular Weight: 170.21. US Biological Life Sciences. | Worldwide |
| Levistilide A | Levistilide A. Group: Biochemicals. Grades: Plant Grade. CAS No. 88182-33-6. Pack Sizes: 20mg. Molecular Formula: C24H28O4, Molecular Weight: 380.48. US Biological Life Sciences. | Worldwide |
| Levistolide A | Levistolide A. Group: Biochemicals. CAS No. 88182-33-6. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Levitide(9ci) | Levitide(9ci). Uses: Designed for use in research and industrial production. Additional or Alternative Names: Levitide, AC1NMWAD, 114281-19-5, pGlu-Gly-Met-Ile-Gly-Thr-Leu-Thr-Ser-Lys-Arg-Ile-Lys-Gln-NH2, 2-[[6-amino-2-[[2-[[2-[[6-amino-2-[[3-hydroxy-2-[[3-hydroxy-2-[[2-[[3-hydroxy-2-[[2-[[3-methyl-2-[[4-methylsulfanyl-2-[[2-[(5-oxopyrrolidine-2-carbonyl)amino]acetyl]amino]butanoyl]amino]pentanoyl]amino]acetyl]amino]butanoyl]amino]-4-methylpentanoyl]amino]butanoyl]amino]propanoyl]amino]hexanoyl]amino]-5-(diaminomethylideneamino)pentanoyl]amino]-3-methylpentanoyl]amino]hexanoyl]amino]pentanediamide. Product Category: Heterocyclic Organic Compound. CAS No. 114281-19-5. Molecular formula: C66H119N21O19S. Mole weight: 1542.8454. Purity: 0.96. IUPACName: 2-[[6-amino-2-[[2-[[2-[[6-amino-2-[[3-hydroxy-2-[[3-hydroxy-2-[[2-[[3-hydroxy-2-[[2-[[3-methyl-2-[[4-methylsulfanyl-2-[[2-[(5-oxopyrrolidine-2-carbonyl)amino]acetyl]amino]butanoyl]amino]pentanoyl]amino]acetyl]amino]butanoyl]amino]-4-methylpentanoyl]amino]. Canonical SMILES: CCC(C)C(C(=O)NCC(=O)NC(C(C)O)C(=O)NC(CC(C)C)C(=O)NC(C(C)O)C(=O)NC(CO)C(=O)NC(CCCCN)C(=O)NC(CCCN=C(N)N)C(=O)NC(C(C)CC)C(=O)NC(CCCCN)C(=O)NC(CCC(=O)N)C(=O)N)NC(=O)C(CCSC)NC(=O)CNC(=O)C1CCC(=O)N1. Density: 1.44 g/cm³. Product ID: ACM114281195. Alfa Chemistry ISO 9001:2015 Certified. | |
| Levobetaxolol HCl | Levobetaxolol exhibits a higher affinity at cloned human β1 and β2 receptors with Ki value of 0.76 nM and 32.6 nM, respectively. Synonyms: AL 1577A; AL-1577A; AL1577A. Grades: >98%. CAS No. 116209-55-3. Molecular formula: C18H29NO3.HCl. Mole weight: 343.89. | |
| Levobetaxolol hydrochloride | Levobetaxolol hydrochloride is a beta-adrenergic receptor inhibitor (beta blocker) that can lower the pressure in the eye. Uses: Scientific research. Group: Signaling pathways. Alternative Names: (S)-Betaxolol hydrochloride; AL-1577A. CAS No. 116209-55-3. Pack Sizes: 10 mM * 1 mL; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B0381B. | |
| Levobunolol | Levobunolol is a nonselective beta-adrenoceptor antagonist used in the treatment of glaucoma. Uses: A nonselective beta-adrenoceptor antagonist. Synonyms: (S)-5-(3-((1,1-Dimethylethyl)amino)-2-hydroxypropoxy)-3,4-dihydro-1(2H)-naphthalenone. Grades: ≥98%. CAS No. 47141-42-4. Molecular formula: C17H25NO3. Mole weight: 291.388. | |
| Levobunolol hydrochloride | Levobunolol hydrochloride, a beta1- and beta2-adregergic blocking agent, has proved to be an effective ocular hypotensive agent to treat glaucoma. Synonyms: 5-[(2R)-3-(tert-butylamino)-2-hydroxypropoxy]-3,4-dihydro-2H-naphthalen-1-one;hydrochloride AKBeta Akorn Brand of Levobunolol Hydrochloride Allergan Brand of Levobunolol Hydrochloride Apo Levobunolol Apo-Levobunolol ApoLevobunolol Apotex Brand of Levobuno. Grades: 95%. CAS No. 27912-14-7. Molecular formula: C17H26ClNO3. Mole weight: 327.85. | |
| Levobunolol hydrochloride | Levobunolol (l-Bunolol) hydrochloride is a potent and nonselective β-adrenergic receptor antagonist. Levobunolol hydrochloride is an ocular hypotensive agent and lowers mean intraocular pressure (IOP). Levobunolol hydrochloride can be used for glaucoma and superior oblique myokymia (SOM) research [1] [2] [3]. Uses: Scientific research. Group: Natural products. Alternative Names: l-Bunolol hydrochloride. CAS No. 27912-14-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg. Product ID: HY-B1035. | |
| Levobupivacaine free base | Levobupivacaine is a local anaesthetic drug belonging to the amino amide group. It is the S-enantiomer of bupivacaine. Levobupivacaine hydrochloride is commonly marketed by Abbott under the trade name Chirocaine. It acts via reversibly binding voltage-gated sodium channels to modulate ionic flux and block the initiation and transmission of nerve impulses. Uses: Local anaesthetic drug. Synonyms: (S)-1-butyl-N-(2,6-dimethylphenyl)piperidine-2-carboxamide; Levobupivacaine free base; (S)-1-Butyl-2',6'-pipecoloxylidide; L(-)-Bupivacaine. Grades: 98%. CAS No. 27262-47-1. Molecular formula: C18H28N2O. Mole weight: 288.44. | |
| Levobupivacaine hydrochloride | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Levobupivacaine hydrochloride | Levobupivacaine hydrochloride ((S)-(-)-Bupivacaine monohydrochloride) is a long-acting amide local agent that can suppress or relieve pain. Levobupivacaine hydrochloride exerts agent that can suppress or relieve pain. and analgesic effects through reversible blockade of neuronal sodium channel. Levobupivacaine hydrochloride can inhibit impulse transmission and conduction in cardiovascular and other tissues, possessing certain cardiac and CNS toxicity. Levobupivacaine hydrochloride is metabolized by hepatic cytochrome P450 (CYP450) enzymes in vivo. Levobupivacaine hydrochloride can also induce ferroptosis by miR-489-3p/SLC7A11 signaling in gastric cancer [1] [2] [3]. Uses: Scientific research. Group: Natural products. Alternative Names: (S)-(-)-Bupivacaine monohydrochloride. CAS No. 27262-48-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg; 500 mg. Product ID: HY-B0653A. | |
| Levobupivacaine hydrochloride | Levobupivacaine hydrochloride. Uses: Designed for use in research and industrial production. Additional or Alternative Names: TIMTEC-BB SBB001337;(S)-(-)-BUPIVACAINE HCL;(S)-(-)-BUPIVACAINE HYDROCHLORIDE;(S)-(-)-1-N-BUTYL-2,6-DIMETHYL-2-PIPERIDINCARBOXANILID HYDROCHLORIDE;(S)-(-)-1-BUTYL-2-(2,6-XYLYLCARBAMOYL)-PIPERIDINE HYDROCHLORIDE;s-(-)-1-butyl-2,6-pipecoloxylidide hydrochloride;(s)-1-butyl-2',6'-piperidinecarboxamidemonohydrochloride;(s)-1-butyl-n-(2,6-dimethylphenyl)-2-piperidinecarboxamidemonohydrochloride. Product Category: Heterocyclic Organic Compound. CAS No. 27262-48-2. Molecular formula: C18H29ClN2O. Mole weight: 324.89. Product ID: ACM27262482. Alfa Chemistry ISO 9001:2015 Certified. | |
| Levobupivacaine Hydrochloride USP | Levobupivacaine Hydrochloride USP. Grades: USP. CAS No. 27262-48-2. Product ID: 8-04518. Molecular formula: C18H28N2O.HCl. Mole weight: 324.89. | |
| Levocabastine | Levocabastine is a selective second-generation Histamine H1 receptor antagonist. It is used for Allergic conjunctivitis and Seasonal allergic rhinitis. Levocabastine is also a potent and selective antagonist for the neurotensin receptor NTS2 and it can be used to characterise the different neurotensin subtypes. Uses: Allergic conjunctivitis; seasonal allergic rhinitis. Synonyms: Levocabastine, Livostin, Bilina;(3S,4R)-1-[4-cyano-4-(4-fluorophenyl)cyclohexyl]-3-methyl-4-phenylpiperidine-4-carboxylic acid. Grades: 98%. CAS No. 79516-68-0. Molecular formula: C26H29FN2O2. Mole weight: 420.52. | |
| Levocabastine HCl | A salt of Levocabastine. Synonyms: 1-[4-cyano-4-(4-fluorophenyl)cyclohexyl]-3-methyl-4-phenylpiperidine-4-carboxylic acid monohydrochloride; 1-(4-Cyano-4-(4-fluorophenyl)cyclohexyl)-3-methyl-4-phenylpiperidine-4-carboxylic acid monohydrochloride; Einecs 279-414-0. Grades: 95%. CAS No. 80185-65-5. Molecular formula: C26H30ClFN2O2. Mole weight: 456.98. | |
| Levocabastine hydrochloride | Levocabastine is a potent and selective second-generation histamine H1 receptor antagonist. It has been utilized in eye drops and nasal sprays for the treatment of allergic conjunctivitis and allergic rhinitis, respectively. Uses: Histamine h1 antagonists, non-sedating. Synonyms: (3S,4R)-1-[cis-4-Cyano-4-(4-fluorophenyl)cyclohexyl]-3-methyl-4-phenyl-4-piperidinecarboxylic Acid Hydrochloride; [3S-[1(cis),3α,4β]]-1-[4-Cyano-4-(4-fluorophenyl)cyclohexyl]-3-methyl-4-phenyl-4-piperidinecarboxylic Acid Monohydrochloride; (3S,4R)-Cabastine Hydrochloride; Livostin. Grades: 98%. CAS No. 79547-78-7. Molecular formula: C26H30ClFN2O2. Mole weight: 456.98. | |
| Levocabastine hydrochloride | Levocabastine (R 50547) hydrochloride is a potent and selective histamine H1-receptor antagonist. Levocabastine hydrochloride is also a selective, high affinity neurotensin receptor subtype 2 (NTR2) antagonist, with a K i of 17 nM for mNTR2. Levocabastine hydrochloride can act as a VLA-4 antagonist, interferes with conjunctival eosinophil infiltration in allergic conjunctivitis (AC) [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: R 50547 hydrochloride. CAS No. 79547-78-7. Pack Sizes: 1 mg; 5 mg. Product ID: HY-14277A. | |
| Levocabastine Impurity 1 | Impurity of Levocabastine. Grades: > 95%. Molecular formula: C26H30FNO4. Mole weight: 439.53. | |
| Levocabastine Impurity 14 | Levocabastine Impurity 14. Uses: For analytical and research use. Group: Impurity standards. CAS No. 105452-51-5. Molecular formula: C26H29FN2O2. Mole weight: 420.53. Catalog: APB105452515. | |
| Levocabastine Impurity 15 | Levocabastine Impurity 15. Uses: For analytical and research use. Group: Impurity standards. CAS No. 105452-52-6. Molecular formula: C26H29FN2O2. Mole weight: 420.53. Catalog: APB105452526. | |
| Levocabastine Impurity 2 | Impurity of Levocabastine. Grades: > 95%. Molecular formula: C26H31FN2O4. Mole weight: 454.55. | |
| Levocabastine Impurity 3 | Impurity of Levocabastine. Grades: > 95%. Molecular formula: C27H31FN2O2. Mole weight: 434.56. | |
| Levocabastine Related Compound A | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
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