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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items Levobunolol, Hydrochloride , Beta-1 adrenergic receptor antagonist, CAS No.27912-14-7, Beta-1 adrenergic receptor antagonist
Synonyms
Levobunolol (hydrochloride) | Levobunolol HCl | Levobunolol, Hydrochloride | CAS-27912-14-7 | D01025 | MLS002154030 | (-)-(S)-5-(3-(TERT-BUTYLAMINO)-2-HYDROXYPROPOXY)-3,4-DIHYDRO-1(2H)-NAPHTHALENONE HYDROCHLORIDE | Betagan (TN) | levobunolol monohydrochlo
Shipped In
Ice chest + Ice pads
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Why this grade for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Descripción general Levobunolol, Hydrochloride is a non-selective β-AR (β-adrenoceptor) antagonist.
Specifications Sinónimos
Levobunolol (hydrochloride) | Levobunolol HCl | Levobunolol, Hydrochloride | CAS-27912-14-7 | D01025 | MLS002154030 | (-)-(S)-5-(3-(TERT-BUTYLAMINO)-2-HYDROXYPROPOXY)-3, 4-DIHYDRO-1(2H)-NAPHTHALENONE HYDROCHLORIDE | Betagan (TN) | levobunolol monohydrochlo
Condiciones de almacenamiento de almacenamiento
Store at -20°C
Enviado en
Ice chest + Ice pads
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Mecanismo de acción
Beta-1 adrenergic receptor antagonist
Nombres e identificadores Sonrisas canónicas CC(C)(C)NCC(COC1=CC=CC2=C1CCCC2=O)O.Cl IUPAC Name 5-[(2S)-3-(tert-butylamino)-2-hydroxypropoxy]-3,4-dihydro-2H-naphthalen-1-one;hydrochloride InChIKey DNTDOBSIBZKFCP-YDALLXLXSA-N INCHI 1S/C17H25NO3.ClH/c1-17(2,3)18-10-12(19)11-21-16-9-5-6-13-14(16)7-4-8-15(13)20;/h5-6,9,12,18-19H,4,7-8,10-11H2,1-3H3;1H/t12-;/m0./s1 Isómeros SMILES CC(C)(C)NC[C@@H](COC1=CC=CC2=C1CCCC2=O)O.Cl Peso molecular 327.84 Reaxy-Rn 6579687 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=6579687&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Benzenoids Clase Tetralins Subclass Not available Intermediate Tree Nodes Not available Direct Parent Tetralins Alternative Parents Aryl alkyl ketones Alkyl aryl ethers Secondary alcohols 1,2-aminoalcohols Dialkylamines Organopnictogen compounds Organic zwitterions Organic oxides Organic chloride salts Hydrocarbon derivatives Molecular Framework Aromatic homopolycyclic compounds Substituents Tetralin - Aryl ketone - Aryl alkyl ketone - Alkyl aryl ether - 1,2-aminoalcohol - Ketone - Secondary alcohol - Secondary aliphatic amine - Ether - Secondary amine - Hydrocarbon derivative - Organic oxygen compound - Organic oxide - Organooxygen compound - Organonitrogen compound - Organopnictogen compound - Alcohol - Organic nitrogen compound - Amine - Organic zwitterion - Organic chloride salt - Organic salt - Aromatic homopolycyclic compound Descripción This compound belongs to the class of organic compounds known as tetralins. These are polycyclic aromatic compounds containing a tetralin moiety, which consists of a benzene fused to a cyclohexane. External Descriptors hydrochloride Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Estructura 3D Objetivos asociados (humanos) Objetivos asociados (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Solubilidad Soluble in Dimethyl Sulfoxide, Hot Ethanol, Methanol and Water Punto de fusión (°C) 209-211° C Peso molecular 327.800 g/mol XLogP3 Hydrogen Bond Donor Count 3 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 6 Exact Mass 327.16 Da Monoisotopic Mass 327.16 Da Topological Polar Surface Area 58.600 Ų Heavy Atom Count 22 Formal Charge 0 Complexity 350.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 1 Undefined Atom Stereocenter Count 0 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 2
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