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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items Zinterol hydrochloride - ≥98%(HPLC) , CAS No.38241-28-0
Synonyms
D06374 | Zinterol HCl | Zinterol hydrochloride [USAN] | Q27261393 | Zinterol hydrochloride (USAN) | Methanesulfonanilide, 5'-(2-((alpha,alpha-dimethylphenethyl)amino)-1-hydroxyethyl)-2'-hydroxy-, monohydrochloride | DTXSID701000591 | NSC284704 | NSC-28470
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Why this grade ≥98%(HPLC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at 2-8°C Ships Wet ice 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.
Specifications Sinónimos
D06374 | Zinterol HCl | Zinterol hydrochloride [USAN] | Q27261393 | Zinterol hydrochloride (USAN) | Methanesulfonanilide, 5'-(2-((alpha, alpha-dimethylphenethyl)amino)-1-hydroxyethyl)-2'-hydroxy-, monohydrochloride | DTXSID701000591 | NSC284704 | NSC-28470
Especificaciones y pureza
≥98%(HPLC)
Mecanismos bioquímicos y fisiológicos
Potent and selectiveβ2-adrenoceptor agonist (pKBvalues are 8.3 and < 5.7 forβ2andβ1receptors respectively, as measured in human artery).
Condiciones de almacenamiento de almacenamiento
Store at 2-8°C
Enviado en
Wet ice
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Nombres e identificadores Pubchem Sid 504753563 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504753563 Sonrisas canónicas CC(C)(CC1=CC=CC=C1)NCC(C2=CC(=C(C=C2)O)NS(=O)(=O)C)O.Cl IUPAC Name N-[2-hydroxy-5-[1-hydroxy-2-[(2-methyl-1-phenylpropan-2-yl)amino]ethyl]phenyl]methanesulfonamide;hydrochloride InChIKey LVNUBJDWJFOMKH-UHFFFAOYSA-N INCHI 1S/C19H26N2O4S.ClH/c1-19(2,12-14-7-5-4-6-8-14)20-13-18(23)15-9-10-17(22)16(11-15)21-26(3,24)25;/h4-11,18,20-23H,12-13H2,1-3H3;1H Isómeros SMILES CC(C)(CC1=CC=CC=C1)NCC(C2=CC(=C(C=C2)O)NS(=O)(=O)C)O.Cl WGK Alemania 3 PubChem CID 37989 Peso molecular 414.95
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 Benzene and substituted derivatives Subclass Phenethylamines Intermediate Tree Nodes Not available Direct Parent Amphetamines and derivatives Alternative Parents Sulfanilides Phenylpropanes Aralkylamines 1-hydroxy-2-unsubstituted benzenoids Organosulfonamides Organic sulfonamides Aminosulfonyl compounds Secondary alcohols 1,2-aminoalcohols Dialkylamines Organopnictogen compounds Organic oxides Hydrochlorides Hydrocarbon derivatives Aromatic alcohols Molecular Framework Aromatic homomonocyclic compounds Substituents Amphetamine or derivatives - Sulfanilide - Phenylpropane - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Aralkylamine - Organic sulfonic acid amide - Organosulfonic acid amide - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Aminosulfonyl compound - Secondary alcohol - 1,2-aminoalcohol - Secondary aliphatic amine - Secondary amine - Organic nitrogen compound - Organic oxide - Hydrocarbon derivative - Organopnictogen compound - Organic oxygen compound - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Alcohol - Hydrochloride - Amine - Aromatic alcohol - Aromatic homomonocyclic compound Descripción This compound belongs to the class of organic compounds known as amphetamines and derivatives. These are organic compounds containing or derived from 1-phenylpropan-2-amine. External Descriptors Not available 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 Solvent:water, Max Conc. mg/mL: 2.07, Max Conc. mM: 5; Solvent:DMSO, Max Conc. mg/mL: 41.49, Max Conc. mM: 100 Peso molecular 414.900 g/mol XLogP3 Hydrogen Bond Donor Count 5 Hydrogen Bond Acceptor Count 6 Rotatable Bond Count 8 Exact Mass 414.138 Da Monoisotopic Mass 414.138 Da Topological Polar Surface Area 107.000 Ų Heavy Atom Count 27 Formal Charge 0 Complexity 526.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 1 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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