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· · COA & SDS available for every product · Same-day shipping on in-stock items Carteolol Hydrochloride - ≥99% , Adrenergic receptor beta antagonist, CAS No.51781-21-6, Adrenergic receptor beta antagonist
Synonyms
BCP28338 | CARTEOLOL HYDROCHLORIDE [VANDF] | WLN: T66 BMVT&J GO1YQ1MX1&1&1 &GH | NCGC00016865-01 | 5-(3-(tert-Butylamino)-2-hydroxypropoxy)-3,4-dihydrocarbostyril monohydrochloride | CARTEOLOL HYDROCHLORIDE [USP MONOGRAPH] | NSC300906 | NSC-300906 | C7542
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Why this grade ≥99% 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.
Overview Carteolol Hydrochloride is a β-Adrenergic blocker which exhibits antihypertensive, antianginal, antiarrhythmic and antiglaucoma properties.
Specifications Synonyms
BCP28338 | CARTEOLOL HYDROCHLORIDE [VANDF] | WLN: T66 BMVT&J GO1YQ1MX1&1&1 &GH | NCGC00016865-01 | 5-(3-(tert-Butylamino)-2-hydroxypropoxy)-3, 4-dihydrocarbostyril monohydrochloride | CARTEOLOL HYDROCHLORIDE [USP MONOGRAPH] | NSC300906 | NSC-300906 | C7542
Specifications & Purity
≥99%
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Mechanism of action
Adrenergic receptor beta antagonist
Names and Identifiers Canonical Smiles CC(C)(C)NCC(COC1=CC=CC2=C1CCC(=O)N2)O.Cl IUPAC Name 5-[3-(tert-butylamino)-2-hydroxypropoxy]-3,4-dihydro-1H-quinolin-2-one;hydrochloride InChIKey FYBXRCFPOTXTJF-UHFFFAOYSA-N INCHI 1S/C16H24N2O3.ClH/c1-16(2,3)17-9-11(19)10-21-14-6-4-5-13-12(14)7-8-15(20)18-13;/h4-6,11,17,19H,7-10H2,1-3H3,(H,18,20);1H Isomeric SMILES CC(C)(C)NCC(COC1=CC=CC2=C1CCC(=O)N2)O.Cl Alternate CAS 51781-06-7 Molecular Weight 328.83 Reaxy-Rn 5784965 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=5784965&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 Organoheterocyclic compounds Class Quinolines and derivatives Subclass Quinolones and derivatives Intermediate Tree Nodes Not available Direct Parent Hydroquinolones Alternative Parents Hydroquinolines Alkyl aryl ethers Benzenoids Secondary carboxylic acid amides Secondary alcohols Lactams Amino acids and derivatives 1,2-aminoalcohols Dialkylamines Azacyclic compounds Organopnictogen compounds Organic oxides Hydrochlorides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aromatic heteropolycyclic compounds Substituents Tetrahydroquinolone - Tetrahydroquinoline - Alkyl aryl ether - Benzenoid - 1,2-aminoalcohol - Amino acid or derivatives - Carboxamide group - Lactam - Secondary alcohol - Secondary carboxylic acid amide - Azacycle - Secondary amine - Carboxylic acid derivative - Secondary aliphatic amine - Ether - Hydrocarbon derivative - Organic oxygen compound - Organopnictogen compound - Amine - Organonitrogen compound - Organic nitrogen compound - Carbonyl group - Organooxygen compound - Organic oxide - Hydrochloride - Alcohol - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as hydroquinolones. These are compounds containing a hydrogenated quinoline bearing a ketone group. 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.
3D Structure Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Solubility Soluble in methanol.insoluble in EtOH; ≥16.44 mg/mL in DMSO; ≥22.25 mg/mL in H2O Sensitivity Moisture sensitive. Melt Point(°C) 269-272° C Molecular Weight 328.830 g/mol XLogP3 Hydrogen Bond Donor Count 4 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 6 Exact Mass 328.155 Da Monoisotopic Mass 328.155 Da Topological Polar Surface Area 70.600 Ų Heavy Atom Count 22 Formal Charge 0 Complexity 354.000 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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