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· · COA & SDS available for every product · Same-day shipping on in-stock items Betaxolol - Moligand™, ≥98% , Antagonist of β 1-adrenoceptor;Antagonist of β 2-adrenoceptor, CAS No.63659-18-7, Antagonist of β 1-adrenoceptor;Antagonist of β 2-adrenoceptor
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥98% Synonyms
1-{4-[2-(Cyclopropylmethoxy)ethyl]phenoxy}-3-[(propan-2-yl)amino]propan-2-ol | NCGC00015159-04 | C75987 | D07526 | NCGC00015159-06 | C07AB05 | GTPL549 | HMS3884L05 | AS-14125 | SCHEMBL23530 | (.+/-.)-1-[p-[2-(Cyclopropylmethoxy)ethyl]phenoxy]-3-(isopropyl
Shipped In
Ice chest + Ice pads
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Why this grade Moligand™, ≥98% Moligand™ 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Overview Betaxolol is a selective beta1 adrenergic receptor blocker used in the treatment of hypertension and glaucoma
Specifications Synonyms
1-{4-[2-(Cyclopropylmethoxy)ethyl]phenoxy}-3-[(propan-2-yl)amino]propan-2-ol | NCGC00015159-04 | C75987 | D07526 | NCGC00015159-06 | C07AB05 | GTPL549 | HMS3884L05 | AS-14125 | SCHEMBL23530 | (.+/-.)-1-[p-[2-(Cyclopropylmethoxy)ethyl]phenoxy]-3-(isopropyl
Specifications & Purity
Moligand™, ≥98%
Biochemical and Physiological Mechanisms
Betaxolol is a cardioselective β1-adrenergic blocker, as well as an antihypertensive and an antiglaucoma
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Mechanism of action
Antagonist of β 1-adrenoceptor;Antagonist of β 2-adrenoceptor
Names and Identifiers Pubchem Sid 488179698 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488179698 Canonical Smiles CC(C)NCC(COC1=CC=C(C=C1)CCOCC2CC2)O IUPAC Name 1-[4-[2-(cyclopropylmethoxy)ethyl]phenoxy]-3-(propan-2-ylamino)propan-2-ol InChIKey NWIUTZDMDHAVTP-UHFFFAOYSA-N INCHI 1S/C18H29NO3/c1-14(2)19-11-17(20)13-22-18-7-5-15(6-8-18)9-10-21-12-16-3-4-16/h5-8,14,16-17,19-20H,3-4,9-13H2,1-2H3 Isomeric SMILES CC(C)NCC(COC1=CC=C(C=C1)CCOCC2CC2)O Molecular Weight 307.43 Reaxy-Rn 1991268 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1991268&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 Class Phenols Subclass Tyrosols and derivatives Intermediate Tree Nodes Not available Direct Parent Tyrosols and derivatives Alternative Parents Phenoxy compounds Phenol ethers Alkyl aryl ethers Secondary alcohols 1,2-aminoalcohols Dialkylamines Dialkyl ethers Organopnictogen compounds Hydrocarbon derivatives Molecular Framework Aromatic homomonocyclic compounds Substituents Tyrosol derivative - Phenoxy compound - Phenol ether - Alkyl aryl ether - Monocyclic benzene moiety - 1,2-aminoalcohol - Secondary alcohol - Dialkyl ether - Secondary amine - Secondary aliphatic amine - Ether - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organopnictogen compound - Amine - Organic oxygen compound - Alcohol - Aromatic homomonocyclic compound Description This compound belongs to the class of organic compounds known as tyrosols and derivatives. These are compounds containing a hydroxyethyl group attached to the C4 carbon of a phenol group. External Descriptors propanolamine 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 Acetone and Chloroform Melt Point(°C) 61-63°C Molecular Weight 307.400 g/mol XLogP3 2.800 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 11 Exact Mass 307.215 Da Monoisotopic Mass 307.215 Da Topological Polar Surface Area 50.700 Ų Heavy Atom Count 22 Formal Charge 0 Complexity 286.000 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 1
Citations of This Product References 1. Wu Jia, Xiao Xue, Li Zhenqun, Jia Li. (2019) Enantioseparation of chiral β-blockers using polynorepinephrine-coated nanoparticles and chiral capillary electrophoresis. ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 411 (10): (2121-2129). [PMID:30734853 ] [10.1007/s00216-019-01641-4 ]
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