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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items 3-Hydroxyphenylboronic acid(contains varying amounts of Anhydride) - ≥97% , CAS No.87199-18-6
Synonyms
EN300-119261 | 3-hydroxy phenyl boronic acid | H1185 | Q-102215 | (3-hydroxyphenyl) boronic acid | 3-Hydroxyphenylboronic acid | 3-hydroxy-phenylboronic acid | 3-hydroxyphenyl-boronic acid | FT-0615831 | (3-hydroxyphenyl)boronicAcid | NCGC00249443-01 | (3
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Why this grade ≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Room temperature Ships Normal 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.
Descripción general Application：
3-Hydroxyphenylboronic acid (3-HPBA) can be used as a reagent:
In Suzuki-Miyaura coupling reactions with aryl halides for the formation of C-C bond in the presence of Pd catalyst.
To synthesize boron/nitrogen-doped polymer nano/microspheres by hydrothermal polymerization with formaldehyde and ammonia.
To prepare carbon quantum dots based on 3-HPBA as selective fructose sensor.
In the development of modified electrodes for electrochemical biosensors.
Specifications Sinónimos
EN300-119261 | 3-hydroxy phenyl boronic acid | H1185 | Q-102215 | (3-hydroxyphenyl) boronic acid | 3-Hydroxyphenylboronic acid | 3-hydroxy-phenylboronic acid | 3-hydroxyphenyl-boronic acid | FT-0615831 | (3-hydroxyphenyl)boronicAcid | NCGC00249443-01 | (3
Especificaciones y pureza
≥97%
Condiciones de almacenamiento de almacenamiento
Room temperature
Nombres e identificadores Pubchem Sid 488192556 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488192556 Sonrisas canónicas B(C1=CC(=CC=C1)O)(O)O IUPAC Name (3-hydroxyphenyl)boronic acid InChIKey WFWQWTPAPNEOFE-UHFFFAOYSA-N INCHI 1S/C6H7BO3/c8-6-3-1-2-5(4-6)7(9)10/h1-4,8-10H Isómeros SMILES B(C1=CC(=CC=C1)O)(O)O WGK Alemania 3 Peso molecular 137.93 Beilstein 16(3)1281 Reaxy-Rn 3240771 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3240771&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 Phenols Subclass 1-hydroxy-4-unsubstituted benzenoids Intermediate Tree Nodes Not available Direct Parent 1-hydroxy-4-unsubstituted benzenoids Alternative Parents 1-hydroxy-2-unsubstituted benzenoids Benzene and substituted derivatives Boronic acids Organic metalloid salts Organooxygen compounds Organoboron compounds Hydrocarbon derivatives Molecular Framework Aromatic homomonocyclic compounds Substituents 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Monocyclic benzene moiety - Boronic acid - Boronic acid derivative - Organic metalloid salt - Organic oxygen compound - Hydrocarbon derivative - Organic salt - Organooxygen compound - Organoboron compound - Aromatic homomonocyclic compound Descripción This compound belongs to the class of organic compounds known as 1-hydroxy-4-unsubstituted benzenoids. These are phenols that are unsubstituted at the 4-position. 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 Slightly soluble in water; Soluble in Methanol Punto de fusión (°C) 210-213°C Peso molecular 137.930 g/mol XLogP3 Hydrogen Bond Donor Count 3 Hydrogen Bond Acceptor Count 3 Rotatable Bond Count 1 Exact Mass 138.049 Da Monoisotopic Mass 138.049 Da Topological Polar Surface Area 60.700 Ų Heavy Atom Count 10 Formal Charge 0 Complexity 107.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 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 1
Citations of This Product Referencias 1. Yu-Xiang Jia, Weizhi Sun, Chai Yin, Chao Xu, Shitao Yu, Xian Mo. (2018) Efficient and selective adsorption of small polyols by boronic acid functionalized polystyrene adsorbent. JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY, 94 (4): (1259-1268). [PMID: [10.1002/jctb.5879 ]
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