4-Aminophenylboronic acid hydrochloride(contains varying amounts of Anhydride) - ≥97%, used for 4-Aminophenylboronic acid hydrochloride can be used to prepare: The modified reduced graphene composite material used as a sugar sensor to detect the analyte i

CAS: 80460-73-7 Cat. No.: A120027 Molecular Weight: 173.41 EC Number: 623-030-1

GRADE & PURITY ≥97%

Synonyms

MFCD03001333 | QBYGJJSFMOVYOA-UHFFFAOYSA-N | (4-aminophenyl)boronicAcidHydrochloride | AC-6979 | SY017592 | 4-Aminophenylboronic acid hydrochloride | 4-aminophenyl-boronic acid hydrochloride | Boronic acid, B-(4-aminophenyl)-, hydrochloride (1:1) | 4-Amin

Storage

Room temperature,Argon charged

Shipped In

Normal

Specifications

Synonyms

MFCD03001333 | QBYGJJSFMOVYOA-UHFFFAOYSA-N | (4-aminophenyl)boronicAcidHydrochloride | AC-6979 | SY017592 | 4-Aminophenylboronic acid hydrochloride | 4-aminophenyl-boronic acid hydrochloride | Boronic acid, B-(4-aminophenyl)-, hydrochloride (1:1) | 4-Amin

Specifications & Purity

≥97%

Application

4-Aminophenylboronic acid hydrochloride can be used to prepare: The modified reduced graphene composite material used as a sugar sensor to detect the analyte in fruit juice. The modified carbon electrode adsorbed with aminophenol, used for the detection o

Storage

Room temperature, Argon charged

Shipped In

Normal

Purity

≥97%

Names and Identifiers

• Pubchem Sid: 488192614
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488192614
• Canonical Smiles: B(C1=CC=C(C=C1)N)(O)O.Cl
• IUPAC Name: (4-aminophenyl)boronic acid;hydrochloride
• InChIKey: QBYGJJSFMOVYOA-UHFFFAOYSA-N
• INCHI: 1S/C6H8BNO2.ClH/c8-6-3-1-5(2-4-6)7(9)10;/h1-4,9-10H,8H2;1H
• Isomeric SMILES: B(C1=CC=C(C=C1)N)(O)O.Cl
• WGK Germany: 1
• Alternate CAS: 89415-43-0
• Molecular Weight: 173.41
• Reaxy-Rn: 10284687
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=10284687&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Class Benzene and substituted derivatives
      • Subclass Aniline and substituted anilines

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Class: Benzene and substituted derivatives
• Subclass: Aniline and substituted anilines
• Intermediate Tree Nodes: Not available
• Direct Parent: Aniline and substituted anilines
• Alternative Parents: Boronic acids Organic metalloid salts Primary amines Organopnictogen compounds Organoboron compounds Organic oxygen compounds Hydrochlorides Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Aniline or substituted anilines - Boronic acid - Boronic acid derivative - Organic metalloid salt - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Hydrochloride - Organic salt - Primary amine - Organonitrogen compound - Organoboron compound - Amine - Aromatic homomonocyclic compound
• Description: This compound belongs to the class of organic compounds known as aniline and substituted anilines. These are organic compounds containing an aminobenzene moiety.
• 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.

DOI: 10.1186/s13321-016-0174-y

Chemical and Physical Properties

• Sensitivity: Hygroscopic;Air sensitive; Light sensitive
• Melt Point(°C): 125-132°C
• Molecular Weight: 173.410 g/mol
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• Exact Mass: 173.041 Da
• Monoisotopic Mass: 173.041 Da
• Topological Polar Surface Area: 66.500 Ų
• Heavy Atom Count: 11
• Formal Charge: 0
• Complexity: 102.000
• 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: 2

XLogP3

References

1. Difei Zhang, Ziyan Wang, Jieyu Gu, Yan Zhang, Jinghua Chen.  (2023)  Phenylboronic acid-functionalized glycogens as dynamic nano-frameworks for conjugation and activation of carbonic anhydrase.  JOURNAL OF POLYMER SCIENCE,      [PMID:] [10.1002/pol.20230058]

2. Huifa Meng, Kaijin Chen, Chuying Li, Longfei Zhang, Yanwei He, Zining Zhao, Peixin Wu, Hai Zhu, Zhenguo Chi, Jiarui Xu, Siwei Liu, Yi Zhang.  (2025)  Innocuous solvent-based, low-temperature curable, and high transparency photosensitive polyimides developed by soluble polyimides containing bio-based magnolol moieties.  Chemical Science,      [PMID:39829980] [10.1039/D4SC07952C]

3. Zhixiong Huang, Jiamin Zhang, Yuyan Qian, Hengxu Liu, Yufen Xiao, Jianzhong Du.  (2025)  Antioxidant glycopolymersomes with dynamic covalent glucose regulation for synergistic pancreatitis-diabetes therapy.  Nano Today,      [PMID:] [10.1016/j.nantod.2025.102871]

4. Xiaonan Qiu, Jiaying Liu, Li Song, Huijun Yu, Yunchao Wu, Qinxin Wang, Mengke Lu, Xuan Gu, Baoding Chen, Miaomiao Zhang, Fengyi Du.  (2025)  Bioorthogonal chemistry-inspired Cu/5-aminolevulinic acid self-assembled nanoparticles-crosslinked in situ hyaluronic acid hydrogel for chemo-photodynamic tumor therapy.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:40939794] [10.1016/j.ijbiomac.2025.147397]