86408-36-8 Purity
96%
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Specification
4-Aminophenylboronic acid (4-APBA) was employed as a key reagent for the fabrication of a portable, disposable electrochemical sensor for sulfide detection. In this study, 4-APBA was electrochemically dimerized on the surface of functionalized multi-walled carbon nanotubes (f-CNTs), forming a robust sensing interface with strong electrocatalytic activity toward sulfide. The dimerized 4-APBA enhanced electron transfer and minimized surface fouling by elemental sulfur, a common challenge in sulfide detection. The modified electrode exhibited a linear detection range of 10 µM to 2 mM and a low detection limit of 2.3 µM, demonstrating high sensitivity and selectivity. Notably, the antifouling properties of the 4-APBA/f-CNT composite allowed for reliable sulfide analysis in serum samples without complex pretreatment. The sensor was successfully applied to assess sulfide levels in clinical samples, revealing significantly lower sulfide concentrations in diabetic patients compared to healthy individuals. Furthermore, the system differentiated cancer cells from normal ones based on intracellular sulfide concentration.
4-Aminophenylboronic acid (APBA) was employed to construct a sensitive electrochemical sensor via incorporation into a reduced graphene oxide (rGO) matrix for sugar detection. The rGO/APBA composite was synthesized by adding 1 mL of a 10 mM APBA ethanol solution to 1 mL of a 0.5 mg/mL aqueous graphene oxide (GO) suspension. The mixture was stirred at 100 °C for 12 hours, facilitating in situ reduction of GO and covalent incorporation of APBA. The resulting black precipitate was collected by centrifugation at 14,000 rpm for 20 minutes, washed three times each with ethanol and water, and dried at 80 °C for 6 hours. This composite was then deposited onto glassy carbon electrodes for differential pulse voltammetry (DPV) analysis. The rGO/APBA-modified electrode demonstrated pH-dependent current responses and was capable of selectively detecting monosaccharides such as fructose, mannose, and glucose via the specific boronic acid-diol interaction
The molecular formula of 4-Aminophenylboronic acid is C6H8BNO2.
The molecular weight of 4-Aminophenylboronic acid is 136.95 g/mol.
The IUPAC name of 4-Aminophenylboronic acid is (4-aminophenyl)boronic acid.
The InChI of 4-Aminophenylboronic acid is InChI=1S/C6H8BNO2/c8-6-3-1-5(2-4-6)7(9)10/h1-4,9-10H,8H2.
The InChIKey of 4-Aminophenylboronic acid is MKPDAJWEBQRQCO-UHFFFAOYSA-N.
The canonical SMILES of 4-Aminophenylboronic acid is B(C1=CC=C(C=C1)N)(O)O.
The CAS number of 4-Aminophenylboronic acid is 89415-43-0.
The European Community (EC) number of 4-Aminophenylboronic acid is 640-548-3.
Yes, 4-Aminophenylboronic acid is a covalently-bonded unit.