A71751
3-Aminophenylboronic acid hemisulfate salt
≥95%
Synonym(s):
(3-Aminophenyl)boric acid hemisulfate, (3-aminophenyl)-boronic acid sulfate (2:1), (m-Aminophenyl)boronic acid hemisulfate, 3-Aminobenzeneboronic acid hemisulfate salt, Bis[3-dihydroxyboranyl)benzenaminium] sulfate
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About This Item
Linear Formula:
H2NC6H4B(OH)2 · 0.5H2SO4
CAS Number:
Molecular Weight:
185.98
UNSPSC Code:
12352103
NACRES:
NA.22
PubChem Substance ID:
EC Number:
266-376-5
Beilstein/REAXYS Number:
8094151
MDL number:
assay
≥95%
form
powder
mp
≥300 °C
SMILES string
OS(O)(=O)=O.Nc1cccc(c1)B(O)O.Nc2cccc(c2)B(O)O
InChI
1S/2C6H8BNO2.H2O4S/c2*8-6-3-1-2-5(4-6)7(9)10;1-5(2,3)4/h2*1-4,9-10H,8H2;(H2,1,2,3,4)
InChI key
UKTAURVTSWDIQR-UHFFFAOYSA-N
Application
3-Aminophenylboronic acid hemisulfate salt is used in the synthesis of:
It can also be used in the preparation of phenylboronic acid (PBA) monolayer-modified Au electrode for the voltammetric sensing of uridine and cytidine.
- Phenylboronic acid-functionalized inverse opal hydrogels within microfluidic flow cells for glucose sensing.
- Phenylboronic acid-salicylhydroxamic acid-derived complexing reagent for protein immobilization on chromatographic support.
It can also be used in the preparation of phenylboronic acid (PBA) monolayer-modified Au electrode for the voltammetric sensing of uridine and cytidine.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Related Content
Glucose-sensitive inverse opal hydrogels: analysis of optical diffraction response
Lee Y, et al.
Langmuir, 20(8), 3096-3106 (2004)
Phenylboronic acid- salicylhydroxamic acid bioconjugates. 1. A novel boronic acid complex for protein immobilization
Stolowitz ML, et al.
Bioconjugate Chemistry, 12(2), 229-239 (2001)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| A71751-25G | 04061833383759 |
| A71751-5G | 04061833383766 |