所有图片(2)
About This Item
线性分子式:
H2NC6H4B(OH)2 · 0.5H2SO4
CAS号:
分子量:
185.98
Beilstein:
8094151
EC 号:
MDL编号:
UNSPSC代码:
12352103
PubChem化学物质编号:
NACRES:
NA.22
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质量水平
方案
≥95%
表单
powder
mp
≥300 °C
SMILES字符串
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
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应用
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.
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
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)
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