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线性分子式:
(HO)2C6H3CH2NH2 · HBr
化学文摘社编号:
分子量:
220.06
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
240-382-8
Beilstein/REAXYS Number:
4002646
MDL number:
Assay:
98%
Form:
crystals
InChI
1S/C7H9NO2.BrH/c8-4-5-1-2-6(9)7(10)3-5;/h1-3,9-10H,4,8H2;1H
InChI key
BVFZTXFCZAXSHN-UHFFFAOYSA-N
SMILES string
Br.NCc1ccc(O)c(O)c1
assay
98%
form
crystals
mp
184-186 °C (lit.)
functional group
amine
Quality Level
Application
<ul>
<li><strong>3,4-二羟基苯乙胺的氧化聚合:</strong>用3,4-二羟基苯乙胺通过氧化聚合制备聚3,4-二羟基苯乙胺(PDHBA),说明本品作为多巴胺的偏小类似物(lower homolog)可用于合成与材料科学(Petran et al., 2023)。</li>
<li><strong>尿游离甲氧基肾上腺素类物质的检测:</strong>以3,4-二羟基苯乙胺为内标,提高尿游离甲氧基肾上腺素类物质检测的准确性,用于嗜铬细胞瘤和副神经节瘤诊断。表明临床诊断应用意义(Wang et al., 2020)。</li>
<li><strong>HPLC-ECD方法开发:</strong>以3,4-二羟基苯乙胺为内标,开发HPLC-ECD方法分析血浆中的维生素C。体现其化学性质有利于生化研究的分析方法改进(Clark and Frank, 2016)。</li>
<li><strong>儿茶酚胺类物质的荧光分析:</strong>用3,4-二羟基苯乙胺作为内标测定大鼠脑组织中的儿茶酚胺及相关物质,体现神经化学分析和研究应用价值(Fonseca et al., 2017)。</li>
</ul>
<li><strong>3,4-二羟基苯乙胺的氧化聚合:</strong>用3,4-二羟基苯乙胺通过氧化聚合制备聚3,4-二羟基苯乙胺(PDHBA),说明本品作为多巴胺的偏小类似物(lower homolog)可用于合成与材料科学(Petran et al., 2023)。</li>
<li><strong>尿游离甲氧基肾上腺素类物质的检测:</strong>以3,4-二羟基苯乙胺为内标,提高尿游离甲氧基肾上腺素类物质检测的准确性,用于嗜铬细胞瘤和副神经节瘤诊断。表明临床诊断应用意义(Wang et al., 2020)。</li>
<li><strong>HPLC-ECD方法开发:</strong>以3,4-二羟基苯乙胺为内标,开发HPLC-ECD方法分析血浆中的维生素C。体现其化学性质有利于生化研究的分析方法改进(Clark and Frank, 2016)。</li>
<li><strong>儿茶酚胺类物质的荧光分析:</strong>用3,4-二羟基苯乙胺作为内标测定大鼠脑组织中的儿茶酚胺及相关物质,体现神经化学分析和研究应用价值(Fonseca et al., 2017)。</li>
</ul>
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
E C Chan et al.
Rapid communications in mass spectrometry : RCM, 14(21), 1959-1964 (2000-11-21)
An assay of norepinephrine (NE), epinephrine (E), dopamine (DA), normetanephrine (NE) and metanephrine (MN) based on high-performance liquid chromatography (HPLC) in combination with atmospheric pressure chemical ionization mass spectrometry (APcI-MS) is described. The catecholamines and metanephrines were extracted from urine
J A Prezioso et al.
Pigment cell research, 3(2), 49-54 (1990-03-01)
The rationale for melanoma specific dihydroxybenzene containing antitumor agents is based in part upon the ability of the enzyme tyrosinase to oxidize these pro drugs to toxic intermediates. In situ tyrosinase activity was demonstrated to be affected by both cell
H B He et al.
Journal of chromatography, 574(2), 213-218 (1992-02-14)
This paper describes the application of a window diagram technique to optimize the four components of eluent (sodium acetate, sodium heptanesulfonate, acetonitrile and pH adjusted by monochloroacetic acid), for complete separation of five catecholamine compounds and the internal standard (3,4-dihydroxybenzylamine
F Boomsma et al.
Journal of cardiovascular pharmacology, 22(2), 198-202 (1993-08-01)
We noted rapid breakdown at 4 degrees and 20 degrees C of dopamine (DA) (but not of (nor)epinephrine and epinine) in pig plasma, but not in human plasma. The enzyme responsible appears to be a semicarbazide-sensitive amine oxidase (SSAO) because
J A Prezioso et al.
The Journal of investigative dermatology, 99(3), 289-293 (1992-09-01)
Buthionine sulfoximine (BSO), a specific inhibitor of glutathione synthesis, showed variable growth-inhibitory activity in different tumor cell lines with a high degree of inhibitory activity against melanoma-derived cell lines. A correlation between BSO growth-inhibitory effects and cellular glutathione peroxidase activity
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