Merck
CN

195464

Sigma-Aldrich

2,5-二羟基-1,4-苯醌

98%

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别名:
2,5-二羟基-2,5-环己二烯-1,4-二酮, 2,5-二羟基-p -苯醌, 2,5-二羟基环己基-2,5-二烯-1,4-二酮, 2,5-二羟基苯醌
线性分子式:
(HO)2C6H2(=O)2
CAS号:
分子量:
140.09
EC 号:
MDL编号:
PubChem化学物质编号:
NACRES:
NA.23

质量水平

检测方案

98%

mp

235 °C (dec.) (lit.)

SMILES string

OC1=CC(=O)C(O)=CC1=O

InChI

1S/C6H4O4/c7-3-1-4(8)6(10)2-5(3)9/h1-2,7,10H

InChI key

QFSYADJLNBHAKO-UHFFFAOYSA-N

象形图

Exclamation mark

警示用语:

Warning

危险分类

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

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


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Nathalie Honorio-Felício et al.
Journal of inorganic biochemistry, 164, 34-41 (2016-09-12)
Conformational changes associated to sensing mechanisms of heme-based protein sensors are a key molecular event that seems to modulate not only the protein activity but also the potential of the Fe
Fengxia Chen et al.
Chemosphere, 250, 126226-126226 (2020-02-24)
A novel catalyst which integrates heterogeneous and homogenous Fenton reactions is designed and fabricated by encapsulating 2,5-dihydroxy-1,4-benzoquinone (2,5-DBQ) in ECDP-Fe3O4, a composite of Fe3O4 nanoparticles immobilized on a β-cyclodextrin polymer (ECDP) with ethylene diamine tetraacetic acid (EDTA) as cross-linking agent.
A Pawlukojć et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 59(3), 537-542 (2003-01-14)
Inelastic neutron scattering (INS) spectra of solid 2,5-dihydroxy-1,4-benzoquinone were measured and compared with IR and Raman data. The INS spectrum is very well reproduced in the region below 1000 cm(-1) by DFT calculations on the B3LYP/6-311++G** level using Gaussian and
P G Jene et al.
Acta crystallographica. Section C, Crystal structure communications, 57(Pt 6), 730-734 (2001-06-16)
The X-ray structure of 1,2,4,5-tetrahydroxybenzene (benzene-1,2,4,5-tetrol) monohydrate, C6H6O4*H2O, (I), reveals columns of 1,2,4,5-tetrahydroxybenzene parallel to the b axis that are separated by 3.364 (12) and 3.453 (11) A. Molecules in adjacent columns are tilted relative to each other by 27.78
Jan Bohuslavek et al.
Biodegradation, 16(4), 353-362 (2005-05-04)
Hydroxyquinol, a common metabolite of aromatic compounds, is readily auto-oxidized to hydroxyquinone. Enzymatic activities that metabolized hydroxyquinone were observed from the cell extracts of Sphingobium chlorophenolicum ATCC 39723. An enzyme capable of transforming hydroxyquinone was partially purified, and its activities

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