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195464

Sigma-Aldrich

2,5-Dihydroxy-1,4-benzoquinone

98%

Sinónimos:

2,5-Dihydroxy-2,5-cyclohexadiene-1,4-dione, 2,5-Dihydroxy-p -benzoquinone, 2,5-Dihydroxycyclohexa-2,5-diene-1,4-dione, Anilic acid

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About This Item

Fórmula lineal:
(HO)2C6H2(=O)2
Número de CAS:
615-94-1
Peso molecular:
140.09
EC Number:
210-454-3
MDL number:
MFCD00001598
UNSPSC Code:
12162002
PubChem Substance ID:
24851694
NACRES:
NA.23

Quality Level

100

assay

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

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number
STBK7968
STBK7214
STBK9724
STBJ8935
STBJ1990

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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
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
M Ahmed et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 56(5), 965-981 (2000-05-16)
The electronic absorption spectra of 1,4-benzoquinone (BQ) and its 2,5-dihydroxy and tetrahydroxy derivatives have been studied in detail. The interpretation of the electronic bands is made on the basis of PPP and CNDO calculations. It is found that the pi
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