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Merck
CN

51386

p-苯醌

pharmaceutical secondary standard; traceable to USP

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线性分子式:
C6H4(=O)2
化学文摘社编号:
分子量:
108.09
EC Number:
203-405-2
UNSPSC Code:
12352005
PubChem Substance ID:
Beilstein/REAXYS Number:
773967
MDL number:
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InChI key

AZQWKYJCGOJGHM-UHFFFAOYSA-N

InChI

1S/C6H4O2/c7-5-1-2-6(8)4-3-5/h1-4H

SMILES string

O=C1C=CC(=O)C=C1

grade

certified reference material, pharmaceutical secondary standard

agency

traceable to USP 1056504

vapor density

3.73 (vs air)

vapor pressure

0.1 mmHg ( 25 °C)

autoignition temp.

815 °F

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

mp

113-115 °C (lit.)

format

neat

storage temp.

2-8°C

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Rozbeh Baradaran et al.
Nature, 494(7438), 443-448 (2013-02-19)
Complex I is the first and largest enzyme of the respiratory chain and has a central role in cellular energy production through the coupling of NADH:ubiquinone electron transfer to proton translocation. It is also implicated in many common human neurodegenerative
Vandana Bhalla et al.
Dalton transactions (Cambridge, England : 2003), 42(4), 975-980 (2012-11-21)
A pentaquinone based compound 3a has been synthesized which undergoes significant fluorescence enhancement in the presence of Zn(2+) ions with a detection limit up to nanomolar range in THF. Further, the zinc ensemble of 3a is evaluated for its anti-oxidizing
Takafumi Hasegawa et al.
Journal of neurochemistry, 87(2), 470-475 (2003-09-27)
Oxidized metabolites of dopamine, known as dopamine quinone derivatives, are thought to play a pivotal role in the degeneration of dopaminergic neurons. Although such quinone derivatives are usually produced via the autoxidation of catecholamines, tyrosinase, which is a key enzyme
K Roberg et al.
Free radical biology & medicine, 27(11-12), 1228-1237 (2000-01-21)
Apoptosis was induced in human foreskin fibroblasts by the redox-cycling quinone naphthazarin (5,8-dihydroxy-1,4-naphthoquinone). Most of the cells displayed ultrastructure typical of apoptosis after 8 h of exposure to naphthazarin. Apoptosis was inhibited in fibroblasts pretreated with the cathepsin D inhibitor
K He et al.
Biochemical pharmacology, 62(2), 191-198 (2001-06-08)
Oxidative ring opening of troglitazone (TGZ)(1) a thiazolidine 2,4-dione derivative used for the treatment of type II diabetes mellitus, leads to the formation of a quinone metabolite. The formation of TGZ quinone was shown to be NADPH dependent and to

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