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About This Item
Linear Formula:
C6H4(OH)2 · C6H4O2
CAS Number:
Molecular Weight:
218.21
Beilstein:
3919222
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Assay
97%
form
powder
composition
Carbon, 63.7-68.4%
mp
167-172 °C (lit.)
functional group
ketone
SMILES string
Oc1ccc(O)cc1.O=C2C=CC(=O)C=C2
InChI
1S/C6H6O2.C6H4O2/c2*7-5-1-2-6(8)4-3-5/h1-4,7-8H;1-4H
InChI key
BDJXVNRFAQSMAA-UHFFFAOYSA-N
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General description
Quinhydrone/methanol treatment for the measurement of carrier lifetime in crystalline silicon substrates has been reported. Surface passivation of silicon substrates by quinhydrone/ethanol treatment has been investigated.
Application
Quinhydrone is a general reagent used in potentiometric titrations. It can also be used as a π-acceptor in the formation of charge-transfer complex of analytes for spectrophotometric analysis.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 3 Oral - Aquatic Acute 1
Storage Class Code
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Surface passivation effect of silicon substrates due to quinhydrone/ethanol treatment.
Takato H, et al.
Jpn J. App. Phys., Part I, 40(10A), L1003-L1003 (2001)
p-Benzosemiquinone radical anion on silver nanoparticles in water.
Tripathi G N R
Journal of the American Chemical Society, 125(5), 1178-1179 (2003)
Photoinduced electron transfer from porphyrin to C60 in a C60| porphyrin double-layer photoelectrochemical cell.
Takahashi K, et al.
Journal of Electroanalytical Chemistry, 426(1-2), 85-90 (1997)
Quinhydrone/methanol treatment for the measurement of carrier lifetime in silicon substrates.
Takato H, et al.
Jpn J. App. Phys., Part I, 41(8A), L870-L870 (2002)
Aldo Bruccoleri
AIDS research and human retroviruses, 29(1), 4-12 (2012-09-04)
Drug resistance is a key cause of failed treatment of HIV infection. The efficacy of nonnucleoside reverse transcriptase-inhibiting (NNRTI) drugs is impaired by the rapid emergence of drug-resistant mutations. The literature supports the idea that purposefully designed flexible NNRTIs at
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