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Sigma-Aldrich

5,12-Naphthacenequinone

97%

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About This Item

Empirical Formula (Hill Notation):
C18H10O2
CAS Number:
1090-13-7
Molecular Weight:
258.27
Beilstein/REAXYS Number:
1880180
EC Number:
214-127-6
MDL number:
MFCD00003701
UNSPSC Code:
12352100
PubChem Substance ID:
24851878
NACRES:
NA.22

assay

97%

mp

282-286 °C (dec.) (lit.)

functional group

ketone

SMILES string

O=C1c2ccccc2C(=O)c3cc4ccccc4cc13

InChI

1S/C18H10O2/c19-17-13-7-3-4-8-14(13)18(20)16-10-12-6-2-1-5-11(12)9-15(16)17/h1-10H

InChI key

LZPBKINTWROMEA-UHFFFAOYSA-N

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General description

The electronic structure of the lowest excited triplet state of 5,12-naphthacenequinone was studied using pulsed electron nuclear double resonance and continuous-wave time-resolved EPR (cw-TREPR).

Application

5,12-Naphthacenequinone was used to study the phototransformation of phenol in aqueous solution.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
MKBR6544V
MKBF3933
05630CH
04406TW
05414BX

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Valter Maurino et al.
Physical chemistry chemical physics : PCCP, 13(23), 11213-11221 (2011-05-17)
The phototransformation of phenol in aqueous solution was studied with different quinoid compounds, which are usually detected on atmospheric particulate matter: 2-ethylanthraquinone (EtAQ), benzanthracene-7,12-dione (BAD), 5,12-naphthacenequinone (NQ), 9,10-anthraquinone (AQ), and 2,6-dihydroxyanthraquinone (DAQ). All the studied quinones were able to sensitise
Takuji Shimokage et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 58(6), 1201-1208 (2002-05-08)
Continuous-wave time-resolved EPR (cw-TREPR) and pulsed electron nuclear double resonance (ENDOR) studies have been carried out to clarify the electronic structure of the lowest excited triplet (Tl) state of 5,12-naphthacenequinone (5,12-NpQ) as well as 1,4-anthraquinone (1,4-AQ) and 6,13-pentacenequinone (6,13-PeQ). The

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