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C84801

Sigma-Aldrich

Coronene

97%

Synonym(s):

Superbenzene, [6]Circulene

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About This Item

Empirical Formula (Hill Notation):
C24H12
CAS Number:
191-07-1
Molecular Weight:
300.35
Beilstein/REAXYS Number:
658468
EC Number:
205-881-7
MDL number:
MFCD00004134
UNSPSC Code:
12352100
PubChem Substance ID:
24893062
NACRES:
NA.22

Quality Level

100

assay

97%

form

powder

bp

525 °C (lit.)

mp

428 °C (lit.)

SMILES string

c1cc2ccc3ccc4ccc5ccc6ccc1c7c2c3c4c5c67

InChI

1S/C24H12/c1-2-14-5-6-16-9-11-18-12-10-17-8-7-15-4-3-13(1)19-20(14)22(16)24(18)23(17)21(15)19/h1-12H

InChI key

VPUGDVKSAQVFFS-UHFFFAOYSA-N

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Application

Coronene can be used
  • To synthesize active materials for organic photovoltaic and optoelectronic applications.
  • As ′nucleation seed′ to synthesize graphene by vapor deposition at low temperatures.
  • To build novel polycyclic aromatic molecular frameworks and architectures.

Incorporation of coronene as ′Carbon Dot′ for bioimaging applications has been reported.

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
06121DP
00909BV

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Persulfurated Coronene: A New Generation of ?Sulflower?.
Dong R, et al.
Journal of the American Chemical Society, 139(6), 2168-2171 (2017)
Continuous graphene films synthesized at low temperatures by introducing coronene as nucleation seeds.
Wu T, et al.
Nanoscale, 5(12), 5456-5461 (2013)
Luminescent Carbon Dot Mimics Assembled on DNA.
Chan KM et al.
Journal of the American Chemical Society, 139(37), 13147-13155 (2017)
Perchlorocoronene: a novel host precursor.
Baird T, et al.
Journal of the Chemical Society. Chemical Communications, (22), 1471-1473 (1988)
Porphyrins fused with unactivated polycyclic aromatic hydrocarbons.
Diev VV, et al.
The Journal of Organic Chemistry, 77(1), 143-159 (2011)
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