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BCR270

Triphenylene

BCR®, certified reference material

Synonym(s):

9,10-Benzophenanthrene

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About This Item

Empirical Formula (Hill Notation):
C18H12
CAS Number:
217-59-4
Molecular Weight:
228.29
Beilstein/REAXYS Number:
1342908
EC Number:
205-922-9
MDL number:
MFCD00001108
UNSPSC Code:
41116107
PubChem Substance ID:
329773803
NACRES:
NA.24

grade

certified reference material

agency

BCR®

manufacturer/tradename

JRC

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

bp

438 °C (lit.)

mp

195-198 °C (lit.)

format

neat

storage temp.

2-8°C

SMILES string

c1ccc2c(c1)c3ccccc3c4ccccc24

InChI

1S/C18H12/c1-2-8-14-13(7-1)15-9-3-4-11-17(15)18-12-6-5-10-16(14)18/h1-12H

InChI key

SLGBZMMZGDRARJ-UHFFFAOYSA-N

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Analysis Note

For more information please see:
BCR270

Legal Information

BCR is a registered trademark of European Commission

pictograms

CorrosionEnvironment
GHS05,GHS09

signalword

Danger

hcodes

H318,H410

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Jeongho Jay Lee et al.
Angewandte Chemie (International ed. in English), 51(34), 8490-8494 (2012-07-24)
Orient and conduct: Triphenylene-based discotic ionic liquid crystals (ILCs) with six imidazolium ion pendants can disperse pristine single-walled carbon nanotubes (SWNTs). When the ILC is columnarly assembled, doping with SWNTs results in macroscopic homeotropic columnar orientation. Combination of shear and
Mahuya Bagui et al.
The journal of physical chemistry. A, 115(9), 1579-1592 (2011-02-12)
A donor-acceptor charge transfer system based on two discotic mesogens has been synthesized. The donor is either a triphenylene (POG0) or a triphenylene-based conjugated dendron (POG1), while the acceptor is a perylene diimide (PDI) core. The donors are covalently linked
Wide-range 2D lattice correlation unveiled for columnarly assembled triphenylene hexacarboxylic esters.
Terutsune Osawa et al.
Angewandte Chemie (International ed. in English), 51(32), 7990-7993 (2012-07-04)
Fabián Vaca Chávez et al.
The journal of physical chemistry. B, 116(8), 2339-2346 (2012-02-23)
The Larmor frequency and temperature dependence of the proton nuclear magnetic resonance (NMR) spin-lattice relaxation time was measured in the isotropic and columnar phases of both chain-end fluorinated triphenylene disk-like and fully hydrogenated molecules. In the columnar phase, the results
Lin Jiang et al.
Organic letters, 13(12), 3020-3023 (2011-05-25)
Triphenylene has been successfully fused to the porphyrin periphery through a convenient oxidative ring-closure reaction. Bistriphenylene-fused porphyrins and a dibenzo[fg,op]tetracene-fused porphyrin have also been obtained using a similar approach. These π-extended porphyrins exhibited broadened and bathochromic shifted UV-vis absorptions.
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