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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:
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

Signal Word

Danger

Hazard Statements

H318,H410

Hazard Classifications

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

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Lucas A Haverkate et al.
The journal of physical chemistry. B, 116(43), 13098-13105 (2012-10-05)
Discotic liquid crystalline (DLC) charge transfer (CT) complexes, which combine visible light absorption with rapid charge transfer characteristics within the CT complex, can have a great potential for photovoltaic applications when they can be made to self-assemble in a bulk
Vandana Bhalla et al.
Dalton transactions (Cambridge, England : 2003), 41(37), 11413-11418 (2012-08-15)
The binding behavior of triphenylene based copper ensemble prepared in situ has been investigated toward various anions (F(-), Cl(-), Br(-), I(-), CH(3)COO(-), H(2)PO(4)(-), NO(3)(-), OH(-), ClO(4)(-), CN(-), CO(3)(-) and SO(4)(-)) by UV-vis and fluorescence spectroscopy. Among various anions tested, 1-Cu(2+)
Ozcan Kocyigit et al.
Journal of hazardous materials, 183(1-3), 334-340 (2010-08-10)
We presented the synthesis of a novel Schiff base and its complexation properties with some transition metal ions in this work. For this, the 2,3,4,6,7,10,11 hexahydroxytriphenylene (HHTP) as starting material was synthesized according to known procedure. Moreover, the 2-((2-chloroethylimino)methyl) phenol
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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