45804
Triphenylene
analytical standard
Synonym(s):
9,10-Benzophenanthrene
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About This Item
Empirical Formula (Hill Notation):
C18H12
CAS Number:
Molecular Weight:
228.29
Beilstein:
1342908
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24
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grade
analytical standard
Quality Level
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable
gas chromatography (GC): suitable
bp
438 °C (lit.)
mp
195-198 °C (lit.)
application(s)
environmental
format
neat
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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General description
Triphenylene belongs to the class of polycyclic aromatic hydrocarbons, which is commonly employed as a substrate for use as a precursor for the synthesis of graphenes, carbon nanotubes, buckminsterfullerenes as well as polycyclic heteroaromatics.
Application
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Triphenylene may be used as an analytical reference standard for the quantification of the analyte in environmental samples using gas chromatography technique.
Recommended products
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Signal Word
Danger
Hazard Statements
Precautionary Statements
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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Analysis of polycyclic aromatic hydrocarbons (PAHs) in environmental samples: a critical review of gas chromatographic (GC) methods
Poster.LD, et al.
Analytical and Bioanalytical Chemistry, 386(4), 859-881 (2006)
Analysis of polycyclic aromatic hydrocarbons (PAHs) in environmental samples: a critical review of gas chromatographic (GC) methods
Prasad RP, et al.
Journal of Chemical Sciences (Bangalore), 126(5), 1311-1321 (2014)
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.
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
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
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