Fluoranthene

Fluoranthene
Names
Preferred IUPAC name
Fluoranthene
Other names
Benzo[jk]fluorene
Tetracyclo[7.6.1.05,16.010,15]hexadeca-1,3,5,7,9(16),10,12,14-octaene
Identifiers
3D model (JSmol)
1907918
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.005.376
EC Number
  • 205-912-4
262216
KEGG
UNII
UN number 1325, 3082
  • InChI=1S/C16H10/c1-2-8-13-12(7-1)14-9-3-5-11-6-4-10-15(13)16(11)14/h1-10H Y
    Key: GVEPBJHOBDJJJI-UHFFFAOYSA-N Y
  • InChI=1/C16H10/c1-2-8-13-12(7-1)14-9-3-5-11-6-4-10-15(13)16(11)14/h1-10H
    Key: GVEPBJHOBDJJJI-UHFFFAOYAL
  • c1ccc-2c(c1)-c3cccc4c3c2ccc4
Properties
C16H10
Molar mass 202.256 g·mol−1
Appearance Yellow to green needles
Density 1.252 g/cm3 (0 °C), solid
Melting point 110.8 °C (231.4 °F; 383.9 K)
Boiling point 375 °C (707 °F; 648 K)
265 μg/L (25 °C)
−138.0·10−6 cm3/mol
Viscosity 0.652 cP at 20 °C
Structure
Planar
0.34 D
Hazards
GHS labelling:
Warning
H302, H410
P273, P501
Flash point 210 °C (410 °F; 483 K)
Related compounds
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YN ?)
Infobox references

Fluoranthene is a polycyclic aromatic hydrocarbon (PAH). The molecule can be viewed as the fusion of naphthalene and benzene unit connected by a five-membered ring. The chemical formula is C16H10. Although samples are often pale yellow, the compound is colorless. It is soluble in nonpolar organic solvents. It is a member of the class of PAHs known as non-alternant PAHs because it has rings other than those with six carbon atoms. It is a structural isomer of the alternant PAH pyrene. It is not as thermodynamically stable as pyrene. Its name is derived from its fluorescence under UV light.