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F807

Sigma-Aldrich

Fluoranthene

98%

Synonym(s):

Benzo[j,k]fluorene

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About This Item

Empirical Formula (Hill Notation):
C16H10
CAS Number:
206-44-0
Molecular Weight:
202.25
Beilstein/REAXYS Number:
1907918
EC Number:
205-912-4
MDL number:
MFCD00001184
UNSPSC Code:
12352100
PubChem Substance ID:
24894957
NACRES:
NA.22

assay

98%

bp

384 °C (lit.)

mp

105-110 °C (lit.)

SMILES string

c1ccc-2c(c1)-c3cccc4cccc-2c34

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

InChI key

GVEPBJHOBDJJJI-UHFFFAOYSA-N

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Application

Fluoranthene can be used as a starting material in the synthesis of:
  • Polyfluoranthene (PFA) based conducting polymer (PFA) by electrochemical anodic oxidation using Lewis acid catalyst.
  • Substituted fluorenones.
  • Fluorescence-emitting oligofluoranthene (OFA) nanorods by oxidative oligomerization.

pictograms

Exclamation markEnvironment
GHS07,GHS09

signalword

Warning

hcodes

H302,H410

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

388.4 °F - closed cup

flash_point_c

198.0 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Synthesis of 1-Substituted Fluorenones
George SRD, et al.
Polycyclic Aromat. Compd., 36(5), 697-715 (2016)
Efficient synthesis of oligofluoranthene nanorods with tunable functionalities
Li X-G, et al.
Chemical Science, 6(12) (2015)
Electrochemical polymerization of fluoranthene and characterization of its polymers
Xu J, et al.
The Journal of Physical Chemistry B, 110(6), 2643-2648 (2006)
Stěpán Zezulka et al.
Aquatic toxicology (Amsterdam, Netherlands), 140-141, 37-47 (2013-06-12)
Polycyclic aromatic hydrocarbons (PAHs) represent one of the major groups of organic contaminants in the aquatic environment. Duckweed (Lemna minor L.) is a common aquatic plant widely used in phytotoxicity tests for xenobiotic substances. The goal of this study was
Marie Kummerová et al.
Chemosphere, 90(2), 665-673 (2012-10-18)
Introduced organic pollutants in all ecosystem compartments can cause stress resulting in a wide range of responses including different root development. In this study, the effects of a polycyclic aromatic hydrocarbon-fluoranthene (FLT; 0.1, 1 and 7 mg L(-1)) on the
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