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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:
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

Signal Word

Warning

Hazard Statements

H302,H410

Hazard Classifications

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

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

388.4 °F - closed cup

Flash Point(C)

198.0 °C - closed cup

Personal Protective Equipment

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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Efficient synthesis of oligofluoranthene nanorods with tunable functionalities
Li X-G, et al.
Chemical Science, 6(12) (2015)
Synthesis of 1-Substituted Fluorenones
George SRD, et al.
Polycyclic Aromat. Compd., 36(5), 697-715 (2016)
Electrochemical polymerization of fluoranthene and characterization of its polymers
Xu J, et al.
The Journal of Physical Chemistry B, 110(6), 2643-2648 (2006)
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
A P Rodrigues et al.
The Science of the total environment, 443, 454-463 (2012-12-12)
Fluoranthene (FLU) is a priority polycyclic aromatic hydrocarbon (PAH) commonly detected in estuarine sediments, water and biota. Despite this, information on FLU detection, accumulation and effects on marine crustaceans is scarce. This work investigated the accumulation of FLU in Carcinus
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