Skip to Content
Merck
All Photos(5)

Documents

F807

Sigma-Aldrich

Fluoranthene

98%

Synonym(s):

Benzo[j,k]fluorene

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C16H10
CAS Number:
Molecular Weight:
202.25
Beilstein:
1907918
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
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

Looking for similar products? Visit Product Comparison Guide

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

Signal Word

Warning

Hazard Statements

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 2

1 of 2

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

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service