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About This Item
Empirical Formula (Hill Notation):
C16H10
CAS Number:
Molecular Weight:
202.25
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
205-912-4
Beilstein/REAXYS Number:
1907918
MDL number:
Product Name
Fluoranthene, 98%
InChI key
GVEPBJHOBDJJJI-UHFFFAOYSA-N
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
SMILES string
c1ccc-2c(c1)-c3cccc4cccc-2c34
assay
98%
bp
384 °C (lit.)
mp
105-110 °C (lit.)
Quality Level
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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.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1
Storage Class
11 - Combustible Solids
wgk
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
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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
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
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