F807
Fluoranthene
98%
Synonym(s):
Benzo[j,k]fluorene
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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:
Assay:
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.)
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.
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
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - PBT - vPvB
Regulatory Information
危险化学品
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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)
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
Sherain N Al-Subiai et al.
Mutation research, 745(1-2), 92-103 (2012-01-11)
Whilst there is growing concern over the potential detrimental impact of engineered nanoparticles (ENPs) on the natural environment, little is known about their interactions with other contaminants. In the present study, marine mussels (Mytilus sp.) were exposed for 3 days
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