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45504

Supelco

Fluoranthene

analytical standard

Synonym(s):

Benzo[j,k]fluorene

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About This Item

Empirical Formula (Hill Notation):
C16H10
CAS Number:
Molecular Weight:
202.25
Beilstein/REAXYS Number:
1907918
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

bp

384 °C (lit.)

mp

105-110 °C (lit.)

application(s)

environmental

format

neat

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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General description

Fluoranthene (FA) belongs to the class of polycyclic aromatic hydrocarbons (PAHs), which are typically generated due to the incomplete burning of organic materials in the presence of oxygen in insufficient quantities. FA is regarded as an environmental indicator and is mainly used in simulation studies. It is also used in the development of a fluorescent chemosensor for the determination of explosive nitroaromatic compounds.

Application

FA may be used as an analytical standard for the determination of the analyte in food samples, oils, fats, and environmental samples by various chromatography techniques.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

pictograms

Exclamation markEnvironment

signalword

Warning

hcodes

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


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Certificates of Analysis (COA)

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Customers Also Viewed

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N Venkatramaiah et al.
Chemical communications (Cambridge, England), 48(41), 5007-5009 (2012-04-19)
A novel fluoranthene based fluorescent chemosensor for the detection of picric acid (PA) at the parts per billion (ppb) level was evaluated. Static fluorescence quenching was the dominant process by intercalative π-π interaction between fluoranthene (S(1)) and nitroaromatics.
L D Gratz et al.
Journal of hazardous materials, 74(1-2), 37-46 (2000-04-27)
For laboratories involved in polycyclic aromatic hydrocarbon (PAH) analyses in environmental samples, it is very useful to participate in interlaboratory comparison studies which provide a mechanism for comparing analytical methods. This is particularly important when PAH analyses are routinely done
Potential groundwater contamination from intentional and nonintentional stormwater infiltration
Ground Water null
G Grimmer et al.
Journal - Association of Official Analytical Chemists, 58(4), 725-733 (1975-07-01)
A method is described for the determination of polycyclic aromatic hydrocarbons (PAHs) with 3-7 rings in (I) meat, poultry, fish, and yeast; and (II) oils and fats. The extraction of PAHs from group I is incomplete, and, therefore, group I
Comparison of a capillary gas chromatographic and a high-performance liquid chromatographic method of analysis for polycyclic aromatic hydrocarbons in food
Dennis MJ, et al.
Journal of Chromatography A, 285, 127-133 (1984)

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