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Merck

392251

Benzo[k]fluoranthene

suitable for fluorescence, ≥99%

Synonym(s):

11,12-Benzofluoranthene, 2,3,1′,8′-Binaphthylene, 8,9-Benzfluoranthene

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About This Item

Empirical Formula (Hill Notation):
C20H12
CAS Number:
Molecular Weight:
252.31
UNSPSC Code:
12352103
NACRES:
NA.23
PubChem Substance ID:
EC Number:
205-916-6
Beilstein/REAXYS Number:
1873745
MDL number:
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Quality Level

assay

≥99%

mp

215-217 °C (lit.)

solubility

95% ethanol: <1 mg/mL at 20 °C, DMSO: <1 mg/mL at 20 °C, H2O: <1 mg/mL at 20 °C, acetone: 1-10 mg/mL at 20 °C, methanol: <1 mg/mL at 20 °C, toluene: 5-10 mg/mL at 20 °C

suitability

suitable for fluorescence

SMILES string

c1ccc2cc-3c(cc2c1)-c4cccc5cccc-3c45

InChI

1S/C20H12/c1-2-6-15-12-19-17-10-4-8-13-7-3-9-16(20(13)17)18(19)11-14(15)5-1/h1-12H

InChI key

HAXBIWFMXWRORI-UHFFFAOYSA-N

Application


  • Enhanced degradation of carcinogenic PAHs benzo (a) pyrene and benzo (k) fluoranthene by a microbial consortia: Bioremediation of high molecular weight PAHs with a combination of microorganisms (S Guntupalli, V Thunuguntla, 2016).

  • Biotransformation of the high‐molecular weight polycyclic aromatic hydrocarbon (PAH) benzofluoranthene by Sphingobium sp. strain KK22 and identification of metabolites: Biotransformation and identification of products from benzo[k]fluoranthene (AH Maeda, S Nishi, Y Hatada, Y Ozeki, 2014).

  • Investigation of the electrochemical properties of benzofluorenthene using a glassy carbon electrode and development of a square-wave voltammetric method for detection: Electrochemical behavior of benzo[k]fluorenthene and development of detection method (A Altun, Y Yardim, A Levent, 2023).

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.


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pictograms

Health hazardEnvironment

signalword

Danger

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

ppe

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 1B - PBT - vPvB



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K L Willett et al.
Toxicology and applied pharmacology, 177(3), 264-271 (2001-12-26)
Certainpolynuclear aromatic hydrocarbons (PAHs) such as benzo[a]pyrene (BaP) induce CYP1A-dependent enzyme activities. Because PAHs are ubiquitous environmental contaminants, and some are aryl hydrocarbon agonists, CYP1A has been used as a biomarker for PAH exposure. However, PAHs exist in the environment
Hiroyuki Masaki et al.
The Analyst, 130(9), 1253-1257 (2005-08-13)
We developed a device and some systems for detecting benzo[a]pyrene (B[a]P) and benzo[k]fluoranthene (B[k]F). The device uses a UV light-emitting diode that emits light with a wavelength of 370 nm and a violet laser diode that emits light with a
G Verrhiest et al.
Ecotoxicology (London, England), 10(6), 363-372 (2002-01-05)
Polycyclic Aromatic Hydrocarbons (PAHs) are ubiquitous pollutants of sediments. Sediment quality criteria often use toxicity data for individual PAHs. However, PAHs always occur in field sediments as a complex mixture of compounds. In this study, the toxicity of phenanthrene (P)