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Safety Information

392251

Sigma-Aldrich

Benzo[k]fluoranthene

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:
207-08-9
Molecular Weight:
252.31
Beilstein:
1873745
EC Number:
205-916-6
MDL number:
MFCD00046287
UNSPSC Code:
12352103
PubChem Substance ID:
24864439
NACRES:
NA.23

grade

for fluorescence

Quality Level

200

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

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

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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.

Pictograms

Health hazardEnvironment
GHS08,GHS09

Signal Word

Danger

Hazard Statements

H350,H410

Hazard Classifications

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

Storage Class Code

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

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

392251-100MG:
392251-BULK:
392251-25MG:
392251-25G:
392251-VAR:

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Certificates of Analysis (COA)

Lot/Batch Number
BCCH2425
BCCG5267
BCCG3781
BCCD6599
BCCC3079

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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
Annekatrin Dreyer et al.
Environmental science & technology, 39(11), 3918-3924 (2005-06-30)
To date, studies about historic PAH (polycyclic aromatic hydrocarbons) deposition at a regional scale have rarely been published. To address this research gap, we sampled 17 ombrotrophic peatlands across eastern Canada. The peat cores from hollows were dated with 210Pb
Petra Booij et al.
Environmental toxicology and chemistry, 30(4), 898-904 (2010-12-31)
In bioassays, exposure concentrations of test compounds are usually expressed as nominal concentrations. As a result of various processes, such as adsorption, degradation, or uptake, the actual freely dissolved concentration of the test compound may differ from the nominal concentration.
Alberto Modelli et al.
The journal of physical chemistry. A, 110(20), 6482-6486 (2006-05-19)
The gas-phase experimental adiabatic electron affinities (AEAs) of the polycyclic aromatic hydrocarbons (PAHs) anthracene, tetracene, pentacene, chrysene, pyrene, benzo[a]pyrene, benzo[e]pyrene, and fluoranthene are well reproduced using the hybrid density functional method B3LYP with the 6-31+G* basis set, indicating that the
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