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49476-U

Supelco

Benzo(k)fluoranthene solution

100 μg/mL in methylene chloride, analytical standard

Synonym(s):

Benzo[k]fluoranthene solution

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About This Item

Empirical Formula (Hill Notation):
C20H12
CAS Number:
207-08-9
Molecular Weight:
252.31
Beilstein:
1873745
MDL number:
MFCD00046287
UNSPSC Code:
77101502
PubChem Substance ID:
329757462
NACRES:
NA.24

grade

analytical standard

CofA

current certificate can be downloaded

packaging

ampule of 1 mL

availability

available only in Italy

concentration

100 μg/mL in methylene chloride

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

environmental

format

single component solution

storage temp.

2-30°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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General description

Benzo(k)fluoranthene belongs to the class of polynuclear aromatic hydrocarbons (PAHs). PAHs are a group of well-known environmental pollutants with both mutagenic and carcinogenic properties. They are released into the environment by the pyrolysis of organic materials.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Pictograms

Health hazardExclamation mark
GHS08,GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H336,H351

Hazard Classifications

Carc. 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Central nervous system

Storage Class Code

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

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
LRAD4329
LRAC6010
LC12658
LB94018
LB69132

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E J LaVoie et al.
Cancer research, 40(12), 4528-4532 (1980-12-01)
The metabolism of the environmental agents benzo(j)-fluoranthene and benzo(k)fluoranthene was investigated using supernatants from the livers of Aroclor 1254-pretreated rats, which are effective in activating benzo(j)fluoranthene and benzo(k)fluoranthene to metabolites mutagenic toward Salmonella typhimurium TA 100. Six bands of metabolites
Hiroyuki Masaki et al.
Environmental sciences : an international journal of environmental physiology and toxicology, 13(6), 353-362 (2007-02-03)
We developed a specific analysis method for benzo[a]pyrene (B[a]P) and benzo[k]fluoranthene (B[k]F) using dual beam fluorometry. B[a]P and B[k]F exhibited two specific fluorescence intensities (up to 10-fold) compared with 22 other polycyclic aromatic hydrocarbons (PAHs) at 370 nm excitation and
Tohru Saitoh et al.
Talanta, 79(2), 177-182 (2009-06-30)
A simple and rapid method for the highly sensitive determination of polycyclic aromatic hydrocarbons (PAHs) in water was developed. Benzo[a]pyrene, benzo[k]fluoranthene, perylene, and pyrene in water were concentrated into sodium dodecyl sulfate (SDS)-alumina admicelles. The collection was performed by adding
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)
Erin E Bessette et al.
Drug metabolism and disposition: the biological fate of chemicals, 33(3), 312-320 (2004-12-04)
Polycyclic aromatic hydrocarbons (PAHs) and heavy metals are often environmental cocontaminants that could interact to alter PAH carcinogenicity. The heavy metal, arsenite, and the PAH, benzo[k]fluoranthene, were used as prototypes to investigate, in human HepG2 cells, mechanisms whereby the bioactivation
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