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49476-U

Supelco

Benzo(k)fluoranthene solution

100 μg/mL in methylene chloride, analytical standard

Sinonimo/i:

Benzo[k]fluoranthene solution

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About This Item

Formula empirica (notazione di Hill):
C20H12
Numero CAS:
Peso molecolare:
252.31
Beilstein:
1873745
Numero MDL:
Codice UNSPSC:
77101502
ID PubChem:
NACRES:
NA.24

Grado

analytical standard

CdA

current certificate can be downloaded

Confezionamento

ampule of 1 mL

Disponibilità

available only in Italy

Concentrazione

100 μg/mL in methylene chloride

tecniche

HPLC: suitable
gas chromatography (GC): suitable

applicazioni

environmental

Formato

single component solution

Temperatura di conservazione

2-30°C

Stringa SMILE

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
HAXBIWFMXWRORI-UHFFFAOYSA-N

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Descrizione generale

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.

Applicazioni

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

Pittogrammi

Health hazardExclamation mark

Avvertenze

Warning

Indicazioni di pericolo

Classi di pericolo

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

Organi bersaglio

Central nervous system

Codice della classe di stoccaggio

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

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable


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Certificati d'analisi (COA)

Lot/Batch Number

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Benzo[a]pyrene ≥96% (HPLC)

Sigma-Aldrich

B1760

Benzo[a]pyrene

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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