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49476-U

Supelco

Benzo(k)fluoranthene solution

100 μg/mL in methylene chloride, analytical standard

Sinônimo(s):

Benzo[k]fluoranthene solution

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About This Item

Fórmula empírica (Notação de Hill):
C20H12
Número CAS:
207-08-9
Peso molecular:
252.31
Beilstein:
1873745
Número MDL:
MFCD00046287
Código UNSPSC:
77101502
ID de substância PubChem:
329757462
NACRES:
NA.24

grau

analytical standard

Certificado de análise (CofA)

current certificate can be downloaded

embalagem

ampule of 1 mL

disponibilidade

available only in Italy

concentração

100 μg/mL in methylene chloride

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

aplicação(ões)

environmental

Formato

single component solution

temperatura de armazenamento

2-30°C

cadeia de caracteres SMILES

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

chave InChI

HAXBIWFMXWRORI-UHFFFAOYSA-N

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Descrição geral

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.[1]

Aplicação

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

Pictogramas

Health hazardExclamation mark
GHS08,GHS07

Palavra indicadora

Warning

Frases de perigo

H315,H319,H336,H351

Classificações de perigo

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

Órgãos-alvo

Central nervous system

Código de classe de armazenamento

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

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Escolha uma das versões mais recentes:

Certificados de análise (COA)

Lot/Batch Number
LC12658
LB94018
LB69132

Não está vendo a versão correta?

Se precisar de uma versão específica, você pode procurar um certificado específico pelo número do lote ou da remessa.

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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
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
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
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