49476-U
苯并[k]荧蒽溶液
100 μg/mL in methylene chloride, analytical standard
别名:
苯并[k]荧蒽 溶液
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关于此项目
经验公式（希尔记法）:
C20H12
化学文摘社编号:
分子量:
252.31
UNSPSC Code:
77101502
NACRES:
NA.24
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1873745
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
SMILES string
c1ccc2cc-3c(cc2c1)-c4cccc5cccc-3c45
InChI key
HAXBIWFMXWRORI-UHFFFAOYSA-N
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
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.
This compound is listed in the SVHC (Substances of very high concern) candidate list of ECHA (European Chemicals Agency)
Application
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
signalword
Warning
hcodes
Hazard Classifications
Carc. 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Central nervous system
存储类别
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
法规信息
危险化学品
此项目有
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
Shan Chen et al.
Environmental science & technology, 42(24), 9431-9436 (2009-01-30)
Japanese medakas (Oryzias latipes) and triolein-embedded cellulose acetate membranes (TECAMs) were exposed simultaneously to benzo[k]fluoranthene (BkF) in the static exposure system containing different concentrations of humic acid (HA). The concentration-response relationships of induced hepatic 7-ethoxysorufin-o-deethylase (EROD) activity were established in
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.
Sandra Martinez-López et al.
Journal of AOAC International, 88(4), 1247-1254 (2005-09-13)
The determination of 15 polycyclic aromatic hydrocarbons (PAHs) in olive oil samples has been improved in order to obtain a fast methodology with a low limit of detection through the combination of liquid-liquid extraction with acetonitrile and preparative gel permeation
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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