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Merck
CN

48492

Supelco

苯并[k]荧蒽

analytical standard

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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:
207-08-9
分子量:
252.31
Beilstein:
1873745
EC 号:
205-916-6
MDL编号:
MFCD00046287
UNSPSC代码:
23151816
PubChem化学物质编号:
24872001

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等级

analytical standard

包装

ampule of 50 mg

技术

HPLC: suitable
gas chromatography (GC): suitable

mp

215-217 °C (lit.)

溶解性

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

应用

cleaning products
cosmetics
environmental
food and beverages
personal care

包装形式

neat

储存温度

2-8°C

SMILES字符串

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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一般描述

Benzo[k]fluoranthene belongs to the class of polycyclic aromatic hydrocarbons. It can find applications as a chemical sensor for nitrated aromatic compounds via fluorescence quenching of benzo[k]fluoranthene in poly(vinyl alcohol) film. It can also serve as a potential candidate in organic light emitting diodes.
This compound is listed in the SVHC (Substances of very high concern) candidate list of ECHA (European Chemicals Agency)

应用

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

象形图

Health hazardEnvironment
GHS08,GHS09

警示用语：

Danger

危险声明

H350,H410

危险分类

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

储存分类代码

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

WGK

WGK 3

个人防护装备

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
LC25169V
LC23841V
LC18307V
LC10008V
LB92853V

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Optical absorption and emission properties of fluoranthene, benzo [k] fluoranthene, and their derivatives. A DFT study
Saranya.G, et al.
The Journal of Physical Chemistry A, 115, 14647-14656 (2011)
Fluorescence quenching of benzo [k] fluoranthene in poly (vinyl alcohol) film: a possible optical sensor for nitro aromatic compounds
Patra D and Mishra.K.A
Sensors and Actuators B, Chemical, 80, 278-282 (2001)
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.
K L Willett et al.
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
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