442475
苯并[e]芘
analytical standard
别名:
1,2-苯并芘, 4,5-苯并芘
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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
Beilstein:
1911334
EC 号:
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
等级
analytical standard
CofA
current certificate can be downloaded
包装
ampule of 25 mg
技术
HPLC: suitable
gas chromatography (GC): suitable
mp
177-180 °C (lit.)
应用
cleaning products
cosmetics
environmental
food and beverages
personal care
包装形式
neat
储存温度
2-30°C
SMILES字符串
c1ccc2c(c1)c3cccc4ccc5cccc2c5c34
InChI
1S/C20H12/c1-2-8-16-15(7-1)17-9-3-5-13-11-12-14-6-4-10-18(16)20(14)19(13)17/h1-12H
InChI key
TXVHTIQJNYSSKO-UHFFFAOYSA-N
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一般描述
苯并[e]芘是一种五环芳烃污染物。 它是强效致癌物苯并[a]芘的结构异构体。
应用
有关合适仪器技术的更多信息，请参考产品′s分析证书。如需进一步支持，请联系技术服务。
警示用语：
Danger
危险声明
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
Formation of sulfate and glucoside conjugates of benzo [e] pyrene by Cunninghamella elegans
Pothuluri.V.J, et al.
Applied Microbiology and Biotechnology, 45, 677-683 (1996)
Photochemical transformations of benzo [e] pyrene in solution and adsorbed on silica gel and alumina surfaces
Fioressi S and Arce R
Environmental Science & Technology, 39, 3646-3655 (2005)
S Faiderbe et al.
Cancer research, 52(10), 2862-2865 (1992-05-15)
High levels of anti-phosphatidylinositol (PtdIns) autoantibodies (autoAb) have been previously described in sera of cancer patients and in plasma of dimethylbenzanthracene-treated female Sprague-Dawley rats. The presence of anti-PtdIns autoAb was tested in a model of highly malignant sarcomas induced by
Daniëlle M J Curfs et al.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 19(10), 1290-1292 (2005-06-09)
Although it has been demonstrated that carcinogenic environmental polycyclic aromatic hydrocarbons (PAHs) cause progression of atherosclerosis, the underlying mechanism remains unclear. In the present study, we aimed to investigate whether DNA binding events are critically involved in the progression of
Gabriela L Borosky et al.
Organic & biomolecular chemistry, 5(14), 2234-2242 (2007-07-05)
A DFT study aimed at understanding structure-reactivity relationships and fluorine substitution effects on carbocation stability in benzo[a]pyrene (BaP), benzo[e]pyrene (BeP), and aza-benzo[a]pyrene (aza-BaP) derivatives are reported. The relative energies of the resulting carbocations are examined and compared, taking into account
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