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442475

Supelco

苯并[e]芘

analytical standard

别名:

1,2-苯并芘, 4,5-苯并芘

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About This Item

经验公式（希尔记法）:
C20H12
CAS号:
192-97-2
分子量:
252.31
Beilstein:
1911334
EC 号:
205-892-7
MDL编号:
MFCD00003605
UNSPSC代码:
12000000
PubChem化学物质编号:
24867865

等级

analytical standard

质量水平

100

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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相关类别

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。

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
MKCX0629
MKCV9270
MKCV0116
MKCR5542
MKCP8988

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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)
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)
Saffar Mansoor et al.
Investigative ophthalmology & visual science, 51(5), 2601-2607 (2009-12-05)
To study the inhibitory effects of some agents or drugs (inhibitors) on benzo(e)pyrene (B(e)P)-induced cell death and apoptosis on human retinal pigment epithelial (ARPE-19) cells in vitro. ARPE-19 cells were pretreated with varying concentrations of different classes of inhibitors (calpain
W H Houser et al.
Molecular carcinogenesis, 5(3), 232-237 (1992-01-01)
In the rat, expression of the CYP1A1 gene is closely associated with arylhydrocarbon hydroxylase (AHH) enzyme activity. AHH is an inducile enzyme activity known to play an important role in the bioactivation of polycyclic aromatic hydrocarbons (PAHs) to mutagenic and
J A Gibbons et al.
Chemico-biological interactions, 83(3), 203-220 (1992-08-28)
The objective of this study was to examine the potential for a specific ligand of carcinogen binding protein (CBP) to induce changes in the overall character of hepatic microsomal cytochromes P-450 (P450) and to compare potential changes with those induced
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