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Supelco

Benzo[e]pyrene

analytical standard

Synonym(s):

1,2-Benzpyrene, 4,5-Benzpyrene

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About This Item

Empirical Formula (Hill Notation):
C20H12
CAS Number:
192-97-2
Molecular Weight:
252.31
Beilstein:
1911334
EC Number:
205-892-7
MDL number:
MFCD00003605
UNSPSC Code:
12000000
PubChem Substance ID:
24867865

grade

analytical standard

Quality Level

100

CofA

current certificate can be downloaded

packaging

ampule of 25 mg

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

mp

177-180 °C (lit.)

application(s)

cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

storage temp.

2-30°C

SMILES string

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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General description

Benzo[e]pyrene is a pentacyclic aromatic hydrocarbon contaminant. It is a structural isomer of the potent carcinogen benzo[a]pyrene.

Application

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

Pictograms

Health hazardEnvironment
GHS08,GHS09

Signal Word

Danger

Hazard Statements

H350,H410

Hazard Classifications

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

Storage Class Code

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

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCV9270
MKCV0116
MKCR5542
MKCP8988
MKCJ7607

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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
Joris J H Haftka et al.
Environmental toxicology and chemistry, 27(7), 1526-1532 (2008-02-12)
The uptake kinetics of fluorene, phenanthrene, fluoranthene, pyrene, and benzo[e]pyrene by solid-phase microextraction fibers was studied in the presence of dissolved organic matter (DOM) obtained from sediment pore water and resulted in increased fiber absorption and desorption rate coefficients. Compared
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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