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BCR050

Benzo[e]pyrene

BCR®, certified reference material

Sinónimos:

1,2-Benzpyrene, 4,5-Benzpyrene

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Fórmula empírica (notación de Hill):
C20H12
Número CAS:
192-97-2
Peso molecular:
252.31
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329774203
EC Number:
205-892-7
Beilstein/REAXYS Number:
1911334
MDL number:
MFCD00003605
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grade

certified reference material

agency

BCR®

manufacturer/tradename

JRC

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

mp

177-180 °C (lit.)

format

neat

storage temp.

2-8°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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Analysis Note

For more information please see:
BCR050

Legal Information

BCR is a registered trademark of European Commission

pictograms

Health hazardEnvironment
GHS08,GHS09

signalword

Danger

hcodes

H350,H410

Hazard Classifications

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

Clase de almacenamiento

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

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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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
D R Davila et al.
Journal of toxicology and environmental health. Part A, 56(4), 249-261 (2000-03-08)
It has been well established that certain polycyclic aromatic hydrocarbons (PAHs), such as 7,12-dimethylbenz[a]anthracene (DMBA), 3-methylcholanthrene (3MC), and benzo[a]pyrene (BaP), produce immunotoxicity and cancer in rodents and that these effects are also likely seen in humans. Our laboratory has found
J A Hardin et al.
Toxicology and applied pharmacology, 117(2), 155-164 (1992-12-01)
The capacity for polycyclic aromatic hydrocarbons (PAH) to suppress immune cell function has been well documented. Nevertheless, mechanisms responsible for PAH immunosuppression and potential effects of PAH on lymphocyte development (lymphopoeisis) remain poorly defined. Murine bone marrow cultures were used
Silvina Fioressi et al.
Environmental science & technology, 39(10), 3646-3655 (2005-06-16)
The photodegradation of benzo[e]pyrene (BeP), a ubiquitous polycyclic aromatic hydrocarbon (PAH) contaminant, was investigated in solution and adsorbed on surfaces modeling the atmospheric particulate matter to provide fundamental information that could help to clarify its fate in the atmosphere. Diones
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