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Benzo[e]pyrene

analytical standard

Sinonimo/i:

1,2-Benzpyrene, 4,5-Benzpyrene

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About This Item

Formula empirica (notazione di Hill):
C20H12
Numero CAS:
192-97-2
Peso molecolare:
252.31
Beilstein:
1911334
Numero CE:
205-892-7
Numero MDL:
MFCD00003605
Codice UNSPSC:
12000000
ID PubChem:
24867865

Grado

analytical standard

Livello qualitativo

100

CdA

current certificate can be downloaded

Confezionamento

ampule of 25 mg

tecniche

HPLC: suitable
gas chromatography (GC): suitable

Punto di fusione

177-180 °C (lit.)

applicazioni

cleaning products
cosmetics
environmental
food and beverages
personal care

Formato

neat

Temperatura di conservazione

2-30°C

Stringa SMILE

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
TXVHTIQJNYSSKO-UHFFFAOYSA-N

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Descrizione generale

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

Applicazioni

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

Pittogrammi

Health hazardEnvironment
GHS08,GHS09

Avvertenze

Danger

Indicazioni di pericolo

H350,H410

Classi di pericolo

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

Codice della classe di stoccaggio

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

Classe di pericolosità dell'acqua (WGK)

WGK 3

Dispositivi di protezione individuale

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

Choose from one of the most recent versions:

Certificati d'analisi (COA)

Lot/Batch Number
MKCV9270
MKCV0116
MKCR5542
MKCP8988
MKCJ7607

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If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

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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)
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
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
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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