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Merck
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ERD-051

Supelco

Dibenzo[a,l]pyrene

vial of 25 mg, Cerilliant®

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About This Item

Formula empirica (notazione di Hill):
C24H14
Numero CAS:
191-30-0
Peso molecolare:
302.37
Beilstein:
2054068
Numero CE:
205-886-4
Numero MDL:
MFCD00467035
Codice UNSPSC:
41116107
ID PubChem:
329799585
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

100

Confezionamento

vial of 25 mg

Produttore/marchio commerciale

Cerilliant®

applicazioni

environmental
forensics and toxicology

Formato

neat

Temperatura di conservazione

room temp

Stringa SMILE

c1ccc2c(c1)cc3ccc4cccc5c6ccccc6c2c3c45

InChI

1S/C24H14/c1-2-8-18-16(6-1)14-17-13-12-15-7-5-11-20-19-9-3-4-10-21(19)24(18)23(17)22(15)20/h1-14H
JNTHRSHGARDABO-UHFFFAOYSA-N

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Descrizione generale

Dibenzo[a,l]pyrene is a polycyclic aromatic hydrocarbon (PAH) found in cigarette smoke condensate and coal combustion. It is an environmental pollutant and a potent carcinogen known to induce tumors in rat mammary gland, mouse skin, lungs and liver.

Applicazioni

Dibenzo[a,l]pyrene may be used as an analytical standard for the determination of the analyte in crude extracts of environmental samples, water samples and Chinese coal fly ash CRM by chromatography and spectrometry techniques.

Note legali

CERILLIANT is a registered trademark of Merck KGaA, Darmstadt, Germany

Pittogrammi

Health hazardCorrosion
GHS08,GHS05

Avvertenze

Danger

Indicazioni di pericolo

H318,H341,H350

Classi di pericolo

Carc. 1B - Eye Dam. 1 - Muta. 2

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

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Direct determination of dibenzo [a, l] pyrene in crude extracts of environmental samples by laser-excited Shpol'skii spectroscopy
Kozin IS, et al.
Analytical Chemistry, 67(9), 1623-1626 (1995)
Fredine T Lauer et al.
Journal of toxicology and environmental health. Part A, 76(1), 16-24 (2012-11-16)
Dibenzo[def,p]chrysene (DBC) is a potent environmental carcinogen in rodents, fish, and human cells examined in culture. There are numerous similarities between the patterns of cytochrome P-450 (P450) activation of DBC and its covalent binding to DNA and proteins with another
Susan Ritger Crowell et al.
Toxicology and applied pharmacology, 257(3), 365-376 (2011-10-18)
Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous environmental contaminants generated as byproducts of natural and anthropogenic combustion processes. Despite significant public health concern, physiologically based pharmacokinetic (PBPK) modeling efforts for PAHs have so far been limited to naphthalene, plus simpler PK
Kun-Ming Chen et al.
International journal of cancer, 133(6), 1300-1309 (2013-03-14)
We previously reported that dibenzo[a,l]pyrene (DB[a,l]P), the most potent known environmental carcinogen among polycyclic aromatic hydrocarbons (PAH) congeners, is carcinogenic in the oral tissues of mice. We have now developed a new mouse model which employs the oral application of
Yijin Tang et al.
Biochemistry, 51(48), 9751-9762 (2012-11-06)
The most potent tumorigen identified among the polycyclic aromatic hydrocarbons (PAH) is the nonplanar fjord region dibenzo[a,l]pyrene (DB[a,l]P). It is metabolically activated in vivo through the widely studied diol epoxide (DE) pathway to form covalent adducts with DNA bases, predominantly
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