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ERD-051

Supelco

Dibenzo[a,l]pyren

vial of 25 mg, Cerilliant®

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About This Item

Empirische Formel (Hill-System):
C24H14
CAS-Nummer:
191-30-0
Molekulargewicht:
302.37
Beilstein:
2054068
EG-Nummer:
205-886-4
MDL-Nummer:
MFCD00467035
UNSPSC-Code:
41116107
PubChem Substanz-ID:
329799585
NACRES:
NA.24

Qualität

analytical standard

Verpackung

vial of 25 mg

Hersteller/Markenname

Cerilliant®

Anwendung(en)

environmental
forensics and toxicology

Format

neat

Lagertemp.

room temp

SMILES String

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

InChIKey

JNTHRSHGARDABO-UHFFFAOYSA-N

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Allgemeine Beschreibung

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.

Anwendung

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.

Rechtliche Hinweise

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

Piktogramme

Health hazardCorrosion
GHS08,GHS05

Signalwort

Danger

Gefahreneinstufungen

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

Lagerklassenschlüssel

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

WGK

WGK 3

Analysenzertifikate (COA)

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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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