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Merck

BCR134

Benzo[c]phenanthrene

BCR®, certified reference material

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About This Item

Fórmula empírica (notación de Hill):
C18H12
Número de CAS:
Peso molecular:
228.29
Beilstein:
1909296
Número CE:
Número MDL:
Código UNSPSC:
41116107
ID de la sustancia en PubChem:
NACRES:
NA.24

grado

certified reference material

Agency

BCR®

fabricante / nombre comercial

JRC

técnicas

HPLC: suitable
gas chromatography (GC): suitable

Formato

neat

temp. de almacenamiento

2-8°C

cadena SMILES

c1ccc2c(c1)ccc3ccc4ccccc4c23

InChI

1S/C18H12/c1-3-7-16-13(5-1)9-11-15-12-10-14-6-2-4-8-17(14)18(15)16/h1-12H

Clave InChI

TUAHORSUHVUKBD-UHFFFAOYSA-N

Nota de análisis

For more information please see:
BCR134

Información legal

BCR is a registered trademark of European Commission

Pictogramas

Exclamation mark

Palabra de señalización

Warning

Clasificaciones de peligro

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Órganos de actuación

Respiratory system

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Equipo de protección personal

dust mask type N95 (US), Eyeshields, Gloves


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R B Roth et al.
Biochemistry, 40(17), 5200-5207 (2001-04-25)
Benzo[c]phenanthrene diol epoxide (B[c]PhDE), the ultimate carcinogenic metabolite of the environmental pollutant benzo[c]phenanthrene, reacts with DNA primarily at the exocyclic amino groups of purines, forming B[c]PhDE-DNA adducts that differ in their stereochemical configurations and their effect on biological processes such
Min Wu et al.
Frontiers in bioscience : a journal and virtual library, 9, 2807-2818 (2004-09-09)
Remarkably different conformations can result when DNA binds with stereoisomeric compounds containing differing absolute configurations of substituents about chiral carbon atoms. Furthermore, the biochemical functions of covalent adducts with DNA are strongly affected by the stereochemistry of the ligands. Such
Carol D Swartz et al.
Mutation research, 661(1-2), 47-56 (2008-12-02)
Sulfur-containing polycyclic aromatic hydrocarbons (thia-PAHs or thiaarenes) are common constituents of air pollution and cigarette smoke, but only a few have been studied for health effects. We evaluated the mutagenicity in Salmonella TA98, TA100, and TA104 of two sulfur-containing derivatives
H J Einolf et al.
Carcinogenesis, 17(10), 2237-2244 (1996-10-01)
Benzo[c]phenanthrene (B[c]Ph) is an environmental contaminant with low carcinogenic activity in rodent bioassays. B[c]Ph-3,4-diol-1,2-epoxides (B[c]PhDE), however, are among the most tumorigenic diol epoxides known. To determine whether human cells are capable of activating B[c]Ph to DNA-binding metabolites, cultures of the
V P Gupta et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 72(1), 82-101 (2008-10-22)
A systematic study has been conducted on the conformation, electronic structure and vibrational spectra of benzo[c]phenanthrene and some of its partially reduced derivatives by experimental infrared spectroscopic and quantum chemical techniques. Electrostatic potential surfaces have been mapped over the electron

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