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BCR134

Benzo[c]phenanthren

BCR®, certified reference material

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About This Item

Empirische Formel (Hill-System):
C18H12
CAS-Nummer:
195-19-7
Molekulargewicht:
228.29
Beilstein:
1909296
EG-Nummer:
205-896-9
MDL-Nummer:
MFCD00019126
UNSPSC-Code:
41116107
PubChem Substanz-ID:
329774224
NACRES:
NA.24

Qualität

certified reference material

Agentur

BCR®

Hersteller/Markenname

JRC

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Format

neat

Lagertemp.

2-8°C

SMILES String

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

InChIKey

TUAHORSUHVUKBD-UHFFFAOYSA-N

Verwandte Kategorien

Hinweis zur Analyse

For more information please see:
BCR134

Rechtliche Hinweise

BCR is a registered trademark of European Commission

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

Gefahreneinstufungen

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

Zielorgane

Respiratory system

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves

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Analysenzertifikate (COA)

Lot/Batch Number

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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
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
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
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
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
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