Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

BCR265

Dibenzo[a,e]fluoranthene

BCR®, certified reference material

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C24H14
CAS Number:
5385-75-1
Molecular Weight:
302.37
Beilstein:
2120920
MDL number:
MFCD00215892
UNSPSC Code:
41116107
PubChem Substance ID:
329773799
NACRES:
NA.24

grade

certified reference material

Agency

BCR®

manufacturer/tradename

JRC

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

format

neat

storage temp.

2-8°C

SMILES string

c1ccc-2c(c1)-c3cc4ccccc4c5cc6ccccc6c-2c35

InChI

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

InChI key

JHOWUOKQHJHGMU-UHFFFAOYSA-N

Analysis Note

For more information please see:
BCR265

Legal Information

BCR is a registered trademark of European Commission

Pictograms

Health hazard
GHS08

Signal Word

Warning

Hazard Statements

H351

Precautionary Statements

P201 - P308 + P313

Hazard Classifications

Carc. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

It looks like we've run into a problem, but you can still download Certificates of Analysis from our Documents section.

If you need assistance, please contact Customer Support.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Metabolic activation of dibenzo(a,e)fluoranthene, a nonalternant carcinogenic polycyclic hydrocarbon, in liver homogenates.
O Perin-Roussel et al.
Cancer research, 40(5), 1742-1749 (1980-05-01)
F Zajdela et al.
Carcinogenesis, 8(3), 461-464 (1987-03-01)
Dibenzofluoranthene-12,13-dihydrodiol (DBF-12,13-DHD) is six times more mutagenic in Salmonella TA100 than dibenzofluoranthene-3,4-dihydrodiol (DBF-3,4-DHD). However, these two major dibenzo[a,e]fluoranthene (DBF) proximate metabolites, which are immediate precursors of the corresponding diolepoxides, showed on an equimolar basis nearly identical initiation activities on mouse
O Perin-Roussel et al.
Cancer letters, 36(2), 169-180 (1987-08-01)
The production by dibenzo[a,e]fluoranthene (DBF) of DNA-protein cross-links in cultured mouse fibroblasts is probably mediated by the activation of proximate metabolites of DBF and not by the DBF molecule itself. In order to test this hypothesis, several agents that enhance
O Périn-Roussel et al.
Carcinogenesis, 13(4), 723-725 (1992-04-01)
Quantitative and qualitative changes in the inhibition of DNA adduct formation in the presence of increasing concentrations of norharman (NH) were investigated in vivo in mouse fibroblasts treated with dibenzo[a,e]fluoranthene (DBF), a potent carcinogen in mice. The nuclease P1 modification
Dibenzo[a,e]fluoranthene.
IARC monographs on the evaluation of the carcinogenic risk of chemicals to humans, 32, 321-325 (1983-12-01)
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service