Skip to Content
Merck
CN
All Photos(1)

Documents

BCR159

Dibenzo[a,h]pyrene

BCR®, certified reference material

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

About This Item

Empirical Formula (Hill Notation):
C24H14
CAS Number:
189-64-0
Molecular Weight:
302.37
Beilstein:
2054067
MDL number:
MFCD00039579
UNSPSC Code:
41116107
PubChem Substance ID:
329773795
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

c1ccc2c(c1)cc3ccc4c5ccccc5cc6ccc2c3c46

InChI

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

InChI key

RXUSYFJGDZFVND-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Analysis Note

For more information please see:
BCR159

Legal Information

BCR is a registered trademark of European Commission

Pictograms

Health hazard
GHS08

Signal Word

Danger

Hazard Statements

H341,H350

Hazard Classifications

Carc. 1B - Muta. 2

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

Sorry, we don't have COAs for this product available online at this time.

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

Dibenzo[a,h]pyrene.
IARC monographs on the evaluation of the carcinogenic risk of chemicals to humans, 32, 331-335 (1983-12-01)
G A Marsch et al.
Chemical research in toxicology, 5(6), 765-772 (1992-11-01)
The in vivo formation of dibenzo[a,h]pyrene-DNA adducts in mouse skin was assessed by laser-excited fluorescence spectroscopy at 77 and 4.2 K. Two adducts were identified with fluorescence origin bands at approximately 383.5 and 407.2 nm, and these were shown to
A W Wood et al.
Cancer research, 41(7), 2589-2597 (1981-07-01)
The mutagenic activities of dibenzo(a,h)(pyrene, dibenzo(a,i)pyrene, and a total of 11 of their benzo-ring derivatives were evaluated in bacterial and mammalian cells in the absence or presence of a mammalian metabolic activation system. trans-1,2-Dihydroxy-1,2-dihydrodibenzo(a,h)pyrene and trans-3,4-dihydroxy-3,4-dihydrodibenzo(a,i)pyrene, the expected dihydrodiol precursors
Tumorigenicity of bay-region diol-epoxides and other benzo-ring derivatives of dibenzo(a,h)pyrene and dibenzo(a,i)pyrene on mouse skin and in newborn mice.
R L Chang et al.
Cancer research, 42(1), 25-29 (1982-01-01)
B S Hass et al.
Cancer research, 42(5), 1646-1649 (1982-05-01)
The polycyclic aromatic hydrocarbons dibenzo(a,i)pyrene and dibenzo(a,h)pyrene, each of which possesses two bay regions, and their bay-region difluorinated derivatives were tested for mutagenicity for ouabain and 6-thioguanine resistance in Chinese hamster V79 cells. Since V79 cells do not metabolize polycyclic
View All Related Papers

Articles

Efficient PAH Analysis (EU 15+1) using an Ascentis® Express PAH HPLC Column

This application note describes the fast and efficient separation of the EU’s list of 15 + 1 polynuclear aromatic hydrocarbons (PAHs) using Ascentis® Express PAH HPLC column.

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