Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

BCR095

Dibenz[a,j]anthracene

BCR®, certified reference material

Sign Into View Organizational & Contract Pricing

Select a Size

100 MG
CHF 664.00

CHF 664.00

Estimated to ship on12 April 2025

Request a Bulk Order
All Photos(1)

Select a Size

Change View
100 MG
CHF 664.00

About This Item

Empirical Formula (Hill Notation):
C22H14
CAS Number:
224-41-9
Molecular Weight:
278.35
Beilstein:
2051201
EC Number:
224-419-5
MDL number:
MFCD00215859
UNSPSC Code:
41116107
PubChem Substance ID:
329774219
NACRES:
NA.24

CHF 664.00

Estimated to ship on12 April 2025

Request a Bulk Order

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)ccc3cc4ccc5ccccc5c4cc23

InChI

1S/C22H14/c1-3-7-19-15(5-1)9-11-17-13-18-12-10-16-6-2-4-8-20(16)22(18)14-21(17)19/h1-14H

InChI key

KLIHYVJAYWCEDM-UHFFFAOYSA-N

Related Categories

Analysis Note

For more information please see:
BCR095

Legal Information

BCR is a registered trademark of European Commission

Storage Class Code

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

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

S V Vulimiri et al.
Chemical research in toxicology, 12(1), 60-67 (1999-01-20)
The formation of DNA adducts in mouse epidermis has been examined following topical application of dibenz[a,j]anthracene (DB[a,j]A) and its metabolites, i.e., DB[a,j]A-3,4-diol, DB[a,j]A-3,4-10, 11-bis-diol, DB[a,j]A-3,4-8,9-bis-diol, 10-OH-DB[a,j]A-3,4-diol, or 11-OH-DB[a,j]A-3,4-diol, using a 32P-postlabeling assay. At initiating doses (400-1600 nmol), DB[a,j]A produced at
R V Nair et al.
Chemical research in toxicology, 4(1), 115-122 (1991-01-01)
Identification of various deoxyribonucleoside adducts formed in primary cultures of mouse keratinocytes exposed to dibenz[a,j]anthracene (DB[a,j]A) is presented. A preliminary analysis of the DNA adducts formed from 7-methyldibenz[a,j]anthracene (7MeDB[a,j]A) also is presented. Cultures of keratinocytes obtained from dorsal skins of
W Baer-Dubowska et al.
Chemical research in toxicology, 8(2), 292-301 (1995-03-01)
The formation of deoxyribonucleoside adducts in mouse epidermis has been examined following topical application of [3H]dibenz[a,j]anthracene (DB[a,j]A) or by 32P-postlabeling following topical application of unlabeled DB[a,j]A, DB[a,j]A trans-3,4-diol or the anti- or syn-3,4-diol 1,2-epoxides. A single topical application of [3H]DB[a,j]A
Dibenz[a,j]anthracene.
IARC monographs on the evaluation of the carcinogenic risk of chemicals to humans, 32, 309-313 (1983-12-01)
R V Nair et al.
Chemical research in toxicology, 5(4), 532-540 (1992-07-01)
The identification of several metabolites formed from dibenz[aj]anthracene (DB[aj]A) and 7-methyldibenz[aj]anthracene (7MeDB[aj]A) in primary cultures of mouse keratinocytes is presented. The metabolites were analyzed by coelution with known synthetic standards using high-pressure liquid chromatography. The metabolite identifications were further facilitated
View All Related Papers

Questions

Reviews

No rating value

Active Filters

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