Skip to Content
Merck
All Photos(1)

Documents

D31206

Sigma-Aldrich

Dibenz[a,c]anthracene

97%

Synonym(s):

1,2:3,4-Dibenzanthracene

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

About This Item

Empirical Formula (Hill Notation):
C22H14
CAS Number:
215-58-7
Molecular Weight:
278.35
Beilstein:
1912415
EC Number:
205-920-8
MDL number:
MFCD00003603
UNSPSC Code:
12352100
PubChem Substance ID:
24893724
NACRES:
NA.22

Assay

97%

form

powder

bp

518 °C (lit.)

mp

205-207 °C (lit.)

SMILES string

c1ccc2cc3c4ccccc4c5ccccc5c3cc2c1

InChI

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

InChI key

RAASUWZPTOJQAY-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Pictograms

Skull and crossbonesEnvironment
GHS06,GHS09

Signal Word

Danger

Hazard Statements

H301 + H311 + H331,H400

Hazard Classifications

Acute Tox. 3 Oral - Aquatic Acute 1

Storage Class Code

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

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

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

Visit the Document Library

I Chouroulinkov et al.
Cancer letters, 19(1), 21-26 (1983-05-01)
The tumor-initiating activities of dibenz[a,c]anthracene (DBA) and of the related trans-1,2-, 3,4- and 10,11-dihydrodiols have been examined on mouse skin subsequently promoted with 12-O-tetradecanoyl-phorbol-13-acetate (TPA). The 1,2- and 10,11-dihydrodiols were active and were more active than equivalent doses of either
M Hall et al.
Carcinogenesis, 9(5), 865-868 (1988-05-01)
Incubation of r-1,t-2-dihydroxy-t-3,4-oxy-1,2,3,4-tetrahydrochrysene (anti-chrysene-1,2-diol 3,4-oxide), the bay-region diol-epoxide of chrysene, with rat liver microsomes in the presence of NADP+ and DNA, followed by 32P-postlabelling analysis of the DNA, revealed the presence of at least two adducts not detected when anti-chrysene-1,2-diol
Dibenz[a,c]anthracene.
IARC monographs on the evaluation of the carcinogenic risk of chemicals to humans, 32, 289-297 (1983-12-01)
S Lecoq et al.
Carcinogenesis, 10(3), 461-469 (1989-03-01)
The comparison of the behaviour of three dibenzoanthracene (DBA) isomers, dibenzo[a,c]anthracene (DB[a,c]A), dibenzo[a,h]anthracene (DB[a,h]A) and dibenzo[a,j]anthracene (DB[a,j]A), polycyclic aromatic hydrocarbons (PAHs), whose carcinogenicity varies from very potent to apparently inactive, has been carried out. Influence of norharman (NH; 9H-pyrido[3,4-b]indol) was
J J Reiners et al.
Molecular carcinogenesis, 21(2), 135-146 (1998-03-13)
Products of several phase I and II genes transcriptionally activated by ligands of the aryl hydrocarbon receptor (AHR) were quantitated in cutaneous samples isolated from non-tumor-bearing SENCAR or SSIN mice, and animals bearing skin tumors generated in initiation-promotion protocols. The
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