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D31206

Sigma-Aldrich

Dibenz[a,c]anthracene

97%

Synonym(s):

1,2:3,4-Dibenzanthracene

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100 MG
$114.00

About This Item

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

$114.00

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Available to ship onMay 05, 2025Details

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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

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pictograms

Skull and crossbonesEnvironment
GHS06,GHS09

signalword

Danger

Hazard Classifications

Acute Tox. 3 Oral - Aquatic Acute 1

Storage Class

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

wgk_germany

WGK 3

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

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Certificates of Analysis (COA)

Lot/Batch Number
10525JE
02013AE
1816AH
0923TE

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S Kumar et al.
Mutation research, 242(4), 337-343 (1990-12-01)
The mutagenic activities of dibenz[a,c]anthracene (DB[a,c]A), and its 11 derivatives, including 3 diols, 6 phenols and 2 oxepines, were studied in the TA100 strain of Salmonella typhimurium at doses varying from 0 to 20 micrograms/plate in the presence of a
Dibenz[a,c]anthracene.
IARC monographs on the evaluation of the carcinogenic risk of chemicals to humans, 32, 289-297 (1983-12-01)
A Hewer et al.
Carcinogenesis, 2(12), 1345-1352 (1981-01-01)
In rat liver microsomal preparations, the 10,11-dihydrodiol of dibenz[a,c]anthracene (DBA) is metabolized to r-10,t-11-dihydroxy-t-12,13-oxy-10,11,12,13-tetrahydrodibenz[a,c]anthracene (anti-DBA 10,11-diol 12,13-oxide), the anti isomer of a non-bay-region diol-epoxide of DBA. When 3H-labelled DBA or trans-10,11-dihydro-10,11-dihydroxydibenz[a,c]anthracene were metabolized in this system in the presence of
A P Koley et al.
Biochemistry, 34(6), 1942-1947 (1995-02-14)
The flash photolysis technique was used to examine the kinetics of CO binding to cytochromes P450 in rat liver microsomes. The effect of polycyclic aromatic hydrocarbons (PAHs) and flavones was used to distinguish the kinetic behavior of the PAH-metabolizing P450
P Bryla et al.
Cancer letters, 65(1), 35-41 (1992-07-31)
The binding of benzo[a]pyrene, 7,12-dimethylbenz[a]anthracene, 3-methylcholanthrene, benz[a]anthracene, dibenz[a,c]anthracene and phenanthrene to calf thymus DNA in vitro in the absence of enzymatic or chemical activation was investigated using the 32P-postlabeling assay. Reactions were performed in the dark or under white light
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