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Merck
CN

D31206

Dibenz[a,c]anthracene

97%

Synonym(s):

1,2:3,4-Dibenzanthracene

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About This Item

Empirical Formula (Hill Notation):
C22H14
CAS Number:
215-58-7
Molecular Weight:
278.35
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24893724
EC Number:
205-920-8
Beilstein/REAXYS Number:
1912415
MDL number:
MFCD00003603
Assay:
97%
Form:
powder

Key Documents

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Product Name

Dibenz[a,c]anthracene, 97%

InChI key

RAASUWZPTOJQAY-UHFFFAOYSA-N

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

SMILES string

c1ccc2cc3c4ccccc4c5ccccc5c3cc2c1

assay

97%

form

powder

bp

518 °C (lit.)

mp

205-207 °C (lit.)

Quality Level

100

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Related Categories

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

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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J R Bend
Ciba Foundation symposium, 76, 83-99 (1980-01-01)
The mechanisms by which administration of polycyclic aromatic hydrocarbons (PAH) stimulates drug-metabolizing enzymes are summarized. The hepatic monooxygenase system of marine and freshwater fish is also induced by PAH-type compounds, including chlorinated dioxins and certain polychlorinated and polybrominated biphenyl isomers
N D Madhavan et al.
Human & experimental toxicology, 14(6), 503-506 (1995-06-01)
Human placenta, umbilical cord blood, maternal blood and breast milk samples from mothers were analysed for the presence of selected polycyclic aromatic hydrocarbons (PAHs). Benzo(a) pyrene (B(a)P), dibenzo(a,c)anthracene (DBA) and chrysene (Chy) were detected in all the four types 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
The metabolic activation of some polycyclic hydrocarbons: the role of dihydrodiols and diol-epoxides.
P Sims
Advances in experimental medicine and biology, 136 Pt A, 487-500 (1981-01-01)
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