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:
Molecular Weight:
278.35
Beilstein:
1912415
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Quality Level
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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Related Categories
Signal Word
Danger
Hazard Statements
Precautionary Statements
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
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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
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)
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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