ERD-014
Dibenz(a,j)acridine
vial of 25 mg, analytical standard, Cerilliant®
Synonym(s):
Dibenz[a,j]acridine, 7-Azadibenz[a,j]anthracene
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About This Item
Empirical Formula (Hill Notation):
C21H13N
CAS Number:
Molecular Weight:
279.33
PubChem Substance ID:
UNSPSC Code:
41116107
Beilstein/REAXYS Number:
18508
MDL number:
SMILES string
c1ccc2c(c1)ccc3nc4ccc5ccccc5c4cc23
InChI key
ANUCHZVCBDOPOX-UHFFFAOYSA-N
InChI
1S/C21H13N/c1-3-7-16-14(5-1)9-11-20-18(16)13-19-17-8-4-2-6-15(17)10-12-21(19)22-20/h1-13H
grade
analytical standard
packaging
vial of 25 mg
manufacturer/tradename
Cerilliant®
application(s)
environmental
forensics and toxicology
format
neat
storage temp.
room temp
General description
Dibenz(a,j)acridine belongs to the class of polycyclic aromatic nitrogen heterocyclic compounds (PANH). PANHs are a group of well-known environmental pollutants with both mutagenic and carcinogenic properties. They are released into the environment by cigarette smoke, industrial effluents, and gasoline engine exhaust.
Application
Dibenz(a,j)acridine may be used as an analytical standard for the determination of the analyte in asphalt and corresponding leachate water and environmental samples by chromatography techniques.
Legal Information
CERILLIANT is a registered trademark of Merck KGaA, Darmstadt, Germany
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Determination of polycyclic aromatic compounds in asphalt and in corresponding leachate water
Kriech AJ, et al.
Polycyclic Aromat. Compd., 22(3-4), 517-535 (2002)
Synthesis of potential metabolites of dibenz [a, j] acridine: dihydro diols and phenols
Rosario CA, et al.
The Journal of Organic Chemistry, 52(6), 1064-1072 (1987)
Development of an analytical method for the simultaneous determination of 15 carcinogenic polycyclic aromatic hydrocarbons and polycyclic aromatic nitrogen heterocyclic compounds. Application to diesel particulates
Sauvain JJ, et al.
Fresenius Journal of Analytical Chemistry, 371(7), 966-974 (2001)
A Kerim et al.
Anticancer research, 17(2A), 1011-1018 (1997-03-01)
Resonance energy per pi-electron (REPE) of azaarenes were calculated by Aihara's theory of resonance energy (TRE). Consequently, it was shown that the REPE values for the cationic species not having the carbon, or nitrogen atom with the highest approximate superdelocalizability
D H Li et al.
Carcinogenesis, 11(12), 2227-2232 (1990-12-01)
I-compounds are age-related bulky DNA modifications that are detected in untreated animals by 32P-postlabeling. To characterize their properties, I-compounds were compared with carcinogen-DNA adducts in liver, kidney and skin of three rodent species. Weanling female Sprague-Dawley rats, ICR mice and
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