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ERD-014

Supelco

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:
224-42-0
Molecular Weight:
279.33
Beilstein:
18508
MDL number:
MFCD00055947
UNSPSC Code:
41116107
PubChem Substance ID:
329799584

grade

analytical standard

packaging

vial of 25 mg

manufacturer/tradename

Cerilliant®

application(s)

environmental
forensics and toxicology

format

neat

storage temp.

room temp

SMILES string

c1ccc2c(c1)ccc3nc4ccc5ccccc5c4cc23

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

InChI key

ANUCHZVCBDOPOX-UHFFFAOYSA-N

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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

Pictograms

Health hazard
GHS08

Signal Word

Warning

Hazard Statements

H351

Precautionary Statements

P281

Hazard Classifications

Carc. 2

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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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)
D Warshawsky et al.
Toxicology, 93(2-3), 135-149 (1994-11-11)
N-Heterocyclic aromatics are by-products of incomplete combustion of organic material. The overall objective of this study was to determine the relative carcinogenic potencies of 7H-dibenzo[c,g]carbazole (DBC) and dibenz[a,j]acridine (DBA) in a bioassay of complete carcinogenicity on mouse skin in a
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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