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DIBENZ(A,J)ACRIDINE

DIBENZ(A,J)ACRIDINE Basic information
Product Name:DIBENZ(A,J)ACRIDINE
Synonyms:DIBENZO(A,J)ACRIDINE;DIBENZ(A,J)ACRIDINE;7-AZADIBENZ[A,J]ANTHRACENE;1,2,7,8-DIBENZACRIDINE;3,4,5,6-dibenzacridine;3,4,6,7-dinaphthacridine;Db(a,j)ac;dibenzacridine
CAS:224-42-0
MF:C21H13N
MW:279.33
EINECS:
Product Categories:Heterocycles;Aromatics Compounds;Aromatics;Mutagenesis Research Chemicals
Mol File:224-42-0.mol
DIBENZ(A,J)ACRIDINE Structure
DIBENZ(A,J)ACRIDINE Chemical Properties
Melting point 218-220°C
Boiling point 412.11°C (rough estimate)
density 1.0343 (rough estimate)
refractive index 1.8240 (estimate)
storage temp. 2-8°C
solubility Chloroform (Slightly), Ethyl Acetate (Slightly, Heated), Methanol (Slightly)
pka4.71±0.30(Predicted)
form neat
BRN 18508
Stability:Light Sensitive
IARC2A (Vol. 32, Sup 7, 103) 2013
EPA Substance Registry SystemDibenz[a,j]acridine (224-42-0)
Safety Information
Hazard Codes Xn
Risk Statements 40
Safety Statements 36/37
RIDADR 2811
WGK Germany 3
RTECS HN1050000
HazardClass 6.1(b)
PackingGroup III
Hazardous Substances Data224-42-0(Hazardous Substances Data)
MSDS Information
DIBENZ(A,J)ACRIDINE Usage And Synthesis
Chemical PropertiesLight Green Solid
UsesA heterocyclic aromatic compound with potent mutagenic and carcinogenic properties
DefinitionChEBI: Dibenz[a,j]acridine is an organonitrogen heterocyclic compound and a polycyclic heteroarene.
Synthesis Reference(s)Journal of Heterocyclic Chemistry, 28, p. 139, 1991 DOI: 10.1002/jhet.5570280125
General DescriptionYellow crystals.
Air & Water ReactionsDust/air mixtures may ignite and explode. Insoluble in water.
Reactivity ProfileDIBENZ(A,J)ACRIDINE neutralizes acids in exothermic reactions to form salts plus water. May be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. May generate hydrogen, a flammable gas, in combination with strong reducing agents such as hydrides.
Safety ProfileConfirmed carcinogen with experimental carcinogenic and tumorigenic data. Experimental reproductive effects. Mutation data reported. When heated to decomposition it emits toxic fumes of NOx. See also ANTHRACENE.
DIBENZ(A,J)ACRIDINE Preparation Products And Raw materials
BENZO(A)ACRIDINE 5,6-BENZOQUINOLINE DIBENZ(A,J)ACRIDINE (D13) SOLUTION 50UG/ML IN TOLUENE 1.2ML DIBENZ(c,h)ACRIDINE, 1,2,3,4-TETRAHYDRO-7-METHYL- DIBENZ(C,G)ACRIDINE DIBENZ(A,H)ACRIDINE SOLUTION 100UG/ML IN METHANOL 5ML DIBENZ(A,H)ACRIDINE 6'-Fluorospiro[dibenz[c,h]acridine-7(14H),3'-[3H]indol]-2'(1'H)-one DIBENZ(A,J)ACRIDINE SOLUTION 100UG/ML IN TOLUENE 5X1ML 4-Hydroxydibenz(a,j)acridine DIBENZ(A,J)ACRIDINE5,6-OXIDE DIBENZ(A,J)ACRIDINE (D13) DIBENZ(A,J)ACRIDINEN-OXIDE TRANS-DIBENZ(A,J)ACRIDINE-3,4-DIHYDRODIOL,Dibenz(a,j)acridine-3,4-diol, 3,4-dihydro-, trans- DIBENZ(A,J)ACRIDINE DIBENZ(A,J)ACRIDINE SOLUTION 100UG/ML IN TOLUENE 5ML TRANS-DIBENZ(A,J)ACRIDINE-1,2-DIHYDRODIOL DIBENZ(A,H)ACRIDINE SOLUTION 100UG/ML IN METHANOL 5X1ML
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