| Identification | Back Directory | [Name]
DIBENZO(A,E)PYRENE | [CAS]
192-65-4 | [Synonyms]
Db(a,e)P
Ccris 212
Brn 2054070
Einecs 205-891-1
DIBENZ(A,E)PYRENE
DIBENZO(A,E)PYRENE
1,2:4,5-DIBENZPYRENE
1,2,4,5-DIBENZOPYRENE
dibenzo[a,e]pyrene(purity)
Naphtho[1,2,3,4-de]chrysene
naptho(1,2,3,4-def)chrysene
naphtho[1,2,3,4-def]chrysene
naphtho(1,2,3,4-def)chrysene
Dibenzo(a,e)pyrene,10mg/L,1ml
Dibenzo(a,e)pyrene,100mg/L,1ml
Dibenzo(a,e)pyrene,200mg/L,1ml
Dibenzo(a,e)pyrene,20mg/L,2x5ml
Dibenzo(a,e)pyrene,100mg/L,2x5ml
Dibenzo(a,e)pyrene,1,000mg/L,1ml
46741, Dibenzo[a,e]pyrene (purity)
Dibenzo(a,e)pyreneSolution,50mg/L,1ml
Dibenz[a,e]pyrene@50 μg/mL in Toluene
Dibenzo[a,e]pyrene Solution, 100μg/mL
Dibenzo(A,E)pyrene [polycyclic aromatic compounds]
Dibenzo(a,e)pyrene: (Naphtho(1,2,3,4-def)chrysene)
Dibenz[a,e]pyrene (OR) Naphtho[1,2,3,4-def]chrysene
Dibenzo(A,E)pyrene [polycyclic aromatic hydrocarbons] | [EINECS(EC#)]
205-891-1 | [Molecular Formula]
C24H14 | [MDL Number]
MFCD00040155 | [MOL File]
192-65-4.mol | [Molecular Weight]
302.37 |
| Chemical Properties | Back Directory | [Melting point ]
233.5°C | [Boiling point ]
378.4°C (rough estimate) | [density ]
1.1762 (estimate) | [refractive index ]
1.9130 (estimate) | [storage temp. ]
2-8°C | [form ]
neat | [BRN ]
2054070 | [InChI]
InChI=1S/C24H14/c1-2-8-17-16(6-1)14-22-19-10-4-3-9-18(19)20-11-5-7-15-12-13-21(17)24(22)23(15)20/h1-14H | [InChIKey]
KGHMWBNEMFNJFZ-UHFFFAOYSA-N | [SMILES]
C1=C2C3=C4C(C=C2)=C2C(C=CC=C2)=CC4=C2C(=C3C=C1)C=CC=C2 | [CAS DataBase Reference]
192-65-4 | [IARC]
3 (Vol. Sup 7, 92) 2010 | [EPA Substance Registry System]
Dibenzo[a,e]pyrene (192-65-4) |
| Hazard Information | Back Directory | [Uses]
Dibenzo[a,e]pyrene is a polyaromatic hydrocarbon with inherent carcinogenic properties. | [General Description]
Yellow crystals. Water insoluble. | [Air & Water Reactions]
Dust/air mixtures may ignite and explode. Insoluble in water. | [Reactivity Profile]
Vigorous reactions, sometimes amounting to explosions, can result from the contact between aromatic hydrocarbons, such as DIBENZO(A,E)PYRENE, and strong oxidizing agents. They can react exothermically with bases and with diazo compounds. Substitution at the benzene nucleus occurs by halogenation (acid catalyst), nitration, sulfonation, and the Friedel-Crafts reaction. | [Definition]
ChEBI: Dibenzo[a,e]pyrene is an ortho- and peri-fused polycyclic arene. | [Carcinogenicity]
Dibenzo[a,e]pyrene was assessed
in two initiation–promotion studies on mouse skin. One
of the studies gave positive results while other gave
negative results. Dibenzo[a,e]pyrene gave negative results
when tested for carcinogenicity by intramamillary administration
to rats. |
|
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J & K SCIENTIFIC LTD.
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https://www.jkchemical.com |
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Spectrum Chemical Manufacturing Corp.
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Finetech Industry Limited
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AFINE CHEMICALS LIMITED
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Energy Chemical
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www.energy-chemical.com |
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