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| | Dibenzo(a,i)pyrene Basic information |
| Product Name: | Dibenzo(a,i)pyrene | | Synonyms: | 3,4,9,10-DIBENZOPYRENE;1,2:7,8-DIBENZPYRENE;DIBENZ(A,I)PYRENE;1,2,7,8-Dibenzopyrene;3,4,9,10-Dibenzpyrene;3,4:9,10-Dibenzpyrene;benzo(rst)pentaphene;Benzo[rst]pentaphene | | CAS: | 189-55-9 | | MF: | C24H14 | | MW: | 302.37 | | EINECS: | 205-877-5 | | Product Categories: | Aromatics;Mutagenesis Research Chemicals | | Mol File: | 189-55-9.mol |  |
| | Dibenzo(a,i)pyrene Chemical Properties |
| Melting point | 281.5°C | | Boiling point | 378.4°C (rough estimate) | | density | 1.1762 (estimate) | | refractive index | 1.9130 (estimate) | | storage temp. | 2-8°C | | solubility | Chloroform (Very Slightly, Heated), Dichloromethane (Slightly, Heated) | | form | Solid | | color | Green-yellow needles from toluene | | Henry's Law Constant | 7.0×102 mol/(m3Pa) at 25℃, HSDB (2015) | | InChI | InChI=1S/C24H14/c1-3-7-19-15(5-1)13-17-9-10-18-14-16-6-2-4-8-20(16)22-12-11-21(19)23(17)24(18)22/h1-14H | | InChIKey | TUGYIJVAYAHHHM-UHFFFAOYSA-N | | SMILES | C1=CC2=C3C=CC4C5=C3C(=CC=C5C=C3C=CC=CC=43)C=C2C=C1 | | IARC | 2B (Vol. 92) 2010 | | EPA Substance Registry System | Dibenzo[a,i]pyrene (189-55-9) |
| | Dibenzo(a,i)pyrene Usage And Synthesis |
| Uses | Dibenzo[a,i]pyrene is a polycyclic aromatic hydrocarbon (PAH) with potent carcinogenic activity. Dibenzo[a,i]pyrene was shown to induce DNA adduction, tumorigenicity as well as Ki-ras oncogene mutations in strain A/J mouse lung. Dibenzo[a,i]pyrene has been shown to be present in cigarette smoke condensate and in automobile exhaust gas in small quantities. | | Definition | ChEBI: Dibenzo[a,i]pyrene is an ortho- and peri-fused polycyclic arene. | | General Description | Colorless solid. Water insoluble. | | Air & Water Reactions | Insoluble in water. | | Reactivity Profile | Vigorous reactions, sometimes amounting to explosions, can result from the contact between aromatic hydrocarbons, such as DIBENZO(A,I)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. | | Health Hazard | Inhalation of material may be harmful. Contact may cause burns to skin and eyes. Inhalation of Asbestos dust may have a damaging effect on the lungs. Fire may produce irritating, corrosive and/or toxic gases. Some liquids produce vapors that may cause dizziness or suffocation. Runoff from fire control may cause pollution. | | Fire Hazard | Some may burn but none ignite readily. Containers may explode when heated. Some may be transported hot. | | Safety Profile | Confirmed carcinogen withexperimental neoplastigenic and tumorigenic data.Mutation data reported. When heated to decomposition itemits acrid smoke and irritating fumes. | | Toxics Screening Level | The IRSL and SRSL were derived from the inhalation unit risk (IUR) factor for B(a)P of 1.76E-3 per μg/m3. |
| | Dibenzo(a,i)pyrene Preparation Products And Raw materials |
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