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Cas Database |
| Name |
PICENE |
EINECS | N/A |
| CAS No. | 213-46-7 | Density | 1.232g/cm3 |
| PSA | 0.00000 | LogP | 6.29940 |
| Solubility | 2.5ug/L(27 oC) | Melting Point |
366-367° |
| Formula | C22H14 | Boiling Point | 519°Cat760mmHg |
| Molecular Weight | 278.353 | Flash Point | 264.5°C |
| Transport Information | N/A | Appearance | N/A |
| Safety | Questionable carcinogen with experimental carcinogenic and neoplastigenic data. When heated to decomposition it emits acrid smoke and irritating fumes. | Risk Codes | N/A |
| Molecular Structure |
|
Hazard Symbols | N/A |
| Synonyms |
1,2:7,8-Dibenzophenanthrene;Benzo[a]chrysene; Dibenzo[a,i]phenanthrene; NSC 406006; [5]Phenacene |
Article Data | 55 |
PICENE Chemical Properties
MF: C22H14
MW: 278.35
EINECS: 205-918-7
IUPAC Name: picene
Storage temp: 2-8°C
Density: 1.232 g/cm3
Flash Point: 264.5 °C
Index of Refraction: 1.811
Enthalpy of Vaporization: 76.18 kJ/mol
Boiling Point: 519 °C at 760 mmHg
Vapour Pressure: 2.34E-10 mmHg at 25°C
Product Categories: Alphabetic ; P ; PER - POLA
Synonyms: 1,2,7,8-Dibenzphenanthrene ; 3,4-Benzchrysene ; Benzo(a)chrysene ; benzo[a]chrysene ; Beta,beta-Binaphthyleneethene ; Dibenzo(a,i)phenanthrene
Following is the molecular structure of Picene (213-46-7):
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PICENE Toxicity Data With Reference
| 1. | skn-mus TDLo:15,142 µg/kg/112W-I:NEO | CRNGDP Carcinogenesis. 11 (1990),1721. | ||
| 2. | scu-mus TDLo:445 µg/kg:CAR | CRNGDP Carcinogenesis. 11 (1990),1721. |
PICENE Safety Profile
Questionable carcinogen with experimental carcinogenic and neoplastigenic data. When heated to decomposition it emits acrid smoke and irritating fumes.
Safety Information of Picene (213-46-7):
RIDADR: 2811
HazardClass: 6.1(b)
PackingGroup: III
PICENE Specification
Picene (213-46-7) is a hydrocarbon found in the pitchy residue obtained in the distillation of peat tar and of petroleum. This is distilled to dryness and the distillate repeatedly recrystallized from cymene. It may be synthetically prepared by the action of anhydrous aluminium chloride on a mixture of naphthalene and 1,2-dibromoethane, or by distilling a-dinaphthostilbene. It crystallizes in large colorless plates which possess a blue fluorescence. It is soluble in concentrated sulfuric acid with a green color. Chromic acid in glacial acetic acid solution oxidizes it to picene-quinone, picene-quinone carboxylic acid, and finally to phthalic acid.
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