What molecule am I?
Anthracene is one of the smaller polynuclear aromatic hydrocarbons. (The only smaller one is naphthalene.) It was isolated from coal tar in 1832 by pioneering French chemists Jean-Baptiste Dumas and Auguste Laurent.
Anthracene can be synthesized by the Elbs reaction, in which o-tolyl phenyl ketone is dehydrated at 400鈥�450 潞C. But most commercial anthracene is still recovered from coal tar.
In commerce, anthracene is mainly used as a starting material for the manufacture of 9,10-anthraquinone, which in turn is used to make colorants such as the red dye alizarin. More recently, crystalline anthracene was found to be a useful wide band-gap semiconductor in devices such as organic field-effect transistors and scintillators for detecting high-energy subatomic particles.聽
Anthracene hazard information*
| Hazard class** | Hazard statement | |
|---|---|---|
| Acute toxicity, dermal, category 4 | H312鈥擧armful in contact with skin |  |
| Skin corrosion/irritation, category 2 | H315鈥擟auses skin irritation | |
| Serious eye damage/eye irritation, category 2A聽 | H319鈥擟auses serious eye irritation | |
| Specific target organ toxicity, single exposure, respiratory tract irritation, category 3 | H335鈥擬ay cause respiratory irritation | |
| Carcinogenicity, category 1A | H350鈥擬ay cause cancer |  |
| Hazardous to the aquatic environment, acute hazard, category 1 | H400鈥擵ery toxic to aquatic life |  |
| Hazardous to the aquatic environment, long-term hazard, category 1 | H410鈥擵ery toxic to aquatic life with long-lasting effects | |
*Combined from multiple safety data sheets.
**Globally Harmonized System of Classification and Labeling of Chemicals.聽
Anthracene聽fast facts
| CAS Reg. No. | 120-12-7 |
nomenclature | Anthracene |
| Empirical formula | C14H10 |
| Molar mass | 178.23 g/mol |
| Appearance | White crystals or powder |
| Melting point | 218 潞C |
| Water solubility | 44 渭g/L |
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