Acenaphthene
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| General | ||||||||||||||||
| Surname | Acenaphthene | |||||||||||||||
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| Molecular formula | C 12 H 10 | |||||||||||||||
| Brief description |
colorless needles |
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| properties | ||||||||||||||||
| Molar mass | 154.21 g mol −1 | |||||||||||||||
| Physical state |
firmly |
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| density |
1.15 g cm −3 (20 ° C) |
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| Melting point |
95 ° C |
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| boiling point |
278 ° C |
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| Vapor pressure |
0.31 Pa (25 ° C) |
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| solubility |
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| Refractive index |
1.6048 (95 ° C) |
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| As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . Refractive index: Na-D line , 20 ° C | ||||||||||||||||
Acenaphthene (1,2-dihydroacenaphthylene; 1,8-ethylene naphthalene) is a white to slightly yellowish solid that belongs to the polycyclic aromatic hydrocarbons . Acenaphthene is found to 0.3% in coal tar .
properties
Acenaphthene is practically insoluble in water, but readily soluble in benzene , ether , chloroform and heated alcohol . The compound decomposes from 476 ° C.
use
Acenaphthene is required for the production of plastics, dyes, insecticides and pharmaceutical products, but mainly for the large-scale production of naphthalic anhydride . Technically, it is obtained by hydrogenating acenaphthylene .
Individual evidence
- ↑ a b c d e Entry on 1,2-dihydroacenaphthylene. In: Römpp Online . Georg Thieme Verlag, accessed on November 12, 2014.
- ↑ a b c d e f Entry on acenaphthene in the GESTIS substance database of the IFA , accessed on June 17, 2016(JavaScript required) .
- ↑ State Institute for Environmental Protection Baden-Württemberg: Substance behavior of gas works-specific PAHs , ISSN 0941-780X , 1997
- ↑ David R. Lide (Ed.): CRC Handbook of Chemistry and Physics . 90th edition. (Internet version: 2010), CRC Press / Taylor and Francis, Boca Raton, FL, Physical Constants of Organic Compounds, pp. 3-4.