Retene | |
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7-Isopropyl-1-methylphenanthrene |
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Other names
Retene |
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Identifiers | |
CAS number | 483-65-8 |
PubChem | 10222 |
Jmol-3D images | Image 1 |
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Properties | |
Molecular formula | C18H18 |
Molar mass | 234.33552 |
Melting point |
98.5 °C |
Boiling point |
390 °C |
(verify) (what is: / ?) Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) |
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Infobox references |
Retene, methyl isopropyl phenanthrene or 1-methyl-7-isopropyl phenanthrene, C18H18, is a polycyclic aromatic hydrocarbon present in the coal tar fraction, boiling above 360 °C. It occurs naturally in the tars obtained by the distillation of resinous woods. It crystallizes in large plates, which melt at 98.5 °C and boil at 390 °C. It is readily soluble in warm ether and in hot glacial acetic acid. Sodium and boiling amyl alcohol reduce it to a tetrahydroretene, whilst if it be heated with phosphorus and hydriodic acid to 260 °C, a dodecahydride is formed. Chromic acid oxidizes it to retene quinone, phthalic acid and acetic acid. It forms a picrate which melts at 123-124 °C.
Retene is derived by degradation of specific diterpenoids biologically produced by conifer trees.
The presence of traces of retene in the air is an indicator of forest fires; it is a major product of pyrolysis of conifer trees.[1] It is also present in effluents from wood pulp and paper mills.[2]
Retene, together with cadalene, simonellite and ip-iHMN, is a biomarker of higher plants, which makes it useful for paleobotanic analysis of rock sediments. Ratio of retene/cadalene in sediments can reveal the ratio of the genus Pinaceae in the biosphere.[3]
This article incorporates text from a publication now in the public domain: Chisholm, Hugh, ed (1911). Encyclopædia Britannica (11th ed.). Cambridge University Press.