Hexane-2,5-dione
| Skeletal formula of hexane-2,5-dione | |
| Names | |
|---|---|
| Other names
1,2-diacetylethane
'α','β'-diacetylethane acetonyl acetone diacetonyl 2,5-dioxohexane 2,5-diketohexane 2,5-hexanedione |
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| Identifiers | |
110-13-4  |
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| ChEBI | CHEBI:85104  |
| ChemSpider | 7744 |
| Jmol 3D model | Interactive image |
| PubChem | 8035 |
| RTECS number | MO3150000 |
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| Properties | |
| C6H10O2 | |
| Molar mass | 114.1438 g mol−1 |
| Appearance | colorless liquid |
| Density | 0.973 g cm−3, liquid |
| Melting point | −5.5 °C (22.1 °F; 267.6 K) |
| Boiling point | 191.4 °C (376.5 °F; 464.5 K) |
| ≥ 10 g/100 mL (22 °C) | |
| Structure | |
| trigonal planar at carbonyl tetrahedral elsewhere |
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| Vapor pressure | {{{value}}} |
| Related compounds | |
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Related diketones
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acetylacetone |
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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| Infobox references | |
Hexane-2,5-dione is an aliphatic diketone. It is a toxic metabolite of hexane and of 2-hexanone.
Symptoms
The initial symptoms of chronic hexane toxicity, attributable to hexane-2,5-dione, are tingling and cramps in the arms and legs, followed by general muscular weakness. In severe cases, atrophy of the skeletal muscles is observed, along with a loss of coordination and problems of vision.[1]
Similar symptoms are observed in animal models. They are associated with a degeneration of the peripheral nervous system (and eventually the central nervous system), starting with the distal portions of the longer and wider nerve axons.
Mechanism of action
It appears that the neurotoxicity of 2,5-hexanedione resides in its γ-diketone structure since 2,3-, 2,4-hexanedione and 2,6-heptanedione are not neurotoxic, while 2,5-heptanedione and 3,6-octanedione and other γ-diketones are neurotoxic.[2] In fact, higher α-diketones, like 2,3-pentanedione and 2,3-hexanedione, are found in small amounts in various foods. They are used as aroma components in alcohol-free beverages and in baked goods.[3]
2,5-Hexanedione reacts with critical lysine residues in axonal proteins by Schiff base formation followed by cyclization to give pyrroles. Oxidation of the pyrrole residues then causes cross-linking between two n-hexane-modified proteins. The resulting denaturation of proteins perturbs axonal transport and function and causes damage to nerve cells.[4]
References
- ↑ Couri D, Milks M. "Toxicity and metabolism of the neurotoxic hexacarbons n-hexane, 2-hexanone, and 2,5-hexanedione" Annual Rev. Pharmacol. Toxicol. 1982;22:145-66.
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