Levoglucosan
Chemical compound From Wikipedia, the free encyclopedia
Levoglucosan (C6H10O5) is an organic compound with a six-carbon ring structure formed from the pyrolysis of carbohydrates, such as starch and cellulose.[1] As a result, levoglucosan is often used as a chemical tracer for biomass burning in atmospheric chemistry studies, particularly with respect to airborne particulate matter. Along with other tracers such as potassium, oxalate, and gaseous acetonitrile,[2] levoglucosan has been shown to be highly correlated with regional fires. This is because the gas emitted by the pyrolysis of wood (biomass) contains significant amounts of levoglucosan.
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Names | |
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IUPAC name
1,6-Anhydro-β-D-glucopyranose | |
Systematic IUPAC name
(1R,2S,3S,4R,5R)-6,8-Dioxabicyclo[3.2.1]octane-2,3,4-triol | |
Other names
Levoglucosan Leucoglucosan | |
Identifiers | |
3D model (JSmol) |
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80998 | |
ChEBI | |
ChemSpider | |
ECHA InfoCard | 100.007.142 |
EC Number |
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MeSH | 1,6-Anhydro-beta-glucopyranose |
PubChem CID |
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UNII | |
CompTox Dashboard (EPA) |
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Properties | |
C6H10O5 | |
Molar mass | 162.141 g·mol−1 |
Appearance | Colorless crystals |
Density | 1.688 g·cm−3 (predicted) |
Melting point | 182 to 184 °C (360 to 363 °F; 455 to 457 K) |
Boiling point | 384 °C (723 °F; 657 K) predicted |
log P | −0.04 (predicted) |
Vapor pressure | 24.1 μPa (predicted) |
Hazards | |
Flash point | 185.9 °C (366.6 °F; 459.0 K) (predicted) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Levoglucosan has been described as "an unequivocal biomass burning tracer" in the context of forest and brush fires.[3] But the anhydrosugar has only been found detectable in low temperature samples (150-350 °C), meaning that its value as an indicator for smoke from controlled biomass combustion in, for instance, modern domestic wood stoves which operate at temperatures above 500 °C, is "very doubtful".[4] Levoglucosan is a marker for coal combustion as well as wood.[5]
The hydrolysis of levoglucosan generates the fermentable sugar glucose. Levoglucosan can be utilized in the synthesis of chiral polymers such as unhydrolysable glucose polymers.
References
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