Glycerol-1,2-carbonate
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Other names
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| Identifiers | |
3D model (JSmol)
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| ChemSpider | |
| ECHA InfoCard | 100.012.032 |
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PubChem CID
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CompTox Dashboard (EPA)
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| Properties | |
| C4H6O4 | |
| Molar mass | 118.088 g·mol−1 |
| Appearance | clear, colourless to light yellow liquid |
| Density | 1.40 g·cm−3 at 25 °C
1.41 g·cm−3 at 20 °C |
| Melting point | −60 °C at 1013 hPa
−69 °C |
| Boiling point | 110–115 °C at 0.1 mmHg 137–140 °C at 0.7 hPa |
| Miscible | |
| Solubility | Miscible in polar solvents such as alcohols
Miscible with tetrahydrofuran |
| Vapor pressure | 0.93 Pa at 25 °C |
Refractive index (nD)
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1,4570 – 1,4610 (20 °C)
1,469 (20 °C) |
| Hazards | |
| NFPA 704 (fire diamond) | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
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Glycerol-1,2-carbonate is formally the cyclic ester of carbonic acid with glycerol and has aroused great interest as a possible product from the "waste materials" carbon dioxide CO2 and glycerol (especially from biodiesel production) with a wide range of applications.
The currently unsatisfactory yields and complex process conditions in direct synthesis stand in the way of a further spread of glycerol carbonate as a solvent and molecular building block from renewable raw materials.