Dibutyl tartrate
From Wikipedia, the free encyclopedia
Dibutyl tartrate, with no stereochemical detail | |
| Names | |
|---|---|
| IUPAC name
dibutyl 2,3-dihydroxybutanedioate | |
| Identifiers | |
3D model (JSmol) |
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| ChemSpider | |
| ECHA InfoCard | 100.001.623 |
| EC Number |
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PubChem CID |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| C12H22O6 | |
| Molar mass | 262.302 g·mol−1 |
| Density | 1.091 |
| Melting point | 21 °C (70 °F; 294 K) |
| Boiling point | 320 °C (608 °F; 593 K) |
Chiral rotation ([α]D) |
+11.5[clarification needed] |
Refractive index (nD) |
1.447 |
| Hazards | |
| Flash point | 91 °C (196 °F; 364 K) |
| 284 °C (543 °F; 557 K) | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Dibutyl tartrate is a di-ester of tartaric acid and butanol.[1] It has been used as a chiral oil to separate enantiomers in chromatography.[2][3] Another use is in farinographs.[4] Yet another use is as a plasticizer.[5] The material is classed as "green" as it is made from natural products, and is biodegradable.[6]
