Diisopropyl tartrate
From Infogalactic: the planetary knowledge core
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Names | |
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IUPAC name
Diisopropyl tartrate
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Other names
Bis(1-methylethyl) ester of 2,3-dihydroxybutanedioic acid, Dipropan-2-yl 2,3-dihydroxybutanedioate, DIPT
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Identifiers | |
2217-15-4 ![]() |
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ChemSpider | 101254 (−)-isomer ![]() |
EC Number | 218-709-0 |
Jmol 3D model | (−)-isomer: Interactive image Interactive image |
PubChem | 102768 (−)-isomer 112972 |
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Properties | |
C10H18O6 | |
Molar mass | 234.25 g/mol |
Boiling point | 152 °C (306 °F; 425 K) at 16 kPa |
Vapor pressure | {{{value}}} |
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 | |
Diisopropyl tartrate (DIPT) is a diester of tartaric acid. It has a two chiral carbon atoms giving rise to three stereoisomeric variants. It is commonly used in asymmetric synthesis as a catalyst and as chiral building block for pharmaceuticals and agrochemicals. Its main application is in Sharpless epoxidation, where it serves as a chiral ligand to titanium after reaction with titanium isopropoxide.[1]
References
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