Triethyl citrate
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Names | |
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IUPAC name
1,2,3-Triethyl 2-hydroxypropane-1,2,3-tricarboxylate | |
Other names
Ethyl citrate E1505 Citric acid ethyl ester | |
Identifiers | |
77-93-0 ![]() | |
ChEMBL | ChEMBL464988 ![]() |
ChemSpider | 13850879 ![]() |
EC number | 201-070-7 |
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Jmol-3D images | Image |
PubChem | 6506 |
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Properties | |
C12H20O7 | |
Molar mass | 276.283 g/mol |
Appearance | Oily liquid |
Density | 1.137 g/mL at 25 °C |
Melting point | −55 °C (−67 °F; 218 K)[2] |
Boiling point | 127 °C (261 °F; 400 K) at 1 mmHg 235 °C at 150 mmHg |
65 g/L[2] | |
Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa) | |
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Infobox references | |
Triethyl citrate is an ester of citric acid. It is a colorless, odorless liquid used as a food additive (E number E1505) to stabilize foams, especially as whipping aid for egg white.[3] It is also used in pharmaceutical coatings and plastics.[4]
Triethyl citrate is also used as a plasticizer for polyvinylchloride and similar plastics.[5]
References
- ↑ Triethyl citrate at Sigma-Aldrich
- ↑ 2.0 2.1 Record of Triethyl citrate in the GESTIS Substance Database of the IFA
- ↑ William J. Stadelman, Owen J. Cotterill (1995). Egg Science and Technology. Haworth Press. ISBN 1-56022-855-5.
- ↑ Pharmaceutical Coatings Bulletin 102-4, morflex.com
- ↑ Hwan-Man Park, Manjusri Misra, Lawrence T. Drzal, and Amar K. Mohanty (2004). ""Green" Nanocomposites from Cellulose Acetate Bioplastic and Clay: Effect of Eco-Friendly Triethyl Citrate Plasticizer". Biomacromolecules 5 (6): 2281–2288. doi:10.1021/bm049690f. PMID 15530043.