![]() | |
| Names | |
|---|---|
| Preferred IUPAC name
Tributyl 2-(acetyloxy)propane-1,2,3-tricarboxylate | |
| Identifiers | |
3D model (JSmol) |
|
| ChemSpider | |
| ECHA InfoCard | 100.000.971 |
PubChem CID |
|
| UNII | |
CompTox Dashboard (EPA) |
|
| |
| |
| Properties | |
| C20H34O8 | |
| Molar mass | 402.484 g·mol−1 |
| Appearance | Colorless liquid |
| Density | 1.046 g/cm3 |
| Melting point | −80 °C (−112 °F; 193 K) |
| Boiling point | 172 to 174 °C (342 to 345 °F; 445 to 447 K) 1 mm Hg |
| 0.02 g/L (20 °C) | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references | |
Acetyltributylcitrate is an organic compound that is used as a plasticizer. As such, it is a potential replacement of DEHP and DINP.[1] It is a colorless liquid that is soluble in organic solvents. It is found in nail polish and other cosmetics. It is prepared by acetylation of tributylcitrate.[2]
References
- ↑ Britt E. Erickson: Regulators And Retailers Raise Pressure On Phthalates, Chemical & Engineering News 93(25), 2015, p. 11–15.
- ↑ Ashford, R.D. Ashford's Dictionary of Industrial Chemicals. London, England: Wavelength Publications Ltd., 1994., p. 902.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.
