|  | |
| Names | |
|---|---|
| IUPAC name Bis(2-ethylhexyl) decanedioate | |
| Systematic IUPAC name [Heptane-3-yl-(-3-methane-1,1-diyl)-] decanedioate | |
| Other names Di(2-ethylhexyl) sebacate, Proviplast 1988, dioctyl sebacate (archaic)[1] | |
| Identifiers | |
| 3D model (JSmol) | |
| ChemSpider | |
| ECHA InfoCard | 100.004.145 | 
| PubChem CID | |
| UNII | |
| CompTox Dashboard (EPA) | |
| 
 | |
| 
 | |
| Properties | |
| C26H50O4 | |
| Molar mass | 426.682 g·mol−1 | 
| Density | 0.9 of water | 
| Melting point | −48 °C (−54 °F; 225 K) | 
| Boiling point | 256 °C (493 °F; 529 K) at 0.7 kPa | 
| none | |
| Vapor pressure | 0.000024 Pa at 37 °C | 
| Hazards | |
| Occupational safety and health (OHS/OSH): | |
| Main hazards | reacts with oxidants | 
| Flash point | 210 °C (410 °F; 483 K) open cup | 
| Lethal dose or concentration (LD, LC): | |
| LD50 (median dose) | 5 g/kg (rat, orally)[2] | 
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references | |
Dioctyl sebacate (also di(2-ethylhexyl) sebacate, commonly abbreviated as DOS, DEHS, and BEHS) is an organic compound which is the diester of sebacic acid and 2-ethylhexanol. It is an oily colorless liquid and is used as a plasticizer, including in the explosive C4.[3] It has also found use in Dot 5 brake fluid, in ester-based engine oils and additives, as seed particle for Particle Image Velocimetry (PIV) and as a model compound that forms stable aerosols.
References
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