|  | |
| Names | |
|---|---|
| Preferred IUPAC name Dodecyl acetate | |
| Other names Lauryl acetate, Dodecan-1-yl acetate, 1-Dodecanol acetate, n-Dodecyl ethanoate, Dodecanol acetate, Dodecanyl acetate, n-Dodecyl acetate | |
| Identifiers | |
| 3D model (JSmol) | |
| ChemSpider | |
| ECHA InfoCard | 100.003.632 | 
| EC Number | 
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| PubChem CID | |
| RTECS number | 
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| UNII | |
| CompTox Dashboard (EPA) | |
| 
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| 
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| Properties | |
| C14H28O2 | |
| Molar mass | 228.376 g·mol−1 | 
| Appearance | Colorless liquid | 
| Odor | Citrus-rose | 
| Density | 0.8652 g/cm3 (22 °C)[1] | 
| Melting point | 0.7 °C (33.3 °F; 273.8 K) at 760 mmHg[1] | 
| Boiling point | 265 °C (509 °F; 538 K) at 760 mmHg 180 °C (356 °F; 453 K) at 40 mmHg[1] 150 °C (302 °F; 423 K) at 15 mmHg[2] | 
| Solubility | Soluble in most organic solvents[2] | 
| Solubility in ethanol | 80% v/v in water: 250 mL/L[2] | 
| log P | 6.1[3] | 
| Vapor pressure | 0.13 Pa[3] | 
| Refractive index (nD) | 1.4439 (20 °C)[1] | 
| Viscosity | 2.81 cP (35 °C)[3] 0.732 cP (70 °C) 0.511 cP (100 °C) 0.224 cP (200 °C)[4] | 
| Hazards | |
| GHS labelling: | |
| H413[5] | |
| NFPA 704 (fire diamond) | |
| Flash point | 113 °C (235 °F; 386 K)[5] | 
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references | |
Dodecyl acetate or lauryl acetate, CH3COO(CH2)11CH3, is the dodecyl ester of acetic acid. It has a floral odor and is useful as a perfume additive.
References
- 1 2 3 4 Lide, David R., ed. (2009). CRC Handbook of Chemistry and Physics (90th ed.). Boca Raton, Florida: CRC Press. ISBN 978-1-4200-9084-0.
- 1 2 3  Compendium of Food Additive Specifications: Addendum 8. Vol. 52. Rome, Italy: FAO. 2000. pp. 134–135. ISBN 92-5-104508-9. {{cite book}}:|work=ignored (help)
- 1 2 3 Kokosa, John M.; Przyjazny, Andrzej; Jeannot, Michael A. (2009). Solvent Microextraction: Theory and Practice. New Jersey: John Wiley & Sons Inc. p. 124. ISBN 978-0-470-27859-8.
- ↑ Yaws, Carl L. (2009). Transport Properties of Chemicals and Hydrocarbons. New York: William Andrew Inc. p. 177. ISBN 978-0-8155-2039-9.
- 1 2 Sigma-Aldrich Co., Lauryl acetate. Retrieved on 2014-05-28.
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