Dodecyl acetate

Last updated
Dodecyl acetate
Skeletal formula of dodecyl acetate Dodecyl acetate.svg
Skeletal formula of dodecyl acetate
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 OOjs UI icon edit-ltr-progressive.svg
EC Number
  • 203-995-1
PubChem CID
RTECS number
  • AH3525000
UNII
  • InChI=1S/C14H28O2/c1-3-4-5-6-7-8-9-10-11-12-13-16-14(2)15/h3-13H2,1-2H3 Yes check.svgY
    Key: VZWGRQBCURJOMT-UHFFFAOYSA-N Yes check.svgY
  • InChI=1S/C14H28O2/c1-3-4-5-6-7-8-9-10-11-12-13-16-14(2)15/h3-13H2,1-2H3
    Key: VZWGRQBCURJOMT-UHFFFAOYSA-N
  • CCCCCCCCCCCCOC(=O)C
Properties
C14H28O2
Molar mass 228.376 g·mol−1
AppearanceColorless 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]
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)
NFPA 704.svgHealth 1: Exposure would cause irritation but only minor residual injury. E.g. turpentineFlammability 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g. canola oilInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
1
1
0
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).

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. 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.
  2. 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)
  3. 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.
  4. ↑ Yaws, Carl L. (2009). Transport Properties of Chemicals and Hydrocarbons. New York: William Andrew Inc. p. 177. ISBN   978-0-8155-2039-9.
  5. 1 2 Sigma-Aldrich Co., Lauryl acetate. Retrieved on 2014-05-28.


This page is based on this Wikipedia article
Text is available under the CC BY-SA 4.0 license; additional terms may apply.
Images, videos and audio are available under their respective licenses.