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D221953

Sigma-Aldrich

Dodecyl acetate

97%

Synonym(s):

Lauryl acetate

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About This Item

Linear Formula:
CH3CO2(CH2)11CH3
CAS Number:
112-66-3
Molecular Weight:
228.37
EC Number:
203-995-1
MDL number:
MFCD00008973
UNSPSC Code:
12352100
PubChem Substance ID:
24893660
NACRES:
NA.22

Quality Level

100

Assay

97%

form

liquid

refractive index

n20/D 1.432 (lit.)

bp

150 °C/15 mmHg (lit.)

density

0.865 g/mL at 25 °C (lit.)

SMILES string

CCCCCCCCCCCCOC(C)=O

InChI

1S/C14H28O2/c1-3-4-5-6-7-8-9-10-11-12-13-16-14(2)15/h3-13H2,1-2H3

InChI key

VZWGRQBCURJOMT-UHFFFAOYSA-N

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Hazard Statements

H413

Hazard Classifications

Aquatic Chronic 4

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

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Kenneth M MacDonald et al.
Journal of chemical ecology, 29(10), 2385-2389 (2003-12-20)
Larvae of the western flower thrips Frankliniella occidentalis are known to produce an anal droplet containing decyl acetate (10Ac) and dodecyl acetate (12Ac), which act as an alarm pheromone. Analysis by GC showed that the combined mass of 10Ac and
Developing new anti-cancer drugs.
Ricardo de Souza Pereira
Recent patents on anti-cancer drug discovery, 6(1), 1-5 (2010-11-30)
K D Philipson et al.
The American journal of physiology, 248(1 Pt 2), H147-H150 (1985-01-01)
We have used charged amphiphiles as phospholipid analogues to modulate the interaction of Ca2+ with myocardial sarcolemma. The amphiphiles were dodecyl sulfate, dodecyltrimethylamine, and lauryl acetate; these are anionic, cationic, and neutral molecules, respectively. The hydrophobic alkyl chain is identical
Ido Yosha et al.
Journal of agricultural and food chemistry, 56(17), 8045-8049 (2008-08-12)
Alginate-gelatin beads with dispersed droplets of a model pheromone, dodecyl acetate, were prepared as a vehicle for slow release of pheromones into the atmosphere over a prolonged period of time. The beads are prepared in two steps, the first being
A M Beedle et al.
Biophysical journal, 79(1), 260-270 (2000-06-27)
We have recently identified farnesol, an intermediate in the mevalonate pathway, as a potent endogenous modulator and blocker of N-type calcium channels (Roullet, J. B., R. L. Spaetgens, T. Burlingame, and G. W. Zamponi. 1999. J. Biol. Chem. 274:25439-25446). Here
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