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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
Daniël Groen et al.
Biochimica et biophysica acta, 1838(1 Pt B), 310-318 (2013-10-16)
This paper describes two synthetic lipid models designed to replace human stratum corneum (SC) in studies of the impact of volatile organic chemicals on the molecular organization of the skin barrier lipids. The models built upon previously developed self-assembled lipid
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
S V B Janardhan Garikipati et al.
Applied and environmental microbiology, 75(20), 6545-6552 (2009-08-25)
Whole-cell biocatalysis to oxidize naphthalene to 1-naphthol in liquid-liquid biphasic systems was performed. Escherichia coli expressing TOM-Green, a variant of toluene ortho-monooxygenase (TOM), was used for this oxidation. Three different solvents, dodecane, dioctyl phthalate, and lauryl acetate, were screened for
Brent L Waguespack et al.
Journal of chromatography. A, 1078(1-2), 171-180 (2005-07-13)
A variety of porous polymer monoliths (PPMs) have been synthesized using the 'conduct-as-cast' format. The resulting polymers have been evaluated for use as separation media in capillary electrochromatography (CEC). The results have shown that substituting a small percentage of the
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