D221953
Dodecyl acetate
97%
Synonym(s):
Lauryl acetate
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About This Item
Linear Formula:
CH3CO2(CH2)11CH3
CAS Number:
Molecular Weight:
228.37
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
203-995-1
MDL number:
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
SMILES string
CCCCCCCCCCCCOC(C)=O
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.)
Quality Level
Related Categories
hcodes
Hazard Classifications
Aquatic Chronic 4
Storage Class
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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Developing new anti-cancer drugs.
Ricardo de Souza Pereira
Recent patents on anti-cancer drug discovery, 6(1), 1-5 (2010-11-30)
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
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
Stephen J Martin et al.
Journal of chemical ecology, 36(8), 855-863 (2010-05-29)
Semiochemicals influence many aspects of insect behavior, including interactions between parasites and their hosts. We studied the chemical recognition system of bumblebees (Bombus) by examining the cuticular hydrocarbon cues of 14 species, including five species of social parasites, known as
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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