D221953
Dodecyl acetate
97%
Sinónimos:
Lauryl acetate
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About This Item
Fórmula lineal:
CH3CO2(CH2)11CH3
Número de CAS:
Peso molecular:
228.37
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Productos recomendados
Quality Level
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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hcodes
Hazard Classifications
Aquatic Chronic 4
Storage Class
10 - Combustible liquids
wgk_germany
WGK 2
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
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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
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
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
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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