L4625
Ethyl dodecanoate
≥99% (TLC)
Synonym(s):
Ethyl laurate, Lauric acid ethyl ester
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About This Item
Linear Formula:
CH3(CH2)10COOC2H5
CAS Number:
Molecular Weight:
228.37
Beilstein/REAXYS Number:
1769671
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
assay
≥99% (TLC)
bp
269 °C (lit.)
density
0.862 g/mL at 20 °C (lit.)
storage temp.
−20°C
SMILES string
CCCCCCCCCCCC(=O)OCC
InChI
1S/C14H28O2/c1-3-5-6-7-8-9-10-11-12-13-14(15)16-4-2/h3-13H2,1-2H3
InChI key
MMXKVMNBHPAILY-UHFFFAOYSA-N
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replaced by
Product No.
Description
Pricing
Storage Class
10 - Combustible liquids
wgk_germany
WGK 2
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
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Hydrocracking of ethyl laurate on bifunctional micro-/mesoporous zeolite catalysts.
Oliver Busse et al.
ChemSusChem, 3(5), 563-565 (2010-05-04)
A Botsi et al.
Carbohydrate research, 241, 37-46 (1993-03-17)
The inclusion complexes of cyclomaltoheptaose (beta CD) and heptakis(2,3,6-tri-O-methyl)cyclomaltoheptaose (TM-beta CD) with the four major components of the pheromone of the olive fruit fly (Dacus oleae), namely 1,7-dioxaspiro[5.5]undecane, (-)-alpha-pinene, nonanal, and ethyl dodecanoate, and the complex of heptakis(2,6-di-O-methyl)cyclomaltoheptaose (DM-beta CD)
Development of an ethyl laurate-based microemulsion for rapid-onset intranasal delivery of diazepam.
Lianli Li et al.
International journal of pharmaceutics, 237(1-2), 77-85 (2002-04-17)
An ethyl laurate-based microemulsion system with Tween 80 as surfactant, propylene glycol and ethanol as cosolvents was developed for intranasal delivery of diazepam. Phase behavior and solubilization capacity of the microemulsion system were characterized and in vivo nasal absorption of
D R Bevan et al.
Cancer letters, 57(2), 173-179 (1991-05-01)
Effects of vehicles and of asbestos on disposition of benzo[a]pyrene (B[a]P) were examined in vivo. [3H]B[a]P dissolved in triethylene glycol, ethyl laurate, or tricaprylin was intratracheally administered to male Sprague-Dawley rats. Excretion was most rapid when triethylene glycol was the
Napaporn Komesvarakul et al.
Journal of cosmetic science, 57(4), 309-325 (2006-09-08)
Microemulsification of triglyceride-based oil is challenging due to the formation of undesirable phases such as macroemulsions, liquid crystals, or sponge phases. This research evaluates the formation of artificial sebum microemulsions using linker molecules, with the addition of co-oil to help
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