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质量水平
方案
≥98.0% (GC)
沸点
269 °C (lit.)
密度
0.862 g/mL at 20 °C (lit.)
官能团
ester
SMILES字符串
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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储存分类代码
10 - Combustible liquids
WGK
WGK 2
闪点(°F)
235.4 °F - closed cup
闪点(°C)
113 °C - closed cup
个人防护装备
Eyeshields, Gloves
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
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
Hydrocracking of ethyl laurate on bifunctional micro-/mesoporous zeolite catalysts.
Oliver Busse et al.
ChemSusChem, 3(5), 563-565 (2010-05-04)
Jun-min Zhang et al.
Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials, 33(2), 215-218 (2010-06-26)
To study the chemical constituents from pine needles of Cedrus deodara. Chemical constituents were isolated by silica gel and Sephadex LH-20 column chromatography. The structures of the isolated compounds were elucidated through spectroscopic analysis. The compounds were identified as 9-hydroxy-dodecanoic
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