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61630

Sigma-Aldrich

Ethyl dodecanoate

≥98.0% (GC)

Synonym(s):

Ethyl laurate, Lauric acid ethyl ester

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About This Item

Linear Formula:
CH3(CH2)10COOC2H5
CAS Number:
106-33-2
Molecular Weight:
228.37
Beilstein:
1769671
EC Number:
203-386-0
MDL number:
MFCD00015065
UNSPSC Code:
12352100
PubChem Substance ID:
57651851
NACRES:
NA.22

Quality Level

100

Assay

≥98.0% (GC)

bp

269 °C (lit.)

density

0.862 g/mL at 20 °C (lit.)

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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Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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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)
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
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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