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Merck
CN

E39600

Ethyl myristate

97%

Synonym(s):

Ethyl tetradecanoate, Myristic acid ethyl ester

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About This Item

Linear Formula:
CH3(CH2)12COOC2H5
CAS Number:
124-06-1
Molecular Weight:
256.42
EC Number:
204-675-4
UNSPSC Code:
12352100
PubChem Substance ID:
24894532
Beilstein/REAXYS Number:
1776382
MDL number:
MFCD00008984

Key Documents

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InChI key

MMKRHZKQPFCLLS-UHFFFAOYSA-N

InChI

1S/C16H32O2/c1-3-5-6-7-8-9-10-11-12-13-14-15-16(17)18-4-2/h3-15H2,1-2H3

SMILES string

CCCCCCCCCCCCCC(=O)OCC

assay

97%

bp

178-180 °C/12 mmHg (lit.)

mp

11-12 °C (lit.)

density

0.86 g/mL at 25 °C (lit.)

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Storage Class

10 - Combustible liquids

wgk

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)

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
01303DH
00503ED
11722MR
10515HO
04101JF

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Woo-kyoung Lee et al.
Journal of controlled release : official journal of the Controlled Release Society, 84(3), 115-123 (2002-12-07)
An oil-in-water solvent evaporation method was used to prepare cyclosporin A (CyA)-loaded particles varying in size (nanoparticles, 'small-sized' microparticles, 'large-sized' microparticles), polymer compositions [poly(D,L-lactide-co-glycolic acid) (PLGA) 50/50, PLGA 85/15, poly(D,L-lactic acid) (PLA)] and additive fatty acid ester (ethyl myristate; EM).
Sven Hartwig et al.
Forensic science international, 131(2-3), 90-97 (2003-02-19)
Fatty acid ethyl esters (FAEE) can be used as alcohol markers in hair. It was investigated in this study whether this diagnostic method is disturbed by hair care and hair cosmetics. Traces of ethyl myristate, ethyl palmitate, ethyl oleate and
Neonatal hair analysis as a biomarker for in utero alcohol exposure.
Julia Klein et al.
The New England journal of medicine, 347(25), 2086-2086 (2002-12-20)
V Auwärter et al.
Clinical chemistry, 47(12), 2114-2123 (2001-11-24)
Fatty acid ethyl esters (FAEEs) are products of nonoxidative ethanol metabolism. After incorporation in hair, they should be suitable long-term markers of alcohol abuse. Hair samples from 19 alcoholics in a treatment program, 10 fatalities with verified excessive alcohol consumption
E Akaho et al.
Journal of pharmaceutical sciences, 70(11), 1225-1228 (1981-11-01)
Interactions of phenolic compounds 4-hexylresorcinol and 3,4-dimethylphenol with esters were studied using hexane-ester cosolvent systems by both phase solubility and partitioning methods. The data obtained by the phase solubility method were variable and could not be analyzed by any mathematical
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