M3650
Methyl myristoleate
≥98.5% (capillary GC), liquid
Synonym(s):
Methyl cis-9-tetradecenoate, Myristoleic acid methyl ester
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About This Item
Empirical Formula (Hill Notation):
C15H28O2
CAS Number:
Molecular Weight:
240.38
UNSPSC Code:
12352211
NACRES:
NA.25
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
2046023
biological source
synthetic (organic)
Quality Level
assay
≥98.5% (capillary GC)
form
liquid
functional group
ester
lipid type
unsaturated FAs
shipped in
ambient
storage temp.
−20°C
SMILES string
[H]\C(CCCC)=C(/[H])CCCCCCCC(=O)OC
InChI
1S/C15H28O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15(16)17-2/h6-7H,3-5,8-14H2,1-2H3/b7-6-
InChI key
RWIPSJUSVXDVPB-SREVYHEPSA-N
Packaging
Sealed ampule
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Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves
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Chang Yi Kong et al.
Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 22(11), 1431-1436 (2006-11-14)
The binary diffusion coefficients, D(12), and retention factors for myristoleic acid and its methyl ester at infinite dilution were measured by the chromatographic impulse response technique in supercritical carbon dioxide at temperatures of 313.2, 333.2 and 343.2 K and pressures
Saskia Thurnhofer et al.
Journal of agricultural and food chemistry, 53(23), 8896-8903 (2005-11-10)
A method using gas chromatography/electron ionization-mass spectrometry (GC/EI-MS) in the selected ion monitoring (SIM) mode was developed for the analysis of fatty acids as methyl esters (FAMEs) in order to determine their percentage contribution to the fatty acid profile in
Zhidong Xu et al.
Lipids, 45(2), 199-208 (2010-01-19)
The existing protocols for analyzing fatty acid methyl esters (FAMEs) using a one-step acetyl chloride (AC) catalyzed transesterification and extraction procedure cannot accurately determine the medium- and long-chain fatty acids simultaneously in clinical (enteral, parenteral) formulations. For example: (1) addition