70130
Methyl myristate
puriss., ≥99.0% (GC)
Synonym(s):
Methyl tetradecanoate, Myristic acid methyl ester
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About This Item
Linear Formula:
CH3(CH2)12COOCH3
CAS Number:
Molecular Weight:
242.40
EC Number:
204-680-1
UNSPSC Code:
12352211
PubChem Substance ID:
Beilstein/REAXYS Number:
1773739
MDL number:
grade
puriss.
assay
≥99.0% (GC)
refractive index
n20/D 1.436 (lit.), n20/D 1.438
bp
323 °C (lit.)
mp
18 °C (lit.)
density
0.855 g/mL at 25 °C (lit.)
SMILES string
CCCCCCCCCCCCCC(=O)OC
InChI
1S/C15H30O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15(16)17-2/h3-14H2,1-2H3
InChI key
ZAZKJZBWRNNLDS-UHFFFAOYSA-N
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Xian-Guo Zou et al.
Journal of agricultural and food chemistry, 62(43), 10594-10603 (2014-10-10)
In the present study, a human milk fat substitute (HMFS) enriched in medium-chain fatty acids (MCFAs) was synthesized through acidolysis reaction from Cinnamomum camphora seed oil (CCSO) with oleic acid in a solvent-free system. A commercial immobilized lipase, Lipozyme RM
Balasubramanian Narasimhan et al.
Bioorganic & medicinal chemistry letters, 16(11), 3023-3029 (2006-03-24)
A series of esters and amides of myristic acid was synthesized and tested in vitro for antibacterial activity against gram-positive and gram-negative bacteria. All the compounds showed activity comparable to that of the standard drug, ciprofloxacin. The structural characteristics governing
Sonja Klee et al.
Rapid communications in mass spectrometry : RCM, 28(14), 1591-1600 (2014-06-05)
Atmospheric pressure chemical ionization (APCI) sources operated with point to plane DC discharges ('Coronas') frequently suffer from point electrode degradation and potentially lead to oxidation and/or fragmentation of the generated analyte ions. It is postulated that these adverse effects are