Skip to Content
Merck
All Photos(4)

Documents

M3378

Sigma-Aldrich

Methyl myristate

≥99% (GC)

Synonym(s):

Methyl tetradecanoate, Myristic acid methyl ester

Sign Into View Organizational & Contract Pricing
All Photos(4)

About This Item

Linear Formula:
CH3(CH2)12COOCH3
CAS Number:
124-10-7
Molecular Weight:
242.40
Beilstein:
1773739
EC Number:
204-680-1
MDL number:
MFCD00008983
UNSPSC Code:
12352211
PubChem Substance ID:
24896834
NACRES:
NA.25

biological source

synthetic (organic)

Assay

≥99% (GC)

form

liquid

refractive index

n20/D 1.436 (lit.)

bp

323 °C (lit.)

mp

18 °C (lit.)

density

0.855 g/mL at 25 °C (lit.)

functional group

ester

lipid type

saturated FAs

shipped in

ambient

storage temp.

2-8°C

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

Looking for similar products? Visit Product Comparison Guide

Application

Methyl myristate may be used as an intermediate polarity oil component of oil-in-water, especially “Pickering-type”, emulsions.

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

233.6 °F - closed cup

Flash Point(C)

112.0 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Tomohiro Imura et al.
Journal of oleo science, 57(8), 415-422 (2008-07-16)
Mannosylerythritol lipid-A (MEL-A) is one of the most promising glycolipid biosurfactants, and abundantly produced by Pseudozyma yeasts. MEL-A gives not only excellent self-assembling properties but also a high binding affinity toward human immunoglobulin G (HIgG). In this study, three kinds
A Walsh et al.
Langmuir : the ACS journal of surfaces and colloids, 26(23), 18039-18048 (2010-11-11)
Sterically stabilized polystyrene latexes were prepared by aqueous emulsion polymerization using a poly(ethylene imine) (PEI) stabilizer in the presence of 4-vinylbenzyl chloride (4-VBC; 1.0 wt % based on styrene). Partial quaternization of the amine groups on the PEI chains by
E S Read et al.
Langmuir : the ACS journal of surfaces and colloids, 20(18), 7422-7429 (2004-08-25)
Sterically stabilized polystyrene latexes (previously described by Amalvy, J. I.; et al. Chem. Commun. 2003, 1826) were evaluated as pH-responsive particulate emulsifiers for the preparation of both oil-in-water and water-in-oil emulsions. The steric stabilizer was a well-defined AB diblock copolymer
Bernard P Binks et al.
Langmuir : the ACS journal of surfaces and colloids, 22(5), 2050-2057 (2006-02-24)
Aqueous dispersions of lightly cross-linked poly(4-vinylpyridine)/silica nanocomposite microgel particles are used as a sole emulsifier of methyl myristate and water (1:1 by volume) at various pH values and salt concentrations at 20 degrees C. These particles become swollen at low
Syuji Fujii et al.
Journal of colloid and interface science, 315(1), 287-296 (2007-08-08)
Hydroxyapatite (HAp) nanoparticles with spherical, rod-shaped or fiber-shaped morphologies were synthesized by wet chemical method in aqueous media. Scanning electron microscopy, dynamic light scattering, helium pycnometry, and aqueous electrophoresis techniques were used to characterize the nanoparticles in terms of their
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service