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Merck
CN

91040

Glyceryl trioctanoate

technical, ≥90% (GC)

Synonym(s):

1,2,3-Tricapryloylglycerol, 1,2,3-Trioctanoylglycerol, Glycerol tricaprylate, Glycerol trioctanoate, Glyceryl tricaprylate, Tricaprylin, Trioctanoin

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About This Item

Linear Formula:
[CH3(CH2)6COOCH2]2CHOCO(CH2)6CH3
CAS Number:
538-23-8
Molecular Weight:
470.68
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
57653420
EC Number:
208-686-5
Beilstein/REAXYS Number:
1717202
MDL number:
MFCD00036236

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InChI key

VLPFTAMPNXLGLX-UHFFFAOYSA-N

InChI

1S/C27H50O6/c1-4-7-10-13-16-19-25(28)31-22-24(33-27(30)21-18-15-12-9-6-3)23-32-26(29)20-17-14-11-8-5-2/h24H,4-23H2,1-3H3

SMILES string

CCCCCCCC(=O)OCC(COC(=O)CCCCCCC)OC(=O)CCCCCCC

grade

technical

assay

≥90% (GC)

form

liquid

bp

233 °C/1 mmHg (lit.)

density

0.956 g/mL at 20 °C (lit.)

functional group

ester

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Storage Class

12 - Non Combustible Liquids

wgk

awg

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
BCCF0616
BCCC4684
BCBW6634
BCBN5142V
BCBK3512V

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Jeong Ho Jeon et al.
Applied microbiology and biotechnology, 81(5), 865-874 (2008-09-06)
To search for new cold-active lipases, a metagenomic library was constructed using cold-sea sediment samples at Edison Seamount and was screened for lipolytic activities by plating on a tricaprylin medium. Subsequently, a fosmid clone was selected, and the whole sequence
Ahmed Aloulou et al.
Biochimica et biophysica acta, 1771(12), 1446-1456 (2007-11-21)
The effects of various detergents and pH on the interfacial binding and activity of two fungal lipases from Yarrowia lipolytica (YLLIP2) and Thermomyces lanuginosus (TLL) were investigated using trioctanoin emulsions as well as monomolecular films spread at the air-water interface.
Maciej Pilarek et al.
Journal of biotechnology, 127(4), 736-744 (2006-09-30)
A new model of enzymatic 1,3-specific alcoholysis of triacylglycerols has been developed. The irreversibility of the acyl bounds cleavage in glycerides, a reversible monoglycerides isomerization and an irreversible enzyme deactivation have been assumed. The Ping Pong Bi Bi mechanism with
Tehila Mishraki et al.
Colloids and surfaces. B, Biointerfaces, 75(1), 47-56 (2009-09-15)
A model protein (lysozyme) was incorporated into monoolein-based reverse hexagonal (H(II)) mesophase and its structure effects were characterized by small angle X-ray scattering, ATR-FTIR spectroscopy, and rheological measurements. Modifications in molecular organization of the H(II) mesophases as well as the
Idit Amar-Yuli et al.
The journal of physical chemistry. B, 112(33), 10171-10180 (2008-07-31)
The solubilization of four bioactive molecules with different polarities, in three reverse hexagonal (HII) systems has been investigated. The three HII systems were a typical reverse hexagonal composed of glycerol monooleate (GMO)/tricaprylin/water and two fluid hexagonal systems containing either 2.75
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