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91040

Sigma-Aldrich

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
Beilstein:
1717202
EC Number:
208-686-5
MDL number:
MFCD00036236
UNSPSC Code:
12352100
PubChem Substance ID:
57653420
NACRES:
NA.22

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

SMILES string

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

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

InChI key

VLPFTAMPNXLGLX-UHFFFAOYSA-N

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Storage Class Code

12 - Non Combustible Liquids

WGK

awg

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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
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
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
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.
Pedro Reis et al.
Langmuir : the ACS journal of surfaces and colloids, 24(14), 7400-7407 (2008-06-13)
Tensiometry (the pendant drop technique), interfacial shear rheology, and ellipsometry have been used to study the effect of polar lipids that are generated during fat digestion on the behavior of lipases at the oil-water interface. Both Sn-1,3 regiospecific and nonregiospecific
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