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Merck
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91040

Sigma-Aldrich

Glyceryl trioctanoate

technical, ≥90% (GC)

Sinonimo/i:

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

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About This Item

Formula condensata:
[CH3(CH2)6COOCH2]2CHOCO(CH2)6CH3
Numero CAS:
538-23-8
Peso molecolare:
470.68
Beilstein:
1717202
Numero CE:
208-686-5
Numero MDL:
MFCD00036236
Codice UNSPSC:
12352100
ID PubChem:
57653420
NACRES:
NA.22

Grado

technical

Saggio

≥90% (GC)

Forma fisica

liquid

P. eboll.

233 °C/1 mmHg (lit.)

Densità

0.956 g/mL at 20 °C (lit.)

Gruppo funzionale

ester

Stringa SMILE

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
VLPFTAMPNXLGLX-UHFFFAOYSA-N

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Codice della classe di stoccaggio

12 - Non Combustible Liquids

Classe di pericolosità dell'acqua (WGK)

awg

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves

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Certificati d'analisi (COA)

Lot/Batch Number
BCCF0616
BCCC4684
BCBW6634
BCBN5142V
BCBK3512V

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Glyceryl trimyristate ≥99%

Sigma-Aldrich

T5141

Glyceryl trimyristate

Lipid standards: triglyceride mixtures certified reference material

Supelco

17811-1AMP

Lipid standards: triglyceride mixtures

Triacetin 99%

Sigma-Aldrich

525073

Triacetin

Glyceryl trioleate ≥99%

Sigma-Aldrich

T7140

Glyceryl trioleate

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
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
Idit Amar-Yuli et al.
The journal of physical chemistry. B, 112(13), 3971-3982 (2008-03-08)
This study reports on the formation of a low viscosity H(II) mesophase at room temperature upon addition of Transcutol (diethylene glycol mono ethyl ether) or ethanol to the ternary mixture of GMO (glycerol monooleate)/TAG (tricaprylin)/water. The microstructure and bulk properties
Gerrit A van Koningsveld et al.
Journal of agricultural and food chemistry, 54(17), 6419-6427 (2006-08-17)
In the present study emulsions were made with various potato protein preparations, which varied in protease inhibitor and patatin content. These emulsions were characterized with respect to average droplet size, plateau surface excess, and the occurrence of droplet aggregation. Droplet
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