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T9517

Sigma-Aldrich

Glyceryl trilinoleate

≥98% (TLC), liquid

Synonym(s):

TG(18:2(9Z,12Z)/18:2(9Z,12Z)/18:2(9Z,12Z)), 1,2,3-Tri-(cis,cis-9,12-octadecadienoyl)glycerol, 1,2,3-Trilinoleoylglycerol, Glycerol trilinoleate, Trilinolein

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About This Item

Empirical Formula (Hill Notation):
C57H98O6
CAS Number:
Molecular Weight:
879.38
Beilstein/REAXYS Number:
1718698
EC Number:
MDL number:
UNSPSC Code:
12352211
PubChem Substance ID:
NACRES:
NA.25

biological source

synthetic (organic)

assay

≥98% (TLC)

form

liquid

density

0.925 g/mL at 20 °C (lit.)

functional group

ester

lipid type

neutral glycerides

shipped in

ambient

storage temp.

−20°C

SMILES string

CCCCC\C=C/C\C=C/CCCCCCCC(=O)OCC(COC(=O)CCCCCCC\C=C/C\C=C/CCCCC)OC(=O)CCCCCCC\C=C/C\C=C/CCCCC

InChI

1S/C57H98O6/c1-4-7-10-13-16-19-22-25-28-31-34-37-40-43-46-49-55(58)61-52-54(63-57(60)51-48-45-42-39-36-33-30-27-24-21-18-15-12-9-6-3)53-62-56(59)50-47-44-41-38-35-32-29-26-23-20-17-14-11-8-5-2/h16-21,25-30,54H,4-15,22-24,31-53H2,1-3H3/b19-16-,20-17-,21-18-,28-25-,29-26-,30-27-

InChI key

HBOQXIRUPVQLKX-BBWANDEASA-N

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Application


  • Gum Arabic-Stabilized Ferric Oxyhydroxide Nanoparticles for Efficient and Targeted Intestinal Delivery of Bioavailable Iron.: This research explores the use of glyceryl trilinoleate in stabilizing nanoparticles for targeted iron delivery, highlighting its potential in improving bioavailability and therapeutic efficiency (Li et al., 2023).

Packaging

Sealed ampule.

hcodes

Hazard Classifications

Aquatic Chronic 4

Storage Class

10 - Combustible liquids

wgk_germany

awg

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves


Certificates of Analysis (COA)

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Ming-Jun Gao et al.
The Plant cell, 21(1), 54-71 (2009-01-22)
The seed maturation program is repressed during germination and seedling development so that embryonic genes are not expressed in vegetative organs. Here, we describe a regulator that represses the expression of embryonic seed maturation genes in vegetative tissues. ASIL1 (for
Hung-Yu Yang et al.
Naunyn-Schmiedeberg's archives of pharmacology, 372(2), 160-167 (2005-09-27)
Trilinolein, isolated from the traditional Chinese herb Sanchi (Panax notoginseng), has been shown to have myocardial protective effects via its antioxidant ability. However, the cellular and molecular mechanisms of the protective effect of trilinolein in the heart remain to be
X Zhang et al.
Archives of biochemistry and biophysics, 405(1), 44-54 (2002-08-15)
Laccase enzymes were investigated for their potential to catalyze the oxidation of trilinolein and methyl linoleate. This study demonstrates that laccase enzymes can oxidize unsaturated fatty acid esters and their associated lipids. The reaction products resulting from laccase-catalyzed reactions with
Pei-Yu Chou et al.
The American journal of Chinese medicine, 39(4), 803-815 (2011-07-02)
Trilinolein has been identified as one of the active constituents isolated from Panax notoginseng used widely in traditional Chinese medicine. Protective actions of Panax notoginseng against cerebral ischemia, beneficial effects on the cardiovascular system, and hemostatic, antioxidant, hypolipidemic, hepatoprotective, renoprotective
Shi-Chung Chen et al.
Planta medica, 71(6), 525-529 (2005-06-23)
Trilinolein, isolated from the traditional Chinese herb Sanchi ( Panax notoginseng), has been shown to have myocardial protective effects via its antioxidant ability. However, the cellular and molecular mechanisms of the protective effect of trilinolein in the heart remain to

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