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T2151

Sigma-Aldrich

Glyceryl triheptadecanoate

≥99%

Synonym(s):

TG(17:0/17:0/17:0), 1,2,3-Triheptadecanoylglycerol, Triheptadecanoin

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About This Item

Linear Formula:
[CH3(CH2)15COOCH2]2CHOCO(CH2)15CH3
CAS Number:
Molecular Weight:
849.40
Beilstein:
1811256
MDL number:
UNSPSC Code:
12352211
PubChem Substance ID:
NACRES:
NA.25

biological source

synthetic (organic)

Assay

≥99%

form

powder

functional group

ester

lipid type

neutral glycerides

shipped in

ambient

storage temp.

−20°C

SMILES string

CCCCCCCCCCCCCCCCC(=O)OCC(COC(=O)CCCCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCCC

InChI

1S/C54H104O6/c1-4-7-10-13-16-19-22-25-28-31-34-37-40-43-46-52(55)58-49-51(60-54(57)48-45-42-39-36-33-30-27-24-21-18-15-12-9-6-3)50-59-53(56)47-44-41-38-35-32-29-26-23-20-17-14-11-8-5-2/h51H,4-50H2,1-3H3

InChI key

FBFWDBGUSMGXPI-UHFFFAOYSA-N

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Application

Glyceryl triheptadecanoate has been used:
  • as an external standard in gas chromatography (GC) analysis for soybean seeds lipid extraction
  • as an internal standard solution to correct the transesterification efficiency during lipid analysis by gas chromatography-flame ionization detector (GC-FID)
  • as an internal standard in chloroform to dissolve total lipids obtained from fresh leaves of N. benthamiana for thin layer chromatography (TLC) analysis and to analyze their fatty acid content using GC

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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’.

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Antoine Delbrut et al.
Molecules (Basel, Switzerland), 23(4) (2018-04-12)
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Kiran-Kumar Shivaiah et al.
Plant physiology, 182(2), 756-775 (2019-12-04)
Arabidopsis (Arabidopsis thaliana), like most dicotyledonous plants, expresses a multicomponent, heteromeric acetyl-CoA carboxylase (htACCase), which catalyzes the generation of the malonyl-CoA precursor of de novo fatty acid biosynthesis. This enzyme consists of four catalytic subunits: biotin carboxylase (BC), carboxyltransferase (CT)-α
Sara Madji et al.
Molecules (Basel, Switzerland), 24(11) (2019-06-12)
This study aims at investigating p-menthane, a novel bio-based solvent resulting from the hydrogenation of d-limonene, as a green alternative to n-hexane or toluene for the extraction and solubilization of natural substances. First, conductor-like combination of quantum chemistry (COSMO) coupled
Shannon E Currie et al.
Conservation physiology, 7(1), coz005-coz005 (2019-02-26)
In order to effectively conserve species, we must understand the structure and function of integral mechanisms at all levels of organismal organisation, from intracellular biochemistry to whole animal ecophysiology. The accuracy of biochemical analyses depend on the quality and integrity
Hyun Uk Kim et al.
FEBS open bio, 4, 25-32 (2013-12-24)
The LEAFY COTYLEDON2 (LEC2) gene plays critically important regulatory roles during both early and late embryonic development. Here, we report the identification of the LEC2 gene from the castor bean plant (Ricinus communis), and characterize the effects of its overexpression

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