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Merck

T2151

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:
2438-40-6
Molecular Weight:
849.40
UNSPSC Code:
12352211
NACRES:
NA.25
PubChem Substance ID:
24900019
MDL number:
MFCD00053740
Beilstein/REAXYS Number:
1811256

Product Name

Glyceryl triheptadecanoate, ≥99%

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

SMILES string

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

InChI key

FBFWDBGUSMGXPI-UHFFFAOYSA-N

biological source

synthetic (organic)

assay

≥99%

form

powder

functional group

ester

lipid type

neutral glycerides

shipped in

ambient

storage temp.

−20°C

Quality Level

200

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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

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
0000483511
0000483511
0000488565
0000488570
0000488570

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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
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
Antoine Delbrut et al.
Molecules (Basel, Switzerland), 23(4) (2018-04-12)
By their autotrophic nature and their molecular richness, microalgae are serious assets in the context of current environmental and societal challenges. Some species produce both omega-3 long chain polyunsaturated fatty acids (PUFAs) and xanthophylls, two molecular families widely studied for
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
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
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