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T3882

Sigma-Aldrich

Glyceryl tritridecanoate

≥99%

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Synonym(s):
TG(13:0/13:0/13:0), 1,2,3-Tritridecanoylglycerol, Tritridecanoin (C13:0)
Empirical Formula (Hill Notation):
C42H80O6
CAS Number:
Molecular Weight:
681.08
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.25

biological source

synthetic

Quality Level

assay

≥99%

form

powder

functional group

ester

lipid type

neutral glycerides

shipped in

ambient

storage temp.

−20°C

SMILES string

CCCCCCCCCCCCC(=O)OCC(COC(=O)CCCCCCCCCCCC)OC(=O)CCCCCCCCCCCC

InChI

1S/C42H80O6/c1-4-7-10-13-16-19-22-25-28-31-34-40(43)46-37-39(48-42(45)36-33-30-27-24-21-18-15-12-9-6-3)38-47-41(44)35-32-29-26-23-20-17-14-11-8-5-2/h39H,4-38H2,1-3H3

InChI key

UDXANBFMQUOKTQ-UHFFFAOYSA-N

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This Item
T2151T5016T5141
Glyceryl tritridecanoate ≥99%

T3882

Glyceryl tritridecanoate

Glyceryl triheptadecanoate ≥99%

T2151

Glyceryl triheptadecanoate

Glyceryl tristearate ≥99%

T5016

Glyceryl tristearate

Glyceryl trimyristate ≥99%

T5141

Glyceryl trimyristate

biological source

synthetic

biological source

synthetic (organic)

biological source

synthetic

biological source

plant (palm)

functional group

ester

functional group

ester

functional group

ester

functional group

ester

form

powder

form

powder

form

powder

form

powder

shipped in

ambient

shipped in

ambient

shipped in

ambient

shipped in

ambient

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

storage temp.

-

Application

Glyceryl tritridecanoate has been used as an internal standard for the extraction of the total lipids from the muscle homogenate. It has also been used in toluene as an internal standard to assess the lipid content and fatty acid (FA) composition of forages and concentrates using a one-step extraction-transesterification procedure.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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Ana Luiza Fontes et al.
Scientific reports, 8(1), 15591-15591 (2018-10-24)
Current research on lipids is highlighting their relevant role in metabolic/signaling pathways. Conjugated fatty acids (CFA), namely isomers of linoleic and linolenic acid (i.e. CLA and CLNA, respectively) can positively modulate inflammation processes and energy metabolism, promoting anti-carcinogenic and antioxidant
Luís M Rodríguez-Alcalá et al.
Journal of agricultural and food chemistry, 65(35), 7680-7686 (2017-08-10)
This study aimed to assess the oral absorption and plasma kinetics of two main isomers contained in commercial conjugated linoleic acid (CLA)-rich oil (Tonalin TG-80), rumenic acid (RA), and C18:2 trans-10, cis-12. The isomer plasma disposition after the single oral
Jimena Lavandera et al.
The British journal of nutrition, 118(11), 906-913 (2017-11-28)
Conjugated linoleic acid (CLA) might regulate the lipid depots in liver and adipose tissue. As there is an association between maternal nutrition, fat depots and risk of offspring chronic disease, the aim was to investigate the effect of maternal CLA
Laura Goracci et al.
Chemical research in toxicology, 33(1), 258-270 (2019-12-11)
The importance of adsorption, distribution, metabolism, excretion, and toxicity (ADMET) analysis is expected to grow substantially due to recent failures in detecting severe toxicity issues of new chemical entities during preclinical/clinical development. Traditionally, safety risk assessment studies for humans have

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