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Merck
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T5141

Sigma-Aldrich

Glyceryl trimyristate

≥99%

Sinónimos:

TG(14:0/14:0/14:0), 1,2,3-Tritetradecanoylglycerol, Glycerol trimyristate, Trimyristin

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About This Item

Fórmula lineal:
[CH3(CH2)12COOCH2]2CHOCO(CH2)12CH3
Número de CAS:
555-45-3
Peso molecular:
723.16
Beilstein/REAXYS Number:
1718242
EC Number:
209-099-7
MDL number:
MFCD00036229
UNSPSC Code:
12352211
PubChem Substance ID:
24900261
NACRES:
NA.25

biological source

plant (palm)

Quality Level

200

assay

≥99%

form

powder

mp

56-57 °C (lit.)

functional group

ester

lipid type

neutral glycerides

shipped in

ambient

SMILES string

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

InChI

1S/C45H86O6/c1-4-7-10-13-16-19-22-25-28-31-34-37-43(46)49-40-42(51-45(48)39-36-33-30-27-24-21-18-15-12-9-6-3)41-50-44(47)38-35-32-29-26-23-20-17-14-11-8-5-2/h42H,4-41H2,1-3H3

InChI key

DUXYWXYOBMKGIN-UHFFFAOYSA-N

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Categorías relacionadas

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Certificados de análisis (COA)

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Sigma-Aldrich

M8005

Sodium myristate

Glyceryl trilinolenate ≥97% (TLC), liquid

Sigma-Aldrich

T6513

Glyceryl trilinolenate

Tripentadecanoin ≥99%

Sigma-Aldrich

T4257

Tripentadecanoin

Maximilian Borgmeyer et al.
Cell reports, 37(1), 109797-109797 (2021-10-06)
Membrane lipids and their metabolism have key functions in neurotransmission. Here we provide a quantitative lipid inventory of mouse and rat synaptic junctions. To this end, we developed a multiomics extraction and analysis workflow to probe the interplay of proteins
W Vogelhuber et al.
Pharmaceutical development and technology, 8(1), 71-79 (2003-04-01)
Matrices made of glyceryl trimyristate as a bioerodible and biocompatible material were manufactured by compression in dimensions that would still allow an application via injection. Pyranine, as a low molecular hydrophilic compound with a low detection limit, and tetramethylrhodamine labeled
S Martins et al.
Journal of biomedical nanotechnology, 5(1), 76-83 (2010-01-09)
Solid lipid nanoparticles (SLN) composed of trimyristin (solid lipid) and poloxamer 407 (surfactant) were prepared by a w/o/w emulsion technique for the incorporation of Salmon calcitonin, and further explored as protein carriers for oral delivery. Trimyristin SLN showed a mean
C Thies et al.
Journal of microencapsulation, 20(1), 87-96 (2003-01-10)
A novel solvent-free particle coating process, based on the solvent properties of supercritical fluids (SCF) is described. It consists of dissolving one or more coating materials in supercritical CO(2) and then adjusting T/P conditions in the autoclave so that the
Carsten Olbrich et al.
International journal of pharmaceutics, 237(1-2), 119-128 (2002-04-17)
In vivo drug release from solid lipid nanoparticles (SLN) takes place by diffusion and degradation of the lipid matrix. SLN with different degree of crystallinity were prepared to study the effect of crystallinity on the degradation velocity. These SLN were
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