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Details

Stereochemistry ACHIRAL
Molecular Formula C39H74O6
Molecular Weight 639.0013
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TRILAURIN

SMILES

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

InChI

InChIKey=VMPHSYLJUKZBJJ-UHFFFAOYSA-N
InChI=1S/C39H74O6/c1-4-7-10-13-16-19-22-25-28-31-37(40)43-34-36(45-39(42)33-30-27-24-21-18-15-12-9-6-3)35-44-38(41)32-29-26-23-20-17-14-11-8-5-2/h36H,4-35H2,1-3H3

HIDE SMILES / InChI

Molecular Formula C39H74O6
Molecular Weight 639.0013
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Development of solid lipid nanoparticles for enhanced solubility of poorly soluble drugs.
2010-12
Short chain saturated fatty acids decrease circulating cholesterol and increase tissue PUFA content in the rat.
2010-11
Myristate is selectively incorporated into surfactant and decreases dipalmitoylphosphatidylcholine without functional impairment.
2010-11
Characterization of an extracellular lipase from the biocontrol fungus, Nomuraea rileyi MJ, and its toxicity toward Spodoptera litura.
2010-11
Progress in antiretroviral drug delivery using nanotechnology.
2010-08-09
X-ray crystallographic and MD simulation studies on the mechanism of interfacial activation of a family I.3 lipase with two lids.
2010-07-02
Modeling the solid-liquid phase transition in saturated triglycerides.
2010-02-07
Pressure-induced phase transitions in triacylglycerides.
2010-02
Formation of biodegradable microcapsules utilizing 3D, selectively surface-modified PDMS microfluidic devices.
2010-02
Psoralea corylifolia Linn.-"Kushtanashini".
2010-01
Enzymatic preparation of structured oils containing short-chain fatty acids.
2010
Fatty acid selectivity of lipases during acidolysis reaction between oleic acid and monoacid triacylglycerols.
2009-11-11
Thermostable lipases from the extreme thermophilic anaerobic bacteria Thermoanaerobacter thermohydrosulfuricus SOL1 and Caldanaerobacter subterraneus subsp. tengcongensis.
2009-09
Influence of structural variations on drug release from lipid/polyethylene glycol matrices.
2009-07-12
Order-disorder phase transformation of triacylglycerols: effect of the structure of the aliphatic chains.
2009-01-29
Understanding the solid-state behaviour of triglyceride solid lipid extrudates and its influence on dissolution.
2009-01
Nanotechnology-based drug delivery systems.
2007-12-01
Isolation of lipase producing Bacillus sp. from olive mill wastewater and improving its enzyme activity.
2007-11-19
Some insights about 1,6-diphenyl-1,3,5-hexatriene-lipid supramolecular assemblies by steady-state fluorescence measurements.
2007-09
Effects of stereospecific positioning of fatty acids in triacylglycerol structures in native and randomized fats: a review of their nutritional implications.
2007-07-12
Development and characterization of amphotericin B bearing emulsomes for passive and active macrophage targeting.
2007-04
Importance of solid lipid nanoparticles (SLN) in various administration routes and future perspectives.
2007
Drug release from lipid-based implants: elucidation of the underlying mass transport mechanisms.
2006-05-18
Development and characterization of emulsomes for sustained and targeted delivery of an antiviral agent to liver.
2006-03
Saturated phospholipids promote crystallization but slow down polymorphic transitions in triglyceride nanoparticles.
2005-10-03
Mutations in the "lid" region affect chain length specificity and thermostability of a Pseudomonas fragi lipase.
2005-04-25
Dialkylphosphatidylcholine and egg yolk lecithin for emulsification of various triglycerides.
2005-04-10
Raman spectroscopy investigation of various saturated monoacid triglycerides.
2005-04
Hydration of an amphiphilic excipient, Gelucire 44/14.
2004-08-20
Enzymatic synthesis of monolaurin.
2004
Maldigestion and malabsorption of dietary lipid during severe childhood malnutrition.
2002-12
Rapid thermogravimetric measurements of boiling points and vapor pressure of saturated medium- and long-chain triglycerides.
2002-08
Saturated triglycerides and fatty acids activate neutrophils depending on carbon chain-length.
2002-04
Process development for production of medium chain triglycerides using immobilized lipase in a solvent-free system.
2002
Final report on the safety assessment of trilaurin, triarachidin, tribehenin, tricaprin, tricaprylin, trierucin, triheptanoin, triheptylundecanoin, triisononanoin, triisopalmitin, triisostearin, trilinolein, trimyristin, trioctanoin, triolein, tripalmitin, tripalmitolein, triricinolein, tristearin, triundecanoin, glyceryl triacetyl hydroxystearate, glyceryl triacetyl ricinoleate, and glyceryl stearate diacetate.
2001
Fatty acids and derivatives as antimicrobial agents.
1972-07
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 19:00:53 GMT 2025
Edited
by admin
on Mon Mar 31 19:00:53 GMT 2025
Record UNII
7FP2Z3RVUV
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DYNASAN 112
Preferred Name English
TRILAURIN
INCI  
INCI  
Official Name English
LAURIC TRIGLYCERIDE
Common Name English
TRILAUROYLGLYCEROL
Systematic Name English
GLYCERIN TRIDODECANOATE
Systematic Name English
TRIDODECANOYL GLYCEROL
Systematic Name English
DODECANOIC ACID, 1,2,3-PROPANETRIYL ESTER
Common Name English
NSC-4061
Code English
GLYCERYL TRILAURATE
Systematic Name English
TRIDODECANOIN
Common Name English
DODECANOIC ACID, 1,1',1''-(1,2,3-PROPANETRIYL) ESTER
Common Name English
GLYCERIN TRILAURATE
Systematic Name English
GLYCERYL TRIDODECANOATE
Systematic Name English
LAURIC ACID TRIGLYCERIDE
Common Name English
Code System Code Type Description
SMS_ID
100000175273
Created by admin on Mon Mar 31 19:00:53 GMT 2025 , Edited by admin on Mon Mar 31 19:00:53 GMT 2025
PRIMARY
CAS
538-24-9
Created by admin on Mon Mar 31 19:00:53 GMT 2025 , Edited by admin on Mon Mar 31 19:00:53 GMT 2025
PRIMARY
NSC
4061
Created by admin on Mon Mar 31 19:00:53 GMT 2025 , Edited by admin on Mon Mar 31 19:00:53 GMT 2025
PRIMARY
RXCUI
1368880
Created by admin on Mon Mar 31 19:00:53 GMT 2025 , Edited by admin on Mon Mar 31 19:00:53 GMT 2025
PRIMARY RxNorm
ECHA (EC/EINECS)
208-687-0
Created by admin on Mon Mar 31 19:00:53 GMT 2025 , Edited by admin on Mon Mar 31 19:00:53 GMT 2025
PRIMARY
MESH
C004565
Created by admin on Mon Mar 31 19:00:53 GMT 2025 , Edited by admin on Mon Mar 31 19:00:53 GMT 2025
PRIMARY
CHEBI
77389
Created by admin on Mon Mar 31 19:00:53 GMT 2025 , Edited by admin on Mon Mar 31 19:00:53 GMT 2025
PRIMARY
PUBCHEM
10851
Created by admin on Mon Mar 31 19:00:53 GMT 2025 , Edited by admin on Mon Mar 31 19:00:53 GMT 2025
PRIMARY
DAILYMED
7FP2Z3RVUV
Created by admin on Mon Mar 31 19:00:53 GMT 2025 , Edited by admin on Mon Mar 31 19:00:53 GMT 2025
PRIMARY
EPA CompTox
DTXSID80904390
Created by admin on Mon Mar 31 19:00:53 GMT 2025 , Edited by admin on Mon Mar 31 19:00:53 GMT 2025
PRIMARY
FDA UNII
7FP2Z3RVUV
Created by admin on Mon Mar 31 19:00:53 GMT 2025 , Edited by admin on Mon Mar 31 19:00:53 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY