U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C12H20O6
Molecular Weight 260.2836
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GLYCERYL TRIPROPANOATE

SMILES

CCC(=O)OCC(COC(=O)CC)OC(=O)CC

InChI

InChIKey=YZWRNSARCRTXDS-UHFFFAOYSA-N
InChI=1S/C12H20O6/c1-4-10(13)16-7-9(18-12(15)6-3)8-17-11(14)5-2/h9H,4-8H2,1-3H3

HIDE SMILES / InChI

Molecular Formula C12H20O6
Molecular Weight 260.2836
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Non-lipolytic and lipolytic sequence-related carboxylesterases: a comparative study of the structure-function relationships of rabbit liver esterase 1 and bovine pancreatic bile-salt-activated lipase.
2010-11
Modeling of solvent-dependent conformational transitions in Burkholderia cepacia lipase.
2009-05-28
Enzymatic hydrolysis of organic-core microcapsules to produce aqueous-core microcapsules.
2008-05
Biochemical characterization, cloning, and molecular modelling of chicken pancreatic lipase.
2006-07-15
Biochemical and molecular characterization of a lipase produced by Rhizopus oryzae.
2006-07
Purification and characterization of a novel lipase from the digestive glands of a primitive animal: the scorpion.
2005-10-30
Biochemical and molecular characterization of Staphylococcus xylosus lipase.
2005-05-25
Expression and characterization of Ca(2+)-independent lipase from Bacillus pumilus B26.
2002-07-11
Distinction between esterases and lipases: a kinetic study with vinyl esters and TAG.
2002-07
Lipase-catalysed hydrolysis of short-chain substrates in solution and in emulsion: a kinetic study.
2001-11-30
Biochemical and molecular characterization of Staphylococcus simulans lipase.
2001-09
Fatty acid steryl, stanyl, and steroid esters by esterification and transesterification in vacuo using Candida rugosa lipase as catalyst.
2001-01
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 18:38:00 GMT 2025
Edited
by admin
on Mon Mar 31 18:38:00 GMT 2025
Record UNII
F8L8EVQ6QB
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
GLYCERYL TRIPROPANOATE
FCC   FHFI  
Systematic Name English
FEMA NO. 3286
Preferred Name English
1,2,3-PROPANETRIOL, 1,2,3-TRIPROPANOATE
Common Name English
GLYCERYL TRIPROPANOATE [FHFI]
Common Name English
PROPIONIN, TRI-
Common Name English
NSC-36744
Code English
TRIPROPIONIN
Common Name English
GLYCERYL TRIPROPANOATE [FCC]
Common Name English
1,2,3-PROPANETRIOL, TRIPROPANOATE
Systematic Name English
Code System Code Type Description
ECHA (EC/EINECS)
205-365-1
Created by admin on Mon Mar 31 18:38:00 GMT 2025 , Edited by admin on Mon Mar 31 18:38:00 GMT 2025
PRIMARY
MESH
C031627
Created by admin on Mon Mar 31 18:38:00 GMT 2025 , Edited by admin on Mon Mar 31 18:38:00 GMT 2025
PRIMARY
FDA UNII
F8L8EVQ6QB
Created by admin on Mon Mar 31 18:38:00 GMT 2025 , Edited by admin on Mon Mar 31 18:38:00 GMT 2025
PRIMARY
CAS
139-45-7
Created by admin on Mon Mar 31 18:38:00 GMT 2025 , Edited by admin on Mon Mar 31 18:38:00 GMT 2025
PRIMARY
JECFA MONOGRAPH
1141
Created by admin on Mon Mar 31 18:38:00 GMT 2025 , Edited by admin on Mon Mar 31 18:38:00 GMT 2025
PRIMARY
EPA CompTox
DTXSID8051702
Created by admin on Mon Mar 31 18:38:00 GMT 2025 , Edited by admin on Mon Mar 31 18:38:00 GMT 2025
PRIMARY
CHEBI
88153
Created by admin on Mon Mar 31 18:38:00 GMT 2025 , Edited by admin on Mon Mar 31 18:38:00 GMT 2025
PRIMARY
PUBCHEM
8763
Created by admin on Mon Mar 31 18:38:00 GMT 2025 , Edited by admin on Mon Mar 31 18:38:00 GMT 2025
PRIMARY
NSC
36744
Created by admin on Mon Mar 31 18:38:00 GMT 2025 , Edited by admin on Mon Mar 31 18:38:00 GMT 2025
PRIMARY