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Details

Stereochemistry ACHIRAL
Molecular Formula C6H14O3
Molecular Weight 134.1736
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TRIMETHYLOLPROPANE

SMILES

CCC(CO)(CO)CO

InChI

InChIKey=ZJCCRDAZUWHFQH-UHFFFAOYSA-N
InChI=1S/C6H14O3/c1-2-6(3-7,4-8)5-9/h7-9H,2-5H2,1H3

HIDE SMILES / InChI

Molecular Formula C6H14O3
Molecular Weight 134.1736
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Layered double hydroxide as nanofiller in the development of polyurethane nanocomposites.
2010-09
Modeling of reaction kinetics for transesterification of palm-based methyl esters with trimethylolpropane.
2010-08
Investigation of thiol-ene and thiol-ene-methacrylate based resins as dental restorative materials.
2010-01
Engineering of cyclodextrin glucanotransferases and the impact for biotechnological applications.
2010-01
Studies on in vitro biostability and blood compatibility of polyurethane potting compound based on aromatic polymeric MDI for extracorporeal devices.
2009-12
Dissociation constants for GABA(A) receptor antagonists determined with neuronal networks on microelectrode arrays.
2008-08-30
Dispersion behavior of zirconia nanocrystals and their surface functionalization with vinyl group-containing ligands.
2007-08-28
High-spin Mn wheels.
2007-08-20
Nanofabricated particles for engineered drug therapies: a preliminary biodistribution study of PRINT nanoparticles.
2007-08-16
Hyperbranched polyesters: synthesis, characterization, and molecular simulations.
2007-08-02
Synthesis and characterization of branched polymers from lipase-catalyzed trimethylolpropane copolymerizations.
2007-06
Co- and terpolyesters based on isosorbide and succinic acid for coating applications: synthesis and characterization.
2006-12
A family of [Mn6] complexes featuring tripodal ligands.
2006-08-21
Control of cardiomyocyte orientation on a microscaffold fabricated by photopolymerization with laser beam interference.
2006-05-06
In situ lubricant degradation in Antarctic marine sediments. 1. Short-term changes.
2006-02
Interactions of bupivacaine with a molecularly imprinted polymer in a monolithic format studied by NMR.
2006-01-15
1,1,1-Tris(hydroxymethyl)propane in manganese carboxylate chemistry: synthesis, structure and magnetic properties of a mixed-valence [MnIII4MnII4] cluster featuring the novel [MnIII4MnII4(mu3-OR)6(mu2-OR)8]6+ core.
2006-01-14
Thiol-ene oligomers as dental restorative materials.
2005-12
Toxicology studies of trimethylolpropane triacrylate (technical grade) (CAS No. 15625-89-5) in F344/N rats, B6C3F1 mice, and genetically modified (FVB Tg.AC hemizygous) mice (dermal studies).
2005-10
Photo-polymerized microarchitectural constructs prepared by microstereolithography (muSL) using liquid acrylate-end-capped trimethylene carbonate-based prepolymers.
2005-05
Tailoring lactide/caprolactone co-oligomers as tissue adhesives.
2004-12
Sensitivity evaluation of the Daphtoxkit and Thamnotoxkit microbiotests on blind samples.
2004-10-13
Synthesis, structure, and magnetic properties of a [Mn22] wheel-like single-molecule magnet.
2004-07-12
Preparation and evaluation of non-bonded hyperbranched polymer-coated columns for capillary electrophoresis.
2004-07-08
[The preparation of chemical-bonded hyperbranched polymer coated column for capillary electrophoresis and their application to separation of basic proteins].
2004-05
Synthetic polymers adsorbing bisphenol A and its analogues prepared by covalent molecular imprinting using bisphenol A dimethacrylate as a template molecule.
2004-04
Telechelic and star-shaped poly(L-lactide)s by means of bismuth(III) acetate as initiator.
2004-03-09
Photocurable biodegradable liquid copolymers: synthesis of acrylate-end-capped trimethylene carbonate-based prepolymers, photocuring, and hydrolysis.
2004-03-09
Preparation of polyol esters based on vegetable and animal fats.
2003-03
Introducing lactide-based biodegradable tissue adhesives.
2003-02
Spectra from 2.5-15 microm of tissue phantom materials, optical clearing agents and ex vivo human skin: implications for depth profiling of human skin.
2003-01-21
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:45:35 GMT 2025
Edited
by admin
on Mon Mar 31 18:45:35 GMT 2025
Record UNII
090GDF4HBD
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TRIMETHYLOLPROPANE
INCI  
INCI  
Official Name English
1,1,1-TRIS(HYDROXYMETHYL)PROPANE
HSDB  
Preferred Name English
PROPYLIDYNETRIMETHANOL
Systematic Name English
PROPANEDIOL, 2-ETHYL-2-(HYDROXYMETHYL)-, 1,3-
Systematic Name English
NSC-3576
Code English
TMP (ALCOHOL)
Common Name English
TRIS(HYDROXYMETHYL)PROPANE
Systematic Name English
1,1,1-TRIMETHYLOLPROPANE
Systematic Name English
1,3-PROPANEDIOL, 2-ETHYL-2-(HYDROXYMETHYL)-
Systematic Name English
2-ETHYL-2-HYDROXYMETHYL-1,3-PROPANEDIOL
Systematic Name English
2-ETHYL-2-(HYDROXYMETHYL)-1,3-PROPANEDIOL
Systematic Name English
1,1,1-TRIS(HYDROXYMETHYL)PROPANE [HSDB]
Common Name English
Classification Tree Code System Code
Food Contact Sustance Notif, (FCN No.) FCN NO. 92
Created by admin on Mon Mar 31 18:45:35 GMT 2025 , Edited by admin on Mon Mar 31 18:45:35 GMT 2025
Food Contact Sustance Notif, (FCN No.) FCN NO. 312
Created by admin on Mon Mar 31 18:45:35 GMT 2025 , Edited by admin on Mon Mar 31 18:45:35 GMT 2025
Food Contact Sustance Notif, (FCN No.) FCN NO. 804
Created by admin on Mon Mar 31 18:45:35 GMT 2025 , Edited by admin on Mon Mar 31 18:45:35 GMT 2025
Food Contact Sustance Notif, (FCN No.) FCN NO. 527
Created by admin on Mon Mar 31 18:45:35 GMT 2025 , Edited by admin on Mon Mar 31 18:45:35 GMT 2025
Food Contact Sustance Notif, (FCN No.) FCN NO. 551
Created by admin on Mon Mar 31 18:45:35 GMT 2025 , Edited by admin on Mon Mar 31 18:45:35 GMT 2025
Code System Code Type Description
NSC
3576
Created by admin on Mon Mar 31 18:45:35 GMT 2025 , Edited by admin on Mon Mar 31 18:45:35 GMT 2025
PRIMARY
DAILYMED
090GDF4HBD
Created by admin on Mon Mar 31 18:45:35 GMT 2025 , Edited by admin on Mon Mar 31 18:45:35 GMT 2025
PRIMARY
CAS
77-99-6
Created by admin on Mon Mar 31 18:45:35 GMT 2025 , Edited by admin on Mon Mar 31 18:45:35 GMT 2025
PRIMARY
EPA CompTox
DTXSID2026448
Created by admin on Mon Mar 31 18:45:35 GMT 2025 , Edited by admin on Mon Mar 31 18:45:35 GMT 2025
PRIMARY
FDA UNII
090GDF4HBD
Created by admin on Mon Mar 31 18:45:35 GMT 2025 , Edited by admin on Mon Mar 31 18:45:35 GMT 2025
PRIMARY
HSDB
5218
Created by admin on Mon Mar 31 18:45:35 GMT 2025 , Edited by admin on Mon Mar 31 18:45:35 GMT 2025
PRIMARY
RXCUI
1368881
Created by admin on Mon Mar 31 18:45:35 GMT 2025 , Edited by admin on Mon Mar 31 18:45:35 GMT 2025
PRIMARY RxNorm
MESH
C018163
Created by admin on Mon Mar 31 18:45:35 GMT 2025 , Edited by admin on Mon Mar 31 18:45:35 GMT 2025
PRIMARY
ECHA (EC/EINECS)
201-074-9
Created by admin on Mon Mar 31 18:45:35 GMT 2025 , Edited by admin on Mon Mar 31 18:45:35 GMT 2025
PRIMARY
WIKIPEDIA
TRIMETHYLOLPROPANE
Created by admin on Mon Mar 31 18:45:35 GMT 2025 , Edited by admin on Mon Mar 31 18:45:35 GMT 2025
PRIMARY
PUBCHEM
6510
Created by admin on Mon Mar 31 18:45:35 GMT 2025 , Edited by admin on Mon Mar 31 18:45:35 GMT 2025
PRIMARY