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Details

Stereochemistry ACHIRAL
Molecular Formula C9H12O
Molecular Weight 136.191
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2,4,6-TRIMETHYLPHENOL

SMILES

CC1=CC(C)=C(O)C(C)=C1

InChI

InChIKey=BPRYUXCVCCNUFE-UHFFFAOYSA-N
InChI=1S/C9H12O/c1-6-4-7(2)9(10)8(3)5-6/h4-5,10H,1-3H3

HIDE SMILES / InChI

Molecular Formula C9H12O
Molecular Weight 136.191
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Structural diversity in polyamine Lewis base stabilised lithium aryloxides.
2010-09-21
Synthesis of fluoro(aryloxo)alkaline earth metal cages by C-F bond activation.
2010-06-28
Reactive photoinduced species in estuarine waters. Characterization of hydroxyl radical, singlet oxygen and dissolved organic matter triplet state in natural oxidation processes.
2010-01
Mono-, di-, tri- and tetranuclear rare earth complexes obtained using a moderately bulky aryloxide ligand.
2009-11-02
Metal based synthetic routes to heavy alkaline earth aryloxo complexes involving ligands of moderate steric bulk.
2009-07-07
Reactivity of a 10-I-3 hypervalent iodine trifluoromethylation reagent with phenols.
2008-10-03
Evaluation of photochemical properties of compost humic-like materials.
2008-07
Characterization of alkylphenol metabolites in fish bile by enzymatic treatment and HPLC-fluorescence analysis.
2008-04
Selective benzylic C-C coupling catalyzed by a bioinspired dicopper complex.
2008-02-28
Chemical composition and biological activity of a new type of Brazilian propolis: red propolis.
2007-09-05
Inhibition of humic substances mediated photooxygenation of furfuryl alcohol by 2,4,6-trimethylphenol. Evidence for reactivity of the phenol with humic triplet excited states.
2007-09-01
Column temperature as an active variable in the isocratic, normal-phase high-performance liquid chromatography separation of lipophilic metabolites of nonylphenol ethoxylates.
2007-07-20
Transformation of polycyclic aromatic hydrocarbons by laccase is strongly enhanced by phenolic compounds present in soil.
2007-04-15
Data processing and classification analysis of proteomic changes: a case study of oil pollution in the mussel, Mytilus edulis.
2006-09-13
Gas-phase acidities and O-H bond dissociation enthalpies of phenol, 3-methylphenol, 2,4,6-trimethylphenol, and ethanoic acid.
2006-09-07
Effect of three different cultivars of Lepidium meyenii (Maca) on learning and depression in ovariectomized mice.
2006-06-23
Synthetic and reaction chemistry of heteroatom stabilized boryl and cationic borylene complexes.
2006-01-14
Selective copper(II)-mediated oxidative coupling of a nucleophilic reagent to the para-methyl group of 2,4,6-trimethylphenol.
2005-11-07
Humic substances mediated phototransformation of 2,4,6-trimethylphenol: a catalytic reaction.
2005-06
Novel cuticular hydrocarbons from the cane beetle Antitrogus parvulus--4,6,8,10,16-penta- and 4,6,8,10,16,18-hexamethyldocosanes-unprecedented anti-anti-anti-stereochemistry in the 4,6,8,10-methyltetrad.
2005-03-04
Photosensitized degradation of bisphenol A by dissolved organic matter.
2004-11-15
Key role of the low molecular size fraction of soil humic acids for fluorescence and photoinductive activity.
2004-04-01
4,6,8,10,16-penta- and 4,6,8,10,16,18-hexamethyldocosanes from the cane beetle antitrogusparvulus--cuticular hydrocarbons with unprecedented structure and stereochemistry.
2003-12-25
The effect of ring nitrogen atoms on the homolytic reactivity of phenolic compounds: understanding the radical-scavenging ability of 5-pyrimidinols.
2003-10-17
Methylphenols removal from water by low-cost adsorbents.
2002-07-01
Thermochemical and kinetic studies of a bisphenol antioxidant.
2001-08-10
Electron-rich phenols for probing the photochemical reactivity of freshwaters.
2001-02-15
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:48:08 GMT 2025
Edited
by admin
on Mon Mar 31 19:48:08 GMT 2025
Record UNII
FPZ32614N6
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FEMA NO. 4329
Preferred Name English
2,4,6-TRIMETHYLPHENOL
FHFI   HSDB  
Systematic Name English
1,3,5-TRIMETHYLPHENOL
Systematic Name English
PHENOL, 2,4,6-TRIMETHYL-
Systematic Name English
2,4,6-TRIMETHYLPHENOL [HSDB]
Common Name English
NSC-5353
Code English
2-HYDROXYMESITYLENE
Systematic Name English
1-HYDROXY-2,4,6-TRIMETHYLBENZENE
Systematic Name English
MESITYL ALCOHOL
Systematic Name English
MESITOL
Systematic Name English
2,4,6-TRIMETHYLPHENOL [FHFI]
Common Name English
Classification Tree Code System Code
JECFA EVALUATION 2,4,6-TRIMETHYLPHENOL
Created by admin on Mon Mar 31 19:48:08 GMT 2025 , Edited by admin on Mon Mar 31 19:48:08 GMT 2025
Code System Code Type Description
NSC
5353
Created by admin on Mon Mar 31 19:48:08 GMT 2025 , Edited by admin on Mon Mar 31 19:48:08 GMT 2025
PRIMARY
JECFA MONOGRAPH
1991
Created by admin on Mon Mar 31 19:48:08 GMT 2025 , Edited by admin on Mon Mar 31 19:48:08 GMT 2025
PRIMARY
WIKIPEDIA
Mesitol
Created by admin on Mon Mar 31 19:48:08 GMT 2025 , Edited by admin on Mon Mar 31 19:48:08 GMT 2025
PRIMARY
FDA UNII
FPZ32614N6
Created by admin on Mon Mar 31 19:48:08 GMT 2025 , Edited by admin on Mon Mar 31 19:48:08 GMT 2025
PRIMARY
EPA CompTox
DTXSID7022049
Created by admin on Mon Mar 31 19:48:08 GMT 2025 , Edited by admin on Mon Mar 31 19:48:08 GMT 2025
PRIMARY
MESH
C505148
Created by admin on Mon Mar 31 19:48:08 GMT 2025 , Edited by admin on Mon Mar 31 19:48:08 GMT 2025
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PUBCHEM
10698
Created by admin on Mon Mar 31 19:48:08 GMT 2025 , Edited by admin on Mon Mar 31 19:48:08 GMT 2025
PRIMARY
ECHA (EC/EINECS)
208-419-2
Created by admin on Mon Mar 31 19:48:08 GMT 2025 , Edited by admin on Mon Mar 31 19:48:08 GMT 2025
PRIMARY
HSDB
5677
Created by admin on Mon Mar 31 19:48:08 GMT 2025 , Edited by admin on Mon Mar 31 19:48:08 GMT 2025
PRIMARY
CAS
527-60-6
Created by admin on Mon Mar 31 19:48:08 GMT 2025 , Edited by admin on Mon Mar 31 19:48:08 GMT 2025
PRIMARY