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

Details

Stereochemistry ACHIRAL
Molecular Formula C14H22O
Molecular Weight 206.3239
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2,6-DI-TERT-BUTYLPHENOL

SMILES

CC(C)(C)C1=CC=CC(=C1O)C(C)(C)C

InChI

InChIKey=DKCPKDPYUFEZCP-UHFFFAOYSA-N
InChI=1S/C14H22O/c1-13(2,3)10-8-7-9-11(12(10)15)14(4,5)6/h7-9,15H,1-6H3

HIDE SMILES / InChI

Molecular Formula C14H22O
Molecular Weight 206.3239
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Determination of antioxidants in new and used lubricant oils by headspace-programmed temperature vaporization-gas chromatography-mass spectrometry.
2010-12
Spike avalanches exhibit universal dynamics across the sleep-wake cycle.
2010-11-30
Prevention of polyurethane oxidative degradation with phenolic antioxidants covalently attached to the hard segments: structure-function relationships.
2010-09-01
Chiral indium alkoxide complexes as initiators for the stereoselective ring-opening polymerization of rac-lactide.
2010-01-18
Antioxidative activity of ferrocenes bearing 2,6-di-tert-butylphenol moieties.
2010
Sterically hindered phenols in negative ion mobility spectrometry-mass spectrometry.
2009-10
Synthesis, structure, and reactivity of low-coordinate 1,1,3,3-tetraethylguanidinate complexes.
2009-08-17
Carbonic anhydrase inhibitors. Inhibition of human erythrocyte isozymes I and II with a series of antioxidant phenols.
2009-04-15
Iron (III) porphyrin bearing 2,6-di-tert-butylphenol pendants deposited onto gold electrodes for amperometric determination of L-histidine.
2009-04-15
Synthesis and evaluation of dithiolethiones as novel cyclooxygenase inhibitors.
2009-01-15
The non-anaesthetic propofol analogue 2,6-di-tert-butylphenol fails to modulate GABA(A) receptor function.
2009
Structural characterization and electrochemical properties of the 3,3'-5,5'-tetra-tert-butyl-4,4'-diphenoquinone.
2008-08
Electron transfer between protonated and unprotonated phenoxyl radicals.
2008-02-01
Synthesis and antioxidative activity of metalloporphyrins bearing 2,6-di-tert-butylphenol pendants.
2007-09-28
Hydrogen atom transfer reactions of imido manganese(V) corrole: one reaction with two mechanistic pathways.
2007-09-19
Biological stability of polyurethane modified with covalent attachment of di-tert-butyl-phenol.
2007-09-15
Synthesis, characterization and properties of some divalent metal(II) complexes: their electrochemical, catalytic, thermal and antimicrobial activity studies.
2007-07
Substituent effect on g-tensor: multifrequency ESR study and DFT calculation of polycrystalline phenoxyl radicals in diamagnetic crystals.
2007-05-31
Synthesis and evaluation of the antiinflammatory activity of N-[2-(3,5-di-tert-butyl-4-hydroxyphenyl)-4-oxo-thiazolidin-3-yl]-nicotinamide.
2007
Calix[4]arene-linked bisporphyrin hosts for fullerenes: binding strength, solvation effects, and porphyrin-fullerene charge transfer bands.
2006-12-13
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.
2006-11
[Effects of two kinds of allelochemicals on photosynthesis and chlorophyll fluorescence parameters of Solanum melongena L. seedlings].
2006-09
New analogues of butylated hydroxytoluene as anti-inflammatory and antioxidant agents.
2006-08-15
Determination of chlorine dioxide in water by gas chromatography-mass spectrometry.
2006-08-04
Synthesis and biological evaluation of acyclic triaryl (Z)-olefins possessing a 3,5-di-tert-butyl-4-hydroxyphenyl pharmacophore: dual inhibitors of cyclooxygenases and lipoxygenases.
2006-08-01
Synthesis and antioxidant activity of [60]fullerene-BHT conjugates.
2006-06-02
Use of SPME-GC-MS in the study of time evolution of the constituents of saffron aroma: modifications of the composition during storage.
2006-01
2,6-di-tert-butylphenol revisited at 110 K.
2005-11
Antioxidant activity of propofol and related monomeric and dimeric compounds.
2005-03
Degradation of 2,6-di-tert-butylphenol by an isolated high-efficiency bacterium strain.
2005
Parallel kinetic resolution of tert-butyl (RS)-3-alkyl-cyclopentene-1-carboxylates for the asymmetric synthesis of 3-alkyl-cispentacin derivatives.
2004-11-21
The effects of conjugation path variation on electron delocalization in phenoxyl-based systems.
2004-08-31
2,6 di-tert-butylphenol, a nonanesthetic propofol analog, modulates alpha1beta glycine receptor function in a manner distinct from propofol.
2004-07
[The degradation characteristics of degrading bacterium of 2,6-di-tert-butylphenol].
2004-05
Evaluation of the antioxidant properties of propofol and its nitrosoderivative. comparison with homologue substituted phenols.
2004-03
Asymmetric synthesis of the stereoisomers of 2-amino-5-carboxymethyl-cyclopentane-1-carboxylate.
2004-02-07
Improving the performance of methylalumoxane: a facile and efficient method to trap "free" trimethylaluminum.
2003-10-15
QSAR study of dual cyclooxygenase and 5-lipoxygenase inhibitors 2,6-di-tert-butylphenol derivatives.
2003-09-15
[Methylated 2-aryl-1,4-naphtoquinone derivatives with diminished antioxidative activity].
2003-08
Percutaneous absorption of 2,6-di-tert-butyl-4-nitrophenol (DBNP) in isolated perfused porcine skin.
2003-06
[Studies on the new antiarthritic drug candidate S-2474].
2003-05
High-affinity block of voltage-operated rat IIA neuronal sodium channels by 2,6 di-tert-butylphenol, a propofol analogue.
2003-03
Structural evidence that propofol stabilizes different GABA(A) receptor states at potentiating and activating concentrations.
2002-09-01
[Determination of 2,4,6-tri-tert-butylphenol and related compounds in foods].
2001-12
Three-coordinate copper(II)-phenolate complexes.
2001-11-19
Autoxidation of substituted phenols catalyzed by cobalt Schiff base complexes in supercritical carbon dioxide.
2001-07-02
[Partially hydrogenated aryl-1,2/1,4-anthraquinone derivatives, 5-lipoxygenase inhibitors with arotinoid structure].
2001-07
General anesthetic potencies of a series of propofol analogs correlate with potency for potentiation of gamma-aminobutyric acid (GABA) current at the GABA(A) receptor but not with lipid solubility.
2001-04
Estrogenic activity of phenolic additives determined by an in vitro yeast bioassay.
2001-02
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:34:04 GMT 2025
Edited
by admin
on Mon Mar 31 18:34:04 GMT 2025
Record UNII
21294V58PF
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2,6-DI-TERT-BUTYLPHENOL
HSDB  
Systematic Name English
NSC-49175
Preferred Name English
DI-TERT-BUTYLPHENOL, 2,6-
Systematic Name English
2,6-DI-TERT-BUTYL-PHENOL
Systematic Name English
2,6-DI-TERT-BUTYLPHENOL [HSDB]
Common Name English
Code System Code Type Description
CAS
128-39-2
Created by admin on Mon Mar 31 18:34:04 GMT 2025 , Edited by admin on Mon Mar 31 18:34:04 GMT 2025
PRIMARY
EPA CompTox
DTXSID6027052
Created by admin on Mon Mar 31 18:34:04 GMT 2025 , Edited by admin on Mon Mar 31 18:34:04 GMT 2025
PRIMARY
ECHA (EC/EINECS)
204-884-0
Created by admin on Mon Mar 31 18:34:04 GMT 2025 , Edited by admin on Mon Mar 31 18:34:04 GMT 2025
PRIMARY
NSC
49175
Created by admin on Mon Mar 31 18:34:04 GMT 2025 , Edited by admin on Mon Mar 31 18:34:04 GMT 2025
PRIMARY
WIKIPEDIA
2,6-DI-TERT-BUTYLPHENOL
Created by admin on Mon Mar 31 18:34:04 GMT 2025 , Edited by admin on Mon Mar 31 18:34:04 GMT 2025
PRIMARY
HSDB
5616
Created by admin on Mon Mar 31 18:34:04 GMT 2025 , Edited by admin on Mon Mar 31 18:34:04 GMT 2025
PRIMARY
FDA UNII
21294V58PF
Created by admin on Mon Mar 31 18:34:04 GMT 2025 , Edited by admin on Mon Mar 31 18:34:04 GMT 2025
PRIMARY
PUBCHEM
31405
Created by admin on Mon Mar 31 18:34:04 GMT 2025 , Edited by admin on Mon Mar 31 18:34:04 GMT 2025
PRIMARY
MESH
C035407
Created by admin on Mon Mar 31 18:34:04 GMT 2025 , Edited by admin on Mon Mar 31 18:34:04 GMT 2025
PRIMARY
Related Record Type Details
PARENT -> IMPURITY