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Details

Stereochemistry ACHIRAL
Molecular Formula C10H14O
Molecular Weight 150.2176
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-TERT-BUTYLPHENOL

SMILES

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

InChI

InChIKey=WJQOZHYUIDYNHM-UHFFFAOYSA-N
InChI=1S/C10H14O/c1-10(2,3)8-6-4-5-7-9(8)11/h4-7,11H,1-3H3

HIDE SMILES / InChI

Molecular Formula C10H14O
Molecular Weight 150.2176
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Photoinduced processes in self-assembled porphyrin/perylene bisimide metallosupramolecular boxes.
2010-11-18
Isolation and characterization of a novel 2-sec-butylphenol-degrading bacterium Pseudomonas sp. strain MS-1.
2010-04
Establishment of yeast reporter assay systems to detect ligands of thyroid hormone receptors alpha and beta.
2010-03
Comparison of relative binding affinities to fish and mammalian estrogen receptors: the regulatory implications.
2010-02-15
In vitro profiling of endocrine disrupting effects of phenols.
2010-02
Sterically hindered phenols in negative ion mobility spectrometry-mass spectrometry.
2009-10
Electrochemical gate-controlled electron transport of redox-active single perylene bisimide molecular junctions.
2008-09-17
A two-hybrid yeast assay to quantify the effects of xenobiotics on retinoid X receptor-mediated gene expression.
2008-02-15
A two-hybrid yeast assay to quantify the effects of xenobiotics on thyroid hormone-mediated gene expression.
2008-01
X-ray and neutron diffraction studies of water-encapsulated inside potassium aryloxide aggregates: complementary host-guest stabilization of mono- and dihydrated cages.
2007-12-10
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.
2006-11
Data processing and classification analysis of proteomic changes: a case study of oil pollution in the mussel, Mytilus edulis.
2006-09-13
In vitro and in vivo analysis of the thyroid system-disrupting activities of brominated phenolic and phenol compounds in Xenopus laevis.
2006-07
Elevated susceptibility of newborn as compared with young rats to 2-tert-butylphenol and 2,4-di-tert-butylphenol toxicity.
2005-12
In vitro and in vivo analysis of the thyroid disrupting activities of phenolic and phenol compounds in Xenopus laevis.
2005-03
Synthesis of 3-tert-butylcatechol by an engineered monooxygenase.
2003-03-05
Quantitative structure-activity relationships for estrogen receptor binding affinity of phenolic chemicals.
2003-03
Changing the substrate reactivity of 2-hydroxybiphenyl 3-monooxygenase from Pseudomonas azelaica HBP1 by directed evolution.
2002-02-15
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:31:22 GMT 2025
Edited
by admin
on Mon Mar 31 19:31:22 GMT 2025
Record UNII
NL2FPV3N0Z
Record Status Validated (UNII)
Record Version
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Name Type Language
2-TERT-BUTYLPHENOL [HSDB]
Preferred Name English
2-TERT-BUTYLPHENOL
HSDB  
Systematic Name English
PHENOL, (1,1-DIMETHYLETHYL)-
Systematic Name English
O-T-BUTYLPHENOL
Systematic Name English
BUTYLPHENOL, 2-TERT-
Systematic Name English
2-T-BUTYLPHENOL
Systematic Name English
PHENOL, O-TERT-BUTYL-
Systematic Name English
PHENOL, 2-(1,1-DIMETHYLETHYL)-
Systematic Name English
O-TERT-BUTYLPHENOL
Systematic Name English
Code System Code Type Description
PUBCHEM
6923
Created by admin on Mon Mar 31 19:31:22 GMT 2025 , Edited by admin on Mon Mar 31 19:31:22 GMT 2025
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WIKIPEDIA
2-tert-Butylphenol
Created by admin on Mon Mar 31 19:31:22 GMT 2025 , Edited by admin on Mon Mar 31 19:31:22 GMT 2025
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FDA UNII
NL2FPV3N0Z
Created by admin on Mon Mar 31 19:31:22 GMT 2025 , Edited by admin on Mon Mar 31 19:31:22 GMT 2025
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EPA CompTox
DTXSID2026525
Created by admin on Mon Mar 31 19:31:22 GMT 2025 , Edited by admin on Mon Mar 31 19:31:22 GMT 2025
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HSDB
5255
Created by admin on Mon Mar 31 19:31:22 GMT 2025 , Edited by admin on Mon Mar 31 19:31:22 GMT 2025
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CAS
88-18-6
Created by admin on Mon Mar 31 19:31:22 GMT 2025 , Edited by admin on Mon Mar 31 19:31:22 GMT 2025
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ECHA (EC/EINECS)
201-807-2
Created by admin on Mon Mar 31 19:31:22 GMT 2025 , Edited by admin on Mon Mar 31 19:31:22 GMT 2025
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MESH
C035406
Created by admin on Mon Mar 31 19:31:22 GMT 2025 , Edited by admin on Mon Mar 31 19:31:22 GMT 2025
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