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D48400

Sigma-Aldrich

2,6-Di-tert-butylphenol

99%

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About This Item

Linear Formula:
[(CH3)3C]2C6H3OH
CAS Number:
128-39-2
Molecular Weight:
206.32
Beilstein:
1841887
EC Number:
204-884-0
MDL number:
MFCD00008820
UNSPSC Code:
12352100
PubChem Substance ID:
24893900
NACRES:
NA.22

vapor pressure

<0.01 mmHg ( 20 °C)

Assay

99%

form

crystals

bp

253 °C (lit.)

mp

34-37 °C (lit.)

SMILES string

CC(C)(C)c1cccc(c1O)C(C)(C)C

InChI

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

InChI key

DKCPKDPYUFEZCP-UHFFFAOYSA-N

Gene Information

human ... GABRA1(2554)

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Pictograms

Exclamation markEnvironment
GHS07,GHS09

Signal Word

Warning

Hazard Statements

H315,H410

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Skin Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

227.3 °F - closed cup

Flash Point(C)

108.5 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Anouar Hafiane et al.
The Canadian journal of cardiology, 35(6), 770-781 (2019-06-04)
Small peptides based on the C-terminal domain of apo E have recently been proposed as ATP-binding cassette transporter A1 (ABCA1) agonist with therapeutic potential. Previous work has shown that a novel synthetic peptide, CS-6253, acts synergistically with apolipoprotein A-I or
Caitlin E Cornell et al.
Biophysical journal, 113(6), 1200-1211 (2017-08-13)
A persistent challenge in membrane biophysics has been to quantitatively predict how membrane physical properties change upon addition of new amphiphiles (e.g., lipids, alcohols, peptides, or proteins) in order to assess whether the changes are large enough to plausibly result
Juan Ruiz et al.
Bioorganic & medicinal chemistry, 11(19), 4207-4216 (2003-09-03)
The dual or selective ability of 24 derived mono- and 2,6-di-tert-butylphenols (DTBP) to act as inhibitors of cyclooxygenase (COX) and/or 5-lipoxygenase (LOX) enzymes is investigated. Firstly, we explored the conformational variability of the compounds. It is found that dual inhibitors
Synthesis and biological evaluation of 2,6-di-tert-butylphenol hydrazones as 5-lipoxygenase inhibitors.
A M Cuadro et al.
Bioorganic & medicinal chemistry, 6(2), 173-180 (1998-04-21)
Jörg Ahrens et al.
Anesthesia and analgesia, 99(1), 91-96 (2004-07-30)
The anesthetic propofol (2,6 diisopropylphenol) mediates some of its effects by activating inhibitory chloride currents in the lower brainstem and spinal cord. The effects comprise direct activation of gamma-aminobutyric acid-A and glycine receptors in the absence of the natural agonist
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