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Merck
CN

D48400

2,6-Di-tert-butylphenol

99%

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About This Item

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

2,6-Di-tert-butylphenol, 99%

InChI key

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

SMILES string

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

vapor pressure

<0.01 mmHg ( 20 °C)

assay

99%

form

crystals

bp

253 °C (lit.)

mp

34-37 °C (lit.)

Gene Information

human ... GABRA1(2554)

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pictograms

Exclamation markEnvironment

signalword

Warning

hcodes

Hazard Classifications

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

Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

227.3 °F - closed cup

flash_point_c

108.5 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves


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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
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
[Regulation by an antioxidant of growth, composition, and physico-chemical features of lipids from Saccharomyces cerevisiae].
O A Reshetnik et al.
Doklady Akademii nauk, 346(5), 705-707 (1996-02-01)
E R Milaeva et al.
Journal of inorganic biochemistry, 102(5-6), 1348-1358 (2008-03-07)
The novel metalloporphyrins (M=HH, Fe, Mn, Co, Cu, Zn) bearing 2,6-di-tert-butylphenol pendants as antioxidant substituents, and a long chain hydrocarbon palmitoyl group have been synthesized. The oxidation of compounds by PbO2 leads to the formation of the corresponding 2,6-di-tert-butylphenoxyl radicals
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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