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About This Item
Linear Formula:
[(CH3)3C]2C6H3OH
CAS Number:
Molecular Weight:
206.32
Beilstein:
1841887
EC Number:
MDL number:
UNSPSC Code:
12352100
Recommended Products
vapor pressure
<0.01 mmHg ( 20 °C)
grade
purum
Assay
≥98.0% (GC)
bp
253 °C (lit.)
mp
34-37 °C (lit.)
34-37 °C
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
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Description
Pricing
Signal Word
Warning
Hazard Statements
Precautionary Statements
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
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QSAR study of dual cyclooxygenase and 5-lipoxygenase inhibitors 2,6-di-tert-butylphenol derivatives.
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
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
Zhen-wei Fang et al.
Huan jing ke xue= Huanjing kexue, 25(3), 98-101 (2004-08-26)
A degrading bacterial strain F-3-4 for 2,6-Di-tert-butylphenol (2,6-DTBP) was isolated from biofilm in acrylic fiber wastewater treatment structures. By acclimation, its capacity for degradation of 2,6-DTBP was enhanced by 26%. It was identified as Alcaligenes sp. according to morphological, physiological
[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)
Jörg Ahrens et al.
Pharmacology, 83(2), 95-98 (2008-12-10)
Modulation of inhibitory synaptic transmission within the central nervous system contributes considerably to the anaesthetic effects of propofol and its analogues in vivo. We have studied the effects of the non-anaesthetic propofol analogue 2,6-di-tert-butylphenol on rat alpha(1)beta(2)gamma(2) GABA(A) receptors expressed
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