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About This Item
Linear Formula:
[(CH3)3C]2C6H3OH
CAS Number:
Molecular Weight:
206.32
Beilstein/REAXYS Number:
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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Product No.
Description
Pricing
signalword
Warning
hcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Skin Irrit. 2
Storage Class
11 - Combustible Solids
wgk_germany
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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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
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)
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
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
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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