2,6-Di-tert-butylphenol
2,6-Di-tert-butylphenol structure
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Common Name | 2,6-Di-tert-butylphenol | ||
|---|---|---|---|---|
| CAS Number | 128-39-2 | Molecular Weight | 206.324 | |
| Density | 0.9±0.1 g/cm3 | Boiling Point | 251.4±9.0 °C at 760 mmHg | |
| Molecular Formula | C14H22O | Melting Point | 34-37 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 118.3±0.0 °C | |
| Symbol |
GHS07, GHS09 |
Signal Word | Warning | |
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Cellular apoptosis and cytotoxicity of phenolic compounds: a quantitative structure-activity relationship study.
J. Med. Chem. 48 , 7234-42, (2005) In this comprehensive study on the caspase-mediated apoptosis-inducing effect of 51 substituted phenols in a murine leukemia cell line (L1210), we determined the concentrations needed to induce caspase activity by 50% (I50) and utilized these data to develop ... |
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Carbonic anhydrase inhibitors. Inhibition of human erythrocyte isozymes I and II with a series of antioxidant phenols.
Bioorg. Med. Chem. 17 , 3207-11, (2009) The inhibition of two human cytosolic carbonic anhydrase (hCA, EC 4.2.1.1) isozymes I and II, with a series of phenol derivatives was investigated by using the esterase assay, with 4-nitrophenyl acetate as substrate. 2,6-Dimethylphenol, 2,6-diisopropylphenol ... |
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Antioxidant activity of propofol and related monomeric and dimeric compounds.
Chem. Pharm. Bull. 53(3) , 344-6, (2005) This study was carried out to investigate the antioxidant activity of propofol (2,6-diisopropylphenol) and its related compounds, butylated hydroxyanisole (BHA), 2,6-dimethylphenol, 2,6-di-t-butylphenol, and their dimeric compounds. The degree of antioxidant ... |
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High-affinity block of voltage-operated rat IIA neuronal sodium channels by 2,6 di-tert-butylphenol, a propofol analogue.
Eur. J. Anaesthesiol. 20(3) , 220-4, (2003) Propofol is a phenol derivative (2,6 di-isopropylphenol) with a unique effect profile including activating effects on GABA(A) and blocking effects on voltage-operated sodium channels. If the substituents in the 2- and the 6-positions are replaced by tert-buty... |
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[Regulation by an antioxidant of growth, composition, and physico-chemical features of lipids from Saccharomyces cerevisiae].
Dokl. Akad. Nauk. 346(5) , 705-7, (1996)
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Lipid peroxidation in erythrocyte membranes: cholesterol product analysis in photosensitized and xanthine oxidase-catalyzed reactions.
Lipids 22(6) , 401-8, (1987) The effects of singlet oxygen- and oxygen radical-induced lipid peroxidation on cell membrane integrity were compared, using the human erythrocyte ghost as a model system. Resealed ghosts underwent lipid peroxidation and lysis (release of trapped glucose-6-P)... |
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Biological stability of polyurethane modified with covalent attachment of di-tert-butyl-phenol.
J. Biomed. Mater. Res. A 82(4) , 1004-11, (2007) Polyurethane cardiovascular implants are subject to oxidation initiated surface degradation, which is mediated by monocyte-derived macrophages (MDM); this often leads to surface cracking and device failure. The present studies examined the hypothesis that cov... |
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Percutaneous absorption of 2,6-di-tert-butyl-4-nitrophenol (DBNP) in isolated perfused porcine skin.
Toxicol. In Vitro 17(3) , 289-92, (2003) DBNP (2,6-di-tert-butyl-4-nitrophenol) has been reported as a potential contaminant in submarines. This yellow substance forms when lubrication oil mist containing the antioxidant additive 2,6-di-tert-butylphenol passes through an electrostatic precipitator a... |
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Degradation of 2,6-di-tert-butylphenol by an isolated high-efficiency bacterium strain.
J. Environ. Sci. (China) 17(2) , 271-5, (2005) An aerobic bacterium strain, F-3-4, capable of effectively degrading 2, 6-ditert-butylphenol (2, 6-DTBP), was isolated and screened out from an acrylic fiber wastewater and the biofilm in the wastewater treatment facilities. This strain was identified as Alca... |
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Structural characterization and electrochemical properties of the 3,3'-5,5'-tetra-tert-butyl-4,4'-diphenoquinone.
Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 70(3) , 477-81, (2008) Crystals of the 3,3'-5,5'-tetra-tert-butyl-4,4'-diphenoquinone (TTBDQ) in the reaction mixture DCM/MeOH (1:1, v/v) were obtained as a result of CC coupling reaction of the sterically hindered phenol (2,6-di-tert-butylphenol, DTBP) using the binuclear Co(II) c... |