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D3292

Sigma-Aldrich

:2,6-二叔丁基苯酚

~99% (GC)

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About This Item

线性分子式:
[(CH3)3C]2C6H3OH
CAS号:
128-39-2
分子量:
206.32
Beilstein:
1841887
EC號碼:
204-884-0
MDL號碼:
MFCD00008820
分類程式碼代碼:
12000000

蒸汽壓力

<0.01 mmHg ( 20 °C)

化驗

~99% (GC)

bp

253 °C (lit.)

mp

34-37 °C (lit.)

儲存溫度

2-8°C

SMILES 字串

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 密鑰

DKCPKDPYUFEZCP-UHFFFAOYSA-N

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象形圖

Exclamation markEnvironment
GHS07,GHS09

訊號詞

Warning

危險聲明

H315,H410

危險分類

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

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 2

閃點（°F）

227.3 °F - closed cup

閃點（°C）

108.5 °C - closed cup

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves

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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
[The effect of antioxidant on the growth and lipid composition of Saccharomyces cerevisiae yeasts at different phases of the development of a culture].
O A Reshetnik et al.
Izvestiia Akademii nauk. Seriia biologicheskaia, (2)(2), 172-176 (1997-03-01)
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
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
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