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Merck

D48400

Sigma-Aldrich

:2,6-二丁基苯酚

99%

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About This Item

线性分子式:
[(CH3)3C]2C6H3OH
CAS号:
分子量:
206.32
Beilstein:
1841887
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

蒸汽壓力

<0.01 mmHg ( 20 °C)

化驗

99%

形狀

crystals

bp

253 °C (lit.)

mp

34-37 °C (lit.)

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

基因資訊

human ... GABRA1(2554)

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象形圖

Exclamation markEnvironment

訊號詞

Warning

危險聲明

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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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
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

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