跳转至内容
Merck
所有图片(1)

主要文件

查看所有文档

D3292

Sigma-Aldrich

:2,6-二叔丁基苯酚

~99% (GC)

登录查看公司和协议定价
所有图片(1)

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

正在寻找类似产品? 访问 产品对比指南

取代透過

产品编号
说明
价格

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

分析证书(COA)

输入产品批号来搜索 分析证书(COA) 。批号可以在产品标签上"批“ （Lot或Batch）字后找到。

已有该产品？

在文件库中查找您最近购买产品的文档。

访问文档库

Mehmet Tümer et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 70(3), 477-481 (2007-09-07)
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) complexes. The oxidation product (TTBDQ), C(28)H(40)O(2), crystallizes in
G Haeseler et al.
European journal of anaesthesiology, 20(3), 220-224 (2003-03-26)
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-butyl groups, the resulting
A W Girotti et al.
Lipids, 22(6), 401-408 (1987-06-01)
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) when irradiated in the
Shinsuke Ishihara et al.
Journal of the American Chemical Society, 133(40), 16119-16126 (2011-08-31)
Porphyrin derivatives bearing 2,6-di-tert-butylphenol substituents at their 5,15-positions undergo reversible photoredox switching between porphyrin and porphodimethene states as revealed by UV-vis spectroscopy, fluorescence spectroscopy, and X-ray single-crystal analyses. Photoredox interconversion is accompanied by substantial variations in electronic absorption and fluorescence
Studies on the synthesis and anti-inflammatory activity of 2,6-di-tert-butylphenols with a heterocyclic group at the 4-position. V. Elimination reaction of the sulfinyl group of 2,3-dihydroimidazo[2,1-b]thiazole 1-oxide.
Y Isomura et al.
Chemical & pharmaceutical bulletin, 32(12), 4726-4730 (1984-12-01)
查看所有相关文献

我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系技术服务部门