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安全信息

B99006

Sigma-Aldrich

2-仲丁基苯酚

98%

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About This Item

线性分子式:
C2H5CH(CH3)C6H4OH
CAS号:
89-72-5
分子量:
150.22
Beilstein:
1210026
EC 号:
201-933-8
MDL编号:
MFCD00002225
UNSPSC代码:
12352100
PubChem化学物质编号:
24892163
NACRES:
NA.22

蒸汽压

0.03 mmHg ( 20 °C)

质量水平

100

方案

98%

表单

liquid

折射率

n20/D 1.522 (lit.)

沸点

226-228 °C (lit.)

mp

12 °C (lit.)

密度

0.982 g/mL at 25 °C (lit.)

SMILES字符串

CCC(C)c1ccccc1O

InChI

1S/C10H14O/c1-3-8(2)9-6-4-5-7-10(9)11/h4-8,11H,3H2,1-2H3

InChI key

NGFPWHGISWUQOI-UHFFFAOYSA-N

基因信息

rat ... Ar(24208)

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相关类别

应用

2-sec-Butylphenol is a precursor to synthesize various coumarin and benzofuran derivatives that are used as lipid-lowering agents and potential bone anabolic agents. It can also be used as a solvent in organic synthesis.

象形图

CorrosionExclamation mark
GHS05,GHS07

警示用语：

Danger

危险声明

H302,H314

危险分类

Acute Tox. 4 Oral - Skin Corr. 1C

储存分类代码

8A - Combustible corrosive hazardous materials

WGK

WGK 2

闪点(°F)

233.6 °F - closed cup

闪点(°C)

112 °C - closed cup

个人防护装备

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

法规信息

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分析证书(COA)

Lot/Batch Number
MKCB1786V
MKBX9303V
MKBX3850V
02806KP
08627LA

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Benzofuran-dihydropyridine hybrids: A new class of potential bone anabolic agents.
Modukuri R K, et al.
Bioorganic & Medicinal Chemistry, 25(24), 6450-6466 (2017)
Spectrophotometric determination of nitrate in vegetable products using 2-sec-butylphenol.
A Tanaka et al.
The Analyst, 107(1271), 190-194 (1982-02-01)
Discovery of coumarin?dihydropyridine hybrids as bone anabolic agents.
Sashidhara K V, et al.
Journal of Medicinal Chemistry, 56(1), 109-122 (2012)
RuSn bimetallic catalysts for selective hydrogenation of levulinic acid to ?-valerolactone.
Wettstein S G, et al.
Applied Catalysis. B, Environmental, 117, 321-329 (2012)
V P Bintoro et al.
The Analyst, 120(11), 2747-2753 (1995-11-01)
A rapid, simple and direct visible spectrophotometric method, based on the quantitative nitration of 2-sec-butylphenol in concentrated sulfuric acid, is described for the determination of nitrate in milk. The nitration product was extracted into toluene and the yellow nitrophenoxide compound
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