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Merck
CN

163031

3-硝基苯酚

99%, ReagentPlus®

别名:

3-NP, -NP, 硝基苯酚

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关于此项目

线性分子式:
O2NC6H4OH
化学文摘社编号:
分子量:
139.11
Beilstein:
1907946
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.21
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产品名称

3-硝基苯酚, ReagentPlus®, 99%

质量水平

产品线

ReagentPlus®

方案

99%

沸点

194 °C/70 mmHg (lit.)

mp

96-98 °C (lit.)

官能团

nitro

SMILES字符串

Oc1cccc(c1)[N+]([O-])=O

InChI

1S/C6H5NO3/c8-6-3-1-2-5(4-6)7(9)10/h1-4,8H

InChI key

RTZZCYNQPHTPPL-UHFFFAOYSA-N

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一般描述

3-硝基苯酚是单硝基苯酚的异构体之一,主要用作制备染料、颜料、木材防腐剂、照相化学品和农药的中间体。它的降解方法包括生物转化、光催化降解和光氧化等。
3-硝基苯酚(硝基苯酚)是硝基芳族化合物。以 3-硝基苯胺为原料,通过重氮化反应可制备 3-硝基苯酚。

应用

3-硝基苯酚可用于制备 3-氨基苯酚。它可以用作毛细管等电聚焦(cIEF)方法中的弱酸。

法律信息

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

象形图

CorrosionExclamation mark

警示用语:

Danger

危险声明

危险分类

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2

储存分类代码

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

个人防护装备

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

法规信息

危险化学品
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分析证书(COA)

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Biotransformation of nitrobenzene by bacteria containing toluene degradative pathways.
Haigler BE and Spain JC.
Applied and Environmental Microbiology, 57(11), 3156-3162 (1991)
Photocatalytic degradation of nitrobenzenes with combustion synthesized nano-TiO 2.
Priya MHl and Madras G.
Journal of Photochemistry and Photobiology A: Chemistry, 178(1), 1-7 (2006)
Thierry Vincent et al.
Environmental science & technology, 38(15), 4233-4240 (2004-09-09)
Hollow chitosan fibers were reacted with chloropalladate solutions and subsequently reduced by hydrogen produced in situ by reaction of sulfuric acid with zinc powder in order to manufacture palladium supported on catalytic hollow chitosan fibers (C2HF-Pd). This catalytic support was
Ali Niazi et al.
Journal of hazardous materials, 146(1-2), 421-427 (2007-04-21)
A simple, novel and sensitive spectrophotometric method was described for simultaneous determination of nitrophenol isomers mixtures. All factors affecting on the sensitivity were optimized and the linear dynamic range for determination of nitrophenol isomers were found. The simultaneous determination of
Z Ioannou et al.
Journal of hazardous materials, 171(1-3), 954-964 (2009-07-25)
Carbonaceous adsorbents prepared from olive stones biomass and novolac resin, as well as a commercial activated carbon for comparison reasons, have been examined for the removal of phenol and 3-nitrophenol from aqueous solutions. All carbonaceous adsorbents have been characterized by

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