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Merck
CN

163031

3-Nitrophenol

99%, ReagentPlus®

Synonym(s):

3-NP, m-NP, m-Nitrophenol

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About This Item

Linear Formula:
O2NC6H4OH
CAS Number:
554-84-7
Molecular Weight:
139.11
NACRES:
NA.21
PubChem Substance ID:
24850022
UNSPSC Code:
12352100
EC Number:
209-073-5
MDL number:
MFCD00007240
Beilstein/REAXYS Number:
1907946
Assay:
99%

Key Documents

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Product Name

3-Nitrophenol, ReagentPlus®, 99%

InChI key

RTZZCYNQPHTPPL-UHFFFAOYSA-N

InChI

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

SMILES string

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

product line

ReagentPlus®

assay

99%

bp

194 °C/70 mmHg (lit.)

mp

96-98 °C (lit.)

functional group

nitro

Quality Level

100

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Application

3-Nitrophenol may be used in the preparation of 3-aminophenol. It may be employed as a weak acid in capillary isoelectric focusing (cIEF) method.

General description

3-Nitrophenol (m-nitrophenol) is a nitroaromatic compound. It can be prepared from 3-nitroaniline, via diazotization reaction.
3-Nitrophenol is one of the isomers of mononitrophenol and is mainly used as an intermediate to prepare dyes, pigments, lumber preservatives, photographic chemicals and pesticides. Some of the methods for its degradation are biotransformation, photocatalytic degradation and photooxidation.

Legal Information

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

pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

Hazard Classifications

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

Storage Class

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

wgk

WGK 3

ppe

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

Regulatory Information

危险化学品
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Certificates of Analysis (COA)

Lot/Batch Number
MKCV9625
MKCR1145
MKCP2626
MKCM3473
MKCK4898

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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)
Drinking water and Health, 4, 230-230 (1982)
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)
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
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
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