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:
Molecular Weight:
139.11
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
209-073-5
MDL number:
Beilstein/REAXYS Number:
1907946
Assay:
99%
Product Name
3-Nitrophenol, ReagentPlus®, 99%
Quality Level
product line
ReagentPlus®
assay
99%
bp
194 °C/70 mmHg (lit.)
mp
96-98 °C (lit.)
functional group
nitro
SMILES string
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
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.
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.
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
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Danger
hcodes
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
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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)
Risky Ayu Kristanti et al.
Environmental science and pollution research international, 19(5), 1852-1858 (2012-03-08)
The accelerated biodegradation of 3-nitrophenol (3-NP) in the rhizosphere of giant duckweed (Spirodela polyrrhiza) was investigated. Biodegradation of 3-nitrophenol in the rhizosphere of a floating aquatic plant, S. polyrrhiza, was investigated by using three river water samples supplemented with 10
Eagleson M.
Concise Encyclopedia Chemistry, 700-700 (1994)