All Photos(3)
Synonym(s):
3-NP, m-NP, m-Nitrophenol
Linear Formula:
O2NC6H4OH
CAS Number:
Molecular Weight:
139.11
Beilstein:
1907946
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.21
Recommended Products
Quality Level
product line
ReagentPlus®
Assay
99%
bp
194 °C/70 mmHg (lit.)
mp
96-98 °C (lit.)
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
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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
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2
WGK
WGK 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
危险化学品
Certificates of Analysis (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)
A Umamaheswari et al.
Ecotoxicology and environmental safety, 58(2), 256-259 (2004-05-26)
Concentration-dependent inhibition of the photosynthetic electron transport chain (photosystem I (PS I), photosystem II (PS II) and whole chain reaction) and ATP content was observed in Nostoc muscorum and Chlorella vulgaris grown with o-nitrophenol, m-nitrophenol, or 2,4-dinitrophenol. Although the extents
Purnendu K Dasgupta
Journal of chromatography. A, 1213(1), 50-55 (2008-09-16)
Resolution of overlapped chromatographic peaks is generally accomplished by modeling the peaks as Gaussian or modified Gaussian functions. It is possible, even preferable, to use actual single analyte input responses for this purpose and a nonlinear least squares minimization routine
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)
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