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163031

Sigma-Aldrich

3-Nitrophenol

ReagentPlus®, 99%

Synonym(e):

3-NP, m-NP, m-Nitrophenol

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About This Item

Lineare Formel:
O2NC6H4OH
CAS-Nummer:
554-84-7
Molekulargewicht:
139.11
Beilstein:
1907946
EG-Nummer:
209-073-5
MDL-Nummer:
MFCD00007240
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24850022
NACRES:
NA.21

Qualitätsniveau

100

Produktlinie

ReagentPlus®

Assay

99%

bp

194 °C/70 mmHg (lit.)

mp (Schmelzpunkt)

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

InChIKey

RTZZCYNQPHTPPL-UHFFFAOYSA-N

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Allgemeine Beschreibung

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.

Anwendung

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.

Rechtliche Hinweise

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

Piktogramme

CorrosionExclamation mark
GHS05,GHS07

Signalwort

Danger

Gefahreneinstufungen

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

Lagerklassenschlüssel

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

WGK

WGK 3

Persönliche Schutzausrüstung

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

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Analysenzertifikate (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)
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)
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
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)
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