35966
2-Nitrophenol
PESTANAL®, analytical standard
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About This Item
Linear Formula:
O2NC6H4OH
CAS Number:
Molecular Weight:
139.11
Beilstein:
775403
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
grade
analytical standard
vapor pressure
1 mmHg ( 49.3 °C)
product line
PESTANAL®
technique(s)
HPLC: suitable
gas chromatography (GC): suitable
application(s)
agriculture
environmental
format
neat
SMILES string
Oc1ccccc1[N+]([O-])=O
InChI
1S/C6H5NO3/c8-6-4-2-1-3-5(6)7(9)10/h1-4,8H
InChI key
IQUPABOKLQSFBK-UHFFFAOYSA-N
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Application
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Legal Information
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
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Wei Guan et al.
Journal of separation science, 35(4), 490-497 (2012-01-28)
The novel surface molecularly imprinted polymer (MIP) with 2-nitrophenol (2-NP) as the template has been prepared and used as the adsorbent for the solid-phase extraction (SPE). The selectivity of the polymer was checked toward several selected nitrophenols (NPs) such as
Qing Wang et al.
Journal of separation science, 35(4), 589-595 (2012-03-06)
Coupling of long-chain ionic liquid (LCIL)-based sweeping and micelle to solvent stacking (MSS) in CZE for anionic compounds was proposed. N-Cetyl-N-methylpyrrolidinium bromide (C16MPYBr) was used as a novel cationic surfactant. The capillary column was conditioned with poly(1-vinyl-3-butylimidazolium) bromide, a kind
Mabel Catalán et al.
Bioelectrochemistry (Amsterdam, Netherlands), 79(2), 162-167 (2010-03-23)
In this study the interaction between new benzimidazole molecules, 2-(2-nitrophenyl)-1H-benzimidazole (NB) and N-benzoyl-2-(2-nitrophenyl)-benzimidazole (BNB), with dsDNA and ssDNA was assessed at pH 7.4. Using differential pulse voltammetry at glassy carbon electrode, both molecules were electrochemically reduced due to the presence
Zhenke Zhu et al.
Chemosphere, 93(1), 29-34 (2013-06-26)
Dissolved organic matter (DOM) is widespread in aquatic and terrestrial environments. Iron is the most abundant transition metal in the Earth's crust. The biogeochemistry of iron and the strength of Fe(II) as a reducing agent while adsorbed on minerals are
D Mahadevan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 86, 139-151 (2011-11-15)
In the present study, the FT-IR and FT-Raman spectra of 3-methyl-2-nitrophenol (C(7)H(7)O(3)N) (3M2NP) have been recorded in the range of 4000-100 cm(-1). The fundamental modes of vibrational frequencies of 3M2NP are assigned. All the geometrical parameters have been calculated by
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