InChI key
IQUPABOKLQSFBK-UHFFFAOYSA-N
InChI
1S/C6H5NO3/c8-6-4-2-1-3-5(6)7(9)10/h1-4,8H
SMILES string
Oc1ccccc1[N+]([O-])=O
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
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Application
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Legal Information
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
法规信息
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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
Lin Li et al.
Talanta, 81(4-5), 1643-1649 (2010-05-06)
A couple of new fluorescent probes, based on diethoxycarbonyl glycoluril, were synthesized and characterized by (1)H NMR, X-ray crystal structure. The probes were found to be relatively highly fluorescence with quantum yields of 0.20 and 0.18, respectively, at room temperature
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
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
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