114693
1-Nitroso-2-naphthol
97%
Synonym(s):
1-Nitroso-2-hydroxynaphthalene
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About This Item
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Assay
97%
form
solid
mp
106-108 °C (dec.) (lit.)
functional group
C-nitroso
nitroso
SMILES string
Oc1ccc2ccccc2c1N=O
InChI
1S/C10H7NO2/c12-9-6-5-7-3-1-2-4-8(7)10(9)11-13/h1-6,12H
InChI key
YXAOOTNFFAQIPZ-UHFFFAOYSA-N
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Application
1-Nitroso-2-naphthol is the chelating ion-exchanger in the synthesis of alumina adsorbents that are of acidic, basic and neutral nature. It is used for the removal and preconcentration of Pb(II), Cu(II), Cr(III) from waste, as well as drinking water. It is also used in the preconcentration of cobalt using C(18) microcolumn with flow injection that is coupled to a flame atomic absorption spectrometry (FI-FAAS) system.
1-Nitroso-2-naphthol is used in the preparation of 1-nitroso-2-naphthol-sodium nitrite reagent.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Muta. 2 - Skin Irrit. 2 - Skin Sens. 1
Storage Class Code
13 - Non Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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European journal of biochemistry, 200(2), 487-493 (1991-09-01)
o-Phenanthroline (1,10-phenanthroline) is a chemical known to chelate iron and other transition metal ions. This compound was added to solid yeast media to reduce the concentration of biologically available iron. Other essential divalent cations, like Zn2+ or Cu2+, which could
Improved fluorometric determination of acetaminophen and its conjugates with 1-nitroso-2-naphthol in whole blood and urine.
Chemical & pharmaceutical bulletin, 30(1), 358-361 (1982-01-01)
Cobalt determination with FI-FAAS after on-line sorbent preconcentration using 1-nitroso-2-naphthol.
Talanta, 57(5), 945-951 (2008-10-31)
The suitability of 1-nitroso-2-naphthol (NN) as a complexing agent for on-line preconcentration of cobalt using C(18) microcolumn with FI-FAAS system has been tested. Various parameters affecting the complex formation and its elution were optimized. Reagent solution (2.5x10(-3) mol l(-1)) and
Fluorometric measurement of tyrosine in serum and plasma.
Clinical chemistry, 20(4), 505-510 (1974-04-01)
Clinical chemistry, 29(11), 1969-1971 (1983-11-01)
1-Nitroso-2-naphthol reacts with various 5-hydroxyindoles as well as para-substituted phenols and guaiacols. Consequently, this reaction has long been used to measure tyrosine in tyrosinosis and tyrosinemia, homovanillic acid in neuroblastoma, and 5-hydroxy-3-indoleacetic acid in the carcinoid tumor. We report here
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