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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Fluorometric measurement of tyrosine in serum and plasma.
Clinical chemistry, 20(4), 505-510 (1974-04-01)
Journal of the American Veterinary Medical Association, 183(3), 318-322 (1983-08-01)
The nitrosonapthol test, which qualitatively measures urinary excretion of 4-hydroxyphenylacetic acid and related compounds, was evaluated as a screening test for small intestinal disease in 60 dogs with chronic diarrhea. Test results were positive in 8 of 13 dogs with
[A modified method of determination of bound 5-hydroxyindoleacetic acid in the urine].
Laboratornoe delo, (7)(7), 25-26 (1983-01-01)
N-acetyl-L-cysteine: an alternative to 2-mercaptoethanol in the reduction of Udenfriend's chromophore used for the determination of urinary 5-hydroxyindoleacetic acid.
Clinica chimica acta; international journal of clinical chemistry, 130(2), 251-256 (1983-05-30)
The Analyst, 115(3), 309-313 (1990-03-01)
The reaction of para- and meta-substituted phenols with 1-nitroso-2-naphthol in the presence of either CeIV or PbIV as an oxidant has been used to develop a fast automated flow injection (Fl) method. A stopped-flow kinetic study of the reaction revealed
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