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品質等級
化驗
97%
形狀
solid
mp
106-108 °C (dec.) (lit.)
SMILES 字串
Oc1ccc2ccccc2c1N=O
InChI
1S/C10H7NO2/c12-9-6-5-7-3-1-2-4-8(7)10(9)11-13/h1-6,12H
InChI 密鑰
YXAOOTNFFAQIPZ-UHFFFAOYSA-N
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應用
1-亚硝基-2-萘酚是氧化铝吸附剂合成中的螯合离子交换剂，具有酸性、碱性和中性性质。它用于从废物及饮用水中去除和预浓缩 Pb（II）、Cu（II）、Cr（III）。它还用于使用 C（18）微柱，联合流动注射与火焰原子吸收光谱（FI-FAAS）系统耦合对钴进行预浓缩。
1-亚硝基-2-萘酚用于制备 1-亚硝基-2-萘酚-亚硝酸钠试剂。
訊號詞
Warning
危險分類
Acute Tox. 4 Oral - Eye Irrit. 2 - Muta. 2 - Skin Irrit. 2 - Skin Sens. 1
儲存類別代碼
13 - Non Combustible Solids
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
N Schnell et al.
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.
J Shibasaki et al.
Chemical & pharmaceutical bulletin, 30(1), 358-361 (1982-01-01)
J A Knight et al.
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
Cobalt determination with FI-FAAS after on-line sorbent preconcentration using 1-nitroso-2-naphthol.
Yingxue Ye et al.
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.
J A Ambrose
Clinical chemistry, 20(4), 505-510 (1974-04-01)
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