114693
1-亚硝基-2-萘酚
97%
别名:
1-Nitroso-2-hydroxynaphthalene
质量水平
方案
97%
表单
solid
mp
106-108 °C (dec.) (lit.)
官能团
C-nitroso
nitroso
SMILES字符串
Oc1ccc2ccccc2c1N=O
InChI
1S/C10H7NO2/c12-9-6-5-7-3-1-2-4-8(7)10(9)11-13/h1-6,12H
InChI key
YXAOOTNFFAQIPZ-UHFFFAOYSA-N
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应用
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。
警示用语:
Warning
危险分类
Acute Tox. 4 Oral - Eye Irrit. 2 - Muta. 2 - Skin Irrit. 2 - Skin Sens. 1
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
Fluorometric measurement of tyrosine in serum and plasma.
J A Ambrose
Clinical chemistry, 20(4), 505-510 (1974-04-01)
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
C F Burrows et al.
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].
N G Shafranova et al.
Laboratornoe delo, (7)(7), 25-26 (1983-01-01)
Nayyef Aljaar et al.
The Journal of organic chemistry, 78(1), 154-166 (2012-11-28)
Reactions between 1-nitroso-2-naphthols and α-functionalized ketones such as α-bromo-, α-chloro-, α-mesyloxy-, α-tosyloxy-, and α-hydroxy ketones under basic conditions delivered 2-substituted naphtho[1,2-d][1,3]oxazoles in a single synthetic operation. The product formation was accompanied by the unexpected loss of the C═O group from
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