33461
N-(1-萘基)乙二胺 二盐酸盐
ACS reagent, ≥98%
别名:
2-(1-萘氨基)乙胺 二盐酸盐
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关于此项目
线性分子式:
C10H7NHCH2CH2NH2 · 2HCl
化学文摘社编号:
分子量:
259.17
Beilstein:
3707471
EC 号:
MDL编号:
UNSPSC代码:
41116105
PubChem化学物质编号:
NACRES:
NA.21
等级
ACS reagent
质量水平
方案
≥98% (calc with ref. to anhyd. subst.)
≥98%
表单
powder
技术
UV/Vis spectroscopy: suitable
杂质
≤5% water (Karl Fischer)
mp
194-198 °C (dec.) (lit.)
适用性
complies for identity
SMILES字符串
Cl.Cl.NCCNc1cccc2ccccc12
InChI
1S/C12H14N2.2ClH/c13-8-9-14-12-7-3-5-10-4-1-2-6-11(10)12;;/h1-7,14H,8-9,13H2;2*1H
InChI key
MZNYWPRCVDMOJG-UHFFFAOYSA-N
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应用
N-（1-萘基）乙二胺二盐酸盐溶解于硫酸-甲醇中可作为测定薄层板上糖的试剂。它也可用于在低 pH 下与对氨基苯磺酸重氮化后，用微分脉冲极谱法测定亚微摩尔浓度的亚硝酸根离子。它也可以用作偶联剂，用于通过重氮化 - 偶联方法分光光度法测定苯胺。
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2
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
法规信息
危险化学品
此项目有
Spectrophotometric determination of aniline by the diazotization-coupling method with N-(1-naphthyl) ethylenediamine as the coupling agent.
Norwitz G and Keliher PN.
Analytical Chemistry, 53 (8), 1238-1240 (1981)
Determination of nitrite ion by differential-pulse polarography using N-(1-naphthyl) ethylenediamine.
Sabharwal S.
Analyst, 115 (10), 1305-1307 (1990)
N-(1-Naphthyl) ethylenediamine dihydrochloride as a new reagent for nanomole quantification of sugars on thin-layer plates by a mathematical calibration process.
Bounias M.
Analytical Chemistry, 106 (2), 291-295 (1980)
J A Cook et al.
Analytical biochemistry, 238(2), 150-158 (1996-07-01)
S-nitrosothiols have been shown to affect a number of physiological functions. Several techniques have been used to detect these species in biological systems, primarily by methods utilizing chemiluminescence. Since the apparatus required for measurement of chemiluminescence are not readily available
Basavaraj Hiremath et al.
Acta pharmaceutica (Zagreb, Croatia), 58(3), 275-285 (2008-12-24)
Two spectrophotometric methods for the determination of ceftazidime (CFZM) in either pure form or in its pharmaceutical formulations are described. The first method is based on the reaction of 3-methylbenzothiazolin-2-one hydrazone (MBTH) with ceftazidime in the presence of ferric chloride
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