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等级
ACS reagent
质量水平
方案
>98%
表单
solid
杂质
≤5% water
mp
194-198 °C (dec.) (lit.)
溶解性
H2O: passes test
适用性
passes test for sensitivity to sulfanilamide
官能团
amine
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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一般描述
N-(1-萘基)乙二胺二盐酸盐(NEDA·2HCl)作为供体分子,与π-受体(醌醇和苦味酸)、σ-受体(碘)和空 轨道 受体(四氯化锡和氯化锌)形成电荷转移复合物。这些复合物可通过正电子湮没寿命谱(PAL)进行研究。
应用
N-(1-萘基)乙二胺二盐酸盐已被用于制备染色溶液,以通过薄层色谱观察淀粉活性酶的反应产物,其中含有α-1, 4连接的和α-1, 6连接的葡萄糖。它也被用于改良型Saville和Griess分析。
在N-(3-二甲氨基丙基)-N′-乙基碳二亚胺盐酸盐和 N-羟基琥珀酰亚胺存在下,N-(1-萘基)乙二胺二盐酸盐可与(±)-1,2-二硫戊环-3-戊酸反应,合成5-[1,2]二硫戊环基-3-戊酸[2-(萘基-1-氨基)-乙基]酰胺(DPAN)。将 N-(1-萘基)乙二胺二盐酸盐溶解在硫酸-甲醇中形成的溶液,可以用作在薄层板上检测纳米级糖的试剂。
分光光度法检测氨基苯酚、苯二胺、二硝基苯胺、氯苯胺、硫醇和磺胺的偶联剂。
溶于硫酸-甲醇的 N-(1-萘基)乙二胺二盐酸盐溶液可用于定量糖。
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
历史批次信息供参考:
分析证书(COA)
Lot/Batch Number
N-(1-naphthyl)ethylenediamine dihydrochloride as a new reagent for nanomole quantification of sugars on thin-layer plates by a mathematical calibration process.
M Bounias
Analytical biochemistry, 106(2), 291-295 (1980-08-01)
Analytica Chimica Acta, 204, 271-271 (1988)
Moamen S Refat et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 122, 34-47 (2013-12-03)
In this work, structural, thermal, morphological, pharmacological screening and positron annihilation lifetime measurements were performed on the interactions between a N-(1-Naphthyl)ethylenediamine dihydrochloride (NEDA·2HCl) donor and three types of acceptors to characterize these CT complexes. The three types of acceptors include
Functionalization of platinum nanoparticles for electrochemical detection of nitrite.
Miao P, et al.
Analytical and Bioanalytical Chemistry, 399(7), 2407-2411 (2011)
K K Verma et al.
Talanta, 38(3), 283-289 (1991-03-01)
A general assay procedure for a wide variety of thiols is described. The technique has three steps: (1) formation of S-nitrosothiols with nitrous acid, (2) destruction of the excess of nitrous acid, (3) hydrolysis of the S-nitrosothiols with mercuric ions
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