N9125
N-(1-萘基)乙二胺 二盐酸盐
≥98%
别名:
2-(1-萘氨基)乙胺 二盐酸盐
质量水平
方案
≥98%
表单
powder
mp
194-198 °C (dec.) (lit.)
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）乙二胺盐酸盐是一种有机化合物，带共轭环结构，在电荷转移配合物中用作强电子供体。它的游离碱形式也称为Bratton-Marshall试剂，广泛用于重氮化-偶联反应检测亚硝酸盐和硝酸盐。
应用
N-1-萘基乙二胺二盐酸盐可作为反应剂合成：
- N
- -1-萘基乙二胺取代的环三磷腈衍生物，用作抗菌剂。
- 荧光化学传感器化合物，以萘基为荧光团，cyclen为金属离子螯合剂，用于检测水溶液中的Zn(II)。
- (N-1-萘基乙二胺)-二氯铂(II)荧光复合物(λmax = 405 nm)。
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
历史批次信息供参考:
分析证书(COA)
Lot/Batch Number
Raquel Morais de Paiva Daibert et al.
PloS one, 15(11), e0241861-e0241861 (2020-11-07)
Macrophages are classified upon activation as classical activated M1 and M2 anti-inflammatory regulatory populations. This macrophage polarization is well characterized in humans and mice, but M1/M2 profile in cattle has been far less explored. Bos primigenius taurus (taurine) and Bos
Improved dye procedure for determining urea concentration by using o-phthalaldehyde and naphthylethylenediamine.
N T Lequang et al.
Clinical chemistry, 33(1), 192-192 (1987-01-01)
C E Davis et al.
Journal - Association of Official Analytical Chemists, 68(3), 485-488 (1985-05-01)
Current methods used for determining residual nitrite concentration in foods involve forming an azo dye that is measured spectrophotometrically. Conventional procedures do not specify control of pH for the final colored solution. Because many indicator dyes are pH-dependent, absorbance of
P K Laikind et al.
Analytical biochemistry, 156(1), 81-90 (1986-07-01)
The Bratton-Marshall reaction can be used to identify patients with adenylosuccinate lyase deficiency. These patients excrete in their urine the dephosphorylated derivative of the de novo purine synthesis intermediate 5'-phosphoribosyl-4-(N-succinylcarboxamide)-5-aminoimidazole (SAICAR). The test described here depends on a coupling reaction
A C Roy et al.
Electrophoresis, 13(6), 396-397 (1992-06-01)
A sensitive staining method for the detection of oxytocinase (EC 3.4.11.3) activity in electrophoresis gels has been described. The method is based on the enzymatic release of p-nitroaniline (PNA) from two specific synthetic oxytocinase substrates, S-benzyl-L-cysteine-p-nitroanilide (BCN) and L-leucine-p-nitroanilide (LN)
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