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Merck
CN

195804

乙二胺 二盐酸盐

98%

别名:

1,2-二氨基乙烷 二盐酸盐

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线性分子式:
NH2CH2CH2NH2 · 2HCl
化学文摘社编号:
分子量:
133.02
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
206-369-6
Beilstein/REAXYS Number:
3665235
MDL number:
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产品名称

乙二胺 二盐酸盐, 98%

InChI key

OHHBFEVZJLBKEH-UHFFFAOYSA-N

InChI

1S/C2H8N2.2ClH/c3-1-2-4;;/h1-4H2;2*1H

SMILES string

Cl[H].Cl[H].NCCN

assay

98%

form

solid

mp

>300 °C (lit.)

solubility

water: soluble 100 mg/mL, clear, colorless to very faintly yellow

functional group

amine

Quality Level

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Application

将二盐酸乙二胺用于改性乙二胺缩合法荧光测定儿茶酚胺 。用它来研究 Eu III 和 Tb III 与乙二胺的配合物的发光属性 。它被用于合成 1,3,5-(4,5-二氢-1 H -咪唑-2-基)苯

pictograms

Health hazardExclamation mark

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Resp. Sens. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


历史批次信息供参考:

分析证书(COA)

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Luminescence spectroscopic study of europium (III) and terbium (III) with ethylenediamine in dimethyl sulfoxide.
Wang Z, et al.
J. Chem. Soc., Dalton Trans., 18, 2791-2796 (1993)
Self-assembled organogels based on two-component system.
Nam SR, et al.
Tetrahedron, 64(46), 10531-10537 (2008)
Modified ethylenediamine condensation method and its application in the analysis of catecholamines by ion-exchange chromatography.
Seki T.
Journal of Chromatography A, 155(2), 415-420 (1978)
Po Ying Yeh et al.
Langmuir : the ACS journal of surfaces and colloids, 28(46), 16227-16236 (2012-11-01)
We report a novel nonfouling passivation method using poly(ethylene glycol) (PEG) engraftment on the surfaces of poly(dimethylsiloxane) (PDMS) microfluidic devices sealed with SU-8. To achieve bonding between the PDMS and SU-8 surfaces, the PDMS surface was first functionalized with amines
Maria V Babak et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 19(13), 4308-4318 (2013-01-24)
With the aim of systematically studying fundamental structure-activity relationships as a basis for the development of Ru(II) arene complexes (arene = p-cymene or biphenyl) bearing mono-, bi-, or tridentate am(m)ine ligands as anticancer agents, a series of ammine, ethylenediamine, and

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