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Merck
CN

654507

氯化镍(II) 六水合物

99.9% trace metals basis

别名:

六水合二氯化镍, 六水合氯化镍2

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关于此项目

线性分子式:
NiCl2 · 6H2O
化学文摘社编号:
分子量:
237.69
MDL编号:
UNSPSC代码:
12352302
PubChem化学物质编号:
NACRES:
NA.23
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质量水平

方案

99.9% trace metals basis

表单

solid

反应适用性

core: nickel

杂质

≤1500.0 ppm Trace Metal Analysis

应用

battery precursors
catalysts
material synthesis precursor

SMILES字符串

[H]O[H].[H]O[H].[H]O[H].[H]O[H].[H]O[H].[H]O[H].Cl[Ni]Cl

InChI

1S/2ClH.Ni.6H2O/h2*1H;;6*1H2/q;;+2;;;;;;/p-2

InChI key

LAIZPRYFQUWUBN-UHFFFAOYSA-L

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一般描述

氯化镍 (II) 六水合物是一种水溶性无机化合物。它是一种经济高效的化合物,可用于电镀、镀镍和防毒面具中的NH3吸附剂。

应用

氯化镍(II)六水合物可用作:      
  • 氧化镍 (NiO) 薄膜的前体,用作染料敏化太阳能电池 (DSSC) 中的空穴传输层。     
  • 钙钛矿太阳能电池中的电子传输层 (ETL) 添加剂,以提高其性能——特别是开路电压。
  • 合成导电聚合物复合材料的有效掺杂剂,有望应用于柔性电子和传感器。     
  • 通过水热法合成镍纳米刺颗粒的前体。

警示用语:

Danger

危险分类

Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 1A Inhalation - Muta. 2 - Repr. 1B - Resp. Sens. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT RE 1 Inhalation

靶器官

Lungs

储存分类代码

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

法规信息

危险化学品
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历史批次信息供参考:

分析证书(COA)

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NiCl2.6H2O: an efficient catalyst precursor for phosphine-free Heck and Sonogashira cross-coupling reactions
Nowrouzi N and Zarei M
Tetrahedron, 71(41), 7847-7852 (2015)
Kariana Moreno-Sader et al.
ACS omega, 4(6), 10834-10844 (2019-08-29)
Nanocomposites composed of polyacrylamide and nanoclay were synthesized via free-radical cross-linking polymerization and used to adsorb Co2+ and Ni2+ ions from water. The polyacrylamide (PAM)/sodium montmorillonite (Na-MMT) nanocomposites were characterized by Fourier transform infrared spectroscopy, X-ray diffraction, and scanning electron
Synthesis of tetra-substituted pyrroles, a potential phosphodiesterase 4B inhibitor, through nickel (II) chloride hexahydrate catalyzed one-pot four-component reaction.
Khan AT, et al.
Tetrahedron Letters, 53(32), 4145-4150 (2012)
Jenilee Way et al.
Nuclear medicine and biology, 40(3), 430-436 (2013-01-12)
4-[(18)F]Fluorobenzylamine ([(18)F]FBA) is an important building block for the synthesis of (18)F-labeled compounds. Synthesis of [(18)F]FBA usually involves application of strong reducing agents like LiAlH4 which is challenging to handle in automated synthesis units (ASUs). Therefore, alternative methods for the
R Prabhakaran et al.
Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry, 18(2), 233-247 (2013-01-01)
Three new nickel(II) thiosemicarbazone complexes have been synthesized and characterized by analytical, spectral, and single-crystal X-ray diffraction studies. In complex 1, the ligand 2-hydroxy-1-naphthaldehydethiosemicarbazone coordinated as a monobasic tridentate donor, whereas in complexes 2 and 3, the ligands salicylaldehyde-4(N)-ethylthiosemicarbazone and

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