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等级
ACS reagent
puriss. p.a.
Agency
USP/NF
reag. ISO
reag. Ph. Eur.
蒸汽压
7.3 mmHg ( 25 °C)
方案
99-102%
表单
crystalline
杂质
≤0.005% in water insoluble matters
≤10 mg/kg total nitrogen (N)
pH值（酸碱度）
3.7-4.5 (20 °C, 5%)
mp
110 °C (dec.) (lit.)
痕量阴离子
chloride (Cl-): ≤10 mg/kg
痕量阳离子
As: ≤0.00005%
Ca: ≤0.001%
Cd: ≤0.001%
Co: ≤0.001%
Fe: ≤0.002%
K: ≤0.001%
Mg: ≤0.0005%
Na: ≤0.002%
Ni: ≤0.002%
Pb: ≤0.002%
Zn: ≤0.030%
SMILES字符串
O.O.O.O.O.[Cu++].[O-]S([O-])(=O)=O
InChI
1S/Cu.H2O4S.5H2O/c;1-5(2,3)4;;;;;/h;(H2,1,2,3,4);5*1H2/q+2;;;;;;/p-2
InChI key
JZCCFEFSEZPSOG-UHFFFAOYSA-L
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一般描述
Copper(II) sulfate pentahydrate (CuSO4·5H2O, Blue vitriol) is a hydrated copper(II) salt. It undergoes hydrothermal reactions with the tripodal ligands to afford metal-organic frameworks (MOFs). CuSO4·5H2O along with metallic copper was employed as a catalyst for the synthesis of different ligand-arm functionalized azoamides. On heating above 560°C, it decomposes to CuO.
应用
Copper(II) sulfate pentahydrate may be employed in the following studies:
- As a catalyst for the acetylation of alcohols and phenols under solvent-free conditions.
- To compose the electrolyte for the electrodeposition of Cu-Zn-Sn precursors, required for the preparation of Cu2ZnSnS4 (CZTS) thin films.
- As catalyst for the dehydration of alcohols.
警示用语：
Danger
危险声明
危险分类
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1
储存分类代码
13 - Non Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
法规信息
新产品
Copper (II) Sulfate.
Hoffman RV, et al.
e-EROS Encyclopedia of Reagents for Organic Synthesis. (2001)
Wei Zhao et al.
Dalton transactions (Cambridge, England : 2003), (8)(8), 1509-1517 (2005-04-13)
Three novel metal-organic frameworks (MOFs), [Cu(1)SO4].H2O (4), [Cu2(2)2(SO4)2].4H2O (5) and [Cu(3)(H2O)]SO4.5.5H2O (6), were obtained by hydrothermal reactions of CuSO4.5H2O with the corresponding ligands, which have different flexibility. The structures of the synthesized complexes were determined by single-crystal X-ray diffraction analyses.
Damijana Urankar et al.
Journal of combinatorial chemistry, 10(6), 981-985 (2008-10-17)
Azoamides, previously established as bioactive intracellular GSH-depleting agents, were decorated with a terminal alkyne moiety to 4 and then were transformed, by copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC), into different ligand-arm functionalized azoamides 6. Azides 5 having ligand-arms amenable for binding to
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