登录 查看组织和合同定价。
选择尺寸
变更视图
关于此项目
线性分子式:
CuSO4 · 5H2O
化学文摘社编号:
分子量:
249.69
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352302
EC Number:
231-847-6
MDL number:
Assay:
≥98.0%, 98.0-102.0% (ACS specification)
Grade:
ACS reagent
Form:
crystals
grade
ACS reagent
vapor pressure
7.3 mmHg ( 25 °C)
assay
≥98.0%, 98.0-102.0% (ACS specification)
form
crystals
reaction suitability
reaction type: click chemistry, reagent type: catalyst
core: copper
pH
3.5-4.5 (20 °C, 50 g/L)
mp
110 °C (dec.) (lit.)
anion traces
chloride (Cl-): ≤0.001%
cation traces
Ca: ≤0.005%, Fe: ≤0.003%, K: ≤0.01%, Na: ≤0.02%, Ni: ≤0.005%
SMILES string
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
General description
五水硫酸铜(II)是一种常用的路易斯酸催化剂，用于促进酸催化的有机转化。它也可与其他混合氧化剂共同组成有效的氧化还原催化剂。
Application
五水硫酸铜(II)可用作催化剂：
还可以用作模板，以乙烯基吡啶和甲基丙烯酸为功能单体合成铜(II)离子印迹聚合物。该聚合物用于通过火焰原子吸收光谱法定量 Cu2+ 离子。
- 在乙酸酐环境下，进行醇和酚的乙酰化反应。
- 通过酰胺与炔基溴的分子内偶联合成多种酰胺。
还可以用作模板，以乙烯基吡啶和甲基丙烯酸为功能单体合成铜(II)离子印迹聚合物。该聚合物用于通过火焰原子吸收光谱法定量 Cu2+ 离子。
Features and Benefits
CuSO4.5H2O 是一种经济、安全的催化剂，可用于各种有机转化。它也可以回收并在另一个反应中重复使用。
Still not finding the right product?
Explore all of our products under 硫酸铜 五水合物
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1
flash_point_f
Not applicable
flash_point_c
Not applicable
存储类别
11 - Combustible Solids
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.
Copper (II) sulfate pentahydrate (CuSO4. 5H2O): a green catalyst for solventless acetylation of alcohols and phenols with acetic anhydride.
Heravi MM, et al.
Journal of the Brazilian Chemical Society, 17(5), 1045-1047 (2006)
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
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 209198-100G | 04061837768453 |
| 209198-2.5KG | 04061835346585 |
| 209198-5G | 04061837768484 |
| 209198-12KG | 04061838770592 |
| 209198-250G | 04061837768460 |
| 209198-25KG | 04061833636473 |
| 209198-500G | 04061837768477 |