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等級
ACS reagent
puriss. p.a.
agency
USP/NF
reag. ISO
reag. Ph. Eur.
蒸汽壓力
7.3 mmHg ( 25 °C)
化驗
99-102%
形狀
solid
雜質
≤0.001% total nitrogen (N)
≤0.005% in water insoluble matters
pH值
3.7-4.5 (20 °C, 5%)
mp
110 °C (dec.) (lit.)
負離子痕跡
chloride (Cl-): ≤10 mg/kg
正離子痕跡
As: ≤0.5 mg/kg
Ca: ≤10 mg/kg
Cd: ≤10 mg/kg
Co: ≤10 mg/kg
Fe: ≤20 mg/kg
K: ≤10 mg/kg
Mg: ≤5 mg/kg
Na: ≤20 mg/kg
Ni: ≤20 mg/kg
Pb: ≤20 mg/kg
Zn: ≤300 mg/kg
SMILES 字串
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 密鑰
JZCCFEFSEZPSOG-UHFFFAOYSA-L
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一般說明
五水硫酸铜(II)(CuSO4·5H2O,胆矾)是一种水合铜(II)盐。它能与三脚架配体发生水热反应,产生金属-有机骨架(MOF)。CuSO4·5H2O 与金属铜能够一起催化不同配体臂官能化偶氮酰胺的合成。当加热到560℃以上后,它会分解成CuO。
應用
五水硫酸铜(II)可用于以下研究:
- 在无溶剂条件下作为醇类和酚类乙酰化的催化剂。
- 制备用于Cu-Zn-Sn前体电沉积的电解质,它是制备Cu2ZnSnS4 (CZTS)薄膜所必需的。
- 作为乙醇的脱水反应的催化剂。
訊號詞
Danger
危險聲明
危險分類
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1
儲存類別代碼
13 - Non Combustible Solids
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
其他客户在看
Copper (II) Sulfate.
e-EROS Encyclopedia of Reagents for Organic Synthesis. (2001)
Materials (Basel, Switzerland), 13(5) (2020-03-11)
Despite the widespread application of activated carbon fiber (ACF) filters in air cleaning owing to their high surface area and low price, they have certain limitations in that they facilitate bacterial growth upon prolonged use as ACF filters can provide
Copper (II) sulfate pentahydrate (CuSO4. 5H2O): a green catalyst for solventless acetylation of alcohols and phenols with acetic anhydride.
Journal of the Brazilian Chemical Society, 17(5), 1045-1047 (2006)
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.
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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