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Sigma-Aldrich

Copper(II) sulfate

puriss., meets analytical specification of Ph. Eur., BP, USP, anhydrous, 99-100.5% (based on anhydrous substance)

Sinónimos:

Cupric sulfate

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About This Item

Fórmula lineal:
CuSO4
Número de CAS:
7758-98-7
Peso molecular:
159.61
EC Number:
231-847-6
MDL number:
MFCD00010981
UNSPSC Code:
12352300
PubChem Substance ID:
329749899
NACRES:
NA.21

vapor pressure

7.3 mmHg ( 25 °C)

Quality Level

200

grade

puriss.

assay

99-100.5% (based on anhydrous substance)

form

solid

quality

meets analytical specification of Ph. Eur., BP, USP

impurities

residual solvents, complies

loss

≤1% loss on drying, 250 °C

pH

3.5-4.5 (20 °C, 50 g/L)

mp

200 °C (dec.) (lit.)

density

3.603 g/mL at 25 °C (lit.)

anion traces

chloride (Cl-): ≤100 mg/kg

cation traces

Ca: ≤50 mg/kg
Fe: ≤30 mg/kg
K: ≤100 mg/kg
Mg: ≤100 mg/kg
Na: ≤200 mg/kg
Ni: ≤50 mg/kg
Pb: ≤80 mg/kg

SMILES string

[Cu++].[O-]S([O-])(=O)=O

InChI

1S/Cu.H2O4S/c;1-5(2,3)4/h;(H2,1,2,3,4)/q+2;/p-2

InChI key

ARUVKPQLZAKDPS-UHFFFAOYSA-L

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General description

Copper(II) sulfate acts as a redox catalyst along with potassium permanganate for the oxidation of alcohols. On heating above 560°C, it decomposes to CuO.5
It can find applications in agriculture as a nutrient for plants. It can also serve as a precursor in the production of foliar bactericides and fungicides.

Application

Copper(II) sulfate may be employed for 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 a Lewis acid catalyst for the dehydration of alcohols.5

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1

Storage Class

13 - Non Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Certificados de análisis (COA)

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Author - Richardson W.H
Handbook of Copper Compounds and Applications (1997)
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
William T Triplett et al.
Magnetic resonance in medicine, 72(1), 8-19 (2013-09-06)
The relationship between fat fractions (FFs) determined based on multiple TE, unipolar gradient echo images and (1) H magnetic resonance spectroscopy (MRS) was evaluated using different models for fat-water decomposition, signal-to-noise ratios, and excitation flip angles. A combination of single-voxel
Preparation of Cu2ZnSnS4 thin films by sulfurization of co-electroplated Cu-Zn-Sn precursors.
Araki H, et al.
Physica Status Solidi, 6(5), 1266-1268 (2009)
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