Copper(II) sulfate

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Copper(II) sulfate
IUPAC name Copper(II) sulfate
pentahydrate
Other names Copper(II) sulfate
Copper(II)sulphate
Cupric sulfate
Blue vitriol
Bluestone
Chalcanthite
Identifiers
CAS number 7758-98-7
EINECS number 231-847-6
RTECS number GL8800000
Properties
Molecular formula CuSO4·5H2O (pentahydrate)
CuSO4 (anhydrous)
Molar mass 249.685 g/mol (pentahydrate)
159.609 g/mol (anhydrous)
Appearance blue crystalline solid (pentahydrate)
gray-white powder (anhydrous)
Melting point

110 °C (− 4H2O)
150 °C (423 K) (− 5H2O)
650 °C decomp.

Solubility in water 31.6 g/100 ml (0 °C)
Structure
Crystal structure Triclinic
Coordination
geometry
Octahedral
Thermochemistry
Standard molar
entropy
So298
109.05 J.K−1.mol−1
Hazards
EU classification Harmful (Xn)
Dangerous for the environment (N)
NFPA 704

0
2
0
 
Flash point non flammable
Related Compounds
Other cations Nickel(II) sulfate
Zinc sulfate
Except where noted otherwise, data are given for
materials in their standard state
(at 25 °C, 100 kPa)

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Overview

Copper(II) sulfate is the chemical compound with the formula CuSO4. This salt exists as a series of compounds that differ in their degree of hydration. The anhydrous form is a pale green or gray-white powder, whereas the pentahydrate, the most commonly encountered salt, is bright blue. This hydrated copper sulfate occurs in nature as the mineral called chalcanthite. Archaic names for copper(II) sulfate are "blue vitriol" and "bluestone".[1]

Preparation

Since it is available commercially, copper sulfate is usually purchased, not prepared in the laboratory. It can be made by the action of sulfuric acid on a variety of copper(II) compounds, for example copper(II) oxide. Copper(II) sulfate pentahydrate decomposes before melting, losing four water molecules at 110 °C and all five at 150 °C. At 650 °C, copper(II) sulfate decomposes into copper(II) oxide (CuO) and sulfur trioxide (SO3). When heated in an open flame the crystals are dehydrated and turn grayish-white.[1]

Uses

As an herbicide, fungicide, pesticide

Copper sulfate pentahydrate is a fungicide. Mixed with lime it is called Bordeaux mixture to control fungus on grapes, melons and other berries,[1] another application is Cheshunt compound, a mixture of copper sulphate and ammonium carbonate used in horticulture to prevent damping off in seedlings. Its use as an herbicide is not agricultural, but instead for control of invasive exotic aquatic plants and the roots of other invasive plants near various pipes that contain water. A dilute solution of copper sulfate is used to treat aquarium fish of various parasitic infections,[1] and is also used to remove snails from aquariums. However, as the copper ions are also highly toxic to the fish, care must be taken with the dosage. Most species of algae can be controlled with very low concentrations of copper sulfate. Copper sulfate inhibits growth of bacteria such as E. coli.

Analytical reagent

Several chemical tests utilize copper sulfate. It is used in Fehling's solution and Benedict's solution to test for reducing sugars, which reduce the soluble blue copper(II) sulfate to insoluble red copper(I) oxide. Copper(II) sulfate is also used in the Biuret reagent to test for proteins.

Copper sulfate is also used to test blood for anemia. The blood is tested by dropping it into a solution of copper sulfate of known specific gravity — blood which contains sufficient hemoglobin sinks rapidly due to its density, whereas blood which does not floats or sinks slowly.[1]

In a flame test, its copper ions emit a deep blue-green light, much more blue than the flame test for barium.

Organic synthesis

Copper sulfate is employed in organic synthesis.[1] The anhydrous salt catalyses the transacetalization in organic synthesis.[1] The hydrated salt reacts with potassium permanganate to give an oxidant for the conversion of primary alcohols.[1]

Chemistry education

Copper sulphate is a commonly included chemical in children's chemistry sets and is often used to grow crystals in schools and in copper plating experiments. Due to its toxicity, it is not recommended for small children. Copper sulfate is often used to demonstrate an exothermic reaction, in which steel wool or magnesium ribbon is placed in an aqueous solution of CuSO4. It is used in school chemistry courses to demonstrate the principle of mineral hydration. The pentahydrate form, which is blue, is heated, turning the copper sulfate into the anhydrous form which is white, while the water that was present in the pentahydrate form evaporates. When water is then added to the anhydrous compound, it turns back into the pentahydrate form, regaining its blue color.

In an illustration of a "single metal replacement reaction," iron is submerged in a solution of copper sulfate. Upon standing, iron dissolves and copper precipitates.

Fe + CuSO4 → FeSO4 + Cu

The copper can also be electroplated to the iron.

Other uses

Other applications include hair dyes, coloring glass, processing of leather and textiles, an ingredient in baby formula milk, and in pyrotechnics as a green colorant.[1]

References

External links



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da:Kobber(II)sulfat de:Kupfersulfatfr:Sulfate de cuivre it:Solfato rameico he:נחושת גופרתית lv:Vara sulfāts hu:Réz-szulfát ms:Kuprum(II) sulfat nl:Koper(II)sulfaat ja:硫酸銅(II) nds:Koppersulfatsk:Síran meďnatý fi:Kuparisulfaatti sv:Kopparsulfat uk:Сульфат міді

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Acknowledgement and Attribution Regarding Sources of Content

Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .

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