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Zinc chloride is an inorganic chemical compound with the ZnCl2· nH2O, with n ranging from 0 to 4.5, forming hydrates. Zinc chloride, anhydrous and its hydrates, are colorless or white solids, and are highly in . Five hydrates of zinc chloride are known, as well as four polymorphs of anhydrous zinc chloride.

All forms of zinc chloride are . They can usually be produced by the reaction of zinc or its compounds with some form of hydrogen chloride. Anhydrous zinc compound is a , readily forming complexes with a variety of Lewis bases. Zinc chloride finds wide application in processing, metallurgical fluxes, chemical synthesis of organic compounds, such as , and processes to produce other compounds of zinc.


History
Zinc chloride has long been known but currently practiced industrial applications all evolved in the latter half of 20th century.

An formed from aqueous zinc chloride and was first investigated in 1855 by . Sorel later went on to investigate the related , which bears his name.

(1993). 9780521372220, Cambridge University Press.

Dilute aqueous zinc chloride was used as a disinfectant under the name "Burnett's Disinfecting Fluid". From 1839 Sir William Burnett promoted its use as a disinfectant as well as a wood preservative. The Royal Navy conducted trials into its use as a disinfectant in the late 1840s, including during the cholera epidemic of 1849; and at the same time experiments were conducted into its preservative properties as applicable to the shipbuilding and railway industries. Burnett had some commercial success with his eponymous fluid. Following his death however, its use was largely superseded by that of and other proprietary products.


Structure and properties
Unlike other metal dichlorides, zinc dichloride adopts several crystalline forms (polymorphs). Four polymorph are known: α, β, γ, and δ. Each features centers surrounded in a tetrahedral manner by four chloride ligands.
(1984). 9780198553700, Clarendon Press.

3.00
3.09
2.98
2.98

Here a, b, and c are lattice constants, Z is the number of structure units per unit cell, and ρ is the density calculated from the structure parameters.

The orthorhombic form (δ) rapidly changes to another polymorph upon exposure to the atmosphere. A possible explanation is that the ions originating from the absorbed water facilitate the rearrangement. Rapid cooling of molten gives a .

Molten has a high viscosity at its melting point and a comparatively low electrical conductivity, which increases markedly with temperature.

(1994). 9780471936206, John Wiley & Sons.
(2025). 9788177648751, Allied Publishers.
As indicated by a study, the viscosity is explained by the presence of polymers,.
(2025). 9780444521163, Elsevier.
Neutron scattering study indicated the presence of tetrahedral centers, which requires aggregation of monomers as well.


Hydrates
A variety of hydrated zinc chloride are known: with n = 1, 1.33, 2.5, 3, and 4.5.
(2025). 9780123526519, Academic Press.
The 1.33-hydrate, previously thought to be the hemitrihydrate, consists of trans-Zn(H2O)4Cl2 centers with the chlorine atoms connected to repeating ZnCl4 chains. The hemipentahydrate, structurally formulated Zn(H2O)5ZnCl4, consists of Zn(H2O)5Cl octahedrons where the chlorine atom is part of a ZnCl42- tetrahedera. The trihydrate consists of distinct hexaaquozinc(II) cations and tetrachlorozincate anions; formulated Zn(H2O)6ZnCl4. Finally, the heminonahydrate, structurally formulated Zn(H2O)6ZnCl4·3H2O also consists of distinct hexaaquozinc(II) cations and tetrachlorozincate anions like the trihydrate but has three extra water molecules. These hydrates can be produced by evaporation of aqueous solutions of zinc chloride at different temperatures.


Preparation and purification
Historically, zinc chlorides are prepared from the reaction of hydrochloric acid with zinc metal or zinc oxide. Aqueous acids cannot be used to produce anhydrous zinc chloride. According to an early procedure, a suspension of powdered zinc in is treated with hydrogen chloride, followed by drying The overall method remains useful in industry, but without the solvent:

Aqueous solutions may be readily prepared similarly by treating Zn metal, zinc carbonate, zinc oxide, and with hydrochloric acid:

(2025). 9780471238966
Hydrates can be produced by evaporation of an aqueous solution of zinc chloride. The temperature of the evaporation determines the hydrates For example, evaporation at room temperature produces the 1.33-hydrate. Lower evaporation temperatures produce higher hydrates.

Commercial samples of zinc chloride typically contain water and products from hydrolysis as impurities. Laboratory samples may be purified by recrystallization from hot . Anhydrous samples can be purified by sublimation in a stream of hydrogen chloride gas, followed by heating the sublimate to 400 °C in a stream of dry gas.

(2025). 9780470842898
A simple method relies on treating the zinc chloride with .


Reactions

Chloride complexes
A number of salts containing the tetrachlorozincate anion, , are known. "Caulton's reagent", , which is used in organic chemistry, is an example of a salt containing .
(1998). 9783527295005, Wiley-VCH.
The compound contains tetrahedral and anions, so, the compound is not caesium pentachlorozincate, but caesium tetrachlorozincate chloride. No compounds containing the ion (hexachlorozincate ion) have been characterized. The compound crystallizes from a solution of in hydrochloric acid. It contains a polymeric anion with balancing monohydrated ions, ions.


Adducts
The adduct with thf illustrates the tendency of zinc chloride to form 1:2 adducts with weak . Being soluble in ethers and lacking acidic protons, this complex is used in the synthesis of organozinc compounds. A related 1:2 complex is (zinc dichloride di(hydroxylamine)). Known as Crismer's salt, this complexes releases upon heating.
(1967). 9780470132401
The distinctive ability of aqueous solutions of to dissolve is attributed to the formation of zinc-cellulose complexes, illustrating the stability of its adducts. Cellulose also dissolves in molten hydrate. Overall, this behavior is consistent with Zn2+ as a Lewis acid.

When solutions of zinc chloride are treated with , diverse ammine complexes are produced. In addition to the tetrahedral 1:2 complex .

(2025). 9781408608401, Read Books.
the complex also has been isolated. The latter contains the ion,. The species in aqueous solution have been investigated and show that is the main species present with also present at lower :Zn ratio.


Aqueous solutions of zinc chloride
Zinc chloride dissolves readily in water to give species and some free chloride. Aqueous solutions of are acidic: a 6 M aqueous solution has a pH of 1. The acidity of aqueous solutions relative to solutions of other Zn2+ salts (say the sulfate) is due to the formation of the tetrahedral chloro such as ZnCl3(H2O).
(2025). 9780199298815, Oxford University Press.
Most metal dichlorides form octahedral complexes, with stronger O-H bonds. The combination of hydrochloric acid and gives a reagent known as "". Such reagents were once used as a test for primary alcohols. Similar reactions are the basis of industrial routes from methanol and ethanol respectively to and .

In alkali solution, zinc chloride converts to various zinc hydroxychlorides. These include , , , and the insoluble . The latter is the mineral .

(1996). 9780306453342, Springer.
When zinc chloride hydrates are heated, hydrogen chloride evolves and hydroxychlorides result.

In aqueous solution , as well as other halides (bromide, iodide), behave interchangeably for the preparation of other zinc compounds. These salts give precipitates of zinc carbonate when treated with aqueous carbonate sources:

reacts with and to form a colored compound "Ruhemann's purple" (RP). Spraying with a zinc chloride solution, which is colorless, forms a 1:1 complex RP:, which is more readily detected as it fluoresces more intensely than RP.
(1999). 9780824719746, CRC Press.


Redox
Anhydrous zinc chloride melts and even boils without any decomposition up to 900 °C. When zinc metal is dissolved in molten at 500–700 °C, a yellow diamagnetic solution is formed consisting of the , which has zinc in the oxidation state +1. The nature of this dizinc dication has been confirmed by Raman spectroscopy. Although is unusual, mercury, a heavy congener of zinc, forms a wide variety of salts.

In the presence of oxygen, zinc chloride oxidizes to above 400 °C. Again, this observation indicates the nonoxidation of Zn2+.


Zinc hydroxychloride
Concentrated aqueous zinc chloride dissolves to form zinc hydroxychloride, which is obtained as colorless crystals:
The same material forms when hydrated zinc chloride is heated.
(2025). 9780123567864, Academic Press.

The ability of zinc chloride to dissolve metal oxides (MO)

(2025). 9783110177701, de Gruyter, Berlin.
is relevant to the utility of as a flux for . It dissolves passivating oxides, exposing the clean metal surface.


Organic syntheses with zinc chloride
Zinc chloride is an occasional laboratory reagent often as a . A dramatic example is the conversion of methanol into hexamethylbenzene using zinc chloride as the solvent and catalyst:
This kind of reactivity has been investigated for the valorization of C1 precursors.

Examples of zinc chloride as a Lewis acid include the Fischer indole synthesis:

Related Lewis-acid behavior is illustrated by a traditional preparation of the dye from phthalic anhydride and , which involves a Friedel-Crafts acylation. This transformation has in fact been accomplished using even the hydrated sample shown in the picture above. Many examples describe the use of zinc chloride in Friedel-Crafts acylation reactions.

Zinc chloride also activates and halides towards substitution by weak such as :

In similar fashion, promotes selective reduction of tertiary, allylic or benzylic halides to the corresponding hydrocarbons.

Zinc , prepared from alkali metal enolates and , provide control of in aldol condensation reactions. This control is attributed to at the zinc. In the example shown below, the product was favored over the by a factor of 5:1 when .


Organozinc precursor
Being inexpensive and anhydrous, ZnCl2 is a widely used for the synthesis of many reagents, such as those used in the palladium catalyzed with or . The prominence of this reaction was highlighted by the award of the 2010 Nobel Prize in Chemistry to .

, a highly reactive form of zinc metal, is generated by reduction of zinc dichloride with . Rieke Zn is useful for the preparation of and for the Reformatsky reaction.


Uses

Industrial organic chemistry
Zinc chloride is used as a catalyst or reagent in diverse reactions conducted on an industrial scale. Benzaldehyde, 20,000 tons of which is produced annually in Western countries, is produced from inexpensive by exploiting the catalytic properties of zinc dichloride. This process begins with the chlorination of toluene to give . In the presence of a small amount of anhydrous zinc chloride, a mixture of benzal chloride are treated continuously with water according to the following stoichiometry:
(2025). 9783527303854
Similarly zinc chloride is employed in hydrolysis of benzotrichloride, the main route to . It serves as a catalyst for the production of methylene-bis(dithiocarbamate).


As a metallurgical flux
The use of zinc chloride as a flux, sometimes in a mixture with ammonium chloride (see also Zinc ammonium chloride), involves the production of HCl and its subsequent reaction with surface oxides.

Zinc chloride forms two salts with ammonium chloride: and , which decompose on heating liberating HCl, just as zinc chloride hydrate does. The action of zinc chloride/ammonium chloride fluxes, for example, in the hot-dip galvanizing process produces gas and ammonia fumes.

(1990). 9780871700216, ASM International.


Other uses
Relevant to its affinity for these paper and textiles, is used as a fireproofing agent and in the process of making , which is made by soaking paper in concentrated zinc chloride. Zinc chloride is also used as a deodorizing agent and to make .


Safety and health
Zinc and chloride are essential for life. Zn2+ is a component of several , e.g., and carbonic anhydrase. Thus, aqueous solutions of zinc chlorides are rarely problematic as an acute poison. Anhydrous zinc chloride is however an aggressive as it can burn skin and other tissues. Ingestion of zinc chloride, often from , requires endoscopic monitoring. Another source of zinc chloride is zinc chloride smoke mixture ("HC") used in . Containing zinc oxide, and powder release zinc chloride, carbon and smoke, an effective .
(1997). 9781428912335, DIANE Publishing.
Such smoke screens can lead to fatalities.
(2025). 9780444594532, Academic Press.


Further reading
  • N. N. Greenwood, A. Earnshaw, Chemistry of the Elements, 2nd ed., Butterworth-Heinemann, Oxford, UK, 1997.
  • The Merck Index, 7th edition, Merck & Co, Rahway, New Jersey, USA, 1960.
  • D. Nicholls, Complexes and First-Row Transition Elements, Macmillan Press, London, 1973.
  • J. March, Advanced Organic Chemistry, 4th ed., p. 723, Wiley, New York, 1992.
  • G. J. McGarvey, in Handbook of Reagents for Organic Synthesis, Volume 1: Reagents, Auxiliaries and Catalysts for C-C Bond Formation, (R. M. Coates, S. E. Denmark, eds.), pp. 220–3, Wiley, New York, 1999.


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