Zinc acetate is a salt with the formula Zn(CH3CO2)2, which commonly occurs as the dihydrate Zn(CH3CO2)2·2H2O. Both the hydrate and the anhydrous forms are colorless solids that are used as dietary supplements. When used as a food additive, it has the E number E650.
Zinc acetate is a component of some medicines, e.g., lozenges for treating the common cold.[1] Zinc acetate can also be used as a dietary supplement.[2] As an oral daily supplement it is used to inhibit the body's absorption of copper as part of the treatment for Wilson's disease.[3] Zinc acetate is also sold as an astringent in the form of an ointment, a topical lotion, or combined with an antibiotic such as erythromycin for the topical treatment of acne.[4] It is commonly sold as a topical anti-itch ointment.
Zinc acetate is used as the catalyst for the industrial production of vinyl acetate from acetylene:
CH3CO2H + C2H2 → CH3CO2CH=CH2. Approximately 1/3 of the worlds production uses this route, which because of its environmental impact, is mainly practiced in countries with relaxed environmental regulations such as China.[5]
In anhydrous zinc acetate the zinc is coordinated to four oxygen atoms to give a tetrahedral environment, these tetrahedral polyhedra are then interconnected by acetate ligands to give a range of polymeric structures.[7][8][9]
In the dihydrate, zinc is octahedral, wherein both acetate groups are bidentate.[10][11]
Heating Zn(CH3CO2)2 in a vacuum results in a loss of acetic anhydride, leaving a residue of "basic zinc acetate," with the formula Zn4O(CH3CO2)6. It can also be prepared by a reaction of glacial acetic acid with zinc oxide.[12] The cluster compound has a tetrahedral structure with an oxide ligand at its center[13] Basic zinc acetate is a common precursor to metal-organic frameworks (MOFs).
^O. F. Wagenknecht; R. Juza (1963). "Zinc Acetate". In G. Brauer (ed.). Handbook of Preparative Inorganic Chemistry, 2nd Ed. Vol. 2pages=1087. NY, NY: Academic Press.
^He, Hongshan (15 November 2006). "A new monoclinic polymorph of anhydrous zinc acetate". Acta Crystallographica Section E. 62 (12): m3291–m3292. doi:10.1107/S1600536806046678.
^Capilla, A. V.; Aranda, R. A. (1979). "Anhydrous Zinc(II) Acetate (CH3-COO)2Zn". Crystal Structure Communications. 8: 795–797.
^Poshkus, Algirdas C. (June 1983). "Improved synthesis of basic zinc acetate, hexakis(.mu.-acetato)-.mu.-oxotetrazinc". Industrial & Engineering Chemistry Product Research and Development. 22 (2): 380–381. doi:10.1021/i300010a041.
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