Zinc acetate

Zinc acetate

Names
IUPAC name Zinc acetate
Other names Acetic acid, Zinc salt Acetic acid, Zinc(II) salt Dicarbomethoxyzinc Zinc diacetate
Identifiers
CAS Number	557-34-6 Y 5970-45-6 N
3D model (Jmol)	Interactive image
ChEMBL	ChEMBL1200928 N
ChemSpider	10719 Y
ECHA InfoCard	100.008.338
E number	E650 (flavour enhancer)
PubChem	11192
RTECS number	ZG8750000
UNII	H2ZEY72PME Y
InChI InChI=1S/2C2H4O2.Zn/c2*1-2(3)4;/h2*1H3,(H,3,4);/q;;+2/p-2 Y Key: DJWUNCQRNNEAKC-UHFFFAOYSA-L Y InChI=1/2C2H4O2.Zn/c2*1-2(3)4;/h2*1H3,(H,3,4);/q;;+2/p-2 Key: DJWUNCQRNNEAKC-NUQVWONBAP
SMILES [Zn+2].[O-]C(=O)C.[O-]C(=O)C
Properties
Chemical formula	ZnC4H6O4 (dihydrate)
Molar mass	219.50 g/mol (dihydrate) 183.48 g/mol (anhydrous)
Appearance	White solid (all forms)
Density	1.735 g/cm3 (dihydrate)
Melting point	Decomposes at 237 °C (459 °F; 510 K) (dihydrate loses water at 100 °C)
Boiling point	decomposes
Solubility in water	43 g/100 mL (20 °C, dihydrate)
Solubility	soluble in alcohol
Structure
Coordination geometry	octahedral (dihydrate)
Molecular shape	tetrahedral
Pharmacology
ATC code	A16AX05 (WHO)
Hazards
Main hazards	mildly toxic
R-phrases	R22 R36 R50/53
S-phrases	S26 S60 S61
Related compounds
Other anions	Zinc chloride
Other cations	Copper(II) acetate
Related compounds	Basic beryllium acetate
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YN ?)
Infobox references

Zinc acetate is a salt with the formula Zn(O₂CCH₃)₂, which commonly occurs as the dihydrate Zn(O₂CCH₃)₂(H₂O)₂. Both the hydrate and the anhydrous forms are colorless solids that are commonly used in chemical synthesis and as dietary supplements. Zinc acetates are prepared by the action of acetic acid on zinc carbonate or zinc metal. When used as a food additive, it has the E number E650.

Basic properties and structures

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.^[1][2][3] In contrast, most metal diacetates feature metals in octahedral coordination with bidentate acetate groups.

In zinc acetate dihydrate the zinc is octahedral, wherein both acetate groups are bidentate.^[4][5]

Basic zinc acetate

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. This cluster compound has the tetrahedral structure shown below. This species closely resembles the corresponding beryllium compound, although it is slightly expanded with Zn-O distances ~1.97 vs ~1.63 Å for Be₄O(OAc)₆.^[6]

Applications

Dietary and medicinal applications

Zinc acetate has been used in lozenges for treating the common cold. Pooling the results of three high dose zinc acetate trials indicates an average 42% reduction in the duration of colds (see figure).^[7]

Zinc acetate is a particularly useful salt in lozenges since acetate has relatively low affinity for zinc, with the result that essentially all zinc from the lozenges is freely released upon solvation in the saliva.^[8][9]

Although zinc acetate lozenges appear to be able to shorten the duration of colds, some zinc lozenges may be more effective than others. Among the factors affecting the usefulness of a zinc lozenge are the total dose of zinc provided as well as the presence of substances like citric acid which may bind up much of the zinc that the lozenge is providing.^[10]

Zinc acetate can also be used to treat zinc deficiencies. 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. 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. It is commonly sold as a topical anti-itch ointment.

In chewing gum, zinc acetate is a breath freshener^[11][12] and, when combined with hexetidine, a plaque inhibitor.^[13]

Industrial applications

Industrial applications include wood preservation, manufacturing other zinc salts, polymers, manufacture of ethylene acetate, as a dye mordant, and analytical reagent. It is used in commercial nuclear power plants as a plating inhibitor on primary water piping.

See also

• Basic beryllium acetate - isostructural

References

1. ↑ Clegg, W.; Little, I. R.; Straughan, B. P. (15 December 1986). "Monoclinic anhydrous zinc(II) acetate". Acta Crystallographica Section C. 42 (12): 1701–1703. doi:10.1107/S010827018609087X. 
2. ↑ 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. 
3. ↑ Capilla, A. V.; Aranda, R. A. (1979). "Anhydrous Zinc(II) Acetate (CH₃-COO)₂Zn". Crystal Structure Communications. 8: 795–797. 
4. ↑ van Niekerk, J. N.; Schoening, F. R. L.; Talbot, J. H. (10 September 1953). "The crystal structure of zinc acetate dihydrate, Zn(CH3COO)2.2H2O". Acta Crystallographica. 6 (8): 720–723. doi:10.1107/S0365110X53002015. 
5. ↑ Ishioka, T.; Murata, A.; Kitagawa, Y.; Nakamura, K. T. (15 August 1997). "Zinc(II) Acetate Dihydrate". Acta Crystallographica Section C. 53 (8): 1029–1031. doi:10.1107/S0108270197004484. 
6. ↑ Koyama, H.; Saito, Y. (1954). "The Crystal Structure of Zinc Oxyacetate, Zn₄O(CH₃COO)₆". Bull. Chem. Soc. Japan. 27 (2): 112–114. doi:10.1246/bcsj.27.112. 
7. ↑ Hemilä, Harri (23 June 2011). "Zinc Lozenges May Shorten the Duration of Colds: A Systematic Review". The Open Respiratory Medicine Journal. 5 (1): 51–58. doi:10.2174/1874306401105010051. PMC 3136969. PMID 21769305. 
8. ↑ Eby, George A. "Zinc Lozenges: Cold Cure or Candy? Solution Chemistry Determinations". Bioscience Reports. 24 (1): 23–39. doi:10.1023/B:BIRE.0000037754.71063.41. 
9. ↑ Eby, George A. (Mar 2010). "Zinc lozenges as cure for the common cold – A review and hypothesis". Medical Hypotheses. 74 (3): 482–492. doi:10.1016/j.mehy.2009.10.017. PMID 19906491. 
10. ↑ Eby G (2009) Zinc Lozenges as a Common Cold Treatment
11. ↑ US 7087255 
12. ↑ US 6592849 
13. ↑ Giertsen E, Svatun B, Saxton A (February 1987). "Plaque inhibition by hexetidine and zinc". Scand J Dent Res. 95 (1): 49–54. doi:10.1111/j.1600-0722.1987.tb01392.x. PMID 3470899.