The pyrithione ligands, which are formally monoanions, are chelated to Zn2+ via oxygen and sulfur centers. In the crystalline state, zinc pyrithione exists as a centrosymmetric dimer (see figure), where each zinc is bonded to two sulfur and three oxygen centers.[3] In solution, however, the dimers dissociate via scission of one Zn-O bond.[citation needed]
This compound was first described in the 1930s.[4]
Because of its low solubilityinwater (8 ppm at neutral pH), zinc pyrithione is suitable for use in outdoor paints and other products that protect against mildew and algae. It is an algaecide. It is chemically incompatible with paints relying on metal carboxylate curing agents. When it is used in latex paints with water containing much iron, a sequestering agent that preferentially binds the iron ions is needed. It is decomposed by ultraviolet light slowly, providing years of protection in direct sunlight.[citation needed]
A process to apply zinc pyrithione to cotton with washable results was patented in the United States in 1984.[12] Zinc pyrithione is used to prevent microbe growth in polyester.[13] Textiles with applied zinc pyrithione protect against odor-causing microorganisms. Export of antimicrobial textiles reached US$497.4 million in 2015.[14]
Its antifungal effect is thought to derive from its ability to disrupt membrane transport by blocking the proton pump that energizes the transport mechanism.[15]
Zinc pyrithione is approved for over-the-counter topical use in the United States as a treatment for dandruff and is the active ingredient in several anti-dandruff shampoos and body wash gels. In its industrial forms and strengths, it may be harmful by contact or ingestion. Zinc pyrithione can in the laboratory setting trigger a variety of responses, such as DNA damage in skin cells.[16]
Use of zinc pyrithione is prohibited within cosmetic products in the European Union since December 2021.[17] The substance was considered safe for use in rinse-off and leave-in products of different tested concentrations, but due to environmental toxicity standard regulation was considered against potential alternatives – and as no submission was made for its use it was automatically prohibited.[17]
A large Swedish study shows that it is broken down in wastewater plants and does not release into waterways.[18] A Danish study shows that it biodegrades quickly, but that a risk of continuous leaching from boat paint may cause environmental toxicity.[19]
^Brayfield, A, ed. (23 September 2011). "Pyrithione Zinc". Martindale: The Complete Drug Reference. Pharmaceutical Press. Archived from the original on 26 March 2020. Retrieved 28 March 2014.
^Barnett, B. L.; Kretschmar, H. C.; Hartman, F. A. (1977). "Structural characterization of bis(N-oxopyridine-2-thionato)zinc(II)". Inorg. Chem.16 (8): 1834–8. doi:10.1021/ic50174a002.
^prof. Mark Draganjac. "Pyrithione zinc". www.cas.astate.edu. Arkansas State University. Archived from the original on 21 June 2007. Retrieved 24 August 2007.
^US US4443222A, Morris; Cletus E. & Welch; Clark M., issued 17 April 1984, assigned to The United States of America as represented by the Secretary of Agriculture
