Zinc pyrithione

Zinc pyrithione
	Zinc pyrithione dimer
Names
	IUPAC name bis(2-pyridylthio)zinc 1,1'-dioxide
	Other names ZnP, Pyrithione Zinc, Zinc OMADINE, ZnPT
Identifiers
CAS Number	13463-41-7 ;
3D model (JSmol)	monomer: Interactive image; dimer: Interactive image;
ChEMBL	ChEMBL1200471;
ChemSpider	21513957 ;
ECHA InfoCard	100.033.324
PubChem CID	3005837;
UNII	R953O2RHZ5 ;
CompTox Dashboard (EPA)	DTXSID7026314 ;
	InChI InChI=1/C5H5NOS.Zn/c7-6-4-2-1-3-5(6)8;/h1-4,7H;/q;+2 Key: YUYSACQNSLQTMI-UHFFFAOYAS;
	SMILES monomer: c1cc[n+]2c(c1)S[Zn-2]3(O2)O[n+]4ccccc4S3; dimer: [O+]01[n+]2ccccc2S[Zn-3]03(O[n+]4ccccc4S3)[O+]5[n+]6ccccc6S[Zn-3]157O[n+]8ccccc8S7;
Properties
Chemical formula	C10H8N2O2S2Zn
Molar mass	317.70 g/mol
Appearance	colourless solid
Melting point	240 °C (464 °F; 513 K) (decomposition)
Boiling point	decomposes
Solubility in water	8 ppm (pH 7)
Pharmacology
ATC code	D11AX12 (WHO)
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Zinc pyrithione (or pyrithione zinc) is a coordination complex of zinc. It has fungistatic (inhibiting the division of fungal cells) and bacteriostatic (inhibiting bacterial cell division) properties and is used in the treatment of seborrhoeic dermatitis^[2] and dandruff.

^ Entry on Zink-Pyrithion. at: Römpp Online. Georg Thieme Verlag, retrieved 5 November 2020.
^ 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.

[Römpp-1] Entry on Zink-Pyrithion. at: Römpp Online. Georg Thieme Verlag, retrieved 5 November 2020.

[MD-2] 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.

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