Selenium disulfide
Names | |
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IUPAC name
Selenium disulfide
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Other names
Selenium sulfide
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Identifiers | |
7488-56-4 | |
ChEMBL | ChEMBL1200680 |
MeSH | Selenium+sulfide |
PubChem | 24087 |
RTECS number | VS8925000 |
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Properties | |
SeS2 | |
Molar mass | 143.09 g/mol |
Appearance | orange to brown powder |
Odor | faint |
Density | 3 g/cm3 |
Melting point | 111 °C (232 °F; 384 K) |
Boiling point | 118 to 119 °C (244 to 246 °F; 391 to 392 K) (decomposes) |
negligible | |
Solubility | soluble in ammonium monosulfide negligible in organic solvents |
Acidity (pKa) | 2-6 |
Pharmacology | |
ATC code | D01 |
Vapor pressure | {{{value}}} |
Related compounds | |
Other anions
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Selenium dioxide Selenic acid Selenious acid |
Other cations
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Hydrogen sulfide |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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verify (what is ?) | |
Infobox references | |
Selenium disulfide is an inorganic compound with the approximate formula SeS2. Both sulfur and selenium catenate[clarification needed] form chains and rings readily, and mixtures of selenium and sulfur likewise give rise to numerous "alloys".[1] This compound is not an analogue of sulfur dioxide.
It is on the WHO Model List of Essential Medicines, the most important medications needed in a basic health system.[2]
Contents
Medical uses
Selenium disulfide is sold as an antifungal agent in shampoos for the treatment of dandruff and seborrheic dermatitis associated in the scalp with Malassezia genus fungi.[3][4][5] In the United States, a 1% strength is available over-the-counter, and a 2.5% strength is also available with a prescription. At the 2.5% strength, selenium disulfide is also used on the body to treat tinea versicolor, a type of fungal skin infection caused by a different species of Malassezia.
Chemical composition
Selenium disulfide has a composition that approximates to SeS2 and is sometimes called selenium sulfide. However, as used in proprietary formulations, it is not a pure chemical compound but is a mixture where the overall Se:S ratio is 1:2. The compounds are cyclic Se–S rings containing a variable number of S and Se atoms, SenS8−n.[1] Selenium disulfide can cause discoloration of the hair and alter the color of hair dyes. It may also discolor metallic jewellery.
Other selenium sulfides
Many selenium sulfides are known. A useful means for characterization is 77Se NMR spectroscopy. Chalcogen ring interconversion pathways.[6] Selenium monosulfide (SeS) is the only selenium compound so far identified as a carcinogen in animals.[7] Selenium monosulfide, along with elemental selenium and sulfur, has been used in medicinal preparations in the past,[8] causing confusion and contradiction[9] as to exactly what form selenium is in any given topical preparation.[10]
See also
- Zinc pyrithione, an antimicrobial agent used in some medicated shampoos
- Selsun Blue, a shampoo with selenium disulfide as its active ingredient
- Ketoconazole, another antifungal agent used in shampoos
References
- ↑ 1.0 1.1 Cyclic selenium sulfides R. Steudel, R. Laitinen, Topics in Current Chemistry, (1982), 102, 177-197
- ↑ Lua error in package.lua at line 80: module 'strict' not found.
- ↑ Selenium(IV) sulfide - pharmacy codes search engine
- ↑ Chemicals of Selenium .Se
- ↑ Accessed Dec. 24, 2007
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Further reading
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- Antifungals
- Cosmetics chemicals
- Selenium compounds
- Sulfides
- Interchalcogens
- World Health Organization essential medicines