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Sulfites (including sulfur dioxide [SO<sub>2</sub>]) are additives used in both wine and beer production for their [[antioxidants|antioxidant]] and anti-microbial effects. These actions make sulfites useful for a variety of tasks including preventing [[oxidation]], inhibiting microbes, quickly [[Remove chlorine from tap water|removing chlorine compounds]] from tap [[water]], and even [[sanitation|sanitizing]] brewing equipment. Sulfites are also a natural product of yeast [[fermentation]], and therefore they are present in every fermented beverage. Forget everything you thought you knew about sulfites; misinformation is rampant in common online sources and even some books.
Sulfites (including sulfur dioxide [SO<sub>2</sub>]) are additives used in both wine and beer production for their [[antioxidants|antioxidant]] and anti-microbial effects. These actions make sulfites useful for a variety of tasks including preventing [[oxidation]], inhibiting microbes, quickly [[Remove chlorine from tap water|removing chlorine compounds]] from tap [[water]], and even [[sanitation|sanitizing]] brewing equipment. Sulfites are also a natural product of yeast [[fermentation]], and therefore they are present in every fermented beverage. Forget everything you thought you knew about sulfites; misinformation is rampant in common online sources and even some books.


Sulfites are NOT directly responsible for the sulfurous/rotten egg/burnt match aroma, as is commonly mistaken — [[hydrogen sulfide]] and/or [[mercaptans|ethyl mercaptan]] are the sources of that off-flavor.<ref>https://www.therealreview.com/2018/07/17/understanding-hydrogen-sulphide-and-sulphur-dioxide/</ref><ref>Williamson, B. [https://williamsonwines.com/recognizing-wine-flaws "Recognizing Wine Flaws."] Williamson Wines. Accessed online March 2020.</ref><ref>Mansfield, AK. [https://cpb-us-e1.wpmucdn.com/blogs.cornell.edu/dist/0/7265/files/2016/11/SulfurOffOdor-1vp1vm4.pdf "Kicking up a Stink: Treatment for Sulfur Off-Odors."] ''Cellar Dweller.'' Cornell University - NYSAES. April 2010.</ref> Sulfites should not be confused with [[sulfate]] or [[hydrogen sulfide|sulfide]].
Sulfites are NOT directly responsible for the sulfurous/rotten egg/burnt match aroma, as is commonly mistaken — [[hydrogen sulfide]] and/or ethyl mercaptan are the sources of that off-flavor.<ref>https://www.therealreview.com/2018/07/17/understanding-hydrogen-sulphide-and-sulphur-dioxide/</ref><ref>Williamson, B. [https://williamsonwines.com/recognizing-wine-flaws "Recognizing Wine Flaws."] Williamson Wines. Accessed online March 2020.</ref><ref>Mansfield, AK. [https://cpb-us-e1.wpmucdn.com/blogs.cornell.edu/dist/0/7265/files/2016/11/SulfurOffOdor-1vp1vm4.pdf "Kicking up a Stink: Treatment for Sulfur Off-Odors."] ''Cellar Dweller.'' Cornell University - NYSAES. April 2010.</ref> Sulfites should not be confused with [[sulfate]] or [[hydrogen sulfide|sulfide]].


Sulfur dioxide (SO2) is a gas that is 85 g L−1 soluble in water at 25 °C and has a boiling point of −10 °C.170 In solution, it undergoes equilibrium reactions with SO2.nH2O, the bisulfite ion (HSO3 −), and the sulfite ion (SO3 −). At beer pH, which is generally 3.8−4.4, the predominant form is the bisulfite ion.158,171 Because all of these species can be converted to, measured as, and reported in terms of SO2, they are often generalized under “SO2” or “sulfites”.<ref name=baedec>Baert JJ, De Clippeleer J, Hughes PS, De Cooman L, Aerts G. [https://pubs.acs.org/doi/abs/10.1021/jf303670z On the origin of free and bound staling aldehydes in beer.] ''J Agric Food Chem.'' 2012;60(46):11449–11472.</ref>
Sulfur dioxide (SO2) is a gas that is 85 g L−1 soluble in water at 25 °C and has a boiling point of −10 °C.170 In solution, it undergoes equilibrium reactions with SO2.nH2O, the bisulfite ion (HSO3 −), and the sulfite ion (SO3 −). At beer pH, which is generally 3.8−4.4, the predominant form is the bisulfite ion.158,171 Because all of these species can be converted to, measured as, and reported in terms of SO2, they are often generalized under “SO2” or “sulfites”.<ref name=baedec>Baert JJ, De Clippeleer J, Hughes PS, De Cooman L, Aerts G. [https://pubs.acs.org/doi/abs/10.1021/jf303670z On the origin of free and bound staling aldehydes in beer.] ''J Agric Food Chem.'' 2012;60(46):11449–11472.</ref>
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