Editing Tin

{{About|the chemical element}}
{{Redirect|Stannum}}
{{For|the chemical compound with formula TiN|Titanium nitride}}
{{Use American English|date=February 2019}}
{{use dmy dates|cs1-dates=ly|date=June 2021}}
{{Infobox tin}}

'''Tin''' is a [[chemical element]]; it has [[chemical symbol|symbol]] '''Sn''' ({{etymology|la|stannum|}}) and [[atomic number]] 50. A silvery-colored metal, tin is soft enough to be cut with little force,<ref>{{cite web |last=Gray|first=Theodore |url=https://theodoregray.com/Periodictable/Ref/050/index.html |work=The Elements |title=Tin Images |publisher=Black Dog & Leventhal |date=2007}}</ref> and a bar of tin can be bent by hand with little effort. When bent, the so-called "[[tin cry]]" can be heard as a result of [[crystal twinning|twinning]] in tin crystals.<ref name="Hol1985">{{cite book |publisher=Walter de&nbsp;Gruyter |date=1985 |edition=91–100 |pages=793–800 |isbn=978-3-11-007511-3 |title=Lehrbuch der Anorganischen Chemie |first1=Arnold F. |last1=Holleman |last2=Wiberg |first2=Egon |last3=Wiberg |first3=Nils |chapter=Tin |language=de}}</ref>

Tin is a [[post-transition metal]] in [[Carbon group|group 14]] of the [[periodic table]] of elements. It is obtained chiefly from the [[mineral]] [[cassiterite]], which contains [[tin(IV) oxide|stannic oxide]], {{chem|SnO|2}}. Tin shows a chemical similarity to both of its neighbors in group 14, [[germanium]] and [[lead]], and has two main [[oxidation state]]s, +2 and the slightly more stable +4. Tin is the 49th most [[abundance of the chemical elements|abundant]] element on Earth, making up 0.00022% of its crust, and with 10 stable isotopes, it has the largest number of stable [[isotope]]s in the periodic table, due to its [[magic number (physics)|magic number]] of protons.

It has two main [[allotropy|allotropes]]: at room temperature, the stable allotrope is β-tin, a silvery-white, [[ductility|malleable]] metal; at low temperatures it is less dense grey α-tin, which has the [[diamond cubic]] structure. Metallic tin does not easily [[redox|oxidize]] in air and water.

The first tin alloy used on a large scale was [[bronze]], made of {{frac|1|8}}&nbsp;tin and {{frac|7|8}}&nbsp;[[copper]] (12.5% and 87.5% respectively), from as early as 3000&nbsp;BC. After 600&nbsp;BC, pure metallic tin was produced. [[Pewter]], which is an alloy of 85–90% tin with the remainder commonly consisting of [[copper]], [[antimony]], bismuth, and sometimes lead and silver, has been used for [[tableware|flatware]] since the [[Bronze Age]]. In modern times, tin is used in many alloys, most notably tin-lead soft [[solder]]s, which are typically 60% or more tin, and in the manufacture of transparent, electrically conducting films of [[indium tin oxide]] in [[optoelectronics|optoelectronic]] applications. Another large application is [[corrosion]]-resistant [[tinning|tin plating]] of [[steel]]. Because of the low toxicity of inorganic tin, tin-plated steel is widely used for [[food packaging]] as "[[steel and tin cans|tin cans]]". Some [[organotin chemistry|organotin compounds]] can be extremely toxic.

{{Toclimit|3}}

==Characteristics==
===Physical===
[[File:Tin-2.jpg|thumb|left|[[Drop (liquid)|Droplet]] of solidified molten tin]]
Tin is a soft, [[malleable]], [[ductile]] and highly [[crystal]]line silvery-white [[metal]]. When a bar of tin is bent a crackling sound known as the "[[tin cry]]" can be heard from the [[Crystal twinning|twinning]] of the crystals.<ref name="Hol1985"/> This trait is shared by [[indium]], [[cadmium]], [[zinc]], and [[mercury (element)|mercury]] in its solid state. Tin melts at about {{convert|232|C|F}}, the lowest in group&nbsp;14, and boils at {{convert|2602|C|F}}, the second lowest (ahead of [[lead]]) in its group. The melting point is further lowered to {{convert|177.3|C|F}} for 11&nbsp;nm particles.<ref>{{cite web|url = http://www.physorg.com/news/2011-04-ink-tin-nanoparticles-future-circuit.html |title=Ink with tin nanoparticles could print future circuit boards |url-status=live |archive-url=https://web.archive.org/web/20110916090032/http://www.physorg.com/news/2011-04-ink-tin-nanoparticles-future-circuit.html |archive-date=2011-09-16 |df=dmy-all |work=Phys.org |date=April 12, 2011}}</ref><ref>{{cite journal |doi=10.1088/0957-4484/22/22/225701 |title=Synthesis and characterization of low temperature Sn nanoparticles for the fabrication of highly conductive ink |year=2011 |last1=Jo |first1=Yun Hwan |last2=Jung |first2=Inyu |last3=Choi |first3=Chung Seok|last4=Kim |first4=Inyoung |last5=Lee |first5=Hyuck Mo |journal=Nanotechnology |volume=22 |issue=22 |page=225701 |pmid=21454937 |bibcode=2011Nanot..22v5701J |s2cid=25202674 }}</ref>

{{external media|width=220px |float=left |video1=[https://www.youtube.com/watch?v=sXB83Heh3_c β–α transition of tin] at −40&nbsp;°C (time lapse; one second of the video is one hour in real time)}}
β-tin, also called ''white tin'', is the [[allotrope]] (structural form) of elemental tin that is stable at and above room temperature. It is metallic and malleable, and has [[Tetragonal crystal system|body-centered tetragonal]] crystal structure. α-tin, or ''gray tin'', is the nonmetallic form. It is stable below {{convert|13.2|C|F}} and is [[brittle]]. α-tin has a [[diamond cubic]] crystal structure, as do [[diamond]] and [[silicon]]. α-tin does not have [[metal]]lic properties because its atoms form a [[covalent]] structure in which electrons cannot move freely. α-tin is a dull-gray powdery material with no common uses other than specialized [[semiconductor]] applications.<ref name="Hol1985" /> γ-tin and σ-tin exist at temperatures above {{convert|161|C|F}}&nbsp; and pressures above several [[Pascal (unit)|GPa]].<ref>{{cite journal |first1=A.M. |last1=Molodets |last2=Nabatov |first2=S.S. |title=Thermodynamic potentials, diagram of state, and phase transitions of tin on shock compression |journal=High Temperature |volume=38 |issue=5 |year=2000 |pages=715–721 |doi=10.1007/BF02755923|bibcode=2000HTemp..38..715M |s2cid=120417927 }}</ref>

In cold conditions β-tin tends to transform spontaneously into α-tin, a phenomenon known as "[[tin pest]]" or "tin disease".<ref>{{Cite web |title=Tin Pests {{!}} Center for Advanced Life Cycle Engineering |url=https://calce.umd.edu/tin-pests |access-date=2022-11-04 |website=calce.umd.edu}}</ref> Some unverifiable sources also say that, during [[Napoleon]]'s Russian campaign of 1812, the temperatures became so cold that the tin buttons on the soldiers' uniforms disintegrated over time, contributing to the defeat of the [[Grande Armée]],<ref>{{cite book |url={{google books |plainurl=y |id=YC4Sm5eL4fsC}}|last1=Le&nbsp;Coureur |first1=Penny |last2=Burreson |first2=Jay |title=Napoleon's Buttons: 17&nbsp;molecules that changed history |place=New York |publisher=Penguin Group, USA |date=2004}}</ref> a persistent legend.<ref>{{cite book| last=Öhrström |first=Lars |title=The Last Alchemist in Paris |year=2013 |publisher=Oxford University Press |location=Oxford |isbn=978-0-19-966109-1}}</ref><ref>{{cite web |url=http://rsc.li/CW_140501 |url-status=dead |title=Book review: The last alchemist in Pari|date=2014-04-29 |first=Simon |last=Cotton |work= [[Chemistry World]] |publisher=[[Royal Society of Chemistry]] |archive-url=https://web.archive.org/web/20140810123922/http://www.rsc.org/chemistryworld/2014/04/last-alchemist-paris-lars-ohrstrom |archive-date=2014-08-10 |df=dmy-all |access-date=November 22, 2019}}</ref><ref>{{cite book |last=Emsley |first=John |date=1 October 2011 |orig-year=2001 |title=Nature's Building Blocks: an A-Z Guide to the Elements |edition=New |location=New York, United States |publisher=[[Oxford University Press]] |page=552 |isbn=978-0-19-960563-7 |author-link=John Emsley |quote=Only officers had metal buttons, and those were made of brass.}}</ref>

The α-β transformation temperature is {{convert|13.2|C|F}}, but impurities (e.g. Al, Zn, etc.) lower it well below {{convert|0|C|F}}. With the addition of [[antimony]] or [[bismuth]] the transformation might not occur at all, increasing durability.<ref name="Schwartz">{{cite book |first=Mel |last=Schwartz |title=Encyclopedia of Materials, Parts and Finishes |edition=2nd |chapter=Tin and alloys, properties |publisher=CRC Press |year=2002 |isbn= 978-1-56676-661-6}}</ref>

Commercial grades of tin (99.8% tin content) resist transformation because of the inhibiting effect of small amounts of bismuth, antimony, lead, and silver present as impurities. Alloying elements such as copper, antimony, bismuth, cadmium, and silver increase the hardness of tin.<ref>{{Cite web |title=Tin Alloys – Characteristics and Uses |url=https://www.nuclear-power.com/nuclear-engineering/metals-what-are-metals/alloys-composition-properties-of-metal-alloys/tin-alloys/ |access-date=2022-11-04 |website=Nuclear Power}}</ref> Tin easily forms hard, brittle intermetallic phases that are typically undesirable. It does not mix into a solution with most metals and elements so tin does not have much solid solubility. Tin mixes well with [[bismuth]], [[gallium]], [[lead]], [[thallium]] and [[zinc]], forming simple [[Eutectic point|eutectic]] systems.<ref name="Schwartz" />

Tin becomes a [[superconductor]] below 3.72&nbsp;[[kelvin|K]]<ref>{{cite journal|doi = 10.1016/S0031-8914(35)90114-8|title = The electrical resistance of cadmium, thallium and tin at low temperatures|date = 1935|last1 = Dehaas|first1 = W.|last2 = Deboer|first2 = J.|last3 = Vandenberg|first3 = G.|journal = Physica|volume = 2|issue = 1–12|page = 453|bibcode=1935Phy.....2..453D}}</ref> and was one of the first superconductors to be studied.<ref name="meissner1">{{cite journal
|volume = 21
|issue = 44
|pages = 787–788
|last = Meissner
|first = W.
|author2=R. Ochsenfeld
|title = Ein neuer effekt bei eintritt der Supraleitfähigkeit
|journal = Naturwissenschaften
|date = 1933
|doi = 10.1007/BF01504252
|bibcode=1933NW.....21..787M
|s2cid = 37842752
}}</ref> The [[Meissner effect]], one of the characteristic features of superconductors, was first discovered in superconducting tin crystals.<ref name="meissner1" />

===Chemical===
Tin resists corrosion from [[water]], but can be corroded by [[acid]]s and [[alkali]]s. Tin can be highly polished and is used as a protective coat for other metals.<ref name="Hol1985" /> When heated in air it oxidizes slowly to form a thin [[Passivation (chemistry)|passivation layer]] of [[stannic oxide]] ({{chem2|SnO2}}) that inhibits further oxidation.<ref>{{cite book| url = {{google books |plainurl=y |id=KXwgAZJBWb0C&pg=RA1-PT126}}| page = 126| title = Handbook of corrosion data| isbn = 978-0-87170-518-1| last1 = Craig| first1 = Bruce D.| last2 = Anderson| first2 = David S.| last3 = International| first3 = A. S. M.| date = January 1995| publisher = ASM International| url-status = live| archive-url = https://web.archive.org/web/20160511021856/https://books.google.com/books?id=KXwgAZJBWb0C&pg=RA1-PT126| archive-date = 2016-05-11}}</ref><ref>{{Cite web |last=Crutchlow |first=Charlotte |date=2021-06-25 |title=Tin-Formation About the Element Tin {{!}} Periodic Table |url=https://chemistrytalk.org/tin-element/ |access-date=2022-11-04 |website=ChemTalk }}</ref>

===Isotopes===
{{Main|Isotopes of tin}}
Tin has ten [[stable isotopes]], the [[List of elements by stability of isotopes|greatest number]] of any element. Their mass numbers are 112, 114, 115, 116, 117, 118, 119, 120, 122, and 124. Tin-120 makes up almost a third of all tin. Tin-118 and tin-116 are also common. Tin-115 is the least common stable isotope.<ref>{{Cite web |title=Tin {{!}} NIDC: National Isotope Development Center |url=https://www.isotopes.gov/products/tin |access-date=2025-04-13 |website=www.isotopes.gov}}</ref> The isotopes with even [[mass number]]s have no [[nuclear spin]], while those with odd mass numbers have a nuclear spin of 1/2. It is thought that tin has such a great multitude of stable isotopes because of tin's [[atomic number]] being 50, which is a "[[Magic number (physics)|magic number]]" in nuclear physics.<ref>{{Cite web |title=Testing the Possible Doubly Magic Nature of Tin-100, Researchers Study the Electromagnetic Properties of Indium Isotopes |url=https://www.energy.gov/science/np/articles/testing-possible-doubly-magic-nature-tin-100-researchers-study-electromagnetic |access-date=2025-04-13 |website=Energy.gov |language=en}}</ref><ref>{{Cite journal |last1=Yang |first1=X. F. |last2=Wang |first2=S. J. |last3=Wilkins |first3=S. G. |last4=Ruiz |first4=R. F. Garcia |date=2023-03-01 |title=Laser spectroscopy for the study of exotic nuclei |url=https://linkinghub.elsevier.com/retrieve/pii/S0146641022000631 |journal=Progress in Particle and Nuclear Physics |volume=129 |pages=104005 |doi=10.1016/j.ppnp.2022.104005 |issn=0146-6410|arxiv=2209.15228 }}</ref>

Tin is one of the easiest elements to detect and analyze by [[NMR spectroscopy]], which relies on molecular weight and its [[chemical shift]]s are referenced against [[tetramethyltin]] ({{chem|SnMe|4}}).{{efn|Only hydrogen, fluorine, phosphorus, thallium and xenon are easier to use NMR analysis with for samples containing isotopes at their natural abundance.}}<ref>{{cite web| url = http://www.nyu.edu/cgi-bin/cgiwrap/aj39/NMRmap.cgi| archive-url = https://web.archive.org/web/20110604130629/http://www.nyu.edu/cgi-bin/cgiwrap/aj39/NMRmap.cgi| archive-date = 2011-06-04| title = Interactive NMR Frequency Map| access-date = 2009-05-05| url-status = dead}}</ref>

Of the stable isotopes, tin-115 has a high [[neutron capture cross section]] for fast neutrons, at 30 [[Barn (unit)|barn]]s. Tin-117 has a cross section of 2.3 barns, one order of magnitude smaller, while tin-119 has a slightly smaller cross section of 2.2 barns.<ref name="crosssections">{{Cite journal |last=Sears |first=Varley F. |date=January 1992 |title=Neutron scattering lengths and cross sections |url=http://www.tandfonline.com/doi/abs/10.1080/10448639208218770 |journal=Neutron News |language=en |volume=3 |issue=3 |pages=26–37 |doi=10.1080/10448639208218770 |issn=1044-8632}} Table of cross sections available at NIST: [https://www.ncnr.nist.gov/resources/n-lengths/elements/sn.html Neutron Scattering Lengths and cross sections].</ref> Before these cross sections were well known, it was proposed to use [[solder#Lead-based|tin-lead solder]] as a [[nuclear reactor coolant|coolant]] for [[fast-neutron reactor|fast reactors]] because of its low melting point. Current studies are for lead or [[lead-bismuth eutectic|lead-bismuth]] reactor coolants because both heavy metals are nearly transparent to fast neutrons, with very low capture cross sections.<ref>{{cite web | url=https://www.westinghousenuclear.com/energy-systems/lead-cooled-fast-reactor | title=Westinghouse Nuclear > Energy Systems > Lead-cooled Fast Reactor }}</ref> In order to use a tin or tin-lead coolant, the tin would first have to go through isotopic separation to remove the isotopes with [[even and odd atomic nuclei|odd]] mass number. Combined, these three isotopes make up about 17% of natural tin but represent nearly all of the capture cross section. Of the remaining seven isotopes tin-112 has a capture cross section of 1 barn. The other six isotopes forming 82.7% of natural tin have capture cross sections of 0.3 barns or less, making them effectively transparent to neutrons.<ref name="crosssections" />

Tin has 33 unstable isotopes, ranging in mass number from 98 to 140<!--32 as per [[Isotopes of tin]]; also the inclusive range [98,140] contains 43 integers.-->. The unstable tin isotopes have half-lives of less than a year except for [[tin-126]], which has a [[half-life]] of about 230,000 years. 
Tin-100 and tin-132 are two of the very few [[nuclide]]s with a "[[Double magic|doubly magic]]" nucleus which despite being unstable, as they have very uneven [[neutron–proton ratio]]s, are the endpoints beyond which tin isotopes lighter than tin-100 and heavier than tin-132 are much less stable.<ref>{{cite journal|first = Phil|last = Walker|title = Doubly Magic Discovery of Tin-100|journal = Physics World|volume = 7|issue = June|date = 1994|pages = 28|doi = 10.1088/2058-7058/7/6/24}}</ref> Another 30 [[metastable isomers]] have been identified for tin isotopes between 111 and 131, the most stable being tin-121m, with a half-life of 43.9 years.<ref name="Audi">{{NUBASE 2003}}</ref>

The relative differences in the abundances of tin's stable isotopes can be explained by how they are formed during [[stellar nucleosynthesis]]. Tin-116 through tin-120, along with tin-122, are formed in the [[s-process|''s''-process]] (slow neutron capture) in most [[star]]s which leads to them being the most common tin isotopes, while tin-124 is only formed in the [[r-process|''r''-process]] (rapid neutron capture) in [[supernovae]] and [[neutron star merger]]s. Tin isotopes 115, 117 through 120, and 122 are produced via both the ''s''-process and the ''r''-process,<ref name=Bragagni23>{{cite journal |journal=Geochimica et Cosmochimica Acta |volume=344 |date=2023 |pages=40–58 |title=Mass-independent Sn isotope fractionation and radiogenic 115Sn in chondrites and terrestrial rocks |first1=Alessandro |last1=Bragagni |first2=Frank |last2=Wombacher |first3=Maria |last3=Kirchenbaur |first4=Ninja |last4=Braukmüller |first5=Carsten |last5=Münker |doi=10.1016/j.gca.2023.01.014|doi-access=free }}</ref> The two lightest stable isotopes, tin-112 and tin-114, cannot be made in significant amounts in the ''s''- or ''r''-processes and are among the [[p-nuclei]] whose origins are not well understood. Some theories about their formation include [[proton capture]] and [[photodisintegration]]. Tin-115 might be partially produced in the ''s''-process, both directly and as the daughter of long-lived [[isotopes of indium|indium-115]], and also from the decay of indium-115 produced via the ''r''-process.<ref name=Bragagni23/><ref name="Cameron">{{cite journal|last1 = Cameron|first1 = A. G. W.|year = 1973|title = Abundance of the Elements in the Solar System|url = http://pubs.giss.nasa.gov/docs/1973/1973_Cameron_1.pdf|journal = Space Science Reviews|volume = 15|issue = 1|pages = 121–146|doi = 10.1007/BF00172440|bibcode = 1973SSRv...15..121C|s2cid = 120201972|url-status = dead|archive-url = https://web.archive.org/web/20111021030549/http://pubs.giss.nasa.gov/docs/1973/1973_Cameron_1.pdf|archive-date = 2011-10-21}}</ref>

==Etymology==
The word ''tin'' is shared among [[Germanic languages]] and can be traced back to [[linguistic reconstruction|reconstructed]] [[Proto-Germanic]] {{lang|mis|*tin-om}}; [[cognate]]s include [[German language|German]] {{lang|de|Zinn}}, [[Swedish language|Swedish]] {{lang|sv|tenn}} and [[Dutch language|Dutch]] {{lang|nl|tin}}. It is not found in other branches of [[Indo-European languages|Indo-European]], except by [[loanword|borrowing]] from Germanic (e.g., [[Irish language|Irish]] {{lang|ga|tinne}} from English).<ref name="oed">{{OED|tin}}</ref><ref>{{etymonline|tin}}</ref>

The [[Latin language|Latin]] name for tin, {{lang|la|stannum}}, originally meant an alloy of silver and lead, and came to mean 'tin' in the fourth century<ref>''Encyclopædia Britannica, 11th Edition'', 1911, ''s.v.'' '[[s:en:1911 Encyclopædia Britannica/Tin|tin]]', citing H. Kopp</ref>—the earlier Latin word for it was {{lang|la|plumbum candidum}}, or "white lead". {{lang|la|Stannum}} apparently came from an earlier {{lang|la|stāgnum}} (meaning the same substance),<ref name="oed" /> the origin of the [[Romance language|Romance]] and [[Celtic languages|Celtic]] terms for ''tin'', such as [[French language|French]] {{lang|fr|étain}}, [[Spanish language|Spanish]] {{lang|es|estaño}}, [[Italian language|Italian]] {{lang|it|stagno}}, and [[Irish language|Irish]] {{lang|ga|stán}}.<ref name="oed" /><ref>{{cite web |access-date=2009-07-07 |url=http://www.oxleigh.freeserve.co.uk/pt77a.htm |archive-url=https://web.archive.org/web/20090403092123/http://www.oxleigh.freeserve.co.uk/pt77a.htm |archive-date=2009-04-03 |title=The Ancient Mining of Tin |work=oxleigh.freeserve.co.uk |url-status=dead }}</ref> The origin of {{lang|la|stannum}}/{{lang|la|stāgnum}} is unknown; it may be pre-[[Indo-European languages|Indo-European]].<ref>''[[American Heritage Dictionary]]''</ref>

The {{lang|de|[[Meyers Konversations-Lexikon]]}} suggests instead that {{lang|la|stannum}} came from [[Cornish language|Cornish]] {{lang|kw|stean}}, and is evidence that [[Cornwall]] in the first centuries AD was the main source of tin.{{citation needed|date=April 2021}}

==History==
{{Main|Tin sources and trade during antiquity}}
[[File:Sword bronze age (2nd version).jpg|thumb|Ceremonial giant bronze [[dirk]] of the Plougrescant-Ommerschans type, Plougrescant, France, 1500–1300 BC]]
Tin extraction and use can be dated to the beginnings of the Bronze Age around 3000&nbsp;BC, when it was observed that [[copper]] objects formed of [[polymetallic]] [[ores]] with different metal contents had different physical properties.<ref>{{Cite book|last1=Cierny|given1=J.|surname2=Weisgerber|given2=G.|date=2003|chapter=The "Bronze Age tin mines in Central Asia|editor1-last= Giumlia-Mair |editor1-first= A.| editor2-last= Lo Schiavo| editor2-first= F.|title=The Problem of Early Tin|pages= 23–31| location= Oxford| publisher= Archaeopress|isbn=978-1-84171-564-3}}</ref> The earliest bronze objects had a tin or arsenic content of less than 2% and are believed to be the result of unintentional [[alloying]] due to trace metal content in the copper ore.<ref name = "pen1986">{{Cite book| last= Penhallurick |first= R. D.|date= 1986| title= Tin in Antiquity: its Mining and Trade Throughout the Ancient World with Particular Reference to Cornwall|location=London|publisher=The Institute of Metals|isbn=978-0-904357-81-3}}</ref> The addition of a second metal to copper increases its hardness, lowers the melting temperature, and improves the [[casting]] process by producing a more fluid melt that cools to a denser, less spongy metal.<ref name = "pen1986" /> This was an important innovation that allowed for the much more complex shapes cast in closed [[Molding (process)|molds]] of the Bronze Age. [[Arsenical bronze]] objects appear first in the Near East where arsenic is commonly found with copper ore, but the [[Arsenic poisoning|health risks]] were quickly realized and the quest for sources of the much less hazardous tin ores began early in the Bronze Age.<ref>{{Cite book|editor1-last=Lamberg-Karlovsky|editor1-first=C. C.|editor2-last=Franklin|editor2-first=Alan D.|editor3-last=Olin|editor3-first=Jacqueline S.|editor4-last=Wertime|editor4-first=Theodore A.|editor4-link=Theodore Wertime|date=July 1980|journal=Technology and Culture|volume=21|issue=3|pages=474|doi=10.2307/3103162|chapter=The development of the usage of tin and tin-bronze: some problems |title=The Search for Ancient Tin|location=Washington D.C.|publisher=A seminar organized by Theodore A. Wertime and held at the Smithsonian Institution and the National Bureau of Standards, Washington D.C. March 14–15, 1977|jstor=3103162}}</ref> This created the demand for rare tin metal and formed a trade network that linked the distant sources of tin to the markets of Bronze Age cultures.<ref>{{cite web |title=Project Ancient Tin |url=https://projectancienttin.wordpress.com/}}</ref>

[[Cassiterite]] ({{chem|SnO|2}}), the oxide form of tin, was most likely the original source of tin. Other tin ores are less common [[sulfide]]s such as [[stannite]] that require a more involved [[smelting]] process. Cassiterite often accumulates in [[alluvial]] channels as [[placer deposits]] because it is harder, heavier, and more chemically resistant than the accompanying [[granite]].<ref name = "pen1986" /> Cassiterite is usually black or dark in color, and these deposits can be easily seen in [[river banks]]. Alluvial ([[placer deposits|placer]]) deposits may incidentally have been collected and separated by methods similar to [[gold panning]].<ref>{{cite journal |last1=Dube |first1=RK |title=Interrelation between gold and tin: A historical perspective |journal=Gold Bulletin |date=September 2006 |volume=39 |issue=3 |pages=103–113 |doi=10.1007/BF03215537 |doi-access=free }}</ref>

==Compounds and chemistry==
{{category see also|Tin compounds}}
In the great majority of its compounds, tin has the [[oxidation state]] II or IV. Compounds containing [[Bivalent (chemistry)|bivalent]] tin are called {{em|[[:wiktionary:stannous|{{visible anchor|stannous}}]]}} while those containing [[tetravalent]] tin are termed {{em|[[:wiktionary:stannic|{{visible anchor|stannic}}]]}}.

===Inorganic compounds===
[[Halide]] compounds are known for both oxidation states. For Sn(IV), all four halides are well known: [[Tin(IV) fluoride|SnF<sub>4</sub>]], [[Tin(IV) chloride|SnCl<sub>4</sub>]], [[Tin(IV) bromide|SnBr<sub>4</sub>]], and [[Tin(IV) iodide|SnI<sub>4</sub>]]. The three heavier members are volatile molecular compounds, whereas the tetrafluoride is polymeric. All four halides are known for Sn(II) also: [[Tin(II) fluoride|SnF<sub>2</sub>]], [[Tin(II) chloride|{{chem|SnCl|2}}]], [[Tin(II) bromide|SnBr<sub>2</sub>]], and [[Tin(II) iodide|SnI<sub>2</sub>]]. All are polymeric solids. Of these eight compounds, only the iodides are colored.<ref name = "Wiberg&Holleman">{{Holleman&Wiberg}}</ref>

[[Tin(II) chloride]] (also known as stannous chloride) is the most important commercial tin halide. Illustrating the routes to such compounds, [[chlorine]] reacts with tin metal to give SnCl<sub>4</sub> whereas the reaction of [[hydrochloric acid]] and tin produces {{chem|SnCl|2}} and hydrogen gas. Alternatively SnCl<sub>4</sub> and Sn combine to stannous chloride by a process called [[comproportionation]]:<ref>{{Greenwood&Earnshaw2nd}}{{page needed|date=June 2021}}</ref>
:SnCl<sub>4</sub> + Sn → 2 {{chem|SnCl|2}}

Tin can form many oxides, sulfides, and other [[chalcogenide]] derivatives. The dioxide {{chem|SnO|2}} (cassiterite) forms when tin is heated in the presence of [[air]].<ref name="Wiberg&Holleman" /> {{chem|SnO|2}} is [[amphoteric]], which means that it dissolves in both acidic and basic solutions.<ref name = "Sherwood">{{cite book| title= Inorganic & Theoretical Chemistry| first= F. Sherwood |last= Taylor| publisher= Heineman| edition= 6th |year= 1942}}</ref> Stannates with the structure [{{chem|Sn(OH)|6}}]<sup>2−</sup>, like {{chem|K|2}}[{{chem|Sn(OH)|6}}], are also known, though the free stannic acid {{chem|H|2}}[{{chem|Sn(OH)|6}}] is unknown.{{Citation needed|date=August 2024}}

[[Sulfide]]s of tin exist in both the +2 and +4 oxidation states: [[tin(II) sulfide]] and [[tin(IV) sulfide]] ([[mosaic gold]]).
[[File:Tin(II)-chloride-xtal-1996-3D-balls-front.png|thumb|[[Ball-and-stick model]]s of the structure of solid [[stannous chloride]] ({{chem|SnCl|2}})<ref>{{cite journal |journal = J. Phys. Chem. Solids|volume = 57|issue = 1|date = 1996|pages = 7–16|title = The high pressure behaviour of the cotunnite and post-cotunnite phases of PbCl<sub>2</sub> and {{chem|SnCl|2}} |author = Leger, J. M. |author2 = Haines, J. |author3 = Atouf, A. |doi = 10.1016/0022-3697(95)00060-7|bibcode = 1996JPCS...57....7L }}</ref>]]

===Hydrides===
[[Stannane]] ({{chem|SnH|4}}), with tin in the +4 oxidation state, is unstable. Organotin hydrides are however well known, e.g. [[tributyltin hydride]] (Sn(C<sub>4</sub>H<sub>9</sub>)<sub>3</sub>H).<ref name="Hol1985" /> These compounds release transient [[Tributyltin|tributyl tin]] radicals, which are rare examples of compounds of tin(III).<ref>{{cite journal | doi = 10.1002/zaac.19733980109 | title = Organic Derivatives of Tin. III. Reactions of Trialkyltin Ethoxide with Alkanolamines | date = 1973 | last1 = Gaur | first1 = D. P.| last2 = Srivastava | first2 = G. | last3 = Mehrotra | first3 = R. C.| journal = Zeitschrift für Anorganische und Allgemeine Chemie | volume = 398 | page = 72}}</ref>

===Organotin compounds===
[[Organotin]] compounds, sometimes called stannanes, are [[chemical compounds]] with tin–carbon bonds.<ref>{{Cite book|last=Elschenbroich|first=Christoph|url=https://www.worldcat.org/oclc/64305455|title=Organometallics.|date=2006|publisher=Wiley-VCH|isbn=3-527-29390-6|edition=3rd, completely rev. and extended|location=Weinheim|oclc=64305455}}</ref> Of the tin compounds, the organic derivatives are commercially the most useful.<ref name="Ullmann" /> Some organotin compounds are highly toxic and have been used as [[biocide]]s. The first organotin compound to be reported was diethyltin diiodide ((C<sub>2</sub>H<sub>5</sub>)<sub>2</sub>SnI<sub>2</sub>), reported by [[Edward Frankland]] in 1849.<ref>{{cite journal|title = Synthetic aspects of tetraorganotins and organotin(IV) halides| first1= Sander H. L.| last1= Thoonen |first2 = Berth-Jan| last2= Deelman| first3 = Gerard |last3= van Koten|journal = [[Journal of Organometallic Chemistry]] |issue = 13|date = 2004| volume= 689|pages = 2145–2157| doi= 10.1016/j.jorganchem.2004.03.027| hdl= 1874/6594| s2cid= 100214292|url = http://igitur-archive.library.uu.nl/chem/2005-0622-182223/13093.pdf |url-status = dead|archive-url = https://web.archive.org/web/20110807042719/http://igitur-archive.library.uu.nl/chem/2005-0622-182223/13093.pdf| archive-date = 2011-08-07|access-date = 2009-07-31}}</ref>

Most organotin compounds are colorless liquids or solids that are stable to air and water. They adopt tetrahedral geometry. Tetraalkyl- and tetraaryltin compounds can be prepared using [[Grignard reagent]]s:<ref name="Ullmann" />
:{{chem|SnCl|4}} + 4 RMgBr → {{chem|R|4|Sn}} + 4 MgBrCl
The mixed halide-alkyls, which are more common and more important commercially than the tetraorgano derivatives, are prepared by [[redistribution reaction]]s:
:{{chem|SnCl|4}} + {{chem|R|4|Sn}} → 2 {{chem|SnCl|2}}R<sub>2</sub>

Divalent organotin compounds are uncommon, although more common than related divalent [[organogermanium]] and [[organosilicon]] compounds. The greater stabilization enjoyed by Sn(II) is attributed to the "[[inert pair effect]]". Organotin(II) compounds include both stannylenes (formula: R<sub>2</sub>Sn, as seen for singlet [[carbene]]s) and distannylenes (R<sub>4</sub>Sn<sub>2</sub>), which are roughly equivalent to [[alkene]]s. Both classes exhibit unusual reactions.<ref>{{cite journal | last1 = Peng | first1 = Yang | last2 = Ellis | first2 = Bobby D. | last3 = Wang | first3 = Xinping | last4 = Fettinger | first4 = James C. | last5 = Power | first5 = P. P.| date = 2009| title = Reversible Reactions of Ethylene with Distannynes Under Ambient Conditions |journal = Science | volume = 325| pages = 1668–1670 | doi = 10.1126/science.1176443 |bibcode = 2009Sci...325.1668P | issue = 5948 | pmid = 19779193 | s2cid = 3011002 }}</ref>

==Occurrence==
{{Category see also|Tin minerals}}
[[File:cassiterite09.jpg|thumb|Sample of cassiterite, the main [[ore]] of tin]]

Tin is generated via the long [[s-process|''s''-process]] in low-to-medium mass stars (with masses of 0.6 to 10 times that of the [[Sun]]), and finally by [[beta decay]] of the heavy isotopes of [[indium]].<ref>{{cite book | url = https://archive.org/details/physicaluniverse00shuf | url-access = registration | pages = [https://archive.org/details/physicaluniverse00shuf/page/n142 119]–121 | title = The physical universe: An introduction to astronomy | publisher = University Science Books | isbn = 978-0-935702-05-7 | last1 = Shu | first1 = Frank H. | date = 1982 }}</ref>

Tin is the 49th most abundant element in [[Earth's crust]], representing 2&nbsp;[[part per million|ppm]] compared with 75&nbsp;ppm for zinc, 50&nbsp;ppm for copper, and 14&nbsp;ppm for lead.{{sfn|Emsley|2001|pp=124, 231, 449 and 503}}

Tin does not occur as the native element but must be extracted from various ores. [[Cassiterite]] ({{chem|SnO|2}}) is the only commercially important source of tin, although small quantities of tin are recovered from complex [[sulfide]]s such as [[stannite]], [[cylindrite]], [[franckeite]], [[canfieldite]], and [[teallite]]. Minerals with tin are almost always associated with [[granite]] rock, usually at a level of 1% tin oxide content.<ref name="I230527">{{cite web|publisher = International Tin Research Institute|title = Tin: From Ore to Ingot|date = 1991|url = http://www.itri.co.uk/pooled/articles/BF_TECHART/view.asp?Q=BF_TECHART_230527|archive-url = https://web.archive.org/web/20090322030548/http://www.itri.co.uk/pooled/articles/BF_TECHART/view.asp?Q=BF_TECHART_230527|archive-date = 2009-03-22|access-date = 2009-03-21|url-status = dead}}</ref>

Because of the higher [[specific gravity]] of tin dioxide, about 80% of mined tin is from secondary deposits found downstream from the primary lodes. Tin is often recovered from granules washed downstream in the past and deposited in valleys or the sea. The most economical ways of mining tin are by [[dredging]], [[Hydraulic mining|hydraulicking]], or [[open cast mining|open pits]]. Most of the world's tin is produced from [[placer mining|placer]] deposits, which can contain as little as 0.015% tin.<ref>{{cite book | url = {{google books |plainurl=y |id=NNlT5of3YikC|page=10}}| page = 9 | title = Tin – International Strategic Minerals Inventory Summary Report | isbn = 978-0-941375-62-7 | last1= Sutphin | first1 = David M. | last3= Reed | first2 = Andrew E. |last2= Sabin | first3= Bruce L.| date = 1992-06-01 | publisher = DIANE | url-status = live | archive-url = https://web.archive.org/web/20160428002413/https://books.google.com/books?id=NNlT5of3YikC&pg=PA10 | archive-date = 2016-04-28 }}</ref>
<div style=display:inline-table>
{| class="wikitable sortable" style="text-align:right;float:right;margin-right:1em;"
|+World tin mine reserves (tonnes, 2011)<ref name="USGS200YB" />
|-
!Country||Reserves
|-
|{{flag|China}}
| style="text-align:right" | 1,500,000
|-
|{{flag|Malaysia}}
| style="text-align:right" | 250,000
|-
|{{flag|Peru}}
| style="text-align:right" | 310,000
|-
|{{flag|Indonesia}}
| style="text-align:right" | 800,000
|-
|{{flag|Brazil}}
| style="text-align:right" | 590,000
|-
|{{flag|Bolivia}}
| style="text-align:right" | 400,000
|-
|{{flag|Russia}}
| style="text-align:right" | 350,000
|-
|{{flag|Australia}}
| style="text-align:right" | 180,000
|-
|{{flag|Thailand}}
| style="text-align:right" | 170,000
|-
|&nbsp;&nbsp;Other
| style="text-align:right" | 180,000
|-
|&nbsp;&nbsp;Total
| style="text-align:right" | 4,800,000
|}
</div><div style=display:inline-table>
{| class="wikitable" style="text-align:right; float:right"
|+Economically recoverable tin reserves<ref name="I230527" />
!Year
!Million tonnes
|-
|1965
| 4,265
|-
|1970
| 3,930
|-
|1975
| 9,060
|-
|1980
| 9,100
|-
|1985
| 3,060
|-
|1990
| 7,100
|-
|2000
| 7,100<ref name="USGS200YB" />
|-
|2010
| 5,200<ref name="USGS200YB" />
|}</div>
About 253,000 tonnes of tin were mined in 2011, mostly in China (110,000&nbsp;t), Indonesia (51,000&nbsp;t), Peru (34,600&nbsp;t), Bolivia (20,700&nbsp;t) and Brazil (12,000&nbsp;t).<ref name="USGS200YB" /> Estimates of tin production have historically varied with the market and mining technology. It is estimated that, at current consumption rates and technologies, the Earth will run out of mine-able tin in 40 years.<ref>{{cite journal|date=May 26, 2007|journal = New Scientist|volume = 194|issue = 2605|pages = 38–39|title = How Long Will it Last?|bibcode = 2007NewSc.194...38R |doi = 10.1016/S0262-4079(07)61508-5|last1=Reilly|first1=Michael }}</ref> In 2006 [[Lester R. Brown|Lester Brown]] suggested tin could run out within 20 years based on conservative estimates of 2% annual growth.<ref name="Brown">{{cite book|last = Brown|first = Lester|title = Plan B 2.0|place = New York|publisher = W.W. Norton|date = 2006|page = 109|isbn = 978-0-393-32831-8|url = https://archive.org/details/planb20rescuingp00brow_0/page/109}}</ref>

Scrap tin is an important source of the metal. Recovery of tin through recycling is increasing rapidly as of 2019.<ref>{{Cite web |last=Alves |first=Bruna |date=February 15, 2024 |title=U.S. annual tin recycling 2023 |url=https://www.statista.com/statistics/209387/recycled-volume-of-tin-in-the-us/#:~:text=The%20amount%20of%20tin%20recycled,comparison%20to%20the%20previous%20year. |access-date=June 23, 2024 |website=Statista}}</ref> Whereas the United States has neither mined (since 1993) nor smelted (since 1989) tin, it was the largest secondary producer, recycling nearly 14,000 tonnes in 2006.<ref name="USGS200YB">{{cite web|publisher = United States Geological Survey|title = Tin: Statistics and Information|url = http://minerals.usgs.gov/minerals/pubs/commodity/tin|access-date = 2008-11-23|first = James F. Jr.|last = Carlin|format = PDF|url-status = live|archive-url = https://web.archive.org/web/20081206004050/http://minerals.usgs.gov/minerals/pubs/commodity/tin/|archive-date = 2008-12-06}}</ref>

New deposits are reported in [[Mongolia]],<ref>{{cite journal  | doi = 10.2113/gsecongeo.90.3.520 | title = Endogenous rare metal ore formations and rare metal metallogeny of Mongolia | date = 1995 | last1 = Kovalenko | first1 = V. I. | last2 = Yarmolyuk | first2 = V. V. | journal = Economic Geology | volume = 90 | page = 520 | issue = 3| bibcode = 1995EcGeo..90..520K }}</ref> and in 2009, new deposits of tin were discovered in Colombia.<ref>{{cite web|url = http://www.freepr101.com/view/52720/Seminole_Group_Colombia_Discovers_High_Grade_Tin_Ore_in_the_Amazons|title = Seminole Group Colombia Discovers High Grade Tin Ore in the Amazon Jungle|publisher = FreePR101 PressRelease|url-status = live|archive-url = https://web.archive.org/web/20140826113831/http://www.freepr101.com/view/52720/Seminole_Group_Colombia_Discovers_High_Grade_Tin_Ore_in_the_Amazons|archive-date = 2014-08-26}}</ref>

==Production==
Tin is produced by [[carbothermic reduction]] of the oxide [[ore]] with [[carbon]] or coke. Both [[reverberatory furnace]] and [[Electric arc furnace|electric furnace]] can be used:<ref>{{cite book|url = {{google books |plainurl=y |id=Nz2wXvmkAF0C|page=89}}|title = Manufacturing processes and materials|isbn = 978-0-87263-517-3|last1 = Schrader|first1 = George F.|last2 = Elshennawy|first2 = Ahmad K.|last3 = Doyle|first3 = Lawrence E.|date = July 2000| publisher=Society of Manufacturing Engineers |url-status = live|archive-url = https://web.archive.org/web/20160511235421/https://books.google.com/books?id=Nz2wXvmkAF0C&pg=PT89|archive-date = 2016-05-11}}</ref><ref>{{cite book|url =https://archive.org/details/metallurgytin01louigoog|title =Metallurgy of tin|last1 =Louis|first1 =Henry|date =1911|publisher =McGraw-Hill book Company}}</ref><ref>{{cite book|url ={{google books |plainurl=y |id=IpuaAAAAIAAJ|page=58}}|title =Tin Under Control|isbn =978-0-8047-2136-3|author =Knorr, Klaus|publisher =Stanford University Press|date =1945|url-status =live|archive-url =https://web.archive.org/web/20160519021151/https://books.google.com/books?id=IpuaAAAAIAAJ&pg=PA58|archive-date =2016-05-19}}</ref>

: SnO<sub>2</sub> + C {{Overset|Arc furnace|→}} Sn + CO<sub>2</sub>↑

===Mining and smelting===
{{Main|Tin mining}}

===Industry===
{{further|List of countries by tin production}}

The ten largest tin-producing companies produced most of the world's tin in 2007.{{Citation needed|date=August 2024}}

Most of the world's tin is traded on LME, from 8 countries, under 17 brands.<ref>{{cite web| publisher= International Tin Research Institute| title= LME Tin Brands| url = http://www.itri.co.uk/pooled/articles/BF_TECHART/view.asp?Q=BF_TECHART_303032| archive-url = https://web.archive.org/web/20081207093543/http://www.itri.co.uk/pooled/articles/BF_TECHART/view.asp?Q=BF_TECHART_303032| archive-date = 2008-12-07|work = ITRI.co.uk |access-date = 2009-05-05|url-status = dead}}</ref>

{| class="wikitable sortable" style="text-align:right;float:right"
|+Largest tin producing companies (tonnes)<ref>{{cite web| publisher= International Tin Research Institute |title= Top Ten Tin Producing Companies |url = http://www.itri.co.uk/pooled/articles/BF_TECHART/view.asp?Q=BF_TECHART_285697 | website= itri.co.uk |archive-url= https://web.archive.org/web/20081207093527/http://www.itri.co.uk/pooled/articles/BF_TECHART/view.asp?Q=BF_TECHART_285697| archive-date = 2008-12-07|access-date = 2009-05-05|url-status = dead}}</ref>
|-
!Company||Polity||2006||2007||2017<ref>{{cite web| url= https://www.thebalance.com/the-10-biggest-tin-producers-2012-2340292| title= The World's Biggest Tin Producers| work= The Balance| date= 13 January 2019}}</ref>||2006–2017<br />% change
|-
| style="text-align:left" | [[Yunnan Tin]]
| style="text-align:left" | China
|52,339||61,129||74,500||42.3
|-
| style="text-align:left" | [[PT Timah]]
| style="text-align:left" | Indonesia
|44,689||58,325||30,200 ||−32.4
|-
| style="text-align:left" | [[Malaysia Smelting Corp]]
| style="text-align:left" | Malaysia
|22,850||25,471||27,200 ||19.0
|-
| style="text-align:left" | [[Yunnan Chengfeng]]
| style="text-align:left" | China
|21,765||18,000||26,800 ||23.1
|-
| style="text-align:left" | [[Minsur]]
| style="text-align:left" | Peru
|40,977||35,940||18,000 ||−56.1
|-
| style="text-align:left" | [[EM Vinto]]
| style="text-align:left" | Bolivia
|11,804||9,448||12,600 ||6.7
|-
| style="text-align:left" | [[Guangxi China Tin]]
| style="text-align:left" | China
|/||/||11,500 ||/
|-
| style="text-align:left" | [[Thaisarco]]
| style="text-align:left" | Thailand
|27,828||19,826||10,600 ||−61.9
|-
| style="text-align:left" | [[Metallo-Chimique]]
| style="text-align:left" | Belgium
|8,049||8,372||9,700 ||20.5
|-
| style="text-align:left" | [[Gejiu Zi Li]]
| style="text-align:left" | China
|/||/||8,700 ||/
|}

The [[International Tin Council]] was established in 1947 to control the price of tin. It collapsed in 1985. In 1984, the Association of Tin Producing Countries was created, with Australia, Bolivia, Indonesia, Malaysia, Nigeria, Thailand, and Zaire as members.<ref>{{cite web |title=Agreement establishing the Association of Tin Producing Countries [1984] ATS 10 |url=http://www3.austlii.edu.au/au/other/dfat/treaties/1984/10.html |website=Australasian Legal Information Institute, Australian Treaties Library }}</ref>

==Price and exchanges==
[[File:SnPrice.png|thumb|World production and price (US exchange) of tin]]
Tin is unique among mineral commodities because of the complex agreements between producer countries and consumer countries dating back to 1921. Earlier agreements tended to be somewhat informal and led to the "First International Tin Agreement" in 1956, the first of a series that effectively collapsed in 1985. Through these agreements, the [[International Tin Council]] (ITC) had a considerable effect on tin prices. ITC supported the price of tin during periods of low prices by buying tin for its buffer stockpile and was able to restrain the price during periods of high prices by selling from the stockpile. This was an anti-free-market approach, designed to assure a sufficient flow of tin to consumer countries and a profit for producer countries. However, the buffer stockpile was not sufficiently large, and during most of those 29 years tin prices rose, sometimes sharply, especially from 1973 through 1980 when rampant inflation plagued many world economies.<ref name="price" />

During the late 1970s and early 1980s, the U.S. reduced its strategic tin stockpile, partly to take advantage of historically high tin prices. The [[Early 1980s recession|1981–82 recession]] damaged the tin industry. Tin consumption declined dramatically. ITC was able to avoid truly steep declines through accelerated buying for its buffer stockpile; this activity required extensive borrowing. ITC continued to borrow until late 1985 when it reached its credit limit. Immediately, a major "tin crisis" ensued—tin was delisted from trading on the [[London Metal Exchange]] for about three years.  ITC dissolved soon afterward, and the price of tin, now in a free-market environment, fell to $4 per pound and remained around that level through the 1990s.<ref name="price">{{cite web| last=Carlin | first=James F. Jr. |year=1998|url=http://minerals.usgs.gov/minerals/pubs/commodity/tin/660798.pdf |title=Significant events affecting tin prices since 1958 |archive-url=https://web.archive.org/web/20111028165126/http://minerals.usgs.gov/minerals/pubs/commodity/tin/660798.pdf |publisher=USGS|archive-date=2011-10-28}}</ref> The price increased again by 2010 with a rebound in consumption following the [[2008 financial crisis]] and the [[Great Recession]], accompanying restocking and continued growth in consumption.<ref name="USGS200YB" />

[[File:Tin Prices.webp|thumb|300px|right|Tin Prices 2008–2022 <br> {{see also|2020s commodities boom}}]]
London Metal Exchange (LME) is tin's principal trading site.<ref name="USGS200YB" /> Other tin contract markets are Kuala Lumpur Tin Market (KLTM) and [[INATIN|Indonesia Tin Exchange]] (INATIN).<ref>{{cite web |url=http://bangka.tribunnews.com/2011/12/15/12-januari-pemasaran-perdana-inatin |title=12 Januari Pemasaran Perdana INATIN |date=December 15, 2011 |url-status=live |archive-url=https://web.archive.org/web/20120426052131/http://bangka.tribunnews.com/2011/12/15/12-januari-pemasaran-perdana-inatin |archive-date=April 26, 2012}}</ref>

Due to factors involved in the [[2021 global supply chain crisis]], tin prices almost doubled during 2020–21 and have had their largest annual rise in over 30 years. Global refined tin consumption dropped 1.6 percent in 2020 as the [[COVID-19 pandemic]] disrupted global manufacturing industries.<ref>{{cite news |last=Daly |first=Tom |url=https://www.reuters.com/markets/commodities/tin-surge-worsens-supply-chain-woes-electronics-solar-auto-firms-2021-12-03/ |title=Tin surge worsens supply chain woes for electronics, solar and auto firms |work=[[Reuters]] |date=2021-12-05 |access-date=2021-12-07 }}</ref>

==Applications==
[[File:tinConsChart.jpg|thumb|right|World consumption of refined tin by end-use, 2006]]
In 2018, just under half of all tin produced was used in solder. The rest was divided between tin plating, tin chemicals, brass and bronze alloys, and niche uses.<ref>{{cite web |url=https://www.mining.com/tin-demand-to-decline-ita/ |title=Tin demand to decline – International Tin Association |website=Mining.com |date=18 October 2019 |access-date=3 July 2021 }}</ref>

===Pigments===

Pigment Yellow 38, [[tin(IV) sulfide]], is known as [[mosaic gold]].<ref>{{cite web |title=The Color of Art Pigment Database – Pigment Yellow – PY |date=2024 |website=artiscreation |url=https://www.artiscreation.com/yellow.html#PY38 |access-date=2024-08-17 }}</ref>

[[Purple of Cassius]], Pigment Red 109, a hydrous double stannate of [[gold]], was mainly, in terms of painting, restricted to miniatures due to its high cost. It was widely used to make [[cranberry glass]]. It has also been used in the arts to stain [[porcelain]].<ref>{{cite web |title=The Color of Art Pigment Database – Pigment Red – PR |date=2024 |website=artiscreation |url=https://www.artiscreation.com/red.html#PR109 |access-date=2024-08-17 }}</ref>

[[Lead-tin yellow]] (which occurs in two yellow forms — a [[stannate]] and a [[silicate]]) was a [[pigment]] that was historically highly important for [[oil painting]] and which had some use in [[fresco]] in its silicate form.<ref>{{cite web |title=The Color of Art Pigment Database – Pigment Yellow – PY |date=2024 |website=artiscreation |url=https://www.artiscreation.com/yellow.html|access-date=2024-08-17 }}</ref> [[Lead]] stannate is also known in orange form but has not seen wide use in the fine arts. It is available for purchase in pigment form from specialist artists' suppliers. There is another minor form, in terms of artistic usage and availability, of lead-tin yellow known as Lead-tin [[Antimony]] Yellow.{{Citation needed|date=August 2024}}

[[Cerulean]] blue, a somewhat dull [[cyan]] chemically known as [[cobalt]] stannate, continues to be an important artists' pigment. Its [[hue]] is similar to that of [[Manganese]] blue, Pigment Blue 33, although it lacks that pigment's [[colorfulness]] and is more opaque.<ref>{{cite web |title=The Color of Art Pigment Database – Pigment Blue – PB |date=2024 |website=artiscreation |url=https://www.artiscreation.com/blue.html#PB35 |access-date=2024-08-17 }}</ref> Artists typically must choose between cobalt stannate and manganese blue imitations made with [[phthalocyanine]] blue green shade (Pigment Blue 15:3), as industrial production of manganese blue pigment ceased in the 1970s.<ref>{{cite web |title=The Color of Art Pigment Database – Pigment Blue – PB |date=2024 |website=artiscreation |url=https://www.artiscreation.com/blue.html#PB33 |access-date=2024-08-17 }}</ref> Cerulean blue made with cobalt stannate, however, was popular with artists prior to the production of Manganese blue.<ref>{{Cite web |date=2021-08-30 |title=Blue pigments |url=https://academicprojects.co.uk/blue-pigments/ |access-date=2025-04-13 |website=Professional development courses, distance learning and consultancy |language=en-GB}}</ref><ref>{{Cite news |last=Hatch |first=Evie |date=2021-10-15 |title=Pigment Colour Index: Blue Pigments - Jackson's Art Blog |url=https://www.jacksonsart.com/blog/2021/10/15/pigment-colour-index-blue-pigments/ |archive-url=http://web.archive.org/web/20250108115045/https://www.jacksonsart.com/blog/2021/10/15/pigment-colour-index-blue-pigments/ |archive-date=2025-01-08 |access-date=2025-04-13 |work=Jackson's Art Blog |language=en-GB}}</ref>

Pigment Red 233, commonly known as Pinkcolor or Potter's Pink and more precisely known as Chrome Tin Pink Sphene, is a historically important pigment in [[watercolor]].<ref>{{cite web |title=The Color of Art Pigment Database – Pigment Red – PR |date=2024 |website=artiscreation |url=https://www.artiscreation.com/red.html#PR233 |access-date=2024-08-17 }}</ref> However, it has enjoyed a large resurgence in popularity due to Internet-based [[word-of-mouth]]. It is fully lightfast and chemically stable in both oil paints and watercolors. Other inorganic mixed metal complex pigments, produced via [[calcination]], often feature tin as a constituent. These pigments are known for their [[lightfastness]], weatherfastness, chemical stability, lack of toxicity, and [[opacity]]. Many are rather dull in terms of colorfulness. However, some possess enough colorfulness to be competitive for use cases that require more than a moderate amount of it. Some are prized for other qualities. For instance, Pinkcolor is chosen by many watercolorists for its strong [[granulation]], even though its chroma is low. Recently, NTP Yellow (a [[pyrochlore]]) has been brought to market as a non-toxic replacement for [[lead(II) chromate]] with greater opacity, lightfastness, and weathering resistance than proposed organic lead chromate replacement pigments possess.<ref>{{cite web |title=The Color of Art Pigment Database – Pigment Yellow – PY |date=2024 |website=artiscreation |url=https://www.artiscreation.com/yellow.html#PY227 |access-date=2024-08-17 }}</ref> NTP Yellow possesses the highest level of color saturation of these contemporary inorganic mixed metal complex pigments. More examples of this group include Pigment Yellow 158 (Tin Vanadium Yellow [[Cassiterite]]),<ref>{{cite web |title=The Color of Art Pigment Database – Pigment Yellow – PY |date=2024 |website=artiscreation |url=https://www.artiscreation.com/yellow.html#PY158 |access-date=2024-08-17 }}</ref> Pigment Yellow 216 (Solaplex Yellow),<ref>{{cite web |title=The Color of Art Pigment Database – Pigment Yellow – PY |date=2024 |website=artiscreation |url=https://www.artiscreation.com/yellow.html#PY216 |access-date=2024-08-17 }}</ref> Pigment Yellow 219 ([[Titanium]] [[Zinc]] [[Antimony]] Stannate),<ref>{{cite web |title=The Color of Art Pigment Database – Pigment Yellow – PY |date=2024 |website=artiscreation |url=https://www.artiscreation.com/yellow.html#PY219 |access-date=2024-08-17 }}</ref> Pigment Orange 82 (Tin Titanium Zinc oxide, also known as Sicopal Orange),<ref>{{cite web |title=The Color of Art Pigment Database – Pigment Orange – PO |date=2024 |website=artiscreation |url=https://www.artiscreation.com/orange.html#PO82 |access-date=2024-08-17 }}</ref> Pigment Red 121 (also known as Tin Violet and [[Chromium]] stannate),<ref>{{cite web |title=The Color of Art Pigment Database – Pigment Red – PR |date=2024 |website=artiscreation |url=https://www.artiscreation.com/red.html#PR121 |access-date=2024-08-17 }}</ref> Pigment Red 230 (Chrome Alumina Pink [[Corundum]]),<ref>{{cite web |title=The Color of Art Pigment Database – Pigment Red – PR |date=2024 |website=artiscreation |url=https://www.artiscreation.com/red.html#PR230 |access-date=2024-08-17 }}</ref> Pigment Red 236 (Chrome Tin Orchid [[Cassiterite]]),<ref>{{cite web |title=The Color of Art Pigment Database – Pigment Red – PR |date=2024 |website=artiscreation |url=https://www.artiscreation.com/red.html#PR236 |access-date=2024-08-17 }}</ref> and Pigment Black 23 (Tin Antimony Grey Cassiterite).<ref>{{cite web |title=The Color of Art Pigment Database – Pigment Black – PBk |date=2024 |website=artiscreation |url=https://www.artiscreation.com/black.html#PBk23 |access-date=2024-08-17 }}</ref> Another blue pigment with tin and cobalt is Pigment Blue 81, Cobalt Tin Alumina Blue [[Spinel]].{{Citation needed|date=August 2024}}

Pigment White 15, tin(IV) oxide, is used for its [[iridescence]], most commonly as a [[ceramic glaze]].<ref>{{cite web |title=The Color of Art Pigment Database – Pigment White – PW |date=2024 |website=artiscreation |url=https://www.artiscreation.com/white.html#PW15 |access-date=2024-08-17 }}</ref> There are no green pigments that have been used by artists that have tin as a constituent and purplish pigments with tin are classified as red, according to the [[Colour Index International]].{{Citation needed|date=August 2024}}

===Solder===
[[File:Ex Lead freesolder.jpg|thumb|left|A coil of lead-free [[solder]] wire]]
Tin has long been used in alloys with lead as [[solder]], in amounts of 5 to 70% w/w. Tin with lead forms a [[eutectic system|eutectic mixture]] at the weight proportion of 61.9% tin and 38.1% lead (the atomic proportion: 73.9% tin and 26.1% lead), with melting temperature of 183&nbsp;°C (361.4&nbsp;°F). Such solders are primarily used for joining [[plumbing|pipes]] or [[electric circuit]]s. Since the European Union [[Waste Electrical and Electronic Equipment Directive]] (WEEE Directive) and [[Restriction of Hazardous Substances Directive]] came into effect on 1 July 2006, the lead content in such alloys has decreased. While lead exposure is associated with [[Lead poisoning|serious health problems]], lead-free solder is not without its challenges, including a higher melting point, and the formation of [[Whisker (metallurgy)|tin whiskers]] that cause electrical problems. [[Tin pest]] can occur in lead-free solders, leading to loss of the soldered joint. Replacement alloys are being found, but the problems of joint integrity remain.<ref>{{cite journal| doi = 10.1289/ehp.113-a682| author = Black, Harvey|title = Getting the Lead Out of Electronics| journal = Environmental Health Perspectives|volume = 113|issue = 10|date = 2005| pmid = 16203230| pages = A682–5| pmc = 1281311}}</ref> A common lead-free alloy is 99% tin, 0.7% copper, and 0.3% silver, with melting temperature of 217&nbsp;°C (422.6&nbsp;°F).<ref>{{cite web |title=Technical data Sheet - Lead free alloy |url=https://docs.rs-online.com/e39d/0900766b81072bac.pdf |website=RS Online |access-date=18 June 2023}}</ref>

===Tin plating===
[[File:Inside of a tin platted can.jpg|thumb|Tin plated metal from a [[Tin can|can]]]]
Tin bonds readily to [[iron]] and is used for coating [[lead]], zinc, and steel to prevent corrosion. [[Tin plating|Tin-plated]] (or tinned) steel containers are widely used for [[food preservation]], and this forms a large part of the market for metallic tin. A tinplate canister for preserving food was first manufactured in London in 1812.<ref>{{cite magazine |last= Childs |first= Peter |date= July 1995 |title= The tin-man's tale |url= http://pubs.rsc.org/historical-collection/products/EIC#!issueid=EIC-1995-32-4 |url-access=subscription |magazine= [[Education in Chemistry]] |volume= 32 |issue= 4 |page= 92 |publisher= [[Royal Society of Chemistry]] |access-date= 19 June 2018 }}</ref><!-- http://www.mirror.co.uk/news/top-stories/2006/02/09/a-canned-history-of-tinned-food-115875-16682285/ https://books.google.com/books?id=EmJRAAAAMAAJ Page 59 https://books.google.com/books?id=qz8rAAAAYAAJ --> Speakers of British English call such containers "tins", while speakers of U.S. English call them "[[tin cans|cans]]" or "tin cans". One derivation of such use is the slang term "[[tinnie]]" or "tinny", meaning "can of beer" in Australia. The [[tin whistle]] is so called because it was mass-produced first in tin-plated steel.<ref>{{cite book | url = {{google books |plainurl=y |id=IpuaAAAAIAAJ|page=13}} | pages = 10–15 | title = Tin Under Control | isbn = 978-0-8047-2136-3 | last1 = Control | first1 = Tin Under | date = 1945 | publisher = Stanford University Press | url-status = live | archive-url = https://web.archive.org/web/20160531012725/https://books.google.com/books?id=IpuaAAAAIAAJ&pg=PA13 | archive-date = 2016-05-31 }}</ref><ref>{{cite book | url = {{google books |plainurl=y |id=IpuaAAAAIAAJ|page=10}} | pages = 10–22 | title = Trends in the use of tin | author1 = Panel On Tin, National Research Council (U.S.). Committee on Technical Aspects of Critical and Strategic Materials | date = 1970 | url-status = live | archive-url = https://web.archive.org/web/20160522102214/https://books.google.com/books?id=qz8rAAAAYAAJ&pg=PA10 | archive-date = 2016-05-22 }}</ref>

Copper cooking vessels such as saucepans and frying pans are frequently lined with a thin plating of tin, by [[electroplating]] or by [[Kalai (process)|traditional chemical]] methods, since use of [[Copper toxicity|copper cookware with acidic foods]] can be toxic.<ref>{{Cite web |title=Cooking utensils and nutrition Information {{!}} Mount Sinai - New York |url=https://www.mountsinai.org/health-library/nutrition/cooking-utensils-and-nutrition#:~:text=The%20FDA%20also%20warns%20against,acidic%20foods,%20causing%20copper%20toxicity. |access-date=2025-04-13 |website=Mount Sinai Health System |language=en-US}}</ref><ref>{{Cite journal |last1=Ali Sultan |first1=Saif Ali |last2=Ahmed Khan |first2=Fawad |last3=Wahab |first3=Abdul |last4=Fatima |first4=Batool |last5=Khalid |first5=Hira |last6=Bahader |first6=Ali |last7=Safi |first7=Sher Zaman |last8=Selvaraj |first8=Chandrabose |last9=Ali |first9=Abid |last10=Alomar |first10=Suliman Yousef |last11=Imran |first11=Muhammad |date=2023-07-24 |title=Assessing Leaching of Potentially Hazardous Elements from Cookware during Cooking: A Serious Public Health Concern |journal=Toxics |volume=11 |issue=7 |pages=640 |doi=10.3390/toxics11070640 |doi-access=free |issn=2305-6304 |pmc=10386729 |pmid=37505605}}</ref>

===Specialized alloys===
[[File:Plate_MET_174927.jpg|thumb|left|[[Pewter]] plate]]
[[File:Alfonso Santiago Leyva and his son Tomás working.jpg|thumb|Artisans working with tin sheets]]

Tin in combination with other elements forms a wide variety of useful alloys. Tin is most commonly alloyed with copper. [[Pewter]] is 85–99% tin,<ref>{{cite book|last = Hull|first = Charles|title = Pewter|publisher = Osprey Publishing|date = 1992|isbn = 978-0-7478-0152-8|pages = 1–5}}</ref> and [[Babbitt metal|bearing metal]] has a high percentage of tin as well.<ref>{{cite book|chapter = Introduction|pages = 1–2|isbn = 978-1-110-11092-6|chapter-url = {{google books |plainurl=y |id=hZ3zGS6by9UC}}|title=Analysis of Babbit|author=Brakes, James|publisher=BiblioBazaar, LLC|date=2009}}</ref><ref>{{cite book|pages = 46–47|isbn = 978-1-4067-4671-6|url = {{google books |plainurl=y |id=KR82QRlAgUwC|page=46}}|title=Principles of Metallography|author=Williams, Robert S.|publisher=Read books|date=2007}}</ref> [[Bronze]] is mostly copper with 12% tin, while the addition of [[phosphorus]] yields [[phosphor bronze]]. [[Bell metal]] is also a copper–tin alloy, containing 22% tin. Tin has sometimes been used in coinage; it once formed a single-digit percentage (usually five percent or less) of American<ref>{{cite web | url = http://www.usmint.gov/about_the_mint/fun_facts/?action=fun_facts2 | publisher = US Mint | access-date = 2011-10-28 | title = The Composition of the Cent | url-status = live | archive-url = https://web.archive.org/web/20111025203152/http://www.usmint.gov/about_the_mint/fun_facts/?action=fun_facts2 | archive-date = 2011-10-25}}</ref> and Canadian<ref>{{cite web | url = http://www.bcscta.ca/resources/hebden/chem/Coin%20Compositions.pdf | publisher = Canadian Mint | access-date = 2011-10-28 | title = Composition of canadian coins | url-status = dead | archive-url = https://web.archive.org/web/20120113112752/http://www.bcscta.ca/resources/hebden/chem/Coin%20Compositions.pdf | archive-date = 2012-01-13 }}</ref> pennies. <!--Because copper is often the major metal in such coins, sometimes including zinc, these could be called bronze, or brass alloys.-->

The [[niobium]]–tin compound [[Niobium–tin|Nb<sub>3</sub>Sn]] is commercially used in [[Electromagnetic coil|coils]] of [[superconducting magnet]]s for its high [[critical temperature#In Superconductivity|critical temperature]] (18&nbsp;K) and critical magnetic field (25&nbsp;[[Tesla (unit)|T]]). A superconducting magnet weighing as little as two [[kilogram]]s is capable of producing the magnetic field of a conventional [[electromagnet]] weighing tons.<ref name="geballe">{{cite journal|last=Geballe|first=Theodore H.|title=Superconductivity: From Physics to Technology|journal=Physics Today|volume=46|issue=10|date=October 1993|pages=52–56|doi=10.1063/1.881384 |bibcode = 1993PhT....46j..52G }}</ref>

A small percentage of tin is added to [[zirconium alloy]]s for the cladding of nuclear fuel.<ref>{{cite book| chapter-url = {{google books |plainurl=y |id=6VdROgeQ5M8C|page=597}}| page =597| chapter =Zirconium| title =Elements of Metallurgy and Engineering Alloys| isbn =978-0-87170-867-0| last1 =Campbell| first1 =Flake C.| date =2008| publisher =ASM International| url-status =live| archive-url =https://web.archive.org/web/20160528212426/https://books.google.com/books?id=6VdROgeQ5M8C&pg=PA597| archive-date =2016-05-28}}</ref>

Most metal pipes in a [[pipe organ]] are of a tin/lead alloy, with 50/50 as the most common composition. The proportion of tin in the pipe defines the pipe's tone, since tin has a desirable tonal resonance. When a tin/lead alloy cools, the lead phase solidifies first, then when the eutectic temperature is reached, the remaining liquid forms the layered tin/lead eutectic structure, which is shiny; contrast with the lead phase produces a mottled or spotted effect. This metal alloy is referred to as spotted metal. Major advantages of using tin for pipes include its appearance, workability, and resistance to corrosion.<ref>{{cite book|chapter-url = {{google books |plainurl=y |id=cgDJaeFFUPoC|page=426}}|isbn = 978-0-415-94174-7|page = [https://archive.org/details/organencyclopedi0000unse/page/411 411]|chapter = Pipe Metal|editor = Robert Palmieri|date = 2006|publisher = Garland|location = New York|title = Encyclopedia of keyboard instruments|url = https://archive.org/details/organencyclopedi0000unse/page/411}}</ref><ref>{{cite book|chapter-url={{google books |plainurl=y |id=I0h525OVoTgC|page=501}}|page=[https://archive.org/details/artoforganbuildi00auds/page/501 501]|title=The Art of Organ Building Audsley, George Ashdown|isbn=978-0-486-21315-6|chapter=Metal Pipes: And the Materials used in their Construction|publisher=Courier Dover Publications|date=1988|author=George Ashdown Audsley|url=https://archive.org/details/artoforganbuildi00auds/page/501}}</ref><!-- https://books.google.com/books?id=aU6giw-OdyUC&pg=PA32-->

=== Manufacturing of chemicals ===
Tin compounds are used in the production of various chemicals, including stabilizers for PVC and catalysts for industrial processes. Tin in form of ingots provide the raw material necessary for these chemical reactions, ensuring consistent quality and performance.{{Citation needed|date=August 2024}}

=== Optoelectronics ===
The [[Indium tin oxide|oxides of indium and tin]] are electrically conductive and transparent, and are used to make transparent electrically conducting films with applications in [[optoelectronics]] devices such as [[liquid crystal displays]].<ref name="Kimetal">{{cite journal|author1=Kim, H. |author2=Gilmore, C. |author3=Pique, A. |author4=Horwitz, J. |author5=Mattoussi, H. |author-link5=Hedi Mattoussi |author6=Murata, H. |author7=Kafafi, Z. |author8=Chrisey, D. |year=1999 |title=Electrical, optical, and structural properties of indium tin oxide thin films for organic light-emitting devices|journal=Journal of Applied Physics|volume=86|issue=11|pages=6451|doi=10.1063/1.371708|bibcode=1999JAP....86.6451K}}</ref>

=== Other applications ===
[[File:Punched tin barn lantern.jpeg|thumb|upright|A 21st-century reproduction barn lantern made of punched tin<!--Barn lanterns were placed over candles and oil lamps to reduce fire hazard when inside barns, and were in use up until the mid-20th century by some farmers.-->]]
Punched tin-plated steel, also called pierced tin, is an artisan technique originating in central Europe for creating functional and decorative housewares. Decorative piercing designs exist in a wide variety, based on local tradition and the artisan. Punched tin lanterns are the most common application of this artisan technique. The light of a candle shining through the pierced design creates a decorative light pattern in the room where it sits. Lanterns and other punched tin articles were created in the New World from the earliest European settlement. A well-known example is the Revere lantern, named after [[Paul Revere]].<ref>{{cite book | url = https://archive.org/details/makingdecorating0000brid | url-access = registration | title = Making & decorating picture frames | publisher = North Light Books | isbn = 978-0-89134-739-2 | last1 = Bridge | first1 = Janet | date = September 1996 }}</ref>

In America, [[pie safe]]s and food safes were in use in the days before refrigeration. These were wooden cupboards of various styles and sizes – either floor standing or hanging cupboards meant to discourage vermin and insects and to keep dust from perishable foodstuffs. These cabinets had tinplate inserts in the doors and sometimes in the sides, punched out by the homeowner, cabinetmaker, or a tinsmith in varying designs to allow for air circulation while excluding flies. Modern reproductions of these articles remain popular in North America.<ref>{{cite web|title=Tin punching|url=http://www.piercedtin.com/about-us.htm|access-date=August 15, 2011|url-status=live|archive-url=https://web.archive.org/web/20110811010659/http://www.piercedtin.com/about-us.htm|archive-date=August 11, 2011}}</ref>

Window glass is most often made by floating molten [[glass]] on molten tin ([[float glass]]), resulting in a flat and flawless surface. This is also called the "[[Pilkington process]]".<ref>{{cite journal|title = Review Lecture. The Float Glass Process.|first = L. A. B.|last = Pilkington|journal = Proceedings of the Royal Society of London. Series A, Mathematical and Physical Sciences|volume = 314|issue = 1516|pages = 1–25|date = 1969|doi = 10.1098/rspa.1969.0212|jstor = 2416528|bibcode = 1969RSPSA.314....1P |s2cid = 109981215}}</ref>

Tin is used as a negative electrode in advanced [[Lithium-ion battery|Li-ion batteries]]. Its application is somewhat limited by the fact that some tin surfaces{{which|date=June 2013}} catalyze decomposition of carbonate-based electrolytes used in Li-ion batteries.<ref>{{cite journal|title=Interfacial processes at single-crystal β-Sn electrodes in organic carbonate electrolytes|journal=Electrochemistry Communications|volume= 13|issue =11|date=2011|pages =1271–1275|doi=10.1016/j.elecom.2011.08.026|last1=Lucas|first1=Ivan T.|last2=Syzdek|first2=Jarosław|last3=Kostecki|first3=Robert}}</ref>

[[Tin(II) fluoride]] is added to some dental care products<ref>{{cite web| url = http://www.colgate.com/app/Colgate/US/OC/Products/FromTheDentist/GelKamStannousFluorideGel.cvsp| title = Colgate Gel-Kam| access-date = 2009-05-05| url-status = live| archive-url = https://web.archive.org/web/20090427101229/http://www.colgate.com/app/Colgate/US/OC/Products/FromTheDentist/GelKamStannousFluorideGel.cvsp| archive-date = 2009-04-27}}</ref> as [[stannous fluoride]] (SnF<sub>2</sub>). Tin(II) fluoride can be mixed with [[calcium]] abrasives while the more common [[sodium fluoride]] gradually becomes biologically inactive in the presence of calcium compounds.<ref>{{cite journal|date=April 1989|journal = Journal of Dentistry|volume = 17|issue = 2|pages = 47–54|pmid = 2732364|title = The State of Fluorides in Toothpastes|doi = 10.1016/0300-5712(89)90129-2|last = Hattab|first = F.}}</ref> It has also been shown to be more effective than [[sodium fluoride]] in controlling [[gingivitis]].<ref>{{cite journal|date=1995|journal = The Journal of Clinical Dentistry|volume = 6|issue = Special Issue|pages = 54–58|pmid = 8593194|title = The clinical effect of a stabilized stannous fluoride dentifrice on plaque formation, gingivitis and gingival bleeding: a six-month study|last1=Perlich|first1=M. A.|last2=Bacca|first2=L. A.|last3=Bollmer|first3=B. W.|last4=Lanzalaco|first4=A. C.|last5=McClanahan|first5=S. F.|last6=Sewak|first6=L. K.|last7=Beiswanger|first7=B. B.|last8=Eichold|first8=W. A.|last9=Hull|first9=J. R.|last10=Jackson |first10=R. D.|display-authors=9}}</ref>

Tin is used as a target to create laser-induced [[Plasma (physics)|plasmas]] that act as the light source for [[extreme ultraviolet lithography]].<ref>{{Cite journal |first=Oscar O. |last=Versolato |title=Physics of laser-driven tin plasma sources of EUV radiation for nanolithography |journal=[[Plasma Sources Science and Technology]] |year=2019 |doi=10.1088/1361-6595/ab3302 |volume=28 |issue=8|bibcode=2019PSST...28h3001V }}</ref>

===Organotin compounds===
{{Main|Organotin chemistry}}
Organotin compounds are [[organometallic compounds]] containing tin–carbon bonds. Worldwide industrial production of organotin compounds likely exceeds 50,000 [[tonne]]s.<ref>{{cite book | chapter-url = {{google books |plainurl=y |id=lAm5e1YVnm4C|page=144}} | page = 144 | chapter = Organotin in Industrial and Domestic Products | title = Trace element speciation for environment, food and health | isbn = 978-0-85404-459-7 | last1 = Ebdon | first1 = L. | last2 = Britain) | first2 = Royal Society of Chemistry (Great | date = 2001 | publisher = Royal Society of Chemistry | url-status = live | archive-url = https://web.archive.org/web/20160521055409/https://books.google.com/books?id=lAm5e1YVnm4C&pg=PA144 | archive-date = 2016-05-21 }}</ref>

====PVC stabilizers====
The major commercial application of organotin compounds is in the stabilization of [[PVC]] plastics. In the absence of such stabilizers, PVC would rapidly degrade under heat, light, and atmospheric oxygen, resulting in discolored, brittle products. Tin scavenges labile [[chloride]] ions (Cl<sup>−</sup>), which would otherwise strip HCl from the plastic material.<ref name="Atkins">{{cite book|pages=343, 345|isbn=978-0-7167-4878-6|title=Inorganic chemistry|author=Atkins, Peter|author2=Shriver, Duward F.|author3=Overton, Tina|author4=Rourke, Jonathan|name-list-style=amp|edition=4th|publisher=W.H. Freeman|date=2006}}</ref> Typical tin compounds are carboxylic acid derivatives of dibutyltin dichloride, such as [[dibutyltin dilaurate]].<ref>{{cite book | url = {{google books |plainurl=y |id=YUkJNI9QYsUC|page=108}} | page = 108 | title = PVC handbook | isbn = 978-1-56990-379-7 | last1 = Wilkes | first1 = Charles E. | last2 = Summers | first2 = James W. | last3 = Daniels | first3 = Charles Anthony | last4 = Berard | first4 = Mark T. | date = August 2005 | publisher = Hanser | url-status = live | archive-url = https://web.archive.org/web/20160509212043/https://books.google.com/books?id=YUkJNI9QYsUC&pg=PA108 | archive-date = 2016-05-09 }}</ref>

====Biocides====
Some organotin compounds are relatively toxic, with both advantages and problems. They are used for [[biocide|biocidal properties]] as [[fungicide]]s, [[pesticide]]s, [[algaecide]]s, [[wood preservative]]s, and [[antifouling agent]]s.<ref name="Atkins" /> [[Tributyltin oxide]] is used as a [[wood preservative]].<ref>{{cite book | chapter-url = {{google books |plainurl=y |id=pKiTzbEDy1QC|page=799}} | page = 799 | isbn = 978-0-8247-0024-9 | chapter = Preservation of Wood | editor =David N.-S. Hon | editor2 =Nobuo Shiraishi | date = 2001 | publisher = Dekker | location = New York, NY | title = Wood and cellulosic chemistry}}</ref> [[Tributyltin]] is used for various industrial purposes such as slime control in paper mills and disinfection of circulating industrial cooling waters.<ref>{{Cite journal|last=Antizar-Ladislao|first=Blanca|date=2008-02-01|title=Environmental levels, toxicity and human exposure to tributyltin (TBT)-contaminated marine environment. A review|journal=Environment International|volume=34|issue=2|pages=292–308|doi=10.1016/j.envint.2007.09.005|pmid=17959247|bibcode=2008EnInt..34..292A }}</ref> Tributyltin was used as additive for ship paint to prevent growth of [[Marine organisms|fouling organisms]] on ships, with use declining after organotin compounds were recognized as [[persistent organic pollutants]] with high toxicity for some marine organisms (the [[dog whelk]], for example).<ref>{{cite web|title = Tin Hazards To Fish, Wildlife, and Invertebrates: A Synoptic Review|first = Ronald|last = Eisler|publisher = U.S. Fish and Wildlife Service Patuxent Wildlife Research Center|url = https://apps.dtic.mil/sti/pdfs/ADA322822.pdf|url-status = live|archive-url = https://web.archive.org/web/20120118204159/http://www.dtic.mil/cgi-bin/GetTRDoc?AD=ADA322822&Location=U2&doc=GetTRDoc.pdf|archive-date = 2012-01-18}}</ref> The EU banned the use of organotin compounds in 2003,<ref>{{cite web| website= europa.eu| url = http://eur-lex.europa.eu/LexUriServ/LexUriServ.do?uri=OJ:L:2003:115:0001:0011:EN:PDF|title = Regulation (EC) No 782/2003 of the European Parliament and of the Council of 14 April 2003 on the prohibition of organotin compounds on ships| access-date = 2009-05-05}}</ref><!--doi 10.1007/s10661-008-0294-6 http://cat.inist.fr/?aModele=afficheN&cpsidt=14491409 --> while concerns over the toxicity of these compounds to marine life and damage to the reproduction and growth of some marine species<ref name="Atkins" /> (some reports describe biological effects to marine life at a concentration of 1 [[nanogram]] per liter) have led to a worldwide ban by the [[International Maritime Organization]].<ref>{{cite book | chapter-url = {{google books |plainurl=y |id=pERX3gKmFy4C|page=227}} | isbn = 978-1-4051-6926-4 | page = 227 | chapter = Fouling on Shipping | editor = Dürr, Simone | editor2 = Thomason, Jeremy | date = 2008 | publisher = Blackwell | location = Oxford | title = Biofouling}}</ref> Many nations now restrict the use of organotin compounds to vessels greater than {{convert|25|m|abbr=on}} long.<ref name="Atkins" /> The persistence of tributyltin in the aquatic environment is dependent upon the nature of the ecosystem.<ref name="Maguire 1987 475–498">{{Cite journal|last=Maguire|first=R. James|date=1987|title=Environmental aspects of tributyltin|journal=Applied Organometallic Chemistry|volume=1|issue=6|pages=475–498|doi=10.1002/aoc.590010602}}</ref> Because of this persistence and its use as an additive in ship paint, high concentrations of tributyltin have been found in marine sediments located near naval docks.<ref>{{Cite journal|last1=de Mora|first1=S. J.|last2=Stewart|first2=C.|last3=Phillips|first3=D.|date=1995-01-01|title=Sources and rate of degradation of tri(n-butyl)tin in marine sediments near Auckland, New Zealand|journal=Marine Pollution Bulletin|volume=30|issue=1|pages=50–57|doi=10.1016/0025-326X(94)00178-C|bibcode=1995MarPB..30...50D }}</ref> Tributyltin has been used as a biomarker for [[imposex]] in [[Neogastropoda|neogastropods]], with at least 82 known species.<ref name="Axiak 743–749">{{Cite journal|last1=Axiak|first1=Victor|last2=Micallef|first2=Diane|last3=Muscat|first3=Joanne|last4=Vella|first4=Alfred|last5=Mintoff|first5=Bernardette|date=2003-03-01|title=Imposex as a biomonitoring tool for marine pollution by tributyltin: some further observations|journal=Environment International|series=Secotox S.I.|volume=28|issue=8|pages=743–749|doi=10.1016/S0160-4120(02)00119-8|pmid=12605923|bibcode=2003EnInt..28..743A }}</ref> With the high levels of TBT in the local inshore areas, due to shipping activities, the shellfish had an adverse effect.<ref name="Maguire 1987 475–498" /> Imposex is the imposition of male sexual characteristics on female specimens where they grow a penis and a pallial [[vas deferens]].<ref name="Axiak 743–749" /><ref name="sciencebuzz.com">{{Cite web|date=2018-11-17|title=The Effects of Tributyltin on the Marine Environment|url=https://www.sciencebuzz.com/the-effects-of-tributyltin-on-the-marine-environment/|access-date=2020-11-17|website=ScienceBuzz|archive-date=2021-01-25 |archive-url=https://web.archive.org/web/20210125103441/https://www.sciencebuzz.com/the-effects-of-tributyltin-on-the-marine-environment/|url-status=dead}}</ref> A high level of TBT can damage mammalian [[endocrine glands]], [[Reproductive system|reproductive]] and [[central nervous system]]s, bone structure and [[gastrointestinal tract]].<ref name="sciencebuzz.com" /> Tributyltin also affect mammals, Including sea otters, whales, dolphins, and humans.<ref name="sciencebuzz.com" />

====Organic chemistry====
Some tin [[reagent]]s are useful in [[organic chemistry]]. In the largest application, stannous chloride is a common reducing agent for the conversion of [[nitro compound|nitro]] and [[oxime]] groups to [[amine]]s. The [[Stille reaction]] couples organotin compounds with organic [[halide]]s or [[pseudohalogen|pseudohalides]].<ref>{{cite book |doi=10.1002/0471264180.or050.01 |chapter=The Stille Reaction |title=Organic Reactions |pages=1–652 |year=1997 |last1=Farina |first1=Vittorio |last2=Krishnamurthy |first2=Venkat |last3=Scott |first3=William J. |isbn=0-471-26418-0 }}</ref>

====Li-ion batteries====
{{main|Lithium-ion battery}}
Tin forms several inter-metallic phases with lithium metal, making it a potentially attractive material for battery applications. Large volumetric expansion of tin upon alloying with lithium and instability of the tin-organic electrolyte interface at low electrochemical potentials are the greatest challenges to employment in commercial cells.<ref>{{Cite journal |last1=Mou |first1=Haoyi |last2=Xiao |first2=Wei |last3=Miao |first3=Chang |last4=Li |first4=Rui |last5=Yu |first5=Liming |date=2020 |title=Tin and Tin Compound Materials as Anodes in Lithium-Ion and Sodium-Ion Batteries: A Review |journal=Frontiers in Chemistry |volume=8 |pages=141 |doi=10.3389/fchem.2020.00141 |pmc=7096543 |pmid=32266205|bibcode=2020FrCh....8..141M |doi-access=free }}</ref> Tin inter-metallic compound with cobalt and carbon was implemented by [[Sony]] in its Nexelion cells released in the late 2000s. The composition of the active material is approximately Sn<sub>0.3</sub>Co<sub>0.4</sub>C<sub>0.3</sub>. Research showed that only some crystalline facets of tetragonal (beta) Sn are responsible for undesirable electrochemical activity.<ref>{{cite journal|first1 = Ivan|title = Interfacial processes at single-crystal β-Sn electrodes in organic carbonate electrolytes|journal = Electrochemistry Communications|last1 = Lucas|last2=Syzdek|first2=Jaroslaw|date = 2011|doi = 10.1016/j.elecom.2011.08.026|volume = 13|issue = 11|page = 1271}}</ref>

==Precautions==
{{Main|Tin poisoning}}
Cases of poisoning from tin metal, its oxides, and its salts are almost unknown. On the other hand, certain [[organotin compound]]s are almost as toxic as [[cyanide]].<ref name="Ullmann">{{Cite book|last=Graf |first=Günter G. |date=15 June 2000 |chapter=Tin, Tin Alloys, and Tin Compounds |title=Ullmann's Encyclopedia of Industrial Chemistry |publisher=Wiley-VCH |location=Weinheim |doi=10.1002/14356007.a27_049|isbn=978-3-527-30385-4 }}</ref>

Exposure to tin in the workplace can occur by inhalation, skin contact, and eye contact. The US [[Occupational Safety and Health Administration]] (OSHA) set the [[permissible exposure limit]] for tin exposure in the workplace as 2&nbsp;mg/m<sup>3</sup> over an 8-hour workday. The [[National Institute for Occupational Safety and Health]] (NIOSH) determined a [[recommended exposure limit]] (REL) of 2&nbsp;mg/m<sup>3</sup> over an 8-hour workday. At levels of 100&nbsp;mg/m<sup>3</sup>, tin is [[IDLH|immediately dangerous to life and health]].<ref>{{Cite web|title =  NIOSH Pocket Guide to Chemical Hazards – Tin|url = https://www.cdc.gov/niosh/npg/npgd0613.html|website = CDC |access-date = 2015-11-24|url-status = live|archive-url = https://web.archive.org/web/20151125105453/http://www.cdc.gov/niosh/npg/npgd0613.html|archive-date = 2015-11-25}}</ref>

==See also==
{{Portal|Chemistry}}
{{Colbegin|colwidth=18em}}
* [[Cassiterides]] (the mythical Tin Islands)
* [[Stannary]]
* [[Terne]]
* [[Tin pest]]
* [[Tin mining in Britain]]
* [[Tinning]]
* [[Whisker (metallurgy)]] (tin whiskers)
{{colend}}

==Notes==
{{Notelist}}

==References==
{{Reflist}}

== Bibliography ==
{{div col |small=yes |colwidth=30em}}
* {{Source-attribution|Carlin, James F., Jr. (1998). [http://minerals.usgs.gov/minerals/pubs/commodity/tin/660798.pdf "Significant events affecting tin prices since 1958"]. [[U.S. National Geodetic Survey]]}}
* <!-- CRC -->{{cite book
|title = Handbook of Chemistry and Physics
|editor = Lide, David R. 
|edition = 87th
|year = 2006
|publisher = CRC Press, Taylor & Francis Group
|location = Boca Raton, Florida
|isbn = 978-0-8493-0487-3
|ref = CITEREFCRC2006}}
* <!-- Em -->{{cite book
|title = Nature's Building Blocks: An A–Z Guide to the Elements
|last = Emsley
|first = John
|publisher = Oxford University Press
|year = 2001
|location = Oxford, England, UK
|isbn = 978-0-19-850340-8
|chapter = Tin
|pages = [https://archive.org/details/naturesbuildingb0000emsl/page/445 445–450]
|chapter-url = {{google books |plainurl=y |id=j-Xu07p3cKwC}}
|url = https://archive.org/details/naturesbuildingb0000emsl/page/445
}}
* <!-- Gr -->{{Greenwood&Earnshaw2nd}}
* <!-- He -->{{cite book
|last = Heiserman
|first = David L.
|title = Exploring Chemical Elements and their Compounds
|location = New York
|publisher = TAB Books
|isbn = 978-0-8306-3018-9
|chapter = Element 50: Tin
|year = 1992
|chapter-url = https://archive.org/details/exploringchemica01heis
}}
* <!-- Mac -->{{cite book
|title = The Encyclopedia of the Chemical Elements
|publisher = Reinhold Book Corporation
|location = New York
|year = 1968
|editor = Clifford A. Hampel
|lccn = 68-29938
|last = MacIntosh
|first = Robert M.
|chapter = Tin
|pages= 722–732
}}
* <!-- Sw -->{{cite book
|title = Guide to the Elements
|chapter-url = https://archive.org/details/guidetoelements00stwe
|chapter-url-access = registration
|edition = Revised
|first = Albert
|last = Stwertka
|publisher = Oxford University Press
|year = 1998
|chapter = Tin
|isbn = 978-0-19-508083-4
}}
{{div col end}}

==External links==
{{Sister project links |wikt=tin |commons=Tin |b=General Chemistry/Chemistries of Various Elements/Group 14#Others |n=no |q=Tin |s=no |v=no |voy=no |species=no |d=no}}
* [http://www.periodicvideos.com/videos/050.htm Tin] at ''[[The Periodic Table of Videos]]'' (University of Nottingham)
* [https://theodoregray.com/PeriodicTable/Elements/050/index.s7.html Theodore Gray's Wooden Periodic Table Table]: Tin samples and castings
* [http://www.basemetals.com/html/sninfo.htm Base Metals: Tin]
* [https://www.cdc.gov/niosh/npg/npgd0613.html CDC – NIOSH Pocket Guide to Chemical Hazards]
* [https://web.archive.org/web/20140222181950/http://helgilibrary.com/indicators/index/tin-usd-cents-per-kg Tin (USD cents per kg) ]

{{Periodic table (navbox)}}
{{Tin compounds}}
{{Authority control}}

[[Category:Tin| ]]
[[Category:Chemical elements]]
[[Category:Post-transition metals]]
[[Category:Native element minerals]]
[[Category:Chemical elements with body-centered tetragonal structure]]
[[Category:Semimetals]]