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==Uses== Choline [[chloride]] and choline [[bitartrate]] are used in [[dietary supplement]]s. Bitartrate is used more often due to its lower hygroscopicity.<ref name=ze/> Certain choline salts are used to supplement chicken, turkey and some other [[animal feed]]s. Some salts are also used as industrial chemicals: for example, in [[photolithography]] to remove [[photoresist]].<ref name="lpi"/> [[Choline theophyllinate]] and choline [[salicylate]] are used as medicines,<ref name="lpi"/><ref>{{Cite book|title=Community pharmacy: symptoms, diagnosis, and treatment|vauthors=Rutter P|publisher=Elsevier|year=2017|isbn=9780702069970|edition=4th|pages=156}}</ref> as well as [[structural analog]]s, like [[methacholine]] and [[carbachol]].<ref name="KOECT">{{cite book | chapter = C2-Chlorocarbons to Combustion Technology |title=Kirk-Othmer encyclopedia of chemical technology | veditors = Howe-Grant M, Kirk RE, Othmer DF |publisher=John Wiley & Sons |year=2000 |isbn=9780471484943 |edition=4th |volume=6 |pages=100–102 |display-authors=etal }}</ref> [[Radiolabeled]] cholines, like [[carbon-11-choline|<sup>11</sup>C-choline]], are used in [[medical imaging]].<ref>{{cite journal | vauthors = Guo Y, Wang L, Hu J, Feng D, Xu L | title = Diagnostic performance of choline PET/CT for the detection of bone metastasis in prostate cancer: A systematic review and meta-analysis | journal = PLOS ONE | volume = 13 | issue = 9 | pages = e0203400 | date = 2018 | pmid = 30192819 | pmc = 6128558 | doi = 10.1371/journal.pone.0203400 | bibcode = 2018PLoSO..1303400G | doi-access = free }}</ref> Other commercially used salts include tricholine [[citrate]] and choline [[bicarbonate]].<ref name="lpi"/> The most common forms of dietary choline supplements are shown in the following table: {{Table alignment}} {| class="wikitable sortable col2center col3center" |- ! Supplement !! weight (g/mol) !! Choline content (%) <!-- "Choline Content (%)" is calculated by Choline weight (104.173 g/mol) divided by the weight of the molecule. --> |- | [[Glycerophosphorylcholine|Αlpha-GPC]] <br/> (Choline alfoscerate) || 257.22 || 40.5% |- | [[Choline bitartrate]] || 253.25 || 41.13 |- | Choline citrate || 295.29 || 35.28% |- | [[Citicoline]] (CDP-choline) || 488.32 || 21.33% |- | [[Phosphatidylcholine]] (PC) ||data-sort-value="500"| Varies || 14-29%<ref>{{Cite web |title=L-α-Phosphatidylcholine - from soybean, Type II-S |url=https://www.sigmaaldrich.com/US/en/product/sigma/p5638 |url-status=live |archive-url=https://web.archive.org/web/20240618181506/https://www.sigmaaldrich.com/FI/en/product/sigma/p5638 |archive-date=2024-06-18 |access-date=2025-02-14 |website=Sigma-Aldrich}}</ref> |- | [[lecithin|Soy lecithin]] <br/> (12.69%–16.7% Phosphatidylcholine)||data-sort-value="5000"| - || 1.67% – 2.20%<ref>{{Cite journal |last=EFSA Panel on Food Additives and Nutrient Sources added to Food|last2=Mortensen |first2=Alicja |last3=Aguilar |first3=Fernando |last4=Crebelli |first4=Riccardo |last5=Di Domenico |first5=Alessandro |last6=Frutos |first6=Maria Jose |last7=Galtier |first7=Pierre |last8=Gott |first8=David |last9=Gundert‐Remy |first9=Ursula |last10=Lambré |first10=Claude |last11=Leblanc |first11=Jean‐Charles |last12=Lindtner |first12=Oliver |last13=Moldeus |first13=Peter |last14=Mosesso |first14=Pasquale |last15=Oskarsson |first15=Agneta |date=2017 |title=Re‐evaluation of lecithins (E 322) as a food additive |journal=EFSA Journal |volume=15 |issue=4 |doi=10.2903/j.efsa.2017.4742 |pmc=7010002 |pmid=32625454 |doi-access=free}}</ref> |}
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