Talk:Sodium erythorbate

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Chemicals Low‑importance

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Another chemical....???

http://chem.sis.nlm.nih.gov/chemidplus/ProxyServlet?objectHandle=DBMaint&actionHandle=default&nextPage=jsp/chemidheavy/ResultScreen.jsp&ROW_NUM=0&TXTSUPERLISTID=007378236

--222.64.25.33 (talk) 10:51, 2 February 2010 (UTC)[reply]

http://product.cheminfo.gov.cn/K0113/K01130401.htm

--222.64.25.33 (talk) 10:55, 2 February 2010 (UTC)[reply]

Get the IUPAC name of the chemical from International Union of Pure and Applied Chemistry --222.64.25.33 (talk) 10:54, 2 February 2010 (UTC)[reply]

http://www.food.gov.uk/safereating/chemsafe/additivesbranch/enumberlist

--222.64.25.33 (talk) 11:01, 2 February 2010 (UTC)[reply]

Little toxicological info is available...

http://scholar.google.com/scholar?start=0&q=allintitle:+sodium+erythorbate&hl=en&as_sdt=2000

--222.64.25.33 (talk) 11:10, 2 February 2010 (UTC)[reply]

I was checking out this article looking for health information about this additive. In this article/on this page dated Dec 2010, it talks about side effects for people sensitive to it, and references a few sources (e.g. Mayo clinic) http://www.livestrong.com/article/340989-sodium-erythorbate-side-effects/. I don't have time right now, but I think it would really improve this article to have a summary of health-related info. — Preceding unsigned comment added by Mspandana (talk • contribs) 20:43, 9 November 2011 (UTC)[reply]

Chemical structure

I am unsure as to the accuracy of the image provided. The erythorbic acid page shows both chiral locations to be R chiral while in the image for sodium erythorbate shows one as R and the second as L. — Preceding unsigned comment added by 174.79.166.77 (talk) 12:00, 19 June 2012 (UTC)[reply]

The chemical structure File:Sodium erythorbate.png appears to be correct to me and matches the structures given at the links in the infobox (Common Chemistry, PubChem, Chemspider, and ChEBI). All display the correct R,R stereochemistry. The image file may appear to be different than File:D-Erythorbic acid.svg because the side chain is oriented differently, but the stereochemistry is the same. -- Ed (Edgar181) 12:23, 19 June 2012 (UTC)[reply]

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External links modified

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Needs to be split into content sections

Currently this article is hard to follow since its just one large intro section 41.133.200.216 (talk) 10:56, 12 June 2024 (UTC)[reply]