Talk:Iodoacetic acid

Latest comment: 7 years ago by InternetArchiveBot in topic External links modified

Untitled

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All the data in the box is for acetyl iodide, including the cas number, and thats why I added an "other name".... ChristianB 19:35, 10 July 2007 (UTC)Reply

Indeed, but this is incorrect because iodoacetate and acetyl iodide are different compounds. I've created an article for acetyl iodide now.
Cheers
Ben 19:44, 10 July 2007 (UTC)Reply
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Hello fellow Wikipedians,

I have just modified one external link on Iodoacetic acid. Please take a moment to review my edit. If you have any questions, or need the bot to ignore the links, or the page altogether, please visit this simple FaQ for additional information. I made the following changes:

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Cheers.—InternetArchiveBot (Report bug) 02:32, 25 April 2017 (UTC)Reply

edit

Hello fellow Wikipedians,

I have just modified one external link on Iodoacetic acid. Please take a moment to review my edit. If you have any questions, or need the bot to ignore the links, or the page altogether, please visit this simple FaQ for additional information. I made the following changes:

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Cheers.—InternetArchiveBot (Report bug) 16:24, 5 May 2017 (UTC)Reply

Toxicity of monohaloacetic acids

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"Monohaloacetic acids are the most toxic, with toxicity increasing with halogen size." Does fluoroacetic acid break this trend, being toxic by a different mechanism? If so should the wording be changed to reflect this? Note that he toxicity seems to increase with halogen size as the carbon-halogen bond becomes easier to cleave, but it is the very stability and unreactivity of the C-F bond that is responsible fot the toxicity of fluoroacetic acid.