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Talk:Trichloroisocyanuric acid

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Requested move

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The following discussion is an archived debate of the proposal. Please do not modify it. Subsequent comments should be made in a new section on the talk page. No further edits should be made to this section.

The result of the debate was uncontroversial, thus moved Patstuarttalk|edits 19:08, 3 January 2007 (UTC)[reply]

SymcloseneTrichloroisocyanuric acid — Google search gives 551 hits for symclosene and +69,000 for trichloroisocyanuric acid. Also consistent with current naming of cyanuric acid, a "parent" chemical compound. Previously discussed at User talk:Smokefoot#Symclosene and dichlor and User talk:Fvasconcellos#Symclosene and dichlor. Fvasconcellos 17:20, 27 December 2006 (UTC) Fvasconcellos 17:20, 27 December 2006 (UTC)[reply]

Survey

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Add  # '''Support'''  or  # '''Oppose'''  on a new line in the appropriate section followed by a brief explanation, then sign your opinion using ~~~~.

Survey - Support votes

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Survey - Oppose votes

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Discussion

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Add any additional comments:
The above discussion is preserved as an archive of the debate. Please do not modify it. Subsequent comments should be made in a new section on this talk page. No further edits should be made to this section.

From nitrile, needs verification

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Nitriles can be obtained from primary amines via oxidation. Common methods include the use of Trichloroisocyanuric acid.[1]

References

  1. ^ Chen, Fen-Er; Kuang, Yun-Yan; Hui-Fang, Dai; Lu, Liang (2003). "A Selective and Mild Oxidation of Primary Amines to Nitriles with Trichloroisocyanuric Acid". Synthesis. 17 (17): 2629–2631. doi:10.1055/s-2003-42431..

Trichloride explosive?

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Can this common chemical react with ammonia to create nitrogen trichloride, an unstable explosive when in concentrated form? The article does not mention this. David Spector (talk) 12:15, 25 December 2021 (UTC)[reply]