Talk:Trichloroisocyanuric acid
 | This article is rated Start-class on Wikipedia's content assessment scale. It is of interest to the following WikiProjects: | ||||||||||
| |||||||||||
Requested move
edit- 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)
Symclosene → Trichloroisocyanuric 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)
Survey
edit- 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
editSurvey - Oppose votes
editDiscussion
edit- 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.
Nitriles can be obtained from primary amines via oxidation. Common methods include the use of Trichloroisocyanuric acid.[1]
References
- ^ 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?
editCan 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)