Dichloroisocyanuric acid
(Redirected from Dichlor)
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| Preferred IUPAC name
1,3-Dichloro-1,3,5-triazinane-2,4,6-trione | |||
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3D model (JSmol)
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| ChemSpider | |||
| ECHA InfoCard | 100.018.625 | ||
| KEGG | |||
PubChem CID
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| UNII | |||
CompTox Dashboard (EPA)
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| Properties | |||
| C3HCl2N3O3 | |||
| Molar mass | 197.96 g/mol | ||
| Density | 2.2 g/cm3 | ||
| Melting point | 225 °C (437 °F; 498 K) | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Dichloroisocyanuric acid, also known as dichlor or dichloro-s-triazinetrione and is marketed under many names (e.g. troclosene), is a chemical compound with the formula (C(O)NCl)2(C(O)NH).
Synthesis
[edit]Dichloroisocyanuric acid is manufactured by chlorination of cyanuric acid:[1]
- (C(O)NH)3 + 2 Cl2 → (C(O)NCl)2(C(O)NH) + 2 HCl
It is a colourless solid.[2]
Mechanism of action
[edit] | This section is missing information about why it is used over hypochlorite — something to do with cyanuric acid?. (January 2022) |
Dichloroisocyanuric acid is an oxidizer, reacting with water to form chlorine gas.[2]
Although the bleaching agent in most chlorine based bleach is sodium hypochlorite, the sodium salt of dichloroisocyanuric acid, sodium dichloroisocyanurate, is the active ingredient in commercial disinfectant bacteriocides, algicides, and cleaning agents[3] such as the pulverized cleanser Comet.[4]
See also
[edit]- Trichloroisocyanuric acid (trichlor)
References
[edit]- ^ Huthmacher, K.; Most, D. "Cyanuric Acid and Cyanuric Chloride". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a08_191. ISBN 978-3527306732.
- ^ a b "Pubchem Dichloroisocyanuric acid". Apr 17, 2021.
- ^ "Alfa Aesar™ Dichloroisocyanuric acid sodium salt, 97% (dry wt.), water <3%". Retrieved April 22, 2021.
- ^ "Procter&Gamble MSDS Comet Powder" (PDF). Oct 15, 2013.