| BCDMH | |
|---|---|
| IUPAC name | 3-bromo-1-chloro-5,5-dimethylimidazolidine-2,4-dione |
| Other names | bromochloro-5,5-dimethylhydantoin, BCDMH, agribrom, aquabrom, aquabrome, bromicide, di-halo, halogene T30, nylate, photobrome, slimicide 78P |
| Identifiers | |
| CAS number | 126-06-7 |
| SMILES |
|
| Properties | |
| Molecular formula | C5H6BrClN2O2 |
| Molar mass | 241.47 g/mol |
| Appearance | White solid |
| Density | 1.9 g/cm3 |
| Melting point |
158 °C - 165 °C |
| Solubility in water | 0.25 g/100 ml (25 °C) |
| Hazards | |
| MSDS | External MSDS |
| Main hazards | Flamability, Inhalation |
| NFPA 704 | |
| R/S statement | S8, S17, S26, S36, S37, S39, S41, S45 |
| Flash point | Decomposes at 160°C |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox references |
|
1-Bromo-3-chloro-5,5-dimethylhydantoin (BCDMH) is a chemical structurally related to hydantoin. It is a white crystalline compound with a slight bromine and acetone odor and is insoluble in water, but soluble in acetone.
BCDMH is an excellent source of both chlorine and bromine as it reacts slowly with water releasing hypochlorous acid and hypobromous acid. It used as a chemical disinfectant used for recreational water and drinking water purification. BCDMH works in the following manner:
The initial BCDMH reacts with water (R = Dimethylhydantoin):
Hypobromous acid partially dissociates in water:
Hypobromous acid oxidizes the substrate, itself being reduced to bromide:
The bromide ions are oxidized with the hypochlorous acid that was formed from the initial BCDMH:
This produces more hypobromous acid. However, it should be noted that the hypochlorous acid itself does act directly as a disinfectant in the process.
| This article's citation style may be unclear. The references used may be clearer with a different or consistent style of citation, footnoting, or external linking. (September 2007) |
No comments have been added.