BCDMH
| Names | |
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| Preferred IUPAC name
1-Bromo-3-chloro-5,5-dimethylimidazolidine-2,4-dione | |
| Other names
bromochloro-5,5-dimethylhydantoin, BCDMH, agribrom, aquabrom, aquabrome, bromicide, bromochlorodimethylhydantoin, di-halo, halogene T30, HarvestCide, nylate, photobrome, slimicide 78P
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| Identifiers | |
3D model (JSmol)
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| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | Lua error in Module:Wikidata at line 880: attempt to index field 'wikibase' (a nil value). Lua error in Module:Wikidata at line 880: attempt to index field 'wikibase' (a nil value).Lua error in Module:EditAtWikidata at line 29: attempt to index field 'wikibase' (a nil value). |
| EC Number |
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| E number | Lua error in Module:Wikidata at line 880: attempt to index field 'wikibase' (a nil value). |
PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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| Properties | |
| C5H6BrClN2O2 | |
| Molar mass | 241.47 g/mol |
| Appearance | White solid |
| Density | 1.9 g/cm3 |
| Melting point | 159 to 163 °C (318 to 325 °F; 432 to 436 K) |
| 0.15 g/100 ml (25 °C) | |
| Hazards | |
| Occupational safety and health (OHS/OSH): | |
Main hazards
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Flamability, Inhalation |
| GHS labelling: | |
| GHS03: OxidizingGHS05: CorrosiveGHS07: Exclamation markGHS09: Environmental hazard | |
| Danger | |
| H272, H302, H312, H314, H317, H332, H400 | |
| P210, P220, P221, P260, P261, P264, P270, P271, P272, P273, P280, P301+P312, P301+P330+P331, P302+P352, P303+P361+P353, P304+P312, P304+P340, P305+P351+P338, P310, P312, P321, P322, P330, P333+P313, P363, P370+P378, P391, P405, P501 | |
| NFPA 704 (fire diamond) | |
| Flash point | Decomposes at 160°C |
| Safety data sheet (SDS) | External MSDS |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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1-Bromo-3-chloro-5,5-dimethylhydantoin (BCDMH or bromochlorodimethylhydantoin) 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 for recreational water sanitation and drinking water purification.[1] BCDMH works in the following manner:[2]
The initial BCDMH reacts with water (R = Dimethylhydantoin):
Hypobromous acid partially dissociates in water:
- HOBr → H+ + OBr−
Hypobromous acid oxidizes the substrate, itself being reduced to bromide:
- HOBr + Live pathogens → Br− + Dead pathogens
The bromide ions are oxidized with the hypochlorous acid that was formed from the initial BCDMH:
- Br− + HOCl → HOBr + Cl−
This produces more hypobromous acid; the hypochlorous acid itself act directly as a disinfectant in the process.
Preparation
[edit | edit source]This compound is prepared by first brominating, then chlorinating 5,5-dimethylhydantoin:[3]
References
[edit | edit source]- ^ Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
- ^ South Australian Health Commission, "Standard for the Operation of Swimming Pools and Spa Pools in South Australia", Supplement C: Bromine Disinfection Archived 2009-05-21 at the Library of Congress Web Archives, page 8. Retrieved on 2009-05-12.
- ^ Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).