BCDMH

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BCDMH
Skeletal formula of BCDMH
Ball-and-stick model of BCDMH
Laboratory sample of BCDMH
Names
IUPAC name
1-bromo-3-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
16079-88-2 YesY
ChemSpider 29069 YesY
Jmol 3D model Interactive image
PubChem 31335
  • InChI=1S/C5H6BrClN2O2/c1-5(2)3(10)8(6)4(11)9(5)7/h1-2H3 YesY
    Key: PQRDTUFVDILINV-UHFFFAOYSA-N YesY
  • InChI=1/C5H6BrClN2O2/c1-5(2)3(10)8(6)4(11)9(5)7/h1-2H3
    Key: PQRDTUFVDILINV-UHFFFAOYAT
  • O=C1N(Br)C(=O)N(Cl)C1(C)C
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)
Vapor pressure {{{value}}}
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
YesY verify (what is YesYN ?)
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:[1]

The initial BCDMH reacts with water (R = Dimethylhydantoin):

BrClR + 2 H2O → HOBr + HOCl + RH2

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. However, the hypochlorous acid itself does act directly as a disinfectant in the process.

Preparation

This compound is prepared by first brominating, then chlorinating 5,5-dimethylhydantoin:[2]

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References

  1. South Australian Health Commission, "Standard for the Operation of Swimming Pools and Spa Pools in South Australia", Supplement C: Bromine Disinfection, page 8. Retrieved on 2009-05-12.
  2. Lua error in package.lua at line 80: module 'strict' not found.

External links