Carbonyl bromide
Appearance
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Names | |||
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Other names
Bromophosgene, carbonic dibromide, carbonyl dibromide
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Identifiers | |||
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3D model (JSmol)
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ChemSpider | |||
PubChem CID
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CompTox Dashboard (EPA)
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Properties | |||
COBr2 | |||
Molar mass | 187.818 g/mol | ||
Appearance | colorless liquid | ||
Density | 2.52 g/ml at 15°C | ||
Boiling point | 64.5°C | ||
reacts with water | |||
Thermochemistry | |||
Heat capacity (C)
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61.8 J·mol-1·K-1 (gas) | ||
Std molar
entropy (S⦵298) |
309.1 J·mol-1·K-1 (gas) | ||
Std enthalpy of
formation (ΔfH⦵298) |
-127.2 kJ·mol-1 (liquid) -96.2 kJ·mol-1 (gas) | ||
Hazards | |||
NFPA 704 (fire diamond) | |||
Related compounds | |||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Carbonyl bromide, also known as bromophosgene by analogy to phosgene, is an organic chemical compound. It is a decomposition product of halon compounds used in fire extinguishers.[2]
Reactions
Carbonyl bromide is formed when carbon tetrabromide is melted and concentrated sulfuric acid is added. Even at low temperatures, carbonyl bromide decomposes to carbon monoxide and elemental bromine.[3]
References
- ^ Lide, David R. (1998), Handbook of Chemistry and Physics (87 ed.), Boca Raton, FL: CRC Press, pp. 3–96, 4–50, 5–26, ISBN 0-8493-0594-2
- ^ US Occupational Safety and Health Administration (May 1996). "Common Fire Extinguishing Agents". Retrieved 2009-11-21.
- ^ Katrizsky, Alan R.; Meth-Cohn, Otto; Wees, Charles W. (1995), Organic Functional Group Transformations, vol. 6, Elsevier, pp. 417–8, ISBN 978-0-08-042704-1, retrieved 2009-11-23