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Names | |||
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IUPAC name Dibromomethane | |||
Other names Methylene bromide, Methylene dibromide, Methyl dibromide, DBM, MDB, Refrigerant-30B2, UN 2664 | |||
Identifiers | |||
CAS Number | |||
3D model (JSmol) | |||
ChEBI | |||
ChemSpider | |||
ECHA InfoCard | 100.000.750 | ||
EC Number |
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PubChem CID | |||
RTECS number |
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CompTox Dashboard (EPA) | |||
InChI
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SMILES
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Properties | |||
Chemical formula | CH2Br2 | ||
Molar mass | 173.83 g/mol | ||
Appearance | Clear colorless to yellowish heavy liquid of low viscosity | ||
Density | 2.4970 g/cm at 20 °C
2.477 g/cm at 25 °C | ||
Melting point | -52.7 °C | ||
Boiling point | 96.95 °C | ||
Solubility in water | 12.5 g/l at 20 °C | ||
Vapor pressure | 60 hPa at 20 °C | ||
Hazards | |||
NFPA 704 (fire diamond) | 2 0 0 | ||
Flash point | None | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Y verify (what is ?) Infobox references |
Dibromomethane or methylene bromide, or methylene dibromide is a halomethane. It is slightly soluble in water, but very soluble in carbon tetrachloride, diethyl ether and methanol. Its refractive index is 1.5419 (20 °C, D).
Preparation
Dibromomethane can be prepared from bromoform by reaction
- CHBr3 + Na3AsO3 + NaOH → CH2Br2 + Na3AsO4 + NaBr
using sodium arsenite and sodium hydroxide.
Another way is to prepare it from diiodomethane and bromine.
Uses
Dibromomethane is used as a solvent, gage fluid, and in organic synthesis.
Natural occurrence
It is naturally produced by marine algae and liberated to the oceans. Releasing on soil causes it to evaporate and leach into the ground. Releasing in water causes it to be lost mainly by volatilisation with a half life of 5.2 hours. It has no significant degradating biological or abiological effects. In the atmosphere it will be lost because of reaction with photochemically produced hydroxyl radicals. The estimated half life of this reaction is 213 days.
References
- Podsiadlo M., Dziubek K., Szafranski M., Katrusiak A. (December 2006). "Molecular interactions in crystalline dibromomethane and diiodomethane, and the stabilities of their high-pressure and low-temperature phases". Acta Cryst. B62 (6): 1090–1098(9). doi:10.1107/S0108768106034963. PMID 17108664. Retrieved 2007-06-29.
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: CS1 maint: multiple names: authors list (link)
External links
- International Chemical Safety Card 0354
- Pesticide residues in food 1979 - Dibromomethane
- MSDS at Oxford University
Halomethanes | |
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Unsubstituted | |
Monosubstituted | |
Disubstituted | |
Trisubstituted | |
Tetrasubstituted | |
* Chiral compound. |