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Dibromomethane

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Dibromomethane
Names
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 Edit this at Wikidata
EC Number
  • 200-824-2
PubChem CID
RTECS number
  • PA7350000
CompTox Dashboard (EPA)
InChI
  • InChI=1S/CH2Br2/c2-1-3/h1H2Key: FJBFPHVGVWTDIP-UHFFFAOYSA-N
  • InChI=1/CH2Br2/c2-1-3/h1H2Key: FJBFPHVGVWTDIP-UHFFFAOYAK
SMILES
  • BrCBr
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)
NFPA 704 four-colored diamondHealth 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g. chloroformFlammability 0: Will not burn. E.g. waterInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
2 0 0
Flash point None
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). checkverify (what is  ?) Infobox references
Chemical compound

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

  1. Methylene bromide preparation

External links

Halomethanes
Unsubstituted
Monosubstituted
Disubstituted
Trisubstituted
Tetrasubstituted
* Chiral compound.
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