Dibromochloromethane

Dibromochloromethane
Skeletal formula of dibromochloromethane
Spacefill model of dibromochloromethane
Names
Preferred IUPAC name
Dibromo(chloro)methane
Other names
  • Dibromochloromethane
  • Chlorodibromomethane[citation needed]
  • Monochlorodibromomethane[citation needed]
Identifiers
CAS Number
  • 124-48-1 checkY
3D model (JSmol)
  • Interactive image
Abbreviations CDBM[citation needed]
Beilstein Reference
1731046
ChEMBL
  • ChEMBL157093 checkY
ChemSpider
  • 29036 checkY
ECHA InfoCard 100.004.277 Edit this at Wikidata
EC Number
  • 204-704-0
KEGG
  • C14692 checkY
MeSH chlorodibromomethane
PubChem CID
  • 31296
RTECS number
  • PA6360000
UNII
  • 3T4AJR1H24 checkY
CompTox Dashboard (EPA)
  • DTXSID1020300 Edit this at Wikidata
InChI
  • InChI=1S/CHBr2Cl/c2-1(3)4/h1H checkY
    Key: GATVIKZLVQHOMN-UHFFFAOYSA-N checkY
  • ClC(Br)Br
Properties
Chemical formula
CHBr2Cl
Molar mass 208.28 g·mol−1
Appearance Colorless liquid
Density 2.451 g mL−1
Melting point −22 °C (−8 °F; 251 K)
Boiling point 119 to 120 °C (246 to 248 °F; 392 to 393 K) at 99.7 kPa
log P 2.206
Henry's law
constant (kH)
8.6 μmol Pa−1 kg−1
Magnetic susceptibility (χ)
-75.1·10−6 cm3/mol
1.547
Hazards
GHS labelling:
GHS07: Exclamation mark
Warning
H302
Lethal dose or concentration (LD, LC):
370 mg kg−1 (oral, rat)
Related compounds
Related alkanes
Related compounds
2-Chloroethanol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references
Chemical compound

Dibromochloromethane is a colorless to yellow, heavy and nonflammable compound with formula CHBr
2
Cl
.[1][2] It is a trihalomethane. The substance has a sweet odour.[3] Small quantities of dibromochloromethane are produced in ocean by algae.[citation needed]

Applications

Dibromochloromethane was formerly used as a flame retardant and as an intermediate in chemicals manufacturing. Today it is used only as a laboratory reagent. Dibromochloromethane is also a disinfection byproduct, formed by the reaction of chlorine with natural organic matter and bromide ions in the raw water supply. As a result, it is commonly found in chlorinated drinking water. Also, it is able to reduce methane production in ruminants by 79 %[4]

See also

References

  1. ^ "Dibromochloromethane". Sigma Aldrich. sigmaaldrich.com. Retrieved 7 June 2017.
  2. ^ "Public Health Statement for Bromoform and Dibromochloromethane". atsdr.cdc.gov. Retrieved 7 June 2017.
  3. ^ "BROMOFORM AND DIBROMOCHLOROMETHANE" (PDF). atsdr.cdc.gov. Retrieved 7 June 2017.
  4. ^ Identification of bioactives from the red seaweed Asparagopsis taxiformis that promote antimethanogenic activity in vitro

External links

  • Dibromochlormethane in greenfacts.org glossary
  • Dibromochloromethane toxicological review
  • ToxFAQ for bromoform at ATSDR
  • v
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Unsubstituted
  • CH4
Monosubstituted
  • CH3F
  • CH3Cl
  • CH3Br
  • CH3I
  • CH3At
Disubstituted
  • CH2F2
  • CH2ClF
  • CH2BrF
  • CH2FI
  • CH2Cl2
  • CH2BrCl
  • CH2ClI
  • CH2Br2
  • CH2BrI
  • CH2I2
Trisubstituted
  • CHF3
  • CHClF2
  • CHBrF2
  • CHF2I
  • CHCl2F
  • C*HBrClF
  • C*HClFI
  • CHBr2F
  • C*HBrFI
  • CHFI2
  • CHCl3
  • CHBrCl2
  • CHCl2I
  • CHBr2Cl
  • C*HBrClI
  • CHClI2
  • CHBr3
  • CHBr2I
  • CHBrI2
  • CHI3
Tetrasubstituted
  • CF4
  • CClF3
  • CBrF3
  • CF3I
  • CCl2F2
  • CBrClF2
  • CClF2I
  • CBr2F2
  • CBrF2I
  • CF2I2
  • CCl3F
  • CBrCl2F
  • CCl2FI
  • CBr2ClF
  • C*BrClFI
  • CClFI2
  • CBr3F
  • CBr2FI
  • CBrFI2
  • CFI3
  • CCl4
  • CBrCl3
  • CCl3I
  • CBr2Cl2
  • CBrCl2I
  • CCl2I2
  • CBr3Cl
  • CBr2ClI
  • CBrClI2
  • CClI3
  • CBr4
  • CBr3I
  • CBr2I2
  • CBrI3
  • CI4
* Chiral compound.
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