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Dibromodifluoromethane

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(Redirected from Halon 1202)
Dibromodifluoromethane
Names
Preferred IUPAC name Dibromo(difluoro)methane
Other names Dibromodifluoromethane
Difluorodibromomethane
Carbon dibromide difluoride
Carbon bromide fluoride
Halon 1202
Fluorocarbon 12-B2
FC 12-B2
R 12B2
UN 1941
Freon 12B2
Identifiers
CAS Number
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard 100.000.805 Edit this at Wikidata
EC Number
  • 200-885-5
PubChem CID
RTECS number
  • PA7525000
UNII
UN number 1941
CompTox Dashboard (EPA)
InChI
  • InChI=1S/CBr2F2/c2-1(3,4)5Key: AZSZCFSOHXEJQE-UHFFFAOYSA-N
  • InChI=1/CBr2F2/c2-1(3,4)5
SMILES
  • BrC(F)(F)Br
Properties
Chemical formula CBr2F2
Molar mass 209.82 g/mol
Appearance Colourless gas/liquid
Density
  • 8.7 kg/m (for gas)
  • 2.27 g/cm (for liquid)
Melting point −101.1 °C (−150.0 °F; 172.1 K)
Boiling point 22.8 °C (73.0 °F; 295.9 K)
Solubility in water insoluble
log P 1.99
Vapor pressure 83 kPa at 20 °C
Hazards
GHS labelling:
Pictograms GHS07: Exclamation mark
Signal word Warning
Hazard statements H420
Precautionary statements P502
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 Non-flammable
NIOSH (US health exposure limits):
PEL (Permissible) TWA 100 ppm (860 mg/m)
REL (Recommended) TWA 100 ppm (860 mg/m)
IDLH (Immediate danger) 2000 ppm
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

Dibromodifluoromethane is a mixed halomethane. It is a colorless non-flammable liquid. Along with Halons 1211, 2402, and 1301, it is one of the most effective fire extinguishers, however, it is also very toxic. It is a class I ozone depleting substance (ODS).

Synthesis

Dibromodifluoromethane can be obtained by vapor phase bromination of difluoromethane.

It is also formed during the fluorination of carbon tetrabromide.

Table of physical properties

Property Value
Density, ρ, at 15 °C (liquid) 2.3063 g/cm
Critical temperature, Tc 198.3 °C, 471.3 K
Critical pressure, pc 4.13 MPa, 40.8 bar
Refractive index, n at 20 °C, D 1.398
Dipole moment 0.7 D
Ozone depletion potential, ODP 0.4, CCl3F is 1
Global warming potential, GWP 231, CO2 is 1

References

  1. ^ NIOSH Pocket Guide to Chemical Hazards. "#0214". National Institute for Occupational Safety and Health (NIOSH).
  2. NLM Hazardous Substances Data Bank entry for
  3. Alan Roy Katritzky, Otto Meth-Cohn, Thomas Lonsdale Gilchrist, Charles Wayne Rees (1995), Comprehensive Organic Functional Group Transformations: Carbon with Three Or ..., Elsevier, p. 226, ISBN 0-08-042704-9{{citation}}: CS1 maint: multiple names: authors list (link)
  4. Hodnebrog, Ø., M. Etminan, J. S. Fuglestvedt, G. Marston, G. Myhre, C. J. Nielsen, K. P. Shine, and T. J. Wallington (2013), ‘Global warming potentials and radiative efficiencies of halocarbons and related compounds: A comprehensive review,’ Reviews of Geophysics, vol. 51, pp. 300-378, doi:10.1002/rog.20013.

External links

Halomethanes
Unsubstituted
Monosubstituted
Disubstituted
Trisubstituted
Tetrasubstituted
* Chiral compound.
Fluorine compounds
Salts and covalent derivatives of the fluoride ion
HF ?HeF2
LiF BeF2 BF
BF3
B2F4
+BO3
CF4
CxFy
+CO3
NF3
FN3
N2F2
NF
N2F4
NF2
?NF5
OF2
O2F2
OF
O3F2
O4F2
?OF4
F2 Ne
NaF MgF2 AlF
AlF3
SiF4 P2F4
PF3
PF5
S2F2
SF2
S2F4
SF3
SF4
S2F10
SF6
+SO4
ClF
ClF3
ClF5
?ArF2
?ArF4
KF CaF
CaF2
ScF3 TiF2
TiF3
TiF4
VF2
VF3
VF4
VF5
CrF2
CrF3
CrF4
CrF5
?CrF6
MnF2
MnF3
MnF4
?MnF5
FeF2
FeF3
FeF4
CoF2
CoF3
CoF4
NiF2
NiF3
NiF4
CuF
CuF2
?CuF3
ZnF2 GaF2
GaF3
GeF2
GeF4
AsF3
AsF5
Se2F2
SeF4
SeF6
+SeO3
BrF
BrF3
BrF5
KrF2
?KrF4
?KrF6
RbF SrF
SrF2
YF3 ZrF2
ZrF3
ZrF4
NbF4
NbF5
MoF4
MoF5
MoF6
TcF4
TcF
5

TcF6
RuF3
RuF
4

RuF5
RuF6
RhF3
RhF4
RhF5
RhF6
PdF2
Pd
PdF4
?PdF6
Ag2F
AgF
AgF2
AgF3
CdF2 InF
InF3
SnF2
SnF4
SbF3
SbF5
TeF4
?Te2F10
TeF6
+TeO3
IF
IF3
IF5
IF7
+IO3
XeF2
XeF4
XeF6
?XeF8
CsF BaF2   LuF3 HfF4 TaF5 WF4
WF5
WF6
ReF4
ReF5
ReF6
ReF7
OsF4
OsF5
OsF6
?OsF
7

?OsF
8
IrF2
IrF3
IrF4
IrF5
IrF6
PtF2
Pt
PtF4
PtF5
PtF6
AuF
AuF3
Au2F10
?AuF6
AuF5•F2
Hg2F2
HgF2
?HgF4
TlF
TlF3
PbF2
PbF4
BiF3
BiF5
?PoF2
PoF4
PoF6
AtF
?AtF3
?AtF5
RnF2
?RnF
4

?RnF
6
FrF RaF2   LrF3 Rf Db Sg Bh Hs Mt Ds Rg Cn Nh Fl Mc Lv Ts Og
LaF3 CeF3
CeF4
PrF3
PrF4
NdF2
NdF3
NdF4
PmF3 SmF2
SmF3
EuF2
EuF3
GdF3 TbF3
TbF4
DyF2
DyF3
DyF4
HoF3 ErF3 TmF2
TmF3
YbF2
YbF3
AcF3 ThF3
ThF4
PaF4
PaF5
UF3
UF4
UF5
UF6
NpF3
NpF4
NpF5
NpF6
PuF3
PuF4
PuF5
PuF6
AmF2
AmF3
AmF4
?AmF6
CmF3
CmF4
 ?CmF6
BkF3
BkF
4
CfF3
CfF4
EsF3
EsF4
?EsF6
Fm Md No
PF−6, AsF−6, SbF−6 compounds
AlF−6 compounds
chlorides, bromides, iodides
and pseudohalogenides
SiF2−6, GeF2−6 compounds
Oxyfluorides
Organofluorides
with transition metal,
lanthanide, actinide, ammonium
nitric acids
bifluorides
thionyl, phosphoryl,
and iodosyl
Chemical formulas
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