1,2,3-Tribromopropane

1,2,3-Tribromopropane
Skeletal formula of 1,2,3-tribromopropane
Names
Preferred IUPAC name
1,2,3-Tribromopropane[1]
Other names
  • Glyceryl tribromohydrin
  • sym-Tribromopropane
Identifiers
3D model (JSmol)
1732082
ChEBI
ChemSpider
ECHA InfoCard 100.002.254 Edit this at Wikidata
EC Number
  • 202-478-8
101184
RTECS number
  • TZ8300000
UNII
  • InChI=1S/C3H5Br3/c4-1-3(6)2-5/h3H,1-2H2 checkY
    Key: FHCLGDLYRUPKAM-UHFFFAOYSA-N checkY
  • BrCC(Br)CBr
Properties
C3H5Br3
Molar mass 280.785 g·mol−1
Appearance Colorless liquid
Density 2.398 g mL−1[2]
Melting point 16.2 °C; 61.1 °F; 289.3 K
Boiling point 220.1 °C; 428.1 °F; 493.2 K
-117.9·10−6 cm3/mol
1.584
Thermochemistry
166.5 J K−1 mol−1
Hazards
GHS labelling:
GHS07: Exclamation mark GHS08: Health hazard
Warning
H302, H312, H315, H319, H332, H335, H351
P261, P280, P305+P351+P338
Flash point 93 °C (199 °F; 366 K)[3]
Related compounds
Related alkanes
Related compounds
 Mitobronitol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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1,2,3-Tribromopropane (TBP) is a toxic organic compound.[4] It is a clear colorless to light yellow liquid.[5]

References

  1. ^ "1,2,3-TRIBROMOPROPANE - Compound Summary". PubChem Compound. USA: National Center for Biotechnology Information. 26 March 2005. Identification. Retrieved 22 June 2012.
  2. ^ "1,2,3-tribromopropane". USA: ChemSynthesis. Physical Properties. Retrieved 28 November 2011.
  3. ^ "1,2,3-Tribromopropane". USA: chemBlink Inc. Properties. Retrieved 28 November 2011.
  4. ^ 1,2,3-Tribromopropane Degradation Pathway. UMBBD (2011-08-15). Retrieved on 2011-11-28.
  5. ^ Johnson, J. R.; McEwen, W. L. (1927). "1,2,3-TRIBROMOPROPANE". Organic Syntheses. 5: 99; Collected Volumes, vol. 1, p. 521.


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