Chemistry:1,2,3-Tribromopropane

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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
EC Number
  • 202-478-8
101184
RTECS number
  • TZ8300000
UNII
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 pictograms GHS07: Harmful GHS08: Health hazard
GHS Signal word WARNING
H302, H312, H315, H319, H332, H335, H351
P261, P280, P305+351+338
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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Infobox references
Tracking categories (test):

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. https://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=7279&loc=ec_rcs#x291. 
  2. "1,2,3-tribromopropane". USA: ChemSynthesis. Physical Properties. http://www.chemsynthesis.com/base/chemical-structure-14677.html. 
  3. "1,2,3-Tribromopropane". USA: chemBlink Inc.. Properties. http://www.chemblink.com/products/96-11-7.htm. 
  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. http://www.orgsyn.org/demo.aspx?prep=CV1P0521. ; Collective Volume, 1, pp. 521