Chemistry:1,2,3-Tribromopropane
From HandWiki
| Names | |
|---|---|
| Preferred IUPAC name
1,2,3-Tribromopropane[1] | |
Other names
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| Identifiers | |
3D model (JSmol)
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| 1732082 | |
| ChEBI | |
| ChemSpider | |
| EC Number |
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| 101184 | |
PubChem CID
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| RTECS number |
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| UNII | |
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| 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 | |
Refractive index (nD)
|
1.584 |
| Thermochemistry | |
Heat capacity (C)
|
166.5 J K−1 mol−1 |
| Hazards | |
| GHS pictograms | |
| 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
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Related compounds
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Mitobronitol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| 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
- ↑ "1,2,3-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.
- ↑ "1,2,3-tribromopropane". USA: ChemSynthesis. Physical Properties. http://www.chemsynthesis.com/base/chemical-structure-14677.html.
- ↑ "1,2,3-Tribromopropane". USA: chemBlink Inc.. Properties. http://www.chemblink.com/products/96-11-7.htm.
- ↑ 1,2,3-Tribromopropane Degradation Pathway. UMBBD (2011-08-15). Retrieved on 2011-11-28.
- ↑ 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

