Chemistry:Vinyl bromide
From HandWiki
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| Names | |
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| Preferred IUPAC name
Bromoethene | |
| Other names
Vinyl bromide
1-Bromoethene Bromoethylene 1-Bromoethylene Monobromoethene Monobromoethylene | |
| Identifiers | |
3D model (JSmol)
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| ChEBI | |
| ChemSpider | |
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| KEGG | |
PubChem CID
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| UNII | |
| UN number | 1085 |
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| Properties | |
| C2H3Br | |
| Molar mass | 106.95 g/mol |
| Appearance | Colorless gas or liquid |
| Odor | pleasant[1] |
| Density | 1.525 g/cm3 at boiling point (liquid)
1.4933 g/cm3 at 20 °C |
| Melting point | −137.8 °C (−216.0 °F; 135.3 K) |
| Boiling point | 15.8 °C (60.4 °F; 288.9 K) |
| Insoluble | |
| log P | 1.57 |
| Vapor pressure | 206.8 kPa at 37.8 °C |
| Hazards | |
| GHS pictograms |  
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| GHS Signal word | Danger |
| H220, H350 | |
| P201, P202, P210, P281, P308+313, P377, P381, P403, P405, P501 | |
| NFPA 704 (fire diamond) | |
| Flash point | 5 °C (41 °F; 278 K) |
| 530 °C (986 °F; 803 K) | |
| Explosive limits | 9%-15%[1] |
| NIOSH (US health exposure limits): | |
PEL (Permissible)
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none[1] |
REL (Recommended)
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Ca[1] |
IDLH (Immediate danger)
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N.D.[1] |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
 verify (what is   ?)
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| Infobox references | |
Tracking categories (test):
Vinyl bromide is the organobromine compound with the formula CH
2=CHBr. Classified as a vinyl halide, it is a colorless gas at room temperature. It is used as a reagent and a comonomer.
Synthesis, reactions, and applications
It is produced from ethylene dibromide:
- CH
2Br–CH
2Br → CH
2=CHBr + HBr
CH
2=CHBr is mainly consumted as a comonomer to confer fire retardant properties to acrylate polymers.[2]
Vinyl bromide reacts with magnesium to give the corresponding Grignard reagent CH
2=CHMgBr.[3][4]
Safety precautions
Vinyl bromide is listed in List of IARC Group 2A carcinogens as a suspected human carcinogen.
See also
References
- ↑ 1.0 1.1 1.2 1.3 1.4 NIOSH Pocket Guide to Chemical Hazards. "#0657". National Institute for Occupational Safety and Health (NIOSH). https://www.cdc.gov/niosh/npg/npgd0657.html.
- ↑ Dagani, M. J.; Barda, H. J.; Benya, T. J.; Sanders, D. C.. "Ullmann's Encyclopedia of Industrial Chemistry". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a04_405.
- ↑ Dietmar Seyferth (1959). "Di-n-butyldivinyltin". Org. Synth. 39: 10. doi:10.15227/orgsyn.039.0010.
- ↑ William J. Scott, G. T. Crisp, J. K. Stille (1990). "Palladium-catalyzed Coupling of Vinyl Triflates with Organostannanes: 4-tert-butyl-1-vinylcyclohexene and 1-(4-tert-butylcyclohexen-1-yl)-2-propen-1-one". Organic Syntheses 68: 116. doi:10.15227/orgsyn.068.0116.
External links
- International Chemical Safety Card 0597
- NIOSH Pocket Guide to Chemical Hazards. "#0657". National Institute for Occupational Safety and Health (NIOSH). https://www.cdc.gov/niosh/npg/npgd0657.html.
- MSDS at Oxford University
- MSDS at mathesontrigas.com
- Vinyl bromide at IRIS
- Vinyl bromide at osha.gov
- IARC Summary & Evaluation of vinyl bromide
- Report on Carcinogens Background Document for Vinyl Bromide
- Synthesis of vinyl bromides
- The Kinetics of Pyrolysis of Vinyl Bromide
- UV absorption spectra
- UV Spectrum and Cross Sections
- 1H NMR spectrum
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