Vinyl bromide
Vinyl bromide is a simple vinyl halide. It is a colorless liquid. It is produced from ethylene dibromide. It is mainly used as a comonomer to confer fire retardant properties to acrylate polymers.[2]
Names | |
---|---|
Preferred IUPAC name
Bromoethene | |
Other names
Vinyl bromide 1-Bromoethene Bromoethylene 1-Bromoethylene Monobromoethene Monobromoethylene | |
Identifiers | |
3D model (JSmol) |
|
ChemSpider | |
ECHA InfoCard | 100.008.911 |
EC Number |
|
KEGG | |
PubChem CID |
|
RTECS number |
|
UNII | |
CompTox Dashboard (EPA) |
|
| |
| |
Properties | |
C2H3Br | |
Molar mass | 106.95 g/mol |
Appearance | Colorless gas |
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 | |
Main hazards | Toxic (T), Highly flammable (F+) |
Safety data sheet | See: data page |
R-phrases (outdated) | R12, R20/21/22, R36/37/38, R45 |
S-phrases (outdated) | S45, S53 |
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) |
none[1] |
REL (Recommended) |
Ca[1] |
IDLH (Immediate danger) |
N.D.[1] |
Supplementary data page | |
Refractive index (n), Dielectric constant (εr), etc. | |
Thermodynamic data |
Phase behaviour solid–liquid–gas |
UV, IR, NMR, MS | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
verify (what is ?) | |
Infobox references | |
Reactions and applications
It reacts with magnesium to give the corresponding Grignard reagent.[3]
Safety precautions
Vinyl bromide is listed in List of IARC Group 2A carcinogens as a suspected human carcinogen.
See also
References
- NIOSH Pocket Guide to Chemical Hazards. "#0657". National Institute for Occupational Safety and Health (NIOSH).
- Dagani, M. J.; Barda, H. J.; Benya, T. J.; Sanders, D. C. "Bromine Compounds". 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.
External links
- International Chemical Safety Card 0597
- NIOSH Pocket Guide to Chemical Hazards. "#0657". National Institute for Occupational Safety and Health (NIOSH).
- 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
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.