1,2-Butadiene
Appearance
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Names | |
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Preferred IUPAC name
Buta-1,2-diene | |
Other names
Methyl allene
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Identifiers | |
3D model (JSmol)
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1730808 | |
ChEBI | |
ChemSpider | |
ECHA InfoCard | 100.008.796 |
EC Number |
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1144 | |
PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
C4H6 | |
Molar mass | 54.092 g·mol−1 |
Density | 0.676 at 4 °C |
Melting point | −136.2 °C (−213.2 °F; 137.0 K) |
Boiling point | 10.9 °C (51.6 °F; 284.0 K) |
Refractive index (nD)
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1.4205 at 1 °C |
Thermochemistry | |
Enthalpy of vaporization (ΔfHvap)
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23.426 kJ/mol |
Hazards | |
Occupational safety and health (OHS/OSH): | |
Main hazards
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Frostbite, flammable |
GHS labelling: | |
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Danger | |
H220, H224, H280, H411 | |
P210, P233, P240, P241, P242, P243, P273, P280, P303+P361+P353, P370+P378, P377, P381, P391, P403, P403+P235, P410+P403, P501 | |
Flash point | −75 °C (−103 °F; 198 K) |
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-Butadiene is the organic compound with the formula CH2=C=CHCH3. It is an isomer of 1,3-butadiene, a common monomer used to make synthetic rubber. It is a colorless flammable gas, one of the simplest substituted allenes.[1]
Production
[edit]![]() | The examples and perspective in this article may not represent a worldwide view of the subject. (August 2024) |
The C4-fraction obtained by cracking and separated by distillation consists of many compounds, predominantly (75%) 1,3-butadiene, isobutene, 1-butene. 1,2-Butadiene comprises less than 1% or this mixture.[2] It is partially purified by extraction with N-methylpyrrolidone. US product is 5,000 -25,000 tons.[1]
References
[edit]- ^ a b "Product Safety Summary 1,2-BUTADIENE". ExxonMobil. March 2016.
- ^ J. Grub; E. Löser (2012). "Butadiene". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a04_431.pub2. ISBN 978-3527306732.