1-Butyne
| Names | |
|---|---|
| Preferred IUPAC name But-1-yne | |
| Other names Ethylacetylene Ethylethyne, UN 2452 | |
| Identifiers | |
| 3D model (JSmol) | |
| ChEBI | |
| ChemSpider | |
| ECHA InfoCard | 100.003.139 | 
| EC Number | 
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| PubChem CID | |
| UNII | |
| UN number | 2452 | 
| CompTox Dashboard (EPA) | |
| 
 | |
| 
 | |
| Properties | |
| C4H6 | |
| Molar mass | 54.091 g/mol | 
| Odor | Acetylenic | 
| Density | 0.6783 g cm−3 | 
| Melting point | −125.7 °C (−194.3 °F; 147.5 K) | 
| Boiling point | 8.08 °C (46.54 °F; 281.23 K) | 
| Hazards | |
| GHS labelling: | |
| Danger | |
| H220 | |
| P210, P377, P381, P403 | |
| Flash point | 7°C (45°F) | 
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references | |
1-Butyne is an organic compound with the formula CH3CH2C≡CH. It is a terminal alkyne. The compound is a common terminal alkyne substrate in diverse studies of catalysis. It is a colorless combustible gas. In 2017, 3.9 million pounds (1,700 long tons) was produced in the USA.
1-Butyne participates in reactions typical for terminal alkynes, such as alkyne metathesis, hydrogenation, condensation with formaldehyde. Based on its heat of combustion, it is slightly more stable than its isomer 2-butyne.
The combustion of 1-Butyne produces propargyl radicals, a pre-cursor to soot and polycyclic aromatic hydrocarbons, as the propargyl radicals can form basic aromatic rings, making butyne's fuel usage a concern for emissions.
1-Butyne is in unsaturated C4 petroleum cuts, and has to be separated out in industrial hydrorefining to make 1-butene, which is used to make low density polyethylene and polybutene. Distillation is impractical due to similar boiling points, so 1-butyne is removed by catalytic hydrogenation. Usually the catalyst is palladium, operated with liquid hydrocarbon and hydrogen gas at 20-60°C and pressures up to 10 bar.