1-Butyne

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
  • 203-451-3
UNII
UN number 2452
  • InChI=1S/C4H6/c1-3-4-2/h1H,4H2,2H3 Y
    Key: KDKYADYSIPSCCQ-UHFFFAOYSA-N Y
  • InChI=1/C4H6/c1-3-4-2/h1H,4H2,2H3
    Key: KDKYADYSIPSCCQ-UHFFFAOYAI
  • C#CCC
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).
Y verify (what is YN ?)
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.