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1-Butyne

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1-Butyne
H C C C | H H | C | H H | H {\displaystyle {\ce {H-C#C}}{-}{\ce {\overset {\displaystyle {H} \atop |}{\underset {| \atop \displaystyle {H}}{C}}}}{-}{\ce {\overset {\displaystyle {H} \atop |}{\underset {| \atop \displaystyle {H}}{C}}}}{\ce {-H}}}
Full displayed formula
Space-filling model
Names
Preferred IUPAC name But-1-yne
Other names Ethylacetylene
Ethylethyne, UN 2452
Identifiers
CAS Number
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.003.139 Edit this at Wikidata
EC Number
  • 203-451-3
PubChem CID
UNII
UN number 2452
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C4H6/c1-3-4-2/h1H,4H2,2H3Key: KDKYADYSIPSCCQ-UHFFFAOYSA-N
  • InChI=1/C4H6/c1-3-4-2/h1H,4H2,2H3Key: KDKYADYSIPSCCQ-UHFFFAOYAI
SMILES
  • C#CCC
Properties
Chemical formula C4H6
Molar mass 54.091 g/mol
Density 0.6783 g cm
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:
Pictograms GHS02: Flammable
Signal word Danger
Hazard statements H220
Precautionary statements P210, P377, P381, P403
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). checkverify (what is  ?) Infobox references
Chemical compound

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.

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.

See also

References

  1. ^ Lide, David R. (2008). CRC Handbook of Chemistry and Physics, 89th Edition. CRC Press. pp. 3–84. ISBN 978-0-8493-0488-0.
  2. Zhang, Wei; Kraft, Stefan; Moore, Jeffrey S. (2004). "Highly Active Trialkoxymolybdenum(VI) Alkylidyne Catalysts Synthesized by a Reductive Recycle Strategy". Journal of the American Chemical Society. 126 (1): 329–335. doi:10.1021/ja0379868. PMID 14709099.
  3. Prosen, E.J.; Maron, F.W.; Rossini, F.D. (1951). "Heats of combustion, formation, and insomerization of ten C4 hydrocarbons". Journal of Research of the National Bureau of Standards. 46 (2): 106. doi:10.6028/jres.046.015.

External links

Alkynes
Preparations
Reactions
Binary compounds of hydrogen
Alkali metal
(Group 1) hydrides
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(Group 2)
earth hydrides
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Group 13
hydrides
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  • NhH
  • NhH3
  • Nh2H6
  • NhH5
Group 14 hydrides
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