1-Butyne
Names | |
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Preferred IUPAC name But-1-yne | |
Other names Ethylacetylene Ethylethyne, UN 2452 | |
Identifiers | |
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ChEBI |
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ChemSpider |
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ECHA InfoCard | 100.003.139 |
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PubChem CID |
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UNII |
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UN number | 2452 |
CompTox Dashboard (EPA) |
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InChI
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Properties[1] | |
Chemical formula | C4H6 |
Molar mass | 54.091 g/mol |
Density | 0.6783 g cm−3[1] |
Melting point | −125.7 °C (−194.3 °F; 147.5 K)[1] |
Boiling point | 8.08 °C (46.54 °F; 281.23 K)[1] |
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Danger | |
Hazard statements | H220, H280 |
Precautionary statements | P210, P377, P381, P403 |
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 |
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]
1-Butyne participates in reactions typical for terminal alkynes, such as alkyne metathesis,[2] hydrogenation, condensation with formaldehyde. Based on its heat of combustion, it is slightly more stable than its isomer 2-butyne.[3]
See also
References
- ^ a b c d e Lide, David R. (2008). CRC Handbook of Chemistry and Physics, 89th Edition. CRC Press. pp. 3–84. ISBN 978-0-8493-0488-0.
- ^ 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.
- ^ 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
- NIST Chemistry WebBook page for 1-butyne
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