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1-Butyne
| [math]\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} }[/math]
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| Names
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| Preferred IUPAC name
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| Other names
Ethylacetylene
Ethylethyne, UN 2452
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| Identifiers
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| ChEBI
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| ChemSpider
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| EC Number
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| UNII
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| UN number
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2452
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InChI=1S/C4H6/c1-3-4-2/h1H,4H2,2H3  YKey: KDKYADYSIPSCCQ-UHFFFAOYSA-N YInChI=1/C4H6/c1-3-4-2/h1H,4H2,2H3 Key: KDKYADYSIPSCCQ-UHFFFAOYAI
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| Properties[1]
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C4H6
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| Molar mass
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54.091 g/mol
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| Density
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0.6783 g cm−3[1]
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| Melting point
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−125.7 °C (−194.3 °F; 147.5 K)[1]
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| Boiling point
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8.08 °C (46.54 °F; 281.23 K)[1]
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| Hazards
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| GHS pictograms
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| GHS Signal word
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Danger
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HH220Script error: No such module "Preview warning".Category:GHS errors, H280
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PP210Script error: No such module "Preview warning".Category:GHS errors, P377, P381, P403
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). |
 Y verify (what is Y N ?)
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| Infobox references
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Tracking categories (test):
1-Butyne is an organic compound with the formula CH
3CH
2C≡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
- ↑ 1.0 1.1 1.2 1.3 1.4 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
 | Original source: https://en.wikipedia.org/wiki/1-Butyne. Read more |
