Date published: 2026-4-5

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1-Phenyl-1-butyne (CAS 622-76-4)

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Alternate Names:
Ethyl phenyl acetylene
CAS Number:
622-76-4
Molecular Weight:
130.19
Molecular Formula:
C10H10
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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1-Phenyl-1-butyne (1-PB) is a highly reactive, colorless liquid with a boiling point of 45°C. It is widely utilized as a versatile organic compound in various applications. 1-Phenyl-1-butyne contributes to the synthesis of polymers such as polyurethanes, polyesters, and polyamides. The mechanism of action of 1-Phenyl-1-butyne is primarily attributed to its ability to form covalent bonds with other molecules, enabling its utilization as an intermediate in the synthesis of diverse compounds. Moreover, the high reactivity of 1-Phenyl-1-butyne enables its application in polymerization processes and as a fuel additive.


1-Phenyl-1-butyne (CAS 622-76-4) References

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  2. Synthesis of tetrasubstituted olefins by Pd-catalyzed addition of arylboronic acids to internal alkynes.  |  Zhou, C. and Larock, RC. 2005. Org Lett. 7: 259-62. PMID: 15646972
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  5. Electronic excitation of [(μ4-η2-alkyne)Rh4(CO)8(μ-CO)2]: an in situ UV/Vis spectroscopy, spectral reconstruction and DFT study.  |  Gao, F., et al. 2012. Chemphyschem. 13: 3139-45. PMID: 22706961
  6. Metalation Reactions XIII.† Effect of the Metalating Agent on the Metalation of Acetylenes  |  J. Y. Becker, S. Brenner, J. Klein. 1972. 10: 827-833.
  7. Oligomerization of alkynes by the RhCl3-aliquat 336 catalyst system: Part 2. formation of 2,3-disubstituted 1-phenylnaphthalenes by cyclodimerization of phenylalkynes  |  Ibrahim Amer, Jochanan Blum 2, K.Peter C. Vollhardt. 1990. Journal of Molecular Catalysis. 60: 323-330.
  8. Synthesis and light-emitting properties of C60-containing poly(1-phenyl-1-butyne)s  |  Hongyao Xu a, Qunhui Sun a, Priscilla Pui-Sze Lee a, Hoi Sing Kwok b, Ben Zhong Tang a b. 2000. Thin Solid Films. 363: 143-145.
  9. Preparation of Organophilic Pd–Montmorillonite, An Efficient Catalyst in Alkyne Semihydrogenation  |  Á. Mastalir a 1, Z. Király b, Gy. Szöllosi a, M. Bartók a. 2000. Journal of Catalysis. 194: 146-152.
  10. A comparative study of Pd supported on MCM-41 and SiO2 in the liquid phase hydrogenation of phenyl alkyl acetylenes mixtures  |  N. Marín-Astorga a, G. Pecchi a, J.L.G. Fierro b, P. Reyes a. 2005. Journal of Molecular Catalysis A: Chemical. 231: 67-74.
  11. Mesostructured silicas as supports for palladium-catalyzed hydrogenation of phenyl acetylene and 1-phenyl-1-hexyne to alkenes  |  Norman Marín-Astorga a, Gina Pecchi a, Thomas J. Pinnavaia b, Gabriela Alvez-Manoli c, Patricio Reyes a. 2006. Journal of Molecular Catalysis A: Chemical. 247: 145-152.
  12. Reaction dynamics of the phenyl radical (C6H5) with 1-butyne (HCCC2H5) and 2-butyne (CH3CCCH3)  |  Ralf I. Kaiser a, Fangtong Zhang a, Xibin Gu a, Vadim V. Kislov b, Alexander M. Mebel b. 2009. Chemical Physics Letters. 481: 46-53.
  13. Ruthenium-Catalyzed Regioselective Cyclization of Aromatic Ketones with Alkynes: An Efficient Route to Indenols and Benzofulvenes  |  Ravi Kiran Chinnagolla, Masilamani Jeganmohan. 2012. European Journal of Organic Chemistry. 2012: 417-423.
  14. Liquid-Phase Hydrogenation of Internal and Terminal Alkynes on Pd–Ag/Al2O3 Catalyst  |  A. V. Rassolov, G. O. Bragina, G. N. Baeva, N. S. Smirnova, A. V. Kazakov, I. S. Mashkovsky & A. Yu. Stakheev. 2019. Kinetics and Catalysis. 60: 642–649.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

1-Phenyl-1-butyne, 10 g

sc-224783
10 g
$53.00