Date published: 2025-10-14

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trans-2-Penten-1-ol (CAS 1576-96-1)

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Alternate Names:
(2E)-2-Penten-1-ol
CAS Number:
1576-96-1
Molecular Weight:
86.13
Molecular Formula:
C5H10O
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Trans-2-Penten-1-ol is a chemical compound that functions as a reactive intermediate in organic synthesis. It acts as a nucleophile in various reactions, participating in the formation of carbon-carbon bonds. Trans-2-Penten-1-Ol can undergo addition reactions with electrophiles, leading to the formation of new chemical compounds. In a research and development applications, trans-2-Penten-1-ol can serve as a building block for the synthesis of more complex organic molecules. Its mechanism of action involves the interaction of its double bond with other molecules, leading to the formation of new chemical bonds. Trans-2-Penten-1-Ol′s reactivity allows for the creation of diverse chemical structures, making it userful in organic chemistry research.


trans-2-Penten-1-ol (CAS 1576-96-1) References

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  2. Initiator structure influence on thermal and rheological properties of oligo(epsilon-caprolactone).  |  Mikhail, A., et al. 2006. J Biomater Sci Polym Ed. 17: 291-301. PMID: 16689016
  3. Partial oxidation of allylic and primary alcohols with O(2) by photoexcited TiO(2).  |  Molinari, A., et al. 2009. Photochem Photobiol Sci. 8: 613-9. PMID: 19424533
  4. Concentrations of aroma compounds and odor activity values of odorant series in different olive cultivars and their oils.  |  Reboredo-Rodríguez, P., et al. 2013. J Agric Food Chem. 61: 5252-9. PMID: 23659432
  5. Improvements in the malaxation process to enhance the aroma quality of extra virgin olive oils.  |  Reboredo-Rodríguez, P., et al. 2014. Food Chem. 158: 534-45. PMID: 24731380
  6. Unveiling the mechanism and selectivity of [3+2] cycloaddition reactions of benzonitrile oxide to ethyl trans-cinnamate, ethyl crotonate and trans-2-penten-1-ol through DFT analysis.  |  Abbiche, K., et al. 2020. J Mol Model. 26: 279. PMID: 32964360
  7. Virgin olive oil odour notes: their relationships with volatile compounds from the lipoxygenase pathway and secoiridoid compounds  |  Franca Angerosa, Roberta Mostallino, Carla Basti, Raffaella Vito. 2000. Food Chemistry. 68: 283-287.
  8. Virgin olive oil differentiation in relation to extraction methodologies  |  F Angerosa, R Mostallino, C Basti, R Vito, A Serraiocco. 2000. 80: 2190-2195.
  9. Influence of malaxation temperature and time on the quality of virgin olive oils  |  Franca Angerosa, Roberta Mostallino, Carla Basti, Raffaella Vito. 2001. Food Chemistry. 72: 19-28.
  10. The effect of cavitating ultrasound on the aqueous phase hydrogenation of cis-2-buten-1-ol and cis-2-penten-1-ol on Pd-black  |  R.S. Disselkamp, K.M. Denslow, T.R. Hart, J.F. White, C.H.F. Peden. 2005. Applied Catalysis A: General. 288: 62-66.
  11. Effect of the matrix in niobium-based aerogel catalysts for the selective oxidation of olefins with hydrogen peroxide  |  Filippo Somma a, Patrizia Canton b, Giorgio Strukul a. 2005. Journal of Catalysis. 229: 490-498.
  12. A selected ion flow tube study of the reactions of H3O+, NO+ and O2+ with a series of C5, C6 and C8 unsaturated biogenic alcohols  |  N. Schoon a, C. Amelynck a, E. Debie b, P. Bultinck b, E. Arijs a ✠. 2007. International Journal of Mass Spectrometry. 263: 127-136.
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  14. Hydrogenation of allyl alcohols catalyzed by aqueous palladium and platinum nanoparticles†  |  Krystel Di Pietrantonio a, Francesca Coccia‡ a, Lucia Tonucci *b, Nicola d'Alessandro a and Mario Bressan a. 2015. RSC Adv. 5: 68493-68499.
  15. Selective Separation of Polar Unsaturated Organics Using a Water Stationary Phase in Gas Chromatography  |  Amberley R. Marno & Kevin B. Thurbide. 2022. Chromatographia. 85: 105–113.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

trans-2-Penten-1-ol, 5 ml

sc-229493
5 ml
$148.00

trans-2-Penten-1-ol, 25 ml

sc-229493A
25 ml
$505.00