Molecular structure of trans-3-Hexen-1-ol, CAS Number: 928-97-2
trans-3-Hexen-1-ol (CAS 928-97-2)
Alternate Names:
trans-3-Hexenol
CAS Number:
928-97-2
Molecular Weight:
100.16
Molecular Formula:
C6H12O
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-3-Hexen-1-ol is a chemical compound characterized by its volatility. It belongs to the category of odorants. It plays a part in the aromatic composition of Tempranillo Blanco wines. Found to be a component to the fragrant character of various flowers, including roses and lavender. Trans-3-Hexen-1-ol has shown to have significant binding affinity to proteins and enzymes, due to its ability to form soluble complexes at the interface between organic and aqueous phases.
trans-3-Hexen-1-ol (CAS 928-97-2) References
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- Volatile composition of Carignan noir wines from ungrafted and grafted onto País (Vitis vinifera L.) grapevines from ten wine-growing sites in Maule Valley, Chile. | Gutiérrez-Gamboa, G., et al. 2018. J Sci Food Agric. 98: 4268-4278. PMID: 29424428
- Characterization of the effect of cis-3-hexen-1-ol on green tea aroma. | Nie, CN., et al. 2020. Sci Rep. 10: 15506. PMID: 32968179
- Asymmetric synthesis of (-)-dehydro-exo-brevicomin with a photoisomerisation-intramolecular acetalisation sequence. | Hirasawa, S., et al. 2021. Org Biomol Chem. 19: 6897-6903. PMID: 34328158
- Gas-Phase Ozone Reaction Kinetics of C5-C8 Unsaturated Alcohols of Biogenic Interest. | Grira, A., et al. 2022. J Phys Chem A. 126: 4413-4423. PMID: 35776765
- Aromatic hydrocarbons: Examination of peach fruit and foliage volatiles | Thomas R. Kemp, L.P. Stoltz, L.V. Packett. 1971. Phytochemistry. 10: 478-479.
- Electroantennogram responses of the carrot fly, Psila rosae, to volatile plant components | P. M. GUERIN, J. H. VISSER. 1980. Physiological Entomology. 5: 111-119.
- Analysis of free and bound aroma compounds of pomegranate (Punica granatum L.) | Jyoti Tripathi a, Suchandra Chatterjee a, Sunita Gamre b, Subrata Chattopadhyay b, Prasad S. Variyar a, Arun Sharma a. 2014. LWT - Food Science and Technology. 59: 461-466.
- Trans-2-hexen-1-ol as a tool for the control of Fusarium verticillioides in stored maize grains | Vanessa Daniela Brito a b, Fernanda Achimón a b, José Sebastian Dambolena a b, Romina Paola Pizzolitto a b, Julio Alberto Zygadlo a b. 2019. Journal of Stored Products Research. 82: 123-130.
- Temperature dependent kinetic study of the gas phase reaction of ozone with 1-penten-3-ol, cis-2-penten-1-ol and trans-3-hexen-1-ol: Experimental and theoretical data | C. Kalalian a, G. El Dib b, H.J. Singh c, P.K. Rao c, E. Roth a, A. Chakir a. 2020. Atmospheric Environment. 223.
- Product investigation of the gas phase ozonolysis of 1-penten-3-ol, cis-2-penten-1-ol and trans-3-hexen-1-ol | C. Kalalian a, E. Roth a, G. El Dib b, H.J. Singh c, P.K. Rao c, A. Chakir a. 2020. Atmospheric Environment. 238.
- Development of lady beetle attractants from floral volatiles and other semiochemicals for the biological control of aphids | Jinhao Zhao a, Zhongyan Wang a, Zhongshan Li a, Jiayu Shi b, Ling Meng b, Guorong Wang c, Jingli Cheng a, Yongjun Du a. 2020. Journal of Asia-Pacific Entomology. 23: 1023-1029.
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| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
trans-3-Hexen-1-ol, 5 g | sc-237186 | 5 g | $65.00 |