Date published: 2025-12-5

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cis-4-Hexen-1-ol (CAS 928-91-6)

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Alternate Names:
(4Z)-Hex-4-en-1-ol
CAS Number:
928-91-6
Molecular Weight:
100.16
Molecular Formula:
C6H12O
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Cis-4-Hexen-1-ol, identified by the CAS number 928-91-6, is an organic compound characterized by a six-carbon chain with a double bond between the fourth and fifth carbons in the cis configuration, and a hydroxyl group attached at the first carbon. This substance falls under the category of green leaf volatiles, which are compounds typically released when plants suffer mechanical damage. Due to its structure, cis-4-Hexen-1-ol exhibits properties typical of alcohols and alkenes, making it a versatile molecule in various non-medical research areas. In research, cis-4-Hexen-1-ol has been extensively used to study plant-insect interactions, as its presence often signals plant distress and can attract or repel specific insect species. Furthermore, this compound is utilized in ecological studies to understand and mimic natural plant signaling, providing insights into ecological balance and plant communication. Additionally, its pleasant, grassy aroma makes it a subject of interest in the fields of flavor and fragrance chemistry, where it is studied for its contributions to the nuances of plant-based scents and its potential applications in crafting fragrances and flavors. In industrial contexts, researchers explore the synthesis and applications of this compound in creating aroma compounds that evoke ′fresh green′ sensory experiences.


cis-4-Hexen-1-ol (CAS 928-91-6) References

  1. Application of HS-SPME and GC-MS to characterization of volatile compounds emitted from Osmanthus flowers.  |  Deng, C., et al. 2004. Ann Chim. 94: 921-7. PMID: 15689028
  2. Relationships between molecular structure and perceived odor quality of ligands for a human olfactory receptor.  |  Sanz, G., et al. 2008. Chem Senses. 33: 639-53. PMID: 18603653
  3. A skin permeability model of insulin in the presence of chemical penetration enhancer.  |  Yerramsetty, KM., et al. 2010. Int J Pharm. 388: 13-23. PMID: 20026200
  4. Effect of different enhancers on the transdermal permeation of insulin analog.  |  Yerramsetty, KM., et al. 2010. Int J Pharm. 398: 83-92. PMID: 20667506
  5. Mechanistic studies of Wacker-type intramolecular aerobic oxidative amination of alkenes catalyzed by Pd(OAc)2/pyridine.  |  Ye, X., et al. 2011. J Org Chem. 76: 1031-44. PMID: 21250706
  6. Evaluation of the volatile profile of wax apple (Syzygium samarangense) wines fermented with different commercial Saccharomyces cerevisiae strains.  |  Lin, X., et al. 2019. Food Sci Biotechnol. 28: 657-667. PMID: 31093423
  7. Delivery of Insulin via Skin Route for the Management of Diabetes Mellitus: Approaches for Breaching the Obstacles.  |  Ahad, A., et al. 2021. Pharmaceutics. 13: PMID: 33466845
  8. Chemical and Antimicrobial Analyses of Juniperus chinensis and Juniperus seravschanica Essential Oils and Comparison with Their Methanolic Crude Extracts.  |  Khamis, AS. and Chai, LC. 2021. Int J Anal Chem. 2021: 9937522. PMID: 34497647
  9. A Comprehensive Review of C. capsularis and C. olitorius: A Source of Nutrition, Essential Phytoconstituents and Pharmacological Activities.  |  Biswas, A., et al. 2022. Antioxidants (Basel). 11: PMID: 35883849
  10. Stress metabolites from Corchorus olitorius L. leaves in response to certain stress agents  |  Abou Zeid, Aisha Hussein Saleh. 2002. Food chemistry. 76: 187-195.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

cis-4-Hexen-1-ol, 100 mg

sc-211109
100 mg
$220.00

cis-4-Hexen-1-ol, 1 g

sc-211109A
1 g
$390.00