Date published: 2026-1-7

1-800-457-3801

SCBT Portrait Logo
Seach Input

5-Hexenoic acid (CAS 1577-22-6)

0.0(0)
Write a reviewAsk a question

CAS Number:
1577-22-6
Molecular Weight:
114.14
Molecular Formula:
C6H10O2
Supplemental Information:
This is 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.

QUICK LINKS

5-Hexenoic acid is a liquid that ranges from colorless to a yellowish hue and emits a strong smell. It′s soluble in water, ethanol, and acetone but has limited solubility in benzene and diethyl ether. This compound is naturally found in several essential oils like basil, thyme, and rosemary, contributing to their distinct flavors and aromas. Additionally, 5-Hexenoic acid plays a critical role in various metabolic processes in organisms, such as the creation of unsaturated fatty acids and the breakdown of amino acids. In scientific research, it serves multiple purposes, including the fabrication of biopolymers, the making of chiral ligands for catalysis, and the formulation of food preservatives. It is also utilized as a reference substance for studying enzymes like aldehyde reductases and aldehyde dehydrogenases.


5-Hexenoic acid (CAS 1577-22-6) References

  1. Biosynthesis of functional polyhydroxyalkanoates by engineered Halomonas bluephagenesis.  |  Yu, LP., et al. 2020. Metab Eng. 59: 119-130. PMID: 32119929
  2. A Novel Family of [1,4]Thiazino[2,3,4-ij]quinolin-4-ium Derivatives: Regioselective Synthesis Based on Unsaturated Heteroatom and Heterocyclic Compounds and Antibacterial Activity.  |  Potapov, VA., et al. 2021. Molecules. 26: PMID: 34577049
  3. Engineered biosynthesis of alkyne-tagged polyketides.  |  Gu, D. and Zhang, W. 2022. Methods Enzymol. 665: 347-373. PMID: 35379442
  4. Influence of ceramide on lipid domain stability studied with small-angle neutron scattering: The role of acyl chain length and unsaturation.  |  DiPasquale, M., et al. 2022. Chem Phys Lipids. 245: 105205. PMID: 35483419
  5. Ni-Catalyzed Enantioselective Dialkyl Carbinol Synthesis via Decarboxylative Cross-Coupling: Development, Scope, and Applications.  |  Gao, Y., et al. 2022. J Am Chem Soc. 144: 10992-11002. PMID: 35671374
  6. The Improvement of Sensory and Bioactive Properties of Yogurt with the Introduction of Tartary Buckwheat.  |  Ye, Y., et al. 2022. Foods. 11: PMID: 35741972
  7. Simultaneous Differentiation of C═C Position Isomerism in Fatty Acids through Ion Mobility and Theoretical Calculations.  |  Wu, F., et al. 2022. Anal Chem. 94: 12213-12220. PMID: 36008361
  8. Electrospun Sulfonatocalix[4]arene Loaded Blended Nanofibers: Process Optimization and In Vitro Studies.  |  Abdul Khodir, WKW., et al. 2022. Pharmaceutics. 14: PMID: 36145660
  9. 'Key Factor' for Baijiu Quality: Research Progress on Acid Substances in Baijiu.  |  Wu, Y., et al. 2022. Foods. 11: PMID: 36230035
  10. One-Pot Terpolymerization of Macrolactones with Limonene Oxide and Phtalic Anhydride to Produce di-Block Semi-Aromatic Polyesters.  |  D'Auria, I., et al. 2022. Polymers (Basel). 14: PMID: 36433038
  11. Quality over quantity: Sampling high probability rare events with the weighted ensemble algorithm.  |  Roussey, NM. and Dickson, A. 2023. J Comput Chem. 44: 935-947. PMID: 36510846
  12. Synthetic study toward the diterpenoid aberrarone.  |  Shi, L., et al. 2022. Beilstein J Org Chem. 18: 1625-1628. PMID: 36530530
  13. Biotechnological Fungal Platforms for the Production of Biosynthetic Cannabinoids.  |  Kosalková, K., et al. 2023. J Fungi (Basel). 9: PMID: 36836348

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

5-Hexenoic acid, 1 g

sc-226972
1 g
$61.00