Date published: 2025-9-21

1-800-457-3801

SCBT Portrait Logo
Seach Input

Hexanal (CAS 66-25-1)

0.0(0)
Write a reviewAsk a question

Alternate Names:
Caproaldehyde; Aldehyde C6; Hexyl aldehyde
CAS Number:
66-25-1
Purity:
≥97%
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.

QUICK LINKS

Hexanal is a volatile organic compound known for its biological properties. It naturally occurs in various compounds like hexenol and caproic acid, which are used in perfume production. Hexanal can be extracted from these sources using solid phase microextraction (SPME) and analyzed through gas chromatography-mass spectrometry. This compound has demonstrated the ability to inhibit transcription activator activity by binding to the DNA at the transcription factor binding site, resulting in reduced intracellular Ca2+ levels and enzyme activities. Hexanal is also used in analytical methods, such as gas chromatography-mass spectrometry, for the detection of dinucleotide phosphate (DNP). In the flavor industry, hexanal is used to create fruity flavors and serves as a flavoring agent in the food industry. Additionally, it is used in Witting and aldol reactions.


Hexanal (CAS 66-25-1) References

  1. Mannanase transfer into hexane and xylene by liquid-liquid extraction.  |  Shipovskov, S., et al. 2010. Appl Biochem Biotechnol. 160: 1124-9. PMID: 19444389
  2. N-hexane and its toxicologic effects: a review.  |  Jørgensen, NK. and Cohr, KH. 1981. Scand J Work Environ Health. 7: 157-68. PMID: 20120580
  3. Paper spray ionization of polar analytes using non-polar solvents.  |  Li, A., et al. 2011. Chem Commun (Camb). 47: 2811-3. PMID: 21286639
  4. Synthesis of S-doped graphene by liquid precursor.  |  Gao, H., et al. 2012. Nanotechnology. 23: 275605. PMID: 22710561
  5. Vesicles protect activated acetic acid.  |  Todd, ZR. and House, CH. 2014. Astrobiology. 14: 859-65. PMID: 25280019
  6. Improvement of biogas production from orange peel waste by leaching of limonene.  |  Wikandari, R., et al. 2015. Biomed Res Int. 2015: 494182. PMID: 25866787
  7. Physicochemical characterization of wet microalgal cells disrupted with instant catapult steam explosion for lipid extraction.  |  Cheng, J., et al. 2015. Bioresour Technol. 191: 66-72. PMID: 25983224
  8. Effects of Hexane in Supercritical Fluid Chromatography for the Separation of Enantiomers.  |  Wu, H., et al. 2016. Chirality. 28: 192-8. PMID: 27280188
  9. Solvation free energies and partition coefficients with the coarse-grained and hybrid all-atom/coarse-grained MARTINI models.  |  Genheden, S. 2017. J Comput Aided Mol Des. 31: 867-876. PMID: 28875361
  10. 2-Methyloxolane (2-MeOx) as Sustainable Lipophilic Solvent to Substitute Hexane for Green Extraction of Natural Products. Properties, Applications, and Perspectives.  |  Rapinel, V., et al. 2020. Molecules. 25: PMID: 32731508
  11. Cuticular hydrocarbons for the identification and geographic assignment of empty puparia of forensically important flies.  |  Moore, H., et al. 2022. Int J Legal Med. 136: 1791-1800. PMID: 35217906
  12. Phytochemical Composition of Lichen Parmotrema hypoleucinum (J. Steiner) Hale from Algeria.  |  Kerboua, M., et al. 2022. Molecules. 27: PMID: 36014465
  13. [Progress on the mechanism of n-hexane induced toxic effects in vitro and in vivo].  |  Zhang, LJ., et al. 2023. Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi. 41: 388-396. PMID: 37248089
  14. Cytogenetic studies on commercial hexane solvent.  |  Daughtrey, WC., et al. 1994. J Appl Toxicol. 14: 161-5. PMID: 8083476

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Hexanal, 2 ml

sc-252885
2 ml
$26.00