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Isopentyl acetate (CAS 123-92-2)

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Application:
Isopentyl acetate is a widely employed ester
CAS Number:
123-92-2
Molecular Weight:
130.18
Molecular Formula:
C7H14O2
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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Isopentyl acetate, also known as isoamyl acetate, bears the CAS number 123-92-2 and is an organic compound that is best known for its distinctive banana-like odor. This ester is formed by the reaction between isopentanol (isoamyl alcohol) and acetic acid, a process commonly catalyzed by acidic conditions. Structurally, isopentyl acetate features an ester functional group, which accounts for its fruity fragrance and makes it a popular ingredient in flavorings and fragrance production. In research contexts, isopentyl acetate has been extensively utilized as a model substance to study esterification reactions, serving as a practical example for teaching organic synthesis and reaction mechanisms in educational settings. Besides its use in flavor and fragrance chemistry, isopentyl acetate has also been studied in entomological research. It is a major component of the pheromone system of the honeybee, acting as an alarm pheromone that signals danger to other bees. This aspect has been explored in various studies examining insect behavior, communication, and pheromone function. Additionally, researchers have investigated its potential as an eco-friendly solvent due to its desirable solvent properties and relatively low toxicity compared to more traditional industrial solvents. This makes isopentyl acetate a multifaceted chemical of interest not only in commercial applications but also in scientific research exploring natural product chemistry and sustainable materials.


Isopentyl acetate (CAS 123-92-2) References:

  1. Identification of isoamyl acetate as an active component in the sting pheromone of the honey bee.  |  BOCH, R., et al. 1962. Nature. 195: 1018-20. PMID: 13870346
  2. Alarm pheromone induces immediate-early gene expression and slow behavioral response in honey bees.  |  Alaux, C. and Robinson, GE. 2007. J Chem Ecol. 33: 1346-50. PMID: 17505874
  3. Discrimination of Chinese vinegars based on headspace solid-phase microextraction-gas chromatography mass spectrometry of volatile compounds and multivariate analysis.  |  Xiao, Z., et al. 2011. J Food Sci. 76: C1125-35. PMID: 22417575
  4. Dynamic labelling of neural connections in multiple colours by trans-synaptic fluorescence complementation.  |  Macpherson, LJ., et al. 2015. Nat Commun. 6: 10024. PMID: 26635273
  5. Comparison of headspace solid-phase microextraction high capacity fiber coatings based on dual mass spectrometric and broadband vacuum ultraviolet absorption detection for untargeted analysis of beer volatiles using gas chromatography.  |  Zanella, D., et al. 2021. Anal Chim Acta. 1141: 91-99. PMID: 33248666
  6. Immobilization of Candida rugosa lipase on magnetic chitosan beads and application in flavor esters synthesis.  |  Bayramoglu, G., et al. 2022. Food Chem. 366: 130699. PMID: 34348221
  7. A surfactant-free microemulsion composed of isopentyl acetate, n-propanol, and water.  |  Liu, Y., et al. 2018. RSC Adv. 8: 1371-1377. PMID: 35540868
  8. Linear and non-linear rheological properties of water-ethanol hybrid pectin gels for aroma enhancement.  |  Tian, Y., et al. 2022. Food Chem X. 14: 100328. PMID: 35601213
  9. Bifunctional intercalation and sequence specificity in the binding of quinomycin and triostin antibiotics to deoxyribonucleic acid.  |  Lee, JS. and Waring, MJ. 1978. Biochem J. 173: 115-28. PMID: 687363

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Isopentyl acetate, 100 ml

sc-250190
100 ml
$105.00

Isopentyl acetate, 500 ml

sc-250190A
500 ml
$221.00