Date published: 2025-10-14

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Octyl acetate (CAS 112-14-1)

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Alternate Names:
Acetic acid octyl ester
Application:
Octyl acetate is a compound found in citrus oils
CAS Number:
112-14-1
Purity:
≥98%
Molecular Weight:
172.26
Molecular Formula:
C10H20O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Octyl acetate is a compound found in citrus oils. Octyl acetate, also referred to as ethyl octanoate, is an organic compound resulting from the combination of octanol and acetic acid. Its distinct characteristic is a pleasant and fruity aroma. This versatile compound finds application in various industries, serving as a flavor and fragrance enhancer in food and beverages, a solvent in paints and coatings, and a plasticizer in pharmaceuticals and cosmetics. Additionally, it plays a pivotal role as a laboratory reagent in the synthesis of other compounds. Furthermore, the scientific community recognizes the broad scope of applications for octyl acetate. In vivo experiments have employed it as a model to investigate the effects of environmental pollutants on the liver and kidney. In vitro studies have also capitalized on its potential to explore the impact of drugs on cell cultures and unravel the intricacies of drug mechanisms. Researchers have unveiled a myriad of pathways influenced by octyl acetate within the human body. Its inhibition of cytochrome P450 enzymes, which play a significant role in metabolizing drugs and various compounds, has been observed. Furthermore, octyl acetate has been found to hinder the activity of cyclooxygenase enzymes, critical in the synthesis of prostaglandins. Additionally, it interferes with acetylcholinesterase, an enzyme responsible for breaking down the neurotransmitter acetylcholine. Octyl acetate serves as a multifaceted compound with broad-ranging uses in both commercial and scientific applications, contributing to advancements in research and development across various fields.


Octyl acetate (CAS 112-14-1) References

  1. Heritability estimates for octyl acetate and octyl butyrate in the mature fruit of the wild parsnip.  |  Carroll, MJ., et al. 2000. J Hered. 91: 68-71. PMID: 10739131
  2. Concentration-detection functions for the odor of homologous n-acetate esters.  |  Cometto-Muñiz, JE., et al. 2008. Physiol Behav. 95: 658-67. PMID: 18950650
  3. [Determination of alpha-pinene and octyl acetate contents in Boswellia serrata].  |  Song, Z., et al. 2012. Zhongguo Zhong Yao Za Zhi. 37: 1431-3. PMID: 22860456
  4. Composition and biological activities of hogweed [Heracleum sphondylium L. subsp. ternatum (Velen.) Brummitt] essential oil and its main components octyl acetate and octyl butyrate.  |  Maggi, F., et al. 2014. Nat Prod Res. 28: 1354-63. PMID: 24697288
  5. Frankincense--therapeutic properties.  |  Al-Yasiry, AR. and Kiczorowska, B. 2016. Postepy Hig Med Dosw (Online). 70: 380-91. PMID: 27117114
  6. Evaluation of the teratogenic potential of octyl acetate in rats.  |  Daughtrey, WC., et al. 1989. Fundam Appl Toxicol. 13: 303-9. PMID: 2792597
  7. Phytotoxic Effect of Invasive Heracleum mantegazzianum Essential Oil on Dicot and Monocot Species.  |  Matoušková, M., et al. 2019. Molecules. 24: PMID: 30682808
  8. Losing the Arms Race: Greater Wax Moths Sense but Ignore Bee Alarm Pheromones.  |  Li, Y., et al. 2019. Insects. 10: PMID: 30909564
  9. Application of Lipase Purified from Aspergillus fumigatus in the Syntheses of Ethyl Acetate and Ethyl Lactate.  |  Mehta, A., et al. 2020. J Oleo Sci. 69: 23-29. PMID: 31902892
  10. Energy-efficient recovery of fermented butyric acid using octyl acetate extraction.  |  Oh, HW., et al. 2022. Biotechnol Biofuels Bioprod. 15: 46. PMID: 35524283
  11. The behavioral sensitivity of mice to acetate esters.  |  Jennings, L., et al. 2022. Chem Senses. 47: PMID: 35816188
  12. Comparison of Volatile Constituents Present in Commercial and Lab-Distilled Frankincense (Boswellia carteri) Essential Oils for Authentication.  |  Ojha, PK., et al. 2022. Plants (Basel). 11: PMID: 36015437
  13. Separation of Mandelic Acid by a Reactive Extraction Method Using Tertiary Amine in Different Organic Diluents.  |  Kiriş, B., et al. 2022. Molecules. 27: PMID: 36144720
  14. Essential Oil Variability in Iranian Populations of Heracleum persicum Desf. ex Fischer: A Rich Source of Hexyl Butyrate and Octyl Acetate.  |  Mustafavi, SH., et al. 2022. Molecules. 27: PMID: 36234832

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Octyl acetate, 5 g

sc-236244
5 g
$24.00