Date published: 2025-10-11

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Pentyl isovalerate (CAS 25415-62-7)

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CAS Number:
25415-62-7
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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Pentyl isovalerate, an ester compound formed by the condensation of pentanol and isovaleric acid, has garnered interest in scientific research due to its applications in flavor and fragrance chemistry, as well as in organic synthesis. Its mechanism of action primarily involves its role as a volatile organic compound imparting fruity and floral aroma characteristics. Researchers have investigated its olfactory properties and sensory perception, contributing to the development of flavors and fragrances for food, cosmetic, and household products. Furthermore, pentyl isovalerate has been utilized as a chemical intermediate in organic synthesis, participating in esterification and transesterification reactions to yield structurally diverse compounds with potential applications in pharmaceuticals, agrochemicals, and materials science. Its versatile nature as a chemical building block has also led to its exploration in green chemistry initiatives, aiming to develop sustainable processes for the synthesis of value-added chemicals. Overall, pentyl isovalerate serves as a valuable tool in research endeavors spanning flavor and fragrance chemistry, organic synthesis, green technology, and materials science, offering opportunities for innovation and advancement in diverse scientific fields.


Pentyl isovalerate (CAS 25415-62-7) References

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  2. Production, partial purification and characterization of organic solvent tolerant lipase from Burkholderia multivorans V2 and its application for ester synthesis.  |  Dandavate, V., et al. 2009. Bioresour Technol. 100: 3374-81. PMID: 19285387
  3. In vitro antileishmanial and cytotoxicity activities of essential oils from Haplophyllum tuberculatum A. Juss leaves, stems and aerial parts.  |  Hamdi, A., et al. 2018. BMC Complement Altern Med. 18: 60. PMID: 29444667
  4. 'Hemping' the drinks: Aromatizing alcoholic beverages with a blend of Cannabis sativa L. flowers.  |  Ascrizzi, R., et al. 2020. Food Chem. 325: 126909. PMID: 32387946
  5. Elucidation of Analytical-Compositional Fingerprinting of Three Different Species of Chili Pepper by Using Headspace Solid-Phase Microextraction Coupled with Gas Chromatography-Mass Spectrometry Analysis, and Sensory Profile Evaluation.  |  Trovato, E., et al. 2022. Molecules. 27: PMID: 35408751
  6. Exploring metabolic dynamics during the fermentation of sea buckthorn beverage: comparative analysis of volatile aroma compounds and non-volatile metabolites using GC-MS and UHPLC-MS.  |  Peng, B., et al. 2023. Front Nutr. 10: 1268633. PMID: 37743927
  7. Influence of harvest season on volatile aroma constituents of two banana cultivars by electronic nose and HS-SPME coupled with GC-MS.  |  Dou, Tong-Xin, et al. 2020. Scientia Horticulturae. 265: 109214.
  8. Monitoring the volatile compounds status of whole seeds and flours of legume cultivars.  |  Rajhi, Imene, et al. 2021. Food Bioscience. 41: 101105.
  9. Essential oils work synergistically to mitigate pathogenic impact of Meloidogyne incognita, Rhizoctonia solani and Sclerotinia rolfsii.  |  Bargali, Pooja, et al. 2024. Biocatalysis and Agricultural Biotechnology. 58: 103160.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Pentyl isovalerate, 25 g

sc-215692
25 g
$200.00