Date published: 2026-4-25

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Hexanoyl chloride (CAS 142-61-0)

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Alternate Names:
Caproyl chloride
CAS Number:
142-61-0
Purity:
≥96%
Molecular Weight:
134.60
Molecular Formula:
C6H11ClO
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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Hexanoyl chloride, or n-hexanoyl chloride, is an organic compound. This colorless liquid possesses volatility and emits a pungent odor. Its applications span various domains, including organic synthesis, and polymer production. Hexanoyl chloride serves as a reagent in scientific research, contributing to the synthesis of diverse organic compounds, such as amino acids, peptides, and carbohydrates. In the realm of scientific research, hexanoyl chloride acts as a reagent, participating in organic synthesis. Through its interactions with alcohols, amines, and other organic compounds, it facilitates the formation of esters, amides, and various other compounds. Its versatile nature extends to the preparation of polymers and other materials, enhancing their synthesis and functionality. As a result, hexanoyl chloride enables the exploration of numerous research avenues and the development of innovative compounds and materials.


Hexanoyl chloride (CAS 142-61-0) References

  1. Synthesis of new sugar-based surfactants and evaluation of their hemolytic activities.  |  Neimert-Andersson, K., et al. 2006. J Org Chem. 71: 3623-6. PMID: 16626152
  2. Pyromellitamide aggregates and their response to anion stimuli.  |  Webb, JE., et al. 2007. J Am Chem Soc. 129: 7155-62. PMID: 17497782
  3. N-hexanoyl chitosan-stabilized magnetic nanoparticles: enhancement of adenoviral-mediated gene expression both in vitro and in vivo.  |  Bhattarai, SR., et al. 2008. Nanomedicine. 4: 146-54. PMID: 18374634
  4. Total synthesis and antibacterial screening of ( ± )-7-butyl-6,8-dihydroxy-3-pentyl-3,4-dihydroisochromen-1-one.  |  Saeed, A., et al. 2013. J Asian Nat Prod Res. 15: 1112-22. PMID: 23869649
  5. Facile synthesis of acyl chitosan isothiocyanates and their application to porphyrin-appended chitosan derivative.  |  Shibano, M., et al. 2014. Carbohydr Polym. 113: 279-85. PMID: 25256486
  6. Hydrophobic cellulose films with excellent strength and toughness via ball milling activated acylation of microfibrillated cellulose.  |  Deng, S., et al. 2016. Carbohydr Polym. 154: 129-38. PMID: 27577904
  7. A Complementary and Revised View on the N-Acylation of Chitosan with Hexanoyl Chloride.  |  Reis, B., et al. 2021. Mar Drugs. 19: PMID: 34356810
  8. Synthesis of thermoplastic chitin hexanoate-graft-poly(ε-caprolactone).  |  Nakashima, A., et al. 2022. Carbohydr Polym. 280: 119024. PMID: 35027126
  9. Esterification of lignin with long chain fatty acids for the stabilization of oil-in-water Pickering emulsions.  |  Shorey, R. and Mekonnen, TH. 2023. Int J Biol Macromol. 230: 123143. PMID: 36641016

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Hexanoyl chloride, 25 ml

sc-250109
25 ml
$45.00

Hexanoyl chloride, 100 ml

sc-250109A
100 ml
$67.00