Date published: 2025-10-4

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Hexanoic anhydride (CAS 2051-49-2)

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Alternate Names:
Caproic anhydride
Application:
Hexanoic anhydride is a reactant in the synthesis of acremomannolipin A
CAS Number:
2051-49-2
Purity:
98%
Molecular Weight:
214.30
Molecular Formula:
C12H22O3
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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Hexanoic anhydride, also known as caproic anhydride, is a versatile reagent used primarily in chemical synthesis and polymer research. This anhydride is particularly valuable in synthesizing modified polymers, acting as an acylating agent to modify hydroxyl or amino groups, thus altering the properties of polymers to confer hydrophobicity or influence mechanical strength. It serves as a critical component in the esterification of polyols, enabling the creation of esters used in plasticizers, lubricants, and coatings. Additionally, its unique structure and reactivity allow researchers to investigate esterification kinetics and mechanisms in various organic substrates. Beyond polymer chemistry, hexanoic anhydride′s role as a derivatization reagent enhances chromatographic analyses of alcohols and amines by forming esters and amides for improved detection and separation. This functionality is crucial for studies aiming to explain the composition of natural products, complex lipid mixtures, or amino acid derivatives. Furthermore, its high reactivity in ring-opening polymerization has made it a valuable candidate for exploring new biodegradable polymers. Thus, hexanoic anhydride′s broad application in research continues to foster innovation in polymer science, chromatographic method development, and the study of organic reaction mechanisms.


Hexanoic anhydride (CAS 2051-49-2) References

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  2. Increase in the growth inhibition of bovine pulmonary artery smooth muscle cells by an O-hexanoyl low-molecular-weight heparin derivative.  |  Garg, HG., et al. 2006. Carbohydr Res. 341: 2607-12. PMID: 16920092
  3. Kinetics and mechanism of imidazole-catalyzed acylation of cellulose in LiCl/N,N-dimethylacetamide.  |  Nawaz, H., et al. 2013. Carbohydr Polym. 92: 997-1005. PMID: 23399120
  4. Separation of formyl-methionyl transfer RNA, methionyl transfer RNA, and transfer RNAfmet using mixed-mode high-performance liquid chromatography on C6-modified aminopropylsilyl-hypersil.  |  Ricker, RD. and Kaji, A. 1988. Anal Biochem. 175: 327-33. PMID: 2469355
  5. One-pot synthesis of anilides, herbicidal activity and molecular docking study.  |  Sartori, SK., et al. 2018. Pest Manag Sci. 74: 1637-1645. PMID: 29318774
  6. Applications of Pyrene Fluorescence to the Characterization of Hydrophobically Modified Starch Nanoparticles.  |  Kim, D., et al. 2018. Langmuir. 34: 8611-8621. PMID: 29936845
  7. Toughening Anhydride-Cured Epoxy Resins Using Fatty Alkyl-Anhydride-Grafted Epoxidized Soybean Oil.  |  Yadav, SK., et al. 2018. ACS Omega. 3: 2641-2651. PMID: 30023843
  8. Synthesis and characterization of thiolated hexanoyl glycol chitosan as a mucoadhesive thermogelling polymer.  |  Cho, IS., et al. 2018. Biomater Res. 22: 30. PMID: 30275973
  9. Simvastatin loaded chitosan guided bone regeneration membranes stimulate bone healing.  |  Murali, VP., et al. 2021. J Periodontal Res. 56: 877-884. PMID: 33830521
  10. Anhydride chemistry-based hexanoylation of polyethylenimine increases transfection efficiency and expression of tagged DNA for therapeutic proteins in cultured cells.  |  Ulgekar, G., et al. 2022. Biotechnol Bioeng. 119: 3275-3283. PMID: 35896515

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Hexanoic anhydride, 50 g

sc-215147
50 g
$40.00

Hexanoic anhydride, 250 g

sc-215147A
250 g
$126.00