Date published: 2025-9-17

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Valeric anhydride (CAS 2082-59-9)

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Alternate Names:
Pentanoic anhydride
Application:
Valeric anhydride is a synthesis reagent
CAS Number:
2082-59-9
Purity:
≥97%
Molecular Weight:
186.25
Molecular Formula:
C10H18O3
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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Valeric anhydride, also known as pentanoic anhydride, is a chemical reagent significant in synthetic organic chemistry, specifically for introducing valeroyl (pentanoyl) groups into target compounds. As a versatile acylating agent, it is particularly useful in modifying alcohols, amines, and phenols via esterification or amidation. In ester synthesis, valeric anhydride facilitates the formation of pentanoate esters, which are valuable intermediates in synthesizing flavors, fragrances, and specialized chemicals. The reagent is also instrumental in studying esterification kinetics, helping to explain the reaction mechanisms and conditions needed for optimal yields. Research involving valeric anhydride extends to the field of polymer science, where it is used to functionalize polymers and modify surface characteristics. By incorporating pentanoyl groups into polymer backbones, scientists investigate how this modification impacts hydrophobicity, compatibility, and flexibility in the resulting materials. Additionally, it is employed in the synthesis of modified cellulose derivatives, yielding cellulose esters with distinctive properties useful in biodegradable films and coatings. Further studies leverage valeric anhydride′s ability to acylate nitrogen-containing compounds to understand structure-activity relationships and to produce N-acyl derivatives for further analysis. Its utility in organic synthesis and polymer science positions valeric anhydride as an important tool for advancing the understanding of functional group transformations and material modifications.


Valeric anhydride (CAS 2082-59-9) References

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  2. Structure-activity relationship of alkyl 9-nitrocamptothecin esters.  |  Cao, ZS., et al. 2003. Acta Pharmacol Sin. 24: 109-19. PMID: 12546717
  3. Synthesis of 2-amido, 2-amino, and 2-azido derivatives of the nitrogen analogue of the naturally occurring glycosidase inhibitor salacinol and their inhibitory activities against O-GlcNAcase and NagZ enzymes.  |  Choubdar, N., et al. 2008. Carbohydr Res. 343: 1766-77. PMID: 18358456
  4. Chitin dipentanoate as the new technologically usable biomaterial.  |  Skołucka-Szary, K., et al. 2015. Mater Sci Eng C Mater Biol Appl. 55: 50-60. PMID: 26117738
  5. Synthesis, functionalisation and post-synthetic modification of bismuth metal-organic frameworks.  |  Köppen, M., et al. 2017. Dalton Trans. 46: 8658-8663. PMID: 28650040
  6. Surface-Anchored Metal-Organic Framework-Cotton Material for Tunable Antibacterial Copper Delivery.  |  Rubin, HN., et al. 2018. ACS Appl Mater Interfaces. 10: 15189-15199. PMID: 29637764
  7. Ionization of carboxylic acid clusters in the gas phase and on free ArN and (H2O)N nanoparticles: valeric acid as a model for small carboxylic acids.  |  Gámez, F., et al. 2019. Phys Chem Chem Phys. 21: 19201-19208. PMID: 31436273
  8. New prodrugs and analogs of the phenazine 5,10-dioxide natural products iodinin and myxin promote selective cytotoxicity towards human acute myeloid leukemia cells.  |  Viktorsson, EÖ., et al. 2021. RSC Med Chem. 12: 767-778. PMID: 34124675
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Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Valeric anhydride, 25 ml

sc-216050
25 ml
$45.00

Valeric anhydride, 100 ml

sc-216050A
100 ml
$60.00