Date published: 2026-4-29

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Cyclododecanone (CAS 830-13-7)

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CAS Number:
830-13-7
Molecular Weight:
182.30
Molecular Formula:
C12H22O
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Cyclododecanone is a macrocyclic ketone that is of particular interest in the field of organic synthesis and material science. In research applications, it is frequently used as a starting material or intermediate in the synthesis of various cyclic compounds and polymers. Its ring structure provides a scaffold for the construction of complex macrocycles, which are studied for their unique properties and potential applications in the development of new materials. Cyclododecanone is also involved in studies aimed at exploring ring-opening polymerization processes, where researchers investigate the polymerizability of this kind of macrocyclic monomers. Additionally, its relatively large ring size makes cyclododecanone a subject of interest in conformational analysis studies, which are integral to understanding the dynamics and stability of cyclic structures in various chemical environments.


Cyclododecanone (CAS 830-13-7) References

  1. Cloning and characterization of a gene cluster for cyclododecanone oxidation in Rhodococcus ruber SC1.  |  Kostichka, K., et al. 2001. J Bacteriol. 183: 6478-86. PMID: 11591693
  2. The gossypol-cyclododecanone (1/2) inclusion complex.  |  Dowd, MK. and Stevens, ED. 2003. Acta Crystallogr C. 59: o397-9. PMID: 12855869
  3. Synthesis and fungicidal activity of novel 2-oxocycloalkylsulfonylureas.  |  Li, XH., et al. 2005. J Agric Food Chem. 53: 2202-6. PMID: 15769157
  4. Beyond the corey reaction: one-step diolefination of cyclic ketones.  |  Butova, ED., et al. 2007. J Org Chem. 72: 5689-96. PMID: 17580903
  5. Bioproduction of lauryl lactone and 4-vinyl guaiacol as value-added chemicals in two-phase biotransformation systems.  |  Yang, J., et al. 2009. Appl Microbiol Biotechnol. 84: 867-76. PMID: 19444442
  6. Enhanced production of γ-cyclodextrin by optimization of reaction of γ-cyclodextrin glycosyltransferase as well as synchronous use of isoamylase.  |  Wang, L., et al. 2013. Food Chem. 141: 3072-6. PMID: 23871061
  7. A Biologically Active Analog of the Sex Pheromone of the Emerald Ash Borer, Agrilus planipennis.  |  Silk, PJ., et al. 2015. J Chem Ecol. 41: 294-302. PMID: 25786893
  8. Technical Synthesis of 1,5,9-Cyclododecatriene Revisited: Surprising Byproducts from a Venerable Industrial Process.  |  Thrun, F., et al. 2019. J Org Chem. 84: 13211-13220. PMID: 31418267
  9. Modification of Bacillus clarkii γ-Cyclodextrin Glycosyltransferase and Addition of Complexing Agents to Increase γ-Cyclodextrin Production.  |  Wang, L., et al. 2020. J Agric Food Chem. 68: 12079-12085. PMID: 33052686
  10. Seven Conformations of the Macrocycle Cyclododecanone Unveiled by Microwave Spectroscopy.  |  Burevschi, E. and Sanz, ME. 2021. Molecules. 26: PMID: 34500596
  11. Microbiological hydroxylation. 8. Cyclododecanone and cyclopentadecanone as substrates for steroid-hydroxylating fungi.  |  Ashton, MJ., et al. 1974. J Chem Soc Perkin 1. 0: 1665-9. PMID: 4472201

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Cyclododecanone, 25 g

sc-239605
25 g
$45.00