Date published: 2025-10-18

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11-Hydroxyundecanoic acid (CAS 3669-80-5)

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CAS Number:
3669-80-5
Molecular Weight:
202.29
Molecular Formula:
C11H22O3
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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11-Hydroxyundecanoic acid, a long-chain fatty acid, exhibits diverse biochemical and physiological impacts. Its synthesis employs various methods, drawing considerable interest in scientific research. Studies have revealed its capacity to impede acyl-CoA synthetase activity, integral to fatty acid metabolism, while concurrently activating peroxisome proliferator-activated receptor alpha (PPARα), pivotal for lipid metabolism regulation.


11-Hydroxyundecanoic acid (CAS 3669-80-5) References

  1. Ordered fabrication of luminescent multilayered thin films of CdSe quantum dots.  |  Vassiltsova, OV., et al. 2009. Dalton Trans. 9426-32. PMID: 19859597
  2. Bioenzymatic and Chemical Derivatization of Renewable Fatty Acids.  |  Akula, RK. and Kwon, YU. 2019. Biomolecules. 9: PMID: 31590242
  3. Bioorganic synthesis, characterization and evaluation of a natural phenolic lipid.  |  Johny, J., et al. 2019. Biotechnol Rep (Amst). 24: e00375. PMID: 31641619
  4. Construction of an engineered biocatalyst system for the production of medium-chain α,ω-dicarboxylic acids from medium-chain ω-hydroxycarboxylic acids.  |  Kim, TH., et al. 2020. Biotechnol Bioeng. 117: 2648-2657. PMID: 32436987
  5. Multienzymatic synthesis of nylon monomers from vegetable oils.  |  Lin, L., et al. 2023. Trends Biotechnol. 41: 150-153. PMID: 36180355
  6. Bis-3-methyl-2-butylborane as a selective reagent for the reduction of representative functional groups  |  Brown, H. C., & Bigley, D. B. 1961. Journal of the American Chemical Society. 83(2): 486-486.
  7. Polymer-supported syntheses of cyclic oligodepsipeptides  |  Cook, A., Hodge, P., Manzini, B., & Ruddick, C. L. 2007. Tetrahedron Letters. 48(37): 6496-6499.
  8. Single-step synthesis of idebenone from Coenzyme Q0 via free-radical alkylation under silver catalysis  |  Wang, J., Li, S., Yang, T., & Yang, J. 2014. Tetrahedron. 70(47): 9029-9032.
  9. Microbial synthesis of medium‐chain α, ω‐dicarboxylic acids and ω‐aminocarboxylic acids from renewable long‐chain fatty acids  |  Song, J. W., Lee, J. H., Bornscheuer, U. T., & Park, J. B. 2014. Advanced Synthesis & Catalysis. 356(8): 1782-1788.
  10. Chemo-enzymatic synthesis of 11-hydroxyundecanoic acid and 1, 11-undecanedioic acid from ricinoleic acid  |  Jang, H. Y., Singha, K., Kim, H. H., Kwon, Y. U., & Park, J. B. 2016. Green Chemistry. 18(4): 1089-1095.
  11. Real-time mass spectrometric identification of metabolites characteristic of chronic obstructive pulmonary disease in exhaled breath  |  Bregy, L., Nussbaumer-Ochsner, Y., Sinues, P. M. L., García-Gómez, D., Suter, Y., Gaisl, T.,.. & Zenobi, R. 2018. Clinical Mass Spectrometry,. 7: 29-35.
  12. Multilayer engineering of enzyme cascade catalysis for one-pot preparation of nylon monomers from renewable fatty acids  |  Kim, T. H., Kang, S. H., Han, J. E., Seo, E. J., Jeon, E. Y., Choi, G. E.,.. & Oh, D. K. 2020. ACS Catalysis. 10(9): 4871-4878.
  13. Pentadecanedioic acid production from 15‐hydroxypentadecanoic acid using an engineered biocatalyst with a co‐factor regeneration system  |  Shin, K. C., Kang, S. H., Lee, T. E., Kim, T. H., & Oh, D. K. 2022. Journal of the American Oil Chemists' Society. 99(8): 675-683.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

11-Hydroxyundecanoic acid, 1 g

sc-223151
1 g
$150.00