Date published: 2025-10-14

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Methyl 10-undecenoate (CAS 111-81-9)

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CAS Number:
111-81-9
Molecular Weight:
198.30
Molecular Formula:
C12H22O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Methyl 10-undecenoate, a chemical compound with the molecular formula C12H22O2, has been the subject of scientific research in various fields, including organic chemistry, fragrance chemistry, and materials science. It is an ester with a fruity, waxy aroma. Research has focused on understanding the synthesis of methyl 10-undecenoate and its mechanisms of formation. Methyl 10-undecenoate can be synthesized through esterification reactions between methanol and 10-undecenoic acid, catalyzed by acid catalysts or enzymes. Studies have explored the factors influencing the yield and selectivity of methyl 10-undecenoate synthesis, such as reaction conditions, catalysts, and reaction kinetics. Furthermore, methyl 10-undecenoate has been used as a fragrance ingredient and flavoring agent. Research has examined its sensory properties, odor thresholds, and contributions to aroma profiles. Methyl 10-undecenoate imparts fruity and waxy notes, making it suitable for various applications in perfumery and flavor formulation. Additionally, its potential as a precursor for materials synthesis has been investigated. The research applications of methyl 10-undecenoate contribute to advancements in organic chemistry, fragrance development, and materials science. By studying the mechanisms and applications of methyl 10-undecenoate, researchers aim to optimize its synthesis methods, explore its sensory impact, and discover new applications in fragrance, flavor, and materials industries.


Methyl 10-undecenoate (CAS 111-81-9) References

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  2. Overcoming Phase-Transfer Limitations in the Conversion of Lipophilic Oleo Compounds in Aqueous Media-A Thermomorphic Approach.  |  Gaide, T., et al. 2016. Angew Chem Int Ed Engl. 55: 2924-8. PMID: 26822502
  3. Semi-Crystalline Polar Polyethylene: Ester-Functionalized Linear Polyolefins Enabled by a Functional-Group-Tolerant, Cationic Nickel Catalyst.  |  Long, BK., et al. 2016. Angew Chem Int Ed Engl. 55: 7106-10. PMID: 27135297
  4. Synthesis and evaluation of anti-oxidant and cytotoxic activities of novel 10-undecenoic acid methyl ester based lipoconjugates of phenolic acids.  |  Narra, N., et al. 2017. Beilstein J Org Chem. 13: 26-32. PMID: 28179945
  5. Phosphine phosphonic amide nickel catalyzed ethylene polymerization and copolymerization with polar monomers.  |  Hong, C., et al. 2018. Dalton Trans. 47: 8264-8267. PMID: 29888779
  6. Accelerating ethylene polymerization using secondary metal ions in tetrahydrofuran.  |  Xiao, D., et al. 2019. Dalton Trans. 48: 17887-17897. PMID: 31782456
  7. Sustainable Fatty Acid Modification of Cellulose in a CO2-Based Switchable Solvent and Subsequent Thiol-Ene Modification.  |  Esen, E., et al. 2021. Biomacromolecules. 22: 586-593. PMID: 33289549
  8. Combining TEMPO and methyl undecenoate to produce an effective anti-mosquito compound with convenient spin-labeling.  |  Doll, KM., et al. 2023. Exp Parasitol. 244: 108440. PMID: 36495953
  9. Study on the Mechanism of Qing-Fei-Shen-Shi Decoction on Asthma Based on Integrated 16S rRNA Sequencing and Untargeted Metabolomics.  |  Hu, H., et al. 2023. Evid Based Complement Alternat Med. 2023: 1456844. PMID: 36846048
  10. Norbornene Copolymerization with Polar Monomers Catalyzed by Palladium Catalysts Containing Imidazolidin-2-imine/Guanidine Ligands.  |  Li, M., et al. 2024. Inorg Chem. 63: 1774-1783. PMID: 38104269

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Methyl 10-undecenoate, 5 ml

sc-215315
5 ml
$210.00