Date published: 2026-4-24

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Undecyl isocyanate (CAS 2411-58-7)

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CAS Number:
2411-58-7
Molecular Weight:
197.32
Molecular Formula:
C12H23NO
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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Undecyl isocyanate is a chemical compound utilized in organic synthesis to introduce isocyanate groups into various substrates, serving as an important reagent in the production of urethanes and ureas. Its reactivity with nucleophiles, such as alcohols and amines, is a key attribute that researchers exploit to create polymers with specific mechanical and chemical properties, making it useful in materials science. In the area of surface chemistry, undecyl isocyanate is used to modify the surfaces of materials, providing insights into the interactions between organic molecules and substrates, which is for the development of advanced coatings and adhesives. Additionally, its role in the synthesis of small molecules is significant for studying structure-activity relationships, particularly in the creation of compounds with potential applications in various industrial fields. The compound′s ability to form strong covalent bonds with a variety of functional groups also makes it a subject for investigation in the study of reaction mechanisms and catalysis within organic chemistry research.


Undecyl isocyanate (CAS 2411-58-7) References

  1. Synthesis and surface-active properties of a new class of surfactants derived from D-gluconic acid.  |  Abert, M., et al. 2002. Carbohydr Res. 337: 997-1006. PMID: 12039540
  2. Stabilization of polymerized vesicular systems: an application of the dynamic molecular shape concept.  |  Wathier, M., et al. 2002. Chem Phys Lipids. 115: 17-37. PMID: 12047896
  3. Discovery of a long-chain carbamoyl aminocarnitine derivative, a reversible carnitine palmitoyltransferase inhibitor with antiketotic and antidiabetic activity.  |  Giannessi, F., et al. 2003. J Med Chem. 46: 303-9. PMID: 12519067
  4. The mechanism of dephosphorylation of bis(2,4-dinitrophenyl) phosphate in mixed micelles of cationic surfactants and lauryl hydroxamic acid.  |  Silva, M., et al. 2009. J Org Chem. 74: 8254-60. PMID: 19788191
  5. From α-nucleophiles to functionalized aggregates: exploring the reactivity of hydroxamate ion towards esterolytic reactions in micelles.  |  Singh, N., et al. 2015. Org Biomol Chem. 13: 2827-48. PMID: 25597899
  6. Investigation of the thermal degradation of alkyl isocyanate polymers by direct pyrolysis mass spectrometry  |  Durairaj, B., Dimock, A. W., Samulski, E. T., & Shaw, M. T. 1989. Journal of Polymer Science Part A: Polymer Chemistry. 27(10): 3211-3225.
  7. Effect of the position of the urea group in the hydrocarbon tail of fatty acid amphiphiles on the physical gelation of organic liquids  |  Pal, A., & Dey, J. 2014. RSC Advances. 4(34): 17521-17525.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Undecyl isocyanate, 2 g

sc-224340
2 g
$99.00