Date published: 2026-5-19

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Tridecanoyl chloride (CAS 17746-06-4)

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CAS Number:
17746-06-4
Molecular Weight:
232.79
Molecular Formula:
C13H25ClO
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Tridecanoyl chloride is a common organic compound with wide range of applications in organic synthesis. It is used in the synthesis of dyes, polymers, surfactants, and analogues of naturally occurring compounds, such as amino acids, peptides, and steroids. Tridecanoyl chloride functions as an acylating agent, facilitating the formation of esters through its reactivity. As an electrophilic reagent, it readily reacts with nucleophilic compounds like alcohols, amines, and carboxylic acids. The resulting reaction yields an ester linkage, connecting the tridecanoyl chloride molecule with the corresponding nucleophilic compound.


Tridecanoyl chloride (CAS 17746-06-4) References

  1. Optimization of benzoxazinones as natural herbicide models by lipophilicity enhancement.  |  Macías, FA., et al. 2006. J Agric Food Chem. 54: 9357-65. PMID: 17147418
  2. Toward controlled spacing in one-dimensional molecular chains: alkyl-chain-functionalized fullerenes in carbon nanotubes.  |  Chamberlain, TW., et al. 2007. J Am Chem Soc. 129: 8609-14. PMID: 17579410
  3. Primary fatty acid amide metabolism: conversion of fatty acids and an ethanolamine in N18TG2 and SCP cells.  |  Farrell, EK., et al. 2012. J Lipid Res. 53: 247-56. PMID: 22095832
  4. Mimicking the lipid peroxidation inhibitory activity of phospholipid hydroperoxide glutathione peroxidase (GPx4) by using fatty acid conjugates of a water-soluble selenolane.  |  Iwaoka, M., et al. 2015. Molecules. 20: 12364-75. PMID: 26198222
  5. Difluoropalmitic acids as potential inhibitors of the biosynthesis of the sex pheromone of the Egyptian armyworm Spodoptera littoralis--IV.  |  Bosch, MP., et al. 1996. Bioorg Med Chem. 4: 467-72. PMID: 8733628
  6. Structure-activity relationship studies of the amide functionality in (p-O-sulfamoyl)-N-alkanoyl tyramines as estrone sulfatase inhibitors.  |  Chu, GH., et al. 1997. Steroids. 62: 530-5. PMID: 9253792
  7. Polymorphism of mixed triglycerides containing odd fatty acids  |  Lutton, E. S., Stewart, C. B., & Fehl, A. J. 1972. Journal of the American Oil Chemists' Society. 49(5): 333-335.
  8. Reaction of organoboranes with 2, 5-dihydroxy-1, 4-benzoquinone and related compounds, and its application to the synthesis of rapanone  |  Maruyama, K., Saimoto, H., & Yamamoto, Y. 1978. The Journal of Organic Chemistry. 43(25): 4895-4898.
  9. Liquid-crystalline solvents as mechanistic probes. 29. Chiral discotic columnar mesophases from the. alpha. and. beta. anomers of penta-On-alkanoylglucopyranoses  |  Morris, N. L., Zimmermann, R. G., Jameson, G. B., Dalziel, A. W., Reuss, P. M., & Weiss, R. G. 1988. Journal of the American Chemical Society. 110(7): 2177-2185.
  10. Structure and dynamics of pyramidic liquid crystals by deuterium NMR and X-ray diffraction  |  Poupko, R., Luz, Z., Spielberg, N., & Zimmermann, H. 1989. Journal of the American Chemical Society. 111(16): 6094-6105.
  11. Synthesis of 6‐and 9‐Ethylocatadecanoic Acids  |  Dragas, D., Tanojo, H., Brussee, J., Junginger, H. E., & Boddé, H. E. 1996. Archiv der Pharmazie. 329(10): 465-467.
  12. Development of a new colloidal drug carrier from chemically-modified cyclodextrins: nanospheres and influence of physicochemical and technological factors on particle size  |  Skiba, M., Duchêne, D., Puisieux, F., & Wouessidjewe, D. 1996. International journal of pharmaceutics. 129(1-2): 113-121.
  13. High-resolution calorimetric study of the phase transitions of tridecylcyanobiphenyl and tetradecylcyanobiphenyl liquid crystals  |  Cordoyiannis, G., Pinto, L. F. V., Godinho, M. H., Glorieux, C., & Thoen, J. 2009. Phase Transitions. 82(3): 280-289.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Tridecanoyl chloride, 1 ml

sc-237290
1 ml
$453.00

Tridecanoyl chloride, 25 ml

sc-237290A
25 ml
$2601.00