Date published: 2025-9-5

1-800-457-3801

SCBT Portrait Logo
Seach Input

Tridecanoic acid (CAS 638-53-9)

0.0(0)
Write a reviewAsk a question

Alternate Names:
Tridecylic acid
Application:
Tridecanoic acid is a saturated fatty acid
CAS Number:
638-53-9
Molecular Weight:
214.34
Molecular Formula:
C13H26O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

Tridecanoic acid (TDA) is a saturated, straight-chain fatty acid. Derived from plant and animal fats and oils, Tridecanoic acid has undergone extensive investigation due to its potential uses. Its biochemical and physiological effects have been explored. In vitro applications have explored Tridecanoic acid′s utility in synthesizing various compounds, including polymers.


Tridecanoic acid (CAS 638-53-9) References

  1. Structures of the high-temperature solid phases of the odd-numbered fatty acids from tridecanoic acid to tricosanoic acid.  |  Gbabode, G., et al. 2007. Chemistry. 13: 3150-9. PMID: 17212366
  2. A microfluidic device for the automated derivatization of free fatty acids to fatty acid methyl esters.  |  Duong, CT. and Roper, MG. 2012. Analyst. 137: 840-6. PMID: 22166918
  3. Functional evolution of duplicated odorant-binding protein genes, Obp57d and Obp57e, in Drosophila.  |  Harada, E., et al. 2012. PLoS One. 7: e29710. PMID: 22238638
  4. Engineering Escherichia coli for odd straight medium chain free fatty acid production.  |  Wu, H. and San, KY. 2014. Appl Microbiol Biotechnol. 98: 8145-54. PMID: 25030454
  5. Drug leads agents from methanol extract of Nigerian bee (Apis mellifera) propolis.  |  Lawal, B., et al. 2016. J Intercult Ethnopharmacol. 5: 43-8. PMID: 27069724
  6. Environmental alterations in biofuel generating molecules in Zilla spinosa.  |  Khattab, H. and El Marid, Z. 2017. Z Naturforsch C J Biosci. 72: 77-91. PMID: 27740933
  7. Fatty acid microemulsion for the treatment of neonatal conjunctivitis: quantification, characterisation and evaluation of antimicrobial activity.  |  Butt, U., et al. 2016. Drug Deliv Transl Res. 6: 722-734. PMID: 27766599
  8. Impact of Terminalia chebula Retz. against Aedes aegypti L. and non-target aquatic predatory insects.  |  Thanigaivel, A., et al. 2017. Ecotoxicol Environ Saf. 137: 210-217. PMID: 27940415
  9. Evolution of Volatile Emission in Rhus coriaria Organs During Different Stages of Growth and Evaluation of the Essential Oil Composition.  |  Reidel, RVB., et al. 2017. Chem Biodivers. 14: PMID: 28742251
  10. Expression, Purification, and Biochemical Characterization of the Flavocytochrome P450 CYP505A30 from Myceliophthora thermophila.  |  Baker, GJ., et al. 2017. ACS Omega. 2: 4705-4724. PMID: 30023729
  11. The role of Lathyrus sativus flower surface wax in short-range attraction and stimulant for nymph laying by an adult viviparous aphid.  |  Mitra, P., et al. 2020. Bull Entomol Res. 110: 231-241. PMID: 31559934
  12. New function of the CD44 gene: Lipid metabolism regulation in bovine mammary epithelial cells.  |  Jiang, P., et al. 2020. J Dairy Sci. 103: 6661-6671. PMID: 32359993
  13. High-resolution metabolomic biomarkers for lung cancer diagnosis and prognosis.  |  Qi, SA., et al. 2021. Sci Rep. 11: 11805. PMID: 34083687
  14. Characterization and cytotoxicity assessment of biosurfactant derived from Lactobacillus pentosus NCIM 2912.  |  Sharma, V., et al. 2022. Braz J Microbiol. 53: 327-340. PMID: 34816387

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Tridecanoic acid, 5 g

sc-216007
5 g
$37.00

Tridecanoic acid, 25 g

sc-216007A
25 g
$88.00