Date published: 2025-10-14

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trans,trans-Farnesol (CAS 106-28-5)

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Alternate Names:
trans,trans-3,7,11-Trimethyl-2,6,10-dodecatrien-1-ol, (E,E)-3,7,11-Trimethyl-2,6,10-dodecatrien-1-ol
CAS Number:
106-28-5
Purity:
96%
Molecular Weight:
222.37
Molecular Formula:
C15H26O
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Trans,trans-Farnesol, a naturally-occurring sesquiterpene alcohol, is found in plant extracts. This colorless, oily liquid possesses a delicate aroma reminiscent of roses. It is widely distributed in various organisms and the environment. Researchers have extensively investigated trans,trans-Farnesol for its potential, revealing its ability to combat inflammation, microbial infections, and cancer. Moreover, its antioxidant properties and gene expression modulation capabilities have been widely studied. Additional trans,trans-Farnesol functionality include the inhibition of specific enzymes involved in the inflammatory response, such as cyclooxygenase-2 (COX-2). Furthermore, trans,trans-Farnesol impedes the growth of bacteria, viruses, and fungi, displaying anti-microbial properties. Its anti-cancer activity manifests through the induction of apoptosis in cancer cells. Lastly, trans,trans-Farnesol demonstrates the ability to modulate gene expression and acts as an antioxidant.


trans,trans-Farnesol (CAS 106-28-5) References

  1. Hydrolysis and isomerization of trans,trans-farnesyl diphosphate by Andrographis tissue-culture enzymes.  |  Mackie, H. and Overton, KH. 1977. Eur J Biochem. 77: 101-6. PMID: 198206
  2. Influences of trans-trans farnesol, a membrane-targeting sesquiterpenoid, on Streptococcus mutans physiology and survival within mixed-species oral biofilms.  |  Jeon, JG., et al. 2011. Int J Oral Sci. 3: 98-106. PMID: 21485314
  3. Study of trans-trans farnesol effect on hyphae formation by Yarrowia lipolytica.  |  Nunes, PM., et al. 2013. Bioprocess Biosyst Eng. 36: 1967-75. PMID: 23715764
  4. Assessment of the antioxidant and antiproliferative effects of sesquiterpenic compounds in in vitro Caco-2 cell models.  |  Vinholes, J., et al. 2014. Food Chem. 156: 204-11. PMID: 24629959
  5. Release behavior of trans,trans-farnesol entrapped in amorphous silica capsules.  |  Sousa, FL., et al. 2012. Results Pharma Sci. 2: 52-6. PMID: 25755994
  6. Effect of Trans, Trans-Farnesol on Pseudogymnoascus destructans and Several Closely Related Species.  |  Raudabaugh, DB. and Miller, AN. 2015. Mycopathologia. 180: 325-32. PMID: 26162644
  7. Purification and Characterization of a Novel NAD(P)+-Farnesol Dehydrogenase from Polygonum minus Leaves.  |  Ahmad-Sohdi, NA., et al. 2015. PLoS One. 10: e0143310. PMID: 26600471
  8. Trans, trans-farnesol as a mevalonate-derived inducer of murine 3T3-F442A pre-adipocyte differentiation.  |  Torabi, S. and Mo, H. 2016. Exp Biol Med (Maywood). 241: 493-500. PMID: 26660152
  9. Trans,trans-farnesol, an antimicrobial natural compound, improves glass ionomer cement properties.  |  de Castilho, ARF., et al. 2019. PLoS One. 14: e0220718. PMID: 31430298
  10. Purification, biochemical characterisation and bioinformatic analysis of recombinant farnesol dehydrogenase from Theobroma cacao.  |  Satyaveanthan, MV., et al. 2021. Plant Physiol Biochem. 161: 143-155. PMID: 33588320
  11. Antimicrobial, modulatory, and antibiofilm activity of tt-farnesol on bacterial and fungal strains of importance to human health.  |  Lopes, AP., et al. 2021. Bioorg Med Chem Lett. 47: 128192. PMID: 34118413
  12. Possible mechanisms involved in the neuroprotective effect of Trans,trans-farnesol on pilocarpine-induced seizures in mice.  |  Araújo Delmondes, G., et al. 2022. Chem Biol Interact. 365: 110059. PMID: 35931201
  13. Biosynthesis of trans, trans- and cis, trans-farnesols by soluble enzymes from tissue cultures of Andrographis paniculata.  |  Overton, KH. and Roberts, FM. 1974. Biochem J. 144: 585-92. PMID: 4468823
  14. Effects of farnesol on the thermotropic behavior of dimyristoylphosphatidylcholine.  |  Bondar, OP., et al. 1994. Chem Phys Lipids. 74: 93-8. PMID: 7820904
  15. Directed cell killing (apoptosis) in human lymphoblastoid cells incubated in the presence of farnesol: effect of phosphatidylcholine.  |  Haug, JS., et al. 1994. Biochim Biophys Acta. 1223: 133-40. PMID: 8061045

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

trans,trans-Farnesol, 1 g

sc-258277
1 g
$29.00