Date published: 2026-4-5

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Dodecane (CAS 112-40-3)

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Alternate Names:
n-Dodecane
Application:
Dodecane is a nonpolar organic solvent
CAS Number:
112-40-3
Molecular Weight:
170.33
Molecular Formula:
C12H26
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Dodecane is a hydrocarbon compound that functions as a solvent in various experimental applications. It has a non-polar nature, allowing it to dissolve non-polar compounds and separate them from polar substances. Dodecane is used to extract and isolate specific compounds from mixtures, aiding in the purification and analysis of various substances. Its mechanism of action involves forming a layer on the surface of the mixture, effectively separating the non-polar compounds from the rest of the solution. This allows for the extraction of the desired compounds, contributing to the process of chemical analysis and synthesis. Dodecane′s ability to selectively dissolve non-polar substances for the separation and purification of compounds without altering their chemical properties.


Dodecane (CAS 112-40-3) References

  1. Effect of n-dodecane on Crypthecodinium cohnii fermentations and DHA production.  |  da Silva, TL., et al. 2006. J Ind Microbiol Biotechnol. 33: 408-16. PMID: 16501933
  2. Hydroconversion of n-dodecane over nanoporous catalysts.  |  Park, YK., et al. 2013. J Nanosci Nanotechnol. 13: 714-7. PMID: 23646804
  3. Hydroisomerization of n-dodecane over Pt/Al-MCM-48 catalysts.  |  Yun, S., et al. 2014. J Nanosci Nanotechnol. 14: 3112-6. PMID: 24734743
  4. Sub-CMC solubilization of dodecane by rhamnolipid in saturated porous media.  |  Zhong, H., et al. 2016. Sci Rep. 6: 33266. PMID: 27619361
  5. High-NOx Photooxidation of n-Dodecane: Temperature Dependence of SOA Formation.  |  Lamkaddam, H., et al. 2017. Environ Sci Technol. 51: 192-201. PMID: 27966908
  6. RIFM fragrance ingredient safety assessment, dodecane, CAS Registry Number 112-40-3.  |  Api, AM., et al. 2020. Food Chem Toxicol. 146 Suppl 1: 111759. PMID: 32966876
  7. Permanganometric Titration for the Quantification of Purified Bis(2,4,4-trimethylpentyl)dithiophosphinic Acid in n-Dodecane.  |  Bessen, NP., et al. 2021. ACS Omega. 6: 8463-8468. PMID: 33817507
  8. Degradation of the mixed organic solvents of tributyl phosphate and n-dodecane by heterogeneous Fenton-like oxidation using nanoscale zero-valent iron as the catalyst.  |  Yang, X., et al. 2022. Chemosphere. 292: 133449. PMID: 34973247
  9. A non-destructive dielectric based approach for the rapid determination of tributyl phosphate in dodecane.  |  Ananthanarayanan, R., et al. 2022. Rev Sci Instrum. 93: 014102. PMID: 35104986
  10. Endothermic Cracking of n-Dodecane in a Flow Reactor using Washcoated Activated Carbon on Metal Foam.  |  Mun, J., et al. 2022. ACS Omega. 7: 8518-8525. PMID: 35309429
  11. Catalytic Cracking of n-Dodecane to Chemicals: Effect of Variable-Morphological ZSM-5 Zeolites Synthesized Using Various Silica Sources.  |  Sanhoob, MA., et al. 2022. ACS Omega. 7: 10317-10329. PMID: 35382321
  12. Removal of single and dual ring thiophene's from dodecane using cavitation based processes.  |  Delaney, P., et al. 2022. Ultrason Sonochem. 89: 106148. PMID: 36063788
  13. Steam Catalytic Cracking of n-Dodecane to Light Olefins over Phosphorous- and Metal-Modified Nanozeolite Y.  |  Al-Shafei, EN., et al. 2022. ACS Omega. 7: 30807-30815. PMID: 36092580
  14. Thermal desorption mechanism of n-dodecane on unsaturated clay: Experimental study and molecular dynamics simulation.  |  Chen, Z., et al. 2023. Environ Pollut. 323: 121228. PMID: 36773689

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Dodecane, 100 ml

sc-397811
100 ml
$81.00