Date published: 2026-4-5

1-800-457-3801

SCBT Portrait Logo
Seach Input

1-Bromododecane (CAS 143-15-7)

0.0(0)
Write a reviewAsk a question

Alternate Names:
Dodecyl bromide; Lauryl bromide
CAS Number:
143-15-7
Molecular Weight:
249.23
Molecular Formula:
CH3(CH2)11Br
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

1-Bromododecane is a long-chain alkyl bromide that functions as an alkylating agent in organic synthesis. It participates in nucleophilic substitution reactions, where the bromine atom is replaced by a nucleophile, leading to the formation of new carbon-carbon or carbon-heteroatom bonds. 1-Bromododecane serves as an electrophile, reacting with various nucleophiles such as amines, thiols, and enolates to introduce the dodecyl group into organic molecules. 1-Bromododecane′s mechanism of action involves the displacement of the bromine atom by a nucleophile, resulting in the formation of a new covalent bond and the incorporation of the dodecyl group into the target molecule.


1-Bromododecane (CAS 143-15-7) References

  1. Catalysis by hydrophobically modified poly(propylenimine) dendrimers having quaternary ammonium and tertiary amine functionality.  |  Murugan, E., et al. 2004. Langmuir. 20: 8307-12. PMID: 15350107
  2. Effects of hydrogen peroxide and hypochlorite on membrane potential of mitochondria in situ in rat heart cells.  |  Konno, N. and Kako, KJ. 1991. Can J Physiol Pharmacol. 69: 1705-12. PMID: 1666537
  3. Synthesis of surfactants based on pentaerythritol. I. Cationic and zwitterionic gemini surfactants.  |  Jahan, N., et al. 2009. J Org Chem. 74: 7762-73. PMID: 19757818
  4. Successful stabilization of functionalized hybrid graphene for high-performance antimicrobial activity.  |  Nam, JA., et al. 2013. Acta Biomater. 9: 7996-8003. PMID: 23602878
  5. Solution properties and electrospinning of phosphonium gemini surfactants.  |  Hemp, ST., et al. 2014. Soft Matter. 10: 3970-7. PMID: 24733359
  6. Synthesis and selected transformations of 2-unsubstituted 1-(adamantyloxy)imidazole 3-oxides: straightforward access to non-symmetric 1,3-dialkoxyimidazolium salts.  |  Mlostoń, G., et al. 2019. Beilstein J Org Chem. 15: 497-505. PMID: 30873233
  7. Adverse Effect of PTFE Stir Bars on the Covalent Functionalization of Carbon and Boron Nitride Nanotubes Using Billups-Birch Reduction Conditions.  |  de Los Reyes, CA., et al. 2019. ACS Omega. 4: 5098-5106. PMID: 31459687
  8. Antimicrobial Nanogels with Nanoinjection Capabilities for Delivery of the Hydrophobic Antibacterial Agent Triclosan.  |  Zu, G., et al. 2020. ACS Appl Polym Mater. 2: 5779-5789. PMID: 33345194
  9. Self-Assembly Nanoparticles of Natural Bioactive Abietane Diterpenes.  |  Ntungwe, E., et al. 2021. Int J Mol Sci. 22: PMID: 34638551
  10. Aliphatic Quaternary Ammonium Functionalized Nanogels for Gene Delivery.  |  Zhang, H., et al. 2021. Pharmaceutics. 13: PMID: 34834380
  11. Covalent organic nanospheres as a fiber coating for solid-phase microextraction of genotoxic impurities followed by analysis using GC-MS.  |  Zhao, Y., et al. 2022. J Pharm Anal. 12: 583-589. PMID: 36105168
  12. Novel dental resin infiltrant containing smart monomer dodecylmethylaminoethyl methacrylate.  |  Huang, X., et al. 2022. Front Cell Infect Microbiol. 12: 1063143. PMID: 36519132
  13. Synthesis and Characterization of Furan-Based Non-Ionic Surfactants (fbnios).  |  Liu, D., et al. 2023. Langmuir. 39: 8974-8983. PMID: 37341578
  14. Synthesis of (-)-muricatacin.  |  Makabe, H., et al. 1993. Biosci Biotechnol Biochem. 57: 1028-9. PMID: 7763871

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

1-Bromododecane, 250 ml

sc-237496
250 ml
$56.00

1-Bromododecane, 1 L

sc-237496A
1 L
$120.00