Date published: 2025-10-31

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Tetrabutylammonium bromide (CAS 1643-19-2)

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Application:
Tetrabutylammonium bromide is used as a phase transfer catalyst
CAS Number:
1643-19-2
Purity:
≥98%
Molecular Weight:
322.37
Molecular Formula:
C16H36NBr
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Tetrabutylammonium bromide (TBAB) is a versatile organic compound extensively utilized as a reagent across various laboratory experiments. This compound consists of a tetrabutylammonium cation and a bromide anion, forming a quaternary ammonium salt. Exhibiting a white, crystalline powder form, Tetrabutylammonium bromide readily dissolves in organic solvents like ethanol and methanol while remaining insoluble in water. The applications of Tetrabutylammonium bromide span a wide range of scientific disciplines, including chromatography, spectroscopy, and organic synthesis. In organic synthesis, Tetrabutylammonium bromide serves as a catalyst, enabling diverse chemical reactions. Furthermore, it acts as a reagent for detecting metals in aqueous solutions and determining anions in aqueous solutions. Chromatographic techniques, such as high-performance liquid chromatography (HPLC), gas chromatography (GC), and thin-layer chromatography (TLC), also make use of Tetrabutylammonium bromide. Notably, Tetrabutylammonium bromide′s structure as a quaternary ammonium salt involves a positively charged nitrogen atom surrounded by four alkyl groups. This positive charge attracts the negatively charged bromide anion, resulting in the formation of an ionic bond. This ionic bond accounts for Tetrabutylammonium bromide′s solubility in organic solvents, contributing to its efficacy as a reagent.


Tetrabutylammonium bromide (CAS 1643-19-2) References

  1. Tetrabutylammonium bromide media aza-Michael addition of 1,2,3,6-tetrahydrophthalimide to symmetrical fumaric esters and acrylic esters under solvent-free conditions.  |  Imanzadeh, G., et al. 2010. Molecules. 15: 7353-62. PMID: 20966877
  2. Tetrabutylammonium bromide (TBABr)-based deep eutectic solvents (DESs) and their physical properties.  |  Yusof, R., et al. 2014. Molecules. 19: 8011-26. PMID: 24932572
  3. Carbonation of Epoxidized Methyl Soyates in Tetrabutylammonium Bromide-Based Deep Eutectic Solvents.  |  Liu, W. and Lu, G. 2018. J Oleo Sci. 67: 609-616. PMID: 29628488
  4. Tetrabutylammonium Bromide-Promoted Metal-Free, Efficient, Rapid, and Scalable Synthesis of N-Aryl Amines.  |  Johnson, CR., et al. 2018. ACS Omega. 3: 10886-10890. PMID: 30288459
  5. Effect of Tetrabutylammonium Bromide-Based Deep Eutectic Solvents on the Aqueous Solubility of Indomethacin at Various Temperatures: Measurement, Modeling, and Prediction with Three-Dimensional Hansen Solubility Parameters.  |  Mokhtarpour, M., et al. 2019. AAPS PharmSciTech. 20: 204. PMID: 31140011
  6. Extraction and ICP-OES determination of heavy metals using tetrabutylammonium bromide aqueous biphasic system and oleophilic collector.  |  Smirnova, SV., et al. 2021. Talanta. 221: 121485. PMID: 33076095
  7. Tetrabutylammonium Bromide (TBAB) Catalyzed Synthesis of Bioactive Heterocycles.  |  Banik, BK., et al. 2020. Molecules. 25: PMID: 33327504
  8. Binding of tetrabutylammonium bromide based deep eutectic solvent to DNA by spectroscopic analysis.  |  Yusof, R., et al. 2021. Spectrochim Acta A Mol Biomol Spectrosc. 253: 119543. PMID: 33636491
  9. Optimization study on deep extractive oxidative desulfurization with tetrabutylammonium bromide/polyethylene glycol DES.  |  Guo, Y., et al. 2021. RSC Adv. 11: 31727-31737. PMID: 35496838
  10. Deep Eutectic Solvents or Eutectic Mixtures? Characterization of Tetrabutylammonium Bromide and Nonanoic Acid Mixtures.  |  Shishov, A., et al. 2022. J Phys Chem B. 126: 3889-3896. PMID: 35608166
  11. Tetrabutylammonium bromide-based hydrophobic deep eutectic solvent for the extraction and separation of dihydromyricetin from vine tea and its inhibitory efficiency against xanthine oxidase.  |  Wang, L., et al. 2022. RSC Adv. 12: 28659-28676. PMID: 36320535
  12. Novel Antireflection Coatings Obtained by Low-Temperature Annealing in the Presence of Tetrabutylammonium Bromide and Gold Nanoparticles.  |  Lokteva, AA., et al. 2022. Materials (Basel). 15: PMID: 36363249
  13. Phase-Transfer-Catalyzed Alkylation of Hydantoins.  |  Keenan, T., et al. 2022. ACS Org Inorg Au. 2: 312-317. PMID: 36855589

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Tetrabutylammonium bromide, 25 g

sc-208427
25 g
$42.00

Tetrabutylammonium bromide, 100 g

sc-208427A
100 g
$63.00