Molecular structure of Tetrabutylammonium chloride hydrate, CAS Number: 37451-68-6
Tetrabutylammonium chloride hydrate (CAS 37451-68-6)
Alternate Names:
TBAC
CAS Number:
37451-68-6
Molecular Weight:
277.92
Molecular Formula:
C16H36ClN
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
QUICK LINKS
Ordering Information
Description
Technical Information
Safety Information
SDS & Certificate of Analysis
Tetrabutylammonium chloride hydrate is a quaternary ammonium salt that functions as a phase-transfer catalyst in organic synthesis. Its mechanism of action involves facilitating the transfer of a reactant from one phase to another, typically from an aqueous phase to an organic phase, by forming an ion pair with the reactant. This allows for reactions between substances that are normally immiscible, enabling the synthesis of various organic compounds. Tetrabutylammonium chloride hydrate acts by increasing the solubility of the reactants in the organic phase, thereby accelerating the reaction rate and improving yield. Its ability to promote phase transfer reactions may be useful in the development of new chemical compounds and materials.
Tetrabutylammonium chloride hydrate (CAS 37451-68-6) References
- Unexpected intermolecular pd-catalyzed cross-coupling reaction employing heteroaromatic carboxylic acids as coupling partners. | Forgione, P., et al. 2006. J Am Chem Soc. 128: 11350-1. PMID: 16939247
- Synthesis of chiral building blocks for use in drug discovery. | Marino, ST., et al. 2004. Molecules. 9: 405-26. PMID: 18007441
- Calcitriol derivatives with two different side chains at C-20. V. Potent inhibitors of mammary carcinogenesis and inducers of leukemia differentiation. | Maehr, H., et al. 2009. J Med Chem. 52: 5505-19. PMID: 19685888
- Poly[[aqua-μ(3)-picolinato-μ(2)-picolinato-dipicolinatopotassium(I)terbium(III)] 2.5-hydrate]. | Cunha-Silva, L., et al. 2008. Acta Crystallogr Sect E Struct Rep Online. 64: m529-30. PMID: 21201993
- Methoxy-derivatization of alkyl chains increases the in vivo efficacy of cationic Mn porphyrins. Synthesis, characterization, SOD-like activity, and SOD-deficient E. coli study of meta Mn(III) N-methoxyalkylpyridylporphyrins. | Tovmasyan, AG., et al. 2011. Dalton Trans. 40: 4111-21. PMID: 21384047
- Cytotoxic effects of Mn(III) N-alkylpyridylporphyrins in the presence of cellular reductant, ascorbate. | Ye, X., et al. 2011. Free Radic Res. 45: 1289-306. PMID: 21859376
- Palladium-Catalyzed Decarboxylative ortho-Amidation of Indole-3-carboxylic Acids with Isothiocyanates Using Carboxyl as a Deciduous Directing Group. | Tulichala, RNP., et al. 2018. J Org Chem. 83: 4375-4383. PMID: 29554415
- In Vitro Antiviral Activity of New Oxazoline Derivatives as Potent Poliovirus Inhibitors. | Madia, VN., et al. 2019. J Med Chem. 62: 798-810. PMID: 30512950
- Arabidopsis MATE45 antagonizes local abscisic acid signaling to mediate development and abiotic stress responses. | Kovinich, N., et al. 2018. Plant Direct. 2: e00087. PMID: 31245687
- Exchange Counterion in Polycationic Hydrogels: Tunability of Hydrophobicity, Water State, and Floating Capability for a Floating pH Device. | Danko, M., et al. 2021. Gels. 7: PMID: 34449591
- Modulating the pro-apoptotic activity of cytochrome c at a biomimetic electrified interface. | Gamero-Quijano, A., et al. 2021. Sci Adv. 7: eabg4119. PMID: 34739310
- The first crystalline hexagonal Si3N4 microtubes† | and Hubert Huppertz, Norbert Stock, Prof. Wolfgang Schnick. October 1996. Advanced Materials. Volume8, Issue10: Pages 844-847.
- Phase equilibrium of ionic semiclathrate hydrates formed with tetrabutylammonium bromide and tetrabutylammonium chloride | K Sato, H Tokutomi, R Ohmura - Fluid Phase Equilibria, 2013 - Elsevier. 15 January 2013,. Fluid Phase Equilibria. Volume 337,: Pages 115-118.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Tetrabutylammonium chloride hydrate, 5 g | sc-237012 | 5 g | $42.00 |