Tetrabutylammonium bromide
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IUPAC name
Tetra-n-butylammonium bromide
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Other names
TBAB
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Identifiers | |
3D model (JSmol)
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ChEBI | |
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.015.182 |
EC Number |
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PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
C16H36BrN | |
Molar mass | 322.368 g/mol |
Appearance | White solid |
Melting point | 103 °C (217 °F; 376 K) Decomposes at 133C[1] |
Hazards | |
Occupational safety and health (OHS/OSH): | |
Main hazards
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Harmful |
GHS labelling: | |
Warning | |
H302, H315, H319, H335, H411, H412 | |
P261, P264, P270, P271, P273, P280, P301+P312, P302+P352, P304+P340, P305+P351+P338, P312, P321, P330, P332+P313, P337+P313, P362, P391, P403+P233, P405, P501 | |
Related compounds | |
Other anions
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Tetrabutylammonium tribromide, Tetra-n-butylammonium fluoride, Tetra-n-butylammonium chloride, Tetra-n-butylammonium iodide, Tetrabutylammonium hydroxide |
Other cations
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Tetramethylammonium bromide, Tetraethylammonium bromide |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Tetra-n-butylammonium bromide (TBAB) is a quaternary ammonium salt with a bromide counterion commonly used as a phase transfer catalyst.[2] It is used to prepare many other tetrabutylammonium salts via salt metathesis reactions.
See also
- Tetrabutylammonium tribromide, with an additional Br2 unit
- Tetrabutylammonium fluoride
- Tetrabutylammonium hydroxide
References
- ^ Applied Catalysis A: General 241 (2003) 227–233
- ^ Henry J. Ledon (1988). "Diazo transfer by means of phase-transfer catalysis: di-tert-butyl diazomalonate". Organic Syntheses; Collected Volumes, vol. 6, p. 414.