Tetraethylammonium bromide, 98%
Tetraethylammonium bromide, 98%
Tetraethylammonium bromide, 98%
Tetraethylammonium bromide, 98%
Thermo Scientific Chemicals

Tetraethylammonium bromide, 98%

CAS: 71-91-0 | C8H20BrN | 210.159 g/mol
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Catalog NumberQuantity
ALFA13835.30250 g
Catalog number ALFA13835.30
Price (MYR)
450.00
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250 g
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Price (MYR)
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Specifications
Chemical Name or MaterialTetraethylammonium bromide
CAS71-91-0
Health Hazard 1Warning
Health Hazard 2GHS H Statement
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
Health Hazard 3GHS P Statement
P261-P280-P305+P351+P338-P304+P340-P405-P501a
Avoid breathing dust/fume/gas/mist/vapors/spray.
Wear protective gloves/protective clothing/eye protection/face protection.
IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.
IF INHALED: Remove to fresh air and keep at rest in a position comfortable for breathing.
Store locked up.
Dispose of contents/container in accordance with local/regional/national/international regulations.
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Tetraethylammonium bromide is used as a phase transfer catalyst. It acts as a source of tetraethylammonium ions in pharmacological and physiological studies. It is also employed in organic chemical synthesis. It plays a major role in the preparation of tetraethylammonium superoxide from potassium superoxide for the conversion of primary alkyl halides to dialkyl peroxides. Furthermore, It is utilized as a catalyst in the oxidation of organic sulfide to sulfoxide using o-iodoxybenzoic acid.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Tetraethylammonium bromide is used as a phase transfer catalyst. It acts as a source of tetraethylammonium ions in pharmacological and physiological studies. It is also employed in organic chemical synthesis. It plays a major role in the preparation of tetraethylammonium superoxide from potassium superoxide for the conversion of primary alkyl halides to dialkyl peroxides. Furthermore, It is utilized as a catalyst in the oxidation of organic sulfide to sulfoxide using o-iodoxybenzoic acid.

Solubility
Soluble in water.

Notes
Hygroscopic. Incompatible with strong oxidizing agents and bases.
RUO – Research Use Only

General References:

  1. Phase-transfer catalyst; see Appendix 2.
  2. For use in combination with anhydrous HBr as a reagent for selective monohydrobromination of an alkyne, see: Org. Synth., 76, 263 (1998).
  3. Takemoto, K.; Yamada, H. Development of rechargeable lithium-bromine batteries with lithium ion conducting solid electrolyte. J. Power Sources 2015, 281, 334-340.
  4. Abdel-Rahman, L. H.; El-Khatib, R. M.; Nassr, L. A.; Abu-Dief, A. M. Salts and Structural Effects on the base Catalyzed Hydrolysis of some Novel and Pharmacologically Active Iron(II) Azomethine Amino Acid Complexes. Int. J. Nano. Chem. 2015, 1 (1), 25-30.