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About This Item
Linear Formula:
(C2H5)4N(Br)
CAS Number:
Molecular Weight:
210.16
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352107
EC Number:
200-769-4
MDL number:
Beilstein/REAXYS Number:
3563430
Assay:
98%
Grade:
reagent grade
Bp:
>310 °C/979.1 hPa
Vapor pressure:
<1 hPa
Product Name
Tetraethylammonium bromide, reagent grade, 98%
grade
reagent grade
Quality Segment
vapor pressure
<1 hPa
assay
98%
form
crystalline
reaction suitability
core: ammonium
greener alternative product characteristics
Catalysis
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sustainability
Greener Alternative Product
dilution
(for analytical testing)
impurities
≤2% triethylamine hydrobromide
pH
6.5 (100 g/L)
bp
>310 °C/979.1 hPa
mp
285 °C (dec.) (lit.)
greener alternative category
SMILES string
[Br-].CC[N+](CC)(CC)CC
InChI
1S/C8H20N.BrH/c1-5-9(6-2,7-3)8-4;/h5-8H2,1-4H3;1H/q+1;/p-1
InChI key
HWCKGOZZJDHMNC-UHFFFAOYSA-M
General description
We are committed to bringing you Greener Alternative Products, which adhere to one of the four categories of Greener Alternatives. This supporting electrolyte is used in electrochemical reactions, enabling efficient ionic conductivity and stability, offering a greener, potentially more sustainable option for electrochemical applications. Click here for more information.
Application
Tetraethylammonium bromide may be used:
- As an organic template for synthesizing zeolite beta via hydrothermal crystallization.
- As a catalyst for the oxidative coupling of aldehydes or alcohols with thiophenols or disulfides to form thioesters.
- In combination with o-iodoxybenzoic acid (IBX) for the oxidative dehomologation of primary carboxamides to nitriles and α,α-disubstituted acetamides to ketones. This reagent combination can also be used for the conversion of sulfides to sulfoxides and N,N-disubstituted glycylamides into corresponding cyanamides.
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hcodes
pcodes
Hazard Classifications
Aquatic Chronic 3
Storage Class
11 - Combustible Solids
flash_point_f
361.4 °F - closed cup
flash_point_c
183 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
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