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86857

Supelco

Tetrabutylammonium bromide

suitable for ion pair chromatography, LiChropur™, ≥99.0%

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About This Item

Linear Formula:
(CH3CH2CH2CH2)4N(Br)
CAS Number:
1643-19-2
Molecular Weight:
322.37
Beilstein:
3570983
EC Number:
216-699-2
MDL number:
MFCD00011633
UNSPSC Code:
12000000
PubChem Substance ID:
329769498
NACRES:
NB.21

description

cationic

Quality Level

100

Assay

≥99.0% (AT)
≥99.0%

form

crystals

quality

LiChropur™

technique(s)

ion pair chromatography: suitable

mp

102-106 °C (lit.)
102-106 °C

λ

10 % in H2O

UV absorption

λ: 240 nm Amax: 0.04
λ: 250 nm Amax: 0.03
λ: 260 nm Amax: 0.02
λ: 500 nm Amax: 0.02

suitability

corresponds to standard for filter test

SMILES string

[Br-].CCCC[N+](CCCC)(CCCC)CCCC

InChI

1S/C16H36N.BrH/c1-5-9-13-17(14-10-6-2,15-11-7-3)16-12-8-4;/h5-16H2,1-4H3;1H/q+1;/p-1

InChI key

JRMUNVKIHCOMHV-UHFFFAOYSA-M

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General description

Tetrabutylammonium bromide, a quaternary ammonium compound widely used as a phase transfer catalyst. TBAB decreases the retention time and removes peak tailing by acting as an ion pair reagent during the chromatographic analysis of quaternary ammonium compounds. In the molten state, TBAB behaves like an ionic liquid, which is a promising green alternative to organic solvents in polymer synthesis.

Application

TBAB may have been used as ion-pairing reagent in phase-transfer catalytic extraction and derivatization procedure during micropollutant determination from water samples using GC technique.

Legal Information

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

Pictograms

Health hazardExclamation mark
GHS08,GHS07

Signal Word

Warning

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Repr. 2 - Skin Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCK1981
BCCG5251
BCCD2226
BCBX5164
BCBR6209V

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Effect of analogue ions in normal-phase ion-pair chromatography of quaternary ammonium compounds.
Bluhm LH and Li T.
Journal of Chromatographic Science, 37.8, 273-276 (1999)
Interfacial chemistry behavior of phase transfer catalysis for hydroxide ion initiated reactions.
Xia L, et al.
Colloids and Surfaces. A, Physicochemical and Engineering Aspects, 317.1, 747-750 (2008)
Novel biobased polyurethanes synthesized from nontoxic phenolic diol containing l-tyrosine moiety under green media.
Mallakpour S, et al.
Journal of Polymers and the Environment, 18.4, 685-695 (2010)
Ion-pair single-drop microextraction versus phase-transfer catalytic extraction for the gas chromatographic determination of phenols as tosylated derivatives.
Fiamegos, Yiannis C., Ageliki-Panayota Kefala, and Constantine D. Stalikas.
Journal of Chromatography A, 1190.1, 44-51 (2008)
Direct polyamidation in molten tetrabutylammonium bromide: novel and efficient green media.
Mallakpour S and Yousefian H.
Polym. Bull., 60.2-3 , 191-198 (2008)
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