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Merck
모든 사진(1)

문서

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:
Molecular Weight:
322.37
Beilstein:
3570983
EC Number:
MDL number:
UNSPSC 코드:
12000000
PubChem Substance ID:
NACRES:
NB.21

설명

cationic

Quality Level

분석

≥99.0% (AT)
≥99.0%

형태

crystals

품질

LiChropur

기술

ion pair chromatography: suitable

mp

102-106 °C (lit.)
102-106 °C

λ

10 % in H2O

UV 흡수

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

적합성

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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일반 설명

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.

애플리케이션

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.

법적 정보

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

픽토그램

Health hazardExclamation mark

신호어

Warning

유해 및 위험 성명서

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

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves


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시험 성적서(COA)

Lot/Batch Number

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문서 라이브러리 방문

Direct polyamidation in molten tetrabutylammonium bromide: novel and efficient green media.
Mallakpour S and Yousefian H.
Polym. Bull., 60.2-3 , 191-198 (2008)
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)
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)
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)
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)

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