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Merck

87297

Tetrahexylammonium bromide

suitable for ion pair chromatography, LiChropur, ≥99.0% (AT)

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About This Item

Linear Formula:
[CH3(CH2)5]4N(Br)
CAS Number:
Molecular Weight:
434.58
UNSPSC Code:
23151817
NACRES:
NB.21
PubChem Substance ID:
EC Number:
224-363-1
Beilstein/REAXYS Number:
3637302
MDL number:
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description

cationic

Quality Level

assay

≥99.0% (AT)

form

crystals

quality

LiChropur

technique(s)

ion pair chromatography: suitable

mp

99-100 °C (lit.)

λ

10 % in methanol

UV absorption

λ: 240 nm Amax: 0.06, λ: 250 nm Amax: 0.04, λ: 260 nm Amax: 0.03, λ: 500 nm Amax: 0.03

suitability

corresponds to standard for filter test

SMILES string

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

InChI

1S/C24H52N.BrH/c1-5-9-13-17-21-25(22-18-14-10-6-2,23-19-15-11-7-3)24-20-16-12-8-4;/h5-24H2,1-4H3;1H/q+1;/p-1

InChI key

SYZCZDCAEVUSPM-UHFFFAOYSA-M

General description

The utilization of ion-pairing reagents as mobile phase additives allows the elution of ionic and highly polar substances using reversed phase HPLC columns. The purity of mobile phase additives is a prime factor to their successful application. Sigma-Aldrich offers an outstanding collection of tailor-made reagents for anionic (quaternary ammonium and phosphonium salts) and cationic (alkanesulfonates) analyzes. All mobile phase additives are rigorously tested with special emphasis on the requirements of modern reversed phase HPLC:

Other Notes

Discover LiChropur reagents ideal for HPLC or LC-MS analysis

Legal Information

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany


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Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves



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A M Lisi et al.
Journal of chromatography, 581(1), 57-63 (1992-10-02)
A simple and efficient procedure has been developed for the derivatization of diuretic agents in human urine by direct extractive alkylation and their detection by gas chromatography-mass spectrometry. The procedure is an improvement over previous extractive alkylation methods because of
Y Uyama et al.
Pflugers Archiv : European journal of physiology, 426(5), 363-370 (1994-03-01)
Effects of tetraalkylammonium ions, having tetraalkyl chains of increasing length from ethyl to octyl, on inositol-trisphosphate (InsP3)-induced Ca2+ release and contractile mechanics were examined in guinea-pig skinned ileal smooth muscle longitudinal strips. Although tetrahexylammonium ions (THexA) appeared to be the
L Zhang et al.
The Journal of pharmacology and experimental therapeutics, 288(3), 1192-1198 (1999-02-23)
Polyspecific organic cation transporters in epithelia play an important role in the elimination of many endogenous bioactive amines and therapeutically important drugs. Recently, the first human organic cation transporter (hOCT1) was cloned from liver. The purpose of the current study