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Tetrahexylammonium hydrogensulfate

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

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5 G
$273.00
25 G
$1,020.00

About This Item

Linear Formula:
[CH3(CH2)5]4N(HSO4)
CAS Number:
Molecular Weight:
451.75
Beilstein/REAXYS Number:
4629729
EC Number:
MDL number:
UNSPSC Code:
23151817
PubChem Substance ID:
NACRES:
NB.21

$273.00


Available to ship onMay 01, 2025Details


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description

cationic

Quality Level

assay

≥99.0% (T)

form

crystals

quality

LiChropur

technique(s)

ion pair chromatography: suitable

mp

98-100 °C (lit.)
99-102 °C

λ

10 % in acetonitrile

UV absorption

λ: 210 nm Amax: 0.10
λ: 220 nm Amax: 0.04
λ: 230 nm Amax: 0.03
λ: 260 nm Amax: 0.02
λ: 500 nm Amax: 0.02

suitability

corresponds to standard for RP gradient test
corresponds to standard for filter test

SMILES string

OS([O-])(=O)=O.CCCCCC[N+](CCCCCC)(CCCCCC)CCCCCC

InChI

1S/C24H52N.H2O4S/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;1-5(2,3)4/h5-24H2,1-4H3;(H2,1,2,3,4)/q+1;/p-1

InChI key

RULHPTADXJPDSN-UHFFFAOYSA-M

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General description

Tetrahexylammonium hydrogensulfate is a quaternary ammonium salt mainly used as an electrolyte.

Application

Tetrahexylammonium hydrogensulfate may have been used as a phase-transfer catalyst during catalysis analysis of benzylic halide to carboxylic acid.[1]

Legal Information

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Selective phase transfer and palladium (0)-catalyzed carbonylation, carbalkoxylation, and reduction reactions.
Alper, Howard, Khaled Hashem, and Josef Heveling.
Organometallics, 1.6, 775-778 (1982)
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
Huiyu Zhou et al.
Journal of pharmaceutical sciences, 91(6), 1502-1511 (2002-07-13)
Inhalation therapy for infectious lung diseases, such as tuberculosis, is currently being explored, with microspheres being used to target alveolar macrophages. One method of drug encapsulation into polymeric microspheres to form hydrophobic ion-paired (HIP) complexes, and then coprecipitate the complex
L G Sayers et al.
Biochimica et biophysica acta, 1152(1), 177-183 (1993-10-10)
In this study we show that the potassium-channel blocker tetrahexyl ammonium chloride (THA+) is able to inhibit inositol 1,4,5-trisphosphate (InsP3)-induced calcium release in an apparently biphasic fashion with a IC50 of 3 microM. This inhibition was not alleviated by valinomycin
Y C Ho et al.
Digestive diseases and sciences, 33(4), 435-442 (1988-04-01)
Our purpose is to develop a standard method for preparing the bile for beta-glucuronidase determination by removal of bile acids and conjugated bilirubin which interfere with its activity. The bile acids and conjugated bilirubin in their purified solutions and in

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