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87299

Tetrahexylammonium hydrogensulfate

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

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About This Item

Linear Formula:
[CH3(CH2)5]4N(HSO4)
CAS Number:
32503-34-7
Molecular Weight:
451.75
UNSPSC Code:
23151817
NACRES:
NB.21
PubChem Substance ID:
329769575
EC Number:
251-069-0
Beilstein/REAXYS Number:
4629729
MDL number:
MFCD00037675
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description

cationic

Quality Level

100

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.

Legal Information

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCN2160
BCCN5276
BCCK8705
BCCB1158
BCCJ6422

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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)
Zeynep S Teksin et al.
Journal of controlled release : official journal of the Controlled Release Society, 116(1), 50-57 (2006-10-20)
Parallel Artificial Membrane Permeability Assay (PAMPA) is a method to screen drug candidates for membrane permeability. The objective was to characterize the transport of a model weak base, metoprolol, across a three lipid-component PAMPA system (denoted A-PAMPA, for anionic-PAMPA) and
The effects of tetrahexylammonium chloride on calcium mobilization from cerebellar microsomes.
L G Sayers et al.
Biochemical Society transactions, 21(2), 105S-105S (1993-05-01)
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
Xuemei Wang et al.
Journal of biomedical materials research. Part A, 80(4), 852-860 (2006-10-31)
Although much effort has been extended to the efficient cancer therapies, the drug resistance is still a major obstacle in cancer chemotherapeutic treatments. Almost 90% of the cancer therapy failure is caused by the relative problems. Recently, the application of
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Global Trade Item Number

SKUGTIN
87299-5G-F04061835570935
87299-25G-F04061835517596

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