87306

Sigma-Aldrich

Tetrahexylammonium hydroxide solution

~40% in H2O (T)

Linear Formula:
[CH3(CH2)5]4N(OH)
CAS Number:
Molecular Weight:
371.68
Beilstein/REAXYS Number:
6019685
MDL number:
PubChem Substance ID:

concentration

~40% in H2O (T)

Quality Level

impurities

≤0.1% halides (as bromide)

anion traces

sulfate (SO42-): ≤1000 mg/kg

SMILES string

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

InChI

1S/C24H52N.H2O/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;1H2/q+1;/p-1

InChI key

JCJNUSDBRRKQPC-UHFFFAOYSA-M

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Application

Tetrahexylammonium hydroxide is a phase-transfer reagent that can be used:
  • To synthesize β-D-xyloside- and β-D-xylobioside-based ionic liquids containing tetrahexylammonium cation.
  • As an alkali-free gelling agent to prepare amorphous microporous silica-alumina.
  • To synthesize tetrahexylammonium prolinate, a promising candidate to prepare a solid supported ionic liquid phase (SILP) carbon dioxide absorber.

Packaging

25, 100 mL in glass bottle

Pictograms

Corrosion

Signal Word

Danger

Hazard Statements

Precautionary Statements

Personal Protective Equipment

dust mask type N95 (US),Eyeshields,Gloves

RIDADR

UN 3267 8 / PGII

WGK Germany

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificate of Analysis

Certificate of Origin

Mesoporous silica-aluminas as catalysts for the alkylation of aromatic hydrocarbons with olefins.
Perego C, et al.
Microporous and Mesoporous Materials : The Official Journal of the International Zeolite Association, 27(2-3), 345-354 (1999)
Detection of diuretic agents in doping control.
Ventura R and Segura J
Journal of Chromatography. B, Biomedical Sciences and Applications, 687(1), 127-144 (1996)
Preparation of new ?-D-xyloside-and ?-D-xylobioside-based ionic liquids through chemical and/or enzymatic reactions.
Gatard S, et al.
Carbohydrate Research, 451, 72-80 (2017)
CO 2 Capture technologies: Current status and new directions using supported ionic liquid phase (SILP) absorbers.
Kolding H, et al.
Science China: Chemistry, 55(8), 1648-1656 (2012)
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...

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