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Sigma-Aldrich

Tetrahexylammonium hydroxide solution

~40% in H2O (T)

Synonym(s):

Tetra(n-hexyl)ammonium hydroxide

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About This Item

Linear Formula:
[CH3(CH2)5]4N(OH)
CAS Number:
Molecular Weight:
371.68
Beilstein:
6019685
MDL number:
UNSPSC Code:
12352106
PubChem Substance ID:
NACRES:
NA.22

form

solution

Quality Level

concentration

~40% in H2O (T)

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.

Pictograms

Corrosion

Signal Word

Danger

Hazard Statements

Precautionary Statements

Hazard Classifications

Skin Corr. 1B

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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)
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)
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)
N Surendran et al.
Journal of chromatography. B, Biomedical sciences and applications, 691(2), 305-312 (1997-04-11)
The objective of this research was to develop a rapid, sensitive and reliable method for the separation of phosphonodipeptide prodrugs and parent compounds to facilitate the evaluation of cell permeation using in vitro cell culture models. Separation was accomplished isocratically

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