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About This Item
Linear Formula:
(CH3CH2CH2CH2)4N(OH) · 30H2O
CAS Number:
Molecular Weight:
799.93
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Beilstein/REAXYS Number:
3571228
Assay:
≥98.0% (T)
Concentration:
≤100%
Form:
crystals or chunks
Product Name
Tetrabutylammonium hydroxide 30-hydrate, ≥98.0% (T)
Quality Level
assay
≥98.0% (T)
form
crystals or chunks
reaction suitability
core: ammonium
concentration
≤100%
impurities
≤0.1% halides (as bromide)
mp
27-30 °C (lit.)
anion traces
sulfate (SO42-): ≤1000 mg/kg
functional group
amine
shipped in
wet ice
storage temp.
2-8°C
SMILES string
O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.[OH-].CCCC[N+](CCCC)(CCCC)CCCC
InChI
1S/C16H36N.31H2O/c1-5-9-13-17(14-10-6-2,15-11-7-3)16-12-8-4;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;/h5-16H2,1-4H3;31*1H2/q+1;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;/p-1
InChI key
DFGIRVKFXSRUOX-UHFFFAOYSA-M
General description
Tetrabutylammonium hydroxide 30-hydrate is commonly used as a strong base and phase-transfer catalyst in organic synthesis. Tetrabutylammonium hydroxide 30-hydrate (TBAH) dissolved in HPLC grade diethyl ether has been used to compose the solvent system in a study.
Application
Tetrabutylammoniumhydroxide 30-hydrate (TBAOH) can be used as:
- A catalyst in the hydroxyalkylation reaction of phenols with cyclic carbonates to synthesize aryl β-hydroxyethylethers.
- A base for the selective degradation of lignins to monomeric aromatics.
- A reactant to synthesize hydroxyfuroxan tetrabutylammonium salts by reacting with nitrofuroxans.
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Solid solutions of the rare earth (RE) cations Pr(3+), Nd(3+), Sm(3+), Gd(3+), Er(3+) and Yb(3+) in anatase TiO2 have been synthesized as mesoporous beads in the concentration range 0.1-0.3% of metal atoms. The solid solutions were have been characterized by
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 86866-100G | 04061835252923 |
| 86866-25G | 04061835252930 |
