Choline hydroxide solution, >97%, 15 wt% in water
Price range: $82.08 through $954.85
Product Code: KI-0058-HPCAS NO: 123-41-1
- Chemical Formula: C5H15NO2
- Synonyms: Chol OH, N,N,N-trimethyl-N-(2-hydroxyethyl)ammonium hydroxide, 1,1,1-trimethyl-1-(2-hydroxyethyl)ammonium hydroxide
- Hydrophilic
**This product will incur a $97.00 HazMat fee when the order is placed.**
SUM Formula: C5H15NO2
Molecular Weight: 121.18
Purity: >97%
- SUM Formula: C5H15NO2
- Molecular Weight: 121.18
Choline hydroxide solution, CAS: 123-41-1
Key Applications:
1. Hydrogen Production and Related Catalysis
- Baseโcatalyzed hydrogen generation
Supports alcohol reforming, ammonia borane hydrolysis, and other hydrogenโrelease reactions where strong, nonโvolatile bases accelerate dehydrogenation.
- Transesterification and biodiesel synthesis
Functions as a greener alternative to sodium or potassium hydroxide, reducing soap formation and simplifying downstream purification.
- Phaseโtransfer and organocatalysis
The hydroxide anion paired with a biocompatible cation enables selective CโC and CโO bondโforming reactions under mild conditions.
2. COโ Capture and Adsorption
- Aqueous COโ absorption
Reacts with COโ to form bicarbonate and carbonate species, enabling reversible COโ uptake in mild, lowโtemperature conditions.
- Hybrid ILโamine sorbent systems
Serves as a tunable alkaline component in ionicโliquidโbased COโ capture formulations, improving absorption kinetics and reducing volatility.
- Regenerable sorbent media
Supports cyclic COโ captureโrelease processes due to its stability and low vapor pressure.
3. Biomass Processing and Green Chemistry
- Lignocellulosic deconstruction
Breaks ester and ether linkages in lignin and hemicellulose, improving sugar release for biofuel production.
- Cellulose dissolution and derivatization
Facilitates swelling, activation, and functionalization of cellulose under milder conditions than inorganic bases.
4. Polymer and Materials Applications
- Polymerization catalyst
Useful in ringโopening polymerizations and curing reactions requiring strong, nonโnucleophilic bases.
- Surface modification
Employed in etching, activation, and functionalization of silica, metal oxides, and polymer surfaces.
5. Electronics and Microfabrication
- Photoresist stripping and cleaning
Provides controlled alkalinity for removing organic residues without the corrosivity of stronger mineral bases.
- Developer solutions
Used in certain lithographic processes where lowโvolatility, aqueous alkaline developers are preferred.
6. General Synthetic and Analytical Uses
- pH control and buffering in alkaline media
Offers stable, lowโvolatility alkalinity for reactions sensitive to inorganic salts.
- Quaternary ammonium precursor
Acts as a building block for synthesizing cholineโderived ionic liquids and functional salts.
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