Tetrabutylammonium Hydroxide (10% in Methanol) TCI T0717

Chemical Identity

Other names: TBAOH
CAS No.: 2052-49-5
PubChem: CID 2723671·SID 87576581
Formula: C16H37NO
Molecular weight: 259.47 g/mol
Reference databases: ChemSpider·ECHA·Wikipedia

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: tetrabutylazanium hydroxide
SMILES: CCCC[N+](CCCC)(CCCC)CCCC.[OH-]
InChIKey: VDZOOKBUILJEDG-UHFFFAOYSA-M

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Tetrabutylammonium Hydroxide (TBAH) is a chemical compound widely used in various synthetic chemical reactions. It is a liquid reagent available in a 10% solution in methanol, making it highly convenient for laboratory use. TBAH serves as a strong base in chemical reactions, particularly in ion separation processes and reactions requiring a basic environment. Its versatility allows it to be employed in substitution reactions, deprotonation, and the synthesis of complex organic compounds.

The properties that make TBAH a preferred choice include its high stability and strong basicity without significant decomposition. It acts as an effective organic base, maintaining its integrity under various reaction conditions. Additionally, TBAH is non-toxic and free from heavy metals, enhancing its safety profile in laboratory settings. The presence of methanol as a solvent simplifies mixing and application across different experimental setups.

In Indonesian laboratories, TBAH is extensively used in chemical research and industrial applications. It is commonly found in academic and industrial settings where precise and stable base reagents are required. Its reliability and safety make it a favored choice for both researchers and professionals working in the chemical industry.

TCI brochures (PDF)

Quaternary Ammonium Salts 2025-11-10 · p. 2
Colloidal Quantum Dot (QD) Research Reagents 2026-05-21 · p. 10

Related TCI products

Ion separation processes benefit from TBAH’s strong basicity and stability, enabling efficient extraction and purification of ions in solution.
Organic synthesis reactions often utilize TBAH due to its ability to act as a non-nucleophilic base, preventing unwanted side reactions during complex molecule formation.
Deprotonation reactions in synthetic chemistry rely on TBAH’s effectiveness in removing protons from organic compounds, facilitating reaction pathways.
Analytical chemistry applications use TBAH as a reagent for pH control and buffer preparation, ensuring accurate and reproducible results.
Environmental testing in laboratories employs TBAH for neutralizing acidic samples, aiding in the analysis of water and soil samples.

Brand	TCI
CAS number	2052-49-5
Molecular formula	—
Purity	—
Category	Chemistry > Synthetic Reagents > Acids, Bases [Synthetic Reagents]
Pack sizes	10% in methanol solution
Physical form	Liquid solution in methanol
Storage	—

Tetrabutylammonium Hydroxide should be stored in a cool, dry place away from direct sunlight and incompatible materials. It is recommended to use airtight containers made of glass or polyethylene to prevent contamination and evaporation. Since it is a liquid solution, it should be kept in a well-ventilated area to avoid exposure to fumes. Proper labeling of containers is essential for safe handling. Laboratory personnel should wear appropriate personal protective equipment, including gloves and safety goggles, when handling this reagent. Regular inspection of storage conditions ensures the reagent remains stable and safe for use in experimental procedures.

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