 
                        Product Details
| Product Name: Triethanolamine borate | CAS No.: 283-56-7 | 
| EC-No.: 206-003-5 | Min. Order: 1kg | 
| Purity: 95.1% | Supply Ability: 1000kg | 
| Release date: 2025/10/31 | 
Triethanolamine borate is a chemical compound formed by the reaction of triethanolamine (a tertiary amine) with boric acid. It is a coordination complex or ester where boron interacts with the hydroxyl groups of triethanolamine, creating a stable compound with unique properties. Below is a detailed overview:
Structure and Synthesis
- Chemical Structure: 
- Triethanolamine (TEA): N(CH2CH2OH)3, a viscous liquid with three ethanol groups attached to a central nitrogen atom. - Borate: Derived from boric acid (H3BO3), boron forms a tetrahedral complex with the hydroxyl groups of TEA. - The resulting compound is a borate ester or coordination complex, often represented as or [B(OCH2CH2)3N]. 
- Synthesis: 
 Produced by mixing triethanolamine and boric acid under mild heating. The reaction involves esterification or Lewis acid-base interactions, where boron (a Lewis acid) binds to the oxygen atoms of TEA’s hydroxyl groups.
Key Properties
Physical State: Typically a clear, viscous liquid or hygroscopic solid.
Solubility: Water-soluble due to polar hydroxyl groups; miscible with many organic solvents.
Stability: Stable under moderate pH and temperature, but may hydrolyze in strongly acidic or alkaline conditions.
pH Buffering: Acts as a buffer in solutions, maintaining pH stability.
Applications
Personal Care Products:
- Used in cosmetics (e.g., creams, lotions) as a pH adjuster, emulsifier, or viscosity modifier. 
- Found in eye drops and contact lens solutions for its mild buffering capacity. - Industrial Uses: 
- Corrosion Inhibition: Protects metal surfaces in cooling systems or lubricants. 
- Polymer Chemistry: Serves as a crosslinker in borate-based gels (e.g., fracturing fluids in oil drilling). 
- Adhesives: Enhances bonding strength in water-based adhesives. - Laboratory Reagent: 
- Used as a boron source or buffer in biochemical assays. - Antifreeze Additive: 
- Occasionally added to antifreeze mixtures for its stabilizing properties. 
Safety and Handling
- Toxicity: Generally low toxicity, but prolonged exposure may cause skin/eye irritation. 
- Environmental Impact: Boron compounds can be toxic to aquatic life at high concentrations. 
- Precautions: Use gloves and goggles; avoid inhalation. Dispose of according to local regulations. 
Differentiation from Similar Compounds
- Unlike simple borate salts (e.g., sodium borate), triethanolamine borate has organic components that enhance solubility and reduce corrosiveness. 
- Compared to other amine borates, TEA borate offers better compatibility with aqueous and organic systems. 
Example Uses
- Oil Industry: Crosslinks guar gum in hydraulic fracturing fluids to create viscous gels. 
- Cosmetics: Stabilizes emulsions in moisturizers. 
- Pharmaceuticals: Buffers ophthalmic solutions. 
This compound bridges organic and inorganic chemistry, offering versatility in industrial, cosmetic, and biomedical applications due to its dual functionality as a buffer and crosslinking agent.



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| $4.00/1000KG | VIP8Y | Career Henan Chemical Co | 2018-08-04 | 
- Since: 2006-04-03
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