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HS Code |
920172 |
| Chemicalname | Trimethyl Borate |
| Casnumber | 121-43-7 |
| Molecularformula | B(OCH3)3 |
| Molarmass | 103.93 g/mol |
| Appearance | Colorless liquid |
| Odor | Mild, alcohol-like |
| Density | 0.935 g/cm³ |
| Boilingpoint | 68.7 °C |
| Meltingpoint | -34.6 °C |
| Solubilityinwater | Reacts with water |
| Flashpoint | 11 °C (closed cup) |
| Refractiveindex | 1.369 at 20 °C |
| Vaporpressure | 108 mmHg (20 °C) |
As an accredited Trimethyl Borate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Trimethyl Borate is packaged in a 500 mL amber glass bottle with a secure screw cap and labeled with hazard warnings. |
| Shipping | Trimethyl Borate should be shipped in tightly sealed containers, away from moisture and sources of ignition, as it is highly flammable. It must be handled as a hazardous material under proper labeling and transport regulations (UN 1993, Class 3). Store and ship in cool, well-ventilated areas, following all relevant safety guidelines. |
| Storage | Trimethyl borate should be stored in a cool, dry, and well-ventilated area, away from heat, sparks, open flames, and incompatible substances such as strong oxidizers and moisture. Keep the container tightly closed and properly labeled. Use approved safety containers and store in a flammable liquids cabinet. Protect from direct sunlight and static discharge to prevent fire or explosion hazards. |
Applications of Trimethyl Borate in Industrial ManufacturingAs the direct manufacturer of Trimethyl Borate, we supply this compound to specialized sectors where it fulfills precise roles throughout various production processes. Below, we outline real-world downstream applications in which Trimethyl Borate contributes unique value, describing compliance requirements, working concentrations, process integration points, and actual finished goods. 1. Boron-Based Optical Glass ProductionSpecialty glassmakers use Trimethyl Borate to introduce boron oxide into the glass matrix during the melt process. Its high purity supports optical clarity and thermal shock resistance for advanced glass types, including borosilicate and high refractive index glasses. By using it as a boron source, manufacturers achieve precise control over final optical and mechanical properties essential for laboratory, photonics, and instrument glass. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Catalyst Synthesis for Olefin PolymerizationChemical producers employ Trimethyl Borate in the synthesis of boron-containing co-catalysts for olefin and diene polymerization. It functions as a methylating agent or boron precursor during the preparation of metallocene and Ziegler-Natta catalysts, enabling controlled catalyst morphology and activity. This improves polymer attributes like melt index, transparency, and toughness in finished product lines. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Flame Retardant Additive SynthesisFormulators of flame-retardant chemicals use Trimethyl Borate as a boron-donor in reactions that yield borate esters and other organoboron compounds. These intermediates serve in the compounding of halogen-free flame retardants for thermoplastics, coatings, and insulation foams. The resulting additives offer thermal stability and low-smoke performance for electronics and construction systems. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Boron Source in Sintered Advanced CeramicsSintered materials manufacturers use Trimethyl Borate as a boron feedstock in the preparation of boron carbide and boron nitride ceramics. It is favored for its clean volatility and minimal residual impurities during high-temperature processing. This supports controlled grain growth and improved densification, which are crucial in producing high-hardness, wear-resistant components for defense, tooling, and electronics sectors. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
5. Reagent in Organic Synthesis of Boronic EstersPharmaceutical and agrochemical manufacturers use Trimethyl Borate in a key reagent role for the preparation of aryl boronic esters and acids. It reacts with Grignard reagents or organolithiums to deliver boronic group transfer, essential for subsequent Suzuki-Miyaura cross-coupling reactions. This pathway produces high-purity intermediates required for complex active ingredients and specialty organics. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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