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HS Code |
542222 |
| Chemical Name | N-[(Trimethylsilyl)Methyl]Benzylamine |
| Molecular Formula | C11H19NSi |
| Molecular Weight | 193.36 g/mol |
| Cas Number | 65696-46-6 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 94-96°C at 6 mmHg |
| Density | 0.862 g/mL at 25°C |
| Refractive Index | n20/D 1.497 |
| Flash Point | 83°C |
| Smiles | C[Si](C)(C)CNCC1=CC=CC=C1 |
| Storage Conditions | Store at 2-8°C, tightly closed |
| Solubility | Soluble in organic solvents such as dichloromethane |
As an accredited N-[(Trimethylsilyl)Methyl]Benzylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g quantity of N-[(Trimethylsilyl)Methyl]Benzylamine is packaged in a sealed amber glass bottle with tamper-evident cap. |
| Shipping | N-[(Trimethylsilyl)methyl]benzylamine should be shipped in tightly sealed containers, protected from moisture and air. Store in a cool, dry place, away from incompatible substances such as oxidizers. Transport must comply with relevant chemical regulations. Utilize appropriate hazard labeling and ensure packaging prevents leaks or spills during transit. Handle with suitable safety measures. |
| Storage | N-[(Trimethylsilyl)Methyl]Benzylamine should be stored in a tightly sealed container under an inert atmosphere, such as nitrogen or argon, to prevent moisture and air exposure. Keep it in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers or acids. Store at room temperature or lower, avoiding direct sunlight and ignition sources. |
Applications of N-[(Trimethylsilyl)Methyl]Benzylamine in Industrial ManufacturingN-[(Trimethylsilyl)Methyl]Benzylamine finds focused use in several advanced chemical production lines, primarily as a structure-directing agent, protected amine, or reactive intermediate. Below we detail specific downstream industrial applications, including technical compliance standards, proportioning, integration within processes, and real finished product outputs. 1. API Synthesis in Pharmaceutical ManufacturingAPI manufacturers frequently use N-[(Trimethylsilyl)Methyl]Benzylamine as an amine source and transient protecting group, particularly for the construction of complex benzylamine-containing pharmaceuticals. The compound participates in sensitive condensation or substitution steps where silylation prevents unwanted side reactions. Its high purity is critical for yield and regulatory acceptance in drug production. Industry compliance standards
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2. Advanced Materials: Liquid Crystal Display IntermediatesManufacturers involved in liquid crystal precursor synthesis apply this raw material as a nucleophilic amine modifier or blocking group, allowing for controlled introduction of functional amine-derived branches into aromatic systems. This facilitates the construction of mesogenic units with precise dielectric or optical properties essential for high-contrast LCDs. Industry compliance standards
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3. Agrochemical Intermediate ProductionChemical plants manufacturing herbicides and pesticides utilize this compound as an amine building block in the multi-step synthesis of substituted benzylamine agrochemical actives. Its silyl substituent enables selective transformations, reducing risk of over-alkylation and permitting controlled N-deprotection for downstream finishing. Industry compliance standards
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4. Fine Chemicals: Synthesis of Functionalized Aromatic AminesIn fine chemical synthesis, this material is valued for its reactivity in generating tailored aromatic amines through mild silylation and subsequent deprotection protocols. Producers of specialty intermediates employ it to achieve temporary protection during multi-step transformations, reducing side product formation and facilitating chromatographic purification of high-value custom molecules. Industry compliance standards
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5. Polymerization Catalysis ModifierPolyolefin and specialty polymer manufacturers incorporate N-[(Trimethylsilyl)Methyl]Benzylamine as a functionalized amine ligand or as a temporary directing group in metal-catalyzed polymerization systems. The material allows for improved catalyst control and offers routes for tuning polymer microstructure, particularly in high-value specialty resins and engineering plastics. Industry compliance standards
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