Trifluoromethanesulfonic Acid Tert-butyldimethylsilyl Ester: Your Premier Silylating Agent Supplier

Discover the critical role of Tert-Butyldimethylsilyl Trifluoromethanesulfonate (CAS 69739-34-0) in driving innovation in organic synthesis. As a leading manufacturer and supplier, we ensure unparalleled quality and availability.

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Key Advantages of Our Silylating Reagents

Exceptional Purity and Reactivity

Our Tert-Butyldimethylsilyl Trifluoromethanesulfonate boasts a purity of ≥95.0%, ensuring predictable and efficient outcomes in your organic synthesis. This high quality makes it ideal for demanding applications where precision is paramount. We understand the importance of reliable reagents for your R&D success.

Versatile Applications in Synthesis

This silylating agent is crucial for introducing tert-butyl dimethylsilyl groups, protecting alcohols and amines, and forming enol silyl ethers. Its utility extends to promoting conjugate additions and activation of carbonyl compounds, making it a versatile reagent for many synthetic strategies. Discover how our product can streamline your chemical processes.

Secure and Stable Supply Chain

As a dedicated manufacturer and supplier, we ensure a stable and consistent supply of Tert-Butyldimethylsilyl Trifluoromethanesulfonate. We cater to bulk purchase requirements, offering competitive prices and dependable delivery, ensuring your production cycles are uninterrupted. Partner with us for your sourcing needs.

Applications Driving Chemical Innovation

Silyl Ether Formation

Easily convert alcohols into robust tert-butyldimethylsilyl (TBDMS) ethers, a common protecting group strategy in multi-step organic synthesis. Rely on our product to buy high-purity silylating agents for your protection needs.

Enol Silyl Ether Synthesis

Generate enol silyl ethers from ketones and lactones, crucial intermediates for C-C bond formation and further functionalization in complex molecule synthesis.

Promoting Conjugate Additions

Catalyze important conjugate addition reactions, enabling efficient carbon-carbon bond formation with various nucleophiles for creating intricate molecular architectures.

Activation of Carbonyl Compounds

Activate carbonyl groups for subsequent nucleophilic attack or cycloaddition reactions, enhancing the scope and efficiency of synthetic routes.