Triethylsulfonium iodide, >98%
Price range: $229.30 through $4,107.56
Product Code: IL-0258-HPCAS NO: 1829-92-1
- Chemical Formula: C6H15IS
- Synonyms: S222 I
- Hydrophilic
SUM Formula: C6H15IS
Molecular Weight: 245.99
Melting Point: 142 °C
Density: 1.416 g/cm³
Purity: >98%
- SUM Formula: C6H15IS
- Molecular Weight: 245.99
- Melting Point: 142 °C
- Density: 1.416 g/cm³
Triethylsulfonium iodide, CAS: 1829-92-1
Key Applications:
Alkylation Reagent in Organic Synthesis
- Acts as a controlled ethylating agent for oxygen-, nitrogen-, and sulfur‑based nucleophiles.
- Supports the synthesis of thioethers, amines, and heterocycles under mild conditions.
- Useful in mechanistic studies of sulfonium‑mediated alkyl transfer pathways.
Phase‑Transfer and Ion‑Exchange Chemistry
- Functions as a sulfonium‑based phase‑transfer catalyst in biphasic systems.
- Facilitates iodide exchange and nucleophile activation in polar–aprotic media.
- Employed in halide metathesis and quaternary onium salt preparation.
Precursor for Sulfur‑Centered Reactive Intermediates
- Generates sulfonium ylides for cyclopropanation, epoxidation, and rearrangement reactions.
- Supports development of sulfur‑based synthetic methodologies and mechanistic probes.
Photoinitiator and Cationic Polymerization Additive
- Serves as a component or precursor in onium‑salt photoinitiator systems.
- Enables cationic polymerization of epoxides, vinyl ethers, and oxetanes under UV exposure.
- Used in coatings, adhesives, and microfabrication resists requiring rapid cure profiles.
Materials and Electrochemical Research
- Investigated as a model sulfonium salt for ion‑pairing, conductivity, and solvation studies.
- Useful in evaluating iodide transport, redox behavior, and ion‑exchange equilibria.
- Supports development of functional materials where controlled cation–anion interactions are critical.
Synthetic Intermediate for Advanced Sulfur Compounds
- Precursor to sulfonium‑based ionic liquids, sulfur(VI) reagents, and functionalized sulfides.
- Enables modular construction of sulfur‑containing ligands and catalysts.
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