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Atomfair Triethylsulphonium iodide C6H15IS
Description Triethylsulphonium Iodide (CAS No. 348-59-4) is a high-purity organosulfur compound with the molecular formula C6H15IS and IUPAC name triethylsulfanium;iodide . This crystalline solid is widely utilized in organic synthesis, catalysis, and as a phase-transfer agent due to its stable sulfonium cation and reactive iodide anion. Our product is rigorously tested to ensure ??98% purity (HPLC/GC), with low levels of heavy metals and residual solvents, making it ideal for sensitive applications. Suitable for use in pharmaceuticals, agrochemicals, and materials science research. Packaged under inert gas to prevent degradation and available in quantities ranging from 1g to 1kg with customizable bulk…
Description
Description
Triethylsulphonium Iodide (CAS No. 348-59-4) is a high-purity organosulfur compound with the molecular formula C6H15IS and IUPAC name triethylsulfanium;iodide. This crystalline solid is widely utilized in organic synthesis, catalysis, and as a phase-transfer agent due to its stable sulfonium cation and reactive iodide anion. Our product is rigorously tested to ensure ??98% purity (HPLC/GC), with low levels of heavy metals and residual solvents, making it ideal for sensitive applications. Suitable for use in pharmaceuticals, agrochemicals, and materials science research. Packaged under inert gas to prevent degradation and available in quantities ranging from 1g to 1kg with customizable bulk options.
- CAS: 348-59-4
- Molecular Weight: 246.16 g/mol
- Appearance: White to off-white crystalline powder
- Melting Point: 180-185??C (dec.)
- Storage: 2-8??C in airtight container, protect from light
- CAS No: 348-59-4
- Molecular Formula: C6H15IS
- Molecular Weight: 246.16
- Exact Mass: 245.99392
- Monoisotopic Mass: 245.99392
- IUPAC Name: triethylsulfanium;iodide
- SMILES: CC[S+](CC)CC.[I-]
- Synonyms: Sulfonium, triethyl-, iodide (1:1), Triethylsulphonium iodide, EINECS 217-383-7, NSC 36719, 217-383-7
Application
Triethylsulphonium iodide serves as a versatile reagent in organic synthesis, particularly in alkylation reactions and as a phase-transfer catalyst for nucleophilic substitutions. It finds specialized use in the preparation of ionic liquids and as a precursor for sulfonium-based photoacid generators (PAGs) in photoresist formulations. Researchers also employ it in electrochemical applications due to its ionic conductivity properties.
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