Diphenyliodonium trifluoromethanesulfonate
98%
- Product Code: 122107
Alias:
Diphenyliodotrifluoromethanesulfonate
CAS:
66003-76-7
| Molecular Weight: | 430.18 g./mol | Molecular Formula: | C₁₃H₁₀F₃IO₃S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00191356 | |
| Melting Point: | 46-49 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | room temperature, away from light |
Product Description:
Diphenyliodonium trifluoromethanesulfonate is widely used as a photoacid generator in photoresist formulations for the semiconductor industry. It plays a critical role in the photolithography process, where it generates strong acids upon exposure to UV light, facilitating the patterning of microelectronic components. Additionally, it is employed in the synthesis of organic compounds, particularly in cationic polymerization reactions, where it acts as an efficient initiator. Its strong oxidizing properties also make it useful in various organic transformations, including cross-coupling reactions and the functionalization of aromatic compounds. In advanced materials science, it is utilized to modify surfaces and create thin films with specific properties.
Product Specification:
| Test | Specification |
|---|---|
| Purity (Ion Exchange Titration) | 97.5-102.5 |
| Melting Point | 177-183 |
| Solubility In Methanol | Almost Transparency |
| Note | This Product Is Low Melting Point Solid, May Change State In Different Environments (Solid, Liquid Or Semi-Solid) |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $26.35 |
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| 5.000 | 10-20 days | $89.27 |
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| 25.000 | 10-20 days | $367.70 |
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Diphenyliodonium trifluoromethanesulfonate
Diphenyliodonium trifluoromethanesulfonate is widely used as a photoacid generator in photoresist formulations for the semiconductor industry. It plays a critical role in the photolithography process, where it generates strong acids upon exposure to UV light, facilitating the patterning of microelectronic components. Additionally, it is employed in the synthesis of organic compounds, particularly in cationic polymerization reactions, where it acts as an efficient initiator. Its strong oxidizing properties also make it useful in various organic transformations, including cross-coupling reactions and the functionalization of aromatic compounds. In advanced materials science, it is utilized to modify surfaces and create thin films with specific properties.
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