Trifluoromethanesulfonic acid
0.1 M CF3SO3H in acetic acid
- Product Code: 67491
Alias:
Trifluoromethanesulfonic acid; trifluoromethanesulfonic acid, perfluoromethanesulfonic acid, triflulic acid, trifluoromethanesulfonic acid
CAS:
1493-13-6
Molecular Weight: | 150.08 g./mol | Molecular Formula: | CF₃SO₃H |
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EC Number: | 216-087-5 | MDL Number: | MFCD00007514 |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | Room temperature, inert gas atmosphere |
Product Description:
Widely used as a superacid catalyst in organic synthesis due to its strong acidic properties. It facilitates various reactions, including esterifications, alkylations, and polymerizations, often at lower temperatures and with higher efficiency. In the pharmaceutical industry, it is employed to synthesize complex molecules and intermediates. It also serves as an electrolyte in fuel cells and batteries, enhancing conductivity and performance. Additionally, it is utilized in the production of specialty chemicals and materials, such as liquid crystals and polymers, where its stability and reactivity are advantageous.
Product Specification:
Test | Specification |
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CONCENTRATION | 0.095-0.105 |
APPEARANCE | Liquid |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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10.000 | 10-20 days | ฿460.00 |
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50.000 | 10-20 days | ฿1,850.00 |
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250.000 | 10-20 days | ฿5,120.00 |
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1000.000 | 10-20 days | ฿11,980.00 |
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Trifluoromethanesulfonic acid
Widely used as a superacid catalyst in organic synthesis due to its strong acidic properties. It facilitates various reactions, including esterifications, alkylations, and polymerizations, often at lower temperatures and with higher efficiency. In the pharmaceutical industry, it is employed to synthesize complex molecules and intermediates. It also serves as an electrolyte in fuel cells and batteries, enhancing conductivity and performance. Additionally, it is utilized in the production of specialty chemicals and materials, such as liquid crystals and polymers, where its stability and reactivity are advantageous.
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