347817
Trifluoromethanesulfonic acid
ReagentPlus®, ≥99%
Manufacturer: Sigma Aldrich
CAS Number: 1493-13-6
Synonym(S): Triflic acid
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 5 G | 347817-5-G | In Stock | ₹ 8,207.90 |
| 25 G | 347817-25-G | In Stock | ₹ 22,819.65 |
| 100 G | 347817-100-G | In Stock | ₹ 44,109.55 |
| 500 G | 347817-500-G | In Stock | ₹ 1,22,369.45 |
347817 - 5 G
In Stock
Quantity
1
Base Price: ₹ 8,207.90
GST (18%): ₹ 1,477.422
Total Price: ₹ 9,685.322
vapor density
5.2 (vs air)
Quality Level
200
vapor pressure
8 mmHg ( 25 °C)
product line
ReagentPlus®
Assay
≥99%
form
liquid
refractive index
n20/D 1.327 (lit.)
bp
162 °C (lit.)
density
1.696 g/mL at 25 °C (lit.)
SMILES string
OS(=O)(=O)C(F)(F)F
Other Options
| Image | Product Name | Manufacturer | Price Range | |
|---|---|---|---|---|
 | Sigma Aldrich Fine Chemicals Biosciences Trifluoromethanesulfonic Acid | 1493-13-6 | MFCD00007514 | 10g | -- | ₹ 4,996.70 | |
| | Strem, An Ascensus Company CAS# 1493-13-6. 50g. Trifluoromethanesulfonic acid, 99+%. MFCD00007514 | -- | ₹ 15,400.80 | |
| | eMolecules Trifluoromethanesulfonic acid | 1493-13-6 | MFCD00007514 | 25g | -- | ₹ 4,343.88 | |
| | Strem, An Ascensus Company CAS# 1493-13-6. 10g. Trifluoromethanesulfonic acid, 99+%. MFCD00007514 | -- | ₹ 5,005.26 | |
| | Trifluoromethanesulfonic acid | -- | ₹ 2,394.85 - ₹ 11,794.90 | |
| | Trifluoromethanesulfonic acid | -- | ₹ 8,207.90 - ₹ 1,22,369.45 | |
| | Trifluoromethanesulfonic acid | -- | ₹ 2,394.85 - ₹ 11,794.90 | |
| | Methanesulfonic acid, 1,1,1-trifluoro- | -- | -- |
Related Products
Description
- General description: Trifluoromethanesulfonic acid is a strong organic acid. It can be prepared by reacting bis(trifluoromethylthio)mercury with H2O2.[1] On mixing with HNO3, it affords a nitrating reagent (a nitronium salt). This reagent is useful for the nitration of aromatic compounds.[2] Its dissociation in various organic solvents has been studied.[3]
- Application: Trifluoromethanesulfonic acid can be used as a catalyst to prepare: Substituted tetrahydrofurans and tetrahydropyrans by cyclization of corresponding unsaturated alcohols under acidic conditions.[4] Nitriles from corresponding aldehydes by Schmidt reaction.[5] Disubstituted five-membered ring lactones by allylboration reaction between 2-alkoxycarbonyl allylboronates and aldehydes.[6] It can also be used as a catalyst in the Fischer glycosylation and Friedel-Crafts acylation reactions.[7][8]
- Legal Information: ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
SAFETY INFORMATION
Pictograms
Signal Word
Danger
Hazard Statements
Precautionary Statements
P234 - P261 - P280 - P301 + P312 - P303 + P361 + P353 - P305 + P351 + P338
Hazard Classifications
Acute Tox. 4 Oral - Met. Corr. 1 - Skin Corr. 1B - STOT SE 3
Target Organs
Respiratory system
WGK
WGK 1
Flash Point(F)
Pensky-Martens closed cup
Flash Point(C)
Pensky-Martens closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves