27619-97-2

Basic information

• Product Name: 1H,1H,2H,2H-PERFLUOROOCTANESULFONIC ACID
• Synonyms: 3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctanesulphonic acid;(1H,1H,2H,2H)-Perfluorooctanesulfonic];1-Octanesulfonic acid, 3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluoro-;1H,1H,2H,2H-Perfluorooctanesulphonic acid 98%;1H,1H,2H,2H-Perfluorooctanesulphonicacid98%;2-(Perfluorohexyl)ethane-1-sulfonic acid;2-(Tridecafluorohexyl)ethanesulfonic acid;3,3,4,4,5,5,6,6,7,7,8,8,8-Tridecafluorooctane-1-sulfonic acid
• CAS NO: 27619-97-2
• Molecular Formula: C₈H₅F₁₃O₃S
• Molecular Weight: 428.17
• EINECS: 248-580-6
• Mol File: 27619-97-2.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 221.2°C at 760 mmHg
• Flash Point: 87.6°C
• Appearance: /
• Density: 1,25 g/cm3
• Vapor Pressure: 0.109mmHg at 25°C
• Refractive Index: 1.491
• PKA: 1.31±0.50(Predicted)
• Water Solubility: 658g/L at 20℃
• CAS DataBase Reference: 1H,1H,2H,2H-PERFLUOROOCTANESULFONIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 1H,1H,2H,2H-PERFLUOROOCTANESULFONIC ACID(27619-97-2)
• EPA Substance Registry System: 1H,1H,2H,2H-PERFLUOROOCTANESULFONIC ACID(27619-97-2)

Safety Data

• Hazard Codes: C,Xi
• Statements: 34
• Safety Statements: 26-36/37/39-45
• RIDADR: 3265
• HazardClass: IRRITANT, CORROSIVE
• Hazardous Substances Data: 27619-97-2(Hazardous Substances Data)

Usage

Flammability and Explosibility

Notclassified

InChI:InChI=1/C10H10F3NO2/c1-2-16-9(15)14-8-5-3-7(4-6-8)10(11,12)13/h3-6H,2H2,1H3,(H,14,15)

Upstream product

• 34451-26-8 2-perfluorohexylethanethiol 
• 26650-09-9 3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl thiocyanate 

Downstream Products

• 27619-89-2 3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctanesulfonyl chloride 

Relevant articles and documents

Preparation method of perfluorohexylethyl sulfonate

The present invention relates to the technical field of fluorocarbon surfactants, and discloses a preparation method of perfluorohexylethyl sulfonate. The preparation method comprises: S1, dissolving sodium hydrosulfide in absolute ethyl alcohol, adding perfluorohexylethyl iodide and a catalyst, and carrying out a reaction under a heating condition to obtain perfluorohexyl ethanethiol; S2, blending perfluorohexyl ethanethiol and nitric acid, and reacting under a heating condition to obtain perfluorohexylethyl sulfonic acid; and S3, reacting the perfluorohexylethyl sulfonic acid with an alkali, purifying, and drying to obtain the perfluorohexylethyl sulfonate. According to the preparation method, perfluorohexylethyl iodide is used as a raw material, and absolute ethyl alcohol is used as a solvent. The method can reduce the production cost, digest production waste, and is safe, environment-friendly and simple to operate.