Molecular Formula | C4F10O2S |
Molar Mass | 302.09 |
Density | 1.682 g/mL at 25 °C (lit.) |
Melting Point | -110°C |
Boling Point | 64 °C (lit.) |
Flash Point | 65-66°C |
Water Solubility | Hydrolyses in water. |
Vapor Presure | 16.665kPa at 20℃ |
Appearance | Liquid |
Specific Gravity | 1.682 |
Color | Colorless to yellow |
BRN | 1813589 |
Storage Condition | Keep in dark place,Sealed in dry,Store in freezer, under -20°C |
Sensitive | Moisture Sensitive |
Refractive Index | n20/D 1.3(lit.) |
Use | For the synthesis of fluorocarbon surfactants, fluorine-containing pesticides, dyes, polycarbonate processing dispersant |
Hazard Symbols | C - Corrosive |
Risk Codes | 34 - Causes burns |
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) S25 - Avoid contact with eyes. |
UN IDs | UN 3265 8/PG 2 |
WGK Germany | 3 |
FLUKA BRAND F CODES | 10-21 |
TSCA | Yes |
HS Code | 29049090 |
Hazard Note | Corrosive |
Hazard Class | 8 |
Packing Group | II |
NIST chemical information | Information provided by: webbook.nist.gov (external link) |
EPA chemical information | Information provided by: ofmpub.epa.gov (external link) |
overview | perfluorobutyl sulfonyl fluoride is a perfluorofluoride, which is a liquid at room temperature and is mainly used for synthesizing fluorocarbon surfactants, fluorine-containing pesticides, dyes, polycarbonate processing dispersants, etc. Its structure and performance are similar to perfluorooctane sulfonyl fluoride. Harmful to water bodies. |
preparation method | butyl sulfonyl chloride is used as the starting material, and butyl sulfonyl chloride is easily prepared by fluorine replacement reaction of butyl sulfonyl chloride, and then butyl sulfonyl fluoride and anhydrous hydrogen fluoride are put into an electrolytic cell together, electrolyzed in a nitrogen atmosphere under normal pressure, and the hydrogen in the alkyl group in butyl sulfonyl fluoride is replaced with fluorine to generate perfluorobutyl sulfonyl fluoride. The reaction formula is as follows. |
use | used to synthesize fluorocarbon surfactants, fluorine-containing pesticides, dyes, polycarbonate processing dispersants, etc. antibacterial synergist, combined with sulfa drugs to enhance antibacterial effect, also used for avian coccidia infection and intestinal bacterial infection; Oral can be used to synthesize a variety of fluorine-containing special surfactants. Its potassium salt potassium perfluorobutylsulfonate is an excellent anionic surfactant and the best flame retardant for polycarbonate. |