846543-00-8

Basic information

• Product Name: 1-Butanone, 1-[4-(heptadecafluorooctyl)phenyl]-
• CAS NO: 846543-00-8
• Molecular Formula: C18H11F17O
• Molecular Weight: 566.258
• Mol File: 846543-00-8.mol

Chemical Properties

• CAS DataBase Reference: 1-Butanone, 1-[4-(heptadecafluorooctyl)phenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Butanone, 1-[4-(heptadecafluorooctyl)phenyl]-(846543-00-8)
• EPA Substance Registry System: 1-Butanone, 1-[4-(heptadecafluorooctyl)phenyl]-(846543-00-8)

Safety Data

• Hazardous Substances Data: 846543-00-8(Hazardous Substances Data)

Usage

General Description

1-Butanone, 1-[4-(heptadecafluorooctyl)phenyl]-, also known as perfluorooctylphenyl ketone, is a fluorinated organic compound with the molecular formula C23H20F17O. It is a colorless liquid with a faint odor and is used as a non-aqueous solvent and in industrial applications such as lubricants, coatings, and electronics. Due to its high thermal stability and chemical inertness, it is often used in high-temperature processes. This chemical is also known for its resistance to grease, oil, and water, making it useful in applications that require durable and long-lasting performance. Additionally, it is considered to be relatively safe for human health and the environment, with no known hazardous effects.

Upstream product

• 591-50-4 iodobenzene 
• 507-63-1 1-iodoheptadecafluorooctane 
• 160565-77-5 1-(4-iodophenyl)butan-1-one 

Downstream Products

• 846543-04-2 phosphoric acid 1-(4-heptadecafluorooctyl-phenyl)-butyl ester diphenyl ester 

Relevant articles and documents

Synthesis of phosphate-type fluorocarbon-hydrocarbon hybrid surfactants and their adsorption onto calcium hydroxyapatite

Five novel phosphate-type hybrid surfactants, Cm F2m+1C6H4CH[OPO2 (OC6H5)Na]CnH2n+1 (FmPHnPPhNa: m = 4, 6, 8; n = 3, 5), have been synthesized. When compared with sulfate-type hybrid surfactants, CmF2m+1C6H4 CH(OSO3Na)CnH2n+1 (C6H4 = p-phenylene), the new hybrid surfactants were found to have comparable abilities to lower the surface tension of water. The critical micelle concentrations of F m PH n PPhNa followed Klevens' rule and their occupied areas per molecule increased with increasing m and n. Calcium hydroxyapatite (CaHAp) pellets modified with FmPH3PPhNa gave high hydro and lipophobic surfaces. The hybrid surfactants are expected to be useful as new dental reagents for oral hygiene.

Synthesis and solution properties of sulfate-type hybrid surfactants with a benzene ring

Nine novel sulfate-type hybrid surfactants, Cm F2m+1C6H4CH(OSO3Na) CnH2n+1 (FmPHnOS: m=4, 6, 8; n=3, 5, 7; C6H4: p-phenylene), with a benzene ring in their molecules were synthesized. Alkanoyl chlorides were allowed to react with iodobenzene in the presence of aluminum chloride to give the corresponding aromatic ketones. The reaction of the ketones with perfluoroalkyl iodides yielded 1-[4-(perfluoroalkyl)phenyl]-1-alkanones as intermediates. The intermediates were allowed to react with methanol in tetrahydrofuran in the presence of sodium borohydride to yield 1-[4-(perfluoroalkyl)phenyl]-1-alkanols. The desired hybrid surfactants were obtained by the reaction of 1-[4-(perfluoroalkyl)phenyl-1-alkanols with sulfur trioxide/pyridine complex in pyridine and by the subsequent neutralization of the products with sodium hydroxide solution. When compared with the conventional hybrid surfactants, Cm F2m+1C6H4COCH(SO3Na) CnH2n+1 (FmHnS: m=4, 6; n=2, 4, 6; C6H4: p-phenylene), the new hybrid surfactants thus synthesized were found to have a comparable ability to lower the surface tension of water and a high hydrophilicity. The cmc of FmPH n OS obeyed Kleven's rule and their occupied areas per molecule increased with increasing m and n with the values between 0.66 and 1.05 nm2. The aggregation number for FmPHnOS micelles ranged from 6 to 45 and the hydrodynamic radius of the micelles was in the range of 1.4-3.1 nm.