355-41-9

Usage

Uses

Used in Chemical Industry:
Perfluorohexyl Chloride is used as a precursor for the synthesis of other fluorinated derivatives, which are essential in various applications due to their unique properties.
Used in Textile Industry:
Perfluorohexyl Chloride is used as a treatment agent for textiles, providing water and oil repellency to fabrics, enhancing their durability and ease of maintenance.
Used in Firefighting Industry:
Perfluorohexyl Chloride is used in the production of firefighting foams, contributing to their effectiveness in extinguishing fires by repelling water and oil.
Used in Aerospace Industry:
Perfluorohexyl Chloride is used in the development of materials with specific properties required for aerospace applications, such as resistance to extreme temperatures and environmental conditions.
However, it is important to note that there are safety concerns associated with the use of Perfluorohexyl Chloride due to its potential toxicity and environmental persistence. Proper handling and disposal measures should be implemented to minimize any adverse effects.

InChI:InChI=1/C6ClF13/c7-5(16,17)3(12,13)1(8,9)2(10,11)4(14,15)6(18,19)20

Upstream product

• 355-37-3 1,1,1,2,2,3,3,4,4,5,5,6,6-tridecafluorohexane 
• 355-43-1 n-perfluorohexyl iodide 
• 375-84-8 2,2,3,3,4,4,5,5,6,6,7,7,7-tridecafluoroheptanoyl fluoride 
• 307-24-4 undecafluorohexanoic acid 

Downstream Products

• 69125-80-0 1-(n-perfluorohexyl)-hexane 
• 120464-27-9 1,1,1,2,2,3,3,4,4,5,5,6,6-tridecafluorohexadec-7-ene 
• 133331-77-8 1,1,1,2,2,3,3,4,4,5,5,6,6-tridecafluorotetradecane 
• 128720-29-6 p-methoxy(tridecafluorohexyl)benzene 
• 128720-28-5 m-methoxy(tridecafluorohexyl)benzene 
• 128720-27-4 o-methoxy(tridecafluorohexyl)benzene 
• 350608-55-8 diethyl 3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctylphosphonate 
• 55009-92-2 (E)-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooct-1-en-1-yl)benzene 
• 355-42-0 tetradecafluorohexane 

Relevant academic research and scientific papers

PERFLUORO DIACYL PEROXIDE, SOLUTION, POLYMERIZATION INITIATOR, POLYMER PREPARATION METHOD, AND PERFLUORO ACYL CHLORIDE

A perfluorodiacyl peroxide represented by the following formula (1): [in-line-formulae](C5F11COO)2 ??(1).[/in-line-formulae] Also disclosed is a solution containing the perfluorodiacyl peroxide, a polymerization initiator containing the perfluorodiacyl peroxide, a method for producing a polymer which includes polymerizing a radically polymerizable monomer with the perfluorodiacyl peroxide, and a perfluoroacyl chloride represent by the following formula (2): [in-line-formulae]C5F11COCl (2).[/in-line-formulae]

Reactivite par voie thermique de RFH

Hydroperfluoroalkanes are well known as being rather inert chemically.Hydroperfluoroalkanes react at high temperature with carbon tetrabromide and carbon tetrachloride to yield bromoperfluoroalkanes and chloroperfluoroalkanes. - Keywords: Hydroperfluoroalkanes; High-temperature reaction; Carbon tetrabromide; Carbon tetrachloride; Bromoperfluoroalkanes; Chloroperfluoroalkanes

PYROLYTIC REACTIONS OF PERFLUORINATED CARBOXYLIC ACID HALIDES

Unlike other acyl halides, perfluoroacyl fluorides only enter into reaction with polar reagents.Perfluoroacyl fluorides, perfluoroacyl bromides, and perfluoroacyl iodides are smoothly decarbonylated at active carbon at elevated temperatures.In the absence of the active carbon the perfluoroacyl fluorides react with halogens, polyhalogenoalkanes, and iodoperfluoroalkanes with the formation of the corresponding halogenoperfluoroalkanes or their mixtures with perfluoroacyl halides; the low yields of the iodoperfluoroalkanes in the reaction of perfluoroacyl fluorides withiodine are explained by their ability to act themselves as reagents in these processes.The catalytic properties of active carbon are due to its ability to transfer electrons to the molecules of the adsorbed reagent and to hold the reaction particles on the surface; graphite and nickel also have specific catalytic activity.

REACTIVITE DES PERFLUOROHALOGENOALCANES EN PRESENCE DE COUPLES METALLIQUES. REACTIVITE DE PERFLUOROIODOALCANES SUR DES DERIVES HALOGENES DANS DES SOLVANTS APROTIQUES DISSOCIANTS (DMSO, DMF).

Perfluoroalkyl iodides (RFI) reacts with organic halide in dissociants solvents (DMF, DMSO) in the presence of zinc-copper couple through an organometallic route; in this way C6F13Cl, C6F13CH2CH2I, (C6F13)2Zn have been prepared.