193529-93-0

Usage

Uses

Used in Surfactant Applications:
Phenol, 4-[(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyl)oxy]is used as a surfactant in various industrial processes for its ability to reduce the surface tension between liquids and solids, facilitating the mixing of substances that would otherwise not combine easily.
Used in Emulsifier Applications:
In the field of emulsification, Phenol, 4-[(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyl)oxy]- serves as an emulsifier, helping to stabilize mixtures of immiscible liquids, such as oil and water, by preventing them from separating into distinct layers.
Used in Plasticizer Applications:
Phenol, 4-[(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyl)oxy]is also utilized as a plasticizer in the manufacturing of plastics, where it increases the flexibility and workability of the material.
Used in Chemical Industry:
In the chemical industry, Phenol, 4-[(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyl)oxy]- is employed for its water and oil repellency properties, making it suitable for applications where resistance to these substances is required, such as in the production of coatings, adhesives, and sealants.
However, it is important to note that the use of fluorinated compounds like Phenol, 4-[(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyl)oxy]raises environmental and health concerns due to their persistence in the environment and potential toxicity to living organisms. As a result, there is a need for careful consideration and responsible use in industrial applications.

Upstream product

• 377048-36-7 benzoic acid 4-(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluoro-decyloxy)-phenyl ester 
• 103-16-2 4-Benzyloxyphenol 
• 678-39-7 3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluoro-1-decanol 
• 507-63-1 1-iodoheptadecafluorooctane 
• 150-76-5 4-methoxy-phenol 
• 1693-14-7 5,5,6,6,7,7,8,8,9,9,10,10,11,11,12,12,12-heptadecafluorododecan-1-ol 
• 123-31-9 hydroquinone 
• 2444-19-1 4-hydroxyphenyl benzoate 

Downstream Products

• 683795-10-0 2-vinyl-cyclopropane-1,1-dicarboxylic acid ethyl ester 4-(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluoro-decyloxy)-phenyl ester 

Relevant academic research and scientific papers

Smectic C Mesogens with Terminal Perfluoroalkyl Chains

The fluorocarbon derivatives were synthesized. Liquid crystalline states were studied by DSC and microscopic observation. TNI of those compounds were from 161.2°C to 191.7°C, which represented those compounds had very good liquid crystalline stability. Sm

Gelation of 1-alkoxy-4-(2-perfluoroalkyl)ethoxybenzenes in organic solvents

This paper describes preparation and physico-chemical properties of 1-alkoxy-4-(2-perfluoroalkyl)ethoxybenzenes (FmOOCn). For FmOOCn, 4-F(CF 2)mCH2CH2O-phenyl-O-(CH 2)nH, three homologues,

Effects of chemical variations on the mesophase behavior of new fluorinated poly(vinylcyclopropane)s

Several new structures of fluorinated polymers poly(1)-poly(9) were prepared by free radical ring opening polymerization of vinylcyclopropane monomers 1-9 containing different fluorinated side groups of the type -(CH2)n(CF2) pF. While in poly(1)-poly(3) p varied from 6 to 10 for a fixed n=2, in poly(4)-poly(6) n increased from 3 to 5 at the given p=8. In poly(7) and poly(8) a phenyl ring was incorporated to elongate the mesogenic side group (n=2; p=6 and 8, respectively), that was further separated from the polymer backbone by a methylene spacer (m=11) in poly(9). Therefore, the effects of various chemical variations of the polymer structure on the mesophase behavior could be assessed. The polymers were in fact co-polymers comprising both 1,5-linear and cyclobutane-ring isomer units. In any case they formed smectic mesophase(s) owing to the special character of the perfluorinated chains. The order and the isotropization temperature (Ti) of the mesophase were enhanced by increasing p, but Ti lowered with increasing n. Extension of the side group by insertion of a phenyl ring improved Ti. Wide angle X-ray diffraction studies clarified the nature of the different smectic phases, the occurrence of which was discussed in terms of the ability of the fluorinated side groups to pack antiparallel in either a partly or fully interdigitated structure. Co-polymers of 3 with a non-mesogenic, not fluorinated co-monomer 10 were also prepared with different chemical compositions. Co-polymerization was found to be another effective means of modifying the mesophase behavior of the poly(vinylcyclopropane)s.