2708-11-4

Usage

Uses

Used in Industrial Applications:
Heptane, 1,1,2,2,3,3,4,4,5,5,6,6,7-tridecafluorois used as a solvent in various industrial processes. Its high thermal and chemical stability make it suitable for use in demanding conditions.
Used in Coating Production:
Heptane, 1,1,2,2,3,3,4,4,5,5,6,6,7-tridecafluorois used in the production of certain types of coatings, where its resistance to degradation and high temperature stability are advantageous.
Used in Lubricant Formulation:
Heptane, 1,1,2,2,3,3,4,4,5,5,6,6,7-tridecafluorois utilized in the formulation of lubricants, taking advantage of its stability and resistance to oxidation.
Used in Surfactant Manufacturing:
It is also used in the manufacturing of surfactants, where its unique properties can enhance the performance of these compounds in various applications.
However, it is important to note that there are concerns about the potential environmental and health impacts of using perfluorinated compounds like Heptane, 1,1,2,2,3,3,4,4,5,5,6,6,7-tridecafluoro-. Some perfluorinated compounds are known to be persistent in the environment and have been associated with adverse effects on human health and the environment. Therefore, the use of Heptane, 1,1,2,2,3,3,4,4,5,5,6,6,7-tridecafluoro- should be carefully considered and managed to minimize any potential risks.

Upstream product

• 56002-71-2 trimethyl-(1H,1H,7H-dodecafluoroheptyloxy)silane 
• 80027-81-2 C₁₁H₁₃F₁₄NOS 
• 78491-62-0 α,α,ω-trihydroperfluoroheptyloxytrifluorosulfurane 

Relevant academic research and scientific papers

PHENYL-α,α,ω-TRIHYDROPOLYFLUOROALKYLIODONIUM FLUOROBORATES

The reaction of difluoroiodo-α,α,ω-trihydropolyfluoroalkanes (I) with boron trifluoride and benzene gave phenyl-α,α,ω-trihydropolyfluoroalkyliodonium fluoroborates (II).It was established that the polyfluoroalkyl radical adds at the sulfur atom in reaction with p-chlorothiophenol, the N-polyfluoroalkylation product is formed with aniline, pyridine is polyfluoroalkylated at the nitrogen atom with the formnation of a quaternary salt, and a mixture of products from polyfluoroalkylation at the nitrogen atom of the dimethylamino group and at the para position of the benzene ring is formed with dimethylaniline.

REACTION OF 1,1,7-TRIHYDRODODECAFLUOROHEPTYLOXYTRIFLUOROSULFURANE WITH ACIDS

1,1,7-Trihydrododecafluoroheptyl esters of carboxylic acids are obtained in the reaction of 1,1,7-trihydrododecafluoroheptyloxytrifluorosulfurane with carboxylic acids.Trimethylsilyl esters of carboxylic acids and also the acids in the presence of sodium fluoride react with 1,1,7-trihydrododecafluoroheptyloxytrifluorosulfurane with the exclusive formation of carboxylic acid fluorides.

(POLYFLUOROALKOXY)-N,N-DIALKYLAMINOFLUOROSULFURANES AND TRIS(POLYFLUOROALKOXY)-N,N-DIALKYLAMINOSULFURANES

(Polyfluoroalkoxy)-N,N-dialkylaminodifluorosulfuranes, bis(polyfluoroalkoxy)-N,N-dialkylaminofluorosulfuranes, and tris(polyfluoroalkoxy)-N,N-dialkylaminosulfuranes were obtained by the reaction of N,N-dialkylaminotrifluorosulfuranes with trimethylsilyloxypolyfluoroalkanes.