73606-19-6 Usage
Uses
Used in Chemical and Manufacturing Industries:
2-[(6-chloro-1,1,2,2,3,3,4,4,5,5,6,6-dodecafluorohexyl)oxyl]-1,1,2,2-tetrafluoroethanesulfonic acid, potassium salt is used as a surfactant for its ability to lower surface tension between two different substances, which is crucial in processes requiring enhanced mixing, emulsification, or stabilization.
Used in Production of Fluorinated Polymers:
In the polymer industry, this potassium salt is utilized as a key component in the synthesis of fluorinated polymers, owing to its capacity to impart unique properties such as increased thermal stability and chemical resistance to the final polymer products.
Used as a Corrosion Inhibitor:
2-[(6-chloro-1,1,2,2,3,3,4,4,5,5,6,6-dodecafluorohexyl)oxyl]-1,1,2,2-tetrafluoroethanesulfonic acid, potassium salt serves as an effective corrosion inhibitor, protecting materials from the degrading effects of chemical reactions, particularly in harsh or corrosive environments.
Used in Manufacturing of Electrochemical Devices:
This chemical is employed as an electrolyte in the production of electrochemical devices, such as batteries and fuel cells, due to its ability to facilitate ionic conduction and contribute to the overall performance and efficiency of these devices.
Used in Solvent Applications:
Given its solubility in a wide range of organic solvents, 2-[(6-chloro-1,1,2,2,3,3,4,4,5,5,6,6-dodecafluorohexyl)oxyl]-1,1,2,2-tetrafluoroethanesulfonic acid, potassium salt is used in solvent applications where its unique solvency properties can be leveraged for specific chemical reactions or processes.
Check Digit Verification of cas no
The CAS Registry Mumber 73606-19-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,6,0 and 6 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 73606-19:
(7*7)+(6*3)+(5*6)+(4*0)+(3*6)+(2*1)+(1*9)=126
126 % 10 = 6
So 73606-19-6 is a valid CAS Registry Number.
InChI:InChI=1/C8HClF16O4S.K/c9-5(18,19)3(14,15)1(10,11)2(12,13)4(16,17)6(20,21)29-7(22,23)8(24,25)30(26,27)28;/h(H,26,27,28);/q;+1/p-1
73606-19-6Relevant academic research and scientific papers
Radical addition of perfluoroalkyl iodides to alkenes and alkynes initiated by sodium dithionite in an aqueous solution in the presence of a novel fluorosurfactant
Xiao, Zhiwei,Hu, Huawei,Ma, Jiaoli,Chen, Qingyun,Guo, Yong
, p. 939 - 944 (2013/08/23)
A new fluorinated anionic surfactant Cl(CF2) 6O(CF2)2SO3N(C2H 5)4 was prepared and characterized. The application of the fluorosurfactant allowed the fluoroalkylation to occur in the water without adding organic solvent. The addition of perfluoroalkyl iodides with olefins and alkynes under the initiation of Na2S2O4 in water in the presence of the fluorosurfactant gave the corresponding adducts in good to excellent yields. The fluorosurfactant was suitable for a radical addition process. A new surfactant Cl(CF2)6O(CF 2)2SO3N(C2H5) 4 was prepared and its properties were measured. The fluorinated surfactant was applied to the fluoroalkylation of perfluoroalkyl iodides with olefins and alkynes. The reactions gave the corresponding adducts in water and avoided the use of organic solvent. The aqueous solution with the surfactant proved to be an effective medium for a radical process. Copyright
