36880-07-6 Usage
Description
6-(PERFLUOROOCTYL)-4-THIAHEXAN-1-OL is a perfluorinated compound that consists of a perfluorooctyl chain, a thiahexan-1-ol group, and a six-carbon chain. It is known for its unique properties, such as being resistant to heat, water, and oils, which make it suitable for various applications.
Uses
Used in Surfactant Applications:
6-(PERFLUOROOCTYL)-4-THIAHEXAN-1-OL is used as a surfactant to reduce the surface tension of liquids, allowing them to spread more easily and mix with other substances. Its resistance to heat and water makes it ideal for use in harsh environments.
Used in Wetting Agent Applications:
As a wetting agent, 6-(PERFLUOROOCTYL)-4-THIAHEXAN-1-OL helps to increase the spreading and absorption of liquids on surfaces. This property is useful in various industries, such as agriculture and textiles, to improve the effectiveness of treatments and coatings.
Used in Lubricant Applications:
6-(PERFLUOROOCTYL)-4-THIAHEXAN-1-OL is used as a lubricant to reduce friction between surfaces, which can help to prevent wear and tear and extend the life of machinery and equipment.
Used in Textile Industry:
In the textile industry, 6-(PERFLUOROOCTYL)-4-THIAHEXAN-1-OL is used to impart water and oil repellency to fabrics, making them more durable and easier to clean.
Used in Coating Industry:
6-(PERFLUOROOCTYL)-4-THIAHEXAN-1-OL is used in the production of coatings to provide a smooth, non-stick surface that is resistant to water, heat, and oils. This makes it suitable for use in various applications, such as cookware and automotive coatings.
However, it is important to note that there is growing concern about the potential environmental and health impacts of perfluorinated compounds, including 6-(perfluorooctyl)-4-thiahexan-1-ol, due to their persistence and bioaccumulative nature in the environment and their association with adverse health effects. As a result, there may be a need to explore alternative compounds or methods to achieve similar results while minimizing potential risks.
Check Digit Verification of cas no
The CAS Registry Mumber 36880-07-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,8,8 and 0 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 36880-07:
(7*3)+(6*6)+(5*8)+(4*8)+(3*0)+(2*0)+(1*7)=136
136 % 10 = 6
So 36880-07-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H11F17OS/c14-6(15,2-5-32-4-1-3-31)7(16,17)8(18,19)9(20,21)10(22,23)11(24,25)12(26,27)13(28,29)30/h31H,1-5H2
36880-07-6Relevant articles and documents
Synthesis of fluoro-substituted acrylic monomers bearing a functionalized lateral chain: Part 1. Preparation of sulfur-containing monomers
Pées,Cahuzac,Sindt,Ameduri,Paul,Boutevin,Mieloszynski
, p. 133 - 142 (2007/10/03)
The synthesis of sulfur-containing fluoroacrylic monomers CmF2m+1(CH2)2S(CH2)n OC(O)CH=CH2 (where m=6, 8 and n=2-4, 11) is presented from a two-step procedure. The first deals with the radical addition of fluorinated mercaptans CmF2m+1(CH2)2SH onto ω-unsaturated alcohols leading to new ω-perfluorinated alcohols containing various polymethylene spacers CmF2m+1(CH2)2S(CH2)n OH according to the nature of the unsaturated alcohols. By-products were noted, resulting from the β-addition of the thiyl radical onto the more hindered side of the alcohol. The proportion of linear and branched isomers is discussed according to the stability of the radical intermediates. These minor products were obtained selectively from other routes to confirm their presence in the reaction media. The second step deals with the acrylation reaction that occurred either in the presence of acryloyl chloride or from a Fisher esterification. Both reactions are described and discussed taking into account the nature of the starting alcohols. The formation of thiiranium ions as intermediates in the esterification of β-sulfur-containing alcohols in acidic medium is established and the formation of regioisomers described according to this thiiranium moieties interposition.
