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1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluoro-N-phenyloctane-1-sulfonamide is a complex organic compound characterized by its unique molecular structure. It consists of an octane chain with a phenyl group attached to the nitrogen atom, and a sulfonamide group at the end. The molecule is highly fluorinated, with 15 fluorine atoms replacing hydrogen atoms in various positions along the octane chain. This extensive fluorination imparts unique properties to the compound, such as increased lipophilicity and resistance to hydrolysis. The compound may have potential applications in various fields, including pharmaceuticals, materials science, and chemical research, due to its unusual structure and properties.

559-05-7

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559-05-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 559-05-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,5 and 9 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 559-05:
(5*5)+(4*5)+(3*9)+(2*0)+(1*5)=77
77 % 10 = 7
So 559-05-7 is a valid CAS Registry Number.

559-05-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluoro-N-phenyloctane-1-sulfonamide

1.2 Other means of identification

Product number -
Other names Heptadecafluor-octan-1-sulfonsaeure-anilid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:559-05-7 SDS

559-05-7Downstream Products

559-05-7Relevant academic research and scientific papers

Synthesis and surface activities of organic solvent-soluble fluorinated surfactants

Li, Guo-Li,Zheng, Li-Qiang,Xiao, Jin-Xin

experimental part, p. 674 - 681 (2009/12/22)

A variety of fluorinated surfactants soluble in organic solvent were prepared, including C8F17SO2NHCnH2n+1 (n = 2, 4, 6, 8, 10), C8F17SO2NHR (R = C6H11, C6H5), C8F17SO2N(CnH2n+1 )2 (n = 1, 2, 3, 4) and C8F17SO2NH(CH2)nN HO2SC8F17 (n = 6, 10). Their surface activities in various organic solvents were determined by surface tension measurement. The results showed that these fluorinated surfactants can reduce the surface tension of both polar and non-polar organic solvents. In general, organic solvents with strong polarity or long alkyl chain are beneficial to increase the surface activity of these polar fluorinated surfactants. By comparing fluorinated surfactants with the same fluorocarbon segment and connecting group, C8F17SO2N(CnH2n+1 )2 (n = 1, 2, 3, 4) showed lower surface activity in organic solvents than C8F17SO2NHCnH2n+1 (n = 2, 4, 6, 8) with an equal carbon number of the solvophilic group. Through surface tension vs. concentration curves given for N-octyl perfluorooctanesulfonamide in various organic solvents, a break point like the critical micelle concentration of ordinary surfactants in aqueous solutions was observed, and the effect of the different types of organic solvents on adsorption and aggregation behavior was also studied.

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