134051-92-6 Usage
Chemical structure
A complex synthetic substance consisting of a long chain of fluorinated carbon atoms with two morpholine rings and a phosphinate group.
Number of fluorinated carbon atoms
19
Resistance to degradation
Highly resistant to heat, chemical, and electrochemical degradation.
Applications
Often used as a flame retardant and as a stabilizer in polymer materials.
Thermal stability
Known for its excellent thermal stability.
Surface energy
Low surface energy.
Resistance to solvents, acids, and bases
Highly resistant.
Industrial applications
Valuable compound in various industrial applications due to its unique properties.
Specific niche
Has a specific niche in the field of material science and engineering.
Complex structure
Due to its complex structure, it is a highly specialized compound.
Check Digit Verification of cas no
The CAS Registry Mumber 134051-92-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,0,5 and 1 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 134051-92:
(8*1)+(7*3)+(6*4)+(5*0)+(4*5)+(3*1)+(2*9)+(1*2)=96
96 % 10 = 6
So 134051-92-6 is a valid CAS Registry Number.
134051-92-6Relevant articles and documents
Synthesis and preliminary data on the biocompatibility and emulsifying properties of perfluoroalkylated phosphoramidates as injectable surfactants
Krafft,Vierling,Riess
, p. 545 - 550 (2007/10/02)
Perfluoroalkylated dimorpholinophosphoramidates, 1-4, were synthesized in 65-80% yield by phosphorylation of the appropriate perfluoroalkylated alcohol by phosphorus oxytrichloride, followed by reaction with morpholine. Preliminary biological tests (effect on cell cultures, hemolysis of red blood cells, and acute in vivo toxicity in mice) performed on compounds 1 to 5 show that the F-alkylated derivatives 1 to 4 are better tolerated than their hydrocarbon analog 5 in spite of their higher surface activity. Where the emulsification of fluorocarbons is concerned, the incorporation of the perfluoroalkylated compounds 1 to 4 in 20% w/v F-decalin/lecithin-based emulsions results in a slight stabilizing effect (not found for the hydrocarbon analog 5), detectable only after one month of storage at 25°C. However, when used as the sole surfactant, the F-alkylated dimorpholinophosphoramidates show no emulsifying properties; this may be assigned to insufficient hydrophilicity of the dimorpholinophosphoramidate head.