338-83-0 Usage
Description
Perfluorotripropylamine is a chemical compound with the formula C9F21N, characterized by its unique perfluorinated structure and amine functional group. It possesses properties such as low surface tension, high thermal stability, and resistance to chemical degradation, making it a versatile reagent for various applications.
Uses
Used in Microfluidics:
Perfluorotripropylamine is used as a reagent for surface modification in droplet polymeric microfluidic devices. Its application is crucial for improving the stable and continuous generation of aqueous droplets, which is essential for the efficient functioning of microfluidic systems.
Used in Surface Coating Industry:
Perfluorotripropylamine is used as a surface-active agent in the development of coatings with enhanced properties. Its low surface tension and chemical resistance contribute to the formation of uniform and durable coatings, which are particularly useful in applications requiring non-stick, anti-fouling, or easy-to-clean surfaces.
Used in Chemical Synthesis:
Perfluorotripropylamine serves as an intermediate or reactant in the synthesis of various perfluorinated compounds. Its unique structure and reactivity make it a valuable building block for the development of specialty chemicals, pharmaceuticals, and materials with tailored properties.
Used in Electronics Industry:
Perfluorotripropylamine is utilized as a component in the fabrication of electronic devices, particularly in the development of high-performance lubricants and thermal interface materials. Its thermal stability and resistance to degradation contribute to the reliable operation and longevity of electronic components.
Used in Environmental Remediation:
Perfluorotripropylamine is employed in the treatment of contaminated water and soil, where its chemical properties enable the efficient removal of pollutants and the decontamination of affected environments. Its resistance to degradation and low toxicity make it a suitable candidate for environmental applications.
Purification Methods
Purify it as for perfluorodimethyl-cyclopropane (see p 220). [Haszeldine J Chem Soc 102 1951, for azeotropes see Simons & Linevsky J Am Chem Soc 74 4750 1972.] IRRITANT.
Check Digit Verification of cas no
The CAS Registry Mumber 338-83-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,3 and 8 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 338-83:
(5*3)+(4*3)+(3*8)+(2*8)+(1*3)=70
70 % 10 = 0
So 338-83-0 is a valid CAS Registry Number.
338-83-0Relevant articles and documents
CORRELATION BETWEEN YIELD AND OPERATING CONDITIONS IN THE ELECTROCHEMICAL FLUORINATION OF TRIPROPYLAMINE
Conte, L.,Napoli, M.,Gambaretto, G. P.
, p. 89 - 96 (1985)
Electrochemical fluorination of tripropylamine in anhydrous hydrogen fluoride was studied in order to verify the correlation between the operating conditions and the yield of the corresponding perfluoroamine.The parameters tested were: temperature, voltage, initial concentration of amine in the bath, constant concentration of amine in the bath and stirring effect.Experimental data show that temperature is the parameter exerting the most remarkable influence over perfluoroamine yield and by-products formation.
An efficient high-yield synthesis for perfluorinated tertiary alkyl amines
Felling, Kyle W.,Lagow, Richard J.
, p. 233 - 236 (2007/10/03)
We wish to report a high-yield synthesis of perfluorinated tertiary amines from their hydrocarbon analogues by direct fluorination. Yields up to 70%, with high purities, have been obtained from certain tertiary amines. This technique will likely develop into a new general method for producing perfluorinated amines.
Technology for the preparation of perfluoro-organic compounds
Moldavskii, Dmitrii D.,Bispen, Tatjana A.,Kaurova, Galina I.,Furin, Georgii G.
, p. 157 - 167 (2007/10/03)
Fluorination by elemental fluorine of fluorine-containing alkenes, alkanes, ethers and tertiary amines was investigated, aimed at obtaining the perfluorinated analogs. The factors affecting yield of the target compounds were studied. Elements of technology were elucidated.
