16165-71-2 Usage
Uses
Used in Flame Retardant Industry:
Diethyl (1-hexadecyl)phosphonate is used as a flame retardant to enhance the fire resistance of materials, providing safety in industries where flammability is a concern.
Used as a Plasticizer:
In the plastics industry, Diethyl (1-hexadecyl)phosphonate is utilized as a plasticizer to increase the flexibility and workability of plastic materials, improving their performance and durability.
Used in Surfactant Formulations:
Diethyl (1-hexadecyl)phosphonate serves as a surfactant in various formulations, reducing surface tension between liquids and solids, and facilitating the mixing and interaction of different substances.
Used as a Corrosion Inhibitor:
Diethyl (1-hexadecyl)phosphonate is employed as a corrosion inhibitor in some applications, protecting materials from degradation and extending their service life.
Used in Pharmaceutical and Biomedical Applications:
Diethyl (1-hexadecyl)phosphonate has been studied for its potential use in the pharmaceutical and biomedical fields, leveraging its unique chemical properties for developing new therapeutic agents and medical devices.
Check Digit Verification of cas no
The CAS Registry Mumber 16165-71-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,1,6 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 16165-71:
(7*1)+(6*6)+(5*1)+(4*6)+(3*5)+(2*7)+(1*1)=102
102 % 10 = 2
So 16165-71-2 is a valid CAS Registry Number.
16165-71-2Relevant academic research and scientific papers
Gaboyard,Hervaud,Boutevin
, p. 877 - 891 (2002)
Long-chain dialkyl alkylphosphonates were synthesized by radical addition of dialkyl hydrogenphosphonates onto alkenes in presence of di(t-butyl) peroxide. This synthetic route leads to high yields between 94 and 97%. We performed chemical modifications of these phosphonates in order to obtain acidic derivatives. The structure of these compounds was characterized by NMR analyses and mass spectroscopy. We also studied their thermal behaviour and various crystalline phases were put in evidence by differential scanning calorimetry and optical microscopy. The thermal stability of these compounds was compared by thermogravimetric analyses.
