17195-46-9 Usage
Uses
Used in Agricultural Formulations:
Phosphonic acid, heptyl-, diethyl ester is used as a surfactant and dispersing agent for enhancing the effectiveness of agricultural products. Its ability to improve the distribution and absorption of active ingredients contributes to the overall performance of these formulations.
Used in Adhesives and Coatings:
In the adhesives and coatings industry, diethyl heptylphosphonate is employed as a surfactant and dispersing agent. It helps in achieving a uniform distribution of components, resulting in improved adhesion and coating properties.
Used in Metal Ion Production:
Phosphonic acid, heptyl-, diethyl ester is used as a chelating agent in the production of metal ions. Its ability to form stable complexes with metal ions aids in the efficient extraction and separation processes.
Used in Polymer Products as a Flame Retardant:
Diethyl heptylphosphonate is incorporated into some polymer products as a flame retardant. It helps in reducing the flammability of these materials, thereby enhancing their safety characteristics.
Safety Considerations:
Although diethyl heptylphosphonate is considered to have low to moderate toxicity and is not classified as a carcinogen, it is essential to handle it with care and follow proper safety protocols to minimize potential risks. This ensures the safe use of Phosphonic acid, heptyl-, diethyl ester in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 17195-46-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,1,9 and 5 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 17195-46:
(7*1)+(6*7)+(5*1)+(4*9)+(3*5)+(2*4)+(1*6)=119
119 % 10 = 9
So 17195-46-9 is a valid CAS Registry Number.
17195-46-9Relevant academic research and scientific papers
A new, effective approach for the C-C bond formation utilizing 1-, 2- and 3-phosphonyl substituted radicals derived from iodoalkylphosphonates and n-Bu3SnH/Et3B/O2 system
Balczewski,Pietrzykowski
, p. 7291 - 7304 (2007/10/03)
A new, practical synthesis of highly substituted phosphonates utilizing 1-, 2- and 3-phosphonyl substituted radicals derived from iodoalkylphosphonates and a catalytic or stoichiometric amounts of the n-Bu3SnH/Et3B/O2 reagent is described.
A free radical approach to functionalization of phosphonates utilizing novel 2- and 3-phosphonyl radicals
Balczewski, Piotr,Pietrzykowski, Witold M.
, p. 13681 - 13694 (2007/10/03)
A general method for the phosphonyl C2-C3-C bond formation under the free radical, reductive conditions is described. The new approach is based on the synthesis of novel 2- and 3-phosphonyl radicals 6, 9 derived from the corresponding 2- and 3-halo (X = Cl, Br, I) substituted phosphonates 7, 10 and their reaction with alkenes 4. Functionalized phosphonates 5, 8 possessing the 2+2 and 3+2 elongated carbon chain were obtained in 24-73% yields.
