13244-67-2 Usage
Uses
Used in Plastic Industry:
Phosphonic acid, phenyl-, monooctyl ester is used as a plasticizer for enhancing the flexibility and durability of plastics. It is particularly effective in materials such as polyvinyl chloride (PVC) and other polymers, improving their overall performance.
Used in Flame Retardant Industry:
Phosphonic acid, phenyl-, monooctyl ester is used as a flame retardant additive, providing fire resistance to various materials. Its inclusion in products like PVC and other polymers helps to slow down the spread of fire and increase safety.
Used in Building Materials Production:
Phosphonic acid, phenyl-, monooctyl ester is used in the manufacturing of building materials to improve their properties, such as flexibility and durability. This makes it a valuable component in the construction industry.
Used in Electrical and Electronic Products Manufacturing:
Phosphonic acid, phenyl-, monooctyl ester is also utilized in the production of electrical and electronic products, where its properties can enhance the performance and safety of these devices.
However, it is crucial to handle Phosphonic acid, phenyl-, monooctyl ester with care, as it can be harmful if ingested, inhaled, or absorbed through the skin. Proper safety measures should be taken to minimize potential health risks.
Check Digit Verification of cas no
The CAS Registry Mumber 13244-67-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,4 and 4 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 13244-67:
(7*1)+(6*3)+(5*2)+(4*4)+(3*4)+(2*6)+(1*7)=82
82 % 10 = 2
So 13244-67-2 is a valid CAS Registry Number.
13244-67-2Relevant academic research and scientific papers
Microwave-assisted esterification of P-acids
ábrányi-Balogh, Péter,Harsági, Nikoletta,Keglevich, Gy?rgy,Kiss, Nóra Zsuzsa
, (2021/10/25)
The possibilities for the preparation of dialky phenylphosphonates were evaluated. On the one hand, the oxidation of phenyl-H-phosphinates gave the corresponding phenylphosphonic acid monoesters. On the other hand, phenylphosphonates may be prepared by MW-assisted direct esterification of phenylphosphonic acid. The reaction with alcohols was performed under MW irradiation in the presence of an ionic liquid as the catalyst. The second ester function was established by alkylating esterification carried out with alkyl halides in the presence of triethylamine under MW conditions.
Solvent Extraction of Trivalent Yttrium, Holmium, and Erbium by Novel Types of Acidic Organophosphonates
Ohto, Keisuke,Inoue, Katsutoshi,Goto, Masahiro,Nakashio, Fumiyuki,Nagasaki, Takeshi,et al.
, p. 2528 - 2535 (2007/10/02)
New types of acidic organophosphonates, HR with different hydrophobic groups, were synthesized in order to investigate their extraction behavior for heavy rare earth elements (Y3+, Ho3+, and Er3+) from aqueous acidic chlor
