563-04-2 Usage
Description
TRI-M-TOLYL PHOSPHATE is a colorless, odorless liquid that is a type of wax. It is characterized by its clear, very slightly yellow to pink appearance and is often mixed with its isomers, ortho and meta, to achieve a consistent and stable formulation.
Uses
Used in Chemical Industry:
TRI-M-TOLYL PHOSPHATE is used as a chemical intermediate for the synthesis of various compounds and materials. Its versatile chemical properties make it suitable for use in the production of plastics, resins, and other polymers.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, TRI-M-TOLYL PHOSPHATE is used as a component in the formulation of certain drugs. Its stability and compatibility with other ingredients make it a valuable addition to the development of new medications.
Used in Agriculture:
TRI-M-TOLYL PHOSPHATE is employed as an additive in the agricultural sector, particularly in the production of pesticides and herbicides. Its ability to enhance the effectiveness of these chemicals while minimizing their environmental impact makes it a valuable asset in this industry.
Used in Lubricant Industry:
TRI-M-TOLYL PHOSPHATE is used as a lubricant additive, providing improved performance and reduced friction in various mechanical applications. Its compatibility with a wide range of materials and its ability to withstand high temperatures make it an ideal choice for use in the lubricant industry.
Used in Flame Retardant Industry:
In the flame retardant industry, TRI-M-TOLYL PHOSPHATE is used as an additive to enhance the fire-resistant properties of materials. Its ability to slow down the spread of flames and reduce the heat release rate makes it a valuable component in the development of safer materials for various applications.
Air & Water Reactions
May hydrolyze under alkaline conditions. . Insoluble in water.
Reactivity Profile
Organophosphates, such as TRI-M-TOLYL PHOSPHATE, are susceptible to formation of highly toxic and flammable phosphine gas in the presence of strong reducing agents such as hydrides. Partial oxidation by oxidizing agents may result in the release of toxic phosphorus oxides.
Check Digit Verification of cas no
The CAS Registry Mumber 563-04-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,6 and 3 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 563-04:
(5*5)+(4*6)+(3*3)+(2*0)+(1*4)=62
62 % 10 = 2
So 563-04-2 is a valid CAS Registry Number.
InChI:InChI=1/C21H21O4P/c1-16-7-4-10-19(13-16)23-26(22,24-20-11-5-8-17(2)14-20)25-21-12-6-9-18(3)15-21/h4-15H,1-3H3
563-04-2Relevant articles and documents
Diphenyl Diselenide-Catalyzed Synthesis of Triaryl Phosphites and Triaryl Phosphates from White Phosphorus
Zhang, Yue,Cai, Ziman,Chi, Yangyang,Zeng, Xiangzhe,Chen, Shuanghui,Liu, Yan,Tang, Guo,Zhao, Yufen
supporting information, p. 5158 - 5163 (2021/07/20)
Industrially important triaryl phosphites, traditionally prepared from PCl3, have been synthesized by a diphenyl diselenide-catalyzed one-step procedure involving white phosphorus and phenols, which provides a halogen- and transition metal-free way to these compounds. Subsequent oxidation of triaryl phosphites produces triaryl phosphates and triaryl thiophosphates. Phosphorotrithioates are also prepared efficiently from aromatic thiols and aliphatic thiols.
Microwave-assisted synthesis of triaryl phosphates
Sagar,Shinde,Bandgar
, p. 269 - 271 (2007/10/03)
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Polymer supported reagents: An efficiant and simple method for the synthesis of triaryl phosphates
Sagar,Thorat,Salunkhe
, p. 2029 - 2033 (2007/10/02)
The reaction of phosphoryl chloride with insoluble polymer-supported phenoxide ion reagents in benzene at room temperature, produced triaryl phosphates in excellent yields. The isolation of pure products by simple filtration and evaporation is an important feature of this method.
