51732-57-1

Basic information

• Product Name: Phosphoric acid,esters,1,4-phenylene tetraphenyl ester
• CAS NO: 51732-57-1
• Molecular Weight: 574.463
• Mol File: 51732-57-1.mol

Chemical Properties

• CAS DataBase Reference: Phosphoric acid,esters,1,4-phenylene tetraphenyl ester (CAS DataBase Reference)
• NIST Chemistry Reference: Phosphoric acid,esters,1,4-phenylene tetraphenyl ester (51732-57-1)
• EPA Substance Registry System: Phosphoric acid,esters,1,4-phenylene tetraphenyl ester (51732-57-1)

Safety Data

• Hazardous Substances Data: 51732-57-1(Hazardous Substances Data)

Usage

Uses

Used in Polymer and Plastic Production:
Phosphoric acid, esters, 1,4-phenylene tetraphenyl ester is used as a flame retardant and plasticizer for improving the fire resistance and flexibility of polymers and plastics. It helps in reducing the flammability of these materials, making them safer for use in various applications.
Used in Electrical Equipment Manufacturing:
In the electrical equipment industry, Phosphoric acid, esters, 1,4-phenylene tetraphenyl ester is used as a flame retardant to enhance the fire safety of products. It is incorporated into the materials used in the manufacturing of electrical components, ensuring they meet the required fire safety standards.
Used in Construction Materials:
Phosphoric acid, esters, 1,4-phenylene tetraphenyl ester is utilized in the production of construction materials to improve their fire resistance. It is incorporated into materials such as insulation, coatings, and adhesives, providing an additional layer of protection against fire hazards in buildings.
Used in Automotive Components:
In the automotive industry, Phosphoric acid, esters, 1,4-phenylene tetraphenyl ester is used as a flame retardant in the manufacturing of various components. It helps in reducing the flammability of materials used in car interiors, wiring, and other parts, ensuring the safety of passengers and the vehicle.
Used in Consumer Products:
Phosphoric acid, esters, 1,4-phenylene tetraphenyl ester can also be found in consumer products such as electronics, furniture, and textiles, where fire safety is a priority. It is used as a flame retardant to reduce the risk of fire hazards and ensure the safety of these products during their usage.
It is crucial to handle Phosphoric acid, esters, 1,4-phenylene tetraphenyl ester with care and follow proper safety measures due to its potential health and environmental hazards.

Upstream product

• 123-31-9 hydroquinone 
• 2524-64-3 chlorophosphoric acid diphenyl ester 

Relevant articles and documents

Triphenyltin(iv) adducts of diphosphoryl ligands: Structural, electronic and energy aspects from X-ray crystallography and theoretical calculations

Some triphenyltin(iv) adducts with a family of diphosphoryl ligands, RR′P(O)-X-P(O)RR′ (R = OPh, Ph, R′ = R, An (aniline)) and X = 1,4-OC6H4O, 1,4-OC6H4NH, 1,4-NHC6H4NH 1,4-(NHCH2)2C6H4, 1,3-(NHCH2)2C6H4 and piperazine have been synthesized and characterized by IR and NMR spectroscopy. X-Ray crystallography reveals that the structure of these complexes comprises a binuclear arrangement with two SnPh3Cl moieties linked via the bridging P(O)-X-P(O) ligands. The influence of the ligand structures on the organization of the crystal structures and the coordination interactions are discussed. Studies of the crystal packing reveal NH...Cl, CH...Cl or CH...O hydrogen bonding interactions, as a function of the X or R groups, to be the main factor controlling the supramolecular architecture in this series of complexes. Based on the results from quantum theory of atoms in molecules (QTAIM) and natural bond orbital (NBO) analyses, Sn-ligand interactions are found to be mainly electrostatic (donor-acceptor-like with charge transfer from the phosphoryl donors to the tin atoms). The stronger coordination bonds are found in the complexes containing Ph substituents with aliphatic spacers, in agreement with the experimental evidence. Binuclear arrangements instead of polymeric or chelating systems may be attributed to the steric demands of SnPh3Cl, regardless of the ligand structures.

WATER MISCIBLE SOLVENT BASED PROCESS FOR PURIFYING A BISPHOSPHATE

There is provided herein a process for purifying bisphosphate comprising solvating a molten bisphosphate in a mixture of water and water miscible solvent; cooling the solution over a period and to a temperature that provides for crystallization of solid product; increasing the pH of the solution prior to, and/or during, and/or after the initiation of crystallization, and/or after crystallization, by the addition of a base; and after crystallization is complete, separating solid product from the solution; washing the separated solid product in the same and/or different mixture of water and water miscible solvent; and, washing the solid product which has been washed in the mixture with water.