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Tris(2-methoxyphenyl) phosphate is a chemical compound with the molecular formula C21H21O6P and a molecular weight of 398.36 g/mol. It is primarily used as a flame retardant in various materials and products, enhancing their fire resistance properties by minimizing the spread of flames and reducing smoke generation in case of a fire.

563-03-1

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563-03-1 Usage

Uses

Used in Plastics Industry:
Tris(2-methoxyphenyl) phosphate is used as a flame retardant in plastics for enhancing their fire resistance properties, ensuring safety and compliance with fire safety regulations.
Used in Resins Industry:
Tris(2-methoxyphenyl) phosphate is used as a flame retardant in resins to improve their fire resistance, making them suitable for applications where fire safety is a concern.
Used in Foams Industry:
Tris(2-methoxyphenyl) phosphate is used as a flame retardant in foams to increase their fire resistance, providing an additional layer of safety in various applications.
However, there are concerns about the potential toxicity and environmental impact of tris(2-methoxyphenyl) phosphate, leading to increased scrutiny and regulation of its use in certain applications.

Check Digit Verification of cas no

The CAS Registry Mumber 563-03-1 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 3 respectively.
Calculate Digit Verification of CAS Registry Number 563-03:
(5*5)+(4*6)+(3*3)+(2*0)+(1*3)=61
61 % 10 = 1
So 563-03-1 is a valid CAS Registry Number.
InChI:InChI=1/C21H21O7P/c1-23-16-10-4-7-13-19(16)26-29(22,27-20-14-8-5-11-17(20)24-2)28-21-15-9-6-12-18(21)25-3/h4-15H,1-3H3

563-03-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name tris(2-methoxyphenyl) phosphate

1.2 Other means of identification

Product number -
Other names Guajacolphosphat

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:563-03-1 SDS

563-03-1Relevant academic research and scientific papers

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

, 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.

NOVEL COMPOUND AND RESIN COMPOSITION CONTAINING THE SAME

-

Paragraph 0023; 0055; 0056; 0057; 0058; 0059, (2014/11/11)

To provide a compound which can demonstrate flame retardancy equal to or higher than V-1 of the UL94 standard by adding a flame retardant to resin containing aromatic polyester and styrene polymer. To provide a compound represented by General Formula (1) of Claim 1. In General Formula (1), R1 to R3 are alkyl groups having 1 to 4 carbon atoms and R1 to R3 may be the same or different from each other.

"One-pot" Synthesis of Triaryl Phosphates a Reaction Calorimetry Approach

Silva, J. F. Cajaiba da,Nakayama, H. T.,Neto, C. Costa

, p. 71 - 82 (2007/10/03)

Triaryl phosphates were obtained in yields ranging from 85-96percent in a "one-pot" synthesis via an alkaline route: an ethanolic solution of sodium hydroxide was added to a solution of substituted phenol in toluene.The mixture was distilled until all ethanol was removed.Phosphorus oxychloride was then added and the toluene was distilled.The triaryl phosphates were characterized by NMR (1H and 31P), MS and FTIR.The heat capacity (Cp), the total heat transfer coefficient (U) and the reaction enthalpy (ΔH) were determined for the synthesis of tris(4-chloro-3-methylphenyl), tris(p-cresyl), tris(o-methoxyphenyl) and tris(p-nitrophenyl) phosphates. - Keywords: Phosphate; NMR spectra; heat capacity; phosphorus oxychloride

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