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Tris(3,5-xylyl) phosphate is an aryl phosphate compound that is primarily recognized for its flame retardant properties. It is characterized by its ability to enhance the fire resistance of materials, making it a valuable additive in various industries.

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  • 25653-16-1 Structure
  • Basic information

    1. Product Name: tris(3,5-xylyl) phosphate
    2. Synonyms: tris(3,5-xylyl) phosphate;3,5-Dimethylphenylphosphate (3:1);Phosphoric acid tri(3,5-dimethylphenyl) ester;3,5-Xylyl phosphate, (C8H9o)3po;Nsc66515;Phenol, 3,5-dimethyl-, phosphate (3:1);3,5-Xylenol Phosphate (3:1)
    3. CAS NO:25653-16-1
    4. Molecular Formula: C24H27O4P
    5. Molecular Weight: 410.442541
    6. EINECS: 247-165-7
    7. Product Categories: N/A
    8. Mol File: 25653-16-1.mol
  • Chemical Properties

    1. Melting Point: 46 °C
    2. Boiling Point: 490.8°Cat760mmHg
    3. Flash Point: 263.8°C
    4. Appearance: /
    5. Density: 1.154g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: tris(3,5-xylyl) phosphate(CAS DataBase Reference)
    10. NIST Chemistry Reference: tris(3,5-xylyl) phosphate(25653-16-1)
    11. EPA Substance Registry System: tris(3,5-xylyl) phosphate(25653-16-1)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 25653-16-1(Hazardous Substances Data)

25653-16-1 Usage

Uses

Used in Plastics and Polymer Industry:
Tris(3,5-xylyl) phosphate is used as an additive for improving the fire resistance of plastics and polymers. Its flame retardant properties help to slow down the spread of fire, providing additional safety measures in the event of a fire.
Used in Lubricant Industry:
In the lubricant industry, tris(3,5-xylyl) phosphate is used as an additive in fireproof OMTI type lubricating oil. Its presence in the lubricant helps to reduce the risk of fire hazards, making it a crucial component in high-risk environments where the potential for fire is increased.

Check Digit Verification of cas no

The CAS Registry Mumber 25653-16-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,6,5 and 3 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 25653-16:
(7*2)+(6*5)+(5*6)+(4*5)+(3*3)+(2*1)+(1*6)=111
111 % 10 = 1
So 25653-16-1 is a valid CAS Registry Number.
InChI:InChI=1/C24H27O4P/c1-16-7-17(2)11-22(10-16)26-29(25,27-23-12-18(3)8-19(4)13-23)28-24-14-20(5)9-21(6)15-24/h7-15H,1-6H3

25653-16-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name tris(3,5-dimethylphenyl) phosphate

1.2 Other means of identification

Product number -
Other names Tris-<3,5-dimethyl-phenyl>-phosphat

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:25653-16-1 SDS

25653-16-1Relevant 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.

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