Tris(3,4-dimethylphenyl) phosphate

Base Information

• Chemical Name: Tris(3,4-dimethylphenyl) phosphate
• CAS No.: 3862-11-1
• Molecular Formula: C24H27O4P
• Molecular Weight: 410.45
• European Community (EC) Number: 654-426-2
• NSC Number: 66431
• UNII: 1G071RJI9Q
• DSSTox Substance ID: DTXSID6022212
• Nikkaji Number: J173.958A
• Wikidata: Q27893893
• Mol file: 3862-11-1.mol

Synonyms:Tris(3,4-dimethylphenyl) phosphate;3862-11-1;Tri-3,4-xylyl phosphate;3,4-Xylenol, phosphate (3:1);TRIS(3,4-DIMETHYLPHENYL)PHOSPHATE;1G071RJI9Q;Phenol, 3,4-dimethyl-, phosphate (3:1);Phosphoric acid, tris(3,4-dimethylphenyl) ester;NSC-66431;Tri-3,4-xylenyl phosphate;HSDB 3911;NSC66431;TRIS(3,4-XYLENYL)PHOSPHATE;NSC 66431;UNII-1G071RJI9Q;SCHEMBL3472021;DTXSID6022212;AKOS024429087;Q27893893

Chemical Property of Tris(3,4-dimethylphenyl) phosphate

Chemical Property:

• Vapor Pressure: 1.65E-09mmHg at 25°C
• Melting Point: 72°C
• Boiling Point: 496.5°Cat760mmHg
• Flash Point: 267.2°C
• Density: 1.154g/cm³
• XLogP3: 7.2
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 6
• Exact Mass: 410.16469634
• Heavy Atom Count: 29
• Complexity: 491

Purity/Quality:

99%min ^*data from raw suppliers

3,4-XylenolPhosphate ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Chemical Classes: Other Classes -> Organophosphates, Other
• Canonical SMILES: CC1=C(C=C(C=C1)OP(=O)(OC2=CC(=C(C=C2)C)C)OC3=CC(=C(C=C3)C)C)C
• Uses: 3,4-Xylenol, phosphate (3:1), is an organo-phosphorus compounds, used as new thermal stabilizers and antifatigue agents for rubber vulcanizates, having applications in plastic and polymer industry.

Technology Process of Tris(3,4-dimethylphenyl) phosphate

There total 1 articles about Tris(3,4-dimethylphenyl) phosphate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

3,4-Dimethylphenol (95-65-8) → phosphoric acid tris-(3,4-dimethyl-phenyl ester) (3862-11-1)

Guidance literature:

With trichlorophosphate;

Reference yield:

phosphoric acid tris-(3,4-dimethyl-phenyl ester) (3862-11-1) + potassium cyanide (151-50-8) → 3,4-dimethylbenzonitrile (22884-95-3)

Guidance literature:

beim Destillieren;

upstream raw materials:

3,4-Dimethylphenol

Downstream raw materials:

3,4-dimethylbenzonitrile