Tris(4-nonylphenyl) phosphite

Base Information

• Chemical Name: Tris(4-nonylphenyl) phosphite
• CAS No.: 3050-88-2
• Deprecated CAS: 221229-36-3
• Molecular Formula: C45H69O3P
• Molecular Weight: 689.015
• Hs Code.: 2920901900
• European Community (EC) Number: 608-492-4
• UNII: E423N4NW2Z
• DSSTox Substance ID: DTXSID60872866
• Nikkaji Number: J175.126C
• Wikidata: Q66501631
• Mol file: 3050-88-2.mol

Synonyms:tris(4-nonylphenyl) phosphite;3050-88-2;Phenol, 4-nonyl-, phosphite (3:1);Tris(p-nonylphenyl) phosphite;Tris[p-nonylphenyl] phosphite;tris(4-nonylphenyl)phosphite;p-Nonylphenol, phosphite (3:1);SUMILIZER TNP;DOVERPHOS 4;trinonyl phenyl phosphite;SCHEMBL77176;tris-(p-nonylphenyl) phosphite;DTXSID60872866;TRIS(NONYLPHENYL)PHOSPHITE [INCI];CS-0160274;D97379;A820410;Tris(nonylphenyl) phosphite;TNNP;Tris(nonylphenol)phosphite;1-[2-[4-(2-phenyl-5,6,7,8-tetrahydrobenzo[f]benzofuran-3-yl)phenoxy]ethyl]pyrrolidine hydrochloride

Chemical Property of Tris(4-nonylphenyl) phosphite

Chemical Property:

• Refractive Index: n20/D 1.528(lit.)
• Boiling Point: 687.5 °C at 760 mmHg
• Flash Point: 467 °C
• PSA: 41.28000
• Density: 0.99 g/mL at 25 °C(lit.)
• LogP: 15.32960
• Storage Temp.: Sealed in dry,Room Temperature
• XLogP3: 19.3
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 30
• Exact Mass: 688.49843306
• Heavy Atom Count: 49
• Complexity: 613

Purity/Quality:

99.9% ^*data from raw suppliers

Tris(4-nonylphenyl)phosphite 97% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCCC1=CC=C(C=C1)OP(OC2=CC=C(C=C2)CCCCCCCCC)OC3=CC=C(C=C3)CCCCCCCCC

Technology Process of Tris(4-nonylphenyl) phosphite

There total 1 articles about Tris(4-nonylphenyl) phosphite 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: 99.56%

triphenyl phosphite (101-02-0) + non-1-ene (124-11-8) → tris(nonylphenyl) phosphite (3050-88-2)

Guidance literature:

triphenyl phosphite; With bis(p-dimethylaminophenyl)methanone; at 120 ℃; for 1h; Inert atmosphere;

non-1-ene; at 130 - 140 ℃; under 750.075 Torr; Reagent/catalyst; Temperature; Pressure; UV-irradiation; Autoclave;

Reference yield:

tris(nonylphenyl) phosphite (3050-88-2) → tri(p-nonylphenyl)phosphate

Guidance literature:

With Cumene hydroperoxide; In benzene; at 20 ℃; Rate constant;

upstream raw materials:

triphenyl phosphite

non-1-ene

Refernces