Trilauryl trithiophosphite

Base Information

• Chemical Name: Trilauryl trithiophosphite
• CAS No.: 1656-63-9
• Molecular Formula: C36H75PS3
• Molecular Weight: 635.163
• Hs Code.: 2931900090
• European Community (EC) Number: 216-751-4
• NSC Number: 44604
• UNII: F99G880I6H
• DSSTox Substance ID: DTXSID7061855
• Nikkaji Number: J56.161D
• Wikidata: Q27277841
• Mol file: 1656-63-9.mol

Synonyms:Trilauryl trithiophosphite;1656-63-9;Tridodecyl trithiophosphite;Phosphorotrithious acid, tridodecyl ester;tris(dodecylsulfanyl)phosphane;Trisdodecyl trithiophosphite;Tris(dodecylthio) phosphite;trilauryltrithiophosphite;UNII-F99G880I6H;F99G880I6H;EINECS 216-751-4;NSC 44604;NSC-44604;Weston TLTTP;Phosphorotrithiousacid, tridodecyl ester;Tris(laurylthio)phosphine;tridodecyl phosphorotrithioite;Tridodecyl Phosphonotrithioite;SCHEMBL284792;DTXSID7061855;C36H75PS3;BAA65663;NSC44604;C36-H75-P-S3;MFCD00015072;Phosphorotrithiousacid,tridodecyl ester;Phosphorotrithious Acid Tridodecyl Ester;FT-0755876;T0460;D92346;Q27277841

Chemical Property of Trilauryl trithiophosphite

Chemical Property:

• Vapor Pressure: 0mmHg at 25°C
• Melting Point: 23 ºC
• Refractive Index: 1.5000 to 1.5050
• Boiling Point: 667.8 ºC at 760 mmHg
• Flash Point: 357.7 ºC
• PSA: 89.49000
• Density: 0.92 g/mL(25/4 ºC)
• LogP: 16.17560
• Solubility.: very soluble in Ethanol,Toluene
• XLogP3: 18
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 36
• Exact Mass: 634.47685291
• Heavy Atom Count: 40
• Complexity: 373

Purity/Quality:

99% ^*data from raw suppliers

Trilauryl Trithiophosphite ^*data from reagent suppliers

Safty Information:

• Statements: 20/21/22-36/37/38
• Safety Statements: 26-36/37/39

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCCCCCSP(SCCCCCCCCCCCC)SCCCCCCCCCCCC
• Uses: Stabilizer, lubricant, chemical intermediate.

Technology Process of Trilauryl trithiophosphite

There total 3 articles about Trilauryl trithiophosphite 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:

1-dodecylthiol (112-55-0) → Tri-n-dodecyl phosphorotrithioite (1656-63-9)

Guidance literature:

With phosphorus trichloride; Heating;

DOI:10.1002/mrc.1260290307

Reference yield:

sodium dodecanethiolate (26960-77-0) → Tri-n-dodecyl phosphorotrithioite (1656-63-9)

Guidance literature:

With diethyl ether; phosphorus trichloride;

DOI:10.1039/jr9570000169

Reference yield:

→ Tri-n-dodecyl phosphorotrithioite (1656-63-9)

Guidance literature:

n-Dodecylmer..., PCl3;

upstream raw materials:

sodium dodecanethiolate

1-dodecylthiol

Downstream raw materials:

tridodecyltetrathiophosphate

S-dodecyl 4-methylbenzenesulfonothioate

Refernces

• 1、 -. "Processes for the production of sulphur-containing esters of phosphoric acid and phosphorous acid". . . Retrieved 2008/06/13.