TRIS(1-METHYLPROPYL) PHOSPHATE)

Base Information

Chemical Name:TRIS(1-METHYLPROPYL) PHOSPHATE)
CAS No.:2528-45-2
Molecular Formula:C12H27 O4 P
Molecular Weight:266.318
Hs Code.:2919900090

Synonyms:Phosphoricacid, tri-sec-butyl ester (8CI); sec-Butyl phosphate ((C4H9O)3PO) (6CI,7CI);Tri-sec-butyl phosphate; Tris(sec-butoxy)phosphine oxide

Suppliers and Price of TRIS(1-METHYLPROPYL) PHOSPHATE)

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 5 raw suppliers

Chemical Property of TRIS(1-METHYLPROPYL) PHOSPHATE)

Chemical Property:

Vapor Pressure:0.0191mmHg at 25°C
Refractive Index:1.427
Boiling Point:261.2°C at 760 mmHg
Flash Point:125.8°C
PSA：54.57000
Density:0.982g/cm³
LogP:4.53980

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of TRIS(1-METHYLPROPYL) PHOSPHATE)

There total 3 articles about TRIS(1-METHYLPROPYL) 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: 90.3%

: 78-92-2,15892-23-6
iso-butanol

: 78-86-4,53178-20-4
s-butyl chloride

: 2528-45-2
Tri-sec-butyl phosphate

Guidance literature:: With zinc(II) phosphide; oxygen; copper dichloride; at 50 ℃; under 750.06 Torr; Title compound not separated from byproducts;

Reference yield: 83.0%

: 78-92-2,15892-23-6
iso-butanol

: 2528-45-2
Tri-sec-butyl phosphate

Guidance literature:: With phosphorous; tetraethylammonium iodide; In water; acetonitrile; at 50 ℃; Electrolysis;
DOI:10.1016/j.jorganchem.2004.11.008