Phosphonium, tributyl(carboxymethyl)-, chloride

Base Information

Chemical Name:Phosphonium, tributyl(carboxymethyl)-, chloride
CAS No.:1519-43-3
Molecular Formula:C₁₄H₃₀O₂P*Cl
Molecular Weight:296.818
Hs Code.:
Mol file:1519-43-3.mol

Synonyms:Phosphonium,tributyl(carboxymethyl)-, chloride (8CI,9CI);Tributyl(carboxymethyl)phosphonium chloride (7CI); NSC 41945

Suppliers and Price of Phosphonium, tributyl(carboxymethyl)-, chloride

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 7 raw suppliers

Chemical Property of Phosphonium, tributyl(carboxymethyl)-, chloride

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
PSA：50.89000
Density:g/cm³
LogP:1.49290

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of Phosphonium, tributyl(carboxymethyl)-, chloride

There total 3 articles about Phosphonium, tributyl(carboxymethyl)-, chloride 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:

: 998-40-3
tributylphosphine

: 79-11-8
chloroacetic acid

: 1519-43-3
tributyl(carboxymethyl)phosphonium chloride

Guidance literature:: at 20 ℃; for 24h; Inert atmosphere;
DOI:10.3184/174751913X13787959859380

Reference yield:

: 998-40-3
tributylphosphine

: 1519-43-3
tributyl(carboxymethyl)phosphonium chloride

Guidance literature:: Multi-step reaction with 2 steps

1: diethyl ether

2: aq. HCl

With hydrogenchloride; In diethyl ether;
DOI:10.1021/jo01023a011