Pyridinium hexafluorophosphate

Base Information

Chemical Name:Pyridinium hexafluorophosphate
CAS No.:16941-15-4
Molecular Formula:C5H6F6NP
Molecular Weight:225.074
Hs Code.:
Mol file:16941-15-4.mol

Synonyms:

Suppliers and Price of Pyridinium hexafluorophosphate

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 6 raw suppliers

Chemical Property of Pyridinium hexafluorophosphate

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
Density:g/cm³

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of Pyridinium hexafluorophosphate

There total 1 articles about Pyridinium hexafluorophosphate 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: 100.0%

: 110-86-1
pyridine

: 16941-15-4
pyridinium hexafluorophosphate

Guidance literature:: With hexafluorophosphoric acid; In methanol; Inert atmosphere;
DOI:10.1002/chem.201801280

Reference yield:

: 16941-15-4
pyridinium hexafluorophosphate

: potassium hydroxide

: 17084-13-8
potassium hexafluorophosphate

Guidance literature:: In ethanol; for 0.166667h;

Reference yield:

: 16941-15-4
pyridinium hexafluorophosphate

: 7647-19-0,874483-74-6
phosphorus pentafluoride

Guidance literature:: With sulfur trioxide; In neat (no solvent); byproducts: pyridinium fluorosulphate; stirring complex salt in flask; evacuation; introduction of SO3 vapour in stages; keeping reactants in contact for 15-20 mins after addn. of last aliquot of SO3; cooling with liquid N2, then with alcohol bath at -50°C; apparatus described;; warming to room temp.; pumping free from excess SO3; filling vessel with dry N2; detn. by IR, 19F-NMR; elem. anal.;;