Bisphenol A bis(2-hydroxypropyl) ether

Base Information

Chemical Name:Bisphenol A bis(2-hydroxypropyl) ether
CAS No.:116-37-0
Deprecated CAS:144834-14-0,2088313-17-9,2099694-66-1
Molecular Formula:C21H28O4
Molecular Weight:344.451
Hs Code.:2909499000
European Community (EC) Number:204-137-9
NSC Number:408494
UNII:S5K2510L3D
DSSTox Substance ID:DTXSID8051592
Nikkaji Number:J39.711C
Wikidata:Q27148853
Mol file:116-37-0.mol

Synonyms:oxypropyldiphenylolpropane

Suppliers and Price of Bisphenol A bis(2-hydroxypropyl) ether

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

AK Scientific
BisphenolAbis(2-hydroxypropyl)ether
2mg
$ 185.00

Total 69 raw suppliers

Chemical Property of Bisphenol A bis(2-hydroxypropyl) ether

Chemical Property:

Vapor Pressure:0Pa at 20℃
Boiling Point:505.4 °C at 760 mmHg
PKA:14.05±0.20(Predicted)
Flash Point:259.5 °C
PSA：58.92000
Density:1.102 g/cm³
LogP:3.53170
Water Solubility.:109mg/L at 20℃
XLogP3:4.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:8
Exact Mass:344.19875937
Heavy Atom Count:25
Complexity:334

Purity/Quality:

99%, ^*data from raw suppliers

BisphenolAbis(2-hydroxypropyl)ether ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Chemical Classes:Other Classes -> Other Aromatic Compounds
Canonical SMILES:CC(COC1=CC=C(C=C1)C(C)(C)C2=CC=C(C=C2)OCC(C)O)O
Uses Bisphenol A bis(2-hydroxypropyl) ether is an engineered material used as a coating for improved adhesion of aminoplasts to metals.

Technology Process of Bisphenol A bis(2-hydroxypropyl) ether

There total 5 articles about Bisphenol A bis(2-hydroxypropyl) ether 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: 99.0%

: 1675-54-3,25085-99-8,55774-85-1,91384-80-4
diphenylolpropane diglycidyl ether

: 116-37-0
Bisphenol A propoxylate

Guidance literature:: With [carbonylchlorohydrido{bis[2-(diphenylphosphinomethyl)ethyl]amino}ethylamino] ruthenium(II); potassium tert-butylate; hydrogen; In toluene; at 75 ℃; for 24h; under 37503.8 Torr; regioselective reaction;
DOI:10.1021/acs.orglett.9b03995

Reference yield:

: 80-05-7
BPA

: 75-56-9,16033-71-9
methyloxirane

: 116-37-0
Bisphenol A propoxylate

Guidance literature:: BPA; With sodium hydroxide; In tetrahydrofuran; at 20 ℃; for 3h; Inert atmosphere;

methyloxirane; In tetrahydrofuran; Inert atmosphere;