3-(2-Hydroxyphenoxy)propane-1,2-diol

Base Information

Chemical Name:3-(2-Hydroxyphenoxy)propane-1,2-diol
CAS No.:19826-87-0
Molecular Formula:C9H12 O4
Molecular Weight:184.192
Hs Code.:2909499000
DSSTox Substance ID:DTXSID50941656
Nikkaji Number:J50.839J
Mol file:19826-87-0.mol

Synonyms:3-(2-hydroxyphenoxy)propane-1,2-diol;19826-87-0;Guaifenesin M (des-methyl);3-(2-hydroxyphenoxy)-1,2-propanediol;3-(o-Hydroxyphenoxy)-1,2-propanediol;1,2-Propanediol, 3-(o-hydroxyphenoxy)-;SCHEMBL6002023;DTXSID50941656;YFTRBASNPFHPAJ-UHFFFAOYSA-N;AKOS020789360

Suppliers and Price of 3-(2-Hydroxyphenoxy)propane-1,2-diol

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 4 raw suppliers

Chemical Property of 3-(2-Hydroxyphenoxy)propane-1,2-diol

Chemical Property:

Vapor Pressure:6.81E-07mmHg at 25°C
Melting Point:87-88 °C
Boiling Point:393.4°C at 760 mmHg
PKA:9.56±0.30(Predicted)
Flash Point:191.7°C
PSA：69.92000
Density:1.313g/cm³
LogP:0.12420
XLogP3:1.1
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:184.07355886
Heavy Atom Count:13
Complexity:140

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C(=C1)O)OCC(CO)O
Uses 3-(2-Hydroxyphenoxy)-1,2-propanediol is a substituted phenol with germicidal activity/properties.

Technology Process of 3-(2-Hydroxyphenoxy)propane-1,2-diol

There total 4 articles about 3-(2-Hydroxyphenoxy)propane-1,2-diol 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: 29.0%