Delmopinol

Base Information Edit

Chemical Name:Delmopinol
CAS No.:79874-76-3
Molecular Formula:C16H33NO2
Molecular Weight:271.444
Hs Code.:
European Community (EC) Number:943-564-1
UNII:DT67WL708F
DSSTox Substance ID:DTXSID10868552
Nikkaji Number:J22.787K
Wikidata:Q13571783
NCI Thesaurus Code:C78112
ChEMBL ID:CHEMBL2104220
Mol file:79874-76-3.mol

Synonyms:Decapinol Oral Rinse;delmopinol

Suppliers and Price of Delmopinol

Supply Marketing:Edit

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

TRC
Delmopinol
1mg
$ 165.00

American Custom Chemicals Corporation
DECAPINOL 95.00%
5MG
$ 502.24

Total 42 raw suppliers

Chemical Property of Delmopinol Edit

Chemical Property:

Vapor Pressure:3.84E-07mmHg at 25°C
Refractive Index:1.462
Boiling Point:374.576 °C at 760 mmHg
Flash Point:180.338 °C
PSA：32.70000
Density:0.924 g/cm³
LogP:3.00410
XLogP3:4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:10
Exact Mass:271.251129295
Heavy Atom Count:19
Complexity:205

Purity/Quality:

99.9% ^*data from raw suppliers

Delmopinol ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCC(CCC)CCCC1COCCN1CCO
Recent EU Clinical Trials:Effect of Delmopinol on treatment of Peri - implant mucositis : a randomised controlled clinical trial
Uses Delmopinol can be used in therapeutic use and biological study for its effect and fluoride on acid adaptation and acid production in dental plaque biofilms.

Technology Process of Delmopinol

There total 15 articles about Delmopinol 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: 89.0%

: methanesulfonic acid 1-[2-(2,2-dimethyl-oxazolidin-3-yl)-ethoxymethyl]-5-propyl-octyl ester

: 79874-76-3
3-(4-propyl-heptyl)-4-(2-hydroxyethyl)-morpholine

Guidance literature:: methanesulfonic acid 1-[2-(2,2-dimethyl-oxazolidin-3-yl)-ethoxymethyl]-5-propyl-octyl ester; With water; at 95 ℃; for 17h;

With sulfuric acid; water; In toluene; pH=1;

With sodium hydroxide; water; at 60 ℃; for 0.166667h; pH=14; Product distribution / selectivity;

Reference yield: 70.7%

: 79874-63-8
3-(4-propyl-heptyl)morpholine

: 107-07-3
2-chloro-ethanol

: 79874-76-3
3-(4-propyl-heptyl)-4-(2-hydroxyethyl)-morpholine

Guidance literature:: 3-(4-propyl-heptyl)morpholine; 2-chloro-ethanol; With potassium iodide; In ethanol; for 5h; Reflux;

With potassium hydroxide; In ethanol; for 11h; Reflux;