Dmrie

Base Information

Chemical Name:Dmrie
CAS No.:153312-64-2
Molecular Formula:Br*C₃₅H₇₄NO₃
Molecular Weight:636.881
Hs Code.:
UNII:PJ9GNX9BOP
DSSTox Substance ID:DTXSID30934728
Wikidata:Q27286590
Mol file:153312-64-2.mol

Synonyms:(3-dimyristyloxypropyl)(dimethyl)(hydroxyethyl)ammonium;dimyristyloxypropyl-3-dimethyl-hydroxyethyl ammonium;DMRIE

Suppliers and Price of Dmrie

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 2 raw suppliers

Chemical Property of Dmrie

Chemical Property:

PSA：38.69000
LogP:6.86310
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:33
Exact Mass:635.48521
Heavy Atom Count:40
Complexity:457

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCCCCCCCCCCCCCOCC(C[N+](C)(C)CCO)OCCCCCCCCCCCCCC.[Br-]

Technology Process of Dmrie

There total 3 articles about Dmrie 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: 58.0%

: 108-01-0
2-(N,N-dimethylamino)ethanol

: 1031848-61-9
rac-1-bromo-1-deoxy-2,3-di-O-tetradecylglycerol

: 153312-64-2
(±)-N-(2-hydroxyethyl)-N,N-dimethyl-2,3-bis(tetradecyloxy)-1-propanammonium bromide

Guidance literature:: In tert-butyl alcohol; for 46h; Reflux;
DOI:10.2174/1570178612666150930222411

Reference yield:

: (±)-2,3-bis-(tetradecyloxy)propyl benzoate

: 153312-64-2
(±)-N-(2-hydroxyethyl)-N,N-dimethyl-2,3-bis(tetradecyloxy)-1-propanammonium bromide

Guidance literature:: Multi-step reaction with 3 steps

1: lithium hydroxide / 12 h / 20 °C

2: triphenylphosphine; carbon tetrabromide / dichloromethane / 4 h / 0 °C / Inert atmosphere

3: tert-butyl alcohol / 46 h / Reflux

With carbon tetrabromide; triphenylphosphine; lithium hydroxide; In dichloromethane; tert-butyl alcohol;
DOI:10.2174/1570178612666150930222411

Reference yield:

: 112-71-0
1-Bromotetradecane

: 153312-64-2
(±)-N-(2-hydroxyethyl)-N,N-dimethyl-2,3-bis(tetradecyloxy)-1-propanammonium bromide

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium hydride / tetrahydrofuran / 13 h / 0 - 20 °C / Inert atmosphere

1.2: 27 h

2.1: lithium hydroxide / 12 h / 20 °C

3.1: triphenylphosphine; carbon tetrabromide / dichloromethane / 4 h / 0 °C / Inert atmosphere

4.1: tert-butyl alcohol / 46 h / Reflux

With carbon tetrabromide; sodium hydride; triphenylphosphine; lithium hydroxide; In tetrahydrofuran; dichloromethane; tert-butyl alcohol;
DOI:10.2174/1570178612666150930222411