Erucylphosphocholine

Base Information Edit

Chemical Name:Erucylphosphocholine
CAS No.:143317-74-2
Molecular Formula:C₂₇H₅₆NO₄P
Molecular Weight:489.72
Hs Code.:
DSSTox Substance ID:DTXSID601315365
ChEMBL ID:CHEMBL229567
Mol file:143317-74-2.mol

Synonyms:EPC;erucylphosphocholine

Suppliers and Price of Erucylphosphocholine

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

American Custom Chemicals Corporation
ERUCYLPHOSPHOCHOLINE 95.00%
5MG
$ 504.48

Total 7 raw suppliers

Chemical Property of Erucylphosphocholine Edit

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
PSA：65.57000
Density:g/cm³
LogP:8.42410
XLogP3:9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:25
Exact Mass:489.39469627
Heavy Atom Count:33
Complexity:483

Purity/Quality:

99% ^*data from raw suppliers

ERUCYLPHOSPHOCHOLINE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCCCC=CCCCCCCCCCCCCOP(=O)([O-])OCC[N+](C)(C)C
Isomeric SMILES:CCCCCCCC/C=C\CCCCCCCCCCCCOP(=O)([O-])OCC[N+](C)(C)C

Technology Process of Erucylphosphocholine

There total 4 articles about Erucylphosphocholine 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:

: 629-98-1
erucyl alcohol

: 143317-74-2
(Z)-13-docosenylphosphocholine

Guidance literature:: Multi-step reaction with 3 steps

1: diisopropylethylamine / CH₂Cl₂ / -20 deg C, 30 min. then room temp., 30 min

2: Br₂ / CH₂Cl₂ / -20 --> 0 deg C, then 0 deg C, 10 min

3: propan-2-ol; acetonitrile; CHCl₃; H₂O

With bromine; N-ethyl-N,N-diisopropylamine; In dichloromethane; chloroform; water; isopropyl alcohol; acetonitrile;
DOI:10.1016/S0040-4039(00)78183-4

Reference yield:

: 2-[((Z)-Docos-13-enyl)oxy]-[1,3,2]dioxaphospholane

: 143317-74-2
(Z)-13-docosenylphosphocholine

Guidance literature:: Multi-step reaction with 2 steps

1: Br₂ / CH₂Cl₂ / -20 --> 0 deg C, then 0 deg C, 10 min

2: propan-2-ol; acetonitrile; CHCl₃; H₂O

With bromine; In dichloromethane; chloroform; water; isopropyl alcohol; acetonitrile;
DOI:10.1016/S0040-4039(00)78183-4