2,3-Bis(palmitoyloxy)propyl dihydrogen phosphate

Base Information

Chemical Name:2,3-Bis(palmitoyloxy)propyl dihydrogen phosphate
CAS No.:19698-29-4
Deprecated CAS:5129-68-0
Molecular Formula:C35H69O8P
Molecular Weight:648.902
Hs Code.:
European Community (EC) Number:243-238-2
DSSTox Substance ID:DTXSID00864003
Nikkaji Number:J225.252J
Wikidata:Q27147644
Metabolomics Workbench ID:75123
ChEMBL ID:CHEMBL1606485

Synonyms:1,2-dipalmitoyl-sn-glycero-3-phosphate;dipalmitoyl phosphatidic acid;dipalmitoylphosphatidic acid;dipalmitoylphosphatidic acid, (+-)-isomer;dipalmitoylphosphatidic acid, (R)-isomer;dipalmitoylphosphatidic acid, ammonium salt;dipalmitoylphosphatidic acid, calcium salt;dipalmitoylphosphatidic acid, sodium salt

Suppliers and Price of 2,3-Bis(palmitoyloxy)propyl dihydrogen phosphate

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 6 raw suppliers

Chemical Property of 2,3-Bis(palmitoyloxy)propyl dihydrogen phosphate

Chemical Property:

Boiling Point:706.9°Cat760mmHg
Flash Point:381.3°C
Density:1.015g/cm³
XLogP3:12.9
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:36
Exact Mass:648.47300615
Heavy Atom Count:44
Complexity:696

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCCCCCCCCCCC(=O)OCC(COP(=O)(O)O)OC(=O)CCCCCCCCCCCCCCC

Technology Process of 2,3-Bis(palmitoyloxy)propyl dihydrogen phosphate

There total 13 articles about 2,3-Bis(palmitoyloxy)propyl dihydrogen phosphate 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:

: 1042289-75-7
rac-1,2-dipalmitoylglycerol

: 19698-29-4
1,2-Dipalmitoylphosphatidic acid

Guidance literature:: With water; triethylamine; trichlorophosphate; Yield given. Multistep reaction; 1.) n-hexane, toluene, room temperature, overnight, 2.) room temperature;
DOI:10.1021/jm00117a020

Reference yield:

: 69176-47-2
1,2-di-O-palmitoyl-3-O-benzyl-rac-glycerol

: 19698-29-4
1,2-Dipalmitoylphosphatidic acid

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogen / 10percent Pd/C / hexane

2: 1.) POCl₃, Et₃N, 2.) water / 1.) n-hexane, toluene, room temperature, overnight, 2.) room temperature

With water; hydrogen; triethylamine; trichlorophosphate; palladium on activated charcoal; In hexane;
DOI:10.1021/jm00117a020

Reference yield:

: 112-67-4
n-hexadecanoyl chloride

: 19698-29-4
1,2-Dipalmitoylphosphatidic acid

Guidance literature:: Multi-step reaction with 3 steps

1: pyridine / benzene / Heating

2: hydrogen / 10percent Pd/C / hexane

3: 1.) POCl₃, Et₃N, 2.) water / 1.) n-hexane, toluene, room temperature, overnight, 2.) room temperature

With pyridine; water; hydrogen; triethylamine; trichlorophosphate; palladium on activated charcoal; In hexane; benzene;
DOI:10.1021/jm00117a020