PALMITOYLCHOLINE IODIDE

Base Information

Chemical Name:PALMITOYLCHOLINE IODIDE
CAS No.:26640-69-7
Molecular Formula:C₂₁H₄₄NO₂*I
Molecular Weight:469.49
Hs Code.:2923900090
Mol file:26640-69-7.mol

Synonyms:Choline,iodide, palmitate (6CI,8CI); Ethanaminium, N,N,N-trimethyl-2-[(1-oxohexadecyl)oxy]-,iodide (9CI); Palmitic acid, ester with choline iodide (8CI); Palmitoylcholineiodide; Trimethyl(palmitoylethyl)ammonium iodide

Suppliers and Price of PALMITOYLCHOLINE IODIDE

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

American Custom Chemicals Corporation
PALMITOYLCHOLINE IODIDE 95.00%
5MG
$ 495.90

Total 4 raw suppliers

Chemical Property of PALMITOYLCHOLINE IODIDE

Chemical Property:

PSA：26.30000
LogP:2.72110
Storage Temp.:?20°C

Purity/Quality:

98%Min ^*data from raw suppliers

PALMITOYLCHOLINE IODIDE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of PALMITOYLCHOLINE IODIDE

There total 4 articles about PALMITOYLCHOLINE IODIDE 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:

: 40817-19-4
Palmitinsaeure-2-(dimethylamino)ethylester

: 74-88-4
methyl iodide

: 26640-69-7
palmitoylcholine iodide

Guidance literature:: With isopropyl alcohol;

Reference yield:

: 57-10-3
1-hexadecylcarboxylic acid

: 26640-69-7
palmitoylcholine iodide

Guidance literature:: Multi-step reaction with 3 steps

1: oxalyl dichloride / dichloromethane / 0.08 h / 65 °C

2: acetonitrile / 0.08 h / 20 °C

3: methanol / 0.08 h / 20 °C

With oxalyl dichloride; In methanol; dichloromethane; acetonitrile;
DOI:10.1021/ac103093w

Reference yield:

: 112-67-4
n-hexadecanoyl chloride

: 26640-69-7
palmitoylcholine iodide

Guidance literature:: Multi-step reaction with 2 steps

1: acetonitrile / 0.08 h / 20 °C

2: methanol / 0.08 h / 20 °C

In methanol; acetonitrile;
DOI:10.1021/ac103093w