1,2-O-DIHEXADECYL-SN-GLYCEROL

Base Information

Chemical Name:1,2-O-DIHEXADECYL-SN-GLYCEROL
CAS No.:67337-03-5
Molecular Formula:C35H72 O3
Molecular Weight:540.955
Hs Code.:
Mol file:67337-03-5.mol

Synonyms:1-Propanol,2,3-bis(hexadecyloxy)-, (S)-; 1,2-Di-O-hexadecyl-sn-glycerol;1,2-Dihexadecyl-sn-glycerol; sn-1,2-Dihexadecylglycerol

Suppliers and Price of 1,2-O-DIHEXADECYL-SN-GLYCEROL

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

TRC
1,2-O-Dihexadecyl-sn-glycerol
1g
$ 250.00

Crysdot
(S)-2,3-Bis(hexadecyloxy)propan-1-ol 97%
5g
$ 673.00

Biosynth Carbosynth
1,2-O-Dihexadecyl-sn-glycerol
1 g
$ 215.00

Biosynth Carbosynth
1,2-O-Dihexadecyl-sn-glycerol
500 mg
$ 135.00

Biosynth Carbosynth
1,2-O-Dihexadecyl-sn-glycerol
250 mg
$ 85.00

Biosynth Carbosynth
1,2-O-Dihexadecyl-sn-glycerol
100 mg
$ 43.00

Biosynth Carbosynth
1,2-O-Dihexadecyl-sn-glycerol
2 g
$ 344.00

AK Scientific
1,2-O-Ddihexadecyl-sn-glycerol
5g
$ 1051.00

AK Scientific
1,2-O-Ddihexadecyl-sn-glycerol
1g
$ 264.00

Total 7 raw suppliers

Chemical Property of 1,2-O-DIHEXADECYL-SN-GLYCEROL

Chemical Property:

Melting Point:48.5 - 49.5 °C
PSA：38.69000
LogP:11.34310
Storage Temp.:-15°C

Purity/Quality:

99% ^*data from raw suppliers

1,2-O-Dihexadecyl-sn-glycerol ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses 1,2-O-Dihexadecyl-sn-glycerol is used to prepare toll-like Receptor-2 Agonistic Diacylthioglycerol Lipopeptides. It is also used to syntheisze phospholipid analogs and evaluation as phosphatidylinositol 4-kinase inhibitors.

Technology Process of 1,2-O-DIHEXADECYL-SN-GLYCEROL

There total 6 articles about 1,2-O-DIHEXADECYL-SN-GLYCEROL 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: 87.0%

: 13071-57-3
(R)-((2,3-bis(hexadecyloxy)propoxy)methyl)benzene

: 67337-03-5
(2R)-3-hydroxy-1,2-di-hexadecyloxypropane

Guidance literature:: With hydrogen; palladium on activated charcoal; In tetrahydrofuran; methanol; for 16h;
DOI:10.1002/(SICI)1521-3765(20000103)6:1<111::AID-CHEM111>3.0.CO;2-X

Reference yield: 67.0%

: 157999-06-9
2,3-Di-O-hexadecyl-sn-glycerol 1-(3'-nitrobenzenesulfonate)

: 67337-03-5
(2R)-3-hydroxy-1,2-di-hexadecyloxypropane

Guidance literature:: With tetra(n-butyl)ammonium hydroxide; In tetrahydrofuran; Heating;
DOI:10.1021/jo00090a011

Reference yield:

: 112-82-3
hexadecanyl bromide

: 67337-03-5
(2R)-3-hydroxy-1,2-di-hexadecyloxypropane

Guidance literature:: Multi-step reaction with 2 steps

1: 68 percent / NaH; tetrabutylammonium iodide / dimethylformamide / 36 h / 20 °C

2: 87 percent / H₂ / 10 percent Pd/C / tetrahydrofuran; methanol / 16 h

With hydrogen; tetra-(n-butyl)ammonium iodide; sodium hydride; palladium on activated charcoal; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; 1: Etherification / 2: Hydrogenolysis;
DOI:10.1002/(SICI)1521-3765(20000103)6:1<111::AID-CHEM111>3.0.CO;2-X