3-Dodecyloxypropane-1,2-diol

Base Information

Chemical Name:3-Dodecyloxypropane-1,2-diol
CAS No.:1561-07-5
Molecular Formula:C₁₅H₃₂O₃
Molecular Weight:260.417
Hs Code.:
European Community (EC) Number:216-334-7
NSC Number:38645
UNII:7P8B67DIVI
DSSTox Substance ID:DTXSID101315691
Nikkaji Number:J206.792G
Wikidata:Q27268674

Synonyms:1-dodecylglycerol;1-O-dodecylglycerol;glycerol monolaurate;lauricidin;monododecylglycerol;monoglycerol laurate;monolaurin;rac-SN-1(3)-dodecylglycerol

Suppliers and Price of 3-Dodecyloxypropane-1,2-diol

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-O-Dodecyl-rac-glycerol
2.5g
$ 240.00

Crysdot
3-(Dodecyloxy)propane-1,2-diol 97%
10g
$ 875.00

Crysdot
3-(Dodecyloxy)propane-1,2-diol 97%
5g
$ 475.00

Total 14 raw suppliers

Chemical Property of 3-Dodecyloxypropane-1,2-diol

Chemical Property:

Vapor Pressure:1.03E-07mmHg at 25°C
Melting Point:62-63 °C
Boiling Point:390.5°C at 760 mmHg
PKA:13.68±0.20(Predicted)
Flash Point:190°C
PSA：49.69000
Density:0.937g/cm³
LogP:3.27710
Storage Temp.:−20°C
XLogP3:4.4
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:14
Exact Mass:260.23514488
Heavy Atom Count:18
Complexity:151

Purity/Quality:

99% ^*data from raw suppliers

1-O-Dodecyl-rac-glycerol ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCCCCCCCOCC(CO)O
Uses 1-O-Dodecylglycerol is a antibacterial agent which stimulates autolysin activity in Streptococcus faecium ATCC 9790. It is also found to be synergistic with amphotericin B against fungi.

Technology Process of 3-Dodecyloxypropane-1,2-diol

There total 35 articles about 3-Dodecyloxypropane-1,2-diol 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: 99.0%

: 478549-98-3
3-O-dodecyl-1,2-O-isopropylidene-sn-glycerol

: 90904-23-7,1561-07-5
3-O-dodecyl-sn-glycerol

Guidance literature:: With 80percent aq. AcOH; at 20 ℃;
DOI:10.1021/ja020396+

Reference yield: 96.3%

: 2461-18-9
dodecyl glycidyl ether

: 100165-14-8,1561-07-5
3-dodecyloxypropane-1,2-diol

Guidance literature:: With formic acid; sodium hydroxide; In diethylene glycol dimethyl ether; at 130 ℃; for 12h;

Reference yield: 73.0%

: 111-82-0
methyl n-dodecanoate

: 56-81-5,25618-55-7,64333-26-2,8013-25-0
glycerol

: 100165-14-8,1561-07-5
3-dodecyloxypropane-1,2-diol

: 17174-67-3
2-dodecyloxy-propane-1,3-diol

Guidance literature:: With 5%-palladium/activated carbon; camphor-10-sulfonic acid; hydrogen; at 120 ℃; for 16h; under 37503.8 Torr; regioselective reaction; Autoclave;
DOI:10.1039/c3gc36907b