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1-Palmitoyl-2-oleoyl-3-linolein

Base Information
  • Chemical Name:1-Palmitoyl-2-oleoyl-3-linolein
  • CAS No.:2680-59-3
  • Molecular Formula:C55H100O6
  • Molecular Weight:857.395
  • Hs Code.:
  • UNII:S6K38J8R5G
  • DSSTox Substance ID:DTXSID801345857
  • Nikkaji Number:J523.829C
  • Mol file:2680-59-3.mol
1-Palmitoyl-2-oleoyl-3-linolein

Synonyms:1-Palmitoyl-2-oleoyl-3-linoleoyl-rac-glycerol;2680-59-3;1587-93-5;1-Palmitoyl-2-oleoyl-3-linolein;S6K38J8R5G;Linolein, 2-oleo-3-palmito-1-;Olein, 1-linoleo-3-palmito-2-;Palmitin, 3-linoleo-2-oleo-1-;UNII-S6K38J8R5G;[1-hexadecanoyloxy-3-[(9Z,12Z)-octadeca-9,12-dienoyl]oxypropan-2-yl] (Z)-octadec-9-enoate;9,12-Octadecadienoic acid (9Z,12Z)-, 3-((1-oxohexadecyl)oxy)-2-(((9Z)-1-oxo-9-octadecen-1-yl)oxy)propyl ester;9,12-Octadecadienoic acid (9Z,12Z)-, 3-((1-oxohexadecyl)oxy)-2-(((9Z)-1-oxo-9-octadecenyl)oxy)propyl ester;9,12-Octadecadienoic acid (Z,Z)-, 3-((1-oxohexadecyl)oxy)-2-((1-oxo-9-octadecenyl)oxy)propyl ester, (Z)-;9,12-Octadecadienoic acid (9Z,12Z)-,3-[(1-oxohexadecyl)oxy]-2-[[(9Z)-1-oxo-9-octadecenyl]oxy]propyl ester;2-Oleo-3-palmito-1-linolein;SCHEMBL2733312;1-Palmitin-2-Olein-3-Linolein;CHEBI:190960;DTXSID801345857;HMS3649G11;Glycerol 1-linolate 2-oleate 3-palmitate;PD020878;SR-01000947057;J-016552;SR-01000947057-1;TG 16:0_18:1_18:2;1-Palmitoyl-2-oleoyl-3-linoleoyl-rac-glycerol, >=98%;(9Z,12Z)-9,12-Octadecadienoic Acid 3-[(1-Oxohexadecyl)oxy]-2-[[(9Z)-1-oxo- 9-octadecen-1-yl]oxy]propyl Ester

Suppliers and Price of 1-Palmitoyl-2-oleoyl-3-linolein
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
  • Usbiological
  • 1-Palmitoyl-2-oleoyl-3-linoleoyl-rac-glycerol
  • 10mg
  • $ 333.00
  • TRC
  • 1-Palmitoyl-2-oleoyl-3-linoleoyl-rac-glycerol
  • 25mg
  • $ 215.00
  • Sigma-Aldrich
  • 1-Palmitoyl-2-oleoyl-3-linoleoyl-rac-glycerol ≥98%
  • 100 mg
  • $ 956.00
  • Cayman Chemical
  • 1-Palmitoyl-2-oleoyl-3-linoleoyl-rac-glycerol ≥85%
  • 50mg
  • $ 328.00
  • Cayman Chemical
  • 1-Palmitoyl-2-oleoyl-3-linoleoyl-rac-glycerol ≥85%
  • 10mg
  • $ 78.00
  • Cayman Chemical
  • 1-Palmitoyl-2-oleoyl-3-linoleoyl-rac-glycerol ≥85%
  • 5mg
  • $ 41.00
  • Cayman Chemical
  • 1-Palmitoyl-2-oleoyl-3-linoleoyl-rac-glycerol ≥85%
  • 100mg
  • $ 574.00
  • AK Scientific
  • 1-Palmitoyl-2-oleoyl-3-linoleoyl-Rac-glycerol
  • 100mg
  • $ 874.00
Total 5 raw suppliers
Chemical Property of 1-Palmitoyl-2-oleoyl-3-linolein
Chemical Property:
  • Boiling Point:801.4±55.0 °C(Predicted) 
  • PSA:78.90000 
  • Density:0.923±0.06 g/cm3(Predicted) 
  • LogP:17.31690 
  • Storage Temp.:−20°C 
  • Solubility.:Chloroform (Slightly), Ethyl Acetate (Slightly) 
  • XLogP3:21.6
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:51
  • Exact Mass:856.75199091
  • Heavy Atom Count:61
  • Complexity:1030
Purity/Quality:

99% *data from raw suppliers

1-Palmitoyl-2-oleoyl-3-linoleoyl-rac-glycerol *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCCCCCCCCCCCCCCC(=O)OCC(COC(=O)CCCCCCCC=CCC=CCCCCC)OC(=O)CCCCCCCC=CCCCCCCCC
  • Isomeric SMILES:CCCCCCCCCCCCCCCC(=O)OCC(COC(=O)CCCCCCC/C=C\C/C=C\CCCCC)OC(=O)CCCCCCC/C=C\CCCCCCCC
  • Description POL is a common triglyceride component in seed and vegetable oils including olive, sesame, soybean, canola, corn, hazelnut, and many others. POL is one of the standard triglyceride components used for the USP analysis of sesame oil for pharmaceutical applications.
  • Uses 1-Palmitoyl-2-oleoyl-3-linoleoyl-rac-glycerol is the major component glycerides of palm oil. The major component glycerides of palm oil.
Technology Process of 1-Palmitoyl-2-oleoyl-3-linolein

There total 4 articles about 1-Palmitoyl-2-oleoyl-3-linolein 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:
Guidance literature:
Multi-step reaction with 2 steps
1: quinoline / benzene
2: quinoline / CHCl3
With quinoline; In chloroform; benzene;
Guidance literature:
Multi-step reaction with 2 steps
1: quinoline / benzene
2: quinoline / CHCl3
With quinoline; In chloroform; benzene;
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