2-Octadecylicosanoic acid

Base Information

Chemical Name:2-Octadecylicosanoic acid
CAS No.:108293-08-9
Molecular Formula:C₃₈H₇₆O₂
Molecular Weight:565.02
Hs Code.:2915900090
DSSTox Substance ID:DTXSID70550683
Wikidata:Q82430110
Mol file:108293-08-9.mol

Synonyms:2-octadecylicosanoic acid;108293-08-9;2-OCTADECYLEICOSANOIC ACID;Eicosanoic acid,2-octadecyl-;2,2-bis-stearyl acetic acid;SCHEMBL4599227;DTXSID70550683;RIQSWUKPKYYGQX-UHFFFAOYSA-N;CS-0098424;D75934

Suppliers and Price of 2-Octadecylicosanoic acid

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
2-OctadecyleicosanoicAcid
50mg
$ 65.00

American Custom Chemicals Corporation
2-OCTADECYLEICOSANOIC ACID 95.00%
5MG
$ 504.36

Total 3 raw suppliers

Chemical Property of 2-Octadecylicosanoic acid

Chemical Property:

PSA：37.30000
LogP:13.99040
Storage Temp.:Refrigerator
Solubility.:Chloroform (Slightly)
XLogP3:18.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:35
Exact Mass:564.58453166
Heavy Atom Count:40
Complexity:438

Purity/Quality:

98% ^*data from raw suppliers

2-OctadecyleicosanoicAcid ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCCCCCCCCCCCCCC(CCCCCCCCCCCCCCCCCC)C(=O)O
Uses 2-Octadecyleicosanoic acid is used as a reagent to synthesize Lipid Oligonucleitide Conjugates, compounds that act as a “drug delivery” system to mutated/infected cells.

Technology Process of 2-Octadecylicosanoic acid

There total 7 articles about 2-Octadecylicosanoic acid 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: 89.0%

: 96873-04-0
2,2-dioctadecylmalonic acid

: 108293-08-9
2-octadecyleicosanoic acid

Guidance literature:: In decane; for 16h; Reflux;

Reference yield:

: 112-89-0
1-Bromooctadecane

: 108293-08-9
2-octadecyleicosanoic acid

Guidance literature:: Multi-step reaction with 4 steps

1: 52 percent / NaOBu / butan-1-ol / 5 h / Heating

2: 68 percent / 18-crown-6, potassium hydroxide / toluene / 12 h / Heating

3: 76 percent / KOH, 18-crown-6 / toluene / 5 h / Heating

4: 6 h / 150 - 170 °C

With potassium hydroxide; 18-crown-6 ether; sodium butanolate; In toluene; butan-1-ol;

Reference yield:

: 42607-83-0
2,2-bis-stearyl diethyl malonate

: 108293-08-9
2-octadecyleicosanoic acid

Guidance literature:: Multi-step reaction with 2 steps

1: potassium hydroxide / isopropyl alcohol; water / 16 h / 80 °C

2: sulfuric acid / water

With sulfuric acid; potassium hydroxide; In water; isopropyl alcohol;
DOI:10.1039/c3tb20357c