9-Octadecenyl acetate

Base Information

• Chemical Name: 9-Octadecenyl acetate
• CAS No.: 693-80-1
• Molecular Formula: C20H38O2
• Molecular Weight: 310.521
• Nikkaji Number: J970.348I
• Metabolomics Workbench ID: 4042
• Mol file: 693-80-1.mol

Synonyms:9-Octadecenyl acetate;Acetic acid, oleyl ester;Z-9-Octadecen-1-ol acetate;[(E)-octadec-9-enyl] acetate;octadec-9-enyl acetate;(e)-9-octadecenyl acetate;E-9-Octadecen-1-ol acetate;SCHEMBL523910;Acetate(Z)-9-Octadecen-1-ol;SCHEMBL1300671;Acetic acid 9-octadecenyl ester;(9E)-9-Octadecenyl acetate #;CHEBI:180266;GYGAZRPDUOHMAF-ZHACJKMWSA-N;LMFA07010397;AKOS015902391

Chemical Property of 9-Octadecenyl acetate

Chemical Property:

• Vapor Pressure: 1.9E-06mmHg at 25°C
• Refractive Index: 1.455
• Boiling Point: 395 °C at 760 mmHg
• Flash Point: 97.4 °C
• PSA: 26.30000
• Density: 0.872 g/cm³
• LogP: 6.58700
• Storage Temp.: −20°C
• Solubility.: Chloroform, Methanol
• XLogP3: 7.9
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 17
• Exact Mass: 310.287180451
• Heavy Atom Count: 22
• Complexity: 258

Purity/Quality:

98% ^*data from raw suppliers

Oleyl Acetate ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: CCCCCCCCC=CCCCCCCCCOC(=O)C
• Isomeric SMILES: CCCCCCCC/C=C/CCCCCCCCOC(=O)C

Technology Process of 9-Octadecenyl acetate

There total 7 articles about 9-Octadecenyl acetate 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: 96.0%

oleoyl alcohol (143-28-2,593-47-5,84286-21-5) + acetic anhydride (108-24-7) → oleyl acetate (693-80-1)

Guidance literature:

With pyridine; dmap; at 0 - 20 ℃; for 12h;

DOI:10.1016/j.bbamem.2015.08.021

Reference yield:

oleoyl alcohol (143-28-2,593-47-5,84286-21-5) + acetyl chloride (75-36-5) → oleyl acetate (693-80-1)

Guidance literature:

With pyridine;

DOI:10.1002/hlca.19520350225

Reference yield:

oleoyl alcohol (143-28-2,593-47-5,84286-21-5) → oleyl acetate (693-80-1)

Guidance literature:

With acetic anhydride;

upstream raw materials:

oleoyl alcohol

acetic anhydride

acetyl chloride

Methyl oleate

Downstream raw materials:

9-Decen-1-ol

9-decen-1-yl acetate

(Z)-9-tetradecenal

(Z)-9-tetradecen-1-ol

Refernces

• 1、 Zheng, Yu,Liu, Xin,Samoshina, Nataliya M.,Samoshin, Vyacheslav V.,Franz, Andreas H.,Guo, Xin. "Trans-2-Aminocyclohexanol-based amphiphiles as highly efficient helper lipids for gene delivery by lipoplexes". . p. 3113 - 3125. Retrieved 2015/10/20.
• 2、 -. "Surface-active hydroxysulfonates". . . Retrieved 2008/06/13.