Octyl laurate

Base Information

• Chemical Name: Octyl laurate
• CAS No.: 5303-24-2
• Molecular Formula: C20H40 O2
• Molecular Weight: 312.536
• Hs Code.: 2915900090
• European Community (EC) Number: 226-149-3
• UNII: I76CUL5YG5
• DSSTox Substance ID: DTXSID7063764
• Nikkaji Number: J115.175D
• Wikidata: Q27280533
• Mol file: 5303-24-2.mol

Synonyms:Octyl laurate;octyl dodecanoate;Dodecanoic acid, octyl ester;5303-24-2;Caprylyl laurate;EINECS 226-149-3;UNII-I76CUL5YG5;I76CUL5YG5;n-octyl n-dodecanoate;TEGOSOFT OL;Lauric acid octyl ester;NIKKOL GS-KL;Lauric acid, octyl ester;SCHEMBL55129;CAPRYLYL LAURATE [INCI];DTXSID7063764;Dodecanoic acid, n.-octyl ester;Q27280533

Chemical Property of Octyl laurate

Chemical Property:

• Vapor Pressure: 1.94E-05mmHg at 25°C
• Boiling Point: 362.4°Cat760mmHg
• Flash Point: 176.4°C
• PSA: 26.30000
• Density: 0.862g/cm³
• LogP: 6.81100
• XLogP3: 8.7
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 18
• Exact Mass: 312.302830514
• Heavy Atom Count: 22
• Complexity: 226

Purity/Quality:

99.9% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCCCCC(=O)OCCCCCCCC

Technology Process of Octyl laurate

There total 5 articles about Octyl laurate 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: 98.0%

lauric acid (143-07-7) + octanol (111-87-5) → octyl laurate (5303-24-2)

Guidance literature:

With nano sulfated-TiO₂; In neat (no solvent); at 80 ℃; for 1.5h; under 760.051 Torr;

DOI:10.1016/j.crci.2012.10.016

Reference yield: 93.0%

octanol (111-87-5) + vinyl laurate (2146-71-6) → octyl laurate (5303-24-2)

Guidance literature:

With carbon dioxide; at 46.02 ℃; for 3.5h; under 66081.6 Torr; Reagent/catalyst; High pressure; Supercritical conditions; Green chemistry;

DOI:10.1016/j.procbio.2015.04.019

Reference yield:

Sodium laurate (629-25-4) → octyl laurate (5303-24-2)

Guidance literature:

Multi-step reaction with 2 steps

1: (COCl)2

With oxalyl dichloride;

DOI:10.1021/ja00437a033

upstream raw materials:

lauric acid

octanol

n-dodecanoyl chloride

Sodium laurate

Refernces

• 1、 Hosseini-Sarvari, Mona,Sodagar, Esmat. "Esterification of free fatty acids (Biodiesel) using nano sulfated-titania as catalyst in solvent-free conditions". . p. 229 - 238. Retrieved 2013/05/09.
• 2、 Tamura, Masazumi,Hakim Siddiki,Shimizu, Ken-Ichi. "CeO2 as a versatile and reusable catalyst for transesterification of esters with alcohols under solvent-free conditions". . p. 1641 - 1646. Retrieved 2013/09/24.