Lauryl myristate

Base Information

• Chemical Name: Lauryl myristate
• CAS No.: 2040-64-4
• Molecular Formula: C26H52 O2
• Molecular Weight: 396.698
• Hs Code.: 2915900090
• European Community (EC) Number: 218-039-9
• UNII: W5V732TTKE
• DSSTox Substance ID: DTXSID1062120
• Nikkaji Number: J298.660D
• Wikidata: Q27292361
• Metabolomics Workbench ID: 3677
• Mol file: 2040-64-4.mol

Synonyms:Lauryl myristate;dodecyl tetradecanoate;2040-64-4;Tetradecanoic acid, dodecyl ester;Dodecyl myristate;dodecanyl tetradecanoate;UNII-W5V732TTKE;W5V732TTKE;EINECS 218-039-9;AI3-31616;WE(12:0/14:0);Dodecyl myristate #;Myristic acid dodecyl ester;lauryl myristate, AldrichCPR;SCHEMBL457143;LAURYL MYRISTATE [INCI];DTXSID1062120;LMFA07010032;Q27292361

Chemical Property of Lauryl myristate

Chemical Property:

• Vapor Pressure: 6.79E-08mmHg at 25°C
• Boiling Point: 438.7°Cat760mmHg
• Flash Point: 225.6°C
• PSA: 26.30000
• Density: 0.86g/cm³
• LogP: 9.15160
• XLogP3: 11.9
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 24
• Exact Mass: 396.396730897
• Heavy Atom Count: 28
• Complexity: 301

Purity/Quality:

99.9% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCCCCCCC(=O)OCCCCCCCCCCCC

Technology Process of Lauryl myristate

There total 2 articles about Lauryl myristate 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: 76.0%

1-dodecyl alcohol (112-53-8) + n-tetradecanoic acid (544-63-8) → tetradecanoic acid, dodecyl ester (2040-64-4)

Guidance literature:

With triphenylphosphine-sulfur trioxide adduct; In neat (no solvent); at 110 ℃; for 2h; Green chemistry;

DOI:10.1080/10426507.2020.1845681

Reference yield:

1-Iodododecane (4292-19-7) → tetradecanoic acid, dodecyl ester (2040-64-4)

Guidance literature:

DOI:10.1039/tf9555101667

upstream raw materials:

1-Iodododecane

1-dodecyl alcohol

n-tetradecanoic acid

Refernces