Ethyl tetradecanoate

Base Information

• Chemical Name: Ethyl tetradecanoate
• CAS No.: 124-06-1
• Molecular Formula: C16H32O2
• Molecular Weight: 256.429
• Hs Code.: 2915900090
• European Community (EC) Number: 204-675-4
• NSC Number: 8917
• UNII: 6995S49749
• DSSTox Substance ID: DTXSID6047654
• Nikkaji Number: J10.056K
• Wikidata: Q27158117
• Metabolomics Workbench ID: 4113
• ChEMBL ID: CHEMBL207555
• Mol file: 124-06-1.mol

Synonyms:ethyl myristate

Chemical Property of Ethyl tetradecanoate

Chemical Property:

• Appearance/Colour: Clear colorless liquid, solidifying in the cold
• Vapor Pressure: 0.00157mmHg at 25°C
• Melting Point: 11-12 °C(lit.)
• Refractive Index: n20/D 1.436(lit.)
• Boiling Point: 295 °C at 760 mmHg
• Flash Point: 135 °C
• PSA: 26.30000
• Density: 0.865 g/cm³
• LogP: 5.25060
• XLogP3: 6.7
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 14
• Exact Mass: 256.240230259
• Heavy Atom Count: 18
• Complexity: 178

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: CCCCCCCCCCCCCC(=O)OCC

Technology Process of Ethyl tetradecanoate

There total 9 articles about Ethyl tetradecanoate 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: 99.6%

→ Ethyl myristate (124-06-1)

Guidance literature:

With toluene-4-sulfonic acid; at 125 ℃; for 3h; under 2052.14 Torr; Sealed tube;

Reference yield: 98.43%

ethanol (64-17-5) + n-tetradecanoic acid (544-63-8) → Ethyl myristate (124-06-1)

Guidance literature:

With sulfuric acid; for 4.5h; Sonication;

DOI:10.3390/molecules23123141

Reference yield: 75.0%

Ethyl 4-bromobutyrate (2969-81-5) + n-decyl magnesium bromide (17049-50-2) → Ethyl myristate (124-06-1)

Guidance literature:

With N,N,N,N,-tetramethylethylenediamine; cobalt(II) chloride; lithium iodide; In tetrahydrofuran; at 10 ℃; for 1h;

DOI:10.1002/adsc.200800166

upstream raw materials:

ethanol

n-tetradecanoic acid

tetradecanoyl chloride

2,2-diethoxypropane

Downstream raw materials:

1-Tetradecanol

tetradecanamide

myristic monoethanolamide

N,N'-ethanediyl-bis-myristamide

Refernces

• 1、 Zhang, Xiaofeng,Jiang, Runze,Cheng, Xu. "Electrochemical Tandem Olefination and Hydrogenation Reaction with Ammonia". . p. 16016 - 16025. Retrieved 2021/08/24.
• 2、 -. "NATURAL BIOSURFACTANT OF ESTER AND MANUFACTURING METHOD THEREOF". Paragraph 0125; 0126; 0129-0132. . Retrieved 2020/12/11.