Myristyl laurate

Base Information

• Chemical Name: Myristyl laurate
• CAS No.: 22412-97-1
• Molecular Formula: C26H52O2
• Molecular Weight: 396.698
• Hs Code.: 2915900090
• European Community (EC) Number: 244-966-3
• UNII: 58U0NZN2BT
• DSSTox Substance ID: DTXSID5066792
• Nikkaji Number: J111.014D
• Wikidata: Q27261618
• RXCUI: 1425923
• Metabolomics Workbench ID: 3678
• Mol file: 22412-97-1.mol

Synonyms:Myristyl laurate;Tetradecyl dodecanoate;22412-97-1;Tetradecyl laurate;Myristyl dodecanoate;Dodecanoic acid, tetradecyl ester;Lauric acid, tetradecyl ester;Dodecanoic acid,tetradecyl ester;Lauric acid myristyl ester;tetradecanyl dodecanoate;UNII-58U0NZN2BT;58U0NZN2BT;EINECS 244-966-3;WE(14:0/12:0);n-tetradecanyl laurate;SCHEMBL443460;Myristyl dodecanoate, >=99%;MYRISTYL LAURATE [INCI];DTXSID5066792;LMFA07010033;AKOS024386305;HY-W127416;LAURIC ACID TETRADECAN-1-YL ESTER;CS-0185650;FT-0638226;J-014695;Q27261618

Chemical Property of Myristyl laurate

Chemical Property:

• Vapor Pressure: 6.79E-08mmHg at 25°C
• Refractive Index: 1.451
• Boiling Point: 438.7 °C at 760 mmHg
• Flash Point: 225.6 °C
• PSA: 26.30000
• Density: 0.86 g/cm³
• LogP: 9.15160
• Storage Temp.: −20°C
• Water Solubility.: 0.35ng/L at 25℃
• 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

MYRISTYL DODECANOATE 95.00% ^*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: CCCCCCCCCCCCCCOC(=O)CCCCCCCCCCC

Technology Process of Myristyl laurate

There total 4 articles about Myristyl 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: 100.0%

lauric acid (143-07-7) + 1-Tetradecanol (112-72-1) → dodecanoic acid tetradecyl ester (22412-97-1)

Guidance literature:

With dodecylbenzene-sulphonic acid; In water; at 40 ℃; for 48h;

DOI:10.1021/ja026241j

Reference yield: 87.0%

tridodecanoylglycerol (538-24-9) + 1-Tetradecanol (112-72-1) → dodecanoic acid tetradecyl ester (22412-97-1)

Guidance literature:

With dodecylbenzene-sulphonic acid; In water; at 40 ℃; for 168h;

DOI:10.1021/ja026241j

Reference yield:

scrap tire → dodecanoic acid tetradecyl ester (22412-97-1) + chrysene (218-01-9) + 9-Phenylfluorene (789-24-2) + 1-methyltriphenylene (2871-91-2)

Guidance literature:

With air; at 650 - 850 ℃; Further byproducts given. Title compound not separated from byproducts; Formation of xenobiotics;

DOI:10.1021/es990883y

upstream raw materials:

lauric acid

1-Tetradecanol

tridodecanoylglycerol