Myristyl palmitate

Base Information

• Chemical Name: Myristyl palmitate
• CAS No.: 4536-26-9
• Molecular Formula: C30H60 O2
• Molecular Weight: 452.805
• Hs Code.: 2915709000
• European Community (EC) Number: 224-884-4
• UNII: 05918JMY6W
• DSSTox Substance ID: DTXSID6063511
• Nikkaji Number: J111.010A
• Wikidata: Q27157444
• Metabolomics Workbench ID: 3647
• Mol file: 4536-26-9.mol

Synonyms:Myristyl palmitate;4536-26-9;Tetradecyl hexadecanoate;Tetradecyl palmitate;Hexadecanoic acid, tetradecyl ester;PALMITIC ACID MYRISTYL ESTER;Palmitic acid, tetradecyl ester;tetradecanyl hexadecanoate;UNII-05918JMY6W;05918JMY6W;EINECS 224-884-4;WE(14:0/16:0);SCHEMBL146506;DTXSID6063511;CHEBI:84064;LMFA07010002;AKOS030254795;FT-0635350;Q27157444

Chemical Property of Myristyl palmitate

Chemical Property:

• Vapor Pressure: 1.47E-09mmHg at 25°C
• Boiling Point: 484.9°Cat760mmHg
• Flash Point: 255.5°C
• PSA: 26.30000
• Density: 0.858g/cm³
• LogP: 10.71200
• Storage Temp.: Refrigerator
• Solubility.: Chloroform (Slightly), Hexane (Slightly)
• XLogP3: 14.1
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 28
• Exact Mass: 452.45933115
• Heavy Atom Count: 32
• Complexity: 353

Purity/Quality:

98%min ^*data from raw suppliers

Myristyl Palmitate ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCCCCCCCCC(=O)OCCCCCCCCCCCCCC
• Uses: Myristyl Palmitate is a wax ester of palmitic acid. Wax esters are esters between long chained fatty alcohols and fatty acids. Wax esters have significance in pharmaceutical and cosmetics applications and occur naturally in plants and animals.

Technology Process of Myristyl palmitate

There total 3 articles about Myristyl palmitate 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: 99.0%

1-Tetradecanol (112-72-1) + 1-hexadecylcarboxylic acid (57-10-3) → myristyl palmitate (4536-26-9)

Guidance literature:

iron(III) chloride; In 1,3,5-trimethyl-benzene; at 162 ℃; for 24h;

DOI:10.1246/cl.2005.1502

Reference yield:

1-Tetradecanol (112-72-1) + n-hexadecanoyl chloride (112-67-4) → myristyl palmitate (4536-26-9)

Guidance literature:

With quinoline; chloroform;

DOI:10.1016/0006-3002(56)90382-1

Reference yield:

→ myristyl palmitate (4536-26-9)

Guidance literature:

Hexadecansaeure, Tetradecylalkohol;

upstream raw materials:

1-Tetradecanol

n-hexadecanoyl chloride

1-hexadecylcarboxylic acid

Downstream raw materials:

1-tetradecene

Refernces

• 1、 Sunitha, Sadula,Kanjilal, Sanjit,Reddy, P. Srinivasa,Prasad, Rachapudi B.N.. "Liquid-liquid biphasic synthesis of long chain wax esters using the Lewis acidic ionic liquid choline chloride·2ZnCl2". . p. 6962 - 6965. Retrieved 2008/02/13.
• 2、 Mantri, Kshudiram,Nakamura, Ryo,Komura, Kenichi,Sugi, Yoshihiro. "Esterification of long chain aliphatic acids with long chain alcohols catalyzed by multi-valent metal salts". . p. 1502 - 1503. Retrieved 2007/10/03.