Methyl hexacosanoate

Base Information

• Chemical Name: Methyl hexacosanoate
• CAS No.: 5802-82-4
• Molecular Formula: C27H54O2
• Molecular Weight: 410.725
• European Community (EC) Number: 227-355-6
• DSSTox Substance ID: DTXSID80206745
• Nikkaji Number: J141.899H
• Wikidata: Q83080603
• Mol file: 5802-82-4.mol

Synonyms:METHYL HEXACOSANOATE;5802-82-4;Hexacosanoic acid methyl ester;Hexacosanoic acid, methyl ester;Cerotic acid methyl ester;EINECS 227-355-6;MFCD00042895;SCHEMBL3504339;DTXSID80206745;CHEBI:192288;AKOS015903232;Methyl hexacosanoate, analytical standard;AS-57418;BP-29849;Hexacosanoic acid methyl ester (FAME MIX);HY-134127;CS-0138229;FT-0751804;Methyl hexacosanoate, >=99% (capillary GC);F3B7AB53-096F-457F-8FC2-5090CC791BBB;Hexacosanoic acid-methyl ester 10 microg/mL in Methyl-tert-butyl ether

Chemical Property of Methyl hexacosanoate

Chemical Property:

• Vapor Pressure: 6.35E-08mmHg at 25°C
• Melting Point: 63-66 °C
• Refractive Index: 1.452
• Boiling Point: 439.5 °C at 760 mmHg
• Flash Point: 220.9 °C
• PSA: 26.30000
• Density: 0.859 g/cm³
• LogP: 9.54170
• Storage Temp.: 2-8°C
• XLogP3: 13.3
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 25
• Exact Mass: 410.412380961
• Heavy Atom Count: 29
• Complexity: 314

Purity/Quality:

98%Min ^*data from raw suppliers

HexacosanoicAcidMethylEster ^*data from reagent suppliers

Safty Information:

• Safety Statements: 22-24/25

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Chemical Classes: Other Classes -> Esters, Other
• Canonical SMILES: CCCCCCCCCCCCCCCCCCCCCCCCCC(=O)OC
• Uses: Hexacosanoic Acid Methyl Ester is the methyl ester derivative of Hexacosanoic Acid (H290910) and is reported to be a grape constituent. Intermediate in special synthesis, medical research, reference standard for gas chromatography.

Technology Process of Methyl hexacosanoate

There total 10 articles about Methyl hexacosanoate 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:

methanol (67-56-1) + C57H104O3 → methyl hexacosanoate (5802-82-4)

Guidance literature:

With sulfuric acid; at 70 ℃; for 4h;

DOI:10.21577/0103-5053.20160308

Reference yield:

methanol (67-56-1) + 1-hexacosanoic acid (506-46-7) → methyl hexacosanoate (5802-82-4)

Guidance literature:

With hydrogenchloride;

Reference yield:

diazomethane (186581-53-3,908094-01-9,334-88-3) + 1-hexacosanoic acid (506-46-7) → methyl hexacosanoate (5802-82-4)

Guidance literature:

With diethyl ether;

upstream raw materials:

diazomethane

1-hexacosanoic acid

methanol

pentadecyl bromide

Downstream raw materials:

hexacosyl alcohol

1-hexacosanoic acid

Refernces

• 1、 De Almeida, Buana C.,Araújo, Bruno Q.,Barros, Elcio D. S.,Freitas, Samya D. L.,Maciel, Dayany S. A.,Ferreira, Ari J. S.,Guadagnin, Rafael C.,Vieira, Gerardo M.,Lago, Jo?o H. G.,Chaves, Mariana H.. "Dammarane triterpenoids from Carnauba, Copernicia prunifera (Miller) H. E. Moore (Arecaceae), wax". . p. 1371 - 1376. Retrieved 2017/07/13.
• 2、 Rao, S. Jagadishwar,Bhalerao, U. T.,Tilak, B. D.. "A New Synthesis of Long Chain Acid Esters and Carbinols". . p. 208 - 211. Retrieved 2007/10/02.