Methyl palmitelaidate

Base Information

• Chemical Name: Methyl palmitelaidate
• CAS No.: 10030-74-7
• Molecular Formula: C17H32O2
• Molecular Weight: 268.44
• Hs Code.: 2916190090
• DSSTox Substance ID: DTXSID101314798
• Nikkaji Number: J47.590D,J600I
• Wikidata: Q63408980
• Mol file: 10030-74-7.mol

Synonyms:Methyl palmitelaidate;10030-74-7;methyl (E)-hexadec-9-enoate;Palmitelaidic acid methyl ester;methyl hexadec-9-enoate;9-Hexadecenoic acid, methyl ester, (9E)-;(E)-9-Hexadecenoic acid methyl ester;Palmitelaidic acid-methyl ester;PALMITELAIDICACIDMETHYLESTER;methyl 9-hexadecenoate;3913-63-1;methyl (9E)-hexadec-9-enoate;9-Hexadecenoic acid, methyl ester, (E)-;9-Hexadecenoic acid methyl;Methyl trans-9-palmitoleate;(E)-methyl hexadec-9-enoate;SCHEMBL161458;9-Hexadecenoic acid methyl ester;CHEBI:167857;DTXSID101314798;AKOS015892989;(E)-9-Hexadecenoic acid, methyl ester;9-Hexadecenoic acid, (E), methyl ester;HY-115362;CS-0035130;J-000093;Q63408980

Chemical Property of Methyl palmitelaidate

Chemical Property:

• Vapor Pressure: 2.01E-06mmHg at 25°C
• Boiling Point: 394.2°Cat760mmHg
• Flash Point: 92.5°C
• PSA: 26.30000
• Density: 0.876g/cm³
• LogP: 5.41670
• Storage Temp.: −20°C
• XLogP3: 6.5
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 14
• Exact Mass: 268.240230259
• Heavy Atom Count: 19
• Complexity: 221

Purity/Quality:

98%,99%, ^*data from raw suppliers

PalmitelaidicAcidMethylEster ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCC=CCCCCCCCC(=O)OC
• Isomeric SMILES: CCCCCC/C=C/CCCCCCCC(=O)OC
• Uses: Palmitelaidic Acid Methyl Ester is a derivative of Palmitoleic Acid (P144900), common constituent of triglycerides of human adipose tissue.

Technology Process of Methyl palmitelaidate

There total 6 articles about Methyl palmitelaidate 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) + soybean oil (8001-22-7) → methyl trans-2-octadecenoate (14663-11-7) + 5,8,11-Eicosatrienoic acid, methyl ester + heneicosapentaenoic acid methyl ester + eicosadienoic acid methyl ester (88400-02-6) + docosapentaenoic acid methyl ester + docosatetraenoic acid methyl ester + docosadienoic acid methyl ester + palmitelaidic acid methyl ester (10030-74-7,3913-63-1) + Methyl oleate (112-62-9) + Methyl linoleate (112-63-0) + methyl cis-13-docosenoate (1120-34-9) + methyl cis-tetracos-15-enate (2733-88-2) + methyl myristoate (124-10-7) + hexadecanoic acid methyl ester (112-39-0) + methyl margarate (1731-92-6) + Methyl stearate (112-61-8) + methyl arachidate (1120-28-1) + behenic acid methyl ester (929-77-1) + methyl tetracosanoate (2442-49-1) + methyl (2E)-eicosenoate (10305-59-6) + methyl (9Z,12Z,15E)-octadeca-9,12,15-trienoate (37929-05-8) + glycerol (56-81-5,25618-55-7,64333-26-2,8013-25-0)

Guidance literature:

With potassium hydroxide; at 48 - 52 ℃; for 4h;

Reference yield:

methanol (67-56-1) + canola oil → methyl trans-2-octadecenoate (14663-11-7) + 5,8,11-Eicosatrienoic acid, methyl ester + heneicosapentaenoic acid methyl ester + eicosadienoic acid methyl ester (88400-02-6) + docosapentaenoic acid methyl ester + docosatetraenoic acid methyl ester + docosadienoic acid methyl ester + palmitelaidic acid methyl ester (10030-74-7,3913-63-1) + Methyl oleate (112-62-9) + Methyl linoleate (112-63-0) + methyl cis-13-docosenoate (1120-34-9) + methyl cis-tetracos-15-enate (2733-88-2) + methyl myristoate (124-10-7) + hexadecanoic acid methyl ester (112-39-0) + methyl margarate (1731-92-6) + Methyl stearate (112-61-8) + methyl arachidate (1120-28-1) + behenic acid methyl ester (929-77-1) + methyl tetracosanoate (2442-49-1) + methyl (2E)-eicosenoate (10305-59-6) + methyl (9Z,12Z,15E)-octadeca-9,12,15-trienoate (37929-05-8) + glycerol (56-81-5,25618-55-7,64333-26-2,8013-25-0)

Guidance literature:

With potassium hydroxide; at 48 - 52 ℃; for 4h;

Reference yield:

methanol (67-56-1) + mustard oil → methyl trans-2-octadecenoate (14663-11-7) + 5,8,11-Eicosatrienoic acid, methyl ester + heneicosapentaenoic acid methyl ester + eicosadienoic acid methyl ester (88400-02-6) + docosapentaenoic acid methyl ester + docosatetraenoic acid methyl ester + docosadienoic acid methyl ester + palmitelaidic acid methyl ester (10030-74-7,3913-63-1) + Methyl oleate (112-62-9) + Methyl linoleate (112-63-0) + methyl cis-13-docosenoate (1120-34-9) + methyl cis-tetracos-15-enate (2733-88-2) + methyl myristoate (124-10-7) + hexadecanoic acid methyl ester (112-39-0) + methyl margarate (1731-92-6) + Methyl stearate (112-61-8) + methyl arachidate (1120-28-1) + behenic acid methyl ester (929-77-1) + methyl tetracosanoate (2442-49-1) + methyl (2E)-eicosenoate (10305-59-6) + methyl (9Z,12Z,15E)-octadeca-9,12,15-trienoate (37929-05-8) + glycerol (56-81-5,25618-55-7,64333-26-2,8013-25-0)

Guidance literature:

With potassium hydroxide; at 48 - 52 ℃; for 4.5h;

upstream raw materials:

(Z)-9-hexadecenoic acid methyl ester

methanol

soybean oil

Downstream raw materials:

(Z)-9-hexadecenoic acid methyl ester

azelaic acid

oenanthic acid

Refernces

• 1、 Tamba, Maurizio,Dajka, Katalin,Ferreri, Carla,Asmus, Klaus-Dieter,Chatgilialoglu, Chryssostomos. "One-electron reduction of methanesulfonyl chloride. The fate of MeSO 2CI?- and MeSO2? intermediates in oxygenated solutions and their role in the cis-trans isomerization of mono-unsaturated fatty acids". . p. 8716 - 8723. Retrieved 2008/02/13.
• 2、 Chatgilialoglu, Chryssostomos,Altieri, Alessio,Fischer, Hanns. "The kinetics of thiyl radical-induced reactions of monounsaturated fatty acid esters". . p. 12816 - 12823. Retrieved 2007/10/03.