Methyl ricinelaidate

Base Information

• Chemical Name: Methyl ricinelaidate
• CAS No.: 7706-01-6
• Molecular Formula: C19H36O3
• Molecular Weight: 312.493
• European Community (EC) Number: 680-556-4
• Nikkaji Number: J64.164B
• Mol file: 7706-01-6.mol

Synonyms:Methyl ricinelaidate;7706-01-6;Methyl (R,E)-12-hydroxyoctadec-9-enoate;(R,Z)-Methyl 12-hydroxyoctadec-9-enoate;methyl (E,12R)-12-hydroxyoctadec-9-enoate;Ricinelaidic acid methyl ester;SCHEMBL1594097;MFCD00069621;AKOS024386336;Methyl trans-12-hydroxy-9-octadecenoate;Methyl ricinelaidate, >=99% (GC), liquid

Chemical Property of Methyl ricinelaidate

Chemical Property:

• PSA: 46.53000
• LogP: 5.16770
• Storage Temp.: −20°C
• XLogP3: 6.1
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 16
• Exact Mass: 312.26644501
• Heavy Atom Count: 22
• Complexity: 274

Purity/Quality:

99% ^*data from raw suppliers

METHYL RICINELAIDATE 95.00% ^*data from reagent suppliers

Safty Information:

• Safety Statements: 23-24/25

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCC(CC=CCCCCCCCC(=O)OC)O
• Isomeric SMILES: CCCCCC[C@H](C/C=C/CCCCCCCC(=O)OC)O

Technology Process of Methyl ricinelaidate

There total 5 articles about Methyl ricinelaidate 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: 95.0%

C58H106O9 → methyl ricinoleate (141-24-2,7706-01-6,23224-20-6,41989-07-5,67529-83-3,84799-82-6,84799-83-7,127062-53-7,127062-89-9)

Guidance literature:

In methanol;

DOI:10.1007/s10600-017-1959-6

Reference yield:

heptanal (111-71-7) + Methyl 10-undecenoate (111-81-9) → methyl ricinoleate (23224-20-6,141-24-2,7706-01-6,41989-07-5,67529-83-3,84799-82-6,84799-83-7,127062-53-7,127062-89-9)

Guidance literature:

With aluminium trichloride;

DOI:10.1002/ejoc.200500701

Reference yield:

methanol (67-56-1) → methyl ricinoleate (23224-20-6,141-24-2,7706-01-6,41989-07-5,67529-83-3,84799-82-6,84799-83-7,127062-53-7,127062-89-9)

Guidance literature:

With hydrogenchloride; ricinolic acid methyl ester;

upstream raw materials:

methanol

Ricinoleic acid

heptanal

Methyl 10-undecenoate

Downstream raw materials:

4-((R)-12-hydroxy-octadec-9t-enoyl)-morpholine

azelaic acid

heptanal

Methyl 10-undecenoate

Refernces

• 1、 Biermann, Ursula,Luetzen, Arne,Metzger, Juergen O.. "Synthesis of enantiomerically pure 2,3,4,6-tetrasubstituted tetrahydropyrans by Prins-type cyclization of methyl ricinoleate and aldehydes". . p. 2631 - 2637. Retrieved 2007/10/03.