Elaidic Anhydride

Base Information

• Chemical Name: Elaidic Anhydride
• CAS No.: 55726-25-5
• Molecular Formula: C36H66O3
• Molecular Weight: 546.918
• Hs Code.: 2916190090
• European Community (EC) Number: 679-946-7
• DSSTox Substance ID: DTXSID701282105
• Nikkaji Number: J421.792F,J534.084E
• Mol file: 55726-25-5.mol

Synonyms:Elaidic Anhydride;octadec-9-enoic anhydride;55726-25-5;6085-36-5;9-Octadecenoic acid anhydride;[(E)-octadec-9-enoyl] (E)-octadec-9-enoate;(E)-octadec-9-enoic anhydride;9-Octadecenoic acid, anhydride;C36H66O3;9-Octadecenoic acid, 1,1'-anhydride;C36-H66-O3;Bis(9-octadecenoic)anhydride;SCHEMBL43556;trans-9-Octadecenoic Anhydride;SCHEMBL10421718;DTXSID701282105;MFCD00070026;AKOS015950698;9-Octadecenoic acid, anhydride, (E,E)-;AS-58515;CS-0453580;E0418;T72616;A914018;J-015721;(9E)-OCTADEC-9-ENOYL (9E)-OCTADEC-9-ENOATE;6-bromo-4-hydroxyquinoline-3-carboxylicacidethylester

Chemical Property of Elaidic Anhydride

Chemical Property:

• Vapor Pressure: 8.57E-15mmHg at 25°C
• Melting Point: 46 °C
• Refractive Index: 1.471
• Boiling Point: 609.4°C at 760 mmHg
• Flash Point: 275.4°C
• PSA: 43.37000
• Density: 0.895g/cm³
• LogP: 12.13120
• XLogP3: 14.9
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 32
• Exact Mass: 546.50119596
• Heavy Atom Count: 39
• Complexity: 528

Purity/Quality:

97% ^*data from raw suppliers

Elaidic Anhydride ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCC=CCCCCCCCC(=O)OC(=O)CCCCCCCC=CCCCCCCCC
• Isomeric SMILES: CCCCCCCC/C=C/CCCCCCCC(=O)OC(=O)CCCCCCC/C=C/CCCCCCCC

Technology Process of Elaidic Anhydride

There total 5 articles about Elaidic Anhydride 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:

trimethylphosphane selenide (20819-54-9) + [Me3POC(O)C17H33][OTf] + cadmium(II) oleate (10468-30-1) → Trimethylphosphine oxide (676-96-0) + oleic anhydride (6085-36-5,55726-25-5,24909-72-6)

Guidance literature:

trimethylphosphane selenide; cadmium(II) oleate; In chloroform-d1; Inert atmosphere;

[Me₃POC(O)C₁₇H₃₃][OTf]; In chloroform-d1; Inert atmosphere;

DOI:10.1021/ja209246z

Reference yield:

cis-Octadecenoic acid (112-80-1,2027-47-6) → oleic anhydride (6085-36-5,55726-25-5,24909-72-6)

Guidance literature:

With 1,1'-carbonyldiimidazole; In chloroform; for 5h; Ambient temperature;

DOI:10.1021/jm950802i

Reference yield:

cis-Octadecenoic acid (112-80-1,2027-47-6) + isobutyl chloroformate (543-27-1) → oleic anhydride (6085-36-5,55726-25-5,24909-72-6)

Guidance literature:

With triethylamine; toluene; Erhitzen des Reaktionsgemisches mit Triaethylamin-oleat;

DOI:10.1021/ja01554a035

upstream raw materials:

cis-Octadecenoic acid

(Z)-9-octadecenoyl chloride

acetic anhydride

isobutyl chloroformate

Downstream raw materials:

dioleoylphosphatidylcholine

cinnamyl 6-deoxy-6-oleamido-1-thio-α-D-mannopyranoside

2-octadec-9'-enoylcyclohexane-1,3-dione

2-oleolylcyclohexane-1,3-dione