DECYL OLEATE

Base Information

• Chemical Name: DECYL OLEATE
• CAS No.: 3687-46-5
• Molecular Formula: C28H54O2
• Molecular Weight: 422.736
• Hs Code.: 2916150000
• European Community (EC) Number: 222-981-6
• UNII: ZGR06DO97T
• DSSTox Substance ID: DTXSID1029259
• Nikkaji Number: J205.598H
• Wikidata: Q297361
• RXCUI: 1307038
• Mol file: 3687-46-5.mol

Synonyms:Oleic acid, decyl ester (7CI,8CI);Ceraphyl 140;Decyl oleate;Estol DCO 3662;Oleic acid n-decyl ester;Standamul CTV;Tegosoft DO;

Chemical Property of DECYL OLEATE

Chemical Property:

• Vapor Pressure: 6.22E-10mmHg at 25°C
• Melting Point: 2.8 °C
• Refractive Index: 1.459
• Boiling Point: 494.847 °C at 760 mmHg
• Flash Point: 77.106 °C
• PSA: 26.30000
• Density: 0.867 g/cm³
• LogP: 9.70780
• Storage Temp.: Sealed in dry,Room Temperature
• Solubility.: Practically insoluble in water, miscible with ethanol (96 per cent), with methylene chloride and with light petroleum (bp: 40-60 °C).
• XLogP3: 12.1
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 25
• Exact Mass: 422.412380961
• Heavy Atom Count: 30
• Complexity: 362

Purity/Quality:

98% ^*data from raw suppliers

DecylOleate ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCCCOC(=O)CCCCCCCC=CCCCCCCCC
• Isomeric SMILES: CCCCCCCCCCOC(=O)CCCCCCC/C=C\CCCCCCCC
• Uses: Decyl Oleate is an emollient used in cosmetics and moisturizing industries. Excipient.

Technology Process of DECYL OLEATE

There total 3 articles about DECYL OLEATE 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: 95.4%

cis-Octadecenoic acid (112-80-1,2027-47-6) + 1-Decanol (112-30-1) → oleic acid decyl ester (3687-46-5)

Guidance literature:

With 1,1,3,3-tetramethylguanidinium hydrogen sulphate; at 150 ℃; for 6h;

DOI:10.1039/c6ra19771j

Reference yield:

Methyl oleate (112-62-9) + 1-Decanol (112-30-1) → oleic acid decyl ester (3687-46-5)

Guidance literature:

With sodium n-decyloxide; at 25 ℃; for 1.5h;

DOI:10.1007/s11746-007-1159-9

Reference yield:

→ etofenamate (30544-47-9) + oleic acid decyl ester (3687-46-5)

Guidance literature:

upstream raw materials:

cis-Octadecenoic acid

1-Decanol

Methyl oleate

Downstream raw materials:

amfenac

Refernces

• 1、 Porwal, Jyoti,Kumar, Subodh,Kaul, Savita,Jain, Suman L.. "Guanidine based task specific ionic liquids for the synthesis of biolubricant range esters under solvent-free condition". . p. 93640 - 93644. Retrieved 2016/10/18.
• 2、 Yao, Linxing,Hammond, Earl,Wang, Tong. "Melting points and viscosities of fatty acid esters that are potential targets for engineered oilseed". . p. 77 - 82. Retrieved 2008/09/19.