Dipropyl sebacate

Base Information

• Chemical Name: Dipropyl sebacate
• CAS No.: 15419-91-7
• Molecular Formula: C16H30O4
• Molecular Weight: 286.412
• Hs Code.: 2917131000
• European Community (EC) Number: 239-430-0
• DSSTox Substance ID: DTXSID10165553
• Nikkaji Number: J190.871E
• Wikidata: Q83034784
• Mol file: 15419-91-7.mol

Synonyms:Dipropyl sebacate;dipropyl decanedioate;15419-91-7;decanedioic acid dipropyl ester;EINECS 239-430-0;Decanedioic acid,1,10-dipropyl ester;Sebacic acid dipropyl ester;SCHEMBL410773;Decanedioic acid, dipropyl ester;DTXSID10165553

Chemical Property of Dipropyl sebacate

Chemical Property:

• Vapor Pressure: 0.000213mmHg at 25°C
• Refractive Index: 1.444
• Boiling Point: 326.6 °C at 760 mmHg
• Flash Point: 146.4 °C
• PSA: 52.60000
• Density: 0.955 g/cm³
• LogP: 4.01360
• XLogP3: 4.5
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 15
• Exact Mass: 286.21440943
• Heavy Atom Count: 20
• Complexity: 225

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCOC(=O)CCCCCCCCC(=O)OCCC

Technology Process of Dipropyl sebacate

There total 2 articles about Dipropyl sebacate 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: 69.0%

propan-1-ol (71-23-8) + 1,10-decanedioic acid (111-20-6,26776-29-4) → bis(propyl) sebacate (15419-91-7)

Guidance literature:

With 6H₂O*Na₃[AlMo₆O₁₈(OH)6]; at 140 ℃; Green chemistry;

DOI:10.1007/s11164-021-04570-z

Reference yield:

→ bis(propyl) sebacate (15419-91-7)

Guidance literature:

Cyclodecen, O3/n-Propylalkohol;

upstream raw materials:

propan-1-ol

1,10-decanedioic acid

Refernces

• 1、 Britton, Joshua,Dalziel, Stuart B.,Raston, Colin L.. "The synthesis of di-carboxylate esters using continuous flow vortex fluidics". . p. 2193 - 2200. Retrieved 2016/04/19.