Diethyl ethyl(hexyl)propanedioate

Base Information

Chemical Name:Diethyl ethyl(hexyl)propanedioate
CAS No.:25234-24-6
Molecular Formula:C15H28 O4
Molecular Weight:272.385
Hs Code.:
NSC Number:46891
DSSTox Substance ID:DTXSID70286657
Wikidata:Q82022429
Mol file:25234-24-6.mol

Synonyms:DIETHYL ETHYLHEXYL MALONATE;25234-24-6;24306-19-2;diethyl ethyl(hexyl)propanedioate;NSC46891;SCHEMBL5860622;diethyl 2-ethyl-2-hexylmalonate;DTXSID70286657;NSC-46891;BENZENEPROPANOICACID,A-HYDROXY-4-METHOXY-

Suppliers and Price of Diethyl ethyl(hexyl)propanedioate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 2 raw suppliers

Chemical Property of Diethyl ethyl(hexyl)propanedioate

Chemical Property:

Vapor Pressure:0.002mmHg at 25°C
Boiling Point:291°C at 760 mmHg
Flash Point:126.4°C
Density:0.961g/cm³
XLogP3:4.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:12
Exact Mass:272.19875937
Heavy Atom Count:19
Complexity:255

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCC(CC)(C(=O)OCC)C(=O)OCC

Technology Process of Diethyl ethyl(hexyl)propanedioate

There total 3 articles about Diethyl ethyl(hexyl)propanedioate 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:

: 111-27-3
hexan-1-ol

: 25234-24-6
ethyl-hexyl-malonic acid diethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: concentrated sulfuric acid; hydrobromic acid

2: sodium ethylate

With sulfuric acid; hydrogen bromide; sodium ethanolate;