Tris(2-methylpropyl) 2-(acetyloxy)propane-1,2,3-tricarboxylate

Base Information

Chemical Name:Tris(2-methylpropyl) 2-(acetyloxy)propane-1,2,3-tricarboxylate
CAS No.:66543-80-4
Molecular Formula:C20H34O8
Molecular Weight:402.485
Hs Code.:
European Community (EC) Number:266-399-0
UNII:9037CNN5JT
DSSTox Substance ID:DTXSID10985152
Nikkaji Number:J310.112F
Wikidata:Q27271271

Synonyms:Acetyltriisobutyl citrate;66543-80-4;Tris(2-methylpropyl) 2-(acetyloxy)propane-1,2,3-tricarboxylate;EINECS 266-399-0;UNII-9037CNN5JT;9037CNN5JT;SCHEMBL722772;ACETYL TRIISOBUTYLCITRATE;ACETYL TRIISOBUTYL CITRATE;DTXSID10985152;Acetylcitric acid triisobutyl ester;tris(2-methylpropyl) 2-acetyloxypropane-1,2,3-tricarboxylate;Q27271271;Tris-(2-methylpropyl)2-(acetyloxy)propane-1,2,3-tricarboxylate;1,2,3-TRIS(2-METHYLPROPYL) 2-(ACETYLOXY)PROPANE-1,2,3-TRICARBOXYLATE

Suppliers and Price of Tris(2-methylpropyl) 2-(acetyloxy)propane-1,2,3-tricarboxylate

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 4 raw suppliers

Chemical Property of Tris(2-methylpropyl) 2-(acetyloxy)propane-1,2,3-tricarboxylate

Chemical Property:

Vapor Pressure:7.85E-07mmHg at 25°C
Boiling Point:406.9°Cat760mmHg
Flash Point:169.6°C
PSA：105.20000
Density:1.076g/cm³
LogP:2.66610
XLogP3:3.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:16
Exact Mass:402.22536804
Heavy Atom Count:28
Complexity:510

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)COC(=O)CC(CC(=O)OCC(C)C)(C(=O)OCC(C)C)OC(=O)C

Technology Process of Tris(2-methylpropyl) 2-(acetyloxy)propane-1,2,3-tricarboxylate

There total 1 articles about Tris(2-methylpropyl) 2-(acetyloxy)propane-1,2,3-tricarboxylate 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: