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Tetracosanedioic acid

Base Information Edit
  • Chemical Name:Tetracosanedioic acid
  • CAS No.:2450-31-9
  • Molecular Formula:C24H46O4
  • Molecular Weight:398.627
  • Hs Code.:2917190090
  • DSSTox Substance ID:DTXSID90369158
  • Nikkaji Number:J937.073K
  • Wikidata:Q82156192
  • Metabolomics Workbench ID:1962
  • Mol file:2450-31-9.mol
Tetracosanedioic acid

Synonyms:Tetracosanedioic acid;2450-31-9;Tetracosanedioicacid;LMFA01170039;SCHEMBL321180;DTXSID90369158;CHEBI:165388;QXGVRGZJILVMDF-UHFFFAOYSA-N;BS-51975;CS-0528825;E83822

Suppliers and Price of Tetracosanedioic acid
Supply Marketing:Edit
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 11 raw suppliers
Chemical Property of Tetracosanedioic acid Edit
Chemical Property:
  • Melting Point:126.9-127.1 °C 
  • Boiling Point:549.4 °C at 760 mmHg 
  • PKA:4.48±0.10(Predicted) 
  • Flash Point:300.1 °C 
  • PSA:74.60000 
  • Density:0.962 g/cm3 
  • LogP:7.73780 
  • XLogP3:9.7
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:23
  • Exact Mass:398.33960994
  • Heavy Atom Count:28
  • Complexity:321
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C(CCCCCCCCCCCC(=O)O)CCCCCCCCCCC(=O)O
Technology Process of Tetracosanedioic acid

There total 14 articles about Tetracosanedioic acid 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:
Guidance literature:
With 5%-palladium/activated carbon; In methanol; at 50 ℃; Inert atmosphere;
DOI:10.1002/chem.201504882
Guidance literature:
Multi-step reaction with 3 steps
1: 1.) triethylamine; 2.) 20percent HCl / 1.) chloroform, 35 deg C, 5 h; 2.) chloroform, reflux, 5 h
2: sodium hydroxide / ethanol / 1 h / Heating
3: 1.) hydrazine hydrate; 2.) potassium hydroxide / 1.) triethanolamine, 130 deg C; reflux, 4 h; 2.) triethanolamine, 200 deg C, 9 h
With hydrogenchloride; potassium hydroxide; sodium hydroxide; hydrazine hydrate; triethylamine; In ethanol;
DOI:10.1021/ja00209a032
Guidance literature:
Multi-step reaction with 4 steps
1: thionyl chloride / 1 h / 50 °C
2: 1.) triethylamine; 2.) 20percent HCl / 1.) chloroform, 35 deg C, 5 h; 2.) chloroform, reflux, 5 h
3: sodium hydroxide / ethanol / 1 h / Heating
4: 1.) hydrazine hydrate; 2.) potassium hydroxide / 1.) triethanolamine, 130 deg C; reflux, 4 h; 2.) triethanolamine, 200 deg C, 9 h
With hydrogenchloride; potassium hydroxide; sodium hydroxide; thionyl chloride; hydrazine hydrate; triethylamine; In ethanol;
DOI:10.1021/ja00209a032
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