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Hexacosanedioic acid

Base Information
  • Chemical Name:Hexacosanedioic acid
  • CAS No.:3365-67-1
  • Molecular Formula:C26H50O4
  • Molecular Weight:426.681
  • Hs Code.:2917190090
  • DSSTox Substance ID:DTXSID70429507
  • Nikkaji Number:J536.096J
  • Wikidata:Q27145891
  • Metabolomics Workbench ID:1963
  • Mol file:3365-67-1.mol
Hexacosanedioic acid

Synonyms:Hexacosanedioic acid;3365-67-1;HEXACOSANEDIOICACID;LMFA01170040;SCHEMBL542366;1,24-Tetracosanedicarboxylicacid;CHEBI:76334;DTXSID70429507;BS-47304;E75841;Q27145891

Suppliers and Price of Hexacosanedioic acid
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
  • American Custom Chemicals Corporation
  • HEXACOSANEDIOIC ACID 95.00%
  • 5MG
  • $ 501.71
  • Ambeed
  • Hexacosanedioicacid 98%
  • 250mg
  • $ 744.00
  • Ambeed
  • Hexacosanedioicacid 98%
  • 25g
  • $ 296.00
Total 15 raw suppliers
Chemical Property of Hexacosanedioic acid
Chemical Property:
  • Melting Point:123.5 °C 
  • Boiling Point:571.3±23.0 °C(Predicted) 
  • PKA:4.48±0.10(Predicted) 
  • PSA:74.60000 
  • Density:0.954±0.06 g/cm3(Predicted) 
  • LogP:8.51800 
  • XLogP3:10.8
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:25
  • Exact Mass:426.37091007
  • Heavy Atom Count:30
  • Complexity:345
Purity/Quality:

98%Min *data from raw suppliers

HEXACOSANEDIOIC ACID 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C(CCCCCCCCCCCCC(=O)O)CCCCCCCCCCCC(=O)O
Technology Process of Hexacosanedioic acid

There total 7 articles about Hexacosanedioic 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:
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
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 2 steps
1: sodium hydroxide / ethanol / 1 h / Heating
2: 1.) hydrazine hydrate; 2.) potassium hydroxide / 1.) triethanolamine, 130 deg C; reflux, 4 h; 2.) triethanolamine, 200 deg C, 9 h
With potassium hydroxide; sodium hydroxide; hydrazine hydrate; In ethanol;
DOI:10.1021/ja00209a032
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