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Dilauryl tartrate

Base Information
  • Chemical Name:Dilauryl tartrate
  • CAS No.:66584-29-0
  • Molecular Formula:C28H54O6
  • Molecular Weight:486.733
  • Hs Code.:2918130000
  • European Community (EC) Number:266-415-6
  • UNII:TBN81RR07P
  • DSSTox Substance ID:DTXSID70216752
  • Nikkaji Number:J310.118E
  • Wikidata:Q27289884
  • Mol file:66584-29-0.mol
Dilauryl tartrate

Synonyms:Dilauryl tartrate;Didodecyl (R-(R*,R*))-tartrate;UNII-TBN81RR07P;66584-29-0;TBN81RR07P;EINECS 266-415-6;L-Tartaric acid didodecyl ester;DTXSID70216752;Q27289884;Butanedioic acid, 2,3-dihydroxy- (2R,3R)-, didodecyl ester;BUTANEDIOIC ACID, 2,3-DIHYDROXY- (2R,3R)-, 1,4-DIDODECYL ESTER

Suppliers and Price of Dilauryl tartrate
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 3 raw suppliers
Chemical Property of Dilauryl tartrate
Chemical Property:
  • Vapor Pressure:1.33E-14mmHg at 25°C 
  • Boiling Point:554.4°Cat760mmHg 
  • Flash Point:163.9°C 
  • PSA:93.06000 
  • Density:0.986g/cm3 
  • LogP:6.63640 
  • XLogP3:10.1
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:27
  • Exact Mass:486.39203944
  • Heavy Atom Count:34
  • Complexity:426
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CCCCCCCCCCCCOC(=O)C(C(C(=O)OCCCCCCCCCCCC)O)O
  • Isomeric SMILES:CCCCCCCCCCCCOC(=O)[C@@H]([C@H](C(=O)OCCCCCCCCCCCC)O)O
Technology Process of Dilauryl tartrate

There total 2 articles about Dilauryl tartrate 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 hydrogenchloride; at 120 ℃; for 36h;
DOI:10.1248/bpb.b16-00007
Guidance literature:
With dmap; dicyclohexyl-carbodiimide; In dichloromethane; at 0 - 20 ℃; for 6h;
DOI:10.1248/bpb.b16-00007
upstream raw materials:

1-dodecyl alcohol

tartaric acid

L-Tartaric acid

Downstream raw materials:

1-dodecyl alcohol

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