Ethyl tetracosanoate

Base Information

• Chemical Name: Ethyl tetracosanoate
• CAS No.: 24634-95-5
• Molecular Formula: C26H52 O2
• Molecular Weight: 396.698
• Hs Code.: 2915900090
• NSC Number: 159289
• DSSTox Substance ID: DTXSID80179384
• Nikkaji Number: J208.665D
• Wikidata: Q83049917
• Mol file: 24634-95-5.mol

Synonyms:Ethyl tetracosanoate;Ethyl Lignocerate;24634-95-5;Lignoceric Acid Ethyl Ester;Ethyl tetracosanate;LIGNOCERICACIDETHYLESTER;Tetracosanoic Acid Ethyl-d5 Ester;Tetracosanoic Acid Ethyl Ester;SCHEMBL3505350;Tetracosanoic acid, ethyl ester;DTXSID80179384;AKXFYSSXNQQBNT-UHFFFAOYSA-N;ZAA63495;MFCD00048673;NSC159289;AKOS015839850;HY-W127425;NSC 159289;NSC-159289;AS-60569;CS-0185659;FT-0735739;L0111;T72151;J-015608

Chemical Property of Ethyl tetracosanoate

Chemical Property:

• Vapor Pressure: 9.16E-07mmHg at 25°C
• Melting Point: 56oC
• Boiling Point: 404.9°Cat760mmHg
• Flash Point: 187.8°C
• PSA: 26.30000
• Density: 0.86g/cm³
• LogP: 9.15160
• Solubility.: almost transparency in Toluene
• XLogP3: 12.1
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 24
• Exact Mass: 396.396730897
• Heavy Atom Count: 28
• Complexity: 301

Purity/Quality:

98%,99%, ^*data from raw suppliers

TetracosanoicAcidEthyl-d5Ester ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCCCCCCCCCCCCCCCCC(=O)OCC
• Uses: Tetracosanoic Acid Ethyl Ester is the ethyl analogue of Tetracosanoic Acid (T291455), a chemical component of a dried mushroom powder exhibiting antioxidant properties. It is a long chain fatty acid present in peanut oil.

Technology Process of Ethyl tetracosanoate

There total 1 articles about Ethyl tetracosanoate 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:

→ ethyl tetracosanoate (24634-95-5)

Guidance literature:

aus CH3(CH2)21CH(COOCH2CH3)2 durch Decarboxylierung mit nassem DMSO/NaCl durch Erhitzen;

Reference yield:

ethyl tetracosanoate (24634-95-5) → tetracosyl alcohol (506-51-4)

Guidance literature:

With sodium; Petroleum ether; butan-1-ol;

Reference yield:

ethyl tetracosanoate (24634-95-5) → ethene (74-85-1) + carbon dioxide (124-38-9,18923-20-1)

Guidance literature:

Destillation; entsteht auch ein Keton und ein Kohlenwasserstoff;

Downstream raw materials:

tetracosyl alcohol

ethene

carbon dioxide