Tricosanoic acid

Base Information

• Chemical Name: Tricosanoic acid
• CAS No.: 2433-96-7
• Molecular Formula: C23H46 O2
• Molecular Weight: 354.617
• Hs Code.: 2915900090
• European Community (EC) Number: 219-419-7
• UNII: MUC9A0MS6V
• DSSTox Substance ID: DTXSID40179067
• Nikkaji Number: J97.994E
• Wikipedia: Tricosylic_acid
• Wikidata: Q4463035
• Metabolomics Workbench ID: 44
• ChEMBL ID: CHEMBL1173462
• Mol file: 2433-96-7.mol

Synonyms:tricosanoic acid;tricosanoic acid, aluminum salt;tricosanoic acid, calcium salt;tricosanoic acid, lead salt

Chemical Property of Tricosanoic acid

Chemical Property:

• Appearance/Colour: white flakes or crystalline powder
• Vapor Pressure: 4.4E-07mmHg at 25°C
• Melting Point: 77-79 °C(lit.)
• Refractive Index: 1.4610 (estimate)
• Boiling Point: 399°C at 760 mmHg
• PKA: 4.78±0.10(Predicted)
• Flash Point: 179.3°C
• PSA: 37.30000
• Density: 0.88g/cm³
• LogP: 8.28300
• Storage Temp.: 2-8°C
• Solubility.: Chloroform (Slightly), Hexanes (Slightly, Heated)
• XLogP3: 10.2
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 21
• Exact Mass: 354.349780706
• Heavy Atom Count: 25
• Complexity: 263

Purity/Quality:

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

Tricosanoic acid ^*data from reagent suppliers

Safty Information:

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36

MSDS Files:

SDS file from LookChem

Useful:

• Chemical Classes: Lipids -> Unambiguous Lipids,Biological Agents -> Fatty Acids and Fats
• Canonical SMILES: CCCCCCCCCCCCCCCCCCCCCCC(=O)O
• Uses: Tricosanoic acid is a purified product is used in medical research and as reference standard for gas chromatography. Tricosanoic Acid is a saturated fatty acid. It may be used to activate orphan G protein-coupled receptor GPR40.

Technology Process of Tricosanoic acid

There total 20 articles about Tricosanoic 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:

Reference yield:

1-Bromodocosane (6938-66-5) + carbon dioxide (124-38-9,18923-20-1) → tricosanoic acid (2433-96-7)

Guidance literature:

With samarium; samarium diiodide; In tetrahydrofuran; at 20 ℃; for 6h; under 760.051 Torr; UV-irradiation;

DOI:10.1016/j.tetlet.2010.10.028

Reference yield:

8-oxo-tricosanoic acid (95490-91-8) → tricosanoic acid (2433-96-7)

Guidance literature:

With potassium hydroxide; hydrazine hydrate; diethylene glycol; at 200 ℃;

DOI:10.1246/bcsj.32.1295

Reference yield:

10-oxo-tricosanoic acid (131288-77-2) → tricosanoic acid (2433-96-7)

Guidance literature:

With potassium hydroxide; hydrazine hydrate; diethylene glycol; at 200 ℃;

DOI:10.1246/bcsj.32.1295

upstream raw materials:

2-hydroxytetracosanoic acid

8-oxo-tricosanoic acid

5-oxo-tricosanoic acid

10-oxo-tricosanoic acid

Downstream raw materials:

tricosanoic acid methyl ester

ethyl tricosanoate

1-tricosanol

tricosylbenzene