Hentriacontan-16-ol

Base Information

• Chemical Name: Hentriacontan-16-ol
• CAS No.: 1070-54-8
• Molecular Formula: C31H64O
• DSSTox Substance ID: DTXSID501315855
• Wikidata: Q27116655
• Metabolomics Workbench ID: 3182
• Mol file: 1070-54-8.mol

Synonyms:hentriacontan-16-ol;16-hentriacontanol;1070-54-8;CHEBI:35985;SCHEMBL3176639;DTXSID501315855;LMFA05000091;Q27116655

Chemical Property of Hentriacontan-16-ol

Chemical Property:

• Vapor Pressure: 0mmHg at 25°C
• XLogP3: 15.1
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 28
• Exact Mass: 452.495716661
• Heavy Atom Count: 32
• Complexity: 284

Purity/Quality:

95% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCCCCCCCCC(CCCCCCCCCCCCCCC)O

Technology Process of Hentriacontan-16-ol

There total 6 articles about Hentriacontan-16-ol 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: 90.0%

palmitone (502-73-8) → 16-hentriacontanol (1070-54-8)

Guidance literature:

With 5% active carbon-supported ruthenium; hydrogen; In water; toluene; at 100 - 150 ℃; for 6h; under 15001.5 Torr; Autoclave; Inert atmosphere;

Reference yield:

1-hexadecylcarboxylic acid (57-10-3) → 16-hentriacontanol (1070-54-8)

Guidance literature:

Multi-step reaction with 2 steps

1: P₂O₅ / 200 - 210 °C

2: alcohol; sodium

With ethanol; sodium; phosphorus pentoxide;

Reference yield:

palmitone (502-73-8) → 16-hentriacontanol (1070-54-8)

Guidance literature:

at 300 ℃; unter Druck;

upstream raw materials:

n-butyl magnesium bromide

diethyl ether

palmitone

i-Amyl alcohol