Dodecanamide, N-octyl-

Base Information

• Chemical Name: Dodecanamide, N-octyl-
• CAS No.: 69943-69-7
• Molecular Formula: C20H41 N O
• Molecular Weight: 311.552
• European Community (EC) Number: 274-233-3
• UNII: 9FTC66QXD5
• DSSTox Substance ID: DTXSID9072024
• Nikkaji Number: J318.098K
• Wikidata: Q81999906
• Mol file: 69943-69-7.mol

Synonyms:Dodecanamide, N-octyl-;N-Octyldodecanamide;69943-69-7;EINECS 274-233-3;9FTC66QXD5;octyl lauramide;UNII-9FTC66QXD5;SCHEMBL6680129;DTXSID9072024;AKOS003864099

Chemical Property of Dodecanamide, N-octyl-

Chemical Property:

• Vapor Pressure: 1.01E-05mmHg at 25°C
• Boiling Point: 371.7°C at 760 mmHg
• Flash Point: 234.1°C
• PSA: 32.59000
• Density: 0.854g/cm³
• LogP: 7.22430
• XLogP3: 8.1
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 17
• Exact Mass: 311.318814931
• Heavy Atom Count: 22
• Complexity: 228

Purity/Quality:

98%Min ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCCCCC(=O)NCCCCCCCC

Technology Process of Dodecanamide, N-octyl-

There total 5 articles about Dodecanamide, N-octyl- 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: 94.0%

n-Octylamine (111-86-4) + C15H27O3S(1-)*Na(1+) (1345092-81-0) → N-octyldodecanamide (69943-69-7)

Guidance literature:

In water; at 20 ℃; for 24h;

DOI:10.1055/s-0030-1261165

Reference yield:

n-Octylamine (111-86-4) + p-Nitrophenyl laurate (1956-11-2) → 4-nitro-phenol (100-02-7,78813-13-5,89830-32-0) + N-octyldodecanamide (69943-69-7)

Guidance literature:

In various solvent(s); at 25 ℃; Kinetics;

Reference yield:

Sodium laurate (629-25-4) + n-octylamine hydrochloride (142-95-0) → N-octyldodecanamide (69943-69-7)

Guidance literature:

With octyl 2-(N-(4,6-dimethoxy-1,3,5-triazin-2-yl)-N,N-dimethylammonio)acetate trifluoromethanesulfonate; n-butylamine hydrochloride; In methanol; at 25 ℃; for 12h; pH=8; aq. phosphate buffer; Micellar solution;

DOI:10.1002/anie.201107706

upstream raw materials:

n-Octylamine

p-Nitrophenyl laurate

n-dodecanoyl chloride

C₁₅H₂₇O₃S^(1-)*Na⁽¹⁺⁾

Refernces

• 1、 Mirgorodskaya,Yatskevich,Kudryashova,Solov'Eva,Antipin,Zakharova,Konovalov. "Catalytic properties of supramolecular systems based on polyoxyethylated calixarenes and amines". scheme or table. p. 529 - 535. Retrieved 2011/10/31.
• 2、 Mirgorodskaya,Kudryavtseva,Shtykova,Bogomolova,Shtykov. "Aminolysis of carboxylic acid esters in direct, bicontinual, and inverse microemulsions based on cetyltrimethylammonium bromide". . p. 1108 - 1112. Retrieved 2007/10/03.