N-(2-Hydroxypropyl)dodecanamide

Base Information

• Chemical Name: N-(2-Hydroxypropyl)dodecanamide
• CAS No.: 142-54-1
• Molecular Formula: C15H31NO2
• Molecular Weight: 257.417
• European Community (EC) Number: 205-541-8
• UNII: 82DUX3RRVU
• DSSTox Substance ID: DTXSID00861815
• Nikkaji Number: J115.345E
• Wikidata: Q27269328
• RXCUI: 2262541
• Mol file: 142-54-1.mol

Synonyms:N-(2-Hydroxypropyl)dodecanamide;142-54-1;Lauramide MIPA;LAURIC ISOPROPANOLAMIDE;Lauroyl isopropanolamide;Dodecanamide, N-(2-hydroxypropyl)-;Dodecanamide,N-(2-hydroxypropyl)-;UNII-82DUX3RRVU;82DUX3RRVU;EINECS 205-541-8;Monoisopropanolamine lauric acid amide;LAURAMIDE MIPA [INCI];SCHEMBL1498601;DTXSID00861815;LAURYL MONOISOPROPANOLAMIDE;CHEBI:182549;N- (2- hydroxypropyl)dodecanamide;AKOS010638772;LAURAMIDE MONOISOPROPANOLAMIDE (MIPA);EN300-15133346;W-109508;Q27269328;Z808916620

Chemical Property of N-(2-Hydroxypropyl)dodecanamide

Chemical Property:

• Appearance/Colour: Colorless and transparent liquid
• Vapor Pressure: 0mmHg at 25°C
• Melting Point: 65-66 °C
• Refractive Index: 1.46
• Boiling Point: 418.277 °C at 760 mmHg
• PKA: 14.56±0.20(Predicted)
• Flash Point: 206.767 °C
• PSA: 49.33000
• Density: 0.92 g/cm³
• LogP: 3.79520
• XLogP3: 4.4
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 12
• Exact Mass: 257.235479232
• Heavy Atom Count: 18
• Complexity: 195

Purity/Quality:

99%, ^*data from raw suppliers

CoconutOilMonoethanolamide ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCCCCC(=O)NCC(C)O

Technology Process of N-(2-Hydroxypropyl)dodecanamide

There total 5 articles about N-(2-Hydroxypropyl)dodecanamide 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:

methyl n-dodecanoate (111-82-0) → lauric acid monoisopropanolamide (142-54-1)

Guidance literature:

With sodium methylate; In (R)-(-)-2-amino-2-propanol;

Reference yield:

lauric acid (143-07-7) → lauric acid monoisopropanolamide (142-54-1)

Guidance literature:

In isopropyl alcohol;

Reference yield:

→ lauric acid monoisopropanolamide (142-54-1)

Guidance literature:

/BRN= 1772239/;

DOI:10.1021/ja01280a026

upstream raw materials:

lauric acid

methyl n-dodecanoate

Refernces