Adelmidrol

Base Information

• Chemical Name: Adelmidrol
• CAS No.: 1675-66-7
• Molecular Formula: C₁₃H₂₆N₂O₄
• Molecular Weight: 274.36
• NSC Number: 27132
• UNII: 1BUC3685QU
• DSSTox Substance ID: DTXSID10168302
• Nikkaji Number: J615.832C
• Wikipedia: Adelmidrol
• Wikidata: Q15633949
• NCI Thesaurus Code: C74098
• ChEMBL ID: CHEMBL2105967
• Mol file: 1675-66-7.mol

Synonyms:adelmidrol;N,N'-bis(2-hydroxyethyl)nonanediamide

Chemical Property of Adelmidrol

Chemical Property:

• Vapor Pressure: 1.04E-16mmHg at 25°C
• Melting Point: 132-134℃
• Boiling Point: 596.4°Cat760mmHg
• PKA: 14.19±0.10(Predicted)
• Flash Point: 314.5°C
• PSA: 98.66000
• Density: 1.097g/cm³
• LogP: 0.71590
• Storage Temp.: 2-8°C
• XLogP3: -0.3
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 12
• Exact Mass: 274.18925731
• Heavy Atom Count: 19
• Complexity: 223

Purity/Quality:

Adelmidrol ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C(CCCC(=O)NCCO)CCCC(=O)NCCO

Technology Process of Adelmidrol

There total 3 articles about Adelmidrol 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: 78.0%

azelaic acid (123-99-9,26776-28-3) + ethanolamine (141-43-5) → Adelmidrol (1675-66-7)

Guidance literature:

Reference yield: 78.0%

ethanolamine (141-43-5) + acrylic acid (79-10-7) → Adelmidrol (1675-66-7)

Guidance literature:

Reference yield:

→ Adelmidrol (1675-66-7)

Guidance literature:

/BRN= 1791966/;

DOI:10.1021/ja01181a534

upstream raw materials:

ethanolamine

acrylic acid

azelaic acid

Refernces

• 1、 -. "Use of N-acyl derivatives of aminoalcohols in the manufacture of a medicament for practicing neuroprotective action in neuropathological states connected with excitotoxicity". . . Retrieved 2008/06/13.
• 2、 -. "Use of N-acyl derivatives of aminoalcohols with polycarboxylic acids for the manufacture of a medicament for the treatment of pathologies relating to mast cells". . . Retrieved 2008/06/13.