5-(Diisopropylamino)amylamine

Base Information

• Chemical Name: 5-(Diisopropylamino)amylamine
• CAS No.: 209803-40-7
• Molecular Formula: C₁₁H₂₆N₂
• Molecular Weight: 186.341
• Hs Code.: 2921290000
• DSSTox Substance ID: DTXSID90396449
• Wikidata: Q82197171
• Mol file: 209803-40-7.mol

Synonyms:5-(DIISOPROPYLAMINO)AMYLAMINE;209803-40-7;N1,N1-Diisopropylpentane-1,5-diamine;N,N-Diisopropyl-1,5-pentanediamine;N',N'-di(propan-2-yl)pentane-1,5-diamine;1,5-Pentanediamine, N1,N1-bis(1-methylethyl)-;MFCD00048285;5-Diisopropylaminoamylamine;5-(Diisopropylamino)pentylamine;SCHEMBL2762075;DTXSID90396449;N1,N1-Dsopropylpentane-1,5-damne;BBL101001;STL554795;AKOS005256166;AS-77124;5-(Diisopropylamino)amylamine, AldrichCPR;N,N-di(propan-2-yl)pentane-1,5-diamine;CS-0324017;FT-0643951;J-523381

Chemical Property of 5-(Diisopropylamino)amylamine

Chemical Property:

• Vapor Pressure: 0.073mmHg at 25°C
• Refractive Index: 1.455
• Boiling Point: 228.5°C at 760 mmHg
• Flash Point: 90.3°C
• PSA: 29.26000
• Density: 0.84g/cm³
• LogP: 2.93450
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• XLogP3: 2
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 7
• Exact Mass: 186.209598838
• Heavy Atom Count: 13
• Complexity: 103

Purity/Quality:

99% ^*data from raw suppliers

5-(Diisopropylamino)amylamine ^*data from reagent suppliers

Safty Information:

• Hazard Codes: C
• Statements: 34-36
• Safety Statements: 26-36/37/39

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C)N(CCCCCN)C(C)C

Technology Process of 5-(Diisopropylamino)amylamine

There total 3 articles about 5-(Diisopropylamino)amylamine 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: 28.0%

C19H28N2O2 → N,N-diisopropylpentane-1,5-diamine (209803-40-7)

Guidance literature:

With hydrazine hydrate; In ethanol; water; for 12h; Reflux;

DOI:10.1016/j.ejmech.2018.08.060

Reference yield:

N-(5-bromopentyl)phthalimide (954-81-4) → N,N-diisopropylpentane-1,5-diamine (209803-40-7)

Guidance literature:

Multi-step reaction with 2 steps

1: potassium carbonate / acetonitrile / 24 h / Reflux

2: hydrazine hydrate / ethanol; water / 12 h / Reflux

With hydrazine hydrate; potassium carbonate; In ethanol; water; acetonitrile; 2: |Gabriel Amine Synthesis;

DOI:10.1016/j.ejmech.2018.08.060

Reference yield:

diisopropylamine (108-18-9) → N,N-diisopropylpentane-1,5-diamine (209803-40-7)

Guidance literature:

Multi-step reaction with 2 steps

1: potassium carbonate / acetonitrile / 24 h / Reflux

2: hydrazine hydrate / ethanol; water / 12 h / Reflux

With hydrazine hydrate; potassium carbonate; In ethanol; water; acetonitrile; 2: |Gabriel Amine Synthesis;

DOI:10.1016/j.ejmech.2018.08.060

upstream raw materials:

N-(5-bromopentyl)phthalimide

diisopropylamine

Refernces