2-Butyloctan-1-amine

Base Information

• Chemical Name: 2-Butyloctan-1-amine
• CAS No.: 217655-07-7
• Molecular Formula: C₁₂H₂₇N
• Molecular Weight: 185.353
• European Community (EC) Number: 833-578-5
• Mol file: 217655-07-7.mol

Synonyms:2-butyloctan-1-amine;2-Butyl-n-octan-1-amine;217655-07-7;2-butyloctylamine;5-(Aminomethyl)undecane;2-butyloctyl amine;2-Butyl-1-n-octylamine;1-Amino-2-butyl-n-octane;SCHEMBL1164854;OOCWTIOGJOIPGS-UHFFFAOYSA-N;MFCD20721903;B5550;T70575;A905869

Chemical Property of 2-Butyloctan-1-amine

Chemical Property:

• Refractive Index: 1.4400 to 1.4440
• Boiling Point: 248.1±8.0 °C(Predicted)
• PKA: 10.87±0.10(Predicted)
• Density: 0.803±0.06 g/cm3(Predicted)
• XLogP3: 4.6
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 9
• Exact Mass: 185.214349865
• Heavy Atom Count: 13
• Complexity: 91.1

Purity/Quality:

98.5% ^*data from raw suppliers

2-Butyl-n-octan-1-amine >98.0%(T) ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: CCCCCCC(CCCC)CN

Technology Process of 2-Butyloctan-1-amine

There total 3 articles about 2-Butyloctan-1-amine 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:

2-(n-butyl)octanol (3913-02-8) → 2-butyloctan-1-amine (217655-07-7)

Guidance literature:

Multi-step reaction with 3 steps

1: triphenylphosphine; bromine / dichloromethane / 0 - 20 °C / Inert atmosphere

2: N,N-dimethyl-formamide / 10 h / 90 °C

3: hydrazine hydrate / methanol / Reflux

With bromine; hydrazine hydrate; triphenylphosphine; In methanol; dichloromethane; N,N-dimethyl-formamide;

DOI:10.1039/c8nj06496b

Reference yield:

5-(bromomethyl)undecane (85531-02-8) → 2-butyloctan-1-amine (217655-07-7)

Guidance literature:

Multi-step reaction with 2 steps

1: N,N-dimethyl-formamide / 10 h / 90 °C

2: hydrazine hydrate / methanol / Reflux

With hydrazine hydrate; In methanol; N,N-dimethyl-formamide;

DOI:10.1039/c8nj06496b

Reference yield:

2-(2-butyloctyl)isoindole-1,3-dione → 2-butyloctan-1-amine (217655-07-7)

Guidance literature:

With hydrazine hydrate; In methanol; Reflux;

DOI:10.1039/c8nj06496b

upstream raw materials:

2-(n-butyl)octanol

5-(bromomethyl)undecane

Refernces