1-Butanamine, 2-methyl-N,N-bis(2-methylbutyl)-

Base Information

• Chemical Name: 1-Butanamine, 2-methyl-N,N-bis(2-methylbutyl)-
• CAS No.: 620-43-9
• Deprecated CAS: 69230-72-4
• Molecular Formula: C₁₅H₃₃N
• Molecular Weight: 227.434
• Hs Code.: 2921199090
• DSSTox Substance ID: DTXSID30883505
• Nikkaji Number: J136.487A
• Mol file: 620-43-9.mol

Synonyms:620-43-9;1-Butanamine, 2-methyl-N,N-bis(2-methylbutyl)-;N,N-bis(2-methylbutyl)-2-methyl-1-butanamine;tris(2-methylbutyl)amine;SCHEMBL2399243;DTXSID30883505;JZFBJRHPXVDQIM-UHFFFAOYSA-N

Chemical Property of 1-Butanamine, 2-methyl-N,N-bis(2-methylbutyl)-

Chemical Property:

• Vapor Pressure: 0.056mmHg at 25°C
• Melting Point: -61.15°C (estimate)
• Refractive Index: 1.4330
• Boiling Point: 233.499°C at 760 mmHg
• Flash Point: 84.441°C
• PSA: 3.24000
• Density: 0.799g/cm³
• LogP: 4.42670
• XLogP3: 5.3
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 9
• Exact Mass: 227.261300057
• Heavy Atom Count: 16
• Complexity: 127

Purity/Quality:

98%min ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCC(C)CN(CC(C)CC)CC(C)CC

Technology Process of 1-Butanamine, 2-methyl-N,N-bis(2-methylbutyl)-

There total 2 articles about 1-Butanamine, 2-methyl-N,N-bis(2-methylbutyl)- 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:

(2S)-2-methyl-1-butanol (1565-80-6) → tri-pentyl-amine (620-43-9)

Guidance literature:

Multi-step reaction with 2 steps

1: Ueberfuehrung in Amylbromid und Erhitzen desselben mit alkoh.Ammoniak auf 100grad

2: Edukt 2 aus linksdrehendem Amylalkohol

Reference yield:

bis(2-methylbutyl)amine (27094-65-1,627-81-6) + 1-Bromopentane (110-53-2) → tri-pentyl-amine (620-43-9)

Guidance literature:

tri-d-pentyl-amine; Edukt 2 aus linksdrehendem Amylalkohol;

Reference yield:

tri-pentyl-amine (620-43-9) + benzyl-methallyl sulfone (502186-60-9) → 1-benzensulfonyl 2-methyl-1-propene (104900-83-6)

Guidance literature:

upstream raw materials:

bis(2-methylbutyl)amine

1-Bromopentane

(2S)-2-methyl-1-butanol

Downstream raw materials:

benzyl 2-propenyl sulfone

1-benzensulfonyl 2-methyl-1-propene