N-isobutyl-N-isopropylamine

Base Information

• Chemical Name: N-isobutyl-N-isopropylamine
• CAS No.: 39099-24-6
• Molecular Formula: C₇H₁₇N
• Molecular Weight: 115.219
• Hs Code.: 2921199090
• DSSTox Substance ID: DTXSID40494929
• Nikkaji Number: J741.311D
• Wikidata: Q82342689
• Mol file: 39099-24-6.mol

Synonyms:N-isobutyl-N-isopropylamine;39099-24-6;2-methyl-N-propan-2-ylpropan-1-amine;N-isopropyl-2-methyl-1-propanamine;(2-methylpropyl)(propan-2-yl)amine;N-Isopropyl-2-methylpropan-1-amine;N-(1-methylethyl)-2-methyl-1-propanamine;N-(Isopropyl-2-methyl)-1-propylamine;N-isobutylisopropylamine;Isobutyl-isopropyl-amine;2-methyl-N-(propan-2-yl)propan-1-amine;1-Propanamine, 2-methyl-N-(1-methylethyl)-;SCHEMBL91192;DTXSID40494929;PHQYHKHLCPPXKT-UHFFFAOYSA-N;MFCD00071496;AKOS000148980;LS-01491;BB 0240798;FT-0678950;EN300-55391

Chemical Property of N-isobutyl-N-isopropylamine

Chemical Property:

• Vapor Pressure: 16.6mmHg at 25°C
• Refractive Index: 1.409
• Boiling Point: 118.5°C at 760 mmHg
• Flash Point: 8.7°C
• PSA: 12.03000
• Density: 0.749g/cm³
• LogP: 2.03130
• XLogP3: 1.9
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 3
• Exact Mass: 115.136099547
• Heavy Atom Count: 8
• Complexity: 48.3

Purity/Quality:

98%Min ^*data from raw suppliers

N-Isobutyl-N-isopropylamine ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: CC(C)CNC(C)C

Technology Process of N-isobutyl-N-isopropylamine

There total 6 articles about N-isobutyl-N-isopropylamine 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: 80.0%

N-isopropylisobutyramide (869-07-8) → N-isopropyl-2-methylpropan-1-amine (39099-24-6)

Guidance literature:

N-isopropylisobutyramide; With bis(trichloromethyl) carbonate; tris(naphthalen-1-yl)phosphine oxide; at 90 ℃;

With tris(2,3,6-trifluorophenyl)borane; hydrogen; at 90 ℃; for 20h; under 60006 Torr;

DOI:10.1055/a-1681-3972

Reference yield:

isobutylamine (78-81-9) + acetone (67-64-1) → N-isopropyl-2-methylpropan-1-amine (39099-24-6)

Guidance literature:

With nickel; at 160 ℃; under 73550.8 Torr; Hydrogenation;

Reference yield:

N-(2-chloro-2-methylpropylidene)-isopropylamine (63364-30-7) → N-isopropyl-2-methylpropan-1-amine (39099-24-6)

Guidance literature:

With lithium aluminium tetrahydride; In diethyl ether;

upstream raw materials:

N-isobutylideneisopropylamine

Acetone methallylimine

isobutylamine

acetone

Refernces

• 1、 Smirnov, Yu. D.,Pavlichenko, V. F.,Tomilov, A. P.. "ELECTROCHEMICAL REDUCTIVE AMINATION. II. AMINATION OF ALIPHATIC ALDEHYDES WITH PRIMARY AMINES". . p. 374 - 380. Retrieved 2007/10/02.