3-Butoxypropanamine

Base Information

• Chemical Name: 3-Butoxypropanamine
• CAS No.: 16499-88-0
• Deprecated CAS: 155634-28-9
• Molecular Formula: C7H17NO
• Molecular Weight: 131.218
• Hs Code.: 29221990
• European Community (EC) Number: 240-566-8
• DSSTox Substance ID: DTXSID6066070
• Nikkaji Number: J116.186E
• Wikidata: Q72513986
• Mol file: 16499-88-0.mol

Synonyms:Propylamine,3-butoxy- (6CI,7CI,8CI);3-(Butyloxy)propylamine;3-(n-Butoxy)propylamine;3-Aminopropyl butyl ether;3-Butoxy-1-propanamine;

Chemical Property of 3-Butoxypropanamine

Chemical Property:

• Appearance/Colour: clear colorless liquid
• Vapor Pressure: 1.52mmHg at 25°C
• Melting Point: -65 °C
• Refractive Index: n20/D 1.426(lit.)
• Boiling Point: 169.7 °C at 760 mmHg
• PKA: 9.77±0.10(Predicted)
• Flash Point: 63.3 °C
• PSA: 35.25000
• Density: 0.851 g/cm³
• LogP: 1.85220
• Storage Temp.: 2-8°C
• Water Solubility.: miscible
• XLogP3: 0.7
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 6
• Exact Mass: 131.131014166
• Heavy Atom Count: 9
• Complexity: 48.2

Purity/Quality:

99% ^*data from raw suppliers

3-Butoxypropan-1-amine ^*data from reagent suppliers

Safty Information:

• Pictogram(s): C
• Hazard Codes: C
• Statements: 34
• Safety Statements: 26-27-36/37/39-45

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: CCCCOCCCN
• Uses: 3-Butoxypropylamine may be used in the synthesis of N-functionalized bis(phosphino)amine ligands with ether, thioether and pyridyl tethers.

Technology Process of 3-Butoxypropanamine

There total 11 articles about 3-Butoxypropanamine 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:

tetrahydrofuran (109-99-9,24979-97-3,77392-70-2) + 3-butoxypropanenitrile (6959-71-3) → 3-butoxypropylamine (16499-88-0) + butan-1-ol (71-36-3)

Guidance literature:

at 30 - 35 ℃; Ausbeute bei unterschiedlichem Mengenverhaeltnis der Reaktionspartner;

DOI:10.1021/ja01604a045 DOI:10.1021/ja01642a067

Reference yield:

diethyl ether (60-29-7,927820-24-4) + 3-butoxypropanenitrile (6959-71-3) → 3-butoxypropylamine (16499-88-0) + butan-1-ol (71-36-3)

Guidance literature:

at 35 ℃; Ausbeute bei unterschiedlichem Mengenverhaeltnis der Reaktionspartner;

DOI:10.1021/ja01604a045 DOI:10.1021/ja01642a067

Reference yield:

acrylonitrile (107-13-1,25014-41-9) + butan-1-ol (71-36-3) → propylamine (107-10-8,42939-71-9) + 3-butoxypropylamine (16499-88-0)

Guidance literature:

upstream raw materials:

3-butoxypropanenitrile

acrylonitrile

butan-1-ol

3-Chloropropionitrile

Downstream raw materials:

N-(3-butoxy-propyl)-N'-(toluene-4-sulfonyl)-urea

3-mercaptopropionic acid

C₁₆H₂₉NO₃

N-[N-[(2S,3S)-3-trans-ethoxycarbonyloxirane-2-carbonyl]-L-phenylalanyl]-1-amino-3-butoxypropane

Refernces